| Name |
|---|
EMWX Geneepisodic muscle weakness, X-linked |
RCHY1 Genering finger and CHY zinc finger domain containing 1, E3 ubiquitin protein ligase The protein encoded by this gene has ubiquitin ligase activity. It mediates E3-dependent ubiquitination and proteasomal degradation of target proteins, including tumor protein 53, histone deacetylase 1, and cyclin-dependent kinase inhibitor 1B, thus regulating their levels and cell cycle progression. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2013] |
LINC01221 Genelong intergenic non-protein coding RNA 1221 |
LINC01227 Genelong intergenic non-protein coding RNA 1227 |
LINC01091 Genelong intergenic non-protein coding RNA 1091 |
LINC01090 Genelong intergenic non-protein coding RNA 1090 |
LINC01093 Genelong intergenic non-protein coding RNA 1093 |
LINC01095 Genelong intergenic non-protein coding RNA 1095 |
LINC01094 Genelong intergenic non-protein coding RNA 1094 |
LINC01097 Genelong intergenic non-protein coding RNA 1097 |
LINC01096 Genelong intergenic non-protein coding RNA 1096 |
LINC01098 Genelong intergenic non-protein coding RNA 1098 |
LINC00320 Genelong intergenic non-protein coding RNA 320 |
LINC00323 Genelong intergenic non-protein coding RNA 323 |
LINC00324 Genelong intergenic non-protein coding RNA 324 |
LINC00326 Genelong intergenic non-protein coding RNA 326 |
LINC00327 Genelong intergenic non-protein coding RNA 327 |
LINC00328 Genelong intergenic non-protein coding RNA 328 |
LINC01215 Genelong intergenic non-protein coding RNA 1215 |
LINC01214 Genelong intergenic non-protein coding RNA 1214 |
LINC00847 Genelong intergenic non-protein coding RNA 847 |
LINC00849 Genelong intergenic non-protein coding RNA 849 |
LINC01251 Genelong intergenic non-protein coding RNA 1251 |
LINC01250 Genelong intergenic non-protein coding RNA 1250 |
LINC01257 Genelong intergenic non-protein coding RNA 1257 |
CCDC26 GeneCCDC26 long non-coding RNA Implicated in brain cancer and high grade glioma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01255 Genelong intergenic non-protein coding RNA 1255 |
LINC01491 Genelong intergenic non-protein coding RNA 1491 |
LINC01490 Genelong intergenic non-protein coding RNA 1490 |
LINC01198 Genelong intergenic non-protein coding RNA 1198 Biomarker of malignant astrocytoma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01194 Genelong intergenic non-protein coding RNA 1194 |
LINC01195 Genelong intergenic non-protein coding RNA 1195 |
LINC01197 Genelong intergenic non-protein coding RNA 1197 |
LINC01191 Genelong intergenic non-protein coding RNA 1191 |
LINC01192 Genelong intergenic non-protein coding RNA 1192 |
LINC01193 Genelong intergenic non-protein coding RNA 1193 |
LINC01360 Genelong intergenic non-protein coding RNA 1360 |
HEIH Genehepatocellular carcinoma up-regulated EZH2-associated long non-coding RNA Biomarker of esophagus squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01365 Genelong intergenic non-protein coding RNA 1365 |
LINC01547 Genelong intergenic non-protein coding RNA 1547 Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01546 Genelong intergenic non-protein coding RNA 1546 |
LINC01545 Genelong intergenic non-protein coding RNA 1545 |
LINC01549 Genelong intergenic non-protein coding RNA 1549 |
LINC01548 Genelong intergenic non-protein coding RNA 1548 |
LINC00633 Genelong intergenic non-protein coding RNA 633 |
LINC00630 Genelong intergenic non-protein coding RNA 630 |
LINC00636 Genelong intergenic non-protein coding RNA 636 |
LINC00637 Genelong intergenic non-protein coding RNA 637 |
LINC00635 Genelong intergenic non-protein coding RNA 635 |
LINC00638 Genelong intergenic non-protein coding RNA 638 |
LINC00639 Genelong intergenic non-protein coding RNA 639 |
LINC01348 Genelong intergenic non-protein coding RNA 1348 |
LINC01550 Genelong intergenic non-protein coding RNA 1550 |
LINC01551 Genelong intergenic non-protein coding RNA 1551 |
LINC01552 Genelong intergenic non-protein coding RNA 1552 |
LINC00879 Genelong intergenic non-protein coding RNA 879 |
LINC00877 Genelong intergenic non-protein coding RNA 877 |
LINC00870 Genelong intergenic non-protein coding RNA 870 |
LINC00871 Genelong intergenic non-protein coding RNA 871 |
LINC00265-3P Genelong intergenic non-protein coding RNA 265-3, pseudogene |
LINC00969 Genelong intergenic non-protein coding RNA 969 |
LINC00404 Genelong intergenic non-protein coding RNA 404 |
LINC00400 Genelong intergenic non-protein coding RNA 400 |
LINC00403 Genelong intergenic non-protein coding RNA 403 |
LINC00402 Genelong intergenic non-protein coding RNA 402 |
LINC00408 Genelong intergenic non-protein coding RNA 408 |
LINC01510 Genelong intergenic non-protein coding RNA 1510 This gene encodes a natural antisense transcript highly expressed in papillary thyroid carcinomas harboring BRAF V600E mutation or RET gene rearrangements. This lncRNA induces the downstream MAPK pathway and is part of a co-expression network including different oncogenes belonging to the MAPK and PI3H/AKT pathways. In thyroid carcinomas, this gene has oncogenic properties associated with increased proliferation and drug resistance. [provided by RefSeq, Jan 2020] |
LINC01114 Genelong intergenic non-protein coding RNA 1114 |
LINC01115 Genelong intergenic non-protein coding RNA 1115 |
LINC01116 Genelong intergenic non-protein coding RNA 1116 |
LINC01117 Genelong intergenic non-protein coding RNA 1117 |
LINC01111 Genelong intergenic non-protein coding RNA 1111 |
LINC01118 Genelong intergenic non-protein coding RNA 1118 |
LINC01514 Genelong intergenic non-protein coding RNA 1514 |
LINC00244 Genelong intergenic non-protein coding RNA 244 |
LINC00243 Genelong intergenic non-protein coding RNA 243 |
LINC00242 Genelong intergenic non-protein coding RNA 242 |
LINC00240 Genelong intergenic non-protein coding RNA 240 |
LINC00939 Genelong intergenic non-protein coding RNA 939 |
LINC00938 Genelong intergenic non-protein coding RNA 938 |
LINC00930 Genelong intergenic non-protein coding RNA 930 |
LINC00933 Genelong intergenic non-protein coding RNA 933 |
LINC00935 Genelong intergenic non-protein coding RNA 935 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and sperm flagellum. Predicted to be active in axonemal A tubule inner sheath. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00934 Genelong intergenic non-protein coding RNA 934 |
LINC00937 Genelong intergenic non-protein coding RNA 937 |
LINC00443 Genelong intergenic non-protein coding RNA 443 |
LINC01099 Genelong intergenic non-protein coding RNA 1099 |
LINC00322 Genelong intergenic non-protein coding RNA 322 |
LINC01327 Genelong intergenic non-protein coding RNA 1327 |
LINC01324 Genelong intergenic non-protein coding RNA 1324 |
LINC01322 Genelong intergenic non-protein coding RNA 1322 |
LINC01320 Genelong intergenic non-protein coding RNA 1320 |
LINC00433 Genelong intergenic non-protein coding RNA 433 |
LINC01424 Genelong intergenic non-protein coding RNA 1424 |
LINC01425 Genelong intergenic non-protein coding RNA 1425 |
LINC01426 Genelong intergenic non-protein coding RNA 1426 |
LINC01427 Genelong intergenic non-protein coding RNA 1427 |
LINC01420 Genelong intergenic non-protein coding RNA 1420 Involved in negative regulation of cytoplasmic mRNA processing body assembly and nuclear-transcribed mRNA catabolic process. Located in P-body. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01422 Genelong intergenic non-protein coding RNA 1422 |
LINC01423 Genelong intergenic non-protein coding RNA 1423 |
LINC01428 Genelong intergenic non-protein coding RNA 1428 |
LINC01280 Genelong intergenic non-protein coding RNA 1280 |
LINC01281 Genelong intergenic non-protein coding RNA 1281 |
LINC01282 Genelong intergenic non-protein coding RNA 1282 |
LINC01284 Genelong intergenic non-protein coding RNA 1284 |
LINC01285 Genelong intergenic non-protein coding RNA 1285 |
LINC01287 Genelong intergenic non-protein coding RNA 1287 |
LINC01288 Genelong intergenic non-protein coding RNA 1288 |
LINC01289 Genelong intergenic non-protein coding RNA 1289 |
LINC00488 Genelong intergenic non-protein coding RNA 488 |
LINC00484 Genelong intergenic non-protein coding RNA 484 |
LINC00487 Genelong intergenic non-protein coding RNA 487 |
LINC00486 Genelong intergenic non-protein coding RNA 486 |
LINC00483 Genelong intergenic non-protein coding RNA 483 |
LINC00482 Genelong intergenic non-protein coding RNA 482 |
SHFLD3 GeneSplit-hand/foot malformation with long bone deficiency 3 |
SPTLC1P1 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 1 |
SPTLC1P2 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 2 |
SPTLC1P5 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 5 |
SPTLC1P4 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 4 |
LINC00266-4P Genelong intergenic non-protein coding RNA 266-4, pseudogene |
LLPH GeneLLP homolog, long-term synaptic facilitation (Aplysia) Enables RNA binding activity. Predicted to be involved in dendrite extension and positive regulation of dendritic spine development. Located in chromosome and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01363 Genelong intergenic non-protein coding RNA 1363 |
LINC00526 Genelong intergenic non-protein coding RNA 526 |
LINC00527 Genelong intergenic non-protein coding RNA 527 |
LINC00524 Genelong intergenic non-protein coding RNA 524 |
LINC00525 Genelong intergenic non-protein coding RNA 525 |
LINC00523 Genelong intergenic non-protein coding RNA 523 |
LINC00520 Genelong intergenic non-protein coding RNA 520 |
LINC00521 Genelong intergenic non-protein coding RNA 521 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00528 Genelong intergenic non-protein coding RNA 528 |
LINC00529 Genelong intergenic non-protein coding RNA 529 |
LINC01499 Genelong intergenic non-protein coding RNA 1499 |
OLMALINC Geneoligodendrocyte maturation-associated long intergenic non-coding RNA |
LINC00200 Genelong intergenic non-protein coding RNA 200 |
LINC00207 Genelong intergenic non-protein coding RNA 207 |
LINC00052 Genelong intergenic non-protein coding RNA 52 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00165 Genelong intergenic non-protein coding RNA 165 |
LINC01252 Genelong intergenic non-protein coding RNA 1252 |
LINC01256 Genelong intergenic non-protein coding RNA 1256 |
LINC01254 Genelong intergenic non-protein coding RNA 1254 |
LINC01258 Genelong intergenic non-protein coding RNA 1258 |
LINC01590 Genelong intergenic non-protein coding RNA 1590 |
LINC01591 Genelong intergenic non-protein coding RNA 1591 |
LINC01592 Genelong intergenic non-protein coding RNA 1592 |
LINC01594 Genelong intergenic non-protein coding RNA 1594 |
LINC01599 Genelong intergenic non-protein coding RNA 1599 |
LINC01046 Genelong intergenic non-protein coding RNA 1046 |
LINC01047 Genelong intergenic non-protein coding RNA 1047 |
LINC01044 Genelong intergenic non-protein coding RNA 1044 |
LINC01043 Genelong intergenic non-protein coding RNA 1043 |
LINC01040 Genelong intergenic non-protein coding RNA 1040 |
LINC01049 Genelong intergenic non-protein coding RNA 1049 |
LINC00311 Genelong intergenic non-protein coding RNA 311 |
LINC00310 Genelong intergenic non-protein coding RNA 310 |
LINC00313 Genelong intergenic non-protein coding RNA 313 |
LINC00312 Genelong intergenic non-protein coding RNA 312 This gene produces an intronless transcript that is thought to function as a tumor suppressor. This transcript is downregulated in nasopharyngeal carcinoma and is a negative regulator of estrogen receptor signaling. A common polymorphism in this transcript allows the production of a 94 aa open reading frame in some individuals, which may interact directly with estrogen receptor 1 (PMID:15474036). This open reading frame does not exist on the reference genome haplotype, which is hypothesized to function through a non-coding RNA product. [provided by RefSeq, Mar 2017] |
LINC00315 Genelong intergenic non-protein coding RNA 315 |
LINC00314 Genelong intergenic non-protein coding RNA 314 |
LINC00316 Genelong intergenic non-protein coding RNA 316 |
LINCMD1 Genelong intergenic non-protein coding RNA, muscle differentiation 1 |
LINC-ROR Genelong intergenic non-protein coding RNA, regulator of reprogramming This gene produces a long non-coding RNA that regulates the reprogramming of pluripotent stem cells. This RNA suppresses induction of tumor protein p53 after DNA damage. It is thought to act as a sponge for microRNAs that regulate stem cell factors POU class 5 homeobox 1, Nanog, and SRY-box 2. This RNA may also have a extracellular role in modulating response to hypoxia in hepatocellular cancer cells. Expression of this transcript is associated with tumor progression and epithelial to mesenchymal transition and metastasis. [provided by RefSeq, Dec 2017] |
LINC00571 Genelong intergenic non-protein coding RNA 571 |
LINC01209 Genelong intergenic non-protein coding RNA 1209 |
LINC01201 Genelong intergenic non-protein coding RNA 1201 |
LINC01202 Genelong intergenic non-protein coding RNA 1202 |
LINC01203 Genelong intergenic non-protein coding RNA 1203 |
LINC01204 Genelong intergenic non-protein coding RNA 1204 |
LINC01205 Genelong intergenic non-protein coding RNA 1205 |
LINC01206 Genelong intergenic non-protein coding RNA 1206 |
LINC01207 Genelong intergenic non-protein coding RNA 1207 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01452 Genelong intergenic non-protein coding RNA 1452 |
LINC01166 Genelong intergenic non-protein coding RNA 1166 |
LINC00415 Genelong intergenic non-protein coding RNA 415 |
LINC00411 Genelong intergenic non-protein coding RNA 411 |
LINC01088 Genelong intergenic non-protein coding RNA 1088 |
LINC01518 Genelong intergenic non-protein coding RNA 1518 |
LINC01519 Genelong intergenic non-protein coding RNA 1519 |
LINC01516 Genelong intergenic non-protein coding RNA 1516 |
LINC00391 Genelong intergenic non-protein coding RNA 391 |
LINC00393 Genelong intergenic non-protein coding RNA 393 |
LINC00392 Genelong intergenic non-protein coding RNA 392 |
LINC00395 Genelong intergenic non-protein coding RNA 395 |
LINC00396 Genelong intergenic non-protein coding RNA 396 |
LINC00399 Genelong intergenic non-protein coding RNA 399 |
LINC00398 Genelong intergenic non-protein coding RNA 398 |
LINC00152 Genelong intergenic non-protein coding RNA 152 This gene produces a long non-coding RNA that is overexpressed in cancer cells and promotes cell proliferation and epithelial-mesenchymal transition. This RNA may bind enhancer of zeste homolog 2 and participate in the transcriptional silencing of tumor suppressor genes. It may act as a sponge for microRNAs. Alternatively spliced variants have been observed. [provided by RefSeq, Dec 2017] |
LINC00159 Genelong intergenic non-protein coding RNA 159 |
LINC00158 Genelong intergenic non-protein coding RNA 158 |
LINC00845 Genelong intergenic non-protein coding RNA 845 |
LINC00844 Genelong intergenic non-protein coding RNA 844 |
LINC00841 Genelong intergenic non-protein coding RNA 841 |
LINC00840 Genelong intergenic non-protein coding RNA 840 |
LINC00843 Genelong intergenic non-protein coding RNA 843 |
LINC00842 Genelong intergenic non-protein coding RNA 842 |
LINC01495 Genelong intergenic non-protein coding RNA 1495 |
LINC01494 Genelong intergenic non-protein coding RNA 1494 |
LINC01497 Genelong intergenic non-protein coding RNA 1497 |
LINC01496 Genelong intergenic non-protein coding RNA 1496 |
LINC01493 Genelong intergenic non-protein coding RNA 1493 |
LINC01492 Genelong intergenic non-protein coding RNA 1492 |
LINC01498 Genelong intergenic non-protein coding RNA 1498 |
LINC00458 Genelong intergenic non-protein coding RNA 458 |
LINC00459 Genelong intergenic non-protein coding RNA 459 |
LINC00452 Genelong intergenic non-protein coding RNA 452 |
LINC00456 Genelong intergenic non-protein coding RNA 456 |
LINC00457 Genelong intergenic non-protein coding RNA 457 |
LINC00454 Genelong intergenic non-protein coding RNA 454 |
LINC00954 Genelong intergenic non-protein coding RNA 954 |
LINC01128 Genelong intergenic non-protein coding RNA 1128 |
LINC01125 Genelong intergenic non-protein coding RNA 1125 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01124 Genelong intergenic non-protein coding RNA 1124 |
LINC01126 Genelong intergenic non-protein coding RNA 1126 |
LINC01121 Genelong intergenic non-protein coding RNA 1121 |
LINC01120 Genelong intergenic non-protein coding RNA 1120 |
LINC01123 Genelong intergenic non-protein coding RNA 1123 |
LINC01122 Genelong intergenic non-protein coding RNA 1122 |
LINC00298 Genelong intergenic non-protein coding RNA 298 |
LINC00299 Genelong intergenic non-protein coding RNA 299 |
LINC00294 Genelong intergenic non-protein coding RNA 294 |
LINC00297 Genelong intergenic non-protein coding RNA 297 |
LINC00293 Genelong intergenic non-protein coding RNA 293 |
LINC00364 Genelong intergenic non-protein coding RNA 364 |
LINC01402 Genelong intergenic non-protein coding RNA 1402 |
LINC01024 Genelong intergenic non-protein coding RNA 1024 |
LINC00643 Genelong intergenic non-protein coding RNA 643 |
LINC00642 Genelong intergenic non-protein coding RNA 642 |
LINC00641 Genelong intergenic non-protein coding RNA 641 |
LINC00640 Genelong intergenic non-protein coding RNA 640 |
LINC00645 Genelong intergenic non-protein coding RNA 645 |
LINC00644 Genelong intergenic non-protein coding RNA 644 |
LINC00649 Genelong intergenic non-protein coding RNA 649 |
LINC00648 Genelong intergenic non-protein coding RNA 648 |
LINC00251 Genelong intergenic non-protein coding RNA 251 |
LINC00929 Genelong intergenic non-protein coding RNA 929 |
LINC00603 Genelong intergenic non-protein coding RNA 603 |
LINC01419 Genelong intergenic non-protein coding RNA 1419 |
LINC01415 Genelong intergenic non-protein coding RNA 1415 |
LINC01416 Genelong intergenic non-protein coding RNA 1416 |
LINC01411 Genelong intergenic non-protein coding RNA 1411 |
LINC01413 Genelong intergenic non-protein coding RNA 1413 |
LINC01412 Genelong intergenic non-protein coding RNA 1412 |
LINC00504 Genelong intergenic non-protein coding RNA 504 |
LINC00505 Genelong intergenic non-protein coding RNA 505 |
LINC00506 Genelong intergenic non-protein coding RNA 506 |
LINC00507 Genelong intergenic non-protein coding RNA 507 |
LINC00501 Genelong intergenic non-protein coding RNA 501 |
LINC00216 Genelong intergenic non-protein coding RNA 216 |
LINC00210 Genelong intergenic non-protein coding RNA 210 |
LINC00211 Genelong intergenic non-protein coding RNA 211 |
LINC00967 Genelong intergenic non-protein coding RNA 967 |
LINC00964 Genelong intergenic non-protein coding RNA 964 |
LINC00965 Genelong intergenic non-protein coding RNA 965 |
LINC00963 Genelong intergenic non-protein coding RNA 963 |
LINC00960 Genelong intergenic non-protein coding RNA 960 |
LINC00961 Genelong intergenic non-protein coding RNA 961 Involved in cellular response to amino acid stimulus and negative regulation of TORC1 signaling. Located in late endosome membrane and lysosomal proton-transporting V-type ATPase complex. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01608 Genelong intergenic non-protein coding RNA 1608 |
LINC01609 Genelong intergenic non-protein coding RNA 1609 |
LINC01604 Genelong intergenic non-protein coding RNA 1604 |
LINC01605 Genelong intergenic non-protein coding RNA 1605 |
LINC01606 Genelong intergenic non-protein coding RNA 1606 |
LINC01607 Genelong intergenic non-protein coding RNA 1607 |
LINC01600 Genelong intergenic non-protein coding RNA 1600 |
LINC01601 Genelong intergenic non-protein coding RNA 1601 |
LINC01602 Genelong intergenic non-protein coding RNA 1602 |
LINC01603 Genelong intergenic non-protein coding RNA 1603 |
LINC00559 Genelong intergenic non-protein coding RNA 559 |
LINC00558 Genelong intergenic non-protein coding RNA 558 |
LINC00557 Genelong intergenic non-protein coding RNA 557 |
LINC00556 Genelong intergenic non-protein coding RNA 556 |
LINC00555 Genelong intergenic non-protein coding RNA 555 |
LINC00552 Genelong intergenic non-protein coding RNA 552 |
LINC00551 Genelong intergenic non-protein coding RNA 551 |
LINC00550 Genelong intergenic non-protein coding RNA 550 |
LINC01337 Genelong intergenic non-protein coding RNA 1337 |
LINC01375 Genelong intergenic non-protein coding RNA 1375 |
LINC01376 Genelong intergenic non-protein coding RNA 1376 |
LINC01377 Genelong intergenic non-protein coding RNA 1377 |
LINC01370 Genelong intergenic non-protein coding RNA 1370 |
LINC01378 Genelong intergenic non-protein coding RNA 1378 |
PARTICL Genepromoter of MAT2A antisense radiation-induced circulating long non-coding RNA Enables dsDNA-RNA triple helix-forming chromatin adaptor activity and mRNA binding activity. Involved in cellular response to ionizing radiation and regulatory ncRNA-mediated heterochromatin formation. Is active in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01484 Genelong intergenic non-protein coding RNA 1484 |
LINC00028 Genelong intergenic non-protein coding RNA 28 |
LINC01483 Genelong intergenic non-protein coding RNA 1483 |
LINC00160 Genelong intergenic non-protein coding RNA 160 |
LINC01039 Genelong intergenic non-protein coding RNA 1039 |
LINC01038 Genelong intergenic non-protein coding RNA 1038 |
LINC01036 Genelong intergenic non-protein coding RNA 1036 |
LINC01033 Genelong intergenic non-protein coding RNA 1033 |
LINC01032 Genelong intergenic non-protein coding RNA 1032 |
LINC01031 Genelong intergenic non-protein coding RNA 1031 |
LINC01030 Genelong intergenic non-protein coding RNA 1030 |
LINC01410 Genelong intergenic non-protein coding RNA 1410 |
LINC01231 Genelong intergenic non-protein coding RNA 1231 |
LINC01230 Genelong intergenic non-protein coding RNA 1230 |
LINC01233 Genelong intergenic non-protein coding RNA 1233 |
LINC01237 Genelong intergenic non-protein coding RNA 1237 |
LINC00184 Genelong intergenic non-protein coding RNA 184 |
LINC00189 Genelong intergenic non-protein coding RNA 189 |
LINC00448 Genelong intergenic non-protein coding RNA 448 |
LSINCT5 Genelong stress-induced non-coding transcript 5 |
LINC01179 Genelong intergenic non-protein coding RNA 1179 |
LINC00441 Genelong intergenic non-protein coding RNA 441 |
LINC00440 Genelong intergenic non-protein coding RNA 440 |
LINC00442 Genelong intergenic non-protein coding RNA 442 |
LINC00445 Genelong intergenic non-protein coding RNA 445 |
LINC00444 Genelong intergenic non-protein coding RNA 444 |
LINC00446 Genelong intergenic non-protein coding RNA 446 |
LINC01234 Genelong intergenic non-protein coding RNA 1234 |
LINC01239 Genelong intergenic non-protein coding RNA 1239 |
LINC01521 Genelong intergenic non-protein coding RNA 1521 |
LINC01520 Genelong intergenic non-protein coding RNA 1520 |
LINC01525 Genelong intergenic non-protein coding RNA 1525 |
LINC01524 Genelong intergenic non-protein coding RNA 1524 |
LINC01527 Genelong intergenic non-protein coding RNA 1527 |
LINC01529 Genelong intergenic non-protein coding RNA 1529 |
LINC00691 Genelong intergenic non-protein coding RNA 691 |
LINC00692 Genelong intergenic non-protein coding RNA 692 |
LINC00693 Genelong intergenic non-protein coding RNA 693 |
LINC00698 Genelong intergenic non-protein coding RNA 698 |
LINC00346 Genelong intergenic non-protein coding RNA 346 |
LINC00347 Genelong intergenic non-protein coding RNA 347 |
LINC00345 Genelong intergenic non-protein coding RNA 345 |
LINC00342 Genelong intergenic non-protein coding RNA 342 Biomarker of Huntington's disease. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00343 Genelong intergenic non-protein coding RNA 343 |
LINC00341 Genelong intergenic non-protein coding RNA 341 |
LINC00348 Genelong intergenic non-protein coding RNA 348 |
LINC01543 Genelong intergenic non-protein coding RNA 1543 |
LINC01541 Genelong intergenic non-protein coding RNA 1541 |
LINC01544 Genelong intergenic non-protein coding RNA 1544 |
LINC00102 Genelong intergenic non-protein coding RNA 102 |
LINC00290 Genelong intergenic non-protein coding RNA 290 |
LINC00266-3 Genelong intergenic non-protein coding RNA 266-3 |
LINC00266-1 Genelong intergenic non-protein coding RNA 266-1 |
LINC00632 Genelong intergenic non-protein coding RNA 632 |
LINC00634 Genelong intergenic non-protein coding RNA 634 Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ACADVL Geneacyl-CoA dehydrogenase, very long chain The protein encoded by this gene is targeted to the inner mitochondrial membrane where it catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. This acyl-Coenzyme A dehydrogenase is specific to long-chain and very-long-chain fatty acids. A deficiency in this gene product reduces myocardial fatty acid beta-oxidation and is associated with cardiomyopathy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
KIR3DL1 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR3DL2 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011] |
KIR3DL3 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. [provided by RefSeq, Jul 2008] |
LINC01176 Genelong intergenic non-protein coding RNA 1176 |
LINC01177 Genelong intergenic non-protein coding RNA 1177 |
LINC01069 Genelong intergenic non-protein coding RNA 1069 |
LINC01065 Genelong intergenic non-protein coding RNA 1065 |
LINC00862 Genelong intergenic non-protein coding RNA 862 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00333 Genelong intergenic non-protein coding RNA 333 |
LINC00331 Genelong intergenic non-protein coding RNA 331 |
LINC01468 Genelong intergenic non-protein coding RNA 1468 |
LINC01003 Genelong intergenic non-protein coding RNA 1003 |
LINC00618 Genelong intergenic non-protein coding RNA 618 |
LINC00619 Genelong intergenic non-protein coding RNA 619 |
LINC00610 Genelong intergenic non-protein coding RNA 610 |
LINC00612 Genelong intergenic non-protein coding RNA 612 |
LINC00613 Genelong intergenic non-protein coding RNA 613 |
LINC00614 Genelong intergenic non-protein coding RNA 614 |
LINC00615 Genelong intergenic non-protein coding RNA 615 |
LINC00616 Genelong intergenic non-protein coding RNA 616 |
LINC01435 Genelong intergenic non-protein coding RNA 1435 |
LINC01151 Genelong intergenic non-protein coding RNA 1151 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00968 Genelong intergenic non-protein coding RNA 968 |
LINC01005 Genelong intergenic non-protein coding RNA 1005 |
LINC00892 Genelong intergenic non-protein coding RNA 892 |
LINC00893 Genelong intergenic non-protein coding RNA 893 |
LINC00890 Genelong intergenic non-protein coding RNA 890 Predicted to be located in membrane. Predicted to be active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00891 Genelong intergenic non-protein coding RNA 891 |
LINC00896 Genelong intergenic non-protein coding RNA 896 |
LINC00894 Genelong intergenic non-protein coding RNA 894 |
LINC00895 Genelong intergenic non-protein coding RNA 895 |
LINC00898 Genelong intergenic non-protein coding RNA 898 |
LINC00899 Genelong intergenic non-protein coding RNA 899 |
LINC01442 Genelong intergenic non-protein coding RNA 1442 |
LINC01443 Genelong intergenic non-protein coding RNA 1443 |
LINC01440 Genelong intergenic non-protein coding RNA 1440 |
LINC01446 Genelong intergenic non-protein coding RNA 1446 |
LINC01447 Genelong intergenic non-protein coding RNA 1447 |
LINC01444 Genelong intergenic non-protein coding RNA 1444 |
LINC01445 Genelong intergenic non-protein coding RNA 1445 |
LINC01448 Genelong intergenic non-protein coding RNA 1448 |
LINC01449 Genelong intergenic non-protein coding RNA 1449 |
LINC00229 Genelong intergenic non-protein coding RNA 229 |
LINC00226 Genelong intergenic non-protein coding RNA 226 |
LINC00221 Genelong intergenic non-protein coding RNA 221 |
LINC00222 Genelong intergenic non-protein coding RNA 222 |
ABALON Geneapoptotic BCL2L1-antisense long non-coding RNA |
LINC00917 Genelong intergenic non-protein coding RNA 917 |
LINC00911 Genelong intergenic non-protein coding RNA 911 |
LINC00910 Genelong intergenic non-protein coding RNA 910 |
LINC01515 Genelong intergenic non-protein coding RNA 1515 |
LINC01349 Genelong intergenic non-protein coding RNA 1349 |
LINC01344 Genelong intergenic non-protein coding RNA 1344 |
LINC01347 Genelong intergenic non-protein coding RNA 1347 |
LINC01346 Genelong intergenic non-protein coding RNA 1346 |
LINC01341 Genelong intergenic non-protein coding RNA 1341 |
LINC01340 Genelong intergenic non-protein coding RNA 1340 |
LINC01343 Genelong intergenic non-protein coding RNA 1343 |
LINC01342 Genelong intergenic non-protein coding RNA 1342 |
LINC01264 Genelong intergenic non-protein coding RNA 1264 |
LINC00710 Genelong intergenic non-protein coding RNA 710 |
LINC00498 Genelong intergenic non-protein coding RNA 498 |
LINC00499 Genelong intergenic non-protein coding RNA 499 |
LINC00997 Genelong intergenic non-protein coding RNA 997 |
LINC00994 Genelong intergenic non-protein coding RNA 994 |
LINC00993 Genelong intergenic non-protein coding RNA 993 |
LINC00992 Genelong intergenic non-protein coding RNA 992 |
LINC00999 Genelong intergenic non-protein coding RNA 999 |
LINC00998 Genelong intergenic non-protein coding RNA 998 Involved in negative regulation of type I interferon-mediated signaling pathway. Located in endoplasmic reticulum membrane and mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00508 Genelong intergenic non-protein coding RNA 508 |
LINC00502 Genelong intergenic non-protein coding RNA 502 |
LINC00696 Genelong intergenic non-protein coding RNA 696 |
SPTLC2 Geneserine palmitoyltransferase, long chain base subunit 2 This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011] |
SPTLC3 Geneserine palmitoyltransferase, long chain base subunit 3 This gene encodes a subunit of the serine palmitoyltransferase complex which catalyzes the rate-limiting step in sphingolipid biosynthesis. This subunit metabolizes lauroyl- and myristoyl-CoA and generates C14 and C16-sphingoid bases. [provided by RefSeq, Mar 2017] |
SPTLC1 Geneserine palmitoyltransferase, long chain base subunit 1 This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013] |
LINC00317 Genelong intergenic non-protein coding RNA 317 |
LINC01372 Genelong intergenic non-protein coding RNA 1372 |
LINC01068 Genelong intergenic non-protein coding RNA 1068 |
LINC01060 Genelong intergenic non-protein coding RNA 1060 |
LINC01061 Genelong intergenic non-protein coding RNA 1061 |
LINC01063 Genelong intergenic non-protein coding RNA 1063 |
LINC00339 Genelong intergenic non-protein coding RNA 339 |
LINC00337 Genelong intergenic non-protein coding RNA 337 |
LINC00336 Genelong intergenic non-protein coding RNA 336 |
LINC00334 Genelong intergenic non-protein coding RNA 334 |
LINC00330 Genelong intergenic non-protein coding RNA 330 |
LINC01220 Genelong intergenic non-protein coding RNA 1220 |
LINC00029 Genelong intergenic non-protein coding RNA 29 |
LINC00674 Genelong intergenic non-protein coding RNA 674 |
LINC01268 Genelong intergenic non-protein coding RNA 1268 |
LINC01266 Genelong intergenic non-protein coding RNA 1266 |
LINC01267 Genelong intergenic non-protein coding RNA 1267 |
LINC01265 Genelong intergenic non-protein coding RNA 1265 |
LINC01260 Genelong intergenic non-protein coding RNA 1260 |
LINC01232 Genelong intergenic non-protein coding RNA 1232 |
LINC00094 Genelong intergenic non-protein coding RNA 94 |
LINC01384 Genelong intergenic non-protein coding RNA 1384 |
LINC00587 Genelong intergenic non-protein coding RNA 587 |
LINC00581 Genelong intergenic non-protein coding RNA 581 |
LINC00582 Genelong intergenic non-protein coding RNA 582 |
LINC00583 Genelong intergenic non-protein coding RNA 583 |
LINC00588 Genelong intergenic non-protein coding RNA 588 |
LINC00589 Genelong intergenic non-protein coding RNA 589 |
LINC01189 Genelong intergenic non-protein coding RNA 1189 |
LINC01183 Genelong intergenic non-protein coding RNA 1183 |
LINC01182 Genelong intergenic non-protein coding RNA 1182 |
LINC01181 Genelong intergenic non-protein coding RNA 1181 |
LINC01187 Genelong intergenic non-protein coding RNA 1187 |
LINC01186 Genelong intergenic non-protein coding RNA 1186 |
LINC01185 Genelong intergenic non-protein coding RNA 1185 |
LINC-PINT Genelong intergenic non-protein coding RNA, p53 induced transcript Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00378 Genelong intergenic non-protein coding RNA 378 |
OPN1LW Geneopsin 1 (cone pigments), long-wave-sensitive This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of partial, protanopic colorblindness. [provided by RefSeq, Jul 2008] |
LINC01119 Genelong intergenic non-protein coding RNA 1119 |
LINC01578 Genelong intergenic non-protein coding RNA 1578 Predicted to be involved in several processes, including adipose tissue development; regulation of gene expression; and thymus development. Predicted to be active in chromatin and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01579 Genelong intergenic non-protein coding RNA 1579 |
LINC01574 Genelong intergenic non-protein coding RNA 1574 |
LINC01572 Genelong intergenic non-protein coding RNA 1572 |
LINC01573 Genelong intergenic non-protein coding RNA 1573 |
LINC01570 Genelong intergenic non-protein coding RNA 1570 |
LINC01571 Genelong intergenic non-protein coding RNA 1571 |
LINC01398 Genelong intergenic non-protein coding RNA 1398 |
LINC01399 Genelong intergenic non-protein coding RNA 1399 |
LINC01392 Genelong intergenic non-protein coding RNA 1392 |
LINC01393 Genelong intergenic non-protein coding RNA 1393 |
LINC01391 Genelong intergenic non-protein coding RNA 1391 |
LINC01396 Genelong intergenic non-protein coding RNA 1396 |
LINC01397 Genelong intergenic non-protein coding RNA 1397 |
LINC01395 Genelong intergenic non-protein coding RNA 1395 |
LINC00621 Genelong intergenic non-protein coding RNA 621 |
LINC00620 Genelong intergenic non-protein coding RNA 620 |
LINC00623 Genelong intergenic non-protein coding RNA 623 |
LINC00624 Genelong intergenic non-protein coding RNA 624 |
LINC00626 Genelong intergenic non-protein coding RNA 626 |
LINC00629 Genelong intergenic non-protein coding RNA 629 |
LINC00628 Genelong intergenic non-protein coding RNA 628 |
SHFLD2 GeneSplit-hand/foot malformation with long deficiency 2 |
LINC00265-2P Genelong intergenic non-protein coding RNA 265-2, pseudogene |
LINC00869 Genelong intergenic non-protein coding RNA 869 |
LINC00868 Genelong intergenic non-protein coding RNA 868 |
LINC00867 Genelong intergenic non-protein coding RNA 867 |
LINC00866 Genelong intergenic non-protein coding RNA 866 |
LINC01180 Genelong intergenic non-protein coding RNA 1180 |
LINC01184 Genelong intergenic non-protein coding RNA 1184 |
LINC00936 Genelong intergenic non-protein coding RNA 936 |
LINC00470 Genelong intergenic non-protein coding RNA 470 |
LINC00472 Genelong intergenic non-protein coding RNA 472 |
LINC00473 Genelong intergenic non-protein coding RNA 473 Involved in DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00474 Genelong intergenic non-protein coding RNA 474 |
LINC00475 Genelong intergenic non-protein coding RNA 475 |
LINC00476 Genelong intergenic non-protein coding RNA 476 |
LINC00477 Genelong intergenic non-protein coding RNA 477 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00479 Genelong intergenic non-protein coding RNA 479 |
LINC01103 Genelong intergenic non-protein coding RNA 1103 |
LINC01102 Genelong intergenic non-protein coding RNA 1102 |
LINC01101 Genelong intergenic non-protein coding RNA 1101 |
LINC01100 Genelong intergenic non-protein coding RNA 1100 |
LINC01107 Genelong intergenic non-protein coding RNA 1107 |
LINC01106 Genelong intergenic non-protein coding RNA 1106 |
LINC01105 Genelong intergenic non-protein coding RNA 1105 |
LINC01104 Genelong intergenic non-protein coding RNA 1104 |
LINC01109 Genelong intergenic non-protein coding RNA 1109 |
LINC01108 Genelong intergenic non-protein coding RNA 1108 |
LINC00278 Genelong intergenic non-protein coding RNA 278 |
LINC00279 Genelong intergenic non-protein coding RNA 279 |
LINC00708 Genelong intergenic non-protein coding RNA 708 |
LINC00709 Genelong intergenic non-protein coding RNA 709 |
LINC00702 Genelong intergenic non-protein coding RNA 702 |
ACADL Geneacyl-CoA dehydrogenase, long chain The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008] |
LINC01312 Genelong intergenic non-protein coding RNA 1312 |
LINC01310 Genelong intergenic non-protein coding RNA 1310 |
LINC01311 Genelong intergenic non-protein coding RNA 1311 |
LINC01314 Genelong intergenic non-protein coding RNA 1314 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01315 Genelong intergenic non-protein coding RNA 1315 |
LINC01235 Genelong intergenic non-protein coding RNA 1235 |
LINC01433 Genelong intergenic non-protein coding RNA 1433 |
LINC01432 Genelong intergenic non-protein coding RNA 1432 |
LINC01431 Genelong intergenic non-protein coding RNA 1431 |
LINC01430 Genelong intergenic non-protein coding RNA 1430 |
LINC01299 Genelong intergenic non-protein coding RNA 1299 |
LINC01293 Genelong intergenic non-protein coding RNA 1293 |
LINC01291 Genelong intergenic non-protein coding RNA 1291 |
LINC01165 Genelong intergenic non-protein coding RNA 1165 |
LINC00944 Genelong intergenic non-protein coding RNA 944 |
LINC00945 Genelong intergenic non-protein coding RNA 945 |
LINC00941 Genelong intergenic non-protein coding RNA 941 Enables promoter-enhancer loop anchoring activity. Involved in chromatin looping and positive regulation of transcription by RNA polymerase II. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00942 Genelong intergenic non-protein coding RNA 942 |
LINC00943 Genelong intergenic non-protein coding RNA 943 |
OVAAL Geneovarian adenocarcinoma amplified long non-coding RNA Predicted to enable pre-mRNA branch point binding activity. Predicted to be involved in mRNA branch site recognition. Predicted to be part of U2 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00535 Genelong intergenic non-protein coding RNA 535 |
LINC00534 Genelong intergenic non-protein coding RNA 534 |
LINC00537 Genelong intergenic non-protein coding RNA 537 Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00536 Genelong intergenic non-protein coding RNA 536 |
LINC00533 Genelong intergenic non-protein coding RNA 533 |
LINC00539 Genelong intergenic non-protein coding RNA 539 |
LINC00538 Genelong intergenic non-protein coding RNA 538 |
LINC01588 Genelong intergenic non-protein coding RNA 1588 |
LINC01585 Genelong intergenic non-protein coding RNA 1585 |
LINC01583 Genelong intergenic non-protein coding RNA 1583 |
LINC01582 Genelong intergenic non-protein coding RNA 1582 |
LINC01581 Genelong intergenic non-protein coding RNA 1581 |
LINC01580 Genelong intergenic non-protein coding RNA 1580 |
LINC01055 Genelong intergenic non-protein coding RNA 1055 |
LINC01057 Genelong intergenic non-protein coding RNA 1057 |
LINC01056 Genelong intergenic non-protein coding RNA 1056 |
LINC01050 Genelong intergenic non-protein coding RNA 1050 |
LINC01053 Genelong intergenic non-protein coding RNA 1053 |
LINC01059 Genelong intergenic non-protein coding RNA 1059 |
LINC01217 Genelong intergenic non-protein coding RNA 1217 |
LINC01216 Genelong intergenic non-protein coding RNA 1216 |
LINC01210 Genelong intergenic non-protein coding RNA 1210 |
LINC01219 Genelong intergenic non-protein coding RNA 1219 |
LINC01218 Genelong intergenic non-protein coding RNA 1218 |
LINC01213 Genelong intergenic non-protein coding RNA 1213 |
LINC00328-2P Genelong intergenic non-protein coding RNA 328-2, pseudogene |
LINC01298 Genelong intergenic non-protein coding RNA 1298 |
LINC01296 Genelong intergenic non-protein coding RNA 1296 |
LINC01507 Genelong intergenic non-protein coding RNA 1507 |
LINC01506 Genelong intergenic non-protein coding RNA 1506 |
LINC01505 Genelong intergenic non-protein coding RNA 1505 |
LINC01503 Genelong intergenic non-protein coding RNA 1503 |
LINC01502 Genelong intergenic non-protein coding RNA 1502 |
LINC01501 Genelong intergenic non-protein coding RNA 1501 |
LINC01500 Genelong intergenic non-protein coding RNA 1500 |
LINC01509 Genelong intergenic non-protein coding RNA 1509 |
LINC01508 Genelong intergenic non-protein coding RNA 1508 |
LINC00368 Genelong intergenic non-protein coding RNA 368 |
LINC00365 Genelong intergenic non-protein coding RNA 365 |
LINC00366 Genelong intergenic non-protein coding RNA 366 |
LINC00367 Genelong intergenic non-protein coding RNA 367 |
LINC00362 Genelong intergenic non-protein coding RNA 362 |
LINC00363 Genelong intergenic non-protein coding RNA 363 |
LINC01144 Genelong intergenic non-protein coding RNA 1144 |
LINC01140 Genelong intergenic non-protein coding RNA 1140 |
MT-LIPCAR Genemitochondrially encoded long non-coding cardiac associated RNA |
LINC00167 Genelong intergenic non-protein coding RNA 167 |
LINC00162 Genelong intergenic non-protein coding RNA 162 |
LINC00163 Genelong intergenic non-protein coding RNA 163 |
LINC00161 Genelong intergenic non-protein coding RNA 161 |
LINC00836 Genelong intergenic non-protein coding RNA 836 |
LINC00837 Genelong intergenic non-protein coding RNA 837 |
LINC00838 Genelong intergenic non-protein coding RNA 838 |
LINC00839 Genelong intergenic non-protein coding RNA 839 |
LOC100422263 Geneserine palmitoyltransferase, long chain base subunit 2 pseudogene |
LINC01158 Genelong intergenic non-protein coding RNA 1158 Predicted to act upstream of or within regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01159 Genelong intergenic non-protein coding RNA 1159 Predicted to act upstream of or within cerebellar cortex structural organization; homeostasis of number of cells within a tissue; and regulation of gene expression. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01150 Genelong intergenic non-protein coding RNA 1150 |
LINC01152 Genelong intergenic non-protein coding RNA 1152 |
LINC01153 Genelong intergenic non-protein coding RNA 1153 |
SPTLC1P3 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 3 |
LINC00283 Genelong intergenic non-protein coding RNA 283 |
LINC00282 Genelong intergenic non-protein coding RNA 282 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00280 Genelong intergenic non-protein coding RNA 280 |
LINC00284 Genelong intergenic non-protein coding RNA 284 |
LINC00678 Genelong intergenic non-protein coding RNA 678 |
LINC00676 Genelong intergenic non-protein coding RNA 676 |
LINC00677 Genelong intergenic non-protein coding RNA 677 |
LINC00675 Genelong intergenic non-protein coding RNA 675 Involved in intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00672 Genelong intergenic non-protein coding RNA 672 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00673 Genelong intergenic non-protein coding RNA 673 This gene produces a long non-protein coding RNA that is involved in the regulation of gene expression during tumor progression. This transcript can promote cell proliferation in gastric cancer through interaction with enhancer of zeste 2 and other epigenetic suppressors of gene expression, thereby downregulating target genes including Kruppel like factors 2 and 4. This transcript may also act as a tumor suppressor by promoting interaction between protein tyrosine phosphatase, non-receptor type 11 (Ptpn11) and ubiquitin ligase, resulting in degradation of Ptpn11 and lowered oncogenic signalling. Naturally-occurring variation at this locus results in the formation of a binding site for miR-1231, which negatively regulates activity of this transcript. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2017] |
LINC00670 Genelong intergenic non-protein coding RNA 670 |
LINC00671 Genelong intergenic non-protein coding RNA 671 |
LINC00092 Genelong intergenic non-protein coding RNA 92 |
LINC01276 Genelong intergenic non-protein coding RNA 1276 |
NKILA GeneNF-kappaB interacting long non-coding RNA |
LINC00863 Genelong intergenic non-protein coding RNA 863 |
LINC00861 Genelong intergenic non-protein coding RNA 861 |
LINC00865 Genelong intergenic non-protein coding RNA 865 |
LINC00864 Genelong intergenic non-protein coding RNA 864 |
PNKY Genelong intergenic non-protein coding RNA PNKY |
GAPLINC Genegastric adenocarcinoma associated, positive CD44 regulator, long intergenic non-coding RNA |
LINC01460 Genelong intergenic non-protein coding RNA 1460 |
LINC01461 Genelong intergenic non-protein coding RNA 1461 |
LINC01465 Genelong intergenic non-protein coding RNA 1465 |
LINC01467 Genelong intergenic non-protein coding RNA 1467 |
LINC00924 Genelong intergenic non-protein coding RNA 924 |
LINC00485 Genelong intergenic non-protein coding RNA 485 |
SHFL1 GeneSplit-hand/foot malformation with long bone deficiency 1 |
LINC00208 Genelong intergenic non-protein coding RNA 208 |
LINC01450 Genelong intergenic non-protein coding RNA 1450 |
LINC00974 Genelong intergenic non-protein coding RNA 974 |
LINC00977 Genelong intergenic non-protein coding RNA 977 |
LINC00971 Genelong intergenic non-protein coding RNA 971 |
LINC00970 Genelong intergenic non-protein coding RNA 970 |
LINC00973 Genelong intergenic non-protein coding RNA 973 |
LINC00972 Genelong intergenic non-protein coding RNA 972 |
LINC00562 Genelong intergenic non-protein coding RNA 562 |
LINC00563 Genelong intergenic non-protein coding RNA 563 |
LINC00560 Genelong intergenic non-protein coding RNA 560 |
LINC00561 Genelong intergenic non-protein coding RNA 561 |
LINC00566 Genelong intergenic non-protein coding RNA 566 |
LINC00567 Genelong intergenic non-protein coding RNA 567 |
LINC00564 Genelong intergenic non-protein coding RNA 564 |
LINC00565 Genelong intergenic non-protein coding RNA 565 |
LINC00471 Genelong intergenic non-protein coding RNA 471 |
KIR2DL5B Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL5A Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
LINC01362 Genelong intergenic non-protein coding RNA 1362 |
LINC01361 Genelong intergenic non-protein coding RNA 1361 |
LINC01366 Genelong intergenic non-protein coding RNA 1366 |
LINC01364 Genelong intergenic non-protein coding RNA 1364 |
LINC01002 Genelong intergenic non-protein coding RNA 1002 |
LINC01000 Genelong intergenic non-protein coding RNA 1000 |
LINC01006 Genelong intergenic non-protein coding RNA 1006 Predicted to be located in cytoplasm and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01007 Genelong intergenic non-protein coding RNA 1007 |
LINC01004 Genelong intergenic non-protein coding RNA 1004 Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01212 Genelong intergenic non-protein coding RNA 1212 |
HELLPAR GeneHELLP associated long non-coding RNA |
LINC01523 Genelong intergenic non-protein coding RNA 1523 |
LINC01522 Genelong intergenic non-protein coding RNA 1522 |
LINC01526 Genelong intergenic non-protein coding RNA 1526 |
LINC01208 Genelong intergenic non-protein coding RNA 1208 |
LINC00202-1 Genelong intergenic non-protein coding RNA 202-1 |
LINC00202-2 Genelong intergenic non-protein coding RNA 202-2 |
LINC00690 Genelong intergenic non-protein coding RNA 690 |
LINC00694 Genelong intergenic non-protein coding RNA 694 |
LINC00349 Genelong intergenic non-protein coding RNA 349 |
SALRNA3 Genesenescence associated long non-coding RNA 3 |
LINC01001 Genelong intergenic non-protein coding RNA 1001 |
LINC01082 Genelong intergenic non-protein coding RNA 1082 |
LINC01080 Genelong intergenic non-protein coding RNA 1080 |
LINC01081 Genelong intergenic non-protein coding RNA 1081 |
LINC01087 Genelong intergenic non-protein coding RNA 1087 |
LINC01085 Genelong intergenic non-protein coding RNA 1085 |
LINC01089 Genelong intergenic non-protein coding RNA 1089 |
LINC00689 Genelong intergenic non-protein coding RNA 689 Implicated in colorectal cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00687 Genelong intergenic non-protein coding RNA 687 |
LINC00686 Genelong intergenic non-protein coding RNA 686 |
LINC00685 Genelong intergenic non-protein coding RNA 685 |
LINC00684 Genelong intergenic non-protein coding RNA 684 |
LINC00682 Genelong intergenic non-protein coding RNA 682 |
LINC00681 Genelong intergenic non-protein coding RNA 681 |
LINC00355 Genelong intergenic non-protein coding RNA 355 |
LINC00354 Genelong intergenic non-protein coding RNA 354 |
LINC00351 Genelong intergenic non-protein coding RNA 351 |
LINC00350 Genelong intergenic non-protein coding RNA 350 |
LINC00353 Genelong intergenic non-protein coding RNA 353 |
LINC00352 Genelong intergenic non-protein coding RNA 352 |
LINC00359 Genelong intergenic non-protein coding RNA 359 |
LINC00358 Genelong intergenic non-protein coding RNA 358 |
LINC00272 Genelong intergenic non-protein coding RNA 272 |
LINC00273 Genelong intergenic non-protein coding RNA 273 |
LINC00271 Genelong intergenic non-protein coding RNA 271 |
LINC00276 Genelong intergenic non-protein coding RNA 276 |
SALRNA1 Genesenescence associated long non-coding RNA 1 |
LINC01246 Genelong intergenic non-protein coding RNA 1246 |
LINC01241 Genelong intergenic non-protein coding RNA 1241 |
LINC01248 Genelong intergenic non-protein coding RNA 1248 |
LINC01249 Genelong intergenic non-protein coding RNA 1249 |
LINC00599 Genelong intergenic non-protein coding RNA 599 Predicted to act upstream of or within several processes, including long-term synaptic potentiation; miRNA-mediated post-transcriptional gene silencing; and sensory perception of sound. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00598 Genelong intergenic non-protein coding RNA 598 |
LINC00116 Genelong intergenic non-protein coding RNA 116 Involved in several processes, including positive regulation of mitochondrial membrane potential; positive regulation of sequestering of calcium ion; and triglyceride homeostasis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00115 Genelong intergenic non-protein coding RNA 115 |
LINC00114 Genelong intergenic non-protein coding RNA 114 |
LINC00113 Genelong intergenic non-protein coding RNA 113 |
LINC00112 Genelong intergenic non-protein coding RNA 112 |
LINC00111 Genelong intergenic non-protein coding RNA 111 |
LINC00996 Genelong intergenic non-protein coding RNA 996 |
HULC Genehepatocellular carcinoma up-regulated long non-coding RNA This gene produces a long RNA that was discovered as upregulated in hepatocellular carcinoma and is associated with cancer progression. Expression of this transcript is regulated by microRNAs and at the transcriptional level by Sp1 family factors. The transcript may regulate gene expression by functioning as a competing RNA for microRNAs. [provided by RefSeq, Dec 2017] |
LINC01160 Genelong intergenic non-protein coding RNA 1160 |
LINC01163 Genelong intergenic non-protein coding RNA 1163 |
LINC01164 Genelong intergenic non-protein coding RNA 1164 |
LINC01167 Genelong intergenic non-protein coding RNA 1167 |
LINC01169 Genelong intergenic non-protein coding RNA 1169 |
LINC01168 Genelong intergenic non-protein coding RNA 1168 |
LINC01554 Genelong intergenic non-protein coding RNA 1554 |
LINC01555 Genelong intergenic non-protein coding RNA 1555 |
LINC01556 Genelong intergenic non-protein coding RNA 1556 |
LINC01553 Genelong intergenic non-protein coding RNA 1553 |
LINC01558 Genelong intergenic non-protein coding RNA 1558 |
LINC01559 Genelong intergenic non-protein coding RNA 1559 |
LINC00607 Genelong intergenic non-protein coding RNA 607 |
LINC00606 Genelong intergenic non-protein coding RNA 606 |
LINC00605 Genelong intergenic non-protein coding RNA 605 |
LINC00602 Genelong intergenic non-protein coding RNA 602 |
LINC00601 Genelong intergenic non-protein coding RNA 601 |
LINC00609 Genelong intergenic non-protein coding RNA 609 |
LINC00608 Genelong intergenic non-protein coding RNA 608 |
LINC00106 Genelong intergenic non-protein coding RNA 106 |
LINC00881 Genelong intergenic non-protein coding RNA 881 |
LINC00880 Genelong intergenic non-protein coding RNA 880 |
LINC00883 Genelong intergenic non-protein coding RNA 883 Predicted to act upstream of or within several processes, including generation of neurons; negative regulation of macromolecule biosynthetic process; and protein stabilization. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00882 Genelong intergenic non-protein coding RNA 882 |
LINC00885 Genelong intergenic non-protein coding RNA 885 Implicated in cervical cancer. Biomarker of cervical cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00884 Genelong intergenic non-protein coding RNA 884 |
LINC00887 Genelong intergenic non-protein coding RNA 887 |
LINC00886 Genelong intergenic non-protein coding RNA 886 |
LINC00889 Genelong intergenic non-protein coding RNA 889 |
LINC00489 Genelong intergenic non-protein coding RNA 489 |
LINC01451 Genelong intergenic non-protein coding RNA 1451 |
LINC01455 Genelong intergenic non-protein coding RNA 1455 |
LINC01473 Genelong intergenic non-protein coding RNA 1473 |
LINC00417 Genelong intergenic non-protein coding RNA 417 |
LINC00412 Genelong intergenic non-protein coding RNA 412 |
LINC00410 Genelong intergenic non-protein coding RNA 410 |
FALEC Genefocally amplified long non-coding RNA in epithelial cancer |
LOC100132304 Genelong intergenic non-protein coding RNA 684 |
LINC00268-2P Genelong intergenic non-protein coding RNA 268-2, pseudogene |
DALIR GeneDNMT1-associated long intergenic non-coding RNA |
LINC00554 Genelong intergenic non-protein coding RNA 554 |
LINC00254 Genelong intergenic non-protein coding RNA 254 |
LINC00437 Genelong intergenic non-protein coding RNA 437 |
SALRNA2 Genesenescence associated long non-coding RNA 2 |
LINC00928 Genelong intergenic non-protein coding RNA 928 |
LINC00922 Genelong intergenic non-protein coding RNA 922 |
LINC00923 Genelong intergenic non-protein coding RNA 923 |
LINC00921 Genelong intergenic non-protein coding RNA 921 |
LINC00926 Genelong intergenic non-protein coding RNA 926 |
LINC00927 Genelong intergenic non-protein coding RNA 927 |
LINC00925 Genelong intergenic non-protein coding RNA 925 |
HAGLR GeneHOXD antisense growth-associated long non-coding RNA |
PTX3 Genepentraxin 3, long This gene encodes a member of the pentraxin protein family. The expression of this protein is induced by inflammatory cytokines in response to inflammatory stimuli in several mesenchymal and epithelial cell types, particularly endothelial cells and mononuclear phagocytes. The protein promotes fibrocyte differentiation and is involved in regulating inflammation and complement activation. It also plays a role in angiogenesis and tissue remodeling. The protein serves as a biomarker for several inflammatory conditions. [provided by RefSeq, Jun 2016] |
PTX4 Genepentraxin 4, long This gene belongs to the pentraxin superfamily, whose members encode highly conserved multifunctional proteins. The encoded protein, like other members of this family, contains a conserved pentraxin domain at the C-terminus. The highest levels of expression of the protein were observed in bone marrow, small intestine and testes. [provided by RefSeq, Jun 2016] |
LINC01338 Genelong intergenic non-protein coding RNA 1338 |
LINC01339 Genelong intergenic non-protein coding RNA 1339 |
LINC01330 Genelong intergenic non-protein coding RNA 1330 |
LINC01331 Genelong intergenic non-protein coding RNA 1331 |
LINC01335 Genelong intergenic non-protein coding RNA 1335 |
LINC01336 Genelong intergenic non-protein coding RNA 1336 |
LINC00051 Genelong intergenic non-protein coding RNA 51 |
LOC100421637 Geneacyl-CoA synthetase long-chain family member 3 pseudogene |
LINC00332 Genelong intergenic non-protein coding RNA 332 |
LINC01317 Genelong intergenic non-protein coding RNA 1317 |
LINC01048 Genelong intergenic non-protein coding RNA 1048 |
LINC00494 Genelong intergenic non-protein coding RNA 494 |
LINC00492 Genelong intergenic non-protein coding RNA 492 |
LINC00493 Genelong intergenic non-protein coding RNA 493 Enables protein kinase binding activity and transmembrane transporter binding activity. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00491 Genelong intergenic non-protein coding RNA 491 |
LINC00920 Genelong intergenic non-protein coding RNA 920 |
LINC01479 Genelong intergenic non-protein coding RNA 1479 |
LINC01387 Genelong intergenic non-protein coding RNA 1387 |
LINC00519 Genelong intergenic non-protein coding RNA 519 |
LINC00518 Genelong intergenic non-protein coding RNA 518 |
LINC00511 Genelong intergenic non-protein coding RNA 511 |
LINC00517 Genelong intergenic non-protein coding RNA 517 |
LINC00515 Genelong intergenic non-protein coding RNA 515 |
LINC00514 Genelong intergenic non-protein coding RNA 514 |
LINC01597 Genelong intergenic non-protein coding RNA 1597 |
THRIL GeneTNF and HNRNPL related immunoregulatory long non-coding RNA |
LINC01333 Genelong intergenic non-protein coding RNA 1333 |
LINC00319 Genelong intergenic non-protein coding RNA 319 |
LINC00237 Genelong intergenic non-protein coding RNA 237 |
LINC01072 Genelong intergenic non-protein coding RNA 1072 |
LINC01070 Genelong intergenic non-protein coding RNA 1070 |
LINC01075 Genelong intergenic non-protein coding RNA 1075 |
LINC00308 Genelong intergenic non-protein coding RNA 308 |
LINC00309 Genelong intergenic non-protein coding RNA 309 |
LINC00302 Genelong intergenic non-protein coding RNA 302 |
LINC00303 Genelong intergenic non-protein coding RNA 303 |
LINC00301 Genelong intergenic non-protein coding RNA 301 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00307 Genelong intergenic non-protein coding RNA 307 |
LINC00304 Genelong intergenic non-protein coding RNA 304 |
LINC00305 Genelong intergenic non-protein coding RNA 305 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01429 Genelong intergenic non-protein coding RNA 1429 |
LINC01170 Genelong intergenic non-protein coding RNA 1170 |
LINC01279 Genelong intergenic non-protein coding RNA 1279 |
LINC01278 Genelong intergenic non-protein coding RNA 1278 |
LINC01277 Genelong intergenic non-protein coding RNA 1277 |
LINC01271 Genelong intergenic non-protein coding RNA 1271 |
LINC01270 Genelong intergenic non-protein coding RNA 1270 |
LINC01273 Genelong intergenic non-protein coding RNA 1273 |
LINC00593 Genelong intergenic non-protein coding RNA 593 |
LINC00592 Genelong intergenic non-protein coding RNA 592 |
LINC00597 Genelong intergenic non-protein coding RNA 597 |
LINC00596 Genelong intergenic non-protein coding RNA 596 |
LINC00595 Genelong intergenic non-protein coding RNA 595 |
LINC00594 Genelong intergenic non-protein coding RNA 594 |
LINC00578 Genelong intergenic non-protein coding RNA 578 |
LINC00570 Genelong intergenic non-protein coding RNA 570 |
LINC01569 Genelong intergenic non-protein coding RNA 1569 |
LINC01568 Genelong intergenic non-protein coding RNA 1568 |
LINC01565 Genelong intergenic non-protein coding RNA 1565 |
LINC01564 Genelong intergenic non-protein coding RNA 1564 |
LINC01567 Genelong intergenic non-protein coding RNA 1567 |
LINC01566 Genelong intergenic non-protein coding RNA 1566 |
LINC01561 Genelong intergenic non-protein coding RNA 1561 |
LINC01560 Genelong intergenic non-protein coding RNA 1560 |
LINC01563 Genelong intergenic non-protein coding RNA 1563 |
LINC01562 Genelong intergenic non-protein coding RNA 1562 |
LINC01389 Genelong intergenic non-protein coding RNA 1389 |
LINC01386 Genelong intergenic non-protein coding RNA 1386 |
LINC00382 Genelong intergenic non-protein coding RNA 382 |
LINC00383 Genelong intergenic non-protein coding RNA 383 |
LINC00380 Genelong intergenic non-protein coding RNA 380 |
LINC00381 Genelong intergenic non-protein coding RNA 381 |
LINC00387 Genelong intergenic non-protein coding RNA 387 |
LINC00384 Genelong intergenic non-protein coding RNA 384 |
LINC00388 Genelong intergenic non-protein coding RNA 388 |
LINC00854 Genelong intergenic non-protein coding RNA 854 |
LINC01436 Genelong intergenic non-protein coding RNA 1436 |
LINC00856 Genelong intergenic non-protein coding RNA 856 |
LINC00857 Genelong intergenic non-protein coding RNA 857 |
LINC00852 Genelong intergenic non-protein coding RNA 852 |
LINC00853 Genelong intergenic non-protein coding RNA 853 |
LINC00850 Genelong intergenic non-protein coding RNA 850 |
LINC00851 Genelong intergenic non-protein coding RNA 851 |
LINC00858 Genelong intergenic non-protein coding RNA 858 |
LINC01486 Genelong intergenic non-protein coding RNA 1486 |
LINC01481 Genelong intergenic non-protein coding RNA 1481 |
LINC01488 Genelong intergenic non-protein coding RNA 1488 |
LINC00469 Genelong intergenic non-protein coding RNA 469 |
LINC00467 Genelong intergenic non-protein coding RNA 467 |
LINC00463 Genelong intergenic non-protein coding RNA 463 |
LINC00462 Genelong intergenic non-protein coding RNA 462 |
LINC00461 Genelong intergenic non-protein coding RNA 461 This is an evolutionarily conserved gene that produces alternatively spliced long non-coding RNAs that may be expressed predominantly in the brain and visual cortex. These transcripts may be involved in tumorigenesis, as depletion by siRNA suppressed glioma cell division. Transcripts may also bind to and regulate the activity of miR-411-5p and argonaut 2, thereby altering the expression of genes involved in tumor growth. [provided by RefSeq, Nov 2017] |
LINC00460 Genelong intergenic non-protein coding RNA 460 |
LINC01127 Genelong intergenic non-protein coding RNA 1127 |
LINC01487 Genelong intergenic non-protein coding RNA 1487 |
LINC01485 Genelong intergenic non-protein coding RNA 1485 |
LINC01482 Genelong intergenic non-protein coding RNA 1482 |
LINC01480 Genelong intergenic non-protein coding RNA 1480 |
LINC01138 Genelong intergenic non-protein coding RNA 1138 |
LINC01139 Genelong intergenic non-protein coding RNA 1139 |
LINC01136 Genelong intergenic non-protein coding RNA 1136 |
LINC01137 Genelong intergenic non-protein coding RNA 1137 |
LINC01134 Genelong intergenic non-protein coding RNA 1134 |
LINC01135 Genelong intergenic non-protein coding RNA 1135 |
LINC01132 Genelong intergenic non-protein coding RNA 1132 |
LINC01133 Genelong intergenic non-protein coding RNA 1133 |
LINC01489 Genelong intergenic non-protein coding RNA 1489 |
LINC00261 Genelong intergenic non-protein coding RNA 261 This gene produces a long non-coding RNA that acts as a negative regulator of cell growth. This transcript may promote differentiation and apoptosis. [provided by RefSeq, Dec 2017] |
LINC00260 Genelong intergenic non-protein coding RNA 260 |
LINC00265 Genelong intergenic non-protein coding RNA 265 |
LINC00264 Genelong intergenic non-protein coding RNA 264 |
LINC00269 Genelong intergenic non-protein coding RNA 269 |
LINC00268 Genelong intergenic non-protein coding RNA 268 |
LINC00466 Genelong intergenic non-protein coding RNA 466 |
LINC00909 Genelong intergenic non-protein coding RNA 909 |
LINC01272 Genelong intergenic non-protein coding RNA 1272 |
LINC00205 Genelong intergenic non-protein coding RNA 205 |
LINC00654 Genelong intergenic non-protein coding RNA 654 |
LINC00656 Genelong intergenic non-protein coding RNA 656 |
LINC00652 Genelong intergenic non-protein coding RNA 652 |
LINC00658 Genelong intergenic non-protein coding RNA 658 |
LINC00659 Genelong intergenic non-protein coding RNA 659 |
LINC01300 Genelong intergenic non-protein coding RNA 1300 |
LINC01304 Genelong intergenic non-protein coding RNA 1304 |
LINC01309 Genelong intergenic non-protein coding RNA 1309 |
LINC01358 Genelong intergenic non-protein coding RNA 1358 |
LINC01356 Genelong intergenic non-protein coding RNA 1356 |
LINC01353 Genelong intergenic non-protein coding RNA 1353 |
LINC01351 Genelong intergenic non-protein coding RNA 1351 |
LINC01478 Genelong intergenic non-protein coding RNA 1478 |
LINC01405 Genelong intergenic non-protein coding RNA 1405 |
LOC646644 GeneLLP homolog, long-term synaptic facilitation (Aplysia) pseudogene |
LINC00959 Genelong intergenic non-protein coding RNA 959 |
LINC00958 Genelong intergenic non-protein coding RNA 958 |
LINC00951 Genelong intergenic non-protein coding RNA 951 |
LINC00950 Genelong intergenic non-protein coding RNA 950 |
LINC00957 Genelong intergenic non-protein coding RNA 957 |
LINC00955 Genelong intergenic non-protein coding RNA 955 |
LINC00540 Genelong intergenic non-protein coding RNA 540 |
LINC00543 Genelong intergenic non-protein coding RNA 543 |
LINC00544 Genelong intergenic non-protein coding RNA 544 |
LINC00545 Genelong intergenic non-protein coding RNA 545 |
LINC00547 Genelong intergenic non-protein coding RNA 547 |
LINC00548 Genelong intergenic non-protein coding RNA 548 |
LINC00683 Genelong intergenic non-protein coding RNA 683 |
LINC00032 Genelong intergenic non-protein coding RNA 32 |
LINC01011 Genelong intergenic non-protein coding RNA 1011 |
LINC01010 Genelong intergenic non-protein coding RNA 1010 |
LINC00940 Genelong intergenic non-protein coding RNA 940 |
LINC01269 Genelong intergenic non-protein coding RNA 1269 |
LINC01020 Genelong intergenic non-protein coding RNA 1020 |
LINC01021 Genelong intergenic non-protein coding RNA 1021 |
LINC01023 Genelong intergenic non-protein coding RNA 1023 |
LINC01028 Genelong intergenic non-protein coding RNA 1028 |
LINC01029 Genelong intergenic non-protein coding RNA 1029 |
LINC01262 Genelong intergenic non-protein coding RNA 1262 |
LINC01222 Genelong intergenic non-protein coding RNA 1222 |
LINC01226 Genelong intergenic non-protein coding RNA 1226 |
LINC01224 Genelong intergenic non-protein coding RNA 1224 |
LINC01225 Genelong intergenic non-protein coding RNA 1225 |
LINC01228 Genelong intergenic non-protein coding RNA 1228 |
LINC01229 Genelong intergenic non-protein coding RNA 1229 |
LINC00266-2P Genelong intergenic non-protein coding RNA 266-2, pseudogene |
LINC01589 Genelong intergenic non-protein coding RNA 1589 |
SENCR Genesmooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA |
LINC01017 Genelong intergenic non-protein coding RNA 1017 |
LINC01247 Genelong intergenic non-protein coding RNA 1247 |
LINC01242 Genelong intergenic non-protein coding RNA 1242 |
LINC01243 Genelong intergenic non-protein coding RNA 1243 |
LINC01532 Genelong intergenic non-protein coding RNA 1532 |
LINC01533 Genelong intergenic non-protein coding RNA 1533 |
LINC01530 Genelong intergenic non-protein coding RNA 1530 |
LINC01531 Genelong intergenic non-protein coding RNA 1531 |
LINC01537 Genelong intergenic non-protein coding RNA 1537 |
LINC01534 Genelong intergenic non-protein coding RNA 1534 |
LINC01535 Genelong intergenic non-protein coding RNA 1535 |
LINC01538 Genelong intergenic non-protein coding RNA 1538 |
LINC01539 Genelong intergenic non-protein coding RNA 1539 |
LINC00379 Genelong intergenic non-protein coding RNA 379 |
LINC00371 Genelong intergenic non-protein coding RNA 371 |
LINC00370 Genelong intergenic non-protein coding RNA 370 |
LINC00377 Genelong intergenic non-protein coding RNA 377 |
LINC00376 Genelong intergenic non-protein coding RNA 376 |
LINC00375 Genelong intergenic non-protein coding RNA 375 |
LINC00707 Genelong intergenic non-protein coding RNA 707 |
LINC00704 Genelong intergenic non-protein coding RNA 704 |
LINC00703 Genelong intergenic non-protein coding RNA 703 |
LINC00174 Genelong intergenic non-protein coding RNA 174 |
LINC00176 Genelong intergenic non-protein coding RNA 176 |
LINC00173 Genelong intergenic non-protein coding RNA 173 |
LINC00824 Genelong intergenic non-protein coding RNA 824 |
TRERNA1 Genetranslation regulatory long non-coding RNA 1 |
LINC01441 Genelong intergenic non-protein coding RNA 1441 |
LINC00706 Genelong intergenic non-protein coding RNA 706 |
LINC01146 Genelong intergenic non-protein coding RNA 1146 |
LINC01143 Genelong intergenic non-protein coding RNA 1143 |
LINC01142 Genelong intergenic non-protein coding RNA 1142 |
LINC01141 Genelong intergenic non-protein coding RNA 1141 |
LINC01149 Genelong intergenic non-protein coding RNA 1149 |
LINC00423 Genelong intergenic non-protein coding RNA 423 |
LINC00421 Genelong intergenic non-protein coding RNA 421 |
LINC00427 Genelong intergenic non-protein coding RNA 427 |
LINC00426 Genelong intergenic non-protein coding RNA 426 |
LINC00424 Genelong intergenic non-protein coding RNA 424 |
LINC00669 Genelong intergenic non-protein coding RNA 669 |
LINC00668 Genelong intergenic non-protein coding RNA 668 |
LINC00665 Genelong intergenic non-protein coding RNA 665 |
LINC00664 Genelong intergenic non-protein coding RNA 664 |
LINC00667 Genelong intergenic non-protein coding RNA 667 |
LINC00661 Genelong intergenic non-protein coding RNA 661 |
LINC00663 Genelong intergenic non-protein coding RNA 663 |
LINC00662 Genelong intergenic non-protein coding RNA 662 |
LINC00083 Genelong intergenic non-protein coding RNA 83 Predicted to enable carbohydrate binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00657 Genelong intergenic non-protein coding RNA 657 Predicted to enable protein sequestering activity. Predicted to be involved in several processes, including determination of adult lifespan; hair follicle development; and skeletal muscle fiber development. Predicted to be active in cytoplasm. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
ELDR GeneEGFR long non-coding downstream RNA Predicted to act upstream of or within regulation of gene expression and response to wounding. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01301 Genelong intergenic non-protein coding RNA 1301 |
LINC01305 Genelong intergenic non-protein coding RNA 1305 |
LINC01307 Genelong intergenic non-protein coding RNA 1307 |
LINC01477 Genelong intergenic non-protein coding RNA 1477 |
LINC01476 Genelong intergenic non-protein coding RNA 1476 |
LINC01475 Genelong intergenic non-protein coding RNA 1475 |
LINC01474 Genelong intergenic non-protein coding RNA 1474 |
LINC01471 Genelong intergenic non-protein coding RNA 1471 |
LINC01470 Genelong intergenic non-protein coding RNA 1470 |
LINC00434 Genelong intergenic non-protein coding RNA 434 |
ACSL3 Geneacyl-CoA synthetase long-chain family member 3 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in brain, and preferentially utilizes myristate, arachidonate, and eicosapentaenoate as substrates. The amino acid sequence of this isozyme is 92% identical to that of rat homolog. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
ACSL1 Geneacyl-CoA synthetase long-chain family member 1 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
ACSL6 Geneacyl-CoA synthetase long-chain family member 6 The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2011] |
LINC00431 Genelong intergenic non-protein coding RNA 431 |
ACSL4 Geneacyl-CoA synthetase long-chain family member 4 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016] |
ACSL5 Geneacyl-CoA synthetase long-chain family member 5 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in uterus and spleen, and in trace amounts in normal brain, but has markedly increased levels in malignant gliomas. This gene functions in mediating fatty acid-induced glioma cell growth. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LINC01511 Genelong intergenic non-protein coding RNA 1511 |
LINC01512 Genelong intergenic non-protein coding RNA 1512 |
LINC01517 Genelong intergenic non-protein coding RNA 1517 |
LINC01504 Genelong intergenic non-protein coding RNA 1504 |
LINC00238 Genelong intergenic non-protein coding RNA 238 |
LINC00239 Genelong intergenic non-protein coding RNA 239 |
LINC00235 Genelong intergenic non-protein coding RNA 235 |
LINC00900 Genelong intergenic non-protein coding RNA 900 |
LINC00901 Genelong intergenic non-protein coding RNA 901 |
LINC00903 Genelong intergenic non-protein coding RNA 903 |
LINC00904 Genelong intergenic non-protein coding RNA 904 |
LINC00905 Genelong intergenic non-protein coding RNA 905 |
LINC00906 Genelong intergenic non-protein coding RNA 906 |
LINC00907 Genelong intergenic non-protein coding RNA 907 |
LINC00908 Genelong intergenic non-protein coding RNA 908 |
LINC00397 Genelong intergenic non-protein coding RNA 397 |
LINC00572 Genelong intergenic non-protein coding RNA 572 |
LINC00575 Genelong intergenic non-protein coding RNA 575 |
LINC00574 Genelong intergenic non-protein coding RNA 574 |
LINC00577 Genelong intergenic non-protein coding RNA 577 |
LINC01587 Genelong intergenic non-protein coding RNA 1587 This gene is expressed in neuroblastoma; however, the function of this gene is not yet determined. [provided by RefSeq, Jul 2008] |
LINC01584 Genelong intergenic non-protein coding RNA 1584 |
LINC00622 Genelong intergenic non-protein coding RNA 622 |
LINC01054 Genelong intergenic non-protein coding RNA 1054 |
LINC01058 Genelong intergenic non-protein coding RNA 1058 |
KIR2DL3 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL2 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL1 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL4 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016] |
LINC00428 Genelong intergenic non-protein coding RNA 428 |
LINC01354 Genelong intergenic non-protein coding RNA 1354 |
LINC01355 Genelong intergenic non-protein coding RNA 1355 |
LINC01350 Genelong intergenic non-protein coding RNA 1350 |
LINC01019 Genelong intergenic non-protein coding RNA 1019 |
LINC01018 Genelong intergenic non-protein coding RNA 1018 |
LINC01013 Genelong intergenic non-protein coding RNA 1013 |
LINC01012 Genelong intergenic non-protein coding RNA 1012 |
LINC01015 Genelong intergenic non-protein coding RNA 1015 |
LINC01014 Genelong intergenic non-protein coding RNA 1014 |
LINC01016 Genelong intergenic non-protein coding RNA 1016 |
LINC00888 Genelong intergenic non-protein coding RNA 888 |
LINC01162 Genelong intergenic non-protein coding RNA 1162 |
LINC00919 Genelong intergenic non-protein coding RNA 919 |
LINC00914 Genelong intergenic non-protein coding RNA 914 |
LINC00705 Genelong intergenic non-protein coding RNA 705 |
LINC00700 Genelong intergenic non-protein coding RNA 700 |
LINC00701 Genelong intergenic non-protein coding RNA 701 |
LINC01359 Genelong intergenic non-protein coding RNA 1359 |
LINC01352 Genelong intergenic non-protein coding RNA 1352 |
LINC01586 Genelong intergenic non-protein coding RNA 1586 |
LINC00989 Genelong intergenic non-protein coding RNA 989 |
LINC00982 Genelong intergenic non-protein coding RNA 982 |
LINC00987 Genelong intergenic non-protein coding RNA 987 |
HAO2 Genehydroxyacid oxidase 2 (long chain) This gene is one of three related genes that have 2-hydroxyacid oxidase activity. The encoded protein localizes to the peroxisome has the highest activity toward the substrate 2-hydroxypalmitate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
LINC02618 Genelong intergenic non-protein coding RNA 2618 |
LINC02249 Genelong intergenic non-protein coding RNA 2249 |
LINC01963 Genelong intergenic non-protein coding RNA 1963 |
LNCTAM34A Genelong non coding transcriptional activator of miR34a |
LINC01833 Genelong intergenic non-protein coding RNA 1833 Predicted to be involved in regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01806 Genelong intergenic non-protein coding RNA 1806 |
LINC01788 Genelong intergenic non-protein coding RNA 1788 |
LINC01843 Genelong intergenic non-protein coding RNA 1843 |
LINC03040 Genelong intergenic non-protein coding RNA 3040 |
LINC01719 Genelong intergenic non-protein coding RNA 1719 |
LINC01772 Genelong intergenic non-protein coding RNA 1772 |
LINC02035 Genelong intergenic non-protein coding RNA 2035 |
LINC01781 Genelong intergenic non-protein coding RNA 1781 |
LINC02044 Genelong intergenic non-protein coding RNA 2044 |
LINC01852 Genelong intergenic non-protein coding RNA 1852 |
LINC01914 Genelong intergenic non-protein coding RNA 1914 |
LINC02102 Genelong intergenic non-protein coding RNA 2102 |
LINC01933 Genelong intergenic non-protein coding RNA 1933 |
LINC02904 Genelong intergenic non-protein coding RNA 2904 |
LINC02910 Genelong intergenic non-protein coding RNA 2910 |
LINC01814 Genelong intergenic non-protein coding RNA 1814 |
LINC02908 Genelong intergenic non-protein coding RNA 2908 |
LINC01829 Genelong intergenic non-protein coding RNA 1829 |
LINC00680 Genelong intergenic non-protein coding RNA 680 |
LINC02019 Genelong intergenic non-protein coding RNA 2019 |
LINC02094 Genelong intergenic non-protein coding RNA 2094 |
LINC02147 Genelong intergenic non-protein coding RNA 2147 |
LINC02012 Genelong intergenic non-protein coding RNA 2012 |
LINC01896 Genelong intergenic non-protein coding RNA 1896 |
LINC02185 Genelong intergenic non-protein coding RNA 2185 |
LINC01828 Genelong intergenic non-protein coding RNA 1828 |
LINC01619 Genelong intergenic non-protein coding RNA 1619 |
LINC01679 Genelong intergenic non-protein coding RNA 1679 |
PRECSIT Genep53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcript |
LINC02208 Genelong intergenic non-protein coding RNA 2208 |
LINC02210 Genelong intergenic non-protein coding RNA 2210 |
LINC03011 Genelong intergenic non-protein coding RNA 3011 |
LINC01702 Genelong intergenic non-protein coding RNA 1702 |
LINC02037 Genelong intergenic non-protein coding RNA 2037 |
LINC02197 Genelong intergenic non-protein coding RNA 2197 |
LINC01595 Genelong intergenic non-protein coding RNA 1595 Implicated in prostate cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC02898 Genelong intergenic non-protein coding RNA 2898 |
LINC02716 Genelong intergenic non-protein coding RNA 2716 |
LINC02116 Genelong intergenic non-protein coding RNA 2116 |
LINC01713 Genelong intergenic non-protein coding RNA 1713 |
LINC02174 Genelong intergenic non-protein coding RNA 2174 |
LINC02052 Genelong intergenic non-protein coding RNA 2052 |
LINC00449 Genelong intergenic non-protein coding RNA 449 |
LINC02084 Genelong intergenic non-protein coding RNA 2084 |
LINC01980 Genelong intergenic non-protein coding RNA 1980 |
LINC01876 Genelong intergenic non-protein coding RNA 1876 |
LINC02167 Genelong intergenic non-protein coding RNA 2167 |
LINC02212 Genelong intergenic non-protein coding RNA 2212 |
LINC02145 Genelong intergenic non-protein coding RNA 2145 |
LINC02905 Genelong intergenic non-protein coding RNA 2905 |
LINC02693 Genelong intergenic non-protein coding RNA 2693 |
LINC01978 Genelong intergenic non-protein coding RNA 1978 |
LINC01979 Genelong intergenic non-protein coding RNA 1979 |
LINC02015 Genelong intergenic non-protein coding RNA 2015 |
LINC01625 Genelong intergenic non-protein coding RNA 1625 |
LINC02202 Genelong intergenic non-protein coding RNA 2202 |
LINC01786 Genelong intergenic non-protein coding RNA 1786 |
LINC01714 Genelong intergenic non-protein coding RNA 1714 |
LINC02028 Genelong intergenic non-protein coding RNA 2028 |
HISLA GeneHIF1A stabilizing long noncoding RNA |
LINC01836 Genelong intergenic non-protein coding RNA 1836 |
LINC01977 Genelong intergenic non-protein coding RNA 1977 |
LINC01907 Genelong intergenic non-protein coding RNA 1907 |
LINC01748 Genelong intergenic non-protein coding RNA 1748 |
ARLNC1 Geneandrogen receptor regulated long noncoding RNA 1 |
LINC01754 Genelong intergenic non-protein coding RNA 1754 |
LINC01770 Genelong intergenic non-protein coding RNA 1770 |
MINCR GeneMYC-induced long non-coding RNA |
LINC02086 Genelong intergenic non-protein coding RNA 2086 |
LINC02193 Genelong intergenic non-protein coding RNA 2193 |
LINC01819 Genelong intergenic non-protein coding RNA 1819 |
LINC02018 Genelong intergenic non-protein coding RNA 2018 |
LINC01869 Genelong intergenic non-protein coding RNA 1869 |
MALINC1 Genemitosis associated long intergenic non-coding RNA 1 |
LINC02106 Genelong intergenic non-protein coding RNA 2106 |
LINC02076 Genelong intergenic non-protein coding RNA 2076 |
LINC02021 Genelong intergenic non-protein coding RNA 2021 |
LINC01915 Genelong intergenic non-protein coding RNA 1915 |
LINC01881 Genelong intergenic non-protein coding RNA 1881 |
LINC01801 Genelong intergenic non-protein coding RNA 1801 |
LINC01750 Genelong intergenic non-protein coding RNA 1750 |
LINC02175 Genelong intergenic non-protein coding RNA 2175 |
LINC02188 Genelong intergenic non-protein coding RNA 2188 |
LINC02913 Genelong intergenic non-protein coding RNA 2913 |
LINC02897 Genelong intergenic non-protein coding RNA 2897 |
LINC02875 Genelong intergenic non-protein coding RNA 2875 |
LINC01238 Genelong intergenic non-protein coding RNA 1238 |
LINC01943 Genelong intergenic non-protein coding RNA 1943 |
LINC02881 Genelong intergenic non-protein coding RNA 2881 |
LINC01345 Genelong intergenic non-protein coding RNA 1345 |
LINC02692 Genelong intergenic non-protein coding RNA 2692 |
LINC02107 Genelong intergenic non-protein coding RNA 2107 |
LINC01874 Genelong intergenic non-protein coding RNA 1874 |
LINC01707 Genelong intergenic non-protein coding RNA 1707 |
LINC01697 Genelong intergenic non-protein coding RNA 1697 |
LINC01684 Genelong intergenic non-protein coding RNA 1684 |
LINC01816 Genelong intergenic non-protein coding RNA 1816 |
LINC01626 Genelong intergenic non-protein coding RNA 1626 |
LINC01623 Genelong intergenic non-protein coding RNA 1623 |
LINC01612 Genelong intergenic non-protein coding RNA 1612 |
LINC01643 Genelong intergenic non-protein coding RNA 1643 |
LINC01647 Genelong intergenic non-protein coding RNA 1647 |
LINC01655 Genelong intergenic non-protein coding RNA 1655 |
LINC01667 Genelong intergenic non-protein coding RNA 1667 |
LINC01749 Genelong intergenic non-protein coding RNA 1749 |
LINC01747 Genelong intergenic non-protein coding RNA 1747 |
LINC01744 Genelong intergenic non-protein coding RNA 1744 |
LINC01743 Genelong intergenic non-protein coding RNA 1743 |
LINC01739 Genelong intergenic non-protein coding RNA 1739 |
LINC01728 Genelong intergenic non-protein coding RNA 1728 |
LINC01723 Genelong intergenic non-protein coding RNA 1723 |
LINC01718 Genelong intergenic non-protein coding RNA 1718 |
LINC01712 Genelong intergenic non-protein coding RNA 1712 |
LINC01704 Genelong intergenic non-protein coding RNA 1704 |
LINC01677 Genelong intergenic non-protein coding RNA 1677 |
LINC01676 Genelong intergenic non-protein coding RNA 1676 |
LINC01673 Genelong intergenic non-protein coding RNA 1673 |
LINC01672 Genelong intergenic non-protein coding RNA 1672 |
LINC01374 Genelong intergenic non-protein coding RNA 1374 |
LINC01297 Genelong intergenic non-protein coding RNA 1297 |
LINC01755 Genelong intergenic non-protein coding RNA 1755 |
LINC01760 Genelong intergenic non-protein coding RNA 1760 |
LINC01763 Genelong intergenic non-protein coding RNA 1763 |
LINC01764 Genelong intergenic non-protein coding RNA 1764 |
LINC02046 Genelong intergenic non-protein coding RNA 2046 |
LINC02045 Genelong intergenic non-protein coding RNA 2045 |
LINC02040 Genelong intergenic non-protein coding RNA 2040 |
LINC02039 Genelong intergenic non-protein coding RNA 2039 |
LINC02034 Genelong intergenic non-protein coding RNA 2034 |
LINC02032 Genelong intergenic non-protein coding RNA 2032 |
LINC02025 Genelong intergenic non-protein coding RNA 2025 |
LINC02022 Genelong intergenic non-protein coding RNA 2022 |
LINC02020 Genelong intergenic non-protein coding RNA 2020 |
LINC02013 Genelong intergenic non-protein coding RNA 2013 |
LINC01999 Genelong intergenic non-protein coding RNA 1999 |
LINC01995 Genelong intergenic non-protein coding RNA 1995 |
LINC01988 Genelong intergenic non-protein coding RNA 1988 |
LINC01986 Genelong intergenic non-protein coding RNA 1986 |
LINC02056 Genelong intergenic non-protein coding RNA 2056 |
LINC02064 Genelong intergenic non-protein coding RNA 2064 |
LINC02166 Genelong intergenic non-protein coding RNA 2166 |
LINC02165 Genelong intergenic non-protein coding RNA 2165 |
LINC02156 Genelong intergenic non-protein coding RNA 2156 |
LINC02152 Genelong intergenic non-protein coding RNA 2152 |
LINC02117 Genelong intergenic non-protein coding RNA 2117 |
LINC02114 Genelong intergenic non-protein coding RNA 2114 |
LINC02113 Genelong intergenic non-protein coding RNA 2113 |
LINC02110 Genelong intergenic non-protein coding RNA 2110 |
LINC02103 Genelong intergenic non-protein coding RNA 2103 |
LINC02096 Genelong intergenic non-protein coding RNA 2096 |
LINC02089 Genelong intergenic non-protein coding RNA 2089 |
LINC02087 Genelong intergenic non-protein coding RNA 2087 |
LINC02079 Genelong intergenic non-protein coding RNA 2079 |
LINC02072 Genelong intergenic non-protein coding RNA 2072 |
LINC02069 Genelong intergenic non-protein coding RNA 2069 |
LINC02059 Genelong intergenic non-protein coding RNA 2059 |
LINC01976 Genelong intergenic non-protein coding RNA 1976 |
LINC01944 Genelong intergenic non-protein coding RNA 1944 |
LINC01855 Genelong intergenic non-protein coding RNA 1855 |
LINC01851 Genelong intergenic non-protein coding RNA 1851 |
LINC01849 Genelong intergenic non-protein coding RNA 1849 |
LINC01846 Genelong intergenic non-protein coding RNA 1846 |
LINC01844 Genelong intergenic non-protein coding RNA 1844 |
LINC01837 Genelong intergenic non-protein coding RNA 1837 |
LINC01818 Genelong intergenic non-protein coding RNA 1818 |
LINC01815 Genelong intergenic non-protein coding RNA 1815 |
LINC01803 Genelong intergenic non-protein coding RNA 1803 |
LINC01799 Genelong intergenic non-protein coding RNA 1799 |
LINC01783 Genelong intergenic non-protein coding RNA 1783 Predicted to enable triplet codon-amino acid adaptor activity. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01778 Genelong intergenic non-protein coding RNA 1778 |
LINC01766 Genelong intergenic non-protein coding RNA 1766 |
LINC01872 Genelong intergenic non-protein coding RNA 1872 |
LINC01962 Genelong intergenic non-protein coding RNA 1962 |
LINC01878 Genelong intergenic non-protein coding RNA 1878 |
LINC01888 Genelong intergenic non-protein coding RNA 1888 |
LINC01938 Genelong intergenic non-protein coding RNA 1938 |
LINC01937 Genelong intergenic non-protein coding RNA 1937 |
LINC01931 Genelong intergenic non-protein coding RNA 1931 |
LINC01927 Genelong intergenic non-protein coding RNA 1927 |
LINC01925 Genelong intergenic non-protein coding RNA 1925 |
LINC01923 Genelong intergenic non-protein coding RNA 1923 |
LINC01919 Genelong intergenic non-protein coding RNA 1919 |
LINC01917 Genelong intergenic non-protein coding RNA 1917 |
LINC01913 Genelong intergenic non-protein coding RNA 1913 |
LINC01912 Genelong intergenic non-protein coding RNA 1912 |
LINC01911 Genelong intergenic non-protein coding RNA 1911 |
LINC01909 Genelong intergenic non-protein coding RNA 1909 |
LINC01905 Genelong intergenic non-protein coding RNA 1905 |
LINC01899 Genelong intergenic non-protein coding RNA 1899 |
LINC01890 Genelong intergenic non-protein coding RNA 1890 |
LINC01884 Genelong intergenic non-protein coding RNA 1884 |
LINC00390 Genelong intergenic non-protein coding RNA 390 |
LINC01052 Genelong intergenic non-protein coding RNA 1052 |
LINC01066 Genelong intergenic non-protein coding RNA 1066 |
LINC02016 Genelong intergenic non-protein coding RNA 2016 |
LINC01694 Genelong intergenic non-protein coding RNA 1694 |
LINC02587 Genelong intergenic non-protein coding RNA 2587 |
LINC02204 Genelong intergenic non-protein coding RNA 2204 |
LINC01785 Genelong intergenic non-protein coding RNA 1785 |
LINC02207 Genelong intergenic non-protein coding RNA 2207 |
LINC02446 Genelong intergenic non-protein coding RNA 2446 |
LINC01857 Genelong intergenic non-protein coding RNA 1857 |
LINC01871 Genelong intergenic non-protein coding RNA 1871 |
GRASLND Geneglycosaminoglycan regulatory associated long non-coding RNA |
LINC01762 Genelong intergenic non-protein coding RNA 1762 |
LINC02027 Genelong intergenic non-protein coding RNA 2027 |
LINC01924 Genelong intergenic non-protein coding RNA 1924 |
LINC01934 Genelong intergenic non-protein coding RNA 1934 |
LINC02251 Genelong intergenic non-protein coding RNA 2251 |
LINC02397 Genelong intergenic non-protein coding RNA 2397 |
LINC01967 Genelong intergenic non-protein coding RNA 1967 |
LINC01357 Genelong intergenic non-protein coding RNA 1357 |
LINC02593 Genelong intergenic non-protein coding RNA 2593 |
LINC02362 Genelong intergenic non-protein coding RNA 2362 |
LINC02523 Genelong intergenic non-protein coding RNA 2523 |
LINC01717 Genelong intergenic non-protein coding RNA 1717 |
LINC02009 Genelong intergenic non-protein coding RNA 2009 |
LINC01724 Genelong intergenic non-protein coding RNA 1724 |
LINC02437 Genelong intergenic non-protein coding RNA 2437 |
LINC01965 Genelong intergenic non-protein coding RNA 1965 |
LINC02836 Genelong intergenic non-protein coding RNA 2836 |
LINC02785 Genelong intergenic non-protein coding RNA 2785 |
LINC01831 Genelong intergenic non-protein coding RNA 1831 |
LINC02053 Genelong intergenic non-protein coding RNA 2053 |
LINC02768 Genelong intergenic non-protein coding RNA 2768 |
LINC02360 Genelong intergenic non-protein coding RNA 2360 |
LINC02237 Genelong intergenic non-protein coding RNA 2237 |
LINC02511 Genelong intergenic non-protein coding RNA 2511 |
LINC01695 Genelong intergenic non-protein coding RNA 1695 |
LINC02901 Genelong intergenic non-protein coding RNA 2901 |
LINC02888 Genelong intergenic non-protein coding RNA 2888 |
LINC02903 Genelong intergenic non-protein coding RNA 2903 |
LINC02899 Genelong intergenic non-protein coding RNA 2899 |
C3ORF86P Genelong intergenic non-protein coding RNA 694 |
LINC02694 Genelong intergenic non-protein coding RNA 2694 |
LINC02902 Genelong intergenic non-protein coding RNA 2902 |
LINC02798 Genelong intergenic non-protein coding RNA 2798 |
LINC02615 Genelong intergenic non-protein coding RNA 2615 |
LINC02696 Genelong intergenic non-protein coding RNA 2696 |
LINC02614 Genelong intergenic non-protein coding RNA 2614 |
LINC02609 Genelong intergenic non-protein coding RNA 2609 |
LINC02981 Genelong intergenic non-protein coding RNA 2981 |
LINC02731 Genelong intergenic non-protein coding RNA 2731 |
LINC02987 Genelong intergenic non-protein coding RNA 2987 |
LINC02544 Genelong intergenic non-protein coding RNA 2544 |
LINC02649 Genelong intergenic non-protein coding RNA 2649 |
LINC02728 Genelong intergenic non-protein coding RNA 2728 |
LINC02803 Genelong intergenic non-protein coding RNA 2803 |
LINC02349 Genelong intergenic non-protein coding RNA 2349 |
LINC02539 Genelong intergenic non-protein coding RNA 2539 |
LINC03002 Genelong intergenic non-protein coding RNA 3002 |
LINC02381 Genelong intergenic non-protein coding RNA 2381 |
LINC02232 Genelong intergenic non-protein coding RNA 2232 |
LINC03100 Genelong intergenic non-protein coding RNA 3100 |
LINC02894 Genelong intergenic non-protein coding RNA 2894 |
LINC02328 Genelong intergenic non-protein coding RNA 2328 |
LINC01779 Genelong intergenic non-protein coding RNA 1779 |
LINC03135 Genelong intergenic non-protein coding RNA 3135 |
LINC02965 Genelong intergenic non-protein coding RNA 2965 |
LINC03052 Genelong intergenic non-protein coding RNA 3052 |
LINC02235 Genelong intergenic non-protein coding RNA 2235 |
LINC02576 Genelong intergenic non-protein coding RNA 2576 |
LINC02560 Genelong intergenic non-protein coding RNA 2560 |
LINC02762 Genelong intergenic non-protein coding RNA 2762 |
LINC02610 Genelong intergenic non-protein coding RNA 2610 |
LINC02854 Genelong intergenic non-protein coding RNA 2854 |
LINC02983 Genelong intergenic non-protein coding RNA 2983 |
LINC02268 Genelong intergenic non-protein coding RNA 2268 |
LINC02893 Genelong intergenic non-protein coding RNA 2893 |
LOC105379427 Genezinc finger protein 717-like |
LOC442041 Genezinc finger protein 532 pseudogene |
RFPL4AL1 Generet finger protein-like 4A-like 1 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF117 Genezinc finger protein 117 This gene encodes a protein containing multiple C2H2-type zinc finger motifs. Readthrough transcription occurs between this gene and the upstream endogenous retrovirus group 3 member 1 (ERV3-1) locus, and may result in additional transcript variants encoding the zinc finger protein. [provided by RefSeq, Jan 2017] |
ZNF114 Genezinc finger protein 114 Enables identical protein binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF112 Genezinc finger protein 112 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P3Y Genezinc finger protein 736 pseudogene 3, Y-linked |
LOC100419801 Genezinc finger protein 532 pseudogene |
LOC100419803 Genezinc finger protein 510 pseudogene |
LOC100419802 Genezinc finger protein 184 pseudogene |
LOC100419806 Genezinc finger protein 519 pseudogene |
ZNF831 Genezinc finger protein 831 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF830 Genezinc finger protein 830 Predicted to enable nucleic acid binding activity and zinc ion binding activity. Predicted to be involved in several processes, including mitotic DNA integrity checkpoint signaling; nuclear DNA replication; and preantral ovarian follicle growth. Predicted to act upstream of or within several processes, including blastocyst growth; chromosome organization; and intestinal epithelial structure maintenance. Predicted to be located in nucleoplasm. Predicted to be part of spliceosomal complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF835 Genezinc finger protein 835 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF837 Genezinc finger protein 837 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF836 Genezinc finger protein 836 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF839 Genezinc finger protein 839 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF304 Genezinc finger protein 304 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein functions as a transcriptional repressor that recruits a corepressor complex to stimulate promoter hypermethylation and transcriptional silencing of target genes. Expression of this gene is upregulated in colorectal, ovarian and breast cancer, and this gene may promote cancer cell survival, growth and invasion. [provided by RefSeq, Jul 2016] |
ZNF302 Genezinc finger protein 302 This gene encodes a member of the zinc-finger protein family. The encoded protein contains seven C2H2-type zinc fingers and a KRAB domain, but its function has yet to be determined. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2014] |
ZNF300 Genezinc finger protein 300 The protein encoded by this gene is a C2H2-type zinc finger DNA binding protein and likely transcriptional regulator. The function of this protein is not yet known. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010] |
LOC100419755 Genezinc finger protein 426 pseudogene |
ZSCAN5CP Genezinc finger and SCAN domain containing 5C, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM5P3 Genezinc finger, SWIM-type containing 5 pseudogene 3 |
ZSWIM5P2 Genezinc finger, SWIM-type containing 5 pseudogene 2 |
ZSWIM5P1 Genezinc finger, SWIM-type containing 5 pseudogene 1 |
ZNF848P Genezinc finger protein 848, pseudogene |
RNF175 Genering finger protein 175 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ERAD pathway. Predicted to be located in membrane. Predicted to be active in Golgi membrane and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF170 Genering finger protein 170 This gene encodes a RING domain-containing protein that resides in the endoplasmic reticulum (ER) membrane. This protein functions as an E3 ubiquitin ligase and mediates ubiquitination and processing of inositol 1,4,5-trisphosphate (IP3) receptors via the ER-associated protein degradation pathway. It is recruited to the activated IP3 receptors by the ERLIN1/ERLIN2 complex to which it is constitutively bound. Mutations in this gene are associated with autosomal dominant sensory ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012] |
ZBTB7A Genezinc finger and BTB domain containing 7A Enables several functions, including SMAD binding activity; nuclear androgen receptor binding activity; and transcription corepressor binding activity. Involved in several processes, including erythrocyte maturation; negative regulation of signal transduction; and regulation of nucleobase-containing compound metabolic process. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB7C Genezinc finger and BTB domain containing 7C Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of cell population proliferation. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB7B Genezinc finger and BTB domain containing 7B This gene encodes a zinc finger-containing transcription factor that acts as a key regulator of lineage commitment of immature T-cell precursors. It is necessary and sufficient for commitment of CD4 lineage, while its absence causes CD8 commitment. It also functions as a transcriptional repressor of type I collagen genes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012] |
ZNF605 Genezinc finger protein 605 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC23 Genezinc finger, CCHC domain containing 23 Predicted to enable nucleic acid binding activity and zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC24 Genezinc finger, CCHC domain containing 24 Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421259 Genezinc finger and BTB domain containing 14 pseudogene |
UNKL Geneunkempt family zinc finger-like This gene encodes a RING finger protein that may function in Rac signaling. It can bind to Brg/Brm-associated factor 60b and can promote its ubiquitination. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2013] |
ZNF733P Genezinc finger protein 733, pseudogene |
ZDHHC3 Genezinc finger, DHHC-type containing 3 Enables palmitoyltransferase activity. Involved in several processes, including protein localization to membrane; protein localization to photoreceptor outer segment; and regulation of signal transduction. Located in membrane. Is active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419888 Genezinc finger protein 331 pseudogene |
ZNF213 Genezinc finger protein 213 C2H2 zinc finger proteins, such as ZNF213, have bipartite structures in which one domain binds DNA or RNA and the other modulates target gene expression.[supplied by OMIM, Apr 2004] |
ZNF419 Genezinc finger protein 419 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF418 Genezinc finger protein 418 Enables DNA-binding transcription repressor activity. Predicted to be involved in microautophagy; regulation of proteasomal ubiquitin-dependent protein catabolic process; and regulation of transcription by RNA polymerase II. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF417 Genezinc finger protein 417 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF416 Genezinc finger protein 416 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in microautophagy; regulation of proteasomal ubiquitin-dependent protein catabolic process; and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within cardiac muscle hypertrophy; negative regulation of cell growth involved in cardiac muscle cell development; and negative regulation of protein phosphorylation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF415 Genezinc finger protein 415 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in fibrillar center and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF414 Genezinc finger protein 414 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF410 Genezinc finger protein 410 Enables DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of gene expression and positive regulation of transcription by RNA polymerase II. Predicted to be located in chromosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF726P1 Genezinc finger protein 726 pseudogene 1 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130632 Genezinc finger protein 530-like |
ZNF658 Genezinc finger protein 658 Enables transcription cis-regulatory region binding activity. Involved in cellular response to zinc ion; negative regulation of DNA-templated transcription; and ribosome biogenesis. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF655 Genezinc finger protein 655 This gene encodes a zinc finger protein. The zinc finger proteins are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
ZNF653 Genezinc finger protein 653 Enables AF-2 domain binding activity; DNA-binding transcription factor binding activity; and transcription corepressor activity. Involved in extracellular negative regulation of signal transduction and negative regulation of transcription by RNA polymerase II. Predicted to be located in extracellular region. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF652 Genezinc finger protein 652 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF384 Genezinc finger protein 384 This gene encodes a C2H2-type zinc finger protein, which may function as a transcription factor. This gene also contains long CAG trinucleotide repeats that encode consecutive glutamine residues. The protein appears to bind and regulate the promoters of the extracellular matrix genes MMP1, MMP3, MMP7 and COL1A1. Studies in mouse suggest that nuclear matrix transcription factors (NP/NMP4) may be part of a general mechanical pathway that couples cell construction and function during extracellular matrix remodeling. Alternative splicing results in multiple transcript variants. Recurrent rearrangements of this gene with the Ewing's sarcoma gene, EWSR1 on chromosome 22, or with the TAF15 gene on chromosome 17, or with the TCF3 (E2A) gene on chromosome 19, have been observed in acute leukemia. A related pseudogene has been identified on chromosome 7. [provided by RefSeq, Apr 2011] |
ZNF383 Genezinc finger protein 383 The protein encoded by this gene is a KRAB-related zinc finger protein that inhibits the transcription of some MAPK signaling pathway genes. The repressor activity resides in the KRAB domain of the encoded protein. [provided by RefSeq, Sep 2016] |
ZFP41 GeneZFP41 zinc finger protein Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP42 GeneZFP42 zinc finger protein Enables sequence-specific double-stranded DNA binding activity. Involved in female gonad development and male gonad development. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RFWD2P1 Genering finger and WD repeat domain 2, E3 ubiquitin protein ligase pseudogene 1 |
LOC100419762 Genezinc finger protein 773 pseudogene |
ZMYND19P1 Genezinc finger, MYND-type containing 19 pseudogene 1 |
ZFHX4 Genezinc finger homeobox 4 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130861 Genezinc finger protein 736 pseudogene |
RFFL Genering finger and FYVE-like domain containing E3 ubiquitin protein ligase Enables enzyme binding activity; p53 binding activity; and ubiquitin protein ligase activity. Involved in several processes, including negative regulation of cysteine-type endopeptidase activity; negative regulation of signal transduction; and protein K48-linked ubiquitination. Located in endosome membrane and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZFHX3 Genezinc finger homeobox 3 This gene encodes a transcription factor with multiple homeodomains and zinc finger motifs, and regulates myogenic and neuronal differentiation. The encoded protein suppresses expression of the alpha-fetoprotein gene by binding to an AT-rich enhancer motif. The protein has also been shown to negatively regulate c-Myb, and transactivate the cell cycle inhibitor cyclin-dependent kinase inhibitor 1A (also known as p21CIP1). This gene is reported to function as a tumor suppressor in several cancers, and sequence variants of this gene are also associated with atrial fibrillation. Multiple transcript variants expressed from alternate promoters and encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
MKRN6P Genemakorin ring finger protein 6, pseudogene |
ZNF192P2 Genezinc finger protein 192 pseudogene 2 |
ZNF192P1 Genezinc finger protein 192 pseudogene 1 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
PHF5EP GenePHD finger protein 5E pseudogene |
RFPL4B Generet finger protein-like 4B Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in several processes, including defense response to symbiont; negative regulation of viral entry into host cell; and negative regulation of viral transcription. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL4A Generet finger protein-like 4A Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be located in female germ cell nucleus. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
MARCH11 Genemembrane-associated ring finger (C3HC4) 11 MARCH11 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). These enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their intracellular transport. March11 appears to have a role in ubiquitin-mediated protein sorting in the trans-Golgi network (TGN)-multivesicular body (MVB) transport pathway (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
MARCH10 Genemembrane-associated ring finger (C3HC4) 10, E3 ubiquitin protein ligase MARCH10 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
LOC730076 Genezinc finger domain containing pseudogene |
ZNF497 Genezinc finger protein 497 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF496 Genezinc finger protein 496 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in positive regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF493 Genezinc finger protein 493 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF490 Genezinc finger protein 490 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105376669 Generet finger protein-like 4A |
LOC646629 Genezinc finger protein 470 pseudogene |
ZNF826P Genezinc finger protein 826, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF20 GenePHD finger protein 20 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nuclear membrane; and nucleoplasm. Part of MLL1 complex and NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
PHF23 GenePHD finger protein 23 Predicted to enable metal ion binding activity. Involved in negative regulation of autophagosome assembly; negative regulation of autophagosome maturation; and positive regulation of protein ubiquitination. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF519P3 Genezinc finger protein 519 pseudogene 3 |
ZIM2 Genezinc finger, imprinted 2 In human, ZIM2 and PEG3 (GeneID:5178) are two distinct genes that share a set of 5' exons and have a common promoter, and both genes are paternally expressed. Alternative splicing events connect the shared exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. This is in contrast to mouse and cow, where ZIM2 and PEG3 genes do not share exons in common, and the imprinting status of ZIM2 is also not conserved amongst mammals. Additional 5' alternatively spliced transcripts encoding the same protein have been found for the human ZIM2 gene. [provided by RefSeq, Oct 2010] |
ZIM3 Genezinc finger, imprinted 3 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
GATAD1 GeneGATA zinc finger domain containing 1 The protein encoded by this gene contains a zinc finger at the N-terminus, and is thought to bind to a histone modification site that regulates gene expression. Mutations in this gene have been associated with autosomal recessive dilated cardiomyopathy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012] |
PYGO1 Genepygopus family PHD finger 1 Enables methylated histone binding activity. Predicted to be involved in kidney development and spermatid nucleus differentiation. Predicted to act upstream of or within several processes, including hematopoietic progenitor cell differentiation; positive regulation of transcription by RNA polymerase II; and spermatid development. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PYGO2 Genepygopus family PHD finger 2 Predicted to enable several functions, including chromatin binding activity; histone acetyltransferase regulator activity; and histone binding activity. Predicted to be involved in kidney development and spermatid nucleus differentiation. Predicted to act upstream of or within several processes, including canonical Wnt signaling pathway; lens development in camera-type eye; and regulation of mammary gland epithelial cell proliferation. Part of beta-catenin-TCF complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF519 Genezinc finger protein 519 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and chromatin binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF512 Genezinc finger protein 512 This gene encodes a protein containing four putative zinc finger motifs. Zinc finger motifs may bind to proteins or nucleic acids. Zinc finger-containing proteins are involved in a variety of processes, including regulation of transcription. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012] |
ZNF513 Genezinc finger protein 513 The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011] |
ZNF510 Genezinc finger protein 510 This gene encodes a krueppel C2H2-type zinc-finger protein family member. The encoded protein is expressed in several cancer cell types and may be a biomarker for early diagnosis of these cancers. [provided by RefSeq, Sep 2015] |
ZNF511 Genezinc finger protein 511 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF516 Genezinc finger protein 516 Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc-finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. [provided by RefSeq, Sep 2012] |
ZNF514 Genezinc finger protein 514 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF208 Genering finger protein 208 Enables ubiquitin-protein transferase activity. Involved in protein autoubiquitination. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF207 Genering finger protein 207 Enables Hsp70 protein binding activity and transmembrane transporter binding activity. Involved in positive regulation of gene expression. Located in perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CNBP GeneCCHC-type zinc finger, nucleic acid binding protein This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion from <30 repeats to 75-11000 repeats in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2016] |
LOC100421122 Genezinc finger protein 106 homolog (mouse) pseudogene |
ZNF75D Genezinc finger protein 75D This gene encodes a protein that likely functions as a transcription factor. The protein, which belongs to the ZNF75 family, includes an N-terminal SCAN domain, a KRAB box, and five C2H2-type zinc finger motifs. Another functional gene belonging to this family is located on chromosome 16, while pseudogenes have been identified on chromosomes 11 and 12. Alternative splicing results in multiple transcripts variants. [provided by RefSeq, Jun 2010] |
LOC100533635 Genezinc finger protein 384 pseudogene |
RNF11P2 Genering finger protein 11 pseudogene 2 |
RNF11P1 Genering finger protein 11 pseudogene 1 |
ZNF750 Genezinc finger protein 750 This gene encodes a protein with a nuclear localization site and a C2H2 zinc finger domain. Mutations in this gene have been associated with seborrhea-like dermatitis with psoriasiform elements. [provided by RefSeq, Jul 2008] |
LOC100533638 Genezinc finger protein 85 pseudogene |
LOC100289442 GenePHD finger protein 5A pseudogene |
LOC647253 Genering finger protein 13 pseudogene |
LOC728376 Genezinc finger protein 430 pseudogene |
ZGLP1 Genezinc finger, GATA-like protein 1 ZGLP1 encodes an evolutionary conserved transcriptional regulator with GATA-like zinc fingers. In females, it is expressed in embryonic germ cells and is essential for oogenic fate determination. It acts downstream of bone morphogenetic protein (BMP) and is involved in the regulation of genes involved in RNA processing, transcription and chromatin modification, retrotransposon regulation, meiotic cell cycle, and oocyte development. In males it is not required for the germ cell sex determination but is required by the spermatogonia for efficiently completing the meiotic prophase. [provided by RefSeq, Jul 2022] |
ZC3H12A Genezinc finger CCCH-type containing 12A ZC3H12A is an MCP1 (CCL2; MIM 158105)-induced protein that acts as a transcriptional activator and causes cell death of cardiomyocytes, possibly via induction of genes associated with apoptosis.[supplied by OMIM, Mar 2008] |
ZC3H12B Genezinc finger CCCH-type containing 12B The protein encoded by this gene belongs to a family of CCCH-type zinc finger proteins that are involved in the proinflammatory activation of macrophages. The exact function of this family member is unknown, but it is thought to function as a ribonuclease. [provided by RefSeq, May 2010] |
ZC3H12C Genezinc finger CCCH-type containing 12C Predicted to enable RNA endonuclease activity and mRNA binding activity. Predicted to be active in cytoplasmic ribonucleoprotein granule and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H12D Genezinc finger CCCH-type containing 12D Predicted to enable RNA endonuclease activity and mRNA binding activity. Involved in negative regulation of G1/S transition of mitotic cell cycle and negative regulation of cell growth. Located in P-body and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TSRM Genezinc finger domain-related protein TSRM |
ZFYVE21 Genezinc finger, FYVE domain containing 21 Predicted to enable metal ion binding activity. Predicted to be located in endosome and focal adhesion. [provided by Alliance of Genome Resources, Mar 2025] |
RNF19BPX Genering finger protein 19B pseudogene, X-linked |
RNF19BPY Genering finger protein 19B pseudogene, Y-linked |
LOC100419752 Genezinc finger protein 251 pseudogene |
DNLZ GeneDNL-type zinc finger Enables protein folding chaperone. Involved in chaperone-mediated protein complex assembly. Located in nucleoplasm. Is active in cytosol; mitochondrion; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF273 Genezinc finger protein 273 This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with 13 C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in transcriptional regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008] |
ZNF277 Genezinc finger protein 277 Predicted to enable RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and metal ion binding activity. Predicted to act upstream of or within cellular response to hydrogen peroxide and regulation of cellular senescence. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF276 Genezinc finger protein 276 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in kinetochore. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF275 Genezinc finger protein 275 This gene encodes a zinc finger protein that appears to be conserved in eutheria. Its function has not yet been established. [provided by RefSeq, Jul 2010] |
ZNF274 Genezinc finger protein 274 This gene encodes a zinc finger protein containing five C2H2-type zinc finger domains, one or two Kruppel-associated box A (KRAB A) domains, and a leucine-rich domain. The encoded protein has been suggested to be a transcriptional repressor. It localizes predominantly to the nucleolus. Alternatively spliced transcript variants encoding different isoforms exist. These variants utilize alternative polyadenylation signals. [provided by RefSeq, Jul 2008] |
ZBTB45P2 Genezinc finger and BTB domain containing 45 pseudogene 2 |
ZBTB45P1 Genezinc finger and BTB domain containing 45 pseudogene 1 |
LOC100652813 Genezinc finger protein 138 pseudogene |
LOC100419830 Genezinc finger protein 337 pseudogene |
LOC100419834 Genezinc finger protein 134 pseudogene |
LOC100419836 Genezinc finger protein 347 pseudogene |
LOC100419838 Genezinc finger protein 860 pseudogene |
LOC100419839 Genezinc finger protein 300 pseudogene |
ZNF815P Genezinc finger protein 815, pseudogene |
LOC644006 Genering finger protein 4 pseudogene |
LOC100131479 Genezinc finger protein 430 pseudogene |
ZNF841 Genezinc finger protein 841 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF843 Genezinc finger protein 843 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF844 Genezinc finger protein 844 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF846 Genezinc finger protein 846 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF592 Genezinc finger protein 592 This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011] |
ZNF593 Genezinc finger protein 593 Enables preribosome binding activity and zinc ion binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF596 Genezinc finger protein 596 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF595 Genezinc finger protein 595 This gene encodes a protein belonging to the Cys2His2 zinc finger protein family, whose members function as transcription factors that can regulate a broad variety of developmental and cellular processes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Oct 2013] |
ZNF598 Genezinc finger protein 598 Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This protein and Grb10-interacting GYF protein 2 have been identified as a components of the mammalian 4EHP (m4EHP) complex. The complex is thought to function as a translation repressor in embryonic development. [provided by RefSeq, Oct 2012] |
ZNF599 Genezinc finger protein 599 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFR2 Genezinc finger RNA binding protein 2 Predicted to enable double-stranded RNA binding activity and single-stranded RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF337 Genezinc finger protein 337 This gene encodes a zinc finger domain containing protein. The function of this protein has yet to be determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ZNF334 Genezinc finger protein 334 This gene encodes a member of the C2H2 zinc finger family. The encoded protein contains a Krueppel-associated box, fourteen C2H2 zinc finger domains, and four C2H2-type/integrase DNA-binding domains. Decreased expression of this gene may be a marker for rheumatoid arthritis. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012] |
ZNF335 Genezinc finger protein 335 The protein encoded by this gene enhances transcriptional activation by ligand-bound nuclear hormone receptors. However, it does this not by direct interaction with the receptor, but by direct interaction with the nuclear hormone receptor transcriptional coactivator NRC. The encoded protein may function by altering local chromatin structure. [provided by RefSeq, Jul 2008] |
ZNF333 Genezinc finger protein 333 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF331 Genezinc finger protein 331 This gene encodes a zinc finger protein containing a KRAB (Kruppel-associated box) domain found in transcriptional repressors. This gene may be methylated and silenced in cancer cells. This gene is located within a differentially methylated region (DMR) and shows allele-specific expression in placenta. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding the same protein. [provided by RefSeq, Nov 2015] |
LOC100419761 Genezinc finger protein 654 pseudogene |
LOC100419763 Genezinc finger with KRAB and SCAN domains 8 pseudogene |
ZNF33B Genezinc finger protein 33B This gene encodes a member of the zinc finger family of proteins. This gene shows decreased expression in cumulus cells derived from patients undergoing controlled ovarian stimulation. This gene is present in a gene cluster with several related zinc finger genes in the pericentromeric region of chromosome 10. Pseudogenes have been identified on chromosomes 7 and 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015] |
ZNF33A Genezinc finger protein 33A Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP92 GeneZFP92 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP90 GeneZFP90 zinc finger protein This gene encodes a member of the zinc finger protein family that modulates gene expression. The encoded protein derepresses the transcription of certain fetal cardiac genes and may contribute to the genetic reprogramming that occurs during the development of heart failure. Genome wide association studies have identified this gene among ulcerative colitis risk loci. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Mar 2015] |
ZFP91 GeneZFP91 zinc finger protein The protein encoded by this gene is a member of the zinc finger family of proteins. The gene product contains C2H2-type domains, which are the classical zinc finger domains found in numerous nucleic acid-binding proteins. This protein functions as a regulator of the non-canonical NF-kappaB pathway in lymphotoxin-beta receptor signaling. Alternative splicing results in multiple transcript variants. A read-through transcript variant composed of ZFP91 and the downstream CNTF gene sequence has been identified, but it is thought to be non-coding. Read-through transcription of ZFP91 and CNTF has also been observed in mouse. A ZFP91-related pseudogene has also been identified on chromosome 2. [provided by RefSeq, Oct 2010] |
ZEB1 Genezinc finger E-box binding homeobox 1 This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010] |
LOC101929991 Genezinc finger protein 93-like |
LOC100505841 Genezinc finger protein 474-like Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
RNF128 Genering finger protein 128, E3 ubiquitin protein ligase The protein encoded by this gene is a type I transmembrane protein that localizes to the endocytic pathway. This protein contains a RING zinc-finger motif and has been shown to possess E3 ubiquitin ligase activity. Expression of this gene in retrovirally transduced T cell hybridoma significantly inhibits activation-induced IL2 and IL4 cytokine production. Induced expression of this gene was observed in anergic CD4(+) T cells, which suggested a role in the induction of anergic phenotype. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
RNF126 Genering finger protein 126 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008] |
RNF125 Genering finger protein 125, E3 ubiquitin protein ligase This gene encodes a novel E3 ubiquitin ligase that contains a RING finger domain in the N-terminus and three zinc-binding and one ubiquitin-interacting motif in the C-terminus. As a result of myristoylation, this protein associates with membranes and is primarily localized to intracellular membrane systems. The encoded protein may function as a positive regulator in the T-cell receptor signaling pathway. [provided by RefSeq, Mar 2012] |
RNF123 Genering finger protein 123 The protein encoded by this gene contains a C-terminal RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions, and an N-terminal SPRY domain. This protein displays E3 ubiquitin ligase activity toward the cyclin-dependent kinase inhibitor 1B which is also known as p27 or KIP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
RNF122 Genering finger protein 122 The encoded protein contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. The encoded protein is localized to the endoplasmic reticulum and golgi apparatus, and may be associated with cell viability. [provided by RefSeq, Jul 2013] |
RNF121 Genering finger protein 121 The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Several alternatively spliced transcript variants have been noted for this gene, however, not all are likely to encode viable protein products. [provided by RefSeq, Sep 2008] |
PDZRN4 GenePDZ domain containing ring finger 4 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
PDZRN3 GenePDZ domain containing ring finger 3 This gene encodes a member of the LNX (Ligand of Numb Protein-X) family of RING-type ubiquitin E3 ligases. This protein may function in vascular morphogenesis and the differentiation of adipocytes, osteoblasts and myoblasts. This protein may be targeted for degradation by the human papilloma virus E6 protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
ZCCHC12 Genezinc finger, CCHC domain containing 12 This gene encodes a downstream effector of bone morphogenetic protein (BMP) signalling. This protein contains a zinc finger domain and functions as a transcriptional coactivator. Variation in this gene may be associated with X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
ZCCHC11 Genezinc finger, CCHC domain containing 11 Enables RNA uridylyltransferase activity. Involved in RNA metabolic process; stem cell population maintenance; and transposable element silencing by mRNA destabilization. Located in cytoplasmic ribonucleoprotein granule; cytosol; and nucleolus. Implicated in liver benign neoplasm. Biomarker of breast cancer. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC10 Genezinc finger, CCHC domain containing 10 Predicted to enable nucleic acid binding activity and zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC17 Genezinc finger, CCHC domain containing 17 Enables identical protein binding activity. Predicted to be involved in RNA stabilization. Predicted to be located in nucleolus. Predicted to be part of cytosolic large ribosomal subunit. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC16 Genezinc finger, CCHC domain containing 16 Predicted to enable nucleic acid binding activity and zinc ion binding activity. Predicted to act upstream of or within cognition and norepinephrine metabolic process. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC14 Genezinc finger, CCHC domain containing 14 Predicted to enable nucleic acid binding activity; phosphatidylinositol binding activity; and zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC18 Genezinc finger, CCHC domain containing 18 Predicted to enable metal ion binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF3 GenePHD finger protein 3 This gene encodes a member of a PHD finger-containing gene family. This gene may function as a transcription factor and may be involved in glioblastomas development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
RNF225 Genering finger protein 225 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF83 Genezinc finger protein 83 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF81 Genezinc finger protein 81 This gene encodes a protein that likely functions as a transcription factor. The protein contains an N-terminal KRAB domain and several C2H2-type zinc finger motifs. Mutations in this gene cause an X-linked form of intellectual disability (MRX45). Microduplication of a region of chromosome X including this gene has also been associated with other forms of intellectual disability. [provided by RefSeq, Jul 2017] |
ZNF80 Genezinc finger protein 80 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF85 Genezinc finger protein 85 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF84 Genezinc finger protein 84 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC440180 Genezinc finger, CCHC domain containing 7 pseudogene |
ZNF736P7Y Genezinc finger protein 736 pseudogene 7, Y-linked |
ZNF863P Genezinc finger protein 863, pseudogene |
WIZP1 Genewidely interspaced zinc finger motifs pseudogene 1 |
HELZ Genehelicase with zinc finger HELZ is a member of the superfamily I class of RNA helicases. RNA helicases alter the conformation of RNA by unwinding double-stranded regions, thereby altering the biologic activity of the RNA molecule and regulating access to other proteins (Wagner et al., 1999 [PubMed 10471385]).[supplied by OMIM, Mar 2008] |
RBAK GeneRB-associated KRAB zinc finger This gene encodes a nuclear protein which interacts with the tumor suppressor retinoblastoma 1. The two interacting proteins are thought to act as a transcriptional repressor for promoters which are activated by the E2F1 transcription factor. This protein contains a Kruppel-associated box (KRAB), which is a transcriptional repressor motif. Read-through transcripts that include exons from the downstream gene LOC389458 are expressed from this locus. [provided by RefSeq, Mar 2011] |
ZNF619P1 Genezinc finger protein 619 pseudogene 1 |
ZNF33BP1 Genezinc finger protein 33B pseudogene 1 |
VEZF1P1 Genevascular endothelial zinc finger 1 pseudogene 1 |
ZDHHC20 Genezinc finger, DHHC-type containing 20 Enables protein-cysteine S-palmitoyltransferase activity and zinc ion binding activity. Involved in peptidyl-L-cysteine S-palmitoylation and positive regulation by host of viral process. Located in Golgi membrane and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC21 Genezinc finger, DHHC-type containing 21 Enables palmitoyltransferase activity. Involved in peptidyl-L-cysteine S-palmitoylation. Located in Golgi apparatus and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC22 Genezinc finger, DHHC-type containing 22 Predicted to enable protein-cysteine S-palmitoyltransferase activity. Involved in protein localization to plasma membrane and protein palmitoylation. Located in Golgi apparatus; endoplasmic reticulum; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC23 Genezinc finger, DHHC-type containing 23 Predicted to enable protein-cysteine S-palmitoyltransferase activity. Involved in protein localization to plasma membrane and protein palmitoylation. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus and endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC24 Genezinc finger, DHHC-type containing 24 Predicted to enable protein-cysteine S-palmitoyltransferase activity. Predicted to be involved in protein targeting to membrane. Predicted to be located in membrane. Predicted to be active in Golgi apparatus and endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF141 Genezinc finger protein 141 The protein encoded by this gene is a zinc finger protein that may be a tumor suppressor. Defects in this gene have been associated with autosomal recessive postaxial polydactyly type A. [provided by RefSeq, Jan 2017] |
ZNF140 Genezinc finger protein 140 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF143 Genezinc finger protein 143 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of snRNA transcription by RNA polymerase II. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF142 Genezinc finger protein 142 The protein encoded by this gene belongs to the Kruppel family of C2H2-type zinc finger proteins. It contains 31 C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013] |
ZNF146 Genezinc finger protein 146 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF148 Genezinc finger protein 148 The protein encoded by this gene is a member of the Kruppel family of zinc finger DNA binding proteins. The encoded protein activates transcription of the T-cell receptor and intestinal alkaline phosphatase genes but represses transcription of the ornithine decarboxylase, vimentin, gastrin, stomelysin, and enolase genes. Increased expression of this gene results in decreased patient survival rates from colorectal cancer, while mutations in this gene have been associated with global developmental delay, hypoplastic corpus callosum, and dysmorphic facies. [provided by RefSeq, Feb 2017] |
ZNF736P4Y Genezinc finger protein 736 pseudogene 4, Y-linked |
ZNF736P12Y Genezinc finger protein 736 pseudogene 12, Y-linked |
LOC100288437 Genering finger and WD repeat domain 2, E3 ubiquitin protein ligase pseudogene |
ZC3HC1 Genezinc finger, C3HC-type containing 1 This gene encodes an F-box-containing protein that is a component of an SCF-type E3 ubiquitin ligase complex that regulates the onset of cell division. The G2/M transition in the cell cycle requires the interaction of the proteins cyclin B1 and cyclin-dependent kinase 1. The activated ubiquitin ligase complex targets the protein cyclin B1 for degradation, preventing this transition to mitosis. [provided by RefSeq, Aug 2013] |
ZNF968P Genezinc finger protein 968, pseudogene |
CTCF GeneCCCTC-binding factor (zinc finger protein) This gene is a member of the BORIS + CTCF gene family and encodes a transcriptional regulator protein with 11 highly conserved zinc finger (ZF) domains. This nuclear protein is able to use different combinations of the ZF domains to bind different DNA target sequences and proteins. Depending upon the context of the site, the protein can bind a histone acetyltransferase (HAT)-containing complex and function as a transcriptional activator or bind a histone deacetylase (HDAC)-containing complex and function as a transcriptional repressor. If the protein is bound to a transcriptional insulator element, it can block communication between enhancers and upstream promoters, thereby regulating imprinted expression. Mutations in this gene have been associated with invasive breast cancers, prostate cancers, and Wilms' tumors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010] |
ZNF426 Genezinc finger protein 426 Kaposi's sarcoma-associated herpesvirus (KSHV) can be reactivated from latency by the viral protein RTA. The protein encoded by this gene is a zinc finger transcriptional repressor that interacts with RTA to modulate RTA-mediated reactivation of KSHV. While the encoded protein can repress KSHV reactivation, RTA can induce degradation of this protein through the ubiquitin-proteasome pathway to overcome the repression. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015] |
ZNF425 Genezinc finger protein 425 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of DNA-templated transcription. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF423 Genezinc finger protein 423 The protein encoded by this gene is a nuclear protein that belongs to the family of Kruppel-like C2H2 zinc finger proteins. It functions as a DNA-binding transcription factor by using distinct zinc fingers in different signaling pathways. Thus, it is thought that this gene may have multiple roles in signal transduction during development. Mutations in this gene are associated with nephronophthisis-14 and Joubert syndrome-19. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2012] |
ZNF420 Genezinc finger protein 420 The protein encoded by this gene is a KRAB-type zinc finger protein that negatively-regulates p53-mediated apoptosis. Under stress conditions, the encoded protein is phosphorylated by ATM and dissociates from p53, which activates p53 and initiates apoptosis. [provided by RefSeq, Jul 2016] |
ZNF428 Genezinc finger protein 428 Predicted to enable metal ion binding activity. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF429 Genezinc finger protein 429 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF969P Genezinc finger protein 969, pseudogene |
ZNF884P Genezinc finger protein 884, pseudogene |
MKRN8P Genemakorin ring finger protein 8, pseudogene |
LOC100421197 Genezinc finger and BTB domain containing 10 pseudogene |
PHF8 GenePHD finger protein 8 The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017] |
PHF6 GenePHD finger protein 6 This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010] |
PHF7 GenePHD finger protein 7 Spermatogenesis is a complex process regulated by extracellular and intracellular factors as well as cellular interactions among interstitial cells of the testis, Sertoli cells, and germ cells. This gene is expressed in the testis in Sertoli cells but not germ cells. The protein encoded by this gene contains plant homeodomain (PHD) finger domains, also known as leukemia associated protein (LAP) domains, believed to be involved in transcriptional regulation. The protein, which localizes to the nucleus of transfected cells, has been implicated in the transcriptional regulation of spermatogenesis. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013] |
PHF2 GenePHD finger protein 2 This gene encodes a protein which contains a zinc finger-like PHD (plant homeodomain) finger, distinct from other classes of zinc finger motifs, and a hydrophobic and highly conserved domain. The PHD finger shows the typical Cys4-His-Cys3 arrangement. PHD finger genes are thought to belong to a diverse group of transcriptional regulators possibly affecting eukaryotic gene expression by influencing chromatin structure. [provided by RefSeq, Jul 2008] |
PHF1 GenePHD finger protein 1 This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009] |
ZC3H6 Genezinc finger CCCH-type containing 6 Predicted to enable RNA binding activity and metal ion binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP14 GeneZFP14 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within blastocyst hatching. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC728743 Genezinc finger protein pseudogene |
LOC100128713 Genezinc finger protein 816A pseudogene |
ZNF735 Genezinc finger protein 735 This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and nine C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017] |
ZNF92P2 Genezinc finger protein 92 pseudogene 2 |
ZNF92P3 Genezinc finger protein 92 pseudogene 3 |
ZNF219 Genezinc finger protein 219 This gene is a member of the Kruppel-like zinc finger gene family. The encoded protein functions as a transcriptional repressor of the high mobility group nucleosome binding domain 1 protein, which is associated with transcriptionally active chromatin. [provided by RefSeq, Apr 2017] |
LOC100419859 Genezinc finger, MYM-type 1 pseudogene |
LOC100419673 GenePHD finger protein 10 pseudogene |
LOC100419678 Genezinc finger, MYM-type 1 pseudogene |
ZFHX2 Genezinc finger homeobox 2 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in regulation of sensory perception of pain. Located in nucleus. Implicated in Marsili syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
HKR1 GeneHKR1, GLI-Kruppel zinc finger family member Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130854 Genezinc finger protein 562 pseudogene |
LOC100419686 Genezinc finger protein 256 pseudogene |
LOC100419685 Genezinc finger protein 555 pseudogene |
LOC100419684 Genezinc finger protein 114 pseudogene |
LOC100419680 Genezinc finger protein 430 pseudogene |
ZFPM2 Genezinc finger protein, FOG family member 2 The zinc finger protein encoded by this gene is a widely expressed member of the FOG family of transcription factors. The family members modulate the activity of GATA family proteins, which are important regulators of hematopoiesis and cardiogenesis in mammals. It has been demonstrated that the protein can both activate and down-regulate expression of GATA-target genes, suggesting different modulation in different promoter contexts. A related mRNA suggests an alternatively spliced product but this information is not yet fully supported by the sequence. [provided by RefSeq, Jul 2008] |
ZNF271P Genezinc finger protein 271, pseudogene Zinc finger proteins interact with nucleic acids and have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Apr 2004] |
ZNF519P1 Genezinc finger protein 519 pseudogene 1 |
ZNF519P2 Genezinc finger protein 519 pseudogene 2 |
ZDHHC20P3 Genezinc finger, DHHC-type containing 20 pseudogene 3 |
PHF5HP GenePHD finger protein 5H pseudogene |
LOC441455 Genemakorin ring finger protein 1 pseudogene |
ZNF355P Genezinc finger protein 355, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF603P Genezinc finger protein 603, pseudogene |
ZNF663P Genezinc finger protein 663, pseudogene |
ZNF252P Genezinc finger protein 252, pseudogene |
ZNF877P Genezinc finger protein 877, pseudogene |
RBCK1 GeneRanBP-type and C3HC4-type zinc finger containing 1 Enables several functions, including protein sequestering activity; transcription coactivator activity; and ubiquitin binding activity. Involved in several processes, including positive regulation of canonical NF-kappaB signal transduction; protein linear polyubiquitination; and regulation of DNA-binding transcription factor activity. Part of LUBAC complex. Implicated in glycogen storage disease. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF722P Genezinc finger protein 722, pseudogene |
ZNF628 Genezinc finger protein 628 Zinc finger proteins (ZNFs), which bind nucleic acids, perform many key functions, the most important of which is regulating transcription. See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Mar 2008] |
ZNF629 Genezinc finger protein 629 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF624 Genezinc finger protein 624 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF625 Genezinc finger protein 625 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF626 Genezinc finger protein 626 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF627 Genezinc finger protein 627 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF620 Genezinc finger protein 620 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF621 Genezinc finger protein 621 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF622 Genezinc finger protein 622 Enables preribosome binding activity. Involved in several processes, including intrinsic apoptotic signaling pathway in response to oxidative stress; positive regulation of JNK cascade; and positive regulation of kinase activity. Located in Golgi apparatus; cytosol; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF623 Genezinc finger protein 623 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SWSAP1 GeneSWIM-type zinc finger 7 associated protein 1 Enables ATP hydrolysis activity and single-stranded DNA binding activity. Involved in double-strand break repair via homologous recombination and protein stabilization. Part of Shu complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN18 Genezinc finger and SCAN domain containing 18 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN10 Genezinc finger and SCAN domain containing 10 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN12 Genezinc finger and SCAN domain containing 12 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN16 Genezinc finger and SCAN domain containing 16 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MKRN1 Genemakorin ring finger protein 1 This gene encodes a protein that belongs to a novel class of zinc finger proteins. The encoded protein functions as a transcriptional co-regulator, and as an E3 ubiquitin ligase that promotes the ubiquitination and proteasomal degradation of target proteins. The protein encoded by this gene is thought to regulate RNA polymerase II-catalyzed transcription. Substrates for this protein's E3 ubiquitin ligase activity include the capsid protein of the West Nile virus and the catalytic subunit of the telomerase ribonucleoprotein. This protein controls cell cycle arrest and apoptosis by regulating p21, a cell cycle regulator, and the tumor suppressor protein p53. Pseudogenes of this gene are present on chromosomes 1, 3, 9, 12 and 20, and on the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014] |
MKRN3 Genemakorin ring finger protein 3 The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene. [provided by RefSeq, Jul 2008] |
MKRN2 Genemakorin ring finger protein 2 This gene encodes a probable E3 ubiquitin ligase containing several zinc finger domains, that is a member of the makorin RING zinc-finger protein family. This gene overlaps the v-raf-1 murine leukemia viral oncogene homolog 1 (RAF1) gene in an antisense orientation and may have a co-regulatory function with RAF1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
LOC100533643 Genezinc finger protein 91 pseudogene |
LOC100533644 Genezinc finger protein 628 pseudogene |
LOC100533646 Genezinc finger protein 135 pseudogene Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF21A GenePHD finger protein 21A The PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron-specific genes through the cis-regulatory element known as repressor element-1 (RE1) or neural restrictive silencer (NRS) (Hakimi et al., 2002 [PubMed 12032298]).[supplied by OMIM, Nov 2010] |
ZNF544 Genezinc finger protein 544 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF547 Genezinc finger protein 547 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF540 Genezinc finger protein 540 Enables mRNA regulatory element binding translation repressor activity. Involved in negative regulation of DNA-templated transcription and negative regulation of translation. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF543 Genezinc finger protein 543 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF549 Genezinc finger protein 549 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF548 Genezinc finger protein 548 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB8A Genezinc finger and BTB domain containing 8A Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II-specific DNA-binding transcription factor binding activity; and transcription coactivator binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB8B Genezinc finger and BTB domain containing 8B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFPM1 Genezinc finger protein, FOG family member 1 Enables RNA polymerase II-specific DNA-binding transcription factor binding activity and transcription corepressor activity. Involved in platelet formation; regulation of definitive erythrocyte differentiation; and regulation of gene expression. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND6P1 Genezinc finger, AN1-type domain 6 pseudogene 1 |
LOC390358 Generet finger protein-like 2 pseudogene |
ZMIZ2 Genezinc finger, MIZ-type containing 2 ZMIZ2 and ZMIZ1 (MIM 607159) are members of a PIAS (see MIM 603566)-like family of proteins that interact with nuclear hormone receptors. ZMIZ2 interacts with androgen receptor (AR; MIM 313700) and enhances AR-mediated transcription (Huang et al., 2005 [PubMed 16051670]).[supplied by OMIM, May 2010] |
ZMIZ1 Genezinc finger, MIZ-type containing 1 This gene encodes a member of the PIAS (protein inhibitor of activated STAT) family of proteins. The encoded protein regulates the activity of various transcription factors, including the androgen receptor, Smad3/4, and p53. The encoded protein may also play a role in sumoylation. A translocation between this locus on chromosome 10 and the protein tyrosine kinase ABL1 locus on chromosome 9 has been associated with acute lymphoblastic leukemia. [provided by RefSeq, Mar 2010] |
RNFT1 Genering finger protein, transmembrane 1 Enables ubiquitin binding activity and ubiquitin protein ligase activity. Involved in positive regulation of ERAD pathway and protein autoubiquitination. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF70P1 Genezinc finger protein 70 pseudogene 1 |
ZNF783 Genezinc finger family member 783 Enables identical protein binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF782 Genezinc finger protein 782 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF781 Genezinc finger protein 781 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF787 Genezinc finger protein 787 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF786 Genezinc finger protein 786 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF785 Genezinc finger protein 785 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF784 Genezinc finger protein 784 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF789 Genezinc finger protein 789 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF788 Genezinc finger family member 788 Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289416 Genezinc finger protein 793 |
ZEB2P1 Genezinc finger E-box binding homeobox 2 pseudogene 1 |
ZBED4 Genezinc finger, BED-type containing 4 Enables identical protein binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100533641 Genezinc finger protein 100 pseudogene |
UHRF1 Geneubiquitin-like with PHD and ring finger domains 1 This gene encodes a member of a subfamily of RING-finger type E3 ubiquitin ligases. The protein binds to specific DNA sequences, and recruits a histone deacetylase to regulate gene expression. Its expression peaks at late G1 phase and continues during G2 and M phases of the cell cycle. It plays a major role in the G1/S transition by regulating topoisomerase IIalpha and retinoblastoma gene expression, and functions in the p53-dependent DNA damage checkpoint. It is regarded as a hub protein for the integration of epigenetic information. This gene is up-regulated in various cancers, and it is therefore considered to be a therapeutic target. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene exists on chromosome 12. [provided by RefSeq, Feb 2014] |
UHRF2 Geneubiquitin-like with PHD and ring finger domains 2, E3 ubiquitin protein ligase This gene encodes a nuclear protein which is involved in cell-cycle regulation. The encoded protein is a ubiquitin-ligase capable of ubiquinating PCNP (PEST-containing nuclear protein), and together they may play a role in tumorigenesis. The encoded protein contains an NIRF_N domain, a PHD finger, a set- and ring-associated (SRA) domain, and a RING finger domain and several of these domains have been shown to be essential for the regulation of cell proliferation. This protein may also have a role in intranuclear degradation of polyglutamine aggregates. Alternative splicing results in multiple transcript variants some of which are non-protein coding. [provided by RefSeq, Feb 2012] |
ZNF248 Genezinc finger protein 248 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
GATAD2A GeneGATA zinc finger domain containing 2A Enables protein-macromolecule adaptor activity. Involved in chromatin remodeling and negative regulation of DNA-templated transcription. Located in nucleoplasm. Part of NuRD complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105378242 Genezinc finger protein 705A-like |
ZDHHC11B Genezinc finger, DHHC-type containing 11B Predicted to enable protein-cysteine S-palmitoyltransferase activity. Predicted to be involved in several processes, including antiviral innate immune response; peptidyl-L-cysteine S-palmitoylation; and positive regulation of defense response to virus by host. Predicted to be located in endosome membrane. Predicted to be active in Golgi apparatus and endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
LOC441711 GeneRING finger protein 145-like |
LOC100419863 Genezinc finger protein 705A pseudogene |
ZFPL1 Genezinc finger protein-like 1 Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101060391 Genezinc finger CCCH domain-containing protein 18-like |
ZNRF4 Genezinc and ring finger 4 Enables ubiquitin protein ligase activity. Involved in negative regulation of nucleotide-binding activity oligomerization domain containing 2 signaling pathway and proteasome-mediated ubiquitin-dependent protein catabolic process. Is active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNRF1 Genezinc and ring finger 1, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin-protein ligase that plays a role in neural-cell differentiation. Overexpression of this gene causes neurite-like elongation. The encoded protein contains both a zinc finger and a RING finger motif and is localized in the endosome/lysosome compartment, indicating that it may be involved in ubiquitin-mediated protein modification, and in synaptic vessicle membranes in neurons. [provided by RefSeq, Feb 2012] |
ZNRF3 Genezinc and ring finger 3 Enables frizzled binding activity and ubiquitin-protein transferase activity. Involved in negative regulation of Wnt signaling pathway; protein ubiquitination; and ubiquitin-dependent protein catabolic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNRF2 Genezinc and ring finger 2, E3 ubiquitin protein ligase Enables ubiquitin protein ligase activity. Involved in positive regulation of autophagosome-lysosome fusion. Located in cytoplasmic vesicle membrane; nuclear lumen; and plasma membrane. Part of protein-containing complex. Is active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF646P1 Genezinc finger protein 646 pseudogene 1 |
LOC100129391 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 pseudogene |
ZNF546 Genezinc finger protein 546 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF541 Genezinc finger protein 541 Predicted to enable transcription corepressor activity. Predicted to be involved in male meiotic nuclear division and regulation of DNA-templated transcription. Predicted to be located in nucleus. Predicted to be part of histone deacetylase complex and transcription regulator complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF138P1 Genering finger protein 138, E3 ubiquitin protein ligase pseudogene 1 |
ZFAND2B Genezinc finger, AN1-type domain 2B This gene encodes a protein containing AN1-type zinc-fingers and ubiquitin-interacting motifs. The encoded protein likely associates with the proteosome to stimulate the degradation of toxic or misfolded proteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012] |
ZFAND2A Genezinc finger, AN1-type domain 2A Predicted to enable zinc ion binding activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process and protein targeting to ER. Predicted to act upstream of or within cellular response to arsenic-containing substance and positive regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleus. Predicted to be part of proteasome complex. Predicted to be active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RSPRY1 Genering finger and SPRY domain containing 1 This gene encodes a glycoprotein that contains a RING-type zinc finger domain and an SPRY domain of unknown function. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015] |
LOC100631330 Genepolycomb group ring finger 6 pseudogene |
LOC101930552 Genezinc finger protein 717-like |
ZNF709 Genezinc finger protein 709 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF708 Genezinc finger protein 708 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in membrane and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF703 Genezinc finger protein 703 Predicted to enable DNA-binding transcription factor binding activity and metal ion binding activity. Involved in several processes, including cellular response to estradiol stimulus; positive regulation of mammary gland epithelial cell proliferation; and regulation of transforming growth factor beta receptor signaling pathway. Located in cytoplasm and nuclear matrix. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF701 Genezinc finger protein 701 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF700 Genezinc finger protein 700 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF707 Genezinc finger protein 707 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF706 Genezinc finger protein 706 Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of DNA-templated transcription and negative regulation of stem cell population maintenance. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF704 Genezinc finger protein 704 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H10 Genezinc finger CCCH-type containing 10 Enables miRNA binding activity. Involved in negative regulation of miRNA processing. Acts upstream of with a positive effect on post-transcriptional regulation of gene expression. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H13 Genezinc finger CCCH-type containing 13 Enables RNA binding activity. Involved in mRNA processing. Located in nuclear speck. Part of RNA N6-methyladenosine methyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF115 Genering finger protein 115 Enables ubiquitin protein ligase activity. Involved in negative regulation of signal transduction; protein ubiquitination; and ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway. Is active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RNF112 Genering finger protein 112 This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
ZC3H14 Genezinc finger CCCH-type containing 14 The protein encoded by this gene is a poly(A)-binding protein that can affect gene expression and poly(A) tail length. The encoded protein may influence mRNA stability, nuclear export, and translation. [provided by RefSeq, May 2016] |
RNF111 Genering finger protein 111 The protein encoded by this gene is a nuclear RING-domain containing E3 ubiquitin ligase. This protein interacts with the transforming growth factor (TGF) -beta/NODAL signaling pathway by promoting the ubiquitination and proteosomal degradation of negative regulators, like SMAD proteins, and thereby enhances TGF-beta target-gene transcription. As a modulator of the nodal signaling cascade, this gene plays a critical role in the induction of mesoderm during embryonic development. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012] |
ZC3H18 Genezinc finger CCCH-type containing 18 Enables mRNA cap binding complex binding activity and protein-macromolecule adaptor activity. Involved in RNA destabilization. Located in nuclear speck. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Mar 2025] |
MGRN1 Genemahogunin ring finger 1, E3 ubiquitin protein ligase Enables ubiquitin-protein transferase activity. Involved in endosome to lysosome transport; negative regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway; and protein monoubiquitination. Located in several cellular components, including early endosome; endoplasmic reticulum; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CHFR Genecheckpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin-protein ligase required for the maintenance of the antephase checkpoint that regulates cell cycle entry into mitosis and, therefore, may play a key role in cell cycle progression and tumorigenesis. The encoded protein has an N-terminal forkhead-associated domain, a central RING-finger domain, and a cysteine-rich C-terminal region. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Mar 2014] |
RFPL1 Generet finger protein-like 1 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Involved in several processes, including negative regulation of G2/M transition of mitotic cell cycle; negative regulation of cell division; and positive regulation of proteolysis. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF56 Genezinc finger protein 56 |
ZNF57 Genezinc finger protein 57 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF7 Genezinc finger protein 7 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF4 Genezinc finger protein-4 |
ZNF5 Genezinc finger protein-5 |
ZNF2 Genezinc finger protein 2 The protein encoded by this gene belongs to the C2H2-type zinc-finger protein family. The exact function of this gene is not known, however, zinc-finger proteins are known to interact with DNA and function as transcription regulators. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014] |
ZNF3 Genezinc finger protein 3 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CTCFL GeneCCCTC-binding factor (zinc finger protein)-like CCCTC-binding factor (CTCF), an 11-zinc-finger factor involved in gene regulation, utilizes different zinc fingers to bind varying DNA target sites. CTCF forms methylation-sensitive insulators that regulate X-chromosome inactivation. This gene is a paralog of CTCF and appears to be expressed primarily in the cytoplasm of spermatocytes, unlike CTCF which is expressed primarily in the nucleus of somatic cells. CTCF and the protein encoded by this gene are normally expressed in a mutually exclusive pattern that correlates with resetting of methylation marks during male germ cell differentiation. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012] |
ZNF8 Genezinc finger protein 8 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within BMP signaling pathway. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN7P1 Genezinc finger with KRAB and SCAN domains 7 pseudogene 1 |
LOC643381 Genezinc finger protein 614 pseudogene |
ZSCAN9 Genezinc finger and SCAN domain containing 9 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN4 Genezinc finger and SCAN domain containing 4 The ZSCAN4 gene encodes a protein involved in telomere maintenance and with a key role in the critical feature of mouse embryonic stem (ES) cells, namely, defying cellular senescence and maintaining normal karyotype for many cell divisions in culture (Zalzman et al., 2010 [PubMed 20336070]).[supplied by OMIM, May 2010] |
ZSCAN1 Genezinc finger and SCAN domain containing 1 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN2 Genezinc finger and SCAN domain containing 2 The protein encoded by this gene contains several copies of zinc finger motif, which is commonly found in transcriptional regulatory proteins. Studies in mice show that this gene is expressed during embryonic development, and specifically in the testis in adult mice, suggesting that it may play a role in regulating genes in germ cells. Alternative splicing of this gene results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
LOC646388 Genezinc finger, CCHC domain containing 9 pseudogene |
LOC100533636 Genezinc finger protein 519 pseudogene |
ZNF138 Genezinc finger protein 138 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in membrane and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF132 Genezinc finger protein 132 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF133 Genezinc finger protein 133 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF134 Genezinc finger protein 134 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF135 Genezinc finger protein 135 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF136 Genezinc finger protein 136 This gene encodes a zinc finger protein containing a Kruppel-associated box (KRAB) A-box domain at its N-terminus, followed by fourteen contiguous C2H2 zinc finger domains and a degenerate zinc finger. The KRAB A-box showed weak transcriptional repressor activity in a reporter gene assay. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
ZNF736P1Y Genezinc finger protein 736 pseudogene 1, Y-linked |
ZNF736P11Y Genezinc finger protein 736 pseudogene 11, Y-linked |
RNF216P1 Genering finger protein 216 pseudogene 1 |
CGRRF1 Genecell growth regulator with ring finger domain 1 Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of cell growth. Located in endoplasmic reticulum and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF813 Genezinc finger protein 813 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF812 Genezinc finger protein 812 |
LOC100287523 Genezinc finger protein 2-like |
ZNF362 Genezinc finger protein 362 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF365 Genezinc finger protein 365 This gene encodes a zinc finger protein that may play a role in the repair of DNA damage and maintenance of genome stability. The N-terminal C2H2 zinc finger motif is required to form a protein complex with PARP1 and MRE11, which are known to be involved in the restart of stalled DNA replication forks. A mutation in this gene may be associated with breast cancer susceptibility. [provided by RefSeq, Mar 2020] |
ZNF367 Genezinc finger protein 367 Enables DNA-binding transcription factor activity. Acts upstream of or within regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF366 Genezinc finger protein 366 Enables nuclear estrogen receptor binding activity and transcription corepressor activity. Involved in negative regulation of intracellular estrogen receptor signaling pathway; negative regulation of transcription by RNA polymerase II; and response to estrogen. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419739 Genezinc finger protein 341 pseudogene |
ZGPAT Genezinc finger, CCCH-type with G patch domain Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of epidermal growth factor-activated receptor activity and negative regulation of transcription by RNA polymerase II. Located in nucleoplasm and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MORC2 GeneMORC family CW-type zinc finger 2 This gene encodes a member of the Microrchidia (MORC) protein superfamily. The encoded protein is known to regulate the condensation of heterochromatin in response to DNA damage and play a role in repressing transcription. The protein has been found to regulate the activity of ATP citrate lyase via specific interaction with this enzyme in the cytosol of lipogenic breast cancer cells. The protein also plays a role in lipogenesis and adipocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016] |
MORC3 GeneMORC family CW-type zinc finger 3 This gene encodes a protein that localizes to the nuclear matrix and forms nuclear bodies via an ATP-dependent mechanism. The protein is predicted to have coiled-coil and zinc finger domains and has RNA binding activity. Alternative splicing produces multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2016] |
MORC1 GeneMORC family CW-type zinc finger 1 This gene encodes the human homolog of mouse morc and like the mouse protein it is testis-specific. Mouse studies support a testis-specific function since only male knockout mice are infertile; infertility is the only apparent defect. These studies further support a role for this protein early in spermatogenesis, possibly by affecting entry into apoptosis because testis from knockout mice show greatly increased numbers of apoptotic cells. [provided by RefSeq, Jan 2009] |
MORC4 GeneMORC family CW-type zinc finger 4 In human, the four current members of the microrchidia (morc) gene family share an N-terminal ATPase-like ATP-binding region and a CW four-cysteine zinc-finger motif. The protein encoded by this gene also has a nuclear matrix binding domain and a two-stranded coiled-coil motif near its C-terminus. This gene is widely expressed at low levels in normal tissues and has elevated expression in placenta and testis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010] |
ZNFX1 Genezinc finger, NFX1-type containing 1 Enables RNA binding activity. Involved in defense response to bacterium and defense response to virus. Is active in cytoplasmic stress granule. Implicated in primary immunodeficiency disease. [provided by Alliance of Genome Resources, Mar 2025] |
RNF19B Genering finger protein 19B This gene encodes a multi-pass membrane protein containing two RING-type and one IBR-type zinc finger motifs. The encoded protin is an E3 ubiquitin-protein ligase that plays a role in the cytotoxic effects of natural killer (NK) cells. Alternative splicing results in multiple transcript variants. There are pseudogenes for this gene on chromosomes X and Y in a possible pseudoautosomal region. [provided by RefSeq, Jul 2014] |
RNF19A Genering finger protein 19A, RBR E3 ubiquitin protein ligase This gene encodes a member of the ring between ring fingers (RBR) protein family, and the encoded protein contains two RING-finger motifs and an in between RING fingers motif. This protein is an E3 ubiquitin ligase that is localized to Lewy bodies, and ubiquitylates synphilin-1, which is an interacting protein of alpha synuclein in neurons. The encoded protein may be involved in amyotrophic lateral sclerosis and Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
RFPL4AP1 Generet finger protein-like 4A pseudogene 1 |
RFPL4AP5 Generet finger protein-like 4A pseudogene 5 |
LOC105379522 Genezinc finger protein 717-like |
RNFT2 Genering finger protein, transmembrane 2 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in positive regulation of ERAD pathway. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421809 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene |
ZNHIT3 Genezinc finger, HIT-type containing 3 Predicted to enable nuclear thyroid hormone receptor binding activity. Predicted to be involved in box C/D snoRNP assembly; maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA); and snoRNA localization. Located in cytoplasm and nucleus. Implicated in PEHO syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT2 Genezinc finger, HIT-type containing 2 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT1 Genezinc finger, HIT-type containing 1 Enables histone binding activity. Involved in muscle cell differentiation and positive regulation of DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT6 Genezinc finger, HIT-type containing 6 Enables ATPase binding activity; TFIID-class transcription factor complex binding activity; and identical protein binding activity. Involved in box C/D snoRNP assembly; protein complex oligomerization; and snoRNA localization. Located in extracellular exosome. Part of pre-snoRNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
FEZF1 GeneFEZ family zinc finger 1 This gene encodes a transcriptional repressor that belongs to the zinc finger double domain protein family. The encoded protein is thought to play a role in the embryonic migration of gonadotropin-releasing hormone neurons into the brain. Mutations in this gene are associated with hypogonadotropic hypogonadism-22 with anosmia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014] |
FEZF2 GeneFEZ family zinc finger 2 Predicted to enable several functions, including DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and chromatin binding activity. Predicted to be involved in regulation of gene expression. Predicted to act upstream of or within several processes, including negative regulation of transcription by RNA polymerase II; nervous system development; and regulation of neuron differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFRP1 Genezinc finger RNA binding protein pseudogene 1 |
ZFP69B GeneZFP69 zinc finger protein B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in Golgi organization. Located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101928508 Genezinc finger Ran-binding domain-containing protein 2 pseudogene |
LOC105369285 Genezinc finger protein 813-like |
ZNF479 Genezinc finger protein 479 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF471 Genezinc finger protein 471 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF470 Genezinc finger protein 470 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF473 Genezinc finger protein 473 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein, a component of the U7 snRNP complex, plays a role in histone 3'-end pre-mRNA processing and may be required for cell cycle progression to S phase. Expression level and methylation status of this gene may be correlated with bone mineral density. [provided by RefSeq, Jul 2016] |
ZNF474 Genezinc finger protein 474 Predicted to enable metal ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100418554 Genezinc finger protein 93 pseudogene |
LOC100418556 Genezinc finger protein 70 pseudogene |
LOC100418550 Genezinc finger protein 93 pseudogene |
LOC100418551 Genezinc finger protein 70 pseudogene |
LOC100418552 Genezinc finger protein 93 pseudogene |
LOC100418553 Genezinc finger protein 70 pseudogene |
ZMYND15 Genezinc finger, MYND-type containing 15 This gene encodes a MYND-containing zinc-binding protein with a nuclear localization sequence. A similar gene in mice has been shown to act as a testis-specific transcriptional repressor by recruiting histone deacetylase enzymes to regulate spatiotemporal expression of many haploid genes. This protein may play an important role in spermatogenesis. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012] |
ZMYND12 Genezinc finger, MYND-type containing 12 Predicted to enable metal ion binding activity. Involved in sperm axoneme assembly. Located in sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYND10 Genezinc finger, MYND-type containing 10 This gene encodes a protein containing a MYND-type zinc finger domain that likely functions in assembly of the dynein motor. Mutations in this gene can cause primary ciliary dyskinesia. This gene is also considered a tumor suppressor gene and is often mutated, deleted, or hypermethylated and silenced in cancer cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
ZMYND11 Genezinc finger, MYND-type containing 11 The protein encoded by this gene was first identified by its ability to bind the adenovirus E1A protein. The protein localizes to the nucleus. It functions as a transcriptional repressor, and expression of E1A inhibits this repression. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
ZMYND19 Genezinc finger, MYND-type containing 19 ZMYND19 is a MYND zinc finger domain-containing protein that binds to the C terminus of melanin-concentrating hormone receptor-1 (MCHR1; MIM 601751) (Bachner et al., 2002 [PubMed 12208518]), and to the N termini of alpha-tubulin (TUBA1; MIM 191110), and beta-tubulin (TUBB; MIM 191130) (Francke et al., 2005 [PubMed 16039987]).[supplied by OMIM, Mar 2008] |
ZKSCAN1 Genezinc finger with KRAB and SCAN domains 1 This gene encodes a member of the Kruppel C2H2-type zinc-finger family of proteins. This encoded protein may function as a transcription factor that regulates the expression of GABA type-A receptors in the brain. Transcripts from this gene have been shown to form stable and abundant circular RNAs. Elevated expression of this gene has been observed in gastric cancer and the encoded protein may stimulate migration and invasion of human gastric cancer cells. [provided by RefSeq, Oct 2016] |
ZKSCAN3 Genezinc finger with KRAB and SCAN domains 3 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and chromatin binding activity. Involved in lysosome organization; negative regulation of metabolic process; and regulation of DNA-templated transcription. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN2 Genezinc finger with KRAB and SCAN domains 2 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN5 Genezinc finger with KRAB and SCAN domains 5 This gene encodes a zinc finger protein of the Kruppel family. The protein contains a SCAN box and a KRAB A domain and may be involved in transcriptional regulation. A similar protein in mouse is differentially expressed in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
ZKSCAN4 Genezinc finger with KRAB and SCAN domains 4 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN7 Genezinc finger with KRAB and SCAN domains 7 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN8 Genezinc finger with KRAB and SCAN domains 8 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF677 Genezinc finger protein 677 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF676 Genezinc finger protein 676 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF675 Genezinc finger protein 675 Enables ubiquitin protein ligase binding activity. Involved in negative regulation of osteoclast differentiation; negative regulation of signal transduction; and regulation of DNA-templated transcription. Located in nucleus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF674 Genezinc finger protein 674 This gene encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 11 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked cognitive disabilities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017] |
ZNF672 Genezinc finger protein 672 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF671 Genezinc finger protein 671 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF670 Genezinc finger protein 670 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Acts upstream of or within lipid metabolic process. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF679 Genezinc finger protein 679 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF678 Genezinc finger protein 678 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP69 GeneZFP69 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of lipid metabolic process and regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP64 GeneZFP64 zinc finger protein Predicted to enable DNA binding activity and metal ion binding activity. Involved in mesenchymal cell differentiation. Located in cytoplasm and megasporocyte nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP62 GeneZFP62 zinc finger protein Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF385C Genezinc finger protein 385C Predicted to enable nucleic acid binding activity and zinc ion binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF385B Genezinc finger protein 385B Enables p53 binding activity. Involved in intrinsic apoptotic signaling pathway by p53 class mediator. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF385A Genezinc finger protein 385A Zinc finger proteins, such as ZNF385A, are regulatory proteins that act as transcription factors, bind single- or double-stranded RNA, or interact with other proteins (Sharma et al., 2004 [PubMed 15527981]).[supplied by OMIM, Oct 2008] |
RNFT1P1 Genering finger protein, transmembrane 1 pseudogene 1 |
RNFT1P2 Genering finger protein, transmembrane 1 pseudogene 2 |
LOC100419583 Genering finger protein 4 pseudogene |
ZNF654 Genezinc finger protein 654 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF382 Genezinc finger protein 382 This gene encodes a KRAB domain zinc finger transcription factor (KZNF). KZNFs play critical roles in the regulation of many cellular processes including differentiation, proliferation and apoptosis. The encoded protein inhibits activating protein 1 (AP-1) and nuclear factor kappa-B (NF-kB) signaling and may function as a tumor suppressor in multiple carcinomas. This gene is found in a cluster with other zinc finger protein genes on the long arm of chromosome 19, and alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012] |
ZNF823 Genezinc finger protein 823 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF5GP GenePHD finger protein 5G pseudogene |
LOC100419913 Genezinc finger protein 678 pseudogene |
ZXDB Genezinc finger, X-linked, duplicated B The ZXDB gene is one of a pair of duplicated zinc finger genes on chromosome Xp11.21 (Greig et al., 1993 [PubMed 8268913]); see also ZXDA (MIM 300235).[supplied by OMIM, Jul 2010] |
ZXDC GeneZXD family zinc finger C Enables C2H2 zinc finger domain binding activity; LRR domain binding activity; and transcription coactivator activity. Involved in positive regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZXDA Genezinc finger, X-linked, duplicated A This gene encodes one of two duplicated zinc finger genes on chromosome Xp11. This gene is the telomeric copy; GeneID 158586 ZXDB is the more centromeric copy. The two genes have 98% nucleotide sequence similarity, and the predicted proteins contain 10 tandem zinc finger motifs. [provided by RefSeq, Nov 2009] |
ZNF702P Genezinc finger protein 702, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105372373 Genezinc finger protein 772 |
LOC100421332 Genezinc finger with KRAB and SCAN domains 1 pseudogene |
ZNF215 Genezinc finger protein 215 This gene is imprinted in a tissue-specific manner with preferential expression in the testis, and encodes a zinc finger protein that belongs to a family of zinc finger transcription factors. The encoded protein contains an N-terminal SRE-ZBP, Ctfin51, AW-1, and Number 18 (SCAN) domain, a kruppel-associated box A (KRABA) domain, and four C-terminal zinc finger domains. This gene is located within one of three regions on chromosome 11p15 associated with Beckwith-Wiedemann syndrome, called Beckwith-Wiedemann syndrome chromosome region-2 (BWSCR2), and is thought to play a role in the etiology of this disease. [provided by RefSeq, Aug 2017] |
ZNF214 Genezinc finger protein 214 This gene is expressed predominantly in the testis and encodes a zinc finger protein that contains an N-terminal kruppel-associated box A (KRABA) domain and twelve zinc finger domains. This gene is located within one of three regions on chromosome 11p15 associated with Beckwith-Wiedemann syndrome, called Beckwith-Wiedemann syndrome chromosome region-2 (BWSCR2), and is thought to play a role in the etiology of this disease. [provided by RefSeq, Aug 2017] |
ZNF217 Genezinc finger protein 217 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in mitochondrion and nuclear speck. Part of histone deacetylase complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF211 Genezinc finger protein 211 This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. This protein may play a role in developmental processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ZNF212 Genezinc finger protein 212 This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008] |
PHF21B GenePHD finger protein 21B Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100132830 Genezinc finger CCCH-type containing 14 pseudogene |
LOC100421641 Genezinc finger CCHC-type and RNA binding motif 1 pseudogene |
LOC391813 Genezinc finger, DHHC-type containing 3 pseudogene |
ZNF534 Genezinc finger protein 534 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF536 Genezinc finger protein 536 The protein encoded by this gene is a highly conserved zinc finger protein. The encoded protein is most abundant in brain, where it negatively regulates neuronal differentiation. [provided by RefSeq, Sep 2015] |
ZNF530 Genezinc finger protein 530 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF532 Genezinc finger protein 532 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB3 Genezinc finger and BTB domain containing 3 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB1 Genezinc finger and BTB domain containing 1 Enables K63-linked polyubiquitin modification-dependent protein binding activity; protein heterodimerization activity; and protein homodimerization activity. Involved in several processes, including negative regulation of transcription by RNA polymerase II; nucleobase-containing compound biosynthetic process; and protein homooligomerization. Located in nuclear body and nuclear membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF220 Genering finger protein 220 Enables beta-catenin binding activity. Involved in positive regulation of canonical Wnt signaling pathway. Acts upstream of or within positive regulation of DNA-binding transcription factor activity and protein monoubiquitination. Located in nuclear lamina. Part of protein-containing complex. Implicated in hypomyelinating leukodystrophy 23. [provided by Alliance of Genome Resources, Mar 2025] |
RNF222 Genering finger protein 222 Predicted to enable metal ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF223 Genering finger protein 223 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF224 Genering finger protein 224 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929206 Genezinc finger protein 708-like |
LOC101929203 GeneRING finger and transmembrane domain-containing protein 1-like |
LOC100133225 Genezinc finger, DHHC-type containing 7 pseudogene |
LOC100421074 GeneZFP14 zinc finger protein pseudogene |
ZC3H8 Genezinc finger CCCH-type containing 8 Enables RNA binding activity. Involved in several processes, including positive regulation of thymocyte apoptotic process; regulation of DNA-templated transcription; and snRNA transcription. Located in Cajal body; euchromatin; and histone locus body. Part of transcription elongation factor complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H3 Genezinc finger CCCH-type containing 3 Predicted to enable DNA binding activity; R-SMAD binding activity; and metal ion binding activity. Predicted to be involved in mRNA transport. Predicted to act upstream of or within mRNA 3'-end processing and positive regulation of activin receptor signaling pathway. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H4 Genezinc finger CCCH-type containing 4 This gene encodes a member of a family of CCCH (C-x8-C-x5-C-x3-H type) zinc finger domain-containing proteins. These zinc finger domains, which coordinate zinc finger binding and are characterized by three cysteine residues and one histidine residue, are nucleic acid-binding. Other family members are known to function in post-transcriptional regulation. [provided by RefSeq, Aug 2011] |
LOC100130881 Genezinc finger protein 12 pseudogene |
ZNF732 Genezinc finger protein 732 This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and sixteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017] |
ZNF730 Genezinc finger protein 730 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736 Genezinc finger protein 736 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF737 Genezinc finger protein 737 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF738 Genezinc finger protein 738 Predicted to enable ubiquitin-protein transferase activity. Predicted to be involved in protein polyubiquitination. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF317P1 Genezinc finger protein 317 pseudogene 1 |
LOC100419679 Genezinc finger protein 670 pseudogene |
LOC100129947 Genezinc finger protein 674 pseudogene |
ZFYVE9P2 Genezinc finger, FYVE domain containing 9 pseudogene 2 |
ZFYVE9P1 Genezinc finger, FYVE domain containing 9 pseudogene 1 |
ZDHHC20P4 Genezinc finger, DHHC-type containing 20 pseudogene 4 |
ZDHHC20P2 Genezinc finger, DHHC-type containing 20 pseudogene 2 |
ZDHHC20P1 Genezinc finger, DHHC-type containing 20 pseudogene 1 |
ZNF69 Genezinc finger protein 69 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF66 Genezinc finger protein 66 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in membrane and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100287477 Genezinc finger protein 420-like |
ZBED1 Genezinc finger, BED-type containing 1 This gene is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. It was earlier identified as a gene with similarity to Ac transposable elements, however, was found not to have transposase activity. Later studies show that this gene product is localized in the nucleus and functions as a transcription factor. It binds to DNA elements found in the promoter regions of several genes related to cell proliferation, such as histone H1, hence may have a role in regulating genes related to cell proliferation. Alternatively spliced transcript variants with different 5' untranslated region have been found for this gene. [provided by RefSeq, Jan 2010] |
ZBED2 Genezinc finger, BED-type containing 2 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of keratinocyte differentiation. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZBED3 Genezinc finger, BED-type containing 3 This gene belongs to a class of genes that arose through hAT DNA transposition and that encode regulatory proteins. This gene is upregulated in lung cancer tissues, where the encoded protein causes an accumulation of beta-catenin and enhanced lung cancer cell invasion. In addition, the encoded protein can be secreted and be involved in resistance to insulin. [provided by RefSeq, Jul 2016] |
ZBED5 Genezinc finger, BED-type containing 5 This gene is unusual in that its coding sequence is mostly derived from Charlie-like DNA transposon; however, it does not appear to be an active DNA transposon as it is not flanked by terminal inverted repeats. The encoded protein is conserved among the mammalian Laurasiatheria branch. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2009] |
ZBED6 Genezinc finger, BED-type containing 6 The protein encoded by this transposon-derived intronless gene is a transcriptional repressor that binds to the consensus sequence 5'-GCTCGC-3'. The encoded protein has been shown to repress IGF2 transcription. This gene is located within the first intron of the ZC3H11A gene. [provided by RefSeq, Jul 2016] |
ZBED8 Genezinc finger, BED-type containing 8 Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBED9 Genezinc finger, BED-type containing 9 Predicted to enable nucleic acid binding activity. Involved in positive regulation of cell cycle and positive regulation of epithelial cell proliferation. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF29P Genezinc finger protein 29, pseudogene |
ZNF736P2Y Genezinc finger protein 736 pseudogene 2, Y-linked |
GATAD2B GeneGATA zinc finger domain containing 2B This gene encodes a zinc finger protein transcriptional repressor. The encoded protein is part of the methyl-CpG-binding protein-1 complex, which represses gene expression by deacetylating methylated nucleosomes. Mutations in this gene are linked to intellectual disability and dysmorphic features associated with cognitive disability. [provided by RefSeq, Jun 2016] |
ZNF296 Genezinc finger protein 296 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of dendrite development; regulation of transcription by RNA polymerase II; and spermatogenesis. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF292 Genezinc finger protein 292 This gene encodes a growth hormone-dependent, zinc finger transcription factor that functions as a tumor suppressor. Naturally occurring mutations in this gene are associated with gastric cancer, colorectal cancer, and chronic lymphocytic leukemia. [provided by RefSeq, May 2017] |
ZNF962P Genezinc finger protein 962, pseudogene |
RFPL4AP4 Generet finger protein-like 4A pseudogene 4 |
RFPL4AP6 Generet finger protein-like 4A pseudogene 6 |
ZNF37CP Genezinc finger protein 37C, pseudogene |
RNF148 Genering finger protein 148 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in Golgi apparatus; endoplasmic reticulum; and late endosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF821 Genezinc finger protein 821 This gene encodes a protein with two C2H2 zinc finger motifs and a score-and-three (23)-amino acid peptide repeat (STPR) domain. The STPR domain of the encoded protein binds to double stranded DNA and may also contain a nuclear localization signal, suggesting that this protein interacts with chromosomal DNA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011] |
ZNF827 Genezinc finger protein 827 Enables NuRD complex binding activity. Involved in several processes, including establishment of protein localization to telomere; negative regulation of shelterin complex assembly; and telomere maintenance. Located in chromatin and chromosome, telomeric region. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF829 Genezinc finger protein 829 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
DBF4P1 GeneDBF4 zinc finger pseudogene 1 |
ZNF311 Genezinc finger protein 311 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF316 Genezinc finger protein 316 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF317 Genezinc finger protein 317 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF318 Genezinc finger protein 318 Predicted to enable protein heterodimerization activity and protein homodimerization activity. Predicted to be involved in negative regulation of DNA-templated transcription and positive regulation of DNA-templated transcription. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF319 Genezinc finger protein 319 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419748 Genezinc finger protein 852 pseudogene |
LOC100419741 Genezinc finger protein 772 pseudogene |
ST18 Genesuppression of tumorigenicity 18, zinc finger Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cytokine-mediated signaling pathway; negative regulation of cell population proliferation; and positive regulation of macromolecule metabolic process. Located in nucleus. Part of protein-DNA complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420347 Genepolycomb group ring finger 3 pseudogene |
DBF4B GeneDBF4 zinc finger B This gene encodes a regulator of the cell division cycle 7 homolog (S. cerevisiae) protein, a serine-threonine kinase which links cell cycle regulation to genome duplication. This protein localizes to the nucleus and, in complex with the cell division cycle 7 homolog (S. cerevisiae) protein, may facilitate M phase progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010] |
RNF149 Genering finger protein 149 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to act upstream of or within cellular response to xenobiotic stimulus; negative regulation of MAPK cascade; and regulation of protein stability. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF141 Genering finger protein 141 The protein encoded by this gene contains a RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. Abundant expression of this gene was found in the testicular tissue of fertile men, but was not detected in azoospermic patients. Studies of the mouse counterpart suggest that this gene may function as a testis specific transcription factor during spermatogenesis. [provided by RefSeq, Jul 2008] |
RNF145 Genering finger protein 145 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in endomembrane system. [provided by Alliance of Genome Resources, Mar 2025] |
RNF146 Genering finger protein 146 Enables poly-ADP-D-ribose binding activity and ubiquitin-protein transferase activity. Involved in positive regulation of canonical Wnt signaling pathway; protein ubiquitination; and ubiquitin-dependent protein catabolic process. Located in cytosol; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF6P1 Genering finger protein (C3H2C3 type) 6 pseudogene 1 |
ZNF818P Genezinc finger protein 818, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3HAV1L Genezinc finger CCCH-type, antiviral 1-like Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
ZFYVE19 Genezinc finger, FYVE domain containing 19 Enables phosphatidylinositol-3-phosphate binding activity. Involved in midbody abscission; mitotic cytokinesis checkpoint signaling; and negative regulation of cytokinesis. Located in centrosome; cleavage furrow; and midbody. Implicated in progressive familial intrahepatic cholestasis. [provided by Alliance of Genome Resources, Mar 2025] |
ZFYVE16 Genezinc finger, FYVE domain containing 16 This gene encodes an endosomal protein that belongs to the FYVE zinc finger family of proteins. The encoded protein is thought to regulate membrane trafficking in the endosome. This protein functions as a scaffold protein in the transforming growth factor-beta signaling pathway and is involved in positive and negative feedback regulation of the bone morphogenetic protein signaling pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
ZC2HC1A Genezinc finger, C2HC-type containing 1A Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF886P Genezinc finger protein 886, pseudogene |
ZNF33AP1 Genezinc finger protein 33A pseudogene 1 |
ZNF259P1 Genezinc finger protein 259 pseudogene 1 |
ZNF165 Genezinc finger protein 165 This gene encodes a member of the Kruppel family of zinc finger proteins. Members of this DNA-binding protein family act as transcriptional regulators. This gene is located within a cluster of zinc finger family members. The encoded protein may play a role in spermatogenesis. [provided by RefSeq, Jul 2008] |
LOC100131411 Genezinc finger protein 28 pseudogene |
BPTF Genebromodomain PHD finger transcription factor This gene was identified by the reactivity of its encoded protein to a monoclonal antibody prepared against brain homogenates from patients with Alzheimer's disease. Analysis of the original protein (fetal Alz-50 reactive clone 1, or FAC1), identified as an 810 aa protein containing a DNA-binding domain and a zinc finger motif, suggested it might play a role in the regulation of transcription. High levels of FAC1 were detected in fetal brain and in patients with neurodegenerative diseases. The protein encoded by this gene is actually much larger than originally thought, and it also contains a C-terminal bromodomain characteristic of proteins that regulate transcription during proliferation. The encoded protein is highly similar to the largest subunit of the Drosophila NURF (nucleosome remodeling factor) complex. In Drosophila, the NURF complex, which catalyzes nucleosome sliding on DNA and interacts with sequence-specific transcription factors, is necessary for the chromatin remodeling required for transcription. Two alternative transcripts encoding different isoforms have been described completely. [provided by RefSeq, Jul 2008] |
LOC100419896 Genezinc finger protein 267 pseudogene |
LOC100419894 Genezinc finger protein 347 pseudogene |
LOC100419895 Genezinc finger protein 670 pseudogene |
LOC100419892 Genezinc finger protein 592 pseudogene |
LOC100419890 Genezinc finger, MYM-type 4 pseudogene |
LOC100419891 Genezinc finger protein 114 pseudogene |
ZNF404 Genezinc finger protein 404 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF126P1 Genering finger protein 126 pseudogene 1 |
ZNF407 Genezinc finger protein 407 This gene encodes a zinc finger protein whose exact function is not known. It may be involved in transcriptional regulation. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
ZNF408 Genezinc finger protein 408 The protein encoded by this gene contains ten tandem zinc fingers and an N-terminal SET domain, so it is likely a DNA binding protein that interacts with other proteins. In adults, the encoded protein is expressed most highly in retina. Consequently, defects in this gene have been associated with familial exudative vitreoretinopathy (FEVR) and retinitis pigmentosa (RP). [provided by RefSeq, Dec 2016] |
BMI1P1 GeneBMI1 proto-oncogene, polycomb ring finger pseudogene 1 |
ZNF648 Genezinc finger protein 648 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF649 Genezinc finger protein 649 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of osteoblast differentiation and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF646 Genezinc finger protein 646 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF644 Genezinc finger protein 644 The protein encoded by this gene is a zinc finger transcription factor that may play a role in eye development. Defects in this gene have been associated with high myopia. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2011] |
ZNF645 Genezinc finger protein 645 This gene encodes a member of the zinc finger domain-containing protein family. This family member contains both a RING-type and a C2H2-type of zinc finger domain, and it may function as an E3 ubiquitin-protein ligase. Protein localization suggests a role in human sperm production and quality control. [provided by RefSeq, Aug 2011] |
ZNF641 Genezinc finger protein 641 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF398 Genezinc finger protein 398 This gene encodes a member of the Kruppel family of C2H2-type zinc-finger transcription factor proteins. The encoded protein acts as a transcriptional activator. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described, but their full length sequence has not been determined. [provided by RefSeq, Jul 2008] |
ZNF391 Genezinc finger protein 391 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF394 Genezinc finger protein 394 The protein encoded by this gene is a zinc finger protein that inhibits the transcription of mitogen-activated protein kinase signaling pathways. The encoded protein may be involved in cardiac function. [provided by RefSeq, Sep 2016] |
ZNF395 Genezinc finger protein 395 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF396 Genezinc finger protein 396 Enables protein heterodimerization activity; protein homodimerization activity; and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of DNA-templated transcription. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF397 Genezinc finger protein 397 This gene encodes a protein with a N-terminal SCAN domain, and the longer isoform contains nine C2H2-type zinc finger repeats in the C-terminal domain. The protein localizes to centromeres during interphase and early prophase, and different isoforms can repress or activate transcription in transfection studies. Multiple transcript variants encoding different isoforms have been found for this gene. Additional variants have been described, but their biological validity has not been determined. [provided by RefSeq, Oct 2009] |
ZBTB8OSP2 Genezinc finger and BTB domain containing 8 opposite strand pseudogene 2 |
ZFP36 GeneZFP36 ring finger protein Enables several functions, including 14-3-3 protein binding activity; heat shock protein binding activity; and mRNA 3'-UTR AU-rich region binding activity. Involved in several processes, including cellular response to cytokine stimulus; cellular response to epidermal growth factor stimulus; and regulation of gene expression. Acts upstream of or within mRNA catabolic process. Located in cytoplasmic ribonucleoprotein granule; cytosol; and nucleus. Part of ribonucleoprotein complex. Biomarker of breast cancer. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP37 GeneZFP37 zinc finger protein This gene encodes a transcription factor that belongs to a large family of zinc finger proteins. A similar protein in mouse is thought to play a role in regulating the structures of the nucleolus and centromere in neurons. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
ZFP30 GeneZFP30 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100129375 Genering finger protein 14 pseudogene |
ZNF774 Genezinc finger protein 774 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF542P Genezinc finger protein 542, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBBX Genezinc finger, B-box domain containing Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF619 Genezinc finger protein 619 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF204P Genezinc finger protein 204, pseudogene This locus represents a transcribed pseudogene, possibly of ZNF79 (GeneID 7633). The protein encoded by this locus would have significant N-terminal truncation, and would lack the KRAB domain and the C2H2 type zinc finger domain, compared to ZNF79. [provided by RefSeq, Jun 2011] |
HELZ2 Genehelicase with zinc finger 2, transcriptional coactivator The protein encoded by this gene is a nuclear transcriptional co-activator for peroxisome proliferator activated receptor alpha. The encoded protein contains a zinc finger and is a helicase that appears to be part of the peroxisome proliferator activated receptor alpha interacting complex. This gene is a member of the DNA2/NAM7 helicase gene family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
ZC3H11B Genezinc finger CCCH-type containing 11B pseudogene Predicted to enable metal ion binding activity. Predicted to be involved in poly(A)+ mRNA export from nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100887072 Genezinc finger protein 470 pseudogene |
LOC100887071 Genezinc finger protein 845 pseudogene |
LOC100887070 Genezinc finger protein 729 pseudogene |
ZFC3H1 Genezinc finger, C3H1-type containing Predicted to enable metal ion binding activity. Predicted to be involved in RNA processing. Located in nucleus. Part of nuclear exosome (RNase complex). [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419796 Genezinc finger protein 146 pseudogene |
LOC100419553 Genezinc finger protein 35 pseudogene |
LOC100419552 Genezinc finger protein 57 pseudogene |
LOC105379260 Geneputative zinc finger protein LOC441666 |
ZNF299P Genezinc finger protein 299, pseudogene |
ZNF93 Genezinc finger protein 93 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific. Involved in transposable element silencing. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF859P Genezinc finger protein 859, pseudogene |
ZFX Genezinc finger protein, X-linked This gene on the X chromosome is structurally similar to a related gene on the Y chromosome. It encodes a member of the krueppel C2H2-type zinc-finger protein family. The full-length protein contains an acidic transcriptional activation domain (AD), a nuclear localization sequence (NLS) and a DNA binding domain (DBD) consisting of 13 C2H2-type zinc fingers. Studies in mouse embryonic and adult hematopoietic stem cells showed that this gene was required as a transcriptional regulator for self-renewal of both stem cell types, but it was dispensable for growth and differentiation of their progeny. Multiple alternatively spliced transcript variants encoding different isoforms have been identified, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2010] |
ZFR Genezinc finger RNA binding protein This gene encodes an RNA-binding protein characterized by its DZF (domain associated with zinc fingers) domain. The encoded protein may play a role in the nucleocytoplasmic shuttling of another RNA-binding protein, Staufen homolog 2, in neurons. Expression of this gene is regulated through alternative polyadenylation that mediates differential microRNA targeting. Elevated expression of this gene has been observed in human patients with pancreatic cancer and knockdown of this gene may result in reduced viability and invasion of pancreatic cancer cells. [provided by RefSeq, Sep 2016] |
ZNF321P Genezinc finger protein 321, pseudogene |
ZC2HC1B Genezinc finger, C2HC-type containing 1B Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZC2HC1C Genezinc finger, C2HC-type containing 1C Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF891 Genezinc finger protein 891 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100287610 Genezinc finger protein 73-like |
ZNF488 Genezinc finger protein 488 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be involved in oligodendrocyte development and regulation of DNA-templated transcription. Predicted to act upstream of or within negative regulation of DNA-templated transcription and positive regulation of oligodendrocyte differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF480 Genezinc finger protein 480 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF483 Genezinc finger protein 483 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF484 Genezinc finger protein 484 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF485 Genezinc finger protein 485 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF486 Genezinc finger protein 486 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF487 Genezinc finger protein 487 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421368 Genezinc finger and SCAN domain containing 5A pseudogene |
RNF138P2 Genering finger protein 138, E3 ubiquitin protein ligase pseudogene 2 |
SNAI2 Genesnail family zinc finger 2 This gene encodes a member of the Snail family of C2H2-type zinc finger transcription factors. The encoded protein acts as a transcriptional repressor that binds to E-box motifs and is also likely to repress E-cadherin transcription in breast carcinoma. This protein is involved in epithelial-mesenchymal transitions and has antiapoptotic activity. Mutations in this gene may be associated with sporatic cases of neural tube defects. [provided by RefSeq, Jul 2008] |
SNAI3 Genesnail family zinc finger 3 SNAI3 is a member of the SNAIL gene family, named for the Drosophila snail gene, which plays roles in mesodermal formation during embryogenesis (Katoh and Katoh, 2003 [PubMed 12579345]).[supplied by OMIM, Apr 2009] |
SNAI1 Genesnail family zinc finger 1 The Drosophila embryonic protein snail is a zinc finger transcriptional repressor which downregulates the expression of ectodermal genes within the mesoderm. The nuclear protein encoded by this gene is structurally similar to the Drosophila snail protein, and is also thought to be critical for mesoderm formation in the developing embryo. At least two variants of a similar processed pseudogene have been found on chromosome 2. [provided by RefSeq, Jul 2008] |
LOC100533634 Genezinc finger protein 737 pseudogene |
DZIP3 GeneDAZ interacting zinc finger protein 3 Enables several functions, including phosphatase binding activity; polyubiquitin modification-dependent protein binding activity; and ubiquitin-protein transferase activity. Involved in protein polyubiquitination. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
DZIP1 GeneDAZ interacting zinc finger protein 1 Enables BBSome binding activity and molecular adaptor activity. Involved in cilium organization; heart development; and protein-containing complex localization to centriolar satellite. Located in cytoplasm; microtubule organizing center; and nucleoplasm. Implicated in mitral valve prolapse and spermatogenic failure 47. [provided by Alliance of Genome Resources, Mar 2025] |
ZNHIT1P1 Genezinc finger, HIT-type containing 1 pseudogene 1 |
ZNF587P1 Genezinc finger protein 587 pseudogene 1 |
ZNF569 Genezinc finger protein 569 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF568 Genezinc finger protein 568 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in embryonic placenta morphogenesis and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF567 Genezinc finger protein 567 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF566 Genezinc finger protein 566 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF565 Genezinc finger protein 565 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF564 Genezinc finger protein 564 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF563 Genezinc finger protein 563 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF562 Genezinc finger protein 562 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF561 Genezinc finger protein 561 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF849P Genezinc finger protein 849, pseudogene |
LOC100996670 Genezinc finger, FYVE domain containing 9 pseudogene |
ZNF169 Genezinc finger protein 169 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF286A Genezinc finger protein 286A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF286B Genezinc finger protein 286B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF160 Genezinc finger protein 160 The protein encoded by this gene is a Kruppel-related zinc finger protein which is characterized by the presence of an N-terminal repressor domain, the Kruppel-associated box (KRAB). The KRAB domain is a potent repressor of transcription; thus this protein may function in transcription regulation. Multiple transcript variants have been found for this gene. [provided by RefSeq, Apr 2016] |
ZNF768 Genezinc finger protein 768 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF765 Genezinc finger protein 765 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF764 Genezinc finger protein 764 Enables transcription coregulator activity. Involved in cellular response to glucocorticoid stimulus. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF766 Genezinc finger protein 766 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF761 Genezinc finger protein 761 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF763 Genezinc finger protein 763 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF34 Genezinc finger protein 34 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF35 Genezinc finger protein 35 Enables DNA-binding transcription factor activity and sequence-specific DNA binding activity. Predicted to be involved in cellular response to retinoic acid; regulation of transcription by RNA polymerase II; and spermatogenesis. Located in nucleus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF32 Genezinc finger protein 32 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF30 Genezinc finger protein 30 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF804A Genezinc finger protein 804A The protein encoded by this gene is a zinc finger binding protein. Polymorphisms in this gene, especially rs1344706, are thought to confer increased susceptibility to schizophrenia, bipolar disorder, and heroin addiciton. [provided by RefSeq, Nov 2015] |
ZNF804B Genezinc finger protein 804B Predicted to enable metal ion binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF658B Genezinc finger protein 658B, pseudogene Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC441528 Genezinc finger protein 839-like |
LOC401261 Genezinc finger protein ZIC 5 |
CIZ1 GeneCDKN1A interacting zinc finger protein 1 The protein encoded by this gene is a zinc finger DNA binding protein that interacts with CIP1, part of a complex with cyclin E. The encoded protein may regulate the cellular localization of CIP1. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012] |
ZC4H2 Genezinc finger, C4H2 domain containing This gene encodes a member of the zinc finger domain-containing protein family. This family member has a C-terminal zinc finger domain that is characterized by four cysteine residues and two histidine residues, and it also includes a coiled-coil region. This protein has been detected as an autoantigen in hepatocellular carcinoma patients. This gene has been identified as a potential candidate for X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011] |
LOC100133252 Genezinc finger protein 131 pseudogene |
ZNF264 Genezinc finger protein 264 This gene encodes a zinc finger protein and belongs to the krueppel C2H2-type zinc-finger protein family. Zinc finger proteins are often localized in the nucleus, bind nucleic acids, and regulate transcription. [provided by RefSeq, Jan 2010] |
ZNF266 Genezinc finger protein 266 This gene encodes a protein containing many tandem zinc-finger motifs. Zinc fingers are protein or nucleic acid-binding domains, and may be involved in a variety of functions, including regulation of transcription. This gene is located in a cluster of similar genes encoding zinc finger proteins on chromosome 19. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012] |
ZNF260 Genezinc finger protein 260 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF263 Genezinc finger protein 263 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and transcription cis-regulatory region binding activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF268 Genezinc finger protein 268 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in several processes, including positive regulation of non-canonical NF-kappaB signal transduction; regulation of apoptotic process; and regulation of primary metabolic process. Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB26 Genezinc finger and BTB domain containing 26 Enables identical protein binding activity and sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB24 Genezinc finger and BTB domain containing 24 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be located in nucleus. Implicated in immunodeficiency-centromeric instability-facial anomalies syndrome 2. [provided by Alliance of Genome Resources, Mar 2025] |
RNF38 Genering finger protein 38 This gene encodes a protein with a coiled-coil motif and a RING-H2 motif (C3H2C2) at its carboxy-terminus. The RING motif is a zinc-binding domain found in a large set of proteins playing roles in diverse cellular processes including oncogenesis, development, signal transduction, and apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008] |
RNF39 Genering finger protein 39 This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
RNF34 Genering finger protein 34, E3 ubiquitin protein ligase The protein encoded by this gene contains a RINF finger, a motif known to be involved in protein-protein and protein-DNA interactions. This protein interacts with DNAJA3/hTid-1, which is a DnaJ protein reported to function as a modulator of apoptosis. Overexpression of this gene in Hela cells was shown to confer the resistance to TNF-alpha induced apoptosis, suggesting an anti-apoptotic function of this protein. This protein can be cleaved by caspase-3 during the induction of apoptosis. This protein also targets p53 and phospho-p53 for degradation. Alternatively splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2012] |
RNF32 Genering finger protein 32 The protein encoded by this gene contains two RING ring finger motifs. RING finger motifs are present in a variety of functionally distinct proteins and are known to be involved in protein-DNA or protein-protein interactions. This gene was found to be expressed during spermatogenesis, most likely in spermatocytes and/or in spermatids. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
RNF31 Genering finger protein 31 The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The encoded protein is the E3 ubiquitin-protein ligase component of the linear ubiquitin chain assembly complex. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015] |
MZF1 Genemyeloid zinc finger 1 Enables DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and protein homodimerization activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419845 Genezinc finger protein 415 pseudogene |
LOC100419844 Genezinc finger protein 610 pseudogene |
LOC100419847 Genezinc finger protein 436 pseudogene |
LOC100419841 Genezinc finger protein 107 pseudogene |
LOC100419840 Genezinc finger protein 446 pseudogene |
LOC100419842 Genezinc finger protein 396 pseudogene |
LOC100128601 Genezinc finger protein 770 pseudogene |
PHF5A GenePHD finger protein 5A This gene encodes a subunit of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence-independent manner and may anchor the U2 snRNP to the pre-mRNA. The protein encoded by this gene contains a PHD-finger-like domain that is flanked by highly basic N- and C-termini. This protein belongs to the PHD-finger superfamily and may act as a chromatin-associated protein. This gene has several pseudogenes on different chromosomes. [provided by RefSeq, Jul 2008] |
ZRSR1 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 1 Predicted to enable pre-mRNA 3'-splice site binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleus. Predicted to be part of U2AF complex and spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
IKZF5 GeneIKAROS family zinc finger 5 (Pegasus) Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Pegasus, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002] |
IKZF4 GeneIKAROS family zinc finger 4 (Eos) Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Eos, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002] |
IKZF1 GeneIKAROS family zinc finger 1 (Ikaros) This gene encodes a transcription factor that belongs to the family of zinc-finger DNA-binding proteins associated with chromatin remodeling. The expression of this protein is restricted to the fetal and adult hemo-lymphopoietic system, and it functions as a regulator of lymphocyte differentiation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. Most isoforms share a common C-terminal domain, which contains two zinc finger motifs that are required for hetero- or homo-dimerization, and for interactions with other proteins. The isoforms, however, differ in the number of N-terminal zinc finger motifs that bind DNA and in nuclear localization signal presence, resulting in members with and without DNA-binding properties. Only a few isoforms contain the requisite three or more N-terminal zinc motifs that confer high affinity binding to a specific core DNA sequence element in the promoters of target genes. The non-DNA-binding isoforms are largely found in the cytoplasm, and are thought to function as dominant-negative factors. Overexpression of some dominant-negative isoforms have been associated with B-cell malignancies, such as acute lymphoblastic leukemia (ALL). [provided by RefSeq, May 2014] |
IKZF3 GeneIKAROS family zinc finger 3 (Aiolos) This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This gene product is a transcription factor that is important in the regulation of B lymphocyte proliferation and differentiation. Both Ikaros and Aiolos can participate in chromatin remodeling. Regulation of gene expression in B lymphocytes by Aiolos is complex as it appears to require the sequential formation of Ikaros homodimers, Ikaros/Aiolos heterodimers, and Aiolos homodimers. Several alternative transcripts encoding different isoforms have been described, as well as some non-protein coding variants. [provided by RefSeq, Apr 2012] |
IKZF2 GeneIKAROS family zinc finger 2 (Helios) This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This protein forms homo- or hetero-dimers with other Ikaros family members, and is thought to function predominantly in early hematopoietic development. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008] |
WIZ Genewidely interspaced zinc finger motifs Enables several functions, including RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; histone methyltransferase binding activity; and transcription corepressor binding activity. Involved in positive regulation of nuclear cell cycle DNA replication and protein stabilization. Located in midbody and nucleoplasm. Biomarker of atherosclerosis. [provided by Alliance of Genome Resources, Mar 2025] |
BRPF3 Genebromodomain and PHD finger containing, 3 Contributes to histone acetyltransferase activity. Involved in positive regulation of DNA replication. Located in nucleus. Part of MOZ/MORF histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
BRPF1 Genebromodomain and PHD finger containing, 1 This gene encodes a bromodomain, PHD finger and chromo/Tudor-related Pro-Trp-Trp-Pro (PWWP) domain containing protein. The encoded protein is a component of the MOZ/MORF histone acetyltransferase complexes which function as a transcriptional regulators. This protein binds to the catalytic MYST domains of the MOZ and MORF proteins and may play a role in stimulating acetyltransferase and transcriptional activity of the complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016] |
ZNF879 Genezinc finger protein 879 This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and thirteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017] |
ZNF878 Genezinc finger protein 878 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF10P1 GenePHD finger protein 10 pseudogene 1 |
LOC100421087 Genezinc finger, CCHC domain containing 9 pseudogene |
RNF114 Genering finger protein 114 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein polyubiquitination and ubiquitin-dependent protein catabolic process. Located in cytosol and plasma membrane. Biomarker of male infertility. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H15 Genezinc finger CCCH-type containing 15 Enables RNA binding activity and cadherin binding activity. Involved in positive regulation of GTPase activity. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP82 GeneZFP82 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF130 Genering finger protein 130 The protein encoded by this gene contains a RING finger motif and is similar to g1, a Drosophila zinc-finger protein that is expressed in mesoderm and involved in embryonic development. The expression of the mouse counterpart was found to be upregulated in myeloblastic cells following IL3 deprivation, suggesting that this gene may regulate growth factor withdrawal-induced apoptosis of myeloid precursor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
RNF133 Genering finger protein 133 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene has no intron. [provided by RefSeq, Jul 2008] |
RNF135 Genering finger protein 135 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene is located in a chromosomal region known to be frequently deleted in patients with neurofibromatosis. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
RNF138 Genering finger protein 138, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008] |
RNF139 Genering finger protein 139 The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP. [provided by RefSeq, Jul 2008] |
TSHZ2 Geneteashirt zinc finger homeobox 2 This gene is a member of the teashirt C2H2-type zinc-finger protein family of transcription factors. This gene encodes a protein with five C2H2-type zinc fingers, a homeobox DNA-binding domain and a coiled-coil domain. This nuclear protein is predicted to act as a transcriptional repressor. This gene is thought to play a role in the development and progression of breast and other types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
TSHZ3 Geneteashirt zinc finger homeobox 3 This gene encodes a zinc-finger transcription factor that regulates smooth muscle cell differentiation in the developing urinary tract. Consistent with this role, mice in which this gene has been inactivated exhibit abnormal gene expression in urinary tract smooth muscle cell precursors and kidney defects including hydronephrosis. The encoded transcription factor comprises a gene silencing complex that inhibits caspase expression. Reduced expression of this gene and consequent caspase upregulation may be correlated with progression of Alzheimer's disease in human patients. [provided by RefSeq, Jul 2016] |
TSHZ1 Geneteashirt zinc finger homeobox 1 This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012] |
RNF7P1 Genering finger protein 7 pseudogene 1 |
ZFAND6 Genezinc finger, AN1-type domain 6 Predicted to enable polyubiquitin modification-dependent protein binding activity. Involved in cellular response to tumor necrosis factor; negative regulation of apoptotic process; and regulation of canonical NF-kappaB signal transduction. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND5 Genezinc finger, AN1-type domain 5 Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to act upstream of or within several processes, including face development; fibroblast migration; and platelet-derived growth factor receptor signaling pathway. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND4 Genezinc finger, AN1-type domain 4 Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND3 Genezinc finger, AN1-type domain 3 Predicted to enable DNA binding activity and zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND1 Genezinc finger, AN1-type domain 1 Enables proteasome binding activity. Involved in cellular response to arsenite ion; positive regulation of intracellular protein transport; and stress granule disassembly. Located in cytoplasmic stress granule. [provided by Alliance of Genome Resources, Mar 2025] |
PIKFYVE Genephosphoinositide kinase, FYVE finger containing Phosphorylated derivatives of phosphatidylinositol (PtdIns) regulate cytoskeletal functions, membrane trafficking, and receptor signaling by recruiting protein complexes to cell- and endosomal-membranes. Humans have multiple PtdIns proteins that differ by the degree and position of phosphorylation of the inositol ring. This gene encodes an enzyme (PIKfyve; also known as phosphatidylinositol-3-phosphate 5-kinase type III or PIPKIII) that phosphorylates the D-5 position in PtdIns and phosphatidylinositol-3-phosphate (PtdIns3P) to make PtdIns5P and PtdIns(3,5)biphosphate. The D-5 position also can be phosphorylated by type I PtdIns4P-5-kinases (PIP5Ks) that are encoded by distinct genes and preferentially phosphorylate D-4 phosphorylated PtdIns. In contrast, PIKfyve preferentially phosphorylates D-3 phosphorylated PtdIns. In addition to being a lipid kinase, PIKfyve also has protein kinase activity. PIKfyve regulates endomembrane homeostasis and plays a role in the biogenesis of endosome carrier vesicles from early endosomes. The protein plays a key role in cell entry of ebola virus and SARS-CoV-2 by endocytosis Mutations in this gene cause corneal fleck dystrophy (CFD); an autosomal dominant disorder characterized by numerous small white flecks present in all layers of the corneal stroma. Histologically, these flecks appear to be keratocytes distended with lipid and mucopolysaccharide filled intracytoplasmic vacuoles. [provided by RefSeq, Jul 2021] |
ZFP36L1 GeneZFP36 ring finger protein-like 1 This gene is a member of the TIS11 family of early response genes, which are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. This gene is well conserved across species and has a promoter that contains motifs seen in other early-response genes. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
ZFP36L2 GeneZFP36 ring finger protein-like 2 This gene is a member of the TIS11 family of early response genes. Family members are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. [provided by RefSeq, Jul 2008] |
ZNF92P1Y Genezinc finger protein 92 pseudogene 1, Y-linked |
LONRF2P2 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene 2 |
LONRF2P1 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene 1 |
ZFYVE27 Genezinc finger, FYVE domain containing 27 This gene encodes a protein with several transmembrane domains, a Rab11-binding domain and a lipid-binding FYVE finger domain. The encoded protein appears to promote neurite formation. A mutation in this gene has been reported to be associated with hereditary spastic paraplegia, however the pathogenicity of the mutation, which may simply represent a polymorphism, is unclear. [provided by RefSeq, Mar 2010] |
ZFYVE26 Genezinc finger, FYVE domain containing 26 This gene encodes a protein which contains a FYVE zinc finger binding domain. The presence of this domain is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane. Mutations in this gene are associated with autosomal recessive spastic paraplegia-15. [provided by RefSeq, Oct 2008] |
ZFYVE28 Genezinc finger, FYVE domain containing 28 Enables phosphatidylinositol-3-phosphate binding activity. Involved in negative regulation of epidermal growth factor-activated receptor activity. Located in cytosol and early endosome membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105372810 Geneputative zinc finger protein 355P |
ZNF157 Genezinc finger protein 157 This gene product is a likely zinc finger family transcription factor. It contains KRAB-A and KRAB-B domains that act as transcriptional repressors in related proteins, and multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. This gene is part of a gene cluster on chromosome Xp11.23. [provided by RefSeq, Jul 2008] |
ZNF154 Genezinc finger protein 154 This gene encodes a protein that belongs to the zinc finger Kruppel family of transcriptional regulators, whose members are thought to function in normal and abnormal cell growth and differentiation. Hypermethylation of this gene is associated with the recurrence of non muscle invasive bladder cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ZNF155 Genezinc finger protein 155 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105369224 Genezinc finger protein 806 pseudogene |
ZNF444P1 Genezinc finger protein 444 pseudogene 1 |
LOC344065 Genezinc finger protein 184 pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF8 Genering finger protein 8, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger motif and an FHA domain. This protein has been shown to interact with several class II ubiquitin-conjugating enzymes (E2), including UBE2E1/UBCH6, UBE2E2, and UBE2E3, and may act as an ubiquitin ligase (E3) in the ubiquitination of certain nuclear proteins. This protein is also known to play a role in the DNA damage response and depletion of this protein causes cell growth inhibition and cell cycle arrest. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
RNF6 Genering finger protein (C3H2C3 type) 6 The protein encoded by this gene contains a RING-H2 finger motif. Deletions and mutations in this gene were detected in esophageal squamous cell carcinoma (ESCC), suggesting that this protein may be a potential tumor suppressor. Studies of the mouse counterpart suggested a role of this protein in the transcription regulation that controls germinal differentiation. Multiple alternatively spliced transcript variants encoding the same protein are observed. [provided by RefSeq, Jul 2008] |
RNF7 Genering finger protein 7 The protein encoded by this gene is a highly conserved ring finger protein. It is an essential subunit of SKP1-cullin/CDC53-F box protein ubiquitin ligases, which are a part of the protein degradation machinery important for cell cycle progression and signal transduction. This protein interacts with, and is a substrate of, casein kinase II (CSNK2A1/CKII). The phosphorylation of this protein by CSNK2A1 has been shown to promote the degradation of IkappaBalpha (CHUK/IKK-alpha/IKBKA) and p27Kip1(CDKN1B). Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
RNF4 Genering finger protein 4 The protein encoded by this gene contains a RING finger motif and acts as a transcription regulator. This protein has been shown to interact with, and inhibit the activity of, TRPS1, a transcription suppressor of GATA-mediated transcription. Transcription repressor ZNF278/PATZ is found to interact with this protein, and thus reduce the enhancement of androgen receptor-dependent transcription mediated by this protein. Studies of the mouse and rat counterparts suggested a role of this protein in spermatogenesis. A pseudogene of this gene is found on chromosome 1.[provided by RefSeq, Jul 2010] |
RNF5 Genering finger protein 5, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008] |
RNF2 Genering finger protein 2 Polycomb group (PcG) of proteins form the multiprotein complexes that are important for the transcription repression of various genes involved in development and cell proliferation. The protein encoded by this gene is one of the PcG proteins. It has been shown to interact with, and suppress the activity of, transcription factor CP2 (TFCP2/CP2). Studies of the mouse counterpart suggested the involvement of this gene in the specification of anterior-posterior axis, as well as in cell proliferation in early development. This protein was also found to interact with huntingtin interacting protein 2 (HIP2), an ubiquitin-conjugating enzyme, and possess ubiquitin ligase activity. [provided by RefSeq, Jul 2008] |
LOC100301990 Genezinc finger protein 610 pseudogene |
ZNF887P Genezinc finger protein 887, pseudogene |
LOC101060181 Genezinc finger protein ZnFP12 |
ZC3H7A Genezinc finger CCCH-type containing 7A Enables miRNA binding activity. Involved in miRNA processing. Acts upstream of with a positive effect on post-transcriptional regulation of gene expression. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LONRF3 GeneLON peptidase N-terminal domain and ring finger 3 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Multiple alternatively spliced transcript variants have been suggested, but their full length natures are not clear. [provided by RefSeq, Jul 2008] |
LONRF2 GeneLON peptidase N-terminal domain and ring finger 2 Predicted to enable ubiquitin protein ligase activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LONRF1 GeneLON peptidase N-terminal domain and ring finger 1 Predicted to enable ubiquitin protein ligase activity. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
RNF5P1 Genering finger protein 5, E3 ubiquitin protein ligase pseudogene 1 |
ZNF699 Genezinc finger protein 699 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF691 Genezinc finger protein 691 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF692 Genezinc finger protein 692 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II and regulation of gluconeogenesis. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF695 Genezinc finger protein 695 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF697 Genezinc finger protein 697 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF696 Genezinc finger protein 696 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419712 Genezinc finger protein 12 pseudogene |
LOC100419715 Genezinc finger protein 626 pseudogene |
LOC100419716 Genezinc finger protein 709 pseudogene |
ZNF343 Genezinc finger protein 343 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF341 Genezinc finger protein 341 Enables DNA binding activity and DNA-binding transcription activator activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. Implicated in hyper IgE recurrent infection syndrome 3. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF347 Genezinc finger protein 347 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF346 Genezinc finger protein 346 The protein encoded by this gene is a nucleolar, zinc finger protein that preferentially binds to double-stranded (ds) RNA or RNA/DNA hybrids, rather than DNA alone. Mutational studies indicate that the zinc finger domains are not only essential for dsRNA binding, but are also required for its nucleolar localization. The encoded protein may be involved in cell growth and survival. It plays a role in protecting neurons by inhibiting cell cycle re-entry via stimulation of p21 gene expression. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
ZNF345 Genezinc finger protein 345 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PCGF1 Genepolycomb group ring finger 1 PCGF1 is a mammalian homolog of the Drosophila polycomb group genes, which act as transcriptional repressors to regulate anterior-posterior patterning in early embryonic development (Nunes et al., 2001 [PubMed 11287196]). See also PCGF2 (MIM 600346).[supplied by OMIM, Aug 2008] |
PCGF3 Genepolycomb group ring finger 3 The protein encoded by this gene contains a C3HC4 type RING finger, which is a motif known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. [provided by RefSeq, Jul 2008] |
PCGF2 Genepolycomb group ring finger 2 The protein encoded by this gene contains a RING finger motif and is similar to the polycomb group (PcG) gene products. PcG gene products form complexes via protein-protein interaction and maintain the transcription repression of genes involved in embryogenesis, cell cycles, and tumorigenesis. This protein was shown to act as a negative regulator of transcription and has tumor suppressor activity. The expression of this gene was detected in various tumor cells, but is limited in neural organs in normal tissues. Knockout studies in mice suggested that this protein may negatively regulate the expression of different cytokines, chemokines, and chemokine receptors, and thus plays an important role in lymphocyte differentiation and migration, as well as in immune responses. [provided by RefSeq, Jul 2008] |
PCGF5 Genepolycomb group ring finger 5 Predicted to enable histone H2AK119 ubiquitin ligase activity. Acts upstream of or within positive regulation of transcription by RNA polymerase II. Located in Golgi apparatus; centrosome; and nucleoplasm. Part of PcG protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
PCGF6 Genepolycomb group ring finger 6 The protein encoded by this gene contains a RING finger motif, which is most closely related to those of polycomb group (PcG) proteins RNF110/MEL-18 and BMI1. PcG proteins are known to form protein complexes and function as transcription repressors. This protein has been shown to interact with some PcG proteins and act as a transcription repressor. The activity of this protein is found to be regulated by cell cycle dependent phosphorylation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
LOC100421071 Genezinc finger, CCHC domain containing 10 pseudogene |
ZBTB39 Genezinc finger and BTB domain containing 39 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB38 Genezinc finger and BTB domain containing 38 The protein encoded by this gene is a zinc finger transcriptional activator that binds methylated DNA. The encoded protein can form homodimers or heterodimers through the zinc finger domains. In mouse, inhibition of this protein has been associated with apoptosis in some cell types. [provided by RefSeq, Jun 2010] |
ZBTB33 Genezinc finger and BTB domain containing 33 This gene encodes a transcriptional regulator with bimodal DNA-binding specificity, which binds to methylated CGCG and also to the non-methylated consensus KAISO-binding site TCCTGCNA. The protein contains an N-terminal POZ/BTB domain and 3 C-terminal zinc finger motifs. It recruits the N-CoR repressor complex to promote histone deacetylation and the formation of repressive chromatin structures in target gene promoters. It may contribute to the repression of target genes of the Wnt signaling pathway, and may also activate transcription of a subset of target genes by the recruitment of catenin delta-2 (CTNND2). Its interaction with catenin delta-1 (CTNND1) inhibits binding to both methylated and non-methylated DNA. It also interacts directly with the nuclear import receptor Importin-α2 (also known as karyopherin alpha2 or RAG cohort 1), which may mediate nuclear import of this protein. Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq, May 2010] |
ZBTB32 Genezinc finger and BTB domain containing 32 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; identical protein binding activity; and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB34 Genezinc finger and BTB domain containing 34 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB37 Genezinc finger and BTB domain containing 37 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in chromatin. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929598 Genezinc finger CCHC domain-containing protein 10 pseudogene |
LOC645749 Genezinc finger protein 131 pseudogene |
LOC100419690 Genezinc finger protein 114 pseudogene |
LOC100419691 Genezinc finger protein 114 pseudogene |
LOC100419692 Genezinc finger protein 791 pseudogene |
LOC100419693 Genezinc finger protein 114 pseudogene |
DBF4 GeneDBF4 zinc finger Predicted to enable protein serine/threonine kinase activator activity. Predicted to be involved in positive regulation of nuclear cell cycle DNA replication and regulation of cell cycle phase transition. Located in nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF75CP Genezinc finger protein 75C, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZGRF1 Genezinc finger, GRF-type containing 1 The encoded protein contains GRF zinc finger (zf-GRF) and transmembrane domains. GRF zinc fingers are found in a number of DNA-binding proteins. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017] |
ZNF354A Genezinc finger protein 354A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nucleolus; and nucleoplasm. Biomarker of in situ carcinoma and seminoma. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF354C Genezinc finger protein 354C Enables DNA-binding transcription repressor activity, RNA polymerase II-specific. Involved in negative regulation of sprouting angiogenesis. Located in cytoplasm; nuclear membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF354B Genezinc finger protein 354B Predicted to enable several functions, including DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and transcription corepressor activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420298 Genemakorin ring finger protein 1 pseudogene |
ZNF602P Genezinc finger protein 602, pseudogene |
ZNF90P2 Genezinc finger protein 90 pseudogene 2 |
ZNF90P3 Genezinc finger protein 90 pseudogene 3 |
ZNF90P1 Genezinc finger protein 90 pseudogene 1 |
GLIS2 GeneGLIS family zinc finger 2 This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this protein's C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys.[provided by RefSeq, Jan 2010] |
GLIS3 GeneGLIS family zinc finger 3 This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear protein with five C2H2-type zinc finger domains. This protein functions as both a repressor and activator of transcription and is specifically involved in the development of pancreatic beta cells, the thyroid, eye, liver and kidney. Mutations in this gene have been associated with neonatal diabetes and congenital hypothyroidism (NDH). Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only two have been determined. [provided by RefSeq, Jul 2008] |
GLIS1 GeneGLIS family zinc finger 1 GLIS1 is a GLI (MIM 165220)-related Kruppel-like zinc finger protein that functions as an activator and repressor of transcription (Kim et al., 2002 [PubMed 12042312]).[supplied by OMIM, Mar 2008] |
ZNF324B Genezinc finger protein 324B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF324 Genezinc finger protein 324 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Acts upstream of or within with a positive effect on G1/S transition of mitotic cell cycle and cell population proliferation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF320 Genezinc finger protein 320 ZNF320 encodes a Kruppel-like zinc finger protein. Members of this protein family are involved in activation or repression of transcription.[supplied by OMIM, Jul 2002] |
FLYWCH1P1 GeneFLYWCH-type zinc finger 1 pseudogene 1 |
LOC100419774 Genezinc finger protein 383 pseudogene |
ZNF451 Genezinc finger protein 451 Enables SUMO ligase activity; transcription corepressor activity; and transcription regulator inhibitor activity. Involved in negative regulation of transcription initiation by RNA polymerase II; negative regulation of transforming growth factor beta receptor signaling pathway; and protein sumoylation. Located in PML body. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF454 Genezinc finger protein 454 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
DBF4P2 GeneDBF4 zinc finger pseudogene 2 |
DZIP1L GeneDAZ interacting zinc finger protein 1-like Predicted to enable metal ion binding activity. Involved in cilium assembly and regulation of protein localization. Located in centriole and ciliary basal body. Implicated in polycystic kidney disease 5. [provided by Alliance of Genome Resources, Mar 2025] |
SH3RF2 GeneSH3 domain containing ring finger 2 Enables protein phosphatase 1 binding activity and ubiquitin protein ligase activity. Involved in several processes, including positive regulation of JNK cascade; protein autoubiquitination; and regulation of protein metabolic process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SH3RF3 GeneSH3 domain containing ring finger 3 Enables ubiquitin protein ligase activity. Involved in positive regulation of JNK cascade and protein autoubiquitination. [provided by Alliance of Genome Resources, Mar 2025] |
SH3RF1 GeneSH3 domain containing ring finger 1 This gene encodes a protein containing an N-terminus RING-finger, four SH3 domains, and a region implicated in binding of the Rho GTPase Rac. Via the RING-finger, the encoded protein has been shown to function as an ubiquitin-protein ligase involved in protein sorting at the trans-Golgi network. The encoded protein may also act as a scaffold for the c-Jun N-terminal kinase signaling pathway, facilitating the formation of a functional signaling module. [provided by RefSeq, Jul 2008] |
ZNF723P Genezinc finger protein 723, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF2P2 GenePHD finger protein 2 pseudogene 2 |
PHF2P1 GenePHD finger protein 2 pseudogene 1 |
ZBTB8OSP1 Genezinc finger and BTB domain containing 8 opposite strand pseudogene 1 |
ZFAT Genezinc finger and AT hook domain containing This gene encodes a protein that likely binds DNA and functions as a transcriptional regulator involved in apoptosis and cell survival. This gene resides in a susceptibility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009] |
ZNF611 Genezinc finger protein 611 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF610 Genezinc finger protein 610 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF613 Genezinc finger protein 613 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF615 Genezinc finger protein 615 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF614 Genezinc finger protein 614 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF616 Genezinc finger protein 616 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF618 Genezinc finger protein 618 Enables identical protein binding activity and transcription coregulator binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in pericentric heterochromatin. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419791 Genezinc finger protein 449 pseudogene |
LOC100419790 Genezinc finger protein 670 pseudogene |
LOC100419795 Genezinc finger, MYM-type 1 pseudogene |
LOC100419794 Genezinc finger protein 449 pseudogene |
ZSCAN29 Genezinc finger and SCAN domain containing 29 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN25 Genezinc finger and SCAN domain containing 25 This gene encodes a protein that bears some similarity to zinc finger proteins, which are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants have been identified, but the full-length nature for most of them has not been determined. [provided by RefSeq, Jul 2008] |
ZSCAN26 Genezinc finger and SCAN domain containing 26 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN20 Genezinc finger and SCAN domain containing 20 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN21 Genezinc finger and SCAN domain containing 21 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN22 Genezinc finger and SCAN domain containing 22 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN23 Genezinc finger and SCAN domain containing 23 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100533637 Genezinc finger protein 83 pseudogene |
LOC100533633 Genezinc finger protein 257 pseudogene |
LOC100533632 Genezinc finger protein 736 pseudogene |
ZNF518B Genezinc finger protein 518B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF518A Genezinc finger protein 518A The protein encoded by this gene is a member of the krueppel C2H2-type zinc finger protein family. The encoded protein contains five zinc fingers and is likely a nuclear transcriptional regulator. Numerous transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2016] |
ANKZF1 Geneankyrin repeat and zinc finger domain containing 1 Enables RNA endonuclease activity and catalytic activity, acting on a tRNA. Involved in cellular response to hydrogen peroxide; protein quality control for misfolded or incompletely synthesized proteins; and rescue of stalled ribosome. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF556 Genezinc finger protein 556 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF557 Genezinc finger protein 557 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF554 Genezinc finger protein 554 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF555 Genezinc finger protein 555 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF552 Genezinc finger protein 552 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF550 Genezinc finger protein 550 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF551 Genezinc finger protein 551 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF558 Genezinc finger protein 558 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF559 Genezinc finger protein 559 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF209P Genezinc finger protein 209, pseudogene |
LOC100131832 GeneZFP91 zinc finger protein pseudogene |
LOC729532 Genezinc finger protein 207 pseudogene |
ZNF790 Genezinc finger protein 790 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF791 Genezinc finger protein 791 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF792 Genezinc finger protein 792 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF793 Genezinc finger protein 793 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. Implicated in Barrett's esophagus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF799 Genezinc finger protein 799 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC346671 Genering finger protein 14 pseudogene |
RFPL3 Generet finger protein-like 3 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be located in nucleus. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL2 Generet finger protein-like 2 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131785 Genering finger protein 181 pseudogene |
ZNF833P Genezinc finger protein 833, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of gene expression. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF185 Genezinc finger protein 185 (LIM domain) Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a LIM-domain zinc finger protein. The LIM domain is composed of two contiguous zinc finger domains, separated by a two-amino acid residue hydrophobic linker. The LIM domain mediates protein:protein interactions. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, May 2010] |
ZNF184 Genezinc finger protein 184 The protein encoded by this gene is predicted to be a Kruppel C2H2-type zinc-finger protein family member. Sequence analysis predicts that the protein contains two Kruppel associated box (KRAB) boxes in the N-terminus and highly conserved zinc finger motifs at the C-terminus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016] |
ZNF181 Genezinc finger protein 181 Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2003] |
ZNF180 Genezinc finger protein 180 Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002] |
ZNF182 Genezinc finger protein 182 Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, May 2010] |
ZNF189 Genezinc finger protein 189 Kruppel-like zinc finger proteins such as ZNF189 contain a conserved stretch of 7 amino acids that connects a variable number of DNA-binding zinc finger repeats of the cys(2)his(2) (C2H2) type (summarized by Odeberg et al., 1998 [PubMed 9653648]). Approximately 30% of human Kruppel-like zinc finger proteins contain an N-terminal Kruppel-associated box (KRAB) domain. The KRAB domain consists of approximately 75 amino acids that may be subdivided into an A box, which is present in every KRAB domain and is essential for transcriptional repression, and a B box, which is not always present.[supplied by OMIM, May 2010] |
ZNF239 Genezinc finger protein 239 MOK2 proteins are DNA- and RNA-binding proteins that are mainly associated with nuclear RNP components, including the nucleoli and extranucleolar structures (Arranz et al., 1997 [PubMed 9121460]).[supplied by OMIM, Mar 2008] |
ZNF236 Genezinc finger protein 236 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cellular response to glucose stimulus. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF235 Genezinc finger protein 235 This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein is a member of the Kruppel family of zinc finger proteins, and contains Kruppel-associated box (KRAB) A and B domains and 15 tandemly arrayed C2H2-type zinc fingers. It is an ortholog of the mouse Zfp93 protein. This gene is located in a cluster of zinc finger genes on 19q13.2. [provided by RefSeq, Jul 2008] |
ZNF234 Genezinc finger protein 234 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF233 Genezinc finger protein 233 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF232 Genezinc finger protein 232 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF230 Genezinc finger protein 230 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100129734 Genezinc finger, AN1-type domain 1 pseudogene |
LOC100419870 Genezinc finger protein 717 pseudogene |
LOC100419872 Genezinc finger, MYM-type 4 pseudogene |
LOC100418549 Genezinc finger protein 93 pseudogene |
ZNF880 Genezinc finger protein 880 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF883 Genezinc finger protein 883 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC644746 Generet finger protein-like 3 pseudogene |
LOC100132599 Genezinc finger protein 114 pseudogene |
ZNF718 Genezinc finger protein 718 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF714 Genezinc finger protein 714 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF716 Genezinc finger protein 716 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF710 Genezinc finger protein 710 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF711 Genezinc finger protein 711 This gene encodes a zinc finger protein of unknown function. It bears similarity to a zinc finger protein which acts as a transcriptional activator. This gene lies in a region of the X chromosome which has been associated with cognitive disability. [provided by RefSeq, Jul 2008] |
ZNF713 Genezinc finger protein 713 The protein encoded by this gene contains C2H2 zinc finger domains. In some individuals, a CGG-repeat expansion from 5-22 repeats to 68-450 repeats has been identified in the first intron of this gene. This mutation is thought to effect the expression of this gene and it has been proposed that it may be associated with Autistic Spectrum Disorder. [provided by RefSeq, Jul 2016] |
ZNF45 Genezinc finger protein 45 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF44 Genezinc finger protein 44 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF43 Genezinc finger protein 43 This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008] |
ZNF41 Genezinc finger protein 41 This gene encodes a protein that contains KRAB-A and KRAB-B domains multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. An initial study suggested that this gene may be associated with X-linked cognitive disability, but a later study has called this finding into question (PMID:23871722).[provided by RefSeq, Apr 2016] |
ZNF48 Genezinc finger protein 48 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF717 Genezinc finger protein 717 This gene encodes a Kruppel-associated box (KRAB) zinc-finger protein, which belongs to a large group of transcriptional regulators in mammals. These proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation and apoptosis, and in regulating viral replication and transcription. A pseudogene of this gene was identified on chromosome 1. [provided by RefSeq, May 2016] |
VEZF1 Genevascular endothelial zinc finger 1 Transcriptional regulatory proteins containing tandemly repeated zinc finger domains are thought to be involved in both normal and abnormal cellular proliferation and differentiation. ZNF161 is a C2H2-type zinc finger protein (Koyano-Nakagawa et al., 1994 [PubMed 8035792]). See MIM 603971 for general information on zinc finger proteins.[supplied by OMIM, Sep 2008] |
LOC100631319 Genezinc finger protein 273 pseudogene |
LOC100631318 Genezinc finger protein 85 pseudogene |
LOC100131257 Genezinc finger protein 655 pseudogene |
ZNF734P Genezinc finger protein 734, pseudogene |
PJA1 Genepraja ring finger 1, E3 ubiquitin protein ligase This gene encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
PJA2 Genepraja ring finger 2, E3 ubiquitin protein ligase Enables protein kinase A catalytic subunit binding activity; protein kinase A regulatory subunit binding activity; and ubiquitin protein ligase activity. Involved in several processes, including proteasome-mediated ubiquitin-dependent protein catabolic process; regulation of macrophage activation; and regulation of signal transduction. Located in cytoplasm; cytoskeleton; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF107 Genezinc finger protein 107 This gene encodes a protein containing multiple C2H2-type zinc finger regions. Proteins containing zinc fingers may act as transcriptional regulators, but may also have other cellular functions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
ZNF106 Genezinc finger protein 106 Enables RNA binding activity. Predicted to be involved in insulin receptor signaling pathway. Predicted to be located in nuclear speck and nucleolus. Predicted to be active in cytosol and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF101 Genezinc finger protein 101 Zinc finger proteins (ZNFs), such as ZNF101, bind nucleic acids and perform many key functions, the most important of which is regulating transcription (summary by Bellefroid et al., 1993 [PubMed 8467795]). See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Nov 2010] |
ZNF100 Genezinc finger protein 100 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TRAFD1 GeneTRAF-type zinc finger domain containing 1 The innate immune system confers host defense against viral and microbial infection, and TRAFD1 is a negative feedback regulator that controls excessive immune responses (Sanada et al., 2008 [PubMed 18849341]).[supplied by OMIM, Dec 2009] |
ZFP64P1 GeneZFP64 zinc finger protein pseudogene 1 |
LOC100289569 Genezinc finger protein 736 pseudogene |
RNF44 Genering finger protein 44 The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008] |
RNF43 Genering finger protein 43 The protein encoded by this gene is a RING-type E3 ubiquitin ligase and is predicted to contain a transmembrane domain, a protease-associated domain, an ectodomain, and a cytoplasmic RING domain. This protein is thought to negatively regulate Wnt signaling, and expression of this gene results in an increase in ubiquitination of frizzled receptors, an alteration in their subcellular distribution, resulting in reduced surface levels of these receptors. Mutations in this gene have been reported in multiple tumor cells, including colorectal and endometrial cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015] |
RNF41 Genering finger protein 41, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin ligase. The encoded protein plays a role in type 1 cytokine receptor signaling by controlling the balance between JAK2-associated cytokine receptor degradation and ectodomain shedding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011] |
LOC645937 Genezinc finger protein 598 pseudogene |
ZNF75A Genezinc finger protein 75a Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MARCH5 Genemembrane-associated ring finger (C3HC4) 5 MARCH5 is a ubiquitin ligase of the mitochondrial outer membrane that plays a role in the control of mitochondrial morphology by regulating mitofusin-2 (MFN2; MIM 608507) and DRP1 (DNM1L; MIM 603850) (Nakamura et al., 2006 [PubMed 16936636]).[supplied by OMIM, Mar 2008] |
MARCH4 Genemembrane-associated ring finger (C3HC4) 4, E3 ubiquitin protein ligase MARCH4 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH4 reduces surface accumulation of several membrane glycoproteins by directing them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
MARCH7 Genemembrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase MARCH7 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Mar 2010] |
MARCH6 Genemembrane-associated ring finger (C3HC4) 6, E3 ubiquitin protein ligase This gene encodes a member of a family of membrane-associated E3 ubiquitin ligases containing RING-CH-type zinc finger motifs. Ubiquitination of type II deiodinase by the encoded protein is an important regulatory step in thyroid hormone signalling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
MARCH1 Genemembrane-associated ring finger (C3HC4) 1, E3 ubiquitin protein ligase MARCH1 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH1 downregulates the surface expression of major histocompatibility complex (MHC) class II molecules (see MIM 142880) and other glycoproteins by directing them to the late endosomal/lysosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Thibodeau et al., 2008 [PubMed 18389477]; De Gassart et al., 2008 [PubMed 18305173]).[supplied by OMIM, Mar 2010] |
MARCH3 Genemembrane-associated ring finger (C3HC4) 3, E3 ubiquitin protein ligase This gene encodes a member of the membrane-associated RING-CH (MARCH) family. The encoded protein is an E3 ubiquitin-protein ligase that may be involved in regulation of the endosomal transport pathway. [provided by RefSeq, Mar 2013] |
MARCH2 Genemembrane-associated ring finger (C3HC4) 2, E3 ubiquitin protein ligase MARCH2 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH2 reduces surface accumulation of several glycoproteins and appears to regulate early endosome-to-trans-Golgi network (TGN) trafficking (Bartee et al., 2004 [PubMed 14722266]; Nakamura et al., 2005 [PubMed 15689499]).[supplied by OMIM, Mar 2010] |
MARCH9 Genemembrane-associated ring finger (C3HC4) 9 MARCH9 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH9 induces internalization of several membrane glycoproteins and directs them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Hoer et al., 2007 [PubMed 17174307]).[supplied by OMIM, Apr 2010] |
MARCH8 Genemembrane-associated ring finger (C3HC4) 8, E3 ubiquitin protein ligase MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
ZNF560 Genezinc finger protein 560 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379617 Genezinc finger protein 430-like |
ZNF808 Genezinc finger protein 808 Enables transcription cis-regulatory region binding activity. Involved in cell differentiation; negative regulation of gene expression; and pancreas development. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF805 Genezinc finger protein 805 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF806 Genezinc finger protein 806 |
ZNF807 Genezinc finger protein 807 |
ZNF800 Genezinc finger protein 800 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to act upstream of or within acinar cell differentiation and endocrine pancreas development. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419721 Genezinc finger protein 670 pseudogene |
ZNF37A Genezinc finger protein 37A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105372319 Geneputative zinc finger protein 56 |
RNF167 Genering finger protein 167 RNF167 is an E3 ubiquitin ligase that interacts with TSSC5 (SLC22A18; MIM 602631) and, together with UBCH6 (UBE2E1; MIM 602916), facilitates TSSC5 polyubiquitylation (Yamada and Gorbsky, 2006 [PubMed 16314844]).[supplied by OMIM, Mar 2008] |
RNF166 Genering finger protein 166 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein polyubiquitination and ubiquitin-dependent protein catabolic process. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF165 Genering finger protein 165 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in motor neuron axon guidance and positive regulation of BMP signaling pathway. Predicted to act upstream of or within several processes, including forelimb morphogenesis; nervous system development; and protein polyubiquitination. Predicted to be part of protein-containing complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF169 Genering finger protein 169 Enables K63-linked polyubiquitin modification-dependent protein binding activity; nucleosome binding activity; and ubiquitin-modified histone reader activity. Involved in double-strand break repair via homologous recombination and negative regulation of double-strand break repair. Located in cytosol; nuclear lumen; and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
RNF168 Genering finger protein 168, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome. [provided by RefSeq, Sep 2011] |
ZBTB40 Genezinc finger and BTB domain containing 40 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Involved in DNA damage response. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB41 Genezinc finger and BTB domain containing 41 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB42 Genezinc finger and BTB domain containing 42 The protein encoded by this gene is a member of the C2H2 zinc finger protein family. This protein is predicted to have a pox virus and zinc finger (POZ) domain at the N-terminus and four zinc finger domains at the C-terminus. In human and mouse, the protein localizes to the nuclei of skeletal muscle cells. Knockdown of this gene in zebrafish results in abnormal skeletal muscle development and myofibrillar disorganization. A novel homozygous variant of the human gene has been associated with lethal congenital contracture syndrome, an autosomal recessive disorder that results in muscle wasting. [provided by RefSeq, Mar 2015] |
ZBTB43 Genezinc finger and BTB domain containing 43 Enables RNA polymerase III general transcription initiation factor binding activity and sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB44 Genezinc finger and BTB domain containing 44 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB45 Genezinc finger and BTB domain containing 45 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB46 Genezinc finger and BTB domain containing 46 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and transcription cis-regulatory region binding activity. Involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB47 Genezinc finger and BTB domain containing 47 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB48 Genezinc finger and BTB domain containing 48 Enables double-stranded telomeric DNA binding activity; identical protein binding activity; and transcription cis-regulatory region binding activity. Involved in positive regulation of DNA-templated transcription and telomere maintenance via telomere lengthening. Located in chromosome, telomeric region. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB49 Genezinc finger and BTB domain containing 49 Enables DNA-binding transcription factor binding activity; sequence-specific DNA binding activity; and transcription coactivator binding activity. Involved in negative regulation of cell population proliferation; positive regulation of transcription by RNA polymerase II; and regulation of cell cycle. Located in cytosol; microtubule cytoskeleton; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF816 Genezinc finger protein 816 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF814 Genezinc finger protein 814 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF101P2 Genezinc finger protein 101 pseudogene 2 |
ZNF101P1 Genezinc finger protein 101 pseudogene 1 |
LOC399783 Genezinc finger protein 532 pseudogene |
LOC100128948 Genezinc finger protein 607 pseudogene |
ZIK1P1 Genezinc finger protein interacting with K protein 1 pseudogene 1 |
ZNF736P8Y Genezinc finger protein 736 pseudogene 8, Y-linked |
ZFY Genezinc finger protein, Y-linked This gene encodes a zinc finger-containing protein that may function as a transcription factor. This gene was once a candidate gene for the testis-determining factor (TDF) and was erroneously referred to as TDF. [provided by RefSeq, Jul 2008] |
ZNF888 Genezinc finger protein 888 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC1 Genezinc finger, DHHC-type containing 1 Enables protein-cysteine S-palmitoyltransferase activity. Involved in antiviral innate immune response; protein palmitoylation; and regulation of defense response. Located in Golgi apparatus and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC2 Genezinc finger, DHHC-type containing 2 Enables protein homodimerization activity and protein-cysteine S-palmitoyltransferase activity. Involved in several processes, including peptidyl-L-cysteine S-palmitoylation; protein localization to membrane raft; and synapse assembly. Located in Golgi apparatus and endoplasmic reticulum membrane. Is active in postsynaptic recycling endosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC5 Genezinc finger, DHHC-type containing 5 Enables protein-cysteine S-palmitoyltransferase activity. Involved in positive regulation of defense response; positive regulation of protein localization to plasma membrane; and protein localization to plasma membrane. Acts upstream of or within protein palmitoylation. Located in nucleoplasm; phagocytic vesicle; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC4 Genezinc finger, DHHC-type containing 4 Enables palmitoyltransferase activity. Involved in positive regulation of innate immune response and protein localization to plasma membrane. Located in Golgi apparatus and endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC7 Genezinc finger, DHHC-type containing 7 Enables protein-cysteine S-palmitoyltransferase activity. Involved in several processes, including nuclear receptor-mediated steroid hormone signaling pathway; regulation of protein localization; and regulation of signal transduction. Located in Golgi apparatus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC6 Genezinc finger, DHHC-type containing 6 Enables palmitoyltransferase activity and protein-cysteine S-stearoyltransferase activity. Involved in positive regulation of mitochondrial fusion; protein palmitoylation; and protein stearoylation. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC9 Genezinc finger, DHHC-type containing 9 This gene encodes an integral membrane protein that is a member of the zinc finger DHHC domain-containing protein family. The encoded protein forms a complex with golgin subfamily A member 7 and functions as a palmitoyltransferase. This protein specifically palmitoylates HRAS and NRAS. Mutations in this gene are associated with X-linked cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, May 2010] |
ZDHHC8 Genezinc finger, DHHC-type containing 8 This gene encodes a four transmembrane protein that is a member of the zinc finger DHHC domain-containing protein family. The encoded protein may function as a palmitoyltransferase. Defects in this gene may be associated with a susceptibility to schizophrenia. Alternate splicing of this gene results in multiple transcript variants. A pseudogene of this gene is found on chromosome 22.[provided by RefSeq, May 2010] |
ZNF468 Genezinc finger protein 468 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF469 Genezinc finger protein 469 This gene encodes a zinc-finger protein. Low-percent homology to certain collagens suggests that it may function as a transcription factor or extra-nuclear regulator factor for the synthesis or organization of collagen fibers. Mutations in this gene cause brittle cornea syndrome. [provided by RefSeq, Jul 2008] |
ZNF462 Genezinc finger protein 462 The protein encoded by this gene belongs to C2H2-type zinc finger family of proteins. It contains multiple C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
ZNF461 Genezinc finger protein 461 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF467 Genezinc finger protein 467 The protein encoded by this gene is a zinc finger protein whose function has not yet been elucidated in humans. However, the mouse ortholog of this protein enhances adipocyte differentiation and suppresses osteoblast differentiation in bone marrow. The mouse protein also is a transcription factor for several genes and can help recruit histone deacetylase complexes. [provided by RefSeq, Aug 2016] |
ZDHHC4P1 Genezinc finger, DHHC-type containing 4 pseudogene 1 |
LOC100130990 Genezinc finger protein 561-like |
ZNF668 Genezinc finger protein 668 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in DNA repair. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF669 Genezinc finger protein 669 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF660 Genezinc finger protein 660 This gene encodes a protein that contains multiple C2H2 zinc finger domains, and is located in a cluster of zinc-finger encoding genes on chromosome 3. Naturally-occurring readthrough transcription is observed between this gene and the downstream zinc finger protein 197 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017] |
ZNF662 Genezinc finger protein 662 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF664 Genezinc finger protein 664 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF665 Genezinc finger protein 665 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF667 Genezinc finger protein 667 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB12P1 Genezinc finger and BTB domain containing 12 pseudogene 1 |
LOC728688 Geneubiquitin-like, containing PHD and RING finger domains, 1 pseudogene |
ZFP57 GeneZFP57 zinc finger protein The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009] |
LOC441666 Genezinc finger protein 91 pseudogene |
ZEB2 Genezinc finger E-box binding homeobox 2 The protein encoded by this gene is a member of the Zfh1 family of 2-handed zinc finger/homeodomain proteins. It is located in the nucleus and functions as a DNA-binding transcriptional repressor that interacts with activated SMADs. Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jan 2010] |
ZNF890P Genezinc finger protein 890, pseudogene |
CXXC1 GeneCXXC finger protein 1 This gene encodes a protein that functions as a transcriptional activator that binds specifically to non-methylated CpG motifs through its CXXC domain. The protein is a component of the SETD1 complex, regulates gene expression and is essential for vertebrate development. [provided by RefSeq, Sep 2015] |
CXXC5 GeneCXXC finger protein 5 The protein encoded by this gene is a retinoid-inducible nuclear protein containing a CXXC-type zinc finger motif. The encoded protein is involved in myelopoiesis, is required for DNA damage-induced p53 activation, regulates the differentiation of C2C12 myoblasts into myocytes, and negatively regulates cutaneous wound healing. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2015] |
CXXC4 GeneCXXC finger protein 4 This gene encodes a CXXC-type zinc finger domain-containing protein that functions as an antagonist of the canonical wingless/integrated signaling pathway. The encoded protein negatively regulates wingless/integrated signaling through interaction with the post synaptic density protein/ Drosophila disc large tumor suppressor/ zonula occludens-1 protein domain of Dishevelled, a scaffolding protein required for the stabilization of the transcriptional co-activator beta-catenin. In addition, the CXXC domain of this protein has been shown to bind unmethylated CpG dinucleotides, localize to promoters and CpG islands, and interact with the catalytic domain of methylcytosine dioxygenase ten-eleven-translocation 2, an iron and alpha-ketoglutarate-dependent dioxygenase that modifies the methylation status of DNA. In humans, a mutation in this gene has been associated with development of malignant renal cell carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
PCGF7P Genepolycomb group ring finger 7 pseudogene |
ZNF652P1 Genezinc finger protein 652 pseudogene 1 |
ZNF587B Genezinc finger protein 587B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBED1P1 Genezinc finger, BED-type containing 1 pseudogene 1 |
MKRN7P Genemakorin ring finger protein 7, pseudogene |
FLYWCH1 GeneFLYWCH-type zinc finger 1 Enables transcription coactivator binding activity and transcription corepressor activity. Involved in DNA damage response and negative regulation of transcription by RNA polymerase II. Located in cytosol; nuclear body; and pericentric heterochromatin. Part of transcription regulator complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419908 Genezinc finger protein 585A pseudogene |
PHF5DP GenePHD finger protein 5D pseudogene |
AZFP GeneAML-associated zinc finger protein |
ZNF415P1 Genezinc finger protein 415 pseudogene 1 |
ZNF207 Genezinc finger protein 207 Enables microtubule binding activity. Involved in mitotic spindle assembly checkpoint signaling; nuclear chromosome segregation; and protein stabilization. Located in kinetochore; nuclear lumen; and spindle matrix. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF205 Genezinc finger protein 205 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II; positive regulation of hydrogen peroxide biosynthetic process; and positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway. Predicted to be located in mitochondrion and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF202 Genezinc finger protein 202 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in chromosome; nuclear body; and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF200 Genezinc finger protein 200 Predicted to enable metal ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF208 Genezinc finger protein 208 Zinc finger proteins (ZNFs), such as ZNF208, bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. A conserved protein motif, termed the Kruppel-associated box (KRAB) domain, mediates protein-protein interactions (Eichler et al., 1998 [PubMed 9724325]). See ZNF91 (MIM 603971) for further information on ZNFs.[supplied by OMIM, Aug 2009] |
ZNF839P1 Genezinc finger protein 839 pseudogene 1 |
ZFYVE9 Genezinc finger, FYVE domain containing 9 This gene encodes a double zinc finger motif-containing protein that participates in the transforming growth factor-beta (TGFB) signalling pathway. The encoded protein interacts directly with SMAD2 and SMAD3, and recruits SMAD2 to the TGFB receptor. There are multiple pseudogenes for this gene on chromosomes 2, 15, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013] |
ZFYVE1 Genezinc finger, FYVE domain containing 1 The FYVE domain mediates the recruitment of proteins involved in membrane trafficking and cell signaling to phosphatidylinositol 3-phosphate-containing membranes. This protein contains two zinc-binding FYVE domains in tandem and is reported to localize to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
ZNF114P1 Genezinc finger protein 114 pseudogene 1 |
ZNF492 Genezinc finger protein 492 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF491 Genezinc finger protein 491 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN5D Genezinc finger and SCAN domain containing 5D Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN5A Genezinc finger and SCAN domain containing 5A Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN5B Genezinc finger and SCAN domain containing 5B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105370704 Geneputative zinc finger protein 355P |
ZNF501 Genezinc finger protein 501 Enables sequence-specific double-stranded DNA binding activity. Involved in Golgi organization. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF500 Genezinc finger protein 500 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF503 Genezinc finger protein 503 Predicted to enable metal ion binding activity. Involved in G1 to G0 transition involved in cell differentiation; negative regulation of cell population proliferation; and negative regulation of gene expression. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF502 Genezinc finger protein 502 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation by host of viral process and viral release from host cell. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF507 Genezinc finger protein 507 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF506 Genezinc finger protein 506 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF847P Genezinc finger protein 847, pseudogene |
ZBTB2 Genezinc finger and BTB domain containing 2 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and identical protein binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB6 Genezinc finger and BTB domain containing 6 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in mitochondrion and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB5 Genezinc finger and BTB domain containing 5 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB4 Genezinc finger and BTB domain containing 4 Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; nucleotide binding activity; and protein homodimerization activity. Involved in DNA damage response and negative regulation of transcription by RNA polymerase II. Located in cytosol and nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB9 Genezinc finger and BTB domain containing 9 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PATZ1 GenePOZ (BTB) and AT hook containing zinc finger 1 The protein encoded by this gene contains an A-T hook DNA binding motif which usually binds to other DNA binding structures to play an important role in chromatin modeling and transcription regulation. Its Poz domain is thought to function as a site for protein-protein interaction and is required for transcriptional repression, and the zinc-fingers comprise the DNA binding domain. Since the encoded protein has typical features of a transcription factor, it is postulated to be a repressor of gene expression. In small round cell sarcoma, this gene is fused to EWS by a small inversion of 22q, then the hybrid is thought to be translocated (t(1;22)(p36.1;q12). The rearrangement of chromosome 22 involves intron 8 of EWS and exon 1 of this gene creating a chimeric sequence containing the transactivation domain of EWS fused to zinc finger domain of this protein. This is a distinct example of an intra-chromosomal rearrangement of chromosome 22. Four alternatively spliced transcript variants are described for this gene. [provided by RefSeq, Jul 2008] |
RNF219 Genering finger protein 219 Enables chromatin binding activity and ubiquitin-protein transferase activity. Involved in protein autoubiquitination; protein monoubiquitination; and regulation of DNA replication. Located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
RNF215 Genering finger protein 215 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF214 Genering finger protein 214 Predicted to enable ubiquitin-protein transferase activity. [provided by Alliance of Genome Resources, Mar 2025] |
RNF217 Genering finger protein 217 This protein encoded by this gene is a member of the RING1-IBR-RING24 (RBR) ubiquitin protein ligase family, and it belongs to a subfamily of these proteins that contain a transmembrane domain. This protein can interact with the HAX1 anti-apoptotic protein via its C-terminal RING finger motif, which suggests a role in apoptosis signaling. It is thought that deregulation of this gene can be a mechanism in leukemogenesis. Mutations in the region encoding the protein GXXXG motif, which appears to be necessary for protein self-association, have been found in human cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016] |
RNF216 Genering finger protein 216 This gene encodes a cytoplasmic protein which specifically colocalizes and interacts with the serine/threonine protein kinase, receptor-interacting protein (RIP). Zinc finger domains of the encoded protein are required for its interaction with RIP and for inhibition of TNF- and IL1-induced NF-kappa B activation pathways. The encoded protein may also function as an E3 ubiquitin-protein ligase which accepts ubiquitin from E2 ubiquitin-conjugating enzymes and transfers it to substrates. Several alternatively spliced transcript variants have been described for this locus but the full-length natures of only some are known. [provided by RefSeq, Jul 2008] |
RNF213 Genering finger protein 213 This gene encodes a protein containing a C3HC4-type RING finger domain, which is a specialized type of Zn-finger that binds two atoms of zinc and is thought to be involved in mediating protein-protein interactions. The protein also contains an AAA domain, which is associated with ATPase activity. This gene is a susceptibility gene for Moyamoya disease, a vascular disorder of intracranial arteries. This gene is also a translocation partner in anaplastic large cell lymphoma and inflammatory myofibroblastic tumor cases, where a t(2;17)(p23;q25) translocation has been identified with the anaplastic lymphoma kinase (ALK) gene on chromosome 2, and a t(8;17)(q24;q25) translocation has been identified with the MYC gene on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011] |
RNF212 Genering finger protein 212 This gene encodes a RING finger protein that may function as a ubiquitin ligase. The encoded protein may be involved in meiotic recombination. This gene is located within a linkage disequilibrium block and polymorphisms in this gene may influence recombination rates. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010] |
LOC100419831 Genezinc finger protein 420 pseudogene |
LOC100419833 Genezinc finger protein 709 pseudogene |
LOC100419835 Genezinc finger protein 160 pseudogene |
ZCCHC9 Genezinc finger, CCHC domain containing 9 Enables RNA binding activity. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC8 Genezinc finger, CCHC domain containing 8 This gene encodes a scaffold protein which serves as an assessory factor to the nuclear RNA exosome complex. The encoded protein forms a trimeric human nuclear exosome targeting (NEXT) complex, together with hMTR4 and the RNA-binding factor RBM7 which promotes the exosomal degradation of non-coding promoter-upstream transcripts, enhancer RNAs and 3'-extended products of histone- and small nuclear RNA transcription. This complex is also thought to recruit the exosome to degrade intronic RNAs via its interaction with both the exosome and the spliceosome. It contains both an N-terminal zinc-knuckle domain and a C-terminal proline-rich domain. [provided by RefSeq, Apr 2017] |
ZCCHC3 Genezinc finger, CCHC domain containing 3 Enables double-stranded DNA binding activity. Involved in cellular response to exogenous dsRNA; detection of virus; and positive regulation of innate immune response. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC2 Genezinc finger, CCHC domain containing 2 Predicted to enable nucleic acid binding activity; phosphatidylinositol binding activity; and zinc ion binding activity. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC7 Genezinc finger, CCHC domain containing 7 Enables RNA binding activity. Predicted to be involved in nuclear RNA surveillance. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC6 Genezinc finger, CCHC domain containing 6 Enables RNA uridylyltransferase activity and miRNA binding activity. Involved in RNA metabolic process and transposable element silencing by mRNA destabilization. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZCCHC5 Genezinc finger, CCHC domain containing 5 This gene is a member of a family of gag-related retrotransposon genes. These genes appear to have lost the ability to retrotranspose; however, their open reading frames have remained intact, which may indicate that these genes have acquired new functions in the cell. [provided by RefSeq, Nov 2009] |
ZCCHC4 Genezinc finger, CCHC domain containing 4 Enables S-adenosyl-L-methionine binding activity; rRNA (adenine-N6-)-methyltransferase activity; and zinc ion binding activity. Involved in positive regulation of translation and rRNA methylation. Located in cytoplasm and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF747 Genezinc finger protein 747 Predicted to enable metal ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF746 Genezinc finger protein 746 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in protein complex oligomerization and regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF740 Genezinc finger protein 740 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF749 Genezinc finger protein 749 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419643 Genering finger protein 14 pseudogene |
LOC100419642 Genezinc finger protein 85 pseudogene |
LOC100419645 Genering finger protein 14 pseudogene |
ZNF18 Genezinc finger protein 18 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF19 Genezinc finger protein 19 The protein encoded by this gene contains a zinc finger, a nucleic acid-binding domain present in many transcription factors. This gene is located in a region next to ZNF23, a gene also encoding a zinc finger protein, on chromosome 16. [provided by RefSeq, Jul 2008] |
ZNF14 Genezinc finger protein 14 The protein encoded by this gene contains a zinc finger and a Kruppel-associated box (KRAB) domain. KRAB domain is known to be involved in the transcriptional repression of a number of zinc finger proteins. [provided by RefSeq, Jul 2008] |
ZNF16 Genezinc finger protein 16 The protein encoded by this gene contains multiple tandem zinc finger motifs. The encoded protein is involved in the differentiation of erythroid and megakaryocytic cells. This gene is located in a cluster of related genes on chromosome 8 encoding zinc finger proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012] |
ZNF17 Genezinc finger protein 17 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF10 Genezinc finger protein 10 The protein encoded by this gene contains a C2H2 zinc finger, and has been shown to function as a transcriptional repressor. The Kruppel-associated box (KRAB) domain of this protein is found to be responsible for its transcriptional repression activity. RING finger containing protein TIF1 was reported to interact with the KRAB domain, and may serve as a mediator for the repression activity of this protein. [provided by RefSeq, Jul 2008] |
ZNF12 Genezinc finger protein 12 This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with eight C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in developmental control of gene expression. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
ZC3H11A Genezinc finger CCCH-type containing 11A Enables RNA binding activity. Involved in poly(A)+ mRNA export from nucleus. Located in transcription export complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100631320 Genezinc finger protein 486 pseudogene |
LOC100631321 Genezinc finger protein 100 pseudogene |
BAZ1B Genebromodomain adjacent to zinc finger domain, 1B This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008] |
ZZEF1 Genezinc finger, ZZ-type with EF-hand domain 1 Enables histone reader activity; lysine-acetylated histone binding activity; and methylated histone binding activity. Predicted to be involved in chromatin organization. Predicted to act upstream of or within several processes, including glutamatergic synaptic transmission; regulation of peptidyl-tyrosine phosphorylation; and visual learning. Predicted to be located in cell surface; postsynapse; and presynaptic active zone. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF287 Genezinc finger protein 287 This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
ZNF284 Genezinc finger protein 284 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF285 Genezinc finger protein 285 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF282 Genezinc finger protein 282 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF283 Genezinc finger protein 283 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF281 Genezinc finger protein 281 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of gene expression; negative regulation of transcription by RNA polymerase II; and positive regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SNAI1P1 Genesnail family zinc finger 1 pseudogene 1 |
ZRSR2 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 This gene encodes an essential splicing factor. The encoded protein associates with the U2 auxiliary factor heterodimer, which is required for the recognition of a functional 3' splice site in pre-mRNA splicing, and may play a role in network interactions during spliceosome assembly. [provided by RefSeq, Jul 2008] |
LOC101930105 Genezinc finger protein 839-like |
RNF14 Genering finger protein 14 The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This protein interacts with androgen receptor (AR) and may function as a coactivator that induces AR target gene expression in prostate. A dominant negative mutant of this gene has been demonstrated to inhibit the AR-mediated growth of prostate cancer. This protein also interacts with class III ubiquitin-conjugating enzymes (E2s) and may act as a ubiquitin-ligase (E3) in the ubiquitination of certain nuclear proteins. Six alternatively spliced transcript variants encoding two distinct isoforms have been reported. [provided by RefSeq, Jan 2011] |
RNF17 Genering finger protein 17 This gene is similar to a mouse gene that encodes a testis-specific protein containing a RING finger domain. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, May 2010] |
RNF10 Genering finger protein 10 The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [provided by RefSeq, Jul 2008] |
RNF11 Genering finger protein 11 The protein encoded by this gene contains a RING-H2 finger motif, which is known to be important for protein-protein interactions. The expression of this gene has been shown to be induced by mutant RET proteins (MEN2A/MEN2B). The germline mutations in RET gene are known to be responsible for the development of multiple endocrine neoplasia (MEN). [provided by RefSeq, Jul 2008] |
RNF13 Genering finger protein 13 The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same protein have been reported. A pseudogene, which is also located on chromosome 3, has been defined for this gene. [provided by RefSeq, Jul 2008] |
LOC100419825 Genezinc finger protein 655 pseudogene |
ZNF37BP Genezinc finger protein 37B, pseudogene |
ZNF780A Genezinc finger protein 780A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF780B Genezinc finger protein 780B Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZMAT1 Genezinc finger, matrin-type 1 This gene encodes a protein containing Cys2-His2 (C2H2)-type zinc fingers, which are similar to those found in the nuclear matrix protein matrin 3. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012] |
ZMAT3 Genezinc finger, matrin-type 3 This gene encodes a protein containing three zinc finger domains and a nuclear localization signal. The mRNA and the protein of this gene are upregulated by wildtype p53 and overexpression of this gene inhibits tumor cell growth, suggesting that this gene may have a role in the p53-dependent growth regulatory pathway. Alternative splicing of this gene results in two transcript variants encoding two isoforms differing in only one amino acid. [provided by RefSeq, Jul 2008] |
ZMAT2 Genezinc finger, matrin-type 2 Predicted to enable DNA binding activity and zinc ion binding activity. Involved in mRNA splicing, via spliceosome. Located in nucleus. Part of U2-type precatalytic spliceosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZMAT5 Genezinc finger, matrin-type 5 Predicted to enable zinc ion binding activity. Predicted to be involved in RNA splicing. Located in nucleoplasm. Part of U12-type spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZMAT4 Genezinc finger, matrin-type 4 Enables identical protein binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF720P1 Genezinc finger protein 720 pseudogene 1 |
ZNF853 Genezinc finger protein 853 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF852 Genezinc finger protein 852 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF850 Genezinc finger protein 850 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF581 Genezinc finger protein 581 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF580 Genezinc finger protein 580 Enables sequence-specific double-stranded DNA binding activity. Involved in several processes, including cellular response to hydrogen peroxide; positive regulation of cell migration; and positive regulation of interleukin-8 production. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF583 Genezinc finger protein 583 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF582 Genezinc finger protein 582 The protein encoded by this gene is a zing finger protein and putative transcription factor that is highly methylated in cervical cancers. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016] |
ZNF584 Genezinc finger protein 584 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF587 Genezinc finger protein 587 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF586 Genezinc finger protein 586 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF589 Genezinc finger protein 589 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF326 Genezinc finger protein 326 Enables RNA polymerase II complex binding activity. Involved in regulation of DNA-templated transcription elongation and regulation of RNA splicing. Located in nucleoplasm. Part of DBIRD complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF322 Genezinc finger protein 322 ZNF322A is a member of the zinc-finger transcription factor family and may regulate transcriptional activation in MAPK (see MAPK1; MIM 176948) signaling pathways (Li et al., 2004 [PubMed 15555580]).[supplied by OMIM, Mar 2008] |
ZNF329 Genezinc finger protein 329 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419779 Genezinc finger protein 195 pseudogene |
LOC100419775 Genezinc finger protein 519 pseudogene |
LOC100419773 Genezinc finger protein 33B pseudogene |
ZNF517 Genezinc finger protein 517 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN12P1 Genezinc finger and SCAN domain containing 12 pseudogene 1 |
PHRF1 GenePHD and ring finger domains 1 Predicted to enable RNA polymerase binding activity. Predicted to be involved in protein ubiquitination. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF123P Genezinc finger protein 123, pseudogene |
RNF152 Genering finger protein 152 Enables small GTPase binding activity and ubiquitin protein ligase activity. Involved in several processes, including cellular response to amino acid starvation; negative regulation of TORC1 signaling; and protein ubiquitination. Located in lysosomal membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF150 Genering finger protein 150 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF151 Genering finger protein 151 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF157 Genering finger protein 157 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in negative regulation of apoptotic process; positive regulation of dendrite extension; and protein ubiquitination. Predicted to be located in cell body. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
GZF1 GeneGDNF-inducible zinc finger protein 1 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289238 Genezinc finger RNA binding protein pseudogene |
LOC100287754 Genezinc finger protein 44 pseudogene |
ZNF90 Genezinc finger protein 90 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF91 Genezinc finger protein 91 The ZNF91 gene encodes a zinc finger protein of the KRAB (Kruppel-associated box) subfamily (Bellefroid et al., 1991, 1993 [PubMed 2023909] [PubMed 8467795]).[supplied by OMIM, May 2010] |
ZNF92 Genezinc finger protein 92 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF98 Genezinc finger protein 98 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF99 Genezinc finger protein 99 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZCWPW2 Genezinc finger, CW type with PWWP domain 2 Enables methylated histone binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZCWPW1 Genezinc finger, CW type with PWWP domain 1 Enables histone reader activity; methyl-CpG binding activity; and methylated histone binding activity. Predicted to be involved in meiosis I; positive regulation of DNA metabolic process; and spermatogenesis. Predicted to act upstream of or within homologous chromosome pairing at meiosis. Predicted to be located in XY body. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101269108 Genezinc finger, FYVE domain containing 9 pseudogene |
ZRANB1 Genezinc finger, RAN-binding domain containing 1 Enables K63-linked polyubiquitin modification-dependent protein binding activity and cysteine-type deubiquitinase activity. Involved in several processes, including positive regulation of Wnt signaling pathway; protein deubiquitination; and regulation of cell morphogenesis. Located in cytosol and nucleoplasm. Is active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZRANB3 Genezinc finger, RAN-binding domain containing 3 Enables ATP-dependent DNA/DNA annealing activity; DNA endonuclease activity; and K63-linked polyubiquitin modification-dependent protein binding activity. Involved in several processes, including DNA metabolic process; DNA rewinding; and negative regulation of DNA recombination. Located in nuclear replication fork and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZRANB2 Genezinc finger, RAN-binding domain containing 2 Enables RNA binding activity. Predicted to be involved in RNA splicing and mRNA processing. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF845 Genezinc finger protein 845 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF731P Genezinc finger protein 731, pseudogene |
ZNF597 Genezinc finger protein 597 This gene encodes a protein with multiple zinc finger domains. Loss of the related gene in rodents results in defects in neural development and embryonic lethality in mutant homozygotes. This gene is adjacent to a differentially methylated region (DMR) and is imprinted and maternally expressed. [provided by RefSeq, Nov 2015] |
ZNF594 Genezinc finger protein 594 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC15 Genezinc finger, DHHC-type containing 15 The protein encoded by this gene belongs to the DHHC palmitoyltransferase family. Mutations in this gene are associated with mental retardatio X-linked type 91 (MRX91). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
ZDHHC14 Genezinc finger, DHHC-type containing 14 Enables palmitoyltransferase activity. Involved in peptidyl-L-cysteine S-palmitoylation. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC17 Genezinc finger, DHHC-type containing 17 Enables identical protein binding activity and protein-cysteine S-palmitoyltransferase activity. Involved in lipoprotein transport; protein palmitoylation; and regulation of programmed cell death. Located in Golgi membrane and Golgi-associated vesicle membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC16 Genezinc finger, DHHC-type containing 16 Enables palmitoyltransferase activity. Involved in protein palmitoylation. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC11 Genezinc finger, DHHC-type containing 11 Enables signaling adaptor activity. Involved in antiviral innate immune response and positive regulation of defense response to virus by host. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC13 Genezinc finger, DHHC-type containing 13 Predicted to enable magnesium ion transmembrane transporter activity and protein-cysteine S-palmitoyltransferase activity. Involved in positive regulation of canonical NF-kappaB signal transduction. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC12 Genezinc finger, DHHC-type containing 12 Enables protein-cysteine S-palmitoyltransferase activity. Involved in gephyrin clustering involved in postsynaptic density assembly; negative regulation of NLRP3 inflammasome complex assembly; and protein palmitoylation. Located in Golgi apparatus and endoplasmic reticulum. Is active in dendritic spine. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC19 Genezinc finger, DHHC-type containing 19 Enables protein-cysteine S-palmitoyltransferase activity. Involved in peptidyl-L-cysteine S-palmitoylation and positive regulation of aggrephagy. Located in Golgi membrane; endoplasmic reticulum; and perinucleolar compartment. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC18 Genezinc finger, DHHC-type containing 18 Enables protein-cysteine S-palmitoyltransferase activity. Involved in negative regulation of cGAS/STING signaling pathway; negative regulation of innate immune response; and peptidyl-L-cysteine S-palmitoylation. Is active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF174 Genezinc finger protein 174 This gene encodes a protein with three Cys2-His2-type zinc fingers in the carboxy-terminus, a putative nuclear localization signal, and an amino-terminus SCAN box which forms homodimers. This protein is believed to function as a transcriptional repressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016] |
ZNF175 Genezinc finger protein 175 Enables DNA-binding transcription activator activity, RNA polymerase II-specific; DNA-binding transcription repressor activity, RNA polymerase II-specific; and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF177 Genezinc finger protein 177 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
ZDBF2 Genezinc finger, DBF-type containing 2 This gene encodes a protein containing DBF4-type zinc finger domains. This gene is imprinted and paternally expressed in lymphocytes but is more stochastically expressed in the placenta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015] |
ZZZ3 Genezinc finger, ZZ-type containing 3 Enables histone reader activity; lysine-acetylated histone binding activity; and methylated histone binding activity. Involved in several processes, including chromatin organization; regulation of cell division; and regulation of primary metabolic process. Located in nucleolus and nucleoplasm. Part of ATAC complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF436 Genezinc finger protein 436 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF431 Genezinc finger protein 431 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein may negatively regulate transcription of target genes, including the hedgehog signaling pathway receptor patched 1, by interacting with histone deacetylases. Mutations in this gene may be associated with non-syndromic facial clefting in human patients. [provided by RefSeq, Jul 2016] |
ZNF430 Genezinc finger protein 430 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in substantia nigra development. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF433 Genezinc finger protein 433 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF432 Genezinc finger protein 432 Enables damaged DNA binding activity and protein-macromolecule adaptor activity. Involved in DNA damage response. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF439 Genezinc finger protein 439 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF438 Genezinc finger protein 438 Enables DNA-binding transcription factor activity. Involved in negative regulation of DNA-templated transcription. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC400682 Genezinc finger protein 100-like |
ZNF885P Genezinc finger protein 885, pseudogene |
LOC100631243 Genezinc finger protein 211 pseudogene |
LOC100631242 Genezinc finger protein 852 pseudogene |
LOC724084 Genezinc finger protein 706 pseudogene |
RC3H1 Genering finger and CCCH-type domains 1 This gene encodes a protein containing RING-type and C3H1-type zinc finger motifs. The encoded protein recognizes and binds to a constitutive decay element (CDE) in the 3' UTR of mRNAs, leading to mRNA deadenylation and degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
RC3H2 Genering finger and CCCH-type domains 2 Enables nucleic acid binding activity and ubiquitin protein ligase activity. Involved in protein polyubiquitination. Located in cell surface; intracellular membrane-bounded organelle; and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP28 GeneZFP28 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P9Y Genezinc finger protein 736 pseudogene 9, Y-linked |
ZNF280D Genezinc finger protein 280D Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF280C Genezinc finger protein 280C This gene encodes a member of the zinc finger domain-containing protein family. This family member contains multiple Cys2-His2(C2H2)-type zinc finger domains, the most common type of zinc finger domain that self-folds to form a beta-beta-alpha structure that binds a zinc ion. [provided by RefSeq, Aug 2011] |
ZNF280B Genezinc finger protein 280B The protein encoded by this gene is a transcription factor that upregulates expression of MDM2, which negatively regulates p53 expression. This gene is highly expressed in prostate cancer cells, which leads to a reduction in p53 levels and an increase in growth of the cancer cells. Several transcript variants have been found for this gene, but only one of them is protein-coding. [provided by RefSeq, Jan 2015] |
ZNF280A Genezinc finger protein 280A This gene encodes a zinc finger protein. The encoded protein contains 4 C2H2-type zinc fingers, which are commonly found in transcription factors. A variety of functions may be performed by this type of zinc finger protein, including the binding of DNA or RNA. [provided by RefSeq, Apr 2014] |
ZBTB12 Genezinc finger and BTB domain containing 12 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB11 Genezinc finger and BTB domain containing 11 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleoplasm. Implicated in autosomal recessive intellectual developmental disorder 69. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB17 Genezinc finger and BTB domain containing 17 This gene encodes a zinc finger protein involved in the regulation of c-myc. The symbol MIZ1 has also been associated with PIAS2 which is a different gene located on chromosome 18. [provided by RefSeq, Jul 2008] |
ZBTB16 Genezinc finger and BTB domain containing 16 This gene is a member of the Krueppel C2H2-type zinc-finger protein family and encodes a zinc finger transcription factor that contains nine Kruppel-type zinc finger domains at the carboxyl terminus. This protein is located in the nucleus, is involved in cell cycle progression, and interacts with a histone deacetylase. Specific instances of aberrant gene rearrangement at this locus have been associated with acute promyelocytic leukemia (APL). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008] |
ZBTB14 Genezinc finger and BTB domain containing 14 Enables DNA-binding transcription factor activity and transcription cis-regulatory region binding activity. Involved in negative regulation of DNA-templated transcription. Located in aggresome; cytosol; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB18 Genezinc finger and BTB domain containing 18 This gene encodes a C2H2-type zinc finger protein which acts a transcriptional repressor of genes involved in neuronal development. The encoded protein recognizes a specific sequence motif and recruits components of chromatin to target genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013] |
LOC100421184 Genezinc finger and BTB domain containing 2 pseudogene |
LOC105372277 Genezinc finger protein 799-like |
LOC100419545 Genezinc finger protein 35 pseudogene |
MKRN4P Genemakorin ring finger protein 4, pseudogene Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM4 Genezinc finger, SWIM-type containing 4 Predicted to enable zinc ion binding activity. Predicted to be part of Cul2-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM5 Genezinc finger, SWIM-type containing 5 Predicted to enable zinc ion binding activity. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM6 Genezinc finger, SWIM-type containing 6 The protein encoded by this gene contains a zinc finger SWI2/SNF2 and MuDR (SWIM) domain. Proteins with SWIM domains have been found in a diverse number of species and are predicted to interact with DNA or proteins. Mutations in this gene result in acromelic frontonasal dysostosis. [provided by RefSeq, Apr 2017] |
ZSWIM7 Genezinc finger, SWIM-type containing 7 Predicted to enable zinc ion binding activity. Involved in double-strand break repair via homologous recombination and protein stabilization. Part of Shu complex. Implicated in 46 XX gonadal dysgenesis and spermatogenic failure 71. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM1 Genezinc finger, SWIM-type containing 1 Predicted to enable zinc ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM2 Genezinc finger, SWIM-type containing 2 Predicted to enable ubiquitin protein ligase activity and zinc ion binding activity. Predicted to be involved in apoptotic process and protein polyubiquitination. Predicted to act upstream of or within positive regulation of extrinsic apoptotic signaling pathway via death domain receptors. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM3 Genezinc finger, SWIM-type containing 3 Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZSWIM8 Genezinc finger, SWIM-type containing 8 Enables ubiquitin-like ligase-substrate adaptor activity. Involved in positive regulation of macromolecule metabolic process; protein ubiquitination; and proteolysis involved in protein catabolic process. Part of Cul3-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
MAZ GeneMYC-associated zinc finger protein (purine-binding transcription factor) Enables DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in several processes, including regulation of gene expression; regulation of signal transduction; and transcription by RNA polymerase II. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB10 Genezinc finger and BTB domain containing 10 Enables telomeric DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Located in chromosome, telomeric region and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
UNK Geneunkempt family zinc finger Enables mRNA CDS binding activity. Involved in cell morphogenesis involved in neuron differentiation and negative regulation of cytoplasmic translation. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421372 Genezinc finger and SCAN domain containing 29 pseudogene |
ZNF876P Genezinc finger protein 876, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL4AP2 Generet finger protein-like 4A pseudogene 2 |
ZNF137P Genezinc finger protein 137, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF40 Genering finger protein 40, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger, a motif known to be involved in protein-protein and protein-DNA interactions. This protein was reported to interact with the tumor suppressor protein RB1. Studies of the rat counterpart suggested that this protein may function as an E3 ubiquitin-protein ligase, and facilitate the ubiquitination and degradation of syntaxin 1, which is an essential component of the neurotransmitter release machinery. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011] |
ZNF639 Genezinc finger protein 639 This gene encodes a member of the Kruppel-like zinc finger family of proteins. Amplification and overexpression of this gene have been observed in esophageal squamous cell carcinoma. The encoded protein has been shown to bind DNA in a sequence-specific manner and may regulate HIV-1 gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
ZNF638 Genezinc finger protein 638 The protein encoded by this gene is a nucleoplasmic protein. It binds cytidine-rich sequences in double-stranded DNA. This protein has three types of domains: MH1, MH2 (repeated three times) and MH3. It is associated with packaging, transferring, or processing transcripts. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008] |
MKRN5P Genemakorin ring finger protein 5, pseudogene |
ZNF630 Genezinc finger protein 630 This gene encodes a protein containing an N-terminal Kruppel-associated box-containing (KRAB) domain and 13 Kruppel-type C2H2 zinc finger domains. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
LOC100418555 Genezinc finger protein 70 pseudogene |
SCRT1 Genescratch family zinc finger 1 This gene encodes a C2H2-type zinc finger transcriptional repressor that binds to E-box motifs. The encoded protein may promote neural differention and may be involved in cancers with neuroendocrine features. [provided by RefSeq, Jul 2013] |
SCRT2 Genescratch family zinc finger 2 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of extrinsic apoptotic signaling pathway via death domain receptors and negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within regulation of neuron migration. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
LOC389906 Genezinc finger protein 839 pseudogene |
LOC730110 Genezinc finger protein 492 pseudogene |
LOC728587 Genezinc finger protein 736 pseudogene |
ZNF570 Genezinc finger protein 570 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF571 Genezinc finger protein 571 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF572 Genezinc finger protein 572 Enables identical protein binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF573 Genezinc finger protein 573 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF574 Genezinc finger protein 574 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF575 Genezinc finger protein 575 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF576 Genezinc finger protein 576 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF577 Genezinc finger protein 577 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF578 Genezinc finger protein 578 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF579 Genezinc finger protein 579 Enables DNA-binding transcription factor activity, RNA polymerase II-specific and transcription cis-regulatory region binding activity. Involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105376056 Geneputative zinc finger protein LOC441666 |
OVOL3 Geneovo-like zinc finger 3 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in epidermal cell differentiation and regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF212B Genering finger protein 212B Predicted to enable SUMO transferase activity and ubiquitin protein ligase activity. Predicted to be involved in chiasma assembly and protein ubiquitination. Predicted to be located in chromosome. Predicted to be active in synaptonemal complex. [provided by Alliance of Genome Resources, Mar 2025] |
JAZF1 GeneJAZF zinc finger 1 This gene encodes a nuclear protein with three C2H2-type zinc fingers, and functions as a transcriptional repressor. Chromosomal aberrations involving this gene are associated with endometrial stromal tumors. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized [provided by RefSeq, Jul 2008] |
ZCCHC13 Genezinc finger, CCHC domain containing 13 This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 3. However, the CDS of this intronless gene remains relatively intact, it is conserved in other mammalian species, it is known to be transcribed, and it is therefore thought to encode a functional protein. The encoded protein contains six CCHC-type zinc fingers, and is thus thought to function as a transcription factor. [provided by RefSeq, May 2010] |
ZNF778 Genezinc finger protein 778 The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011] |
ZNF776 Genezinc finger protein 776 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF777 Genezinc finger protein 777 Predicted to enable DNA-binding transcription factor activity. Involved in negative regulation of DNA-templated transcription; negative regulation of cell population proliferation; and protein heterooligomerization. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF775 Genezinc finger protein 775 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF772 Genezinc finger protein 772 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF773 Genezinc finger protein 773 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF770 Genezinc finger protein 770 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF771 Genezinc finger protein 771 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421810 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene |
BAZ2A Genebromodomain adjacent to zinc finger domain, 2A Enables histone binding activity. Contributes to RNA polymerase I core promoter sequence-specific DNA binding activity. Predicted to be involved in DNA methylation-dependent constitutive heterochromatin formation; negative regulation of transcription by RNA polymerase I; and rDNA heterochromatin formation. Predicted to act upstream of or within heterochromatin formation. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
BAZ2B Genebromodomain adjacent to zinc finger domain, 2B This gene belongs to the bromodomain gene family. Members of this gene family encode proteins that are integral components of chromatin remodeling complexes. The encoded protein showed strong preference for the activating H3K14Ac mark in a histone peptide screen, suggesting a potential role in transcriptional activation. This gene may be associated with susceptibility to sudden cardiac death (SCD). [provided by RefSeq, Aug 2016] |
RNF10P1 Genering finger protein 10 pseudogene 1 |
BMI1 GeneBMI1 proto-oncogene, polycomb ring finger This gene encodes a ring finger protein that is major component of the polycomb group complex 1 (PRC1). This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells. This protein also plays a central role in DNA damage repair. This gene is an oncogene and aberrant expression is associated with numerous cancers and is associated with resistance to certain chemotherapies. A pseudogene of this gene is found on chromosome X. Read-through transcription also exists between this gene and the upstream COMM domain containing 3 (COMMD3) gene. [provided by RefSeq, Sep 2015] |
PHF5CP GenePHD finger protein 5C pseudogene |
RLIMP2 Genering finger protein, LIM domain interacting pseudogene 2 |
RLIMP3 Genering finger protein, LIM domain interacting pseudogene 3 |
RLIMP1 Genering finger protein, LIM domain interacting pseudogene 1 |
ZNF25 Genezinc finger protein 25 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF24 Genezinc finger protein 24 Enables DNA-binding transcription activator activity, RNA polymerase II-specific; identical protein binding activity; and sequence-specific DNA binding activity. Involved in negative regulation of DNA-templated transcription and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF26 Genezinc finger protein 26 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF20 Genezinc finger protein 20 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF23 Genezinc finger protein 23 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF22 Genezinc finger protein 22 Predicted to enable DNA binding activity. Predicted to be involved in odontogenesis and regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF28 Genezinc finger protein 28 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF113B Genering finger protein 113B Predicted to enable metal ion binding activity. Predicted to be involved in snoRNA splicing. Predicted to be part of U2-type spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF113A Genering finger protein 113A This intronless gene encodes a protein which contains a C3H1-type zinc finger domain and a C3HC4 Ring-type (Really Interesting New Gene-type) zinc finger domain. The Ring-type zinc finger domain is identified in various tumor suppressors, DNA repair genes and cytokine receptor-associated molecules, and is probably involved in mediating protein-protein interactions. [provided by RefSeq, May 2010] |
RFWD2 Genering finger and WD repeat domain 2, E3 ubiquitin protein ligase Enables ubiquitin protein ligase activity. Involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process; proteasome-mediated ubiquitin-dependent protein catabolic process; and response to ionizing radiation. Part of Cul4A-RING E3 ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
RFWD3 Genering finger and WD repeat domain 3 Enables MDM2/MDM4 family protein binding activity; p53 binding activity; and ubiquitin protein ligase activity. Involved in several processes, including DNA metabolic process; regulation of cell cycle phase transition; and response to ionizing radiation. Located in nucleoplasm and site of double-strand break. Implicated in Fanconi anemia complementation group W. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF251 Genezinc finger protein 251 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within hematopoietic stem cell homeostasis. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF250 Genezinc finger protein 250 Enables identical protein binding activity and sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF253 Genezinc finger protein 253 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF254 Genezinc finger protein 254 Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002] |
ZNF257 Genezinc finger protein 257 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF256 Genezinc finger protein 256 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF25 Genering finger protein 25 The protein encoded by this gene contains a RING finger motif. The mouse counterpart of this protein has been shown to interact with Rela, the p65 subunit of NF-kappaB (NFKB), and modulate NFKB-mediated transcription activity. The mouse protein also binds ubiquitin-conjugating enzymes (E2s) and is a substrate for E2-dependent ubiquitination. [provided by RefSeq, Jul 2008] |
RNF24 Genering finger protein 24 This gene encodes an integral membrane protein that contains a RING-type zinc finger. The encoded protein may interact with multiple transient receptor potential cation channel subfamily C (TRPC) proteins and regulate the trafficking and insertion of these proteins into the plasma membrane. [provided by RefSeq, Mar 2016] |
RNF26 Genering finger protein 26 The protein encoded by this intronless gene contains a C3HC5 type of RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. The expression of this gene was found to be upregulated in cancer cell lines derived from different types of cancer. [provided by RefSeq, Jul 2008] |
RNF20 Genering finger protein 20, E3 ubiquitin protein ligase The protein encoded by this gene shares similarity with BRE1 of S. cerevisiae. The protein encoded by this human gene is an E3 ubiquitin ligase that regulates chromosome structure by monoubiquitinating histone H2B. This protein acts as a putative tumor suppressor and positively regulates the p53 tumor suppressor as well as numerous histone H2A and H2B genes. In contrast, this protein also suppresses the expression of several protooncogenes and growth-related genes, including many genes that are induced by epidermal growth factor. This gene selectively suppresses the expression of some genes by interfering with chromatin recruitment of transcription elongation factor SII (TFIIS). [provided by RefSeq, Feb 2012] |
ZIK1 Genezinc finger protein interacting with K protein 1 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF725P Genezinc finger protein 725, pseudogene |
LOC732229 GeneAN1-type zinc finger protein 5 pseudogene |
LOC100129144 Genezinc finger protein 681 pseudogene |
ZMYND8 Genezinc finger, MYND-type containing 8 The protein encoded by this gene is a receptor for activated C-kinase (RACK) protein. The encoded protein has been shown to bind in vitro to activated protein kinase C beta I. In addition, this protein is a cutaneous T-cell lymphoma-associated antigen. Finally, the protein contains a bromodomain and two zinc fingers, and is thought to be a transcriptional regulator. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
OVOL2 Geneovo-like zinc finger 2 This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy. [provided by RefSeq, Apr 2016] |
OVOL1 Geneovo-like zinc finger 1 This gene encodes a putative zinc finger containing transcription factor that is highly similar to homologous protein in Drosophila and mouse. Based on known functions in these species, this protein is likely involved in hair formation and spermatogenesis in human as well. [provided by RefSeq, Aug 2011] |
ZNF865 Genezinc finger protein 865 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF862 Genezinc finger protein 862 Predicted to enable metal ion binding activity and protein dimerization activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF860 Genezinc finger protein 860 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF512B Genezinc finger protein 512B Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of miRNA transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP1 GeneZFP1 zinc finger protein This gene belongs to the zinc finger protein family. Some members of this family bind to DNA by zinc-mediated secondary structures called zinc fingers, and are involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
ZFP2 GeneZFP2 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP3 GeneZFP3 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419706 Genezinc finger protein 84 pseudogene |
ZNF840P Genezinc finger protein 840, pseudogene |
GLI2 GeneGLI family zinc finger 2 This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008] |
GLI3 GeneGLI family zinc finger 3 This gene encodes a protein which belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008] |
GLI1 GeneGLI family zinc finger 1 This gene encodes a member of the Kruppel family of zinc finger proteins. The encoded transcription factor is activated by the sonic hedgehog signal transduction cascade and regulates stem cell proliferation. The activity and nuclear localization of this protein is negatively regulated by p53 in an inhibitory loop. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009] |
GLI4 GeneGLI family zinc finger 4 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF970P Genezinc finger protein 970, pseudogene |
FIZ1 GeneFLT3-interacting zinc finger 1 This gene encodes zinc finger protein, which interacts with a receptor tyrosine kinase involved in the regulation of hematopoietic and lymphoid cells. This gene product also interacts with a transcription factor that regulates the expression of rod-specific genes in retina. [provided by RefSeq, Jul 2008] |
RNF103 Genering finger protein 103 The protein encoded by this gene contains a RING-H2 finger, a motif known to be involved in protein-protein and protein-DNA interactions. This gene is highly expressed in normal cerebellum, but not in the cerebral cortex. The expression of the rat counterpart in the frontal cortex and hippocampus was shown to be induced by elctroconvulsive treatment (ECT) as well as chronic antidepressant treatment, suggesting that this gene may be a molecular target for ECT and antidepressants. The protein is a ubiquitin ligase that functions in the endoplasmic reticulum-associated degradation pathway. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream CHMP3 (charged multivesicular body protein 3) gene. [provided by RefSeq, Oct 2011] |
ZNF402P Genezinc finger protein 402, pseudogene |
ZNF861P Genezinc finger protein 861, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF460 Genezinc finger protein 460 Zinc finger proteins, such as ZNF272, interact with nucleic acids and have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, May 2004] |
LOC100420774 Genezinc finger, DHHC-type containing 6 pseudogene |
RING1 Genering finger protein 1 This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008] |
ZNF124 Genezinc finger protein 124 This gene encodes a protein with an amino-terminal KRAB-A box and multiple repeated Kruppel-type (C2H2) zinc finger motifs at its carboxy terminus. The encoded protein may function as a transcription factor. Expression of this gene is increased after vascular endothelial growth factor (VEGF) stimulation in human leukemia cell lines and results in inhibition of apoptotic cell death induced by irradiation or exposure to etoposide. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2014] |
ZNF121 Genezinc finger protein 121 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P6Y Genezinc finger protein 736 pseudogene 6, Y-linked |
LOC101928592 Genezinc finger protein OZF-like |
LOC101928044 Genezinc finger CCHC domain-containing protein 9 pseudogene |
LOC100289500 Genezinc finger, AN1-type domain 1 pseudogene |
ZNF736P10Y Genezinc finger protein 736 pseudogene 10, Y-linked |
RNF144A Genering finger protein 144A This gene encodes a member of a family of RING finger domain-containing E3 ubiquitin ligases that also includes parkin and parc. The expression of this gene is induced by DNA damage. The encoded protein interacts with the cytoplasmic DNA-dependent protein kinase, catalytic subunit (DNA-PKcs) and promotes its degradation through ubiquitination. The orthologous mouse protein has been shown to interact with a ubiquitin-conjugating enzyme involved in embryonic development. [provided by RefSeq, Mar 2017] |
ZNF688 Genezinc finger protein 688 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF689 Genezinc finger protein 689 Enables histone binding activity. Involved in regulation of transcription by RNA polymerase II. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF682 Genezinc finger protein 682 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF683 Genezinc finger protein 683 Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in T cell receptor signaling pathway; cellular response to ionomycin; and regulation of gene expression. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF680 Genezinc finger protein 680 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF681 Genezinc finger protein 681 This gene encodes a protein containing the krueppel associated box (KRAB) and zinc-finger domains, which may be involved in transcriptional regulation. Non-functional alleles of this gene are present in alternate genome assemblies including T2T-CHM13v1.1, resulting from a 'TG' deletion (rs61397759) which causes a frameshift and a premature stop codon. [provided by RefSeq, Sep 2022] |
ZNF687 Genezinc finger protein 687 This gene encodes C2H2 zinc finger protein. The encoded protein may play a role in bone differentiation and development. Mutations in this gene are the cause of Paget disease of bone-6. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
ZNF684 Genezinc finger protein 684 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within innate immune response and negative regulation of single stranded viral RNA replication via double stranded DNA intermediate. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419707 Genezinc finger protein 41 pseudogene |
LOC100419704 Genezinc finger protein 57 pseudogene |
ZNF350 Genezinc finger protein 350 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II intronic transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nuclear body. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF358 Genezinc finger protein 358 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in several processes, including embryonic forelimb morphogenesis; neural tube development; and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC401805 Genering finger protein 145 pseudogene |
RNF185 Genering finger protein 185 Enables ubiquitin binding activity; ubiquitin protein ligase activity; and ubiquitin-like protein conjugating enzyme binding activity. Involved in several processes, including positive regulation of ERAD pathway; protein ubiquitination; and proteolysis involved in protein catabolic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RNF187 Genering finger protein 187 Enables ubiquitin-protein transferase activity. Involved in positive regulation of DNA-templated transcription; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF186 Genering finger protein 186 Enables ubiquitin protein ligase activity and ubiquitin protein ligase binding activity. Involved in several processes, including intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Acts upstream of with a positive effect on regulation of autophagosome assembly. Located in endoplasmic reticulum membrane. Is active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RNF181 Genering finger protein 181 RNF181 binds the integrin alpha-IIb (ITGA2B; MIM 607759)/beta-3 (ITGB3; MIM 173470) complex and has E3 ubiquitin ligase activity (Brophy et al., 2008 [PubMed 18331836]).[supplied by OMIM, Dec 2008] |
RNF180 Genering finger protein 180 Predicted to enable ubiquitin conjugating enzyme binding activity and ubiquitin protein ligase activity. Predicted to be involved in norepinephrine metabolic process; positive regulation of proteasomal ubiquitin-dependent protein catabolic process; and serotonin metabolic process. Predicted to act upstream of or within several processes, including adult behavior; positive regulation of protein ubiquitination; and protein polyubiquitination. Predicted to be located in endoplasmic reticulum; membrane; and nuclear envelope. Predicted to be active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF183 Genering finger protein 183 Enables ubiquitin protein ligase activity. Involved in positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway; protein ubiquitination; and response to endoplasmic reticulum stress. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF182 Genering finger protein 182 Enables ubiquitin-protein transferase activity. Involved in protein ubiquitination. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB22 Genezinc finger and BTB domain containing 22 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB20 Genezinc finger and BTB domain containing 20 This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017] |
ZBTB21 Genezinc finger and BTB domain containing 21 Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; POZ domain binding activity; and methyl-CpG binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZBTB25 Genezinc finger and BTB domain containing 25 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
UHRF2P1 Geneubiquitin-like with PHD and ring finger domains 2 pseudogene 1 |
LOC100419515 Genezinc finger protein 41 pseudogene |
LOC100419512 Genezinc finger protein 19 pseudogene |
LOC100419511 Genezinc finger protein 79 pseudogene |
CXXC1P1 GeneCXXC finger protein 1 pseudogene 1 |
ZNF75BP Genezinc finger protein 75B, pseudogene |
ZNF705G Genezinc finger protein 705G Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705F Genezinc finger protein 705F |
ZNF705E Genezinc finger protein 705E Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705D Genezinc finger protein 705D Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705C Genezinc finger protein 705C, pseudogene |
ZNF705B Genezinc finger protein 705B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705A Genezinc finger protein 705A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420804 Genezinc finger CCCH-type containing 14 pseudogene |
LOC100419451 Genezinc finger protein 3 pseudogene |
ZNF601P Genezinc finger protein 601, pseudogene |
ZNF267 Genezinc finger protein 267 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF444 Genezinc finger protein 444 This gene encodes a zinc finger protein which activates transcription of a scavenger receptor gene involved in the degradation of acetylated low density lipoprotein (Ac-LDL) (PMID: 11978792). This gene is located in a cluster of zinc finger genes on chromosome 19 at q13.4. A pseudogene of this gene is located on chromosome 15. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] |
ZNF445 Genezinc finger protein 445 Enables double-stranded methylated DNA binding activity. Involved in epigenetic programing of female pronucleus and negative regulation of gene expression via chromosomal CpG island methylation. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF446 Genezinc finger protein 446 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF440 Genezinc finger protein 440 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF441 Genezinc finger protein 441 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF442 Genezinc finger protein 442 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF443 Genezinc finger protein 443 Zinc finger proteins (ZNFs) bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. For a general description of these proteins, see ZNF91 (MIM 603971).[supplied by OMIM, Jul 2002] |
ZNF449 Genezinc finger protein 449 This gene encodes a nuclear protein that likely functions as a transcription factor. The protein includes an N-terminal SCAN domain, and seven C2H2-type zinc finger motifs. [provided by RefSeq, May 2010] |
LOC100418548 Genezinc finger protein 70 pseudogene |
LOC100418547 Genezinc finger protein 93 pseudogene |
LOC100418546 Genezinc finger protein 70 pseudogene |
LOC100288844 Genezinc finger protein 133-like |
ZNF385D Genezinc finger protein 385D Enables sequence-specific double-stranded DNA binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZDHHC8P1 Genezinc finger, DHHC-type containing 8 pseudogene 1 |
ZNF322P1 Genezinc finger protein 322 pseudogene 1 |
ZNF724P Genezinc finger protein 724, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF600 Genezinc finger protein 600 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF606 Genezinc finger protein 606 This gene encodes a zinc finger protein containing a Kruppel-associated box (KRAB) domain at its N-terminus, followed by contiguous C2H2 zinc finger motifs. The encoded protein is a nuclear protein that can act as a transcriptional repressor of growth factor-mediated signaling pathways in a reporter gene assay. This protein has been shown to interact with the SRY-box 9 gene product, and suppresses its transcriptional activity by inhibiting its DNA binding activity. Reduced expression of this gene promotes chondrocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
ZNF607 Genezinc finger protein 607 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in mitochondrial inner membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF608 Genezinc finger protein 608 Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF609 Genezinc finger protein 609 Predicted to enable promoter-specific chromatin binding activity. Involved in regulation of myoblast proliferation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419786 Genezinc finger protein 670 pseudogene |
LOC100419784 Genezinc finger protein 484 pseudogene |
LOC100419782 Genezinc finger protein 717 pseudogene |
LOC100419783 Genezinc finger protein 831 pseudogene |
LOC100419780 Genezinc finger protein 479 pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419781 Genezinc finger protein 267 pseudogene |
ZSCAN32 Genezinc finger and SCAN domain containing 32 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZSCAN31 Genezinc finger and SCAN domain containing 31 This gene encodes a protein containing multiple C2H2-type zinc finger motifs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016] |
ZSCAN30 Genezinc finger and SCAN domain containing 30 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF152P1 Genering finger protein 152 pseudogene 1 |
ZPR1 GeneZPR1 zinc finger The protein encoded by this gene is found in the cytoplasm of quiescent cells but translocates to the nucleolus in proliferating cells. The encoded protein interacts with survival motor neuron protein (SMN1) to enhance pre-mRNA splicing and to induce neuronal differentiation and axonal growth. Defects in this gene or the SMN1 gene can cause spinal muscular atrophy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
ZNF285B Genezinc finger protein 285B, pseudogene |
ZUFSP Genezinc finger with UFM1-specific peptidase domain This gene encodes a protein containing zinc finger motifs and a cysteine peptidase domain. The encoded protein functions as a K63-specific de-ubiquitinating enzyme that specifically cleaves long K63-linked polyubiquitin chains in the middle of a chain (i.e. `endo cleavage) rather than by removing the terminal ubiquitin from a chain. This enzyme is thought to be involved in the regulation of DNA repair by cleaving K63-linked ubiquitin chains at repair foci. This protein is related to proteases for the ubiquitin-like modifiers Ufm1 (ubiquitin fold modifier 1) and Atg8/Gabarapl2, but does not have any activity on these modifiers. [provided by RefSeq, Mar 2018] |
ZNF729 Genezinc finger protein 729 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL4AP7 Generet finger protein-like 4A pseudogene 7 |
ZNF585A Genezinc finger protein 585A Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF585B Genezinc finger protein 585B Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419848 Genezinc finger protein 250 pseudogene |
LOC645481 Genezinc finger protein 248 pseudogene |
ZMYM2 Genezinc finger, MYM-type 2 The protein encoded by this gene is a zinc finger protein that may act as a transcription factor. The encoded protein may be part of a BHC histone deacetylase complex. Translocation of this gene with the fibroblast growth factor receptor-1 gene (FGFR1) results in a fusion gene, which may be a cause of stem cell leukemia lymphoma syndrome (SCLL). Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010] |
ZMYM3 Genezinc finger, MYM-type 3 This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010] |
ZMYM1 Genezinc finger, MYM-type 1 Predicted to enable protein dimerization activity and zinc ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYM6 Genezinc finger, MYM-type 6 Predicted to enable DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYM4 Genezinc finger, MYM-type 4 Predicted to enable DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYM5 Genezinc finger, MYM-type 5 Predicted to enable zinc ion binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC392264 Genezinc finger protein 532 pseudogene |
LOC100129265 Genezinc finger protein 66-like |
RNF2P1 Genering finger protein 2 pseudogene 1 |
BAZ1A Genebromodomain adjacent to zinc finger domain, 1A The BAZ1A gene encodes the accessory subunit of the ATP-dependent chromatin assembly factor (ACF), a member of the ISWI ('imitation switch') family of chromatin remodeling complexes (summarized by Racki et al., 2009 [PubMed 20033039]).[supplied by OMIM, Apr 2010] |
RLIM Genering finger protein, LIM domain interacting The protein encoded by this gene is a RING-H2 zinc finger protein. It has been shown to be an E3 ubiquitin protein ligase that targets LIM domain binding 1 (LDB1/CLIM), and causes proteasome-dependent degradation of LDB1. This protein and LDB1 are co-repressors of LHX1/LIM-1, a homeodomain transcription factor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Feb 2009] |
PHF5FP GenePHD finger protein 5F pseudogene |
CASZ1 Genecastor zinc finger 1 The protein encoded by this gene is a zinc finger transcription factor. The encoded protein may function as a tumor suppressor, and single nucleotide polymorphisms in this gene are associated with blood pressure variation. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012] |
LOC645135 Genezinc finger protein 532 pseudogene |
JADE3 Genejade family PHD finger 3 This gene encodes a member of a family of large proteins containing PHD (plant homeo domain)-type zinc fingers. The encoded protein may be associated in a nuclear complex that functions in histone H4 acetylation. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Aug 2013] |
JADE2 Genejade family PHD finger 2 Enables histone H4K12 acetyltransferase activity; histone H4K5 acetyltransferase activity; and histone H4K8 acetyltransferase activity. Contributes to histone H3K14 acetyltransferase activity. Involved in regulation of DNA biosynthetic process; regulation of DNA replication; and regulation of cell cycle. Located in nucleoplasm. Part of histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
JADE1 Genejade family PHD finger 1 Enables transcription coactivator activity. Contributes to histone acetyltransferase activity. Involved in several processes, including negative regulation of canonical Wnt signaling pathway; regulation of cell growth; and regulation of nucleobase-containing compound metabolic process. Acts upstream of or within negative regulation of G1/S transition of mitotic cell cycle. Located in several cellular components, including cytosol; microtubule organizing center; and nuclear speck. Part of histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF300P1 Genezinc finger protein 300 pseudogene 1 (functional) |
ZNF197 Genezinc finger protein 197 This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein contains 20 tandemly arrayed C2H2-type zinc fingers, a Kruppel-associated box (KRAB) domain, and a SCAN box. This transcript turns over rapidly and contains 3' UTR AUUUA motifs, which are often a hallmark of rapid turnover. It is overexpressed in some thyroid papillary carcinomas. This gene is located in a cluster of zinc finger genes at 3p21. Naturally-occurring readthrough transcription is observed between this gene and the upstream zinc finger protein 660 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017] |
ZNF195 Genezinc finger protein 195 This gene encodes a protein belonging to the Krueppel C2H2-type zinc-finger protein family. These family members are transcription factors that are implicated in a variety of cellular processes. This gene is located near the centromeric border of chromosome 11p15.5, next to an imprinted domain that is associated with maternal-specific loss of heterozygosity in Wilms' tumors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
ZNF221 Genezinc finger protein 221 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF222 Genezinc finger protein 222 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF223 Genezinc finger protein 223 This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. The function of this protein has yet to be determined. [provided by RefSeq, Mar 2014] |
ZNF224 Genezinc finger protein 224 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein represses transcription of the aldolase A gene, which encodes a key enzyme in glycolysis. The encoded zinc-finger protein may also function as a transcriptional co-activator with Wilms' tumor protein 1 to regulate apoptotic genes in leukemia. [provided by RefSeq, Jul 2016] |
ZNF225 Genezinc finger protein 225 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF226 Genezinc finger protein 226 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF227 Genezinc finger protein 227 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF229 Genezinc finger protein 229 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105377200 Genezinc finger protein Rlf-like |
ZNF965P Genezinc finger protein 965, pseudogene |
PHF14 GenePHD finger protein 14 Enables histone binding activity. Predicted to be involved in several processes, including germinal center B cell differentiation; lung development; and negative regulation of mesenchymal cell proliferation involved in lung development. Located in chromatin; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF10 GenePHD finger protein 10 This gene contains a predicted ORF that encodes a protein with two zinc finger domains. The function of the encoded protein is not known. Sequence analysis suggests that multiple alternatively spliced transcript variants are derived from this gene but the full-length nature of only two of them is known. These two splice variants encode different isoforms. A pseudogene for this gene is located on Xq28. [provided by RefSeq, Jul 2008] |
PHF11 GenePHD finger protein 11 This gene encodes a protein containing a PHD (plant homeodomain) type zinc finger. This gene has been identified in some studies as a candidate gene for asthma. Naturally-occurring readthrough transcription may occur from the upstream SETDB2 (SET domain bifurcated 2) gene to this locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
PHF12 GenePHD finger protein 12 Enables phosphatidylinositol binding activity and transcription corepressor activity. Involved in negative regulation of DNA-templated transcription. Acts upstream of or within negative regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of Sin3-type complex and transcription repressor complex. [provided by Alliance of Genome Resources, Mar 2025] |
PHF13 GenePHD finger protein 13 Enables chromatin binding activity; chromatin-protein adaptor activity; and methylated histone binding activity. Involved in mitotic chromosome condensation and regulation of DNA repair. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF19 GenePHD finger protein 19 Enables methylated histone binding activity. Involved in negative regulation of gene expression, epigenetic. Located in ESC/E(Z) complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3HAV1 Genezinc finger CCCH-type, antiviral 1 This gene encodes a CCCH-type zinc finger protein. This antiviral protein inhibits viral replication by recruiting cellular RNA degradation machineries to degrade viral mRNAs. The encoded protein plays an important role in the innate immune response against multiple DNA and RNA viruses, including Ebola virus, HIV and SARS-CoV-2 (which causes COVID-19). [provided by RefSeq, Sep 2021] |
LOC100131556 Genezinc finger CCHC-type and RNA binding motif 1 pseudogene |
LOC100419792 Genezinc finger protein 622 pseudogene |
ZNF521 Genezinc finger protein 521 Enables protein domain specific binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within neuron fate commitment. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZCRB1 Genezinc finger CCHC-type and RNA binding motif 1 Pre-mRNA splicing is catalyzed by the spliceosome. U12-type spliceosome binds U12-type pre-mRNAs and recognizes the 5' splice site and branch-point sequence. U11 and U12 snRNPs are components of U12-type spliceosome and function as a molecular bridge connecting both ends of the intron. The protein encoded by this gene contains a RNA recognition motif. It was identified as one of the protein components of U11/U12 snRNPs. This protein and many other U11/U12 snRNP proteins are highly conserved in organisms known to contain U12-type introns. These proteins have been shown to be essential for cell viability, suggesting the key roles in U12-type splicing. [provided by RefSeq, Jul 2008] |
ZNF527 Genezinc finger protein 527 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF526 Genezinc finger protein 526 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF525 Genezinc finger protein 525 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF524 Genezinc finger protein 524 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF529 Genezinc finger protein 529 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF528 Genezinc finger protein 528 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF144B Genering finger protein 144B Enables ubiquitin-protein transferase activity. Involved in negative regulation of apoptotic process and ubiquitin-dependent protein catabolic process. Located in mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025] |
BCL11A GeneB-cell CLL/lymphoma 11A (zinc finger protein) This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
BCL11B GeneB-cell CLL/lymphoma 11B (zinc finger protein) This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function of this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
LOC441155 Genezinc finger CCCH-type domain-containing-like Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102724436 Geneputative zinc finger protein 66 |
ZNF721 Genezinc finger protein 721 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF720 Genezinc finger protein 720 Predicted to enable metal ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF727 Genezinc finger protein 727 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF726 Genezinc finger protein 726 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF728 Genezinc finger protein 728 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF72P Genezinc finger protein 72, pseudogene |
ZC3H7B Genezinc finger CCCH-type containing 7B This gene encodes a protein that contains a tetratricopeptide repeat domain. The encoded protein also interacts with the rotavirus non-structural protein NSP3. [provided by RefSeq, Jul 2008] |
MKRN9P Genemakorin ring finger protein 9, pseudogene |
LOC100533707 GeneZFP37 zinc finger protein pseudogene |
ZNF79 Genezinc finger protein 79 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF73 Genezinc finger protein 73 |
ZNF70 Genezinc finger protein 70 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytoplasm and megasporocyte nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF71 Genezinc finger protein 71 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF76 Genezinc finger protein 76 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF77 Genezinc finger protein 77 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF74 Genezinc finger protein 74 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in actin cytoskeleton and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF767P Genezinc finger family member 767, pseudogene |
PHF20L1 GenePHD finger protein 20-like 1 Enables methylation-dependent protein binding activity. Involved in negative regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleoplasm. Predicted to be part of NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNRF2P1 Genezinc and ring finger 2 pseudogene 1 |
ZNRF2P3 Genezinc and ring finger 2 pseudogene 3 |
ZNRF2P2 Genezinc and ring finger 2 pseudogene 2 |
PHF24 GenePHD finger protein 24 Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to act upstream of or within several processes, including detection of mechanical stimulus involved in sensory perception of pain; gamma-aminobutyric acid signaling pathway; and regulation of GABAergic synaptic transmission. Predicted to be active in glutamatergic synapse; nucleus; and synaptic vesicle membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF1 Genemembrane associated ring-CH-type finger 1 MARCH1 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH1 downregulates the surface expression of major histocompatibility complex (MHC) class II molecules (see MIM 142880) and other glycoproteins by directing them to the late endosomal/lysosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Thibodeau et al., 2008 [PubMed 18389477]; De Gassart et al., 2008 [PubMed 18305173]).[supplied by OMIM, Mar 2010] |
MARCHF7 Genemembrane associated ring-CH-type finger 7 MARCH7 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Mar 2010] |
ZSWIM9 Genezinc finger SWIM-type containing 9 Predicted to act upstream of or within hematopoietic progenitor cell differentiation. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF6 Genemembrane associated ring-CH-type finger 6 This gene encodes a member of a family of membrane-associated E3 ubiquitin ligases containing RING-CH-type zinc finger motifs. Ubiquitination of type II deiodinase by the encoded protein is an important regulatory step in thyroid hormone signalling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
ZNF724 Genezinc finger protein 724 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZUP1 Genezinc finger containing ubiquitin peptidase 1 This gene encodes a protein containing zinc finger motifs and a cysteine peptidase domain. The encoded protein functions as a K63-specific de-ubiquitinating enzyme that specifically cleaves long K63-linked polyubiquitin chains in the middle of a chain (i.e. `endo cleavage) rather than by removing the terminal ubiquitin from a chain. This enzyme is thought to be involved in the regulation of DNA repair by cleaving K63-linked ubiquitin chains at repair foci. This protein is related to proteases for the ubiquitin-like modifiers Ufm1 (ubiquitin fold modifier 1) and Atg8/Gabarapl2, but does not have any activity on these modifiers. [provided by RefSeq, Mar 2018] |
MARCHF5 Genemembrane associated ring-CH-type finger 5 MARCH5 is a ubiquitin ligase of the mitochondrial outer membrane that plays a role in the control of mitochondrial morphology by regulating mitofusin-2 (MFN2; MIM 608507) and DRP1 (DNM1L; MIM 603850) (Nakamura et al., 2006 [PubMed 16936636]).[supplied by OMIM, Mar 2008] |
LOC122513141 Genering finger protein-like |
LOC122539214 GeneZinc finger protein LOC122539214 |
MARCHF3 Genemembrane associated ring-CH-type finger 3 This gene encodes a member of the membrane-associated RING-CH (MARCH) family. The encoded protein is an E3 ubiquitin-protein ligase that may be involved in regulation of the endosomal transport pathway. [provided by RefSeq, Mar 2013] |
MARCHF8 Genemembrane associated ring-CH-type finger 8 MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
MARCHF2 Genemembrane associated ring-CH-type finger 2 MARCH2 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH2 reduces surface accumulation of several glycoproteins and appears to regulate early endosome-to-trans-Golgi network (TGN) trafficking (Bartee et al., 2004 [PubMed 14722266]; Nakamura et al., 2005 [PubMed 15689499]).[supplied by OMIM, Mar 2010] |
MARCHF10 Genemembrane associated ring-CH-type finger 10 MARCH10 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
ZFTA Genezinc finger translocation associated Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF227 Genering finger protein 227 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF9 Genemembrane associated ring-CH-type finger 9 MARCH9 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH9 induces internalization of several membrane glycoproteins and directs them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Hoer et al., 2007 [PubMed 17174307]).[supplied by OMIM, Apr 2010] |
ZSCAN5DP Genezinc finger and SCAN domain containing 5D pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFTRAF1 Genezinc finger TRAF-type containing 1 Predicted to enable zinc ion binding activity. Predicted to be located in nuclear envelope and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF723 Genezinc finger protein 723 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF11 Genemembrane associated ring-CH-type finger 11 MARCH11 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). These enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their intracellular transport. March11 appears to have a role in ubiquitin-mediated protein sorting in the trans-Golgi network (TGN)-multivesicular body (MVB) transport pathway (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
ZSCAN5C Genezinc finger and SCAN domain containing 5C Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF4 Genemembrane associated ring-CH-type finger 4 MARCH4 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH4 reduces surface accumulation of several membrane glycoproteins by directing them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
ZNF875 Genezinc finger protein 875 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZBED10P Genezinc finger BED-type containing 10, pseudogene |
ZNF788P Genezinc finger family member 788, pseudogene Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF812P Genezinc finger protein 812, pseudogene |
ZNF807P Genezinc finger protein 807, pseudogene |
ZBTB12BP Genezinc finger and BTB domain containing 12B, pseudogene |
BPTFP1 Genebromodomain PHD finger transcription factor pseudogene 1 |
LOC124904660 Geneputative zinc finger protein 826 |
RNF228 Genering finger protein 228 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF475 Genezinc finger protein 475 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF892 Genezinc finger protein 892 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H11C Genezinc finger CCCH-type containing 11C Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ARK2C Genearkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in motor neuron axon guidance and positive regulation of BMP signaling pathway. Predicted to act upstream of or within several processes, including forelimb morphogenesis; nervous system development; and protein polyubiquitination. Predicted to be part of protein-containing complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
NOAZFP Genenucleolar atypical zinc finger Predicted to enable metal ion binding activity. Located in chromosome, centromeric region; midbody; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025] |
ZBED11 Genezinc finger BED-type containing 11 |
ZBTB35 Genezinc finger and BTB domain containing 35 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in intermediate filament cytoskeleton and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3H11D Genezinc finger CCCH-type containing 11D Predicted to be involved in poly(A)+ mRNA export from nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
weakness of long finger extensor muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of long finger extensor muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Weakness Of Long Finger Extensor Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Long Finger Extensor Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
paresis of extensor muscles of the big toe Gene SetFrom HPO Gene-Disease Associations genes associated with the paresis of extensor muscles of the big toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness of the intrinsic hand muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of the intrinsic hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness of muscles of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of muscles of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Fatigable Weakness Of Neck Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Neck Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Bulbar Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Bulbar Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Distal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Distal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Respiratory Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Respiratory Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatiguable Weakness Of Proximal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatiguable Weakness Of Proximal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Weakness Of Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Weakness Of Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Facial Muscle Weakness Of Muscles Innervated By Cn Vii Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Muscle Weakness Of Muscles Innervated By Cn Vii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of The Intrinsic Hand Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of The Intrinsic Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Swallowing Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Swallowing Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Skeletal Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Skeletal Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Muscles Of Respiration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Muscles Of Respiration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Speech Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Speech Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Zinc finger, PHD-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PHD-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
long proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Long Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Proximal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
extensor Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term extensor in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
toe extensor amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the toe extensor amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal extensor digitorum longus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal extensor digitorum longus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased extensor digitorum longus weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased extensor digitorum longus weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal extensor digitorum longus weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
extensor digitorum communis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue extensor digitorum communis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
extensor Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue extensor in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
extensor digitorum brevis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue extensor digitorum brevis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
extensor digitorum longus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue extensor digitorum longus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Toe Extensor Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Extensor Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Extensor Rigidity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extensor Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
increased extensor digitorum longus weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased extensor digitorum longus weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased extensor digitorum longus weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased extensor digitorum longus weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal extensor digitorum longus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extensor digitorum longus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Extensor Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Extensor in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Extensor digitorum longus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Extensor digitorum longus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Extensor digitorum communis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Extensor digitorum communis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Extensor digitorum brevis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Extensor digitorum brevis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Long Chain/Very Long Chain Acyl Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain/Very Long Chain Acyl Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis of extraocular muscles, congenital, 3b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset. |
Fibrosis of Extraocular Muscles, Congenital, 3B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles, Congenital, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset. |
congenital fibrosis of extraocular muscles type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of extraocular muscles type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital fibrosis of the extraocular muscles Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of the extraocular muscles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscles Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term muscles in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
DMD_Deficiency_GDS2996_613_mouse_Cardiac muscles from 8-week (mdx animals) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DMD_Deficiency_GDS2996_613_mouse_Cardiac muscles from 8-week (mdx animals) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
DMD_Deficiency_GDS2996_614_mouse_Cardiac muscles from 10.5-month (mdx animals) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DMD_Deficiency_GDS2996_614_mouse_Cardiac muscles from 10.5-month (mdx animals) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PPARGC1B_Hypomorphic Mutation_GDS2515_695_mouse_Skeletal muscle - (quadriceps muscles) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PPARGC1B_Hypomorphic Mutation_GDS2515_695_mouse_Skeletal muscle - (quadriceps muscles) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
DES_KO_GDS4804_171_mouse_young skeletal muscles Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the DES_KO_GDS4804_171_mouse_young skeletal muscles gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PPARalpha_OE_GDS2289_244_mouse_Skeletal muscles Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PPARalpha_OE_GDS2289_244_mouse_Skeletal muscles gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypotrophy of the small hand muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the hypotrophy of the small hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spasticity of pharyngeal muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the spasticity of pharyngeal muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spasticity of facial muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the spasticity of facial muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
firm muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the firm muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital fibrosis of extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased collagen deposition in the muscles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fibrosis of extraocular muscles, congenital, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 3b Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3b phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 3a Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3a phenotype from the curated OMIM Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Fibrosis Of The Extraocular Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Fibrosis Of The Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypotrophy Of The Small Hand Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypotrophy Of The Small Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Masticatory Muscles, Hypertrophy Of Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Masticatory Muscles, Hypertrophy Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Floppy Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Floppy Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spasticity Of Facial Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spasticity Of Facial Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spasticity Of Pharyngeal Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spasticity Of Pharyngeal Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Jaw Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Jaw Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Firm Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Firm Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Of Extraocular Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Extraocular Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weak Extraocular Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weak Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
absent extraocular muscles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent extraocular muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased collagen deposition in the muscles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent eye muscles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Congenital fibrosis of the extraocular muscles Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital fibrosis of the extraocular muscles from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles 3A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of extraocular muscles Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fibrosis of extraocular muscles Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle Weakness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscle Weakness from the curated CTD Gene-Disease Associations dataset. |
Episodic Muscle Weakness, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Muscle Weakness, X-Linked from the curated CTD Gene-Disease Associations dataset. |
deglutition disorders; muscle weakness; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deglutition disorders; muscle weakness; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
weakness Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term weakness in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abdominal wall muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal wall muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
foot dorsiflexor weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the foot dorsiflexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peroneal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the peroneal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
first dorsal interossei muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic flaccid weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic flaccid weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scapuloperoneal weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the scapuloperoneal weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder girdle muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
respiratory insufficiency due to muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neck flexor weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the neck flexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness due to upper motor neuron dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neck muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the neck muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intercostal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the intercostal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lower limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness in lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness in lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diaphragmatic weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the diaphragmatic weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fatigable weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the fatigable weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thenar muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the thenar muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
quadriceps muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the quadriceps muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pelvic girdle muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the pelvic girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
axial muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the axial muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness in upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness in upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
limb-girdle muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the limb-girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intermittent episodes of respiratory insufficiency due to muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hand muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the hand muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Muscle Weakness Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscle Weakness phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
progressive muscle weakness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscle weakness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
weakness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene SetFrom OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic muscle weakness, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic muscle weakness, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
Bulbar Weakness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bulbar Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Facial Muscle Weakness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Facial Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Foot Dorsiflexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Dorsiflexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Muscle Weakness, Ctcae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shoulder Girdle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Girdle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Axial Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Limb-Girdle Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limb-Girdle Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Weakness Of Limb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Weakness Of Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neck Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neck Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neck Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neck Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Respiratory Insufficiency Due To Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Lower Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Lower Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Upper Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Upper Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Quadriceps Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Quadriceps Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Triceps Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Triceps Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ankle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ankle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Frontalis Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontalis Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hip Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Favorable Response Of Weakness To Acetylcholine Esterase Inhibitors Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Favorable Response Of Weakness To Acetylcholine Esterase Inhibitors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Calf Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Calf Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Girdle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Girdle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness In Lower Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Lower Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness In Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hand Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
First Dorsal Interossei Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype First Dorsal Interossei Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thenar Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thenar Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tibialis Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tibialis Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Flaccid Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Flaccid Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Due To Upper Motor Neuron Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Wall Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Wall Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unfavorable Response Of Muscle Weakness To Acetylcholine Esterase Inhibitors Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unfavorable Response Of Muscle Weakness To Acetylcholine Esterase Inhibitors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Pain Or Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Pain Or Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Worsened Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Worsened in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Scapuloperoneal Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scapuloperoneal Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intercostal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intercostal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peroneal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peroneal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Orbicularis Oculi Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Orbicularis Oculi Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
weakness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
muscle weakness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
progressive muscle weakness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Lower limb muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive proximal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Shoulder girdle muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Shoulder girdle muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Limb-girdle muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Scapuloperoneal weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Generalized muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pelvic girdle muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pelvic girdle muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic flaccid weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic flaccid weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hip flexor weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hip flexor weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal muscle weakness in lower limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness in lower limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Foot dorsiflexor weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Foot dorsiflexor weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
finger agnosia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease finger agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
finger Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term finger in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
c3hc4-type ring finger domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the c3hc4-type ring finger domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ring-like zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ring-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
c2h2 zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the c2h2 zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sclerosis of finger phalanx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the sclerosis of finger phalanx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
radial deviation of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
macrodactyly of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the macrodactyly of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapering pointed ends of distal finger phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
camptodactyly of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the camptodactyly of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism of middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism of middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent middle phalanx of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the absent middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pseudoepiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
patchy sclerosis of finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the patchy sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interphalangeal joint contracture of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the interphalangeal joint contracture of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger clinodactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the finger clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
3-4 finger cutaneous syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 3-4 finger cutaneous syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sclerosis of distal finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism of middle phalanx of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism of middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
joint contracture of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the joint contracture of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypersegmentation of proximal phalanx of second finger Gene SetFrom HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of second finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of phalanx of 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of phalanx of 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent proximal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the absent proximal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphyses of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphyses of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pseudoepiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of phalanx of 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of phalanx of 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased finger mobility Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased finger mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cutaneous finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the cutaneous finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
clinodactyly of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the clinodactyly of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fifth finger distal phalanx clinodactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
polydactyly affecting the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the polydactyly affecting the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
2-3 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 2-3 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
4-5 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 4-5 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
single interphalangeal crease of fifth finger Gene SetFrom HPO Gene-Disease Associations genes associated with the single interphalangeal crease of fifth finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger joint hypermobility Gene SetFrom HPO Gene-Disease Associations genes associated with the finger joint hypermobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flexion contracture of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the flexion contracture of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
2-4 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 2-4 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital finger flexion contractures Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital finger flexion contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism affecting the proximal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
1-5 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 1-5 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
contracture of the proximal interphalangeal joint of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the contracture of the proximal interphalangeal joint of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypersegmentation of proximal phalanx of third finger Gene SetFrom HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of third finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger joint hyperextensibility Gene SetFrom HPO Gene-Disease Associations genes associated with the finger joint hyperextensibility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered distal phalanges of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
streaks of hyperkeratosis along each finger onto the palm Gene SetFrom HPO Gene-Disease Associations genes associated with the streaks of hyperkeratosis along each finger onto the palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
1-5 finger complete cutaneous syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 1-5 finger complete cutaneous syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperextensibility of the finger joints Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperextensibility of the finger joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sclerosis of finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
polydactyly affecting the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the polydactyly affecting the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
3-4 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 3-4 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent fourth finger distal interphalangeal crease Gene SetFrom HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
PR domain zinc finger protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR domain zinc finger protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, NHR/GATA-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, NHR/GATA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FYVE-type, endofin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FYVE-type, endofin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C6HC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C6HC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, MYND-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, MYND-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, H2C2-type, histone UAS binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, H2C2-type, histone UAS binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DBF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DBF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
C2H2- zinc finger protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the C2H2- zinc finger protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNA glycosylase/AP lyase/isoleucyl tRNA synthetase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNA glycosylase/AP lyase/isoleucyl tRNA synthetase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TRM13/UPF0224 family, U11-48K-like CHHC zinc finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRM13/UPF0224 family, U11-48K-like CHHC zinc finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PARP-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PARP-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, double-stranded RNA binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, double-stranded RNA binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TFIIS-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TFIIS-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, ZZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, ZZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3669, zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3669, zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, U1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, U1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RDM domain, Ret finger protein-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RDM domain, Ret finger protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein PLAGL1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein PLAGL1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 446 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 446 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 174 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 174 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, N-recognin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, N-recognin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Putative treble-clef, zinc-finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Putative treble-clef, zinc-finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR-domain zinc finger protein PRDM5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR-domain zinc finger protein PRDM5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PMZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PMZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2HC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2HC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Replication termination factor 2, RING-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Replication termination factor 2, RING-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, MIZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, MIZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING/FYVE/PHD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING/FYVE/PHD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 131 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 131 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-CH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-CH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, LIM-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, LIM-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cip1-interacting zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cip1-interacting zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNA-directed DNA polymerase, family B, alpha Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNA-directed DNA polymerase, family B, alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Sec23/Sec24-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Sec23/Sec24-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger homeobox protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger homeobox protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, NF-X1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, NF-X1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2CH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2CH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 496 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 496 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR-domain zinc finger protein PRDM4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR-domain zinc finger protein PRDM4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DPH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DPH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C4H2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C4H2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger CCCH-type antiviral protein 1-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger CCCH-type antiviral protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 18 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 18 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, AN1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, AN1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CXXC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CXXC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2, LYAR-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2, LYAR-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FLYWCH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FLYWCH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TRAF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TRAF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger transcription factor Trps1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger transcription factor Trps1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNA glycosylase/AP lyase-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNA glycosylase/AP lyase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
C4-type zinc-finger of DNA polymerase delta Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the C4-type zinc-finger of DNA polymerase delta protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein GLIS1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein GLIS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C3HC-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C3HC-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Mcm10/DnaG-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Mcm10/DnaG-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Transcription factor IIIC, putative zinc-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transcription factor IIIC, putative zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FYVE/PHD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FYVE/PHD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, SWIM-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, SWIM-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PHD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PHD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RING-type zinc-finger, LisH dimerisation motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RING-type zinc-finger, LisH dimerisation motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CTCHY-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CTCHY-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, U1-C type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, U1-C type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PHD-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PHD-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger C2HC domain-containing protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger C2HC domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spt4/RpoE2 zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spt4/RpoE2 zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2, APLF-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2, APLF-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA topoisomerase, type IA, zn finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, zn finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DHHC-type, palmitoyltransferase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DHHC-type, palmitoyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, N-recognin, metazoa Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, N-recognin, metazoa protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, ZPR1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, ZPR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor-transporting protein/CXXC-type zinc finger protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor-transporting protein/CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger and BTB domain-containing protein 22 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger and BTB domain-containing protein 22 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein PLAG1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein PLAG1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, MYM-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, MYM-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TFIIB-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TFIIB-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, SIAH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, SIAH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, piccolo-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, piccolo-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bromodomain adjacent to zinc finger domain protein 2A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bromodomain adjacent to zinc finger domain protein 2A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Putative zinc-finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Putative zinc-finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, nuclear hormone receptor-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, nuclear hormone receptor-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FYVE-finger-containing Rab5 effector protein rabenosyn-5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FYVE-finger-containing Rab5 effector protein rabenosyn-5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C5HC2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C5HC2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, GATA-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, GATA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CCCH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CCCH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised conserved protein UCP037948, zinc finger MYND-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised conserved protein UCP037948, zinc finger MYND-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, AD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, AD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein Gfi-1b Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein Gfi-1b protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised conserved protein UCP037956, zinc finger Ran-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised conserved protein UCP037956, zinc finger Ran-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, GRF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, GRF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FLYWCH-type zinc finger-containing protein, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FLYWCH-type zinc finger-containing protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger C2H2-type/integrase DNA-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger C2H2-type/integrase DNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger and BTB domain-containing protein 40 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger and BTB domain-containing protein 40 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, HIT-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, HIT-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2HC5-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2HC5-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2-type matrin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2-type matrin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, B-box, chordata Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, B-box, chordata protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CXXC-type zinc finger protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR domain zinc finger protein 16 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR domain zinc finger protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RanBP2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RanBP2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TTF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TTF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger C2HC domain-containing protein 1C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger C2HC domain-containing protein 1C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CCHC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CCHC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, XPA-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, XPA-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FYVE-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FYVE-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
KRAB domain C2H2 zinc finger family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the KRAB domain C2H2 zinc finger family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CW-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CW-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CHCC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CHCC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, V(D)J recombination-activating protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, V(D)J recombination-activating protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, UBP-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, UBP-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CCCH-type, TRM13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CCCH-type, TRM13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FYVE zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FYVE zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR-domain zinc finger protein PRDM12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR-domain zinc finger protein PRDM12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 518A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 518A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tim10/DDP family zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tim10/DDP family zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C3HC4 RING-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C3HC4 RING-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FCS-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FCS-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, B-box Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, B-box protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA glycosylase/AP lyase, zinc finger domain, DNA-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA glycosylase/AP lyase, zinc finger domain, DNA-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-H2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-H2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc-finger domain of monoamine-oxidase A repressor R1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc-finger domain of monoamine-oxidase A repressor R1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, A20-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, A20-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Interferon regulatory factor 2-binding protein 1 & 2, zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Interferon regulatory factor 2-binding protein 1 & 2, zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 518B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 518B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, BED-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, BED-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNL-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNL-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein NOA36 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein NOA36 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, nanos-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, nanos-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CHHC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CHHC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CHY-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CHY-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger FYVE domain-containing protein 26 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger FYVE domain-containing protein 26 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Btk motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Btk motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TAZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TAZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Rad18-type putative Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Rad18-type putative protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
N-acetyltransferase ESCO, zinc-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the N-acetyltransferase ESCO, zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histone deacetylase complex subunit SAP30 zinc-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histone deacetylase complex subunit SAP30 zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA polymerase, Y-family, little finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase, Y-family, little finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
finger Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term finger in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
finger Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue finger in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Joint Contracture Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Joint Contracture Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fifth Finger Distal Phalanx Clinodactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Finger Flexion Contractures Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Finger Flexion Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Finger Syndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Finger Syndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Middle Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Middle Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tapering Pointed Ends Of Distal Finger Phalanges Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tapering Pointed Ends Of Distal Finger Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ectopic Accessory Finger-Like Appendage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ectopic Accessory Finger-Like Appendage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Finger Symphalangism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Finger Symphalangism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radial Deviation Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radial Deviation Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Deformity Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Deformity Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypersegmentation Of Proximal Phalanx Of Second Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Second Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypersegmentation Of Proximal Phalanx Of Third Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Third Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Finger Syndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Finger Syndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radial Deviation Of The 4Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radial Deviation Of The 4Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Slender Proximal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Slender Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Interphalangeal Joint Contracture Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Interphalangeal Joint Contracture Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Trigger Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Trigger Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Trigger Finger Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Trigger Finger Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Fourth Finger Distal Interphalangeal Crease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Phalanges Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Phalanges Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Agnosia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Agnosia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radial Deviation Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radial Deviation Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flexion Contracture Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flexion Contracture Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Finger Flexion Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Finger Flexion Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Spasticity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Syndactyly Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Syndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radial Deviation Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radial Deviation Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Joint Hypermobility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Joint Hypermobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hyperextensibility Of The Finger Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperextensibility Of The Finger Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Proximal Finger Flexion Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Proximal Finger Flexion Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deviation Of The 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Complete Duplication Of The Middle Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of The Middle Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Streaks Of Hyperkeratosis Along Each Finger Onto The Palm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Streaks Of Hyperkeratosis Along Each Finger Onto The Palm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tapered Distal Phalanges Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapered Distal Phalanges Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Finger Mobility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Finger Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Middle Phalanx Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Middle Phalanx Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Patchy Sclerosis Of Finger Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Sclerosis Of Finger Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Middle Phalanx Of The 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Middle Phalanx Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Small Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Single Interphalangeal Crease Of Fifth Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Single Interphalangeal Crease Of Fifth Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Swelling Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Swelling Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Contracture Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Contracture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deviation Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Symphalangism Of The 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Symphalangism Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
C3HC4-type RING finger domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the C3HC4-type RING finger domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
C2H2 zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the C2H2 zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
RING-like zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the RING-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
C3HC4-type RING finger domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the C3HC4-type RING finger domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
C2H2 zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the C2H2 zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
RING-like zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the RING-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Finger agnosia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Finger agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Finger Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Finger in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Congenital finger flexion contractures Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital finger flexion contractures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Clinodactyly of the 5th finger Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Clinodactyly of the 5th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Symphalangism affecting the proximal phalanx of the 4th finger Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Symphalangism affecting the proximal phalanx of the 4th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Finger syndactyly Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Finger syndactyly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal finger morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal finger morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short 5th finger Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short 5th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Zinc finger transcription factors Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Zinc finger transcription factors assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Trigger finger Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trigger finger phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Finger osteoarthritis severity (hand Klsum) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Finger osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
long insular gyri, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in long insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
long insular gyri, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in long insular gyri, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
the prc2 complex sets long-term gene silencing through modification of histone tails Gene SetFrom Biocarta Pathways proteins participating in the the prc2 complex sets long-term gene silencing through modification of histone tails pathway from the Biocarta Pathways dataset. |
Long QT syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acquired long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LONG QT SYNDROME 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LONG QT SYNDROME 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long Qt Syndrome 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 9 from the curated CTD Gene-Disease Associations dataset. |
LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset. |
Long QT Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long QT Syndrome from the curated CTD Gene-Disease Associations dataset. |
Long QT syndrome type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long QT syndrome type 3 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 5 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 6 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 10 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 11 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 12 from the curated CTD Gene-Disease Associations dataset. |
LONG QT SYNDROME 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LONG QT SYNDROME 13 from the curated CTD Gene-Disease Associations dataset. |
Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset. |
Split-hand/foot malformation with long bone deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset. |
long qt syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease long qt syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
long qt syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease long qt syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
long qt syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease long qt syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
long bone adamantinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease long bone adamantinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
human long-term memory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease human long-term memory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inherited cardiac arrhythmia long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inherited cardiac arrhythmia long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
drug-induced long-qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease drug-induced long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome; torsades de pointes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long-qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; heart arrest; long qt syndrome; syncope Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; heart arrest; long qt syndrome; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disease models, animal; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delayed graft function acute rejection episodes and long-term graft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; death, sudden; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome; sinus tachycardia; tachycardia, sinus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; sinus tachycardia; tachycardia, sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression ; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression ; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long-term kidney allograft survival Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long-term kidney allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term long in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty-acyl-coa biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty-acyl-coa biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty-acyl-coa metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty-acyl-coa metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty-acyl-coa metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty-acyl-coa metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-term memory Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-term memory biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty-acyl-coa catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty-acyl-coa catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset. |
long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset. |
peroxisomal long-chain fatty acid import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peroxisomal long-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain-enoyl-coa hydratase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-enoyl-coa hydratase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain acyl-coa hydrolase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acid-coa ligase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acid-coa ligase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very-long-chain-(s)-2-hydroxy-acid oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very-long-chain-(s)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acid binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acid binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol o-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol o-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-fatty-acyl-coa reductase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-fatty-acyl-coa reductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very long chain acyl-coa hydrolase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very long chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very-long-chain-acyl-coa dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very-long-chain-acyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-3-hydroxyacyl-coa dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-3-hydroxyacyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acyl-coa binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acyl-coa binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very long-chain fatty acid-coa ligase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very long-chain fatty acid-coa ligase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-acyl-coa dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-acyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acid transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long qt syndrome Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease long qt syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
increased density of long bones Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased density of long bones phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thickened cortex of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the thickened cortex of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long face Gene SetFrom HPO Gene-Disease Associations genes associated with the long face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fractures of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the fractures of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortically dense long tubular bones Gene SetFrom HPO Gene-Disease Associations genes associated with the cortically dense long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dumbbell-shaped long bone Gene SetFrom HPO Gene-Disease Associations genes associated with the dumbbell-shaped long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long neck Gene SetFrom HPO Gene-Disease Associations genes associated with the long neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long foot Gene SetFrom HPO Gene-Disease Associations genes associated with the long foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the long metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the long fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long coccyx Gene SetFrom HPO Gene-Disease Associations genes associated with the long coccyx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
periosteal thickening of long tubular bones Gene SetFrom HPO Gene-Disease Associations genes associated with the periosteal thickening of long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical thickening of long bone diaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical thickening of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of long bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of long bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long fibula Gene SetFrom HPO Gene-Disease Associations genes associated with the long fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long penis Gene SetFrom HPO Gene-Disease Associations genes associated with the long penis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long palm Gene SetFrom HPO Gene-Disease Associations genes associated with the long palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the long hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased density of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the increased density of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
crumpled long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the crumpled long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long second metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the long second metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the broad long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skin dimple over apex of long bone angulation Gene SetFrom HPO Gene-Disease Associations genes associated with the skin dimple over apex of long bone angulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
very long chain fatty acid accumulation Gene SetFrom HPO Gene-Disease Associations genes associated with the very long chain fatty acid accumulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
stenosis of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the stenosis of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long clavicles Gene SetFrom HPO Gene-Disease Associations genes associated with the long clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bowing of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the bowing of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long chain 3 hydroxyacyl coa dehydrogenase deficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the long chain 3 hydroxyacyl coa dehydrogenase deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the long upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-segment aganglionic megacolon Gene SetFrom HPO Gene-Disease Associations genes associated with the long-segment aganglionic megacolon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased density of long bone diaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the increased density of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender long bone Gene SetFrom HPO Gene-Disease Associations genes associated with the slender long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated long chain fatty acids Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated long chain fatty acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long nose Gene SetFrom HPO Gene-Disease Associations genes associated with the long nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long toe Gene SetFrom HPO Gene-Disease Associations genes associated with the long toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the long thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-tract signs Gene SetFrom HPO Gene-Disease Associations genes associated with the long-tract signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the long palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior bowing of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior bowing of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of long-chain fatty-acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of long-chain fatty-acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
overtubulated long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the overtubulated long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long ear Gene SetFrom HPO Gene-Disease Associations genes associated with the long ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
protuberances at ends of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the protuberances at ends of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short long bone Gene SetFrom HPO Gene-Disease Associations genes associated with the short long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the long philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-chain dicarboxylic aciduria Gene SetFrom HPO Gene-Disease Associations genes associated with the long-chain dicarboxylic aciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long eyelashes in irregular rows Gene SetFrom HPO Gene-Disease Associations genes associated with the long eyelashes in irregular rows phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the long eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long eyebrows Gene SetFrom HPO Gene-Disease Associations genes associated with the long eyebrows phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Memory, Long-Term Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Memory, Long-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Long QT Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Long QT Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Long hematopoietin receptor, single chain, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Long hematopoietin receptor, single chain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Long hematopoietin receptor, Gp130 family 2, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Long hematopoietin receptor, Gp130 family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Long hematopoietin receptor, soluble alpha chain, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Long hematopoietin receptor, soluble alpha chain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PLUNC, long form Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PLUNC, long form protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peroxysomal long chain fatty acyl transporter Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxysomal long chain fatty acyl transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acyl-CoA thioesterase, long chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA thioesterase, long chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Anaphase-promoting complex subunit 4 long domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Anaphase-promoting complex subunit 4 long domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
long term depression Gene SetFrom KEGG Pathways proteins participating in the long term depression pathway from the KEGG Pathways dataset. |
long term potentiation Gene SetFrom KEGG Pathways proteins participating in the long term potentiation pathway from the KEGG Pathways dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enhanced long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enhanced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long nails Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased length of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone diaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone diaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased long bone epiphyseal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long snout Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long snout phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased diameter of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long fibula Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased length of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long gestation period Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long gestation period phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphyseal plate proliferative zone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal plate proliferative zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term object recognition memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased diameter of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long radius Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone hypertrophic chondrocyte zone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone hypertrophic chondrocyte zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long ribs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long lived plasma cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long lived plasma cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased long bone epiphyseal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal limb long bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal limb long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long tibia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long tibia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphyseal ossification zone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long mandible Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long mandible phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long tail Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long femur Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long stride length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long stride length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term spatial reference memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long ulna Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long humerus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long humerus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphyseal plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thickened long bone epiphysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
disorganized long bone epiphyseal plate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long limbs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long limbs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long incisors Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long toenails Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long toenails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long qt syndrome 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 1, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 1, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome-11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome-11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome-10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome-10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 2, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome, acquired, reduced susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome-3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome-3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Beta-oxidation of very long chain fatty acids Gene Setproteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways dataset. |
Repair synthesis of patch ~27-30 bases long by DNA polymerase Gene Setproteins participating in the Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway from the Reactome Pathways dataset. |
Synthesis of very long-chain fatty acyl-CoAs Gene Setproteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways dataset. |
long bone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue long bone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Acquired Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Chain Acyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain Acyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Very Long Chain Acyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Very Long Chain Acyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Narrow Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Narrow Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Split-Hand-Foot Malformation With Long Bone Deficiency 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Long Bone Deficiency 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Thickening Of Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Thickening Of Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Chain Dicarboxylic Aciduria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long-Chain Dicarboxylic Aciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Osteochondroma Of Long Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Osteochondroma Of Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Deletion Of Long Arm Of Chromosome 18 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Deletion Of Long Arm Of Chromosome 18 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Segment Aganglionic Megacolon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long-Segment Aganglionic Megacolon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Tract Signs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long-Tract Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Philtrum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Philtrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Very Long Chain Fatty Acid Accumulation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Very Long Chain Fatty Acid Accumulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Palpebral Fissure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Palpebral Fissure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Face Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Foot Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skin Dimple Over Apex Of Long Bone Angulation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skin Dimple Over Apex Of Long Bone Angulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bowing Of The Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bowing Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thickened Cortex Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thickened Cortex Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Toe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Upper Lip Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Long Bones With Narrow Diaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Long Bones With Narrow Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Overtubulated Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Overtubulated Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Thorax Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Thorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Fibula Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Fibula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Ulna Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Ulna in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Sleeper Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Sleeper Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Clavicle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Clavicle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fractures Of The Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fractures Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dumbbell-Shaped Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dumbbell-Shaped Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Crumpled Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Crumpled Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Periosteal Thickening Of Long Tubular Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periosteal Thickening Of Long Tubular Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Ear Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Long-Bone Exostoses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Long-Bone Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Protuberances At Ends Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Protuberances At Ends Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Medullary Cavity Of The Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Medullary Cavity Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thin Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thin Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Density Of Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Density Of Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Long Bone Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Long Bone Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Bowing Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Bowing Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Eyelashes In Irregular Rows Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Eyelashes In Irregular Rows in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Palm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Palm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Qt Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Eyebrows Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Eyebrows in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Curly Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Curly Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long, Smooth Philtrum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long, Smooth Philtrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Second Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Second Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Density Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Density Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortically Dense Long Tubular Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortically Dense Long Tubular Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Coccyx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Coccyx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
long-chain fatty-acyl-CoA biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty-acyl-CoA biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term memory Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term memory biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty-acyl-CoA catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty-acyl-CoA metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty-acyl-CoA metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid import into peroxisome Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid import into peroxisome biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty-acyl-CoA catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty-acyl-CoA metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty-acyl-CoA metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid beta-oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid beta-oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acyl-CoA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acyl-CoA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain acyl-CoA hydrolase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain fatty acid omega-hydroxylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acid omega-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain fatty acid omega-1 hydroxylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acid omega-1 hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain fatty acid binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acid binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-acyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
very-long-chain-acyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the very-long-chain-acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-aldehyde dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
N-(long-chain-acyl)ethanolamine deacylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the N-(long-chain-acyl)ethanolamine deacylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-3-hydroxyacyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-3-hydroxyacyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
very long chain acyl-CoA hydrolase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the very long chain acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-fatty-acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-fatty-acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol O-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
very-long-chain enoyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the very-long-chain enoyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal long bone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphyseal plate morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal plate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased length of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphyseal ossification zone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone diaphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone diaphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased long bone epiphyseal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone hypertrophic chondrocyte zone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone hypertrophic chondrocyte zone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphyseal plate proliferative zone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal plate proliferative zone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased diameter of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased diameter of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long nails Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long nails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term object recognition memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term object recognition memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized long bone epiphyseal plate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long gestation period Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long gestation period phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased long bone epiphyseal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased diameter of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thickened long bone epiphysis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term spatial reference memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term spatial reference memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long tail Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long tail phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long ribs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long ribs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long toenails Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long toenails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal limb long bone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal limb long bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal incus long process morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal incus long process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long fibula Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long fibula phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long tibia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long tibia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long stride length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long stride length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long femur Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long femur phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long lower incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long lower incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long humerus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long humerus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased length of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased length of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long mandible Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long mandible phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long snout Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long snout phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long ulna Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long ulna phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long radius Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long radius phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long limbs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long limbs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone internal diameter Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone internal diameter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long lived plasma cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long lived plasma cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long photoreceptor outer segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long photoreceptor outer segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long tibia Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the long tibia phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Long-term hematopoietic stem cell_Bone marrow_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Long-term hematopoietic stem cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Long-projecting GABAergic cell_Brain_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Long-projecting GABAergic cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Long Descending Limb (Outer Medulla) cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Long Descending Limb (Outer Medulla) cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mitochondrial long chain fatty acid beta oxidation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mitochondrial long chain fatty acid beta oxidation pathway from the WikiPathways Pathways 2024 dataset. |
Beta-oxidation of very long chain fatty acids Gene Setproteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways 2024 dataset. |
Long-term potentiation Gene Setproteins participating in the Long-term potentiation pathway from the Reactome Pathways 2024 dataset. |
PCNA-Dependent Long Patch Base Excision Repair Gene Setproteins participating in the PCNA-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
POLB-Dependent Long Patch Base Excision Repair Gene Setproteins participating in the POLB-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
Synthesis of very long-chain fatty acyl-CoAs Gene Setproteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways 2024 dataset. |
long-chain fatty-acyl-CoA biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-chain fatty-acyl-CoA biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
very long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
long-term memory Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-term memory biological process from the curated GO Biological Process Annotations 2025 dataset. |
long-chain fatty-acyl-CoA catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |