Multiple Osteochondroma Of Long Bone

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Results for "Multiple Osteochondroma Of Long Bone": 1344 genes, 1001 gene sets

Name
MS Gene multiple sclerosis
SHANK3 Gene SH3 and multiple* ankyrin repeat domains 3* This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]
SHANK2 Gene SH3 and multiple* ankyrin repeat domains 2* This gene encodes a protein that is a member of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses. Shank proteins contain multiple domains for protein-protein interaction, including ankyrin repeats, and an SH3 domain. This particular family member contains a PDZ domain, a consensus sequence for cortactin SH3 domain-binding peptides and a sterile alpha motif. The alternative splicing demonstrated in Shank genes has been suggested as a mechanism for regulating the molecular structure of Shank and the spectrum of Shank-interacting proteins in the postsynaptic densities of the adult and developing brain. Alterations in the encoded protein may be associated with susceptibility to autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]
SHANK1 Gene SH3 and multiple* ankyrin repeat domains 1* This gene encodes a member of the SHANK (SH3 domain and ankyrin repeat containing) family of proteins. Members of this family act as scaffold proteins that are required for the development and function of neuronal synapses. Deletions in this gene may be associated with autism spectrum disorder in males. [provided by RefSeq, Apr 2016]
EXT3 Gene exostoses (multiple) 3
MMDFS Gene Multiple mitochondrial dysfunctions syndrome
MEN1 Gene multiple endocrine neoplasia I This gene encodes menin, a tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. Menin is a scaffold protein that functions in histone modification and epigenetic gene regulation. It is thought to regulate several pathways and processes by altering chromatin structure through the modification of histones. [provided by RefSeq, May 2019]
MCTP1 Gene multiple C2 domains, transmembrane 1 Enables calcium ion binding activity. Predicted to be involved in several processes, including modulation of chemical synaptic transmission; negative regulation of endocytosis; and negative regulation of response to oxidative stress. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
MCTP2 Gene multiple C2 domains, transmembrane 2 Enables calcium ion binding activity. Predicted to be involved in regulation of neurotransmitter secretion. Located in cytosol; membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]
MMEDF Gene Macrocephaly with multiple* epiphyseal dysplasia and distinctive facies*
MEGF8 Gene multiple EGF-like-domains 8 The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
CNC2 Gene Carney complex type 2, multiple* neoplasia and lentiginosis*
RBPMS2 Gene RNA binding protein with multiple* splicing 2* The protein encoded by this gene is a member of the RNA recognition motif (RRM)-containing protein family and is involved in the development and dedifferentiation of digestive smooth muscle cells. The encoded protein functions as a homodimer and indirectly inhibits the bone morphogenetic protein pathway. [provided by RefSeq, Aug 2016]
MCFD2P1 Gene multiple coagulation factor deficiency 2 pseudogene 1
MINPP1 Gene multiple inositol-polyphosphate phosphatase 1 This gene encodes multiple inositol polyphosphate phosphatase; an enzyme that removes 3-phosphate from inositol phosphate substrates. It is the only enzyme known to hydrolzye inositol pentakisphosphate and inositol hexakisphosphate. This enzyme also converts 2,3 bisphosphoglycerate (2,3-BPG) to 2-phosphoglycerate; an activity formerly thought to be exclusive to 2,3-BPG synthase/2-phosphatase (BPGM) in the Rapoport-Luebering shunt of the glycolytic pathway.[provided by RefSeq, Sep 2009]
RBPMSLP Gene RNA binding protein with multiple* splicing-like pseudogene*
MS4 Gene Multiple sclerosis, susceptiblity to, 4
MS3 Gene Multiple sclerosis, susceptibility to, 3
MS2 Gene Multiple sclerosis, susceptibility to, 2
CSMD2 Gene CUB and Sushi multiple* domains 2* The protein encoded by this gene is thought to be involved in the control of complement cascade of the immune system. Defects in this gene have been associated with schizophrenia. This gene may act as a tumor suppressor for colorectal cancer. [provided by RefSeq, Jan 2020]
CSMD3 Gene CUB and Sushi multiple* domains 3* Predicted to be involved in regulation of dendrite development. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]
CSMD1 Gene CUB and Sushi multiple* domains 1* Predicted to act upstream of or within several processes, including learning or memory; mammary gland branching involved in pregnancy; and reproductive structure development. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LOC105373985 Gene multiple epidermal growth factor-like domains protein 6
MFT2 Gene Trichoepithelioma, multiple* familial, 2*
EGFL7 Gene EGF-like-domain, multiple* 7* This gene encodes a secreted endothelial cell protein that contains two epidermal growth factor-like domains. The encoded protein may play a role in regulating vasculogenesis. This protein may be involved in the growth and proliferation of tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]
EGFL6 Gene EGF-like-domain, multiple* 6* This gene encodes a member of the epidermal growth factor (EGF) repeat superfamily. Members of this superfamily are characterized by the presence of EGF-like repeats and are often involved in the regulation of cell cycle, proliferation, and developmental processes. The gene product contains a signal peptide, suggesting that it is secreted; an EGF repeat region consisting of 4 complete EGF-like repeats and 1 partial EGF-like repeat, 3 of which have a calcium-binding consensus sequence; an arg-gly-asp integrin association motif; and a MAM domain, which is believed to have an adhesive function. This gene is expressed early during development, and its expression has been detected in lung and meningioma tumors. [provided by RefSeq, Jul 2008]
EGFL8 Gene EGF-like-domain, multiple* 8* Predicted to enable signaling receptor binding activity. Predicted to be involved in vasculogenesis. Predicted to be active in cell surface and extracellular region. [provided by Alliance of Genome Resources, Mar 2025]
MEGF9 Gene multiple EGF-like-domains 9 Predicted to enable small GTPase binding activity. Predicted to be involved in regulation of actin filament polymerization. Predicted to be located in basement membrane and membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]
MEGF6 Gene multiple EGF-like-domains 6 Predicted to enable calcium ion binding activity and scavenger receptor activity. Predicted to be involved in vesicle-mediated transport. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025]
CHDT3 Gene Congenital heart defects, multiple* types, 3*
EXTL2P1 Gene exostoses (multiple)-like 2 pseudogene 1
ODPF Gene Osseous dysplasia, digital, with facial pigmentary defects and multiple* frenula*
MPDZ Gene multiple PDZ domain protein The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]
RBPMS Gene RNA binding protein with multiple* splicing* This gene encodes a member of the RNA recognition motif family of RNA-binding proteins. The RNA recognition motif is between 80-100 amino acids in length and family members contain one to four copies of the motif. The RNA recognition motif consists of two short stretches of conserved sequence, as well as a few highly conserved hydrophobic residues. The encoded protein has a single, putative RNA recognition motif in its N-terminus. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]
MCFD2 Gene multiple coagulation factor deficiency 2 This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D); a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2016]
MEGF10 Gene multiple EGF-like-domains 10 This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]
MEGF11 Gene multiple EGF-like-domains 11 Predicted to be involved in homotypic cell-cell adhesion and retina layer formation. Predicted to be located in basolateral plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC01221 Gene long intergenic non-protein coding RNA 1221
LINC01227 Gene long intergenic non-protein coding RNA 1227
LINC01091 Gene long intergenic non-protein coding RNA 1091
LINC01090 Gene long intergenic non-protein coding RNA 1090
LINC01093 Gene long intergenic non-protein coding RNA 1093
LINC01095 Gene long intergenic non-protein coding RNA 1095
LINC01094 Gene long intergenic non-protein coding RNA 1094
LINC01097 Gene long intergenic non-protein coding RNA 1097
LINC01096 Gene long intergenic non-protein coding RNA 1096
LINC01098 Gene long intergenic non-protein coding RNA 1098
LINC00320 Gene long intergenic non-protein coding RNA 320
LINC00323 Gene long intergenic non-protein coding RNA 323
LINC00324 Gene long intergenic non-protein coding RNA 324
LINC00326 Gene long intergenic non-protein coding RNA 326
LINC00327 Gene long intergenic non-protein coding RNA 327
LINC00328 Gene long intergenic non-protein coding RNA 328
LINC01215 Gene long intergenic non-protein coding RNA 1215
LINC01214 Gene long intergenic non-protein coding RNA 1214
LINC00847 Gene long intergenic non-protein coding RNA 847
LINC00849 Gene long intergenic non-protein coding RNA 849
LINC01251 Gene long intergenic non-protein coding RNA 1251
LINC01250 Gene long intergenic non-protein coding RNA 1250
LINC01257 Gene long intergenic non-protein coding RNA 1257
CCDC26 Gene CCDC26 long* non-coding RNA* Implicated in brain cancer and high grade glioma. [provided by Alliance of Genome Resources, Mar 2025]
LINC01255 Gene long intergenic non-protein coding RNA 1255
LINC01491 Gene long intergenic non-protein coding RNA 1491
LINC01490 Gene long intergenic non-protein coding RNA 1490
LINC01198 Gene long intergenic non-protein coding RNA 1198 Biomarker of malignant astrocytoma. [provided by Alliance of Genome Resources, Mar 2025]
LINC01194 Gene long intergenic non-protein coding RNA 1194
LINC01195 Gene long intergenic non-protein coding RNA 1195
LINC01197 Gene long intergenic non-protein coding RNA 1197
LINC01191 Gene long intergenic non-protein coding RNA 1191
LINC01192 Gene long intergenic non-protein coding RNA 1192
LINC01193 Gene long intergenic non-protein coding RNA 1193
LINC01360 Gene long intergenic non-protein coding RNA 1360
HEIH Gene hepatocellular carcinoma up-regulated EZH2-associated long* non-coding RNA* Biomarker of esophagus squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025]
LINC01365 Gene long intergenic non-protein coding RNA 1365
LINC01547 Gene long intergenic non-protein coding RNA 1547 Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025]
LINC01546 Gene long intergenic non-protein coding RNA 1546
LINC01545 Gene long intergenic non-protein coding RNA 1545
LINC01549 Gene long intergenic non-protein coding RNA 1549
LINC01548 Gene long intergenic non-protein coding RNA 1548
LINC00633 Gene long intergenic non-protein coding RNA 633
LINC00630 Gene long intergenic non-protein coding RNA 630
LINC00636 Gene long intergenic non-protein coding RNA 636
LINC00637 Gene long intergenic non-protein coding RNA 637
LINC00635 Gene long intergenic non-protein coding RNA 635
LINC00638 Gene long intergenic non-protein coding RNA 638
LINC00639 Gene long intergenic non-protein coding RNA 639
LINC01348 Gene long intergenic non-protein coding RNA 1348
LINC01550 Gene long intergenic non-protein coding RNA 1550
LINC01551 Gene long intergenic non-protein coding RNA 1551
LINC01552 Gene long intergenic non-protein coding RNA 1552
LINC00879 Gene long intergenic non-protein coding RNA 879
LINC00877 Gene long intergenic non-protein coding RNA 877
LINC00870 Gene long intergenic non-protein coding RNA 870
LINC00871 Gene long intergenic non-protein coding RNA 871
LINC00265-3P Gene long intergenic non-protein coding RNA 265-3, pseudogene
LINC00969 Gene long intergenic non-protein coding RNA 969
LINC00404 Gene long intergenic non-protein coding RNA 404
LINC00400 Gene long intergenic non-protein coding RNA 400
LINC00403 Gene long intergenic non-protein coding RNA 403
LINC00402 Gene long intergenic non-protein coding RNA 402
LINC00408 Gene long intergenic non-protein coding RNA 408
LINC01510 Gene long 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 Gene long intergenic non-protein coding RNA 1114
LINC01115 Gene long intergenic non-protein coding RNA 1115
LINC01116 Gene long intergenic non-protein coding RNA 1116
LINC01117 Gene long intergenic non-protein coding RNA 1117
LINC01111 Gene long intergenic non-protein coding RNA 1111
LINC01118 Gene long intergenic non-protein coding RNA 1118
LINC01514 Gene long intergenic non-protein coding RNA 1514
LINC00244 Gene long intergenic non-protein coding RNA 244
LINC00243 Gene long intergenic non-protein coding RNA 243
LINC00242 Gene long intergenic non-protein coding RNA 242
LINC00240 Gene long intergenic non-protein coding RNA 240
LINC00939 Gene long intergenic non-protein coding RNA 939
LINC00938 Gene long intergenic non-protein coding RNA 938
LINC00930 Gene long intergenic non-protein coding RNA 930
LINC00933 Gene long intergenic non-protein coding RNA 933
LINC00935 Gene long 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 Gene long intergenic non-protein coding RNA 934
LINC00937 Gene long intergenic non-protein coding RNA 937
LINC00443 Gene long intergenic non-protein coding RNA 443
LINC01099 Gene long intergenic non-protein coding RNA 1099
LINC00322 Gene long intergenic non-protein coding RNA 322
LINC01327 Gene long intergenic non-protein coding RNA 1327
LINC01324 Gene long intergenic non-protein coding RNA 1324
LINC01322 Gene long intergenic non-protein coding RNA 1322
LINC01320 Gene long intergenic non-protein coding RNA 1320
LINC00433 Gene long intergenic non-protein coding RNA 433
LINC01424 Gene long intergenic non-protein coding RNA 1424
LINC01425 Gene long intergenic non-protein coding RNA 1425
LINC01426 Gene long intergenic non-protein coding RNA 1426
LINC01427 Gene long intergenic non-protein coding RNA 1427
LINC01420 Gene long 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 Gene long intergenic non-protein coding RNA 1422
LINC01423 Gene long intergenic non-protein coding RNA 1423
LINC01428 Gene long intergenic non-protein coding RNA 1428
LINC01280 Gene long intergenic non-protein coding RNA 1280
LINC01281 Gene long intergenic non-protein coding RNA 1281
LINC01282 Gene long intergenic non-protein coding RNA 1282
LINC01284 Gene long intergenic non-protein coding RNA 1284
LINC01285 Gene long intergenic non-protein coding RNA 1285
LINC01287 Gene long intergenic non-protein coding RNA 1287
LINC01288 Gene long intergenic non-protein coding RNA 1288
LINC01289 Gene long intergenic non-protein coding RNA 1289
LINC00488 Gene long intergenic non-protein coding RNA 488
LINC00484 Gene long intergenic non-protein coding RNA 484
LINC00487 Gene long intergenic non-protein coding RNA 487
LINC00486 Gene long intergenic non-protein coding RNA 486
LINC00483 Gene long intergenic non-protein coding RNA 483
LINC00482 Gene long intergenic non-protein coding RNA 482
SHFLD3 Gene Split-hand/foot malformation with long* bone deficiency 3*
SPTLC1P1 Gene serine palmitoyltransferase, long* chain base subunit 1 pseudogene 1*
SPTLC1P2 Gene serine palmitoyltransferase, long* chain base subunit 1 pseudogene 2*
SPTLC1P5 Gene serine palmitoyltransferase, long* chain base subunit 1 pseudogene 5*
SPTLC1P4 Gene serine palmitoyltransferase, long* chain base subunit 1 pseudogene 4*
LINC00266-4P Gene long intergenic non-protein coding RNA 266-4, pseudogene
LLPH Gene LLP 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 Gene long intergenic non-protein coding RNA 1363
LINC00526 Gene long intergenic non-protein coding RNA 526
LINC00527 Gene long intergenic non-protein coding RNA 527
LINC00524 Gene long intergenic non-protein coding RNA 524
LINC00525 Gene long intergenic non-protein coding RNA 525
LINC00523 Gene long intergenic non-protein coding RNA 523
LINC00520 Gene long intergenic non-protein coding RNA 520
LINC00521 Gene long intergenic non-protein coding RNA 521 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00528 Gene long intergenic non-protein coding RNA 528
LINC00529 Gene long intergenic non-protein coding RNA 529
LINC01499 Gene long intergenic non-protein coding RNA 1499
OLMALINC Gene oligodendrocyte maturation-associated long* intergenic non-coding RNA*
LINC00200 Gene long intergenic non-protein coding RNA 200
LINC00207 Gene long intergenic non-protein coding RNA 207
LINC00052 Gene long intergenic non-protein coding RNA 52 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00165 Gene long intergenic non-protein coding RNA 165
LINC01252 Gene long intergenic non-protein coding RNA 1252
LINC01256 Gene long intergenic non-protein coding RNA 1256
LINC01254 Gene long intergenic non-protein coding RNA 1254
LINC01258 Gene long intergenic non-protein coding RNA 1258
LINC01590 Gene long intergenic non-protein coding RNA 1590
LINC01591 Gene long intergenic non-protein coding RNA 1591
LINC01592 Gene long intergenic non-protein coding RNA 1592
LINC01594 Gene long intergenic non-protein coding RNA 1594
LINC01599 Gene long intergenic non-protein coding RNA 1599
LINC01046 Gene long intergenic non-protein coding RNA 1046
LINC01047 Gene long intergenic non-protein coding RNA 1047
LINC01044 Gene long intergenic non-protein coding RNA 1044
LINC01043 Gene long intergenic non-protein coding RNA 1043
LINC01040 Gene long intergenic non-protein coding RNA 1040
LINC01049 Gene long intergenic non-protein coding RNA 1049
LINC00311 Gene long intergenic non-protein coding RNA 311
LINC00310 Gene long intergenic non-protein coding RNA 310
LINC00313 Gene long intergenic non-protein coding RNA 313
LINC00312 Gene long 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 Gene long intergenic non-protein coding RNA 315
LINC00314 Gene long intergenic non-protein coding RNA 314
LINC00316 Gene long intergenic non-protein coding RNA 316
LINCMD1 Gene long intergenic non-protein coding RNA, muscle differentiation 1
LINC-ROR Gene long 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 Gene long intergenic non-protein coding RNA 571
LINC01209 Gene long intergenic non-protein coding RNA 1209
LINC01201 Gene long intergenic non-protein coding RNA 1201
LINC01202 Gene long intergenic non-protein coding RNA 1202
LINC01203 Gene long intergenic non-protein coding RNA 1203
LINC01204 Gene long intergenic non-protein coding RNA 1204
LINC01205 Gene long intergenic non-protein coding RNA 1205
LINC01206 Gene long intergenic non-protein coding RNA 1206
LINC01207 Gene long intergenic non-protein coding RNA 1207 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC01452 Gene long intergenic non-protein coding RNA 1452
LINC01166 Gene long intergenic non-protein coding RNA 1166
LINC00415 Gene long intergenic non-protein coding RNA 415
LINC00411 Gene long intergenic non-protein coding RNA 411
LINC01088 Gene long intergenic non-protein coding RNA 1088
LINC01518 Gene long intergenic non-protein coding RNA 1518
LINC01519 Gene long intergenic non-protein coding RNA 1519
LINC01516 Gene long intergenic non-protein coding RNA 1516
LINC00391 Gene long intergenic non-protein coding RNA 391
LINC00393 Gene long intergenic non-protein coding RNA 393
LINC00392 Gene long intergenic non-protein coding RNA 392
LINC00395 Gene long intergenic non-protein coding RNA 395
LINC00396 Gene long intergenic non-protein coding RNA 396
LINC00399 Gene long intergenic non-protein coding RNA 399
LINC00398 Gene long intergenic non-protein coding RNA 398
LINC00152 Gene long 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 Gene long intergenic non-protein coding RNA 159
LINC00158 Gene long intergenic non-protein coding RNA 158
LINC00845 Gene long intergenic non-protein coding RNA 845
LINC00844 Gene long intergenic non-protein coding RNA 844
LINC00841 Gene long intergenic non-protein coding RNA 841
LINC00840 Gene long intergenic non-protein coding RNA 840
LINC00843 Gene long intergenic non-protein coding RNA 843
LINC00842 Gene long intergenic non-protein coding RNA 842
LINC01495 Gene long intergenic non-protein coding RNA 1495
LINC01494 Gene long intergenic non-protein coding RNA 1494
LINC01497 Gene long intergenic non-protein coding RNA 1497
LINC01496 Gene long intergenic non-protein coding RNA 1496
LINC01493 Gene long intergenic non-protein coding RNA 1493
LINC01492 Gene long intergenic non-protein coding RNA 1492
LINC01498 Gene long intergenic non-protein coding RNA 1498
LINC00458 Gene long intergenic non-protein coding RNA 458
LINC00459 Gene long intergenic non-protein coding RNA 459
LINC00452 Gene long intergenic non-protein coding RNA 452
LINC00456 Gene long intergenic non-protein coding RNA 456
LINC00457 Gene long intergenic non-protein coding RNA 457
LINC00454 Gene long intergenic non-protein coding RNA 454
LINC00954 Gene long intergenic non-protein coding RNA 954
LINC01128 Gene long intergenic non-protein coding RNA 1128
LINC01125 Gene long intergenic non-protein coding RNA 1125 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC01124 Gene long intergenic non-protein coding RNA 1124
LINC01126 Gene long intergenic non-protein coding RNA 1126
LINC01121 Gene long intergenic non-protein coding RNA 1121
LINC01120 Gene long intergenic non-protein coding RNA 1120
LINC01123 Gene long intergenic non-protein coding RNA 1123
LINC01122 Gene long intergenic non-protein coding RNA 1122
LINC00298 Gene long intergenic non-protein coding RNA 298
LINC00299 Gene long intergenic non-protein coding RNA 299
LINC00294 Gene long intergenic non-protein coding RNA 294
LINC00297 Gene long intergenic non-protein coding RNA 297
LINC00293 Gene long intergenic non-protein coding RNA 293
LINC00364 Gene long intergenic non-protein coding RNA 364
LINC01402 Gene long intergenic non-protein coding RNA 1402
LINC01024 Gene long intergenic non-protein coding RNA 1024
LINC00643 Gene long intergenic non-protein coding RNA 643
LINC00642 Gene long intergenic non-protein coding RNA 642
LINC00641 Gene long intergenic non-protein coding RNA 641
LINC00640 Gene long intergenic non-protein coding RNA 640
LINC00645 Gene long intergenic non-protein coding RNA 645
LINC00644 Gene long intergenic non-protein coding RNA 644
LINC00649 Gene long intergenic non-protein coding RNA 649
LINC00648 Gene long intergenic non-protein coding RNA 648
LINC00251 Gene long intergenic non-protein coding RNA 251
LINC00929 Gene long intergenic non-protein coding RNA 929
LINC00603 Gene long intergenic non-protein coding RNA 603
LINC01419 Gene long intergenic non-protein coding RNA 1419
LINC01415 Gene long intergenic non-protein coding RNA 1415
LINC01416 Gene long intergenic non-protein coding RNA 1416
LINC01411 Gene long intergenic non-protein coding RNA 1411
LINC01413 Gene long intergenic non-protein coding RNA 1413
LINC01412 Gene long intergenic non-protein coding RNA 1412
LINC00504 Gene long intergenic non-protein coding RNA 504
LINC00505 Gene long intergenic non-protein coding RNA 505
LINC00506 Gene long intergenic non-protein coding RNA 506
LINC00507 Gene long intergenic non-protein coding RNA 507
LINC00501 Gene long intergenic non-protein coding RNA 501
LINC00216 Gene long intergenic non-protein coding RNA 216
LINC00210 Gene long intergenic non-protein coding RNA 210
LINC00211 Gene long intergenic non-protein coding RNA 211
LINC00967 Gene long intergenic non-protein coding RNA 967
LINC00964 Gene long intergenic non-protein coding RNA 964
LINC00965 Gene long intergenic non-protein coding RNA 965
LINC00963 Gene long intergenic non-protein coding RNA 963
LINC00960 Gene long intergenic non-protein coding RNA 960
LINC00961 Gene long 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 Gene long intergenic non-protein coding RNA 1608
LINC01609 Gene long intergenic non-protein coding RNA 1609
LINC01604 Gene long intergenic non-protein coding RNA 1604
LINC01605 Gene long intergenic non-protein coding RNA 1605
LINC01606 Gene long intergenic non-protein coding RNA 1606
LINC01607 Gene long intergenic non-protein coding RNA 1607
LINC01600 Gene long intergenic non-protein coding RNA 1600
LINC01601 Gene long intergenic non-protein coding RNA 1601
LINC01602 Gene long intergenic non-protein coding RNA 1602
LINC01603 Gene long intergenic non-protein coding RNA 1603
LINC00559 Gene long intergenic non-protein coding RNA 559
LINC00558 Gene long intergenic non-protein coding RNA 558
LINC00557 Gene long intergenic non-protein coding RNA 557
LINC00556 Gene long intergenic non-protein coding RNA 556
LINC00555 Gene long intergenic non-protein coding RNA 555
LINC00552 Gene long intergenic non-protein coding RNA 552
LINC00551 Gene long intergenic non-protein coding RNA 551
LINC00550 Gene long intergenic non-protein coding RNA 550
LINC01337 Gene long intergenic non-protein coding RNA 1337
LINC01375 Gene long intergenic non-protein coding RNA 1375
LINC01376 Gene long intergenic non-protein coding RNA 1376
LINC01377 Gene long intergenic non-protein coding RNA 1377
LINC01370 Gene long intergenic non-protein coding RNA 1370
LINC01378 Gene long intergenic non-protein coding RNA 1378
PARTICL Gene promoter 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 Gene long intergenic non-protein coding RNA 1484
LINC00028 Gene long intergenic non-protein coding RNA 28
LINC01483 Gene long intergenic non-protein coding RNA 1483
LINC00160 Gene long intergenic non-protein coding RNA 160
LINC01039 Gene long intergenic non-protein coding RNA 1039
LINC01038 Gene long intergenic non-protein coding RNA 1038
LINC01036 Gene long intergenic non-protein coding RNA 1036
LINC01033 Gene long intergenic non-protein coding RNA 1033
LINC01032 Gene long intergenic non-protein coding RNA 1032
LINC01031 Gene long intergenic non-protein coding RNA 1031
LINC01030 Gene long intergenic non-protein coding RNA 1030
LINC01410 Gene long intergenic non-protein coding RNA 1410
LINC01231 Gene long intergenic non-protein coding RNA 1231
LINC01230 Gene long intergenic non-protein coding RNA 1230
LINC01233 Gene long intergenic non-protein coding RNA 1233
LINC01237 Gene long intergenic non-protein coding RNA 1237
LINC00184 Gene long intergenic non-protein coding RNA 184
LINC00189 Gene long intergenic non-protein coding RNA 189
LINC00448 Gene long intergenic non-protein coding RNA 448
LSINCT5 Gene long stress-induced non-coding transcript 5
LINC01179 Gene long intergenic non-protein coding RNA 1179
LINC00441 Gene long intergenic non-protein coding RNA 441
LINC00440 Gene long intergenic non-protein coding RNA 440
LINC00442 Gene long intergenic non-protein coding RNA 442
LINC00445 Gene long intergenic non-protein coding RNA 445
LINC00444 Gene long intergenic non-protein coding RNA 444
LINC00446 Gene long intergenic non-protein coding RNA 446
LINC01234 Gene long intergenic non-protein coding RNA 1234
LINC01239 Gene long intergenic non-protein coding RNA 1239
LINC01521 Gene long intergenic non-protein coding RNA 1521
LINC01520 Gene long intergenic non-protein coding RNA 1520
LINC01525 Gene long intergenic non-protein coding RNA 1525
LINC01524 Gene long intergenic non-protein coding RNA 1524
LINC01527 Gene long intergenic non-protein coding RNA 1527
LINC01529 Gene long intergenic non-protein coding RNA 1529
LINC00691 Gene long intergenic non-protein coding RNA 691
LINC00692 Gene long intergenic non-protein coding RNA 692
LINC00693 Gene long intergenic non-protein coding RNA 693
LINC00698 Gene long intergenic non-protein coding RNA 698
LINC00346 Gene long intergenic non-protein coding RNA 346
LINC00347 Gene long intergenic non-protein coding RNA 347
LINC00345 Gene long intergenic non-protein coding RNA 345
LINC00342 Gene long intergenic non-protein coding RNA 342 Biomarker of Huntington's disease. [provided by Alliance of Genome Resources, Mar 2025]
LINC00343 Gene long intergenic non-protein coding RNA 343
LINC00341 Gene long intergenic non-protein coding RNA 341
LINC00348 Gene long intergenic non-protein coding RNA 348
LINC01543 Gene long intergenic non-protein coding RNA 1543
LINC01541 Gene long intergenic non-protein coding RNA 1541
LINC01544 Gene long intergenic non-protein coding RNA 1544
LINC00102 Gene long intergenic non-protein coding RNA 102
LINC00290 Gene long intergenic non-protein coding RNA 290
LINC00266-3 Gene long intergenic non-protein coding RNA 266-3
LINC00266-1 Gene long intergenic non-protein coding RNA 266-1
LINC00632 Gene long intergenic non-protein coding RNA 632
LINC00634 Gene long intergenic non-protein coding RNA 634 Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]
ACADVL Gene acyl-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 Gene killer 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 Gene killer 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 Gene killer 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 Gene long intergenic non-protein coding RNA 1176
LINC01177 Gene long intergenic non-protein coding RNA 1177
LINC01069 Gene long intergenic non-protein coding RNA 1069
LINC01065 Gene long intergenic non-protein coding RNA 1065
LINC00862 Gene long intergenic non-protein coding RNA 862 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00333 Gene long intergenic non-protein coding RNA 333
LINC00331 Gene long intergenic non-protein coding RNA 331
LINC01468 Gene long intergenic non-protein coding RNA 1468
LINC01003 Gene long intergenic non-protein coding RNA 1003
LINC00618 Gene long intergenic non-protein coding RNA 618
LINC00619 Gene long intergenic non-protein coding RNA 619
LINC00610 Gene long intergenic non-protein coding RNA 610
LINC00612 Gene long intergenic non-protein coding RNA 612
LINC00613 Gene long intergenic non-protein coding RNA 613
LINC00614 Gene long intergenic non-protein coding RNA 614
LINC00615 Gene long intergenic non-protein coding RNA 615
LINC00616 Gene long intergenic non-protein coding RNA 616
LINC01435 Gene long intergenic non-protein coding RNA 1435
LINC01151 Gene long 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 Gene long intergenic non-protein coding RNA 968
LINC01005 Gene long intergenic non-protein coding RNA 1005
LINC00892 Gene long intergenic non-protein coding RNA 892
LINC00893 Gene long intergenic non-protein coding RNA 893
LINC00890 Gene long 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 Gene long intergenic non-protein coding RNA 891
LINC00896 Gene long intergenic non-protein coding RNA 896
LINC00894 Gene long intergenic non-protein coding RNA 894
LINC00895 Gene long intergenic non-protein coding RNA 895
LINC00898 Gene long intergenic non-protein coding RNA 898
LINC00899 Gene long intergenic non-protein coding RNA 899
LINC01442 Gene long intergenic non-protein coding RNA 1442
LINC01443 Gene long intergenic non-protein coding RNA 1443
LINC01440 Gene long intergenic non-protein coding RNA 1440
LINC01446 Gene long intergenic non-protein coding RNA 1446
LINC01447 Gene long intergenic non-protein coding RNA 1447
LINC01444 Gene long intergenic non-protein coding RNA 1444
LINC01445 Gene long intergenic non-protein coding RNA 1445
LINC01448 Gene long intergenic non-protein coding RNA 1448
LINC01449 Gene long intergenic non-protein coding RNA 1449
LINC00229 Gene long intergenic non-protein coding RNA 229
LINC00226 Gene long intergenic non-protein coding RNA 226
LINC00221 Gene long intergenic non-protein coding RNA 221
LINC00222 Gene long intergenic non-protein coding RNA 222
ABALON Gene apoptotic BCL2L1-antisense long* non-coding RNA*
LINC00917 Gene long intergenic non-protein coding RNA 917
LINC00911 Gene long intergenic non-protein coding RNA 911
LINC00910 Gene long intergenic non-protein coding RNA 910
LINC01515 Gene long intergenic non-protein coding RNA 1515
LINC01349 Gene long intergenic non-protein coding RNA 1349
LINC01344 Gene long intergenic non-protein coding RNA 1344
LINC01347 Gene long intergenic non-protein coding RNA 1347
LINC01346 Gene long intergenic non-protein coding RNA 1346
LINC01341 Gene long intergenic non-protein coding RNA 1341
LINC01340 Gene long intergenic non-protein coding RNA 1340
LINC01343 Gene long intergenic non-protein coding RNA 1343
LINC01342 Gene long intergenic non-protein coding RNA 1342
LINC01264 Gene long intergenic non-protein coding RNA 1264
LINC00710 Gene long intergenic non-protein coding RNA 710
LINC00498 Gene long intergenic non-protein coding RNA 498
LINC00499 Gene long intergenic non-protein coding RNA 499
LINC00997 Gene long intergenic non-protein coding RNA 997
LINC00994 Gene long intergenic non-protein coding RNA 994
LINC00993 Gene long intergenic non-protein coding RNA 993
LINC00992 Gene long intergenic non-protein coding RNA 992
LINC00999 Gene long intergenic non-protein coding RNA 999
LINC00998 Gene long 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 Gene long intergenic non-protein coding RNA 508
LINC00502 Gene long intergenic non-protein coding RNA 502
LINC00696 Gene long intergenic non-protein coding RNA 696
SPTLC2 Gene serine 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 Gene serine 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 Gene serine 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 Gene long intergenic non-protein coding RNA 317
LINC01372 Gene long intergenic non-protein coding RNA 1372
LINC01068 Gene long intergenic non-protein coding RNA 1068
LINC01060 Gene long intergenic non-protein coding RNA 1060
LINC01061 Gene long intergenic non-protein coding RNA 1061
LINC01063 Gene long intergenic non-protein coding RNA 1063
LINC00339 Gene long intergenic non-protein coding RNA 339
LINC00337 Gene long intergenic non-protein coding RNA 337
LINC00336 Gene long intergenic non-protein coding RNA 336
LINC00334 Gene long intergenic non-protein coding RNA 334
LINC00330 Gene long intergenic non-protein coding RNA 330
LINC01220 Gene long intergenic non-protein coding RNA 1220
LINC00029 Gene long intergenic non-protein coding RNA 29
LINC00674 Gene long intergenic non-protein coding RNA 674
LINC01268 Gene long intergenic non-protein coding RNA 1268
LINC01266 Gene long intergenic non-protein coding RNA 1266
LINC01267 Gene long intergenic non-protein coding RNA 1267
LINC01265 Gene long intergenic non-protein coding RNA 1265
LINC01260 Gene long intergenic non-protein coding RNA 1260
LINC01232 Gene long intergenic non-protein coding RNA 1232
LINC00094 Gene long intergenic non-protein coding RNA 94
LINC01384 Gene long intergenic non-protein coding RNA 1384
LINC00587 Gene long intergenic non-protein coding RNA 587
LINC00581 Gene long intergenic non-protein coding RNA 581
LINC00582 Gene long intergenic non-protein coding RNA 582
LINC00583 Gene long intergenic non-protein coding RNA 583
LINC00588 Gene long intergenic non-protein coding RNA 588
LINC00589 Gene long intergenic non-protein coding RNA 589
LINC01189 Gene long intergenic non-protein coding RNA 1189
LINC01183 Gene long intergenic non-protein coding RNA 1183
LINC01182 Gene long intergenic non-protein coding RNA 1182
LINC01181 Gene long intergenic non-protein coding RNA 1181
LINC01187 Gene long intergenic non-protein coding RNA 1187
LINC01186 Gene long intergenic non-protein coding RNA 1186
LINC01185 Gene long intergenic non-protein coding RNA 1185
LINC-PINT Gene long 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 Gene long intergenic non-protein coding RNA 378
OPN1LW Gene opsin 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 Gene long intergenic non-protein coding RNA 1119
LINC01578 Gene long 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 Gene long intergenic non-protein coding RNA 1579
LINC01574 Gene long intergenic non-protein coding RNA 1574
LINC01572 Gene long intergenic non-protein coding RNA 1572
LINC01573 Gene long intergenic non-protein coding RNA 1573
LINC01570 Gene long intergenic non-protein coding RNA 1570
LINC01571 Gene long intergenic non-protein coding RNA 1571
LINC01398 Gene long intergenic non-protein coding RNA 1398
LINC01399 Gene long intergenic non-protein coding RNA 1399
LINC01392 Gene long intergenic non-protein coding RNA 1392
LINC01393 Gene long intergenic non-protein coding RNA 1393
LINC01391 Gene long intergenic non-protein coding RNA 1391
LINC01396 Gene long intergenic non-protein coding RNA 1396
LINC01397 Gene long intergenic non-protein coding RNA 1397
LINC01395 Gene long intergenic non-protein coding RNA 1395
LINC00621 Gene long intergenic non-protein coding RNA 621
LINC00620 Gene long intergenic non-protein coding RNA 620
LINC00623 Gene long intergenic non-protein coding RNA 623
LINC00624 Gene long intergenic non-protein coding RNA 624
LINC00626 Gene long intergenic non-protein coding RNA 626
LINC00629 Gene long intergenic non-protein coding RNA 629
LINC00628 Gene long intergenic non-protein coding RNA 628
SHFLD2 Gene Split-hand/foot malformation with long* deficiency 2*
LINC00265-2P Gene long intergenic non-protein coding RNA 265-2, pseudogene
LINC00869 Gene long intergenic non-protein coding RNA 869
LINC00868 Gene long intergenic non-protein coding RNA 868
LINC00867 Gene long intergenic non-protein coding RNA 867
LINC00866 Gene long intergenic non-protein coding RNA 866
LINC01180 Gene long intergenic non-protein coding RNA 1180
LINC01184 Gene long intergenic non-protein coding RNA 1184
LINC00936 Gene long intergenic non-protein coding RNA 936
LINC00470 Gene long intergenic non-protein coding RNA 470
LINC00472 Gene long intergenic non-protein coding RNA 472
LINC00473 Gene long intergenic non-protein coding RNA 473 Involved in DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025]
LINC00474 Gene long intergenic non-protein coding RNA 474
LINC00475 Gene long intergenic non-protein coding RNA 475
LINC00476 Gene long intergenic non-protein coding RNA 476
LINC00477 Gene long intergenic non-protein coding RNA 477 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00479 Gene long intergenic non-protein coding RNA 479
LINC01103 Gene long intergenic non-protein coding RNA 1103
LINC01102 Gene long intergenic non-protein coding RNA 1102
LINC01101 Gene long intergenic non-protein coding RNA 1101
LINC01100 Gene long intergenic non-protein coding RNA 1100
LINC01107 Gene long intergenic non-protein coding RNA 1107
LINC01106 Gene long intergenic non-protein coding RNA 1106
LINC01105 Gene long intergenic non-protein coding RNA 1105
LINC01104 Gene long intergenic non-protein coding RNA 1104
LINC01109 Gene long intergenic non-protein coding RNA 1109
LINC01108 Gene long intergenic non-protein coding RNA 1108
LINC00278 Gene long intergenic non-protein coding RNA 278
LINC00279 Gene long intergenic non-protein coding RNA 279
LINC00708 Gene long intergenic non-protein coding RNA 708
LINC00709 Gene long intergenic non-protein coding RNA 709
LINC00702 Gene long intergenic non-protein coding RNA 702
ACADL Gene acyl-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 Gene long intergenic non-protein coding RNA 1312
LINC01310 Gene long intergenic non-protein coding RNA 1310
LINC01311 Gene long intergenic non-protein coding RNA 1311
LINC01314 Gene long intergenic non-protein coding RNA 1314 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC01315 Gene long intergenic non-protein coding RNA 1315
LINC01235 Gene long intergenic non-protein coding RNA 1235
LINC01433 Gene long intergenic non-protein coding RNA 1433
LINC01432 Gene long intergenic non-protein coding RNA 1432
LINC01431 Gene long intergenic non-protein coding RNA 1431
LINC01430 Gene long intergenic non-protein coding RNA 1430
LINC01299 Gene long intergenic non-protein coding RNA 1299
LINC01293 Gene long intergenic non-protein coding RNA 1293
LINC01291 Gene long intergenic non-protein coding RNA 1291
LINC01165 Gene long intergenic non-protein coding RNA 1165
LINC00944 Gene long intergenic non-protein coding RNA 944
LINC00945 Gene long intergenic non-protein coding RNA 945
LINC00941 Gene long 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 Gene long intergenic non-protein coding RNA 942
LINC00943 Gene long intergenic non-protein coding RNA 943
OVAAL Gene ovarian 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 Gene long intergenic non-protein coding RNA 535
LINC00534 Gene long intergenic non-protein coding RNA 534
LINC00537 Gene long 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 Gene long intergenic non-protein coding RNA 536
LINC00533 Gene long intergenic non-protein coding RNA 533
LINC00539 Gene long intergenic non-protein coding RNA 539
LINC00538 Gene long intergenic non-protein coding RNA 538
LINC01588 Gene long intergenic non-protein coding RNA 1588
LINC01585 Gene long intergenic non-protein coding RNA 1585
LINC01583 Gene long intergenic non-protein coding RNA 1583
LINC01582 Gene long intergenic non-protein coding RNA 1582
LINC01581 Gene long intergenic non-protein coding RNA 1581
LINC01580 Gene long intergenic non-protein coding RNA 1580
LINC01055 Gene long intergenic non-protein coding RNA 1055
LINC01057 Gene long intergenic non-protein coding RNA 1057
LINC01056 Gene long intergenic non-protein coding RNA 1056
LINC01050 Gene long intergenic non-protein coding RNA 1050
LINC01053 Gene long intergenic non-protein coding RNA 1053
LINC01059 Gene long intergenic non-protein coding RNA 1059
LINC01217 Gene long intergenic non-protein coding RNA 1217
LINC01216 Gene long intergenic non-protein coding RNA 1216
LINC01210 Gene long intergenic non-protein coding RNA 1210
LINC01219 Gene long intergenic non-protein coding RNA 1219
LINC01218 Gene long intergenic non-protein coding RNA 1218
LINC01213 Gene long intergenic non-protein coding RNA 1213
LINC00328-2P Gene long intergenic non-protein coding RNA 328-2, pseudogene
LINC01298 Gene long intergenic non-protein coding RNA 1298
LINC01296 Gene long intergenic non-protein coding RNA 1296
LINC01507 Gene long intergenic non-protein coding RNA 1507
LINC01506 Gene long intergenic non-protein coding RNA 1506
LINC01505 Gene long intergenic non-protein coding RNA 1505
LINC01503 Gene long intergenic non-protein coding RNA 1503
LINC01502 Gene long intergenic non-protein coding RNA 1502
LINC01501 Gene long intergenic non-protein coding RNA 1501
LINC01500 Gene long intergenic non-protein coding RNA 1500
LINC01509 Gene long intergenic non-protein coding RNA 1509
LINC01508 Gene long intergenic non-protein coding RNA 1508
LINC00368 Gene long intergenic non-protein coding RNA 368
LINC00365 Gene long intergenic non-protein coding RNA 365
LINC00366 Gene long intergenic non-protein coding RNA 366
LINC00367 Gene long intergenic non-protein coding RNA 367
LINC00362 Gene long intergenic non-protein coding RNA 362
LINC00363 Gene long intergenic non-protein coding RNA 363
LINC01144 Gene long intergenic non-protein coding RNA 1144
LINC01140 Gene long intergenic non-protein coding RNA 1140
MT-LIPCAR Gene mitochondrially encoded long* non-coding cardiac associated RNA*
LINC00167 Gene long intergenic non-protein coding RNA 167
LINC00162 Gene long intergenic non-protein coding RNA 162
LINC00163 Gene long intergenic non-protein coding RNA 163
LINC00161 Gene long intergenic non-protein coding RNA 161
LINC00836 Gene long intergenic non-protein coding RNA 836
LINC00837 Gene long intergenic non-protein coding RNA 837
LINC00838 Gene long intergenic non-protein coding RNA 838
LINC00839 Gene long intergenic non-protein coding RNA 839
LOC100422263 Gene serine palmitoyltransferase, long* chain base subunit 2 pseudogene*
LINC01158 Gene long 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 Gene long 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 Gene long intergenic non-protein coding RNA 1150
LINC01152 Gene long intergenic non-protein coding RNA 1152
LINC01153 Gene long intergenic non-protein coding RNA 1153
SPTLC1P3 Gene serine palmitoyltransferase, long* chain base subunit 1 pseudogene 3*
LINC00283 Gene long intergenic non-protein coding RNA 283
LINC00282 Gene long intergenic non-protein coding RNA 282 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00280 Gene long intergenic non-protein coding RNA 280
LINC00284 Gene long intergenic non-protein coding RNA 284
LINC00678 Gene long intergenic non-protein coding RNA 678
LINC00676 Gene long intergenic non-protein coding RNA 676
LINC00677 Gene long intergenic non-protein coding RNA 677
LINC00675 Gene long 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 Gene long intergenic non-protein coding RNA 672 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00673 Gene long 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 Gene long intergenic non-protein coding RNA 670
LINC00671 Gene long intergenic non-protein coding RNA 671
LINC00092 Gene long intergenic non-protein coding RNA 92
LINC01276 Gene long intergenic non-protein coding RNA 1276
NKILA Gene NF-kappaB interacting long* non-coding RNA*
LINC00863 Gene long intergenic non-protein coding RNA 863
LINC00861 Gene long intergenic non-protein coding RNA 861
LINC00865 Gene long intergenic non-protein coding RNA 865
LINC00864 Gene long intergenic non-protein coding RNA 864
PNKY Gene long intergenic non-protein coding RNA PNKY
GAPLINC Gene gastric adenocarcinoma associated, positive CD44 regulator, long* intergenic non-coding RNA*
LINC01460 Gene long intergenic non-protein coding RNA 1460
LINC01461 Gene long intergenic non-protein coding RNA 1461
LINC01465 Gene long intergenic non-protein coding RNA 1465
LINC01467 Gene long intergenic non-protein coding RNA 1467
LINC00924 Gene long intergenic non-protein coding RNA 924
LINC00485 Gene long intergenic non-protein coding RNA 485
SHFL1 Gene Split-hand/foot malformation with long* bone deficiency 1*
LINC00208 Gene long intergenic non-protein coding RNA 208
LINC01450 Gene long intergenic non-protein coding RNA 1450
LINC00974 Gene long intergenic non-protein coding RNA 974
LINC00977 Gene long intergenic non-protein coding RNA 977
LINC00971 Gene long intergenic non-protein coding RNA 971
LINC00970 Gene long intergenic non-protein coding RNA 970
LINC00973 Gene long intergenic non-protein coding RNA 973
LINC00972 Gene long intergenic non-protein coding RNA 972
LINC00562 Gene long intergenic non-protein coding RNA 562
LINC00563 Gene long intergenic non-protein coding RNA 563
LINC00560 Gene long intergenic non-protein coding RNA 560
LINC00561 Gene long intergenic non-protein coding RNA 561
LINC00566 Gene long intergenic non-protein coding RNA 566
LINC00567 Gene long intergenic non-protein coding RNA 567
LINC00564 Gene long intergenic non-protein coding RNA 564
LINC00565 Gene long intergenic non-protein coding RNA 565
LINC00471 Gene long intergenic non-protein coding RNA 471
KIR2DL5B Gene killer 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 Gene killer 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 Gene long intergenic non-protein coding RNA 1362
LINC01361 Gene long intergenic non-protein coding RNA 1361
LINC01366 Gene long intergenic non-protein coding RNA 1366
LINC01364 Gene long intergenic non-protein coding RNA 1364
LINC01002 Gene long intergenic non-protein coding RNA 1002
LINC01000 Gene long intergenic non-protein coding RNA 1000
LINC01006 Gene long intergenic non-protein coding RNA 1006 Predicted to be located in cytoplasm and membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC01007 Gene long intergenic non-protein coding RNA 1007
LINC01004 Gene long 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 Gene long intergenic non-protein coding RNA 1212
HELLPAR Gene HELLP associated long* non-coding RNA*
LINC01523 Gene long intergenic non-protein coding RNA 1523
LINC01522 Gene long intergenic non-protein coding RNA 1522
LINC01526 Gene long intergenic non-protein coding RNA 1526
LINC01208 Gene long intergenic non-protein coding RNA 1208
LINC00202-1 Gene long intergenic non-protein coding RNA 202-1
LINC00202-2 Gene long intergenic non-protein coding RNA 202-2
LINC00690 Gene long intergenic non-protein coding RNA 690
LINC00694 Gene long intergenic non-protein coding RNA 694
LINC00349 Gene long intergenic non-protein coding RNA 349
SALRNA3 Gene senescence associated long* non-coding RNA 3*
LINC01001 Gene long intergenic non-protein coding RNA 1001
LINC01082 Gene long intergenic non-protein coding RNA 1082
LINC01080 Gene long intergenic non-protein coding RNA 1080
LINC01081 Gene long intergenic non-protein coding RNA 1081
LINC01087 Gene long intergenic non-protein coding RNA 1087
LINC01085 Gene long intergenic non-protein coding RNA 1085
LINC01089 Gene long intergenic non-protein coding RNA 1089
LINC00689 Gene long intergenic non-protein coding RNA 689 Implicated in colorectal cancer. [provided by Alliance of Genome Resources, Mar 2025]
LINC00687 Gene long intergenic non-protein coding RNA 687
LINC00686 Gene long intergenic non-protein coding RNA 686
LINC00685 Gene long intergenic non-protein coding RNA 685
LINC00684 Gene long intergenic non-protein coding RNA 684
LINC00682 Gene long intergenic non-protein coding RNA 682
LINC00681 Gene long intergenic non-protein coding RNA 681
LINC00355 Gene long intergenic non-protein coding RNA 355
LINC00354 Gene long intergenic non-protein coding RNA 354
LINC00351 Gene long intergenic non-protein coding RNA 351
LINC00350 Gene long intergenic non-protein coding RNA 350
LINC00353 Gene long intergenic non-protein coding RNA 353
LINC00352 Gene long intergenic non-protein coding RNA 352
LINC00359 Gene long intergenic non-protein coding RNA 359
LINC00358 Gene long intergenic non-protein coding RNA 358
LINC00272 Gene long intergenic non-protein coding RNA 272
LINC00273 Gene long intergenic non-protein coding RNA 273
LINC00271 Gene long intergenic non-protein coding RNA 271
LINC00276 Gene long intergenic non-protein coding RNA 276
SALRNA1 Gene senescence associated long* non-coding RNA 1*
LINC01246 Gene long intergenic non-protein coding RNA 1246
LINC01241 Gene long intergenic non-protein coding RNA 1241
LINC01248 Gene long intergenic non-protein coding RNA 1248
LINC01249 Gene long intergenic non-protein coding RNA 1249
LINC00599 Gene long 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 Gene long intergenic non-protein coding RNA 598
LINC00116 Gene long 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 Gene long intergenic non-protein coding RNA 115
LINC00114 Gene long intergenic non-protein coding RNA 114
LINC00113 Gene long intergenic non-protein coding RNA 113
LINC00112 Gene long intergenic non-protein coding RNA 112
LINC00111 Gene long intergenic non-protein coding RNA 111
LINC00996 Gene long intergenic non-protein coding RNA 996
HULC Gene hepatocellular 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 Gene long intergenic non-protein coding RNA 1160
LINC01163 Gene long intergenic non-protein coding RNA 1163
LINC01164 Gene long intergenic non-protein coding RNA 1164
LINC01167 Gene long intergenic non-protein coding RNA 1167
LINC01169 Gene long intergenic non-protein coding RNA 1169
LINC01168 Gene long intergenic non-protein coding RNA 1168
LINC01554 Gene long intergenic non-protein coding RNA 1554
LINC01555 Gene long intergenic non-protein coding RNA 1555
LINC01556 Gene long intergenic non-protein coding RNA 1556
LINC01553 Gene long intergenic non-protein coding RNA 1553
LINC01558 Gene long intergenic non-protein coding RNA 1558
LINC01559 Gene long intergenic non-protein coding RNA 1559
LINC00607 Gene long intergenic non-protein coding RNA 607
LINC00606 Gene long intergenic non-protein coding RNA 606
LINC00605 Gene long intergenic non-protein coding RNA 605
LINC00602 Gene long intergenic non-protein coding RNA 602
LINC00601 Gene long intergenic non-protein coding RNA 601
LINC00609 Gene long intergenic non-protein coding RNA 609
LINC00608 Gene long intergenic non-protein coding RNA 608
LINC00106 Gene long intergenic non-protein coding RNA 106
LINC00881 Gene long intergenic non-protein coding RNA 881
LINC00880 Gene long intergenic non-protein coding RNA 880
LINC00883 Gene long 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 Gene long intergenic non-protein coding RNA 882
LINC00885 Gene long intergenic non-protein coding RNA 885 Implicated in cervical cancer. Biomarker of cervical cancer. [provided by Alliance of Genome Resources, Mar 2025]
LINC00884 Gene long intergenic non-protein coding RNA 884
LINC00887 Gene long intergenic non-protein coding RNA 887
LINC00886 Gene long intergenic non-protein coding RNA 886
LINC00889 Gene long intergenic non-protein coding RNA 889
LINC00489 Gene long intergenic non-protein coding RNA 489
LINC01451 Gene long intergenic non-protein coding RNA 1451
LINC01455 Gene long intergenic non-protein coding RNA 1455
LINC01473 Gene long intergenic non-protein coding RNA 1473
LINC00417 Gene long intergenic non-protein coding RNA 417
LINC00412 Gene long intergenic non-protein coding RNA 412
LINC00410 Gene long intergenic non-protein coding RNA 410
FALEC Gene focally amplified long* non-coding RNA in epithelial cancer*
LOC100132304 Gene long intergenic non-protein coding RNA 684
LINC00268-2P Gene long intergenic non-protein coding RNA 268-2, pseudogene
DALIR Gene DNMT1-associated long* intergenic non-coding RNA*
LINC00554 Gene long intergenic non-protein coding RNA 554
LINC00254 Gene long intergenic non-protein coding RNA 254
LINC00437 Gene long intergenic non-protein coding RNA 437
SALRNA2 Gene senescence associated long* non-coding RNA 2*
LINC00928 Gene long intergenic non-protein coding RNA 928
LINC00922 Gene long intergenic non-protein coding RNA 922
LINC00923 Gene long intergenic non-protein coding RNA 923
LINC00921 Gene long intergenic non-protein coding RNA 921
LINC00926 Gene long intergenic non-protein coding RNA 926
LINC00927 Gene long intergenic non-protein coding RNA 927
LINC00925 Gene long intergenic non-protein coding RNA 925
HAGLR Gene HOXD antisense growth-associated long* non-coding RNA*
PTX3 Gene pentraxin 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 Gene pentraxin 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 Gene long intergenic non-protein coding RNA 1338
LINC01339 Gene long intergenic non-protein coding RNA 1339
LINC01330 Gene long intergenic non-protein coding RNA 1330
LINC01331 Gene long intergenic non-protein coding RNA 1331
LINC01335 Gene long intergenic non-protein coding RNA 1335
LINC01336 Gene long intergenic non-protein coding RNA 1336
LINC00051 Gene long intergenic non-protein coding RNA 51
LOC100421637 Gene acyl-CoA synthetase long-chain family member 3 pseudogene
LINC00332 Gene long intergenic non-protein coding RNA 332
LINC01317 Gene long intergenic non-protein coding RNA 1317
LINC01048 Gene long intergenic non-protein coding RNA 1048
LINC00494 Gene long intergenic non-protein coding RNA 494
LINC00492 Gene long intergenic non-protein coding RNA 492
LINC00493 Gene long 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 Gene long intergenic non-protein coding RNA 491
LINC00920 Gene long intergenic non-protein coding RNA 920
LINC01479 Gene long intergenic non-protein coding RNA 1479
LINC01387 Gene long intergenic non-protein coding RNA 1387
LINC00519 Gene long intergenic non-protein coding RNA 519
LINC00518 Gene long intergenic non-protein coding RNA 518
LINC00511 Gene long intergenic non-protein coding RNA 511
LINC00517 Gene long intergenic non-protein coding RNA 517
LINC00515 Gene long intergenic non-protein coding RNA 515
LINC00514 Gene long intergenic non-protein coding RNA 514
LINC01597 Gene long intergenic non-protein coding RNA 1597
THRIL Gene TNF and HNRNPL related immunoregulatory long* non-coding RNA*
LINC01333 Gene long intergenic non-protein coding RNA 1333
LINC00319 Gene long intergenic non-protein coding RNA 319
LINC00237 Gene long intergenic non-protein coding RNA 237
LINC01072 Gene long intergenic non-protein coding RNA 1072
LINC01070 Gene long intergenic non-protein coding RNA 1070
LINC01075 Gene long intergenic non-protein coding RNA 1075
LINC00308 Gene long intergenic non-protein coding RNA 308
LINC00309 Gene long intergenic non-protein coding RNA 309
LINC00302 Gene long intergenic non-protein coding RNA 302
LINC00303 Gene long intergenic non-protein coding RNA 303
LINC00301 Gene long intergenic non-protein coding RNA 301 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]
LINC00307 Gene long intergenic non-protein coding RNA 307
LINC00304 Gene long intergenic non-protein coding RNA 304
LINC00305 Gene long intergenic non-protein coding RNA 305 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025]
LINC01429 Gene long intergenic non-protein coding RNA 1429
LINC01170 Gene long intergenic non-protein coding RNA 1170
LINC01279 Gene long intergenic non-protein coding RNA 1279
LINC01278 Gene long intergenic non-protein coding RNA 1278
LINC01277 Gene long intergenic non-protein coding RNA 1277
LINC01271 Gene long intergenic non-protein coding RNA 1271
LINC01270 Gene long intergenic non-protein coding RNA 1270
LINC01273 Gene long intergenic non-protein coding RNA 1273
LINC00593 Gene long intergenic non-protein coding RNA 593
LINC00592 Gene long intergenic non-protein coding RNA 592
LINC00597 Gene long intergenic non-protein coding RNA 597
LINC00596 Gene long intergenic non-protein coding RNA 596
LINC00595 Gene long intergenic non-protein coding RNA 595
LINC00594 Gene long intergenic non-protein coding RNA 594
LINC00578 Gene long intergenic non-protein coding RNA 578
LINC00570 Gene long intergenic non-protein coding RNA 570
LINC01569 Gene long intergenic non-protein coding RNA 1569
LINC01568 Gene long intergenic non-protein coding RNA 1568
LINC01565 Gene long intergenic non-protein coding RNA 1565
LINC01564 Gene long intergenic non-protein coding RNA 1564
LINC01567 Gene long intergenic non-protein coding RNA 1567
LINC01566 Gene long intergenic non-protein coding RNA 1566
LINC01561 Gene long intergenic non-protein coding RNA 1561
LINC01560 Gene long intergenic non-protein coding RNA 1560
LINC01563 Gene long intergenic non-protein coding RNA 1563
LINC01562 Gene long intergenic non-protein coding RNA 1562
LINC01389 Gene long intergenic non-protein coding RNA 1389
LINC01386 Gene long intergenic non-protein coding RNA 1386
LINC00382 Gene long intergenic non-protein coding RNA 382
LINC00383 Gene long intergenic non-protein coding RNA 383
LINC00380 Gene long intergenic non-protein coding RNA 380
LINC00381 Gene long intergenic non-protein coding RNA 381
LINC00387 Gene long intergenic non-protein coding RNA 387
LINC00384 Gene long intergenic non-protein coding RNA 384
LINC00388 Gene long intergenic non-protein coding RNA 388
LINC00854 Gene long intergenic non-protein coding RNA 854
LINC01436 Gene long intergenic non-protein coding RNA 1436
LINC00856 Gene long intergenic non-protein coding RNA 856
LINC00857 Gene long intergenic non-protein coding RNA 857
LINC00852 Gene long intergenic non-protein coding RNA 852
LINC00853 Gene long intergenic non-protein coding RNA 853
LINC00850 Gene long intergenic non-protein coding RNA 850
LINC00851 Gene long intergenic non-protein coding RNA 851
LINC00858 Gene long intergenic non-protein coding RNA 858
LINC01486 Gene long intergenic non-protein coding RNA 1486
LINC01481 Gene long intergenic non-protein coding RNA 1481
LINC01488 Gene long intergenic non-protein coding RNA 1488
LINC00469 Gene long intergenic non-protein coding RNA 469
LINC00467 Gene long intergenic non-protein coding RNA 467
LINC00463 Gene long intergenic non-protein coding RNA 463
LINC00462 Gene long intergenic non-protein coding RNA 462
LINC00461 Gene long 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 Gene long intergenic non-protein coding RNA 460
LINC01127 Gene long intergenic non-protein coding RNA 1127
LINC01487 Gene long intergenic non-protein coding RNA 1487
LINC01485 Gene long intergenic non-protein coding RNA 1485
LINC01482 Gene long intergenic non-protein coding RNA 1482
LINC01480 Gene long intergenic non-protein coding RNA 1480
LINC01138 Gene long intergenic non-protein coding RNA 1138
LINC01139 Gene long intergenic non-protein coding RNA 1139
LINC01136 Gene long intergenic non-protein coding RNA 1136
LINC01137 Gene long intergenic non-protein coding RNA 1137
LINC01134 Gene long intergenic non-protein coding RNA 1134
LINC01135 Gene long intergenic non-protein coding RNA 1135
LINC01132 Gene long intergenic non-protein coding RNA 1132
LINC01133 Gene long intergenic non-protein coding RNA 1133
LINC01489 Gene long intergenic non-protein coding RNA 1489
LINC00261 Gene long 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 Gene long intergenic non-protein coding RNA 260
LINC00265 Gene long intergenic non-protein coding RNA 265
LINC00264 Gene long intergenic non-protein coding RNA 264
LINC00269 Gene long intergenic non-protein coding RNA 269
LINC00268 Gene long intergenic non-protein coding RNA 268
LINC00466 Gene long intergenic non-protein coding RNA 466
LINC00909 Gene long intergenic non-protein coding RNA 909
LINC01272 Gene long intergenic non-protein coding RNA 1272
LINC00205 Gene long intergenic non-protein coding RNA 205
LINC00654 Gene long intergenic non-protein coding RNA 654
LINC00656 Gene long intergenic non-protein coding RNA 656
LINC00652 Gene long intergenic non-protein coding RNA 652
LINC00658 Gene long intergenic non-protein coding RNA 658
LINC00659 Gene long intergenic non-protein coding RNA 659
LINC01300 Gene long intergenic non-protein coding RNA 1300
LINC01304 Gene long intergenic non-protein coding RNA 1304
LINC01309 Gene long intergenic non-protein coding RNA 1309
LINC01358 Gene long intergenic non-protein coding RNA 1358
LINC01356 Gene long intergenic non-protein coding RNA 1356
LINC01353 Gene long intergenic non-protein coding RNA 1353
LINC01351 Gene long intergenic non-protein coding RNA 1351
LINC01478 Gene long intergenic non-protein coding RNA 1478
LINC01405 Gene long intergenic non-protein coding RNA 1405
LOC646644 Gene LLP homolog, long-term synaptic facilitation (Aplysia) pseudogene
LINC00959 Gene long intergenic non-protein coding RNA 959
LINC00958 Gene long intergenic non-protein coding RNA 958
LINC00951 Gene long intergenic non-protein coding RNA 951
LINC00950 Gene long intergenic non-protein coding RNA 950
LINC00957 Gene long intergenic non-protein coding RNA 957
LINC00955 Gene long intergenic non-protein coding RNA 955
LINC00540 Gene long intergenic non-protein coding RNA 540
LINC00543 Gene long intergenic non-protein coding RNA 543
LINC00544 Gene long intergenic non-protein coding RNA 544
LINC00545 Gene long intergenic non-protein coding RNA 545
LINC00547 Gene long intergenic non-protein coding RNA 547
LINC00548 Gene long intergenic non-protein coding RNA 548
LINC00683 Gene long intergenic non-protein coding RNA 683
LINC00032 Gene long intergenic non-protein coding RNA 32
LINC01011 Gene long intergenic non-protein coding RNA 1011
LINC01010 Gene long intergenic non-protein coding RNA 1010
LINC00940 Gene long intergenic non-protein coding RNA 940
LINC01269 Gene long intergenic non-protein coding RNA 1269
LINC01020 Gene long intergenic non-protein coding RNA 1020
LINC01021 Gene long intergenic non-protein coding RNA 1021
LINC01023 Gene long intergenic non-protein coding RNA 1023
LINC01028 Gene long intergenic non-protein coding RNA 1028
LINC01029 Gene long intergenic non-protein coding RNA 1029
LINC01262 Gene long intergenic non-protein coding RNA 1262
LINC01222 Gene long intergenic non-protein coding RNA 1222
LINC01226 Gene long intergenic non-protein coding RNA 1226
LINC01224 Gene long intergenic non-protein coding RNA 1224
LINC01225 Gene long intergenic non-protein coding RNA 1225
LINC01228 Gene long intergenic non-protein coding RNA 1228
LINC01229 Gene long intergenic non-protein coding RNA 1229
LINC00266-2P Gene long intergenic non-protein coding RNA 266-2, pseudogene
LINC01589 Gene long intergenic non-protein coding RNA 1589
SENCR Gene smooth muscle and endothelial cell enriched migration/differentiation-associated long* non-coding RNA*
LINC01017 Gene long intergenic non-protein coding RNA 1017
LINC01247 Gene long intergenic non-protein coding RNA 1247
LINC01242 Gene long intergenic non-protein coding RNA 1242
LINC01243 Gene long intergenic non-protein coding RNA 1243
LINC01532 Gene long intergenic non-protein coding RNA 1532
LINC01533 Gene long intergenic non-protein coding RNA 1533
LINC01530 Gene long intergenic non-protein coding RNA 1530
LINC01531 Gene long intergenic non-protein coding RNA 1531
LINC01537 Gene long intergenic non-protein coding RNA 1537
LINC01534 Gene long intergenic non-protein coding RNA 1534
LINC01535 Gene long intergenic non-protein coding RNA 1535
LINC01538 Gene long intergenic non-protein coding RNA 1538
LINC01539 Gene long intergenic non-protein coding RNA 1539
LINC00379 Gene long intergenic non-protein coding RNA 379
LINC00371 Gene long intergenic non-protein coding RNA 371
LINC00370 Gene long intergenic non-protein coding RNA 370
LINC00377 Gene long intergenic non-protein coding RNA 377
LINC00376 Gene long intergenic non-protein coding RNA 376
LINC00375 Gene long intergenic non-protein coding RNA 375
LINC00707 Gene long intergenic non-protein coding RNA 707
LINC00704 Gene long intergenic non-protein coding RNA 704
LINC00703 Gene long intergenic non-protein coding RNA 703
LINC00174 Gene long intergenic non-protein coding RNA 174
LINC00176 Gene long intergenic non-protein coding RNA 176
LINC00173 Gene long intergenic non-protein coding RNA 173
LINC00824 Gene long intergenic non-protein coding RNA 824
TRERNA1 Gene translation regulatory long* non-coding RNA 1*
LINC01441 Gene long intergenic non-protein coding RNA 1441
LINC00706 Gene long intergenic non-protein coding RNA 706
LINC01146 Gene long intergenic non-protein coding RNA 1146
LINC01143 Gene long intergenic non-protein coding RNA 1143
LINC01142 Gene long intergenic non-protein coding RNA 1142
LINC01141 Gene long intergenic non-protein coding RNA 1141
LINC01149 Gene long intergenic non-protein coding RNA 1149
LINC00423 Gene long intergenic non-protein coding RNA 423
LINC00421 Gene long intergenic non-protein coding RNA 421
LINC00427 Gene long intergenic non-protein coding RNA 427
LINC00426 Gene long intergenic non-protein coding RNA 426
LINC00424 Gene long intergenic non-protein coding RNA 424
LINC00669 Gene long intergenic non-protein coding RNA 669
LINC00668 Gene long intergenic non-protein coding RNA 668
LINC00665 Gene long intergenic non-protein coding RNA 665
LINC00664 Gene long intergenic non-protein coding RNA 664
LINC00667 Gene long intergenic non-protein coding RNA 667
LINC00661 Gene long intergenic non-protein coding RNA 661
LINC00663 Gene long intergenic non-protein coding RNA 663
LINC00662 Gene long intergenic non-protein coding RNA 662
LINC00083 Gene long intergenic non-protein coding RNA 83 Predicted to enable carbohydrate binding activity. [provided by Alliance of Genome Resources, Mar 2025]
LINC00657 Gene long 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 Gene EGFR 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 Gene long intergenic non-protein coding RNA 1301
LINC01305 Gene long intergenic non-protein coding RNA 1305
LINC01307 Gene long intergenic non-protein coding RNA 1307
LINC01477 Gene long intergenic non-protein coding RNA 1477
LINC01476 Gene long intergenic non-protein coding RNA 1476
LINC01475 Gene long intergenic non-protein coding RNA 1475
LINC01474 Gene long intergenic non-protein coding RNA 1474
LINC01471 Gene long intergenic non-protein coding RNA 1471
LINC01470 Gene long intergenic non-protein coding RNA 1470
LINC00434 Gene long intergenic non-protein coding RNA 434
ACSL3 Gene acyl-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 Gene acyl-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 Gene acyl-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 Gene long intergenic non-protein coding RNA 431
ACSL4 Gene acyl-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 Gene acyl-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 Gene long intergenic non-protein coding RNA 1511
LINC01512 Gene long intergenic non-protein coding RNA 1512
LINC01517 Gene long intergenic non-protein coding RNA 1517
LINC01504 Gene long intergenic non-protein coding RNA 1504
LINC00238 Gene long intergenic non-protein coding RNA 238
LINC00239 Gene long intergenic non-protein coding RNA 239
LINC00235 Gene long intergenic non-protein coding RNA 235
LINC00900 Gene long intergenic non-protein coding RNA 900
LINC00901 Gene long intergenic non-protein coding RNA 901
LINC00903 Gene long intergenic non-protein coding RNA 903
LINC00904 Gene long intergenic non-protein coding RNA 904
LINC00905 Gene long intergenic non-protein coding RNA 905
LINC00906 Gene long intergenic non-protein coding RNA 906
LINC00907 Gene long intergenic non-protein coding RNA 907
LINC00908 Gene long intergenic non-protein coding RNA 908
LINC00397 Gene long intergenic non-protein coding RNA 397
LINC00572 Gene long intergenic non-protein coding RNA 572
LINC00575 Gene long intergenic non-protein coding RNA 575
LINC00574 Gene long intergenic non-protein coding RNA 574
LINC00577 Gene long intergenic non-protein coding RNA 577
LINC01587 Gene long 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 Gene long intergenic non-protein coding RNA 1584
LINC00622 Gene long intergenic non-protein coding RNA 622
LINC01054 Gene long intergenic non-protein coding RNA 1054
LINC01058 Gene long intergenic non-protein coding RNA 1058
KIR2DL3 Gene killer 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 Gene killer 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 Gene killer 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 Gene killer 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 Gene long intergenic non-protein coding RNA 428
LINC01354 Gene long intergenic non-protein coding RNA 1354
LINC01355 Gene long intergenic non-protein coding RNA 1355
LINC01350 Gene long intergenic non-protein coding RNA 1350
LINC01019 Gene long intergenic non-protein coding RNA 1019
LINC01018 Gene long intergenic non-protein coding RNA 1018
LINC01013 Gene long intergenic non-protein coding RNA 1013
LINC01012 Gene long intergenic non-protein coding RNA 1012
LINC01015 Gene long intergenic non-protein coding RNA 1015
LINC01014 Gene long intergenic non-protein coding RNA 1014
LINC01016 Gene long intergenic non-protein coding RNA 1016
LINC00888 Gene long intergenic non-protein coding RNA 888
LINC01162 Gene long intergenic non-protein coding RNA 1162
LINC00919 Gene long intergenic non-protein coding RNA 919
LINC00914 Gene long intergenic non-protein coding RNA 914
LINC00705 Gene long intergenic non-protein coding RNA 705
LINC00700 Gene long intergenic non-protein coding RNA 700
LINC00701 Gene long intergenic non-protein coding RNA 701
LINC01359 Gene long intergenic non-protein coding RNA 1359
LINC01352 Gene long intergenic non-protein coding RNA 1352
LINC01586 Gene long intergenic non-protein coding RNA 1586
LINC00989 Gene long intergenic non-protein coding RNA 989
LINC00982 Gene long intergenic non-protein coding RNA 982
LINC00987 Gene long intergenic non-protein coding RNA 987
HAO2 Gene hydroxyacid 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 Gene long intergenic non-protein coding RNA 2618
LINC02249 Gene long intergenic non-protein coding RNA 2249
LINC01963 Gene long intergenic non-protein coding RNA 1963
LNCTAM34A Gene long non coding transcriptional activator of miR34a
LINC01833 Gene long intergenic non-protein coding RNA 1833 Predicted to be involved in regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025]
LINC01806 Gene long intergenic non-protein coding RNA 1806
LINC01788 Gene long intergenic non-protein coding RNA 1788
LINC01843 Gene long intergenic non-protein coding RNA 1843
LINC03040 Gene long intergenic non-protein coding RNA 3040
LINC01719 Gene long intergenic non-protein coding RNA 1719
LINC01772 Gene long intergenic non-protein coding RNA 1772
LINC02035 Gene long intergenic non-protein coding RNA 2035
LINC01781 Gene long intergenic non-protein coding RNA 1781
LINC02044 Gene long intergenic non-protein coding RNA 2044
LINC01852 Gene long intergenic non-protein coding RNA 1852
LINC01914 Gene long intergenic non-protein coding RNA 1914
LINC02102 Gene long intergenic non-protein coding RNA 2102
LINC01933 Gene long intergenic non-protein coding RNA 1933
LINC02904 Gene long intergenic non-protein coding RNA 2904
LINC02910 Gene long intergenic non-protein coding RNA 2910
LINC01814 Gene long intergenic non-protein coding RNA 1814
LINC02908 Gene long intergenic non-protein coding RNA 2908
LINC01829 Gene long intergenic non-protein coding RNA 1829
LINC00680 Gene long intergenic non-protein coding RNA 680
LINC02019 Gene long intergenic non-protein coding RNA 2019
LINC02094 Gene long intergenic non-protein coding RNA 2094
LINC02147 Gene long intergenic non-protein coding RNA 2147
LINC02012 Gene long intergenic non-protein coding RNA 2012
LINC01896 Gene long intergenic non-protein coding RNA 1896
LINC02185 Gene long intergenic non-protein coding RNA 2185
LINC01828 Gene long intergenic non-protein coding RNA 1828
LINC01619 Gene long intergenic non-protein coding RNA 1619
LINC01679 Gene long intergenic non-protein coding RNA 1679
PRECSIT Gene p53 regulated carcinoma associated Stat3 activating long* intergenic non-protein coding transcript*
LINC02208 Gene long intergenic non-protein coding RNA 2208
LINC02210 Gene long intergenic non-protein coding RNA 2210
LINC03011 Gene long intergenic non-protein coding RNA 3011
LINC01702 Gene long intergenic non-protein coding RNA 1702
LINC02037 Gene long intergenic non-protein coding RNA 2037
LINC02197 Gene long intergenic non-protein coding RNA 2197
LINC01595 Gene long intergenic non-protein coding RNA 1595 Implicated in prostate cancer. [provided by Alliance of Genome Resources, Mar 2025]
LINC02898 Gene long intergenic non-protein coding RNA 2898
LINC02716 Gene long intergenic non-protein coding RNA 2716
LINC02116 Gene long intergenic non-protein coding RNA 2116
LINC01713 Gene long intergenic non-protein coding RNA 1713
LINC02174 Gene long intergenic non-protein coding RNA 2174
LINC02052 Gene long intergenic non-protein coding RNA 2052
LINC00449 Gene long intergenic non-protein coding RNA 449
LINC02084 Gene long intergenic non-protein coding RNA 2084
LINC01980 Gene long intergenic non-protein coding RNA 1980
LINC01876 Gene long intergenic non-protein coding RNA 1876
LINC02167 Gene long intergenic non-protein coding RNA 2167
LINC02212 Gene long intergenic non-protein coding RNA 2212
LINC02145 Gene long intergenic non-protein coding RNA 2145
LINC02905 Gene long intergenic non-protein coding RNA 2905
LINC02693 Gene long intergenic non-protein coding RNA 2693
LINC01978 Gene long intergenic non-protein coding RNA 1978
LINC01979 Gene long intergenic non-protein coding RNA 1979
LINC02015 Gene long intergenic non-protein coding RNA 2015
LINC01625 Gene long intergenic non-protein coding RNA 1625
LINC02202 Gene long intergenic non-protein coding RNA 2202
LINC01786 Gene long intergenic non-protein coding RNA 1786
LINC01714 Gene long intergenic non-protein coding RNA 1714
LINC02028 Gene long intergenic non-protein coding RNA 2028
HISLA Gene HIF1A stabilizing long* noncoding RNA*
LINC01836 Gene long intergenic non-protein coding RNA 1836
LINC01977 Gene long intergenic non-protein coding RNA 1977
LINC01907 Gene long intergenic non-protein coding RNA 1907
LINC01748 Gene long intergenic non-protein coding RNA 1748
ARLNC1 Gene androgen receptor regulated long* noncoding RNA 1*
LINC01754 Gene long intergenic non-protein coding RNA 1754
LINC01770 Gene long intergenic non-protein coding RNA 1770
MINCR Gene MYC-induced long* non-coding RNA*
LINC02086 Gene long intergenic non-protein coding RNA 2086
LINC02193 Gene long intergenic non-protein coding RNA 2193
LINC01819 Gene long intergenic non-protein coding RNA 1819
LINC02018 Gene long intergenic non-protein coding RNA 2018
LINC01869 Gene long intergenic non-protein coding RNA 1869
MALINC1 Gene mitosis associated long* intergenic non-coding RNA 1*
LINC02106 Gene long intergenic non-protein coding RNA 2106
LINC02076 Gene long intergenic non-protein coding RNA 2076
LINC02021 Gene long intergenic non-protein coding RNA 2021
LINC01915 Gene long intergenic non-protein coding RNA 1915
LINC01881 Gene long intergenic non-protein coding RNA 1881
LINC01801 Gene long intergenic non-protein coding RNA 1801
LINC01750 Gene long intergenic non-protein coding RNA 1750
LINC02175 Gene long intergenic non-protein coding RNA 2175
LINC02188 Gene long intergenic non-protein coding RNA 2188
LINC02913 Gene long intergenic non-protein coding RNA 2913
LINC02897 Gene long intergenic non-protein coding RNA 2897
LINC02875 Gene long intergenic non-protein coding RNA 2875
LINC01238 Gene long intergenic non-protein coding RNA 1238
LINC01943 Gene long intergenic non-protein coding RNA 1943
LINC02881 Gene long intergenic non-protein coding RNA 2881
LINC01345 Gene long intergenic non-protein coding RNA 1345
LINC02692 Gene long intergenic non-protein coding RNA 2692
LINC02107 Gene long intergenic non-protein coding RNA 2107
LINC01874 Gene long intergenic non-protein coding RNA 1874
LINC01707 Gene long intergenic non-protein coding RNA 1707
LINC01697 Gene long intergenic non-protein coding RNA 1697
LINC01684 Gene long intergenic non-protein coding RNA 1684
LINC01816 Gene long intergenic non-protein coding RNA 1816
LINC01626 Gene long intergenic non-protein coding RNA 1626
LINC01623 Gene long intergenic non-protein coding RNA 1623
LINC01612 Gene long intergenic non-protein coding RNA 1612
LINC01643 Gene long intergenic non-protein coding RNA 1643
LINC01647 Gene long intergenic non-protein coding RNA 1647
LINC01655 Gene long intergenic non-protein coding RNA 1655
LINC01667 Gene long intergenic non-protein coding RNA 1667
LINC01749 Gene long intergenic non-protein coding RNA 1749
LINC01747 Gene long intergenic non-protein coding RNA 1747
LINC01744 Gene long intergenic non-protein coding RNA 1744
LINC01743 Gene long intergenic non-protein coding RNA 1743
LINC01739 Gene long intergenic non-protein coding RNA 1739
LINC01728 Gene long intergenic non-protein coding RNA 1728
LINC01723 Gene long intergenic non-protein coding RNA 1723
LINC01718 Gene long intergenic non-protein coding RNA 1718
LINC01712 Gene long intergenic non-protein coding RNA 1712
LINC01704 Gene long intergenic non-protein coding RNA 1704
LINC01677 Gene long intergenic non-protein coding RNA 1677
LINC01676 Gene long intergenic non-protein coding RNA 1676
LINC01673 Gene long intergenic non-protein coding RNA 1673
LINC01672 Gene long intergenic non-protein coding RNA 1672
LINC01374 Gene long intergenic non-protein coding RNA 1374
LINC01297 Gene long intergenic non-protein coding RNA 1297
LINC01755 Gene long intergenic non-protein coding RNA 1755
LINC01760 Gene long intergenic non-protein coding RNA 1760
LINC01763 Gene long intergenic non-protein coding RNA 1763
LINC01764 Gene long intergenic non-protein coding RNA 1764
LINC02046 Gene long intergenic non-protein coding RNA 2046
LINC02045 Gene long intergenic non-protein coding RNA 2045
LINC02040 Gene long intergenic non-protein coding RNA 2040
LINC02039 Gene long intergenic non-protein coding RNA 2039
LINC02034 Gene long intergenic non-protein coding RNA 2034
LINC02032 Gene long intergenic non-protein coding RNA 2032
LINC02025 Gene long intergenic non-protein coding RNA 2025
LINC02022 Gene long intergenic non-protein coding RNA 2022
LINC02020 Gene long intergenic non-protein coding RNA 2020
LINC02013 Gene long intergenic non-protein coding RNA 2013
LINC01999 Gene long intergenic non-protein coding RNA 1999
LINC01995 Gene long intergenic non-protein coding RNA 1995
LINC01988 Gene long intergenic non-protein coding RNA 1988
LINC01986 Gene long intergenic non-protein coding RNA 1986
LINC02056 Gene long intergenic non-protein coding RNA 2056
LINC02064 Gene long intergenic non-protein coding RNA 2064
LINC02166 Gene long intergenic non-protein coding RNA 2166
LINC02165 Gene long intergenic non-protein coding RNA 2165
LINC02156 Gene long intergenic non-protein coding RNA 2156
LINC02152 Gene long intergenic non-protein coding RNA 2152
LINC02117 Gene long intergenic non-protein coding RNA 2117
LINC02114 Gene long intergenic non-protein coding RNA 2114
LINC02113 Gene long intergenic non-protein coding RNA 2113
LINC02110 Gene long intergenic non-protein coding RNA 2110
LINC02103 Gene long intergenic non-protein coding RNA 2103
LINC02096 Gene long intergenic non-protein coding RNA 2096
LINC02089 Gene long intergenic non-protein coding RNA 2089
LINC02087 Gene long intergenic non-protein coding RNA 2087
LINC02079 Gene long intergenic non-protein coding RNA 2079
LINC02072 Gene long intergenic non-protein coding RNA 2072
LINC02069 Gene long intergenic non-protein coding RNA 2069
LINC02059 Gene long intergenic non-protein coding RNA 2059
LINC01976 Gene long intergenic non-protein coding RNA 1976
LINC01944 Gene long intergenic non-protein coding RNA 1944
LINC01855 Gene long intergenic non-protein coding RNA 1855
LINC01851 Gene long intergenic non-protein coding RNA 1851
LINC01849 Gene long intergenic non-protein coding RNA 1849
LINC01846 Gene long intergenic non-protein coding RNA 1846
LINC01844 Gene long intergenic non-protein coding RNA 1844
LINC01837 Gene long intergenic non-protein coding RNA 1837
LINC01818 Gene long intergenic non-protein coding RNA 1818
LINC01815 Gene long intergenic non-protein coding RNA 1815
LINC01803 Gene long intergenic non-protein coding RNA 1803
LINC01799 Gene long intergenic non-protein coding RNA 1799
LINC01783 Gene long 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 Gene long intergenic non-protein coding RNA 1778
LINC01766 Gene long intergenic non-protein coding RNA 1766
LINC01872 Gene long intergenic non-protein coding RNA 1872
LINC01962 Gene long intergenic non-protein coding RNA 1962
LINC01878 Gene long intergenic non-protein coding RNA 1878
LINC01888 Gene long intergenic non-protein coding RNA 1888
LINC01938 Gene long intergenic non-protein coding RNA 1938
LINC01937 Gene long intergenic non-protein coding RNA 1937
LINC01931 Gene long intergenic non-protein coding RNA 1931
LINC01927 Gene long intergenic non-protein coding RNA 1927
LINC01925 Gene long intergenic non-protein coding RNA 1925
LINC01923 Gene long intergenic non-protein coding RNA 1923
LINC01919 Gene long intergenic non-protein coding RNA 1919
LINC01917 Gene long intergenic non-protein coding RNA 1917
LINC01913 Gene long intergenic non-protein coding RNA 1913
LINC01912 Gene long intergenic non-protein coding RNA 1912
LINC01911 Gene long intergenic non-protein coding RNA 1911
LINC01909 Gene long intergenic non-protein coding RNA 1909
LINC01905 Gene long intergenic non-protein coding RNA 1905
LINC01899 Gene long intergenic non-protein coding RNA 1899
LINC01890 Gene long intergenic non-protein coding RNA 1890
LINC01884 Gene long intergenic non-protein coding RNA 1884
LINC00390 Gene long intergenic non-protein coding RNA 390
LINC01052 Gene long intergenic non-protein coding RNA 1052
LINC01066 Gene long intergenic non-protein coding RNA 1066
LINC02016 Gene long intergenic non-protein coding RNA 2016
LINC01694 Gene long intergenic non-protein coding RNA 1694
LINC02587 Gene long intergenic non-protein coding RNA 2587
LINC02204 Gene long intergenic non-protein coding RNA 2204
LINC01785 Gene long intergenic non-protein coding RNA 1785
LINC02207 Gene long intergenic non-protein coding RNA 2207
LINC02446 Gene long intergenic non-protein coding RNA 2446
LINC01857 Gene long intergenic non-protein coding RNA 1857
LINC01871 Gene long intergenic non-protein coding RNA 1871
GRASLND Gene glycosaminoglycan regulatory associated long* non-coding RNA*
LINC01762 Gene long intergenic non-protein coding RNA 1762
LINC02027 Gene long intergenic non-protein coding RNA 2027
LINC01924 Gene long intergenic non-protein coding RNA 1924
LINC01934 Gene long intergenic non-protein coding RNA 1934
LINC02251 Gene long intergenic non-protein coding RNA 2251
LINC02397 Gene long intergenic non-protein coding RNA 2397
LINC01967 Gene long intergenic non-protein coding RNA 1967
LINC01357 Gene long intergenic non-protein coding RNA 1357
LINC02593 Gene long intergenic non-protein coding RNA 2593
LINC02362 Gene long intergenic non-protein coding RNA 2362
LINC02523 Gene long intergenic non-protein coding RNA 2523
LINC01717 Gene long intergenic non-protein coding RNA 1717
LINC02009 Gene long intergenic non-protein coding RNA 2009
LINC01724 Gene long intergenic non-protein coding RNA 1724
LINC02437 Gene long intergenic non-protein coding RNA 2437
LINC01965 Gene long intergenic non-protein coding RNA 1965
LINC02836 Gene long intergenic non-protein coding RNA 2836
LINC02785 Gene long intergenic non-protein coding RNA 2785
LINC01831 Gene long intergenic non-protein coding RNA 1831
LINC02053 Gene long intergenic non-protein coding RNA 2053
LINC02768 Gene long intergenic non-protein coding RNA 2768
LINC02360 Gene long intergenic non-protein coding RNA 2360
LINC02237 Gene long intergenic non-protein coding RNA 2237
LINC02511 Gene long intergenic non-protein coding RNA 2511
LINC01695 Gene long intergenic non-protein coding RNA 1695
LINC02901 Gene long intergenic non-protein coding RNA 2901
LINC02888 Gene long intergenic non-protein coding RNA 2888
LINC02903 Gene long intergenic non-protein coding RNA 2903
LINC02899 Gene long intergenic non-protein coding RNA 2899
C3ORF86P Gene long intergenic non-protein coding RNA 694
LINC02694 Gene long intergenic non-protein coding RNA 2694
LINC02902 Gene long intergenic non-protein coding RNA 2902
LINC02798 Gene long intergenic non-protein coding RNA 2798
LINC02615 Gene long intergenic non-protein coding RNA 2615
LINC02696 Gene long intergenic non-protein coding RNA 2696
LINC02614 Gene long intergenic non-protein coding RNA 2614
LINC02609 Gene long intergenic non-protein coding RNA 2609
LINC02981 Gene long intergenic non-protein coding RNA 2981
LINC02731 Gene long intergenic non-protein coding RNA 2731
LINC02987 Gene long intergenic non-protein coding RNA 2987
LINC02544 Gene long intergenic non-protein coding RNA 2544
LINC02649 Gene long intergenic non-protein coding RNA 2649
LINC02728 Gene long intergenic non-protein coding RNA 2728
LINC02803 Gene long intergenic non-protein coding RNA 2803
LINC02349 Gene long intergenic non-protein coding RNA 2349
LINC02539 Gene long intergenic non-protein coding RNA 2539
LINC03002 Gene long intergenic non-protein coding RNA 3002
LINC02381 Gene long intergenic non-protein coding RNA 2381
LINC02232 Gene long intergenic non-protein coding RNA 2232
LINC03100 Gene long intergenic non-protein coding RNA 3100
LINC02894 Gene long intergenic non-protein coding RNA 2894
LINC02328 Gene long intergenic non-protein coding RNA 2328
LINC01779 Gene long intergenic non-protein coding RNA 1779
LINC03135 Gene long intergenic non-protein coding RNA 3135
LINC02965 Gene long intergenic non-protein coding RNA 2965
LINC03052 Gene long intergenic non-protein coding RNA 3052
LINC02235 Gene long intergenic non-protein coding RNA 2235
LINC02576 Gene long intergenic non-protein coding RNA 2576
LINC02560 Gene long intergenic non-protein coding RNA 2560
LINC02762 Gene long intergenic non-protein coding RNA 2762
LINC02610 Gene long intergenic non-protein coding RNA 2610
LINC02854 Gene long intergenic non-protein coding RNA 2854
LINC02983 Gene long intergenic non-protein coding RNA 2983
LINC02268 Gene long intergenic non-protein coding RNA 2268
LINC02893 Gene long intergenic non-protein coding RNA 2893
Multiple Osteochondroma Of Long Bone Gene Set From 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.
Multiple Long-Bone Exostoses Gene Set From 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.
Osteochondroma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteochondroma from the curated CTD Gene-Disease Associations dataset.
osteochondroma Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term osteochondroma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
increased osteochondroma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased osteochondroma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
osteochondroma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue osteochondroma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
increased osteochondroma incidence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased osteochondroma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Osteochondroma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Osteochondroma cell 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 Set From 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 Set From 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.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; multiple trauma; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; multiple trauma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Multiple synapse bouton, contacting multiple dendrites Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton, contacting multiple dendrites cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set From 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 Set From 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.
Split-hand/foot malformation with long bone deficiency Gene Set From 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 bone adamantinoma Gene Set From 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.
abnormality of long bone morphology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
dumbbell-shaped long bone Gene Set From 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.
cortical thickening of long bone diaphyses Gene Set From 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 Set From 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.
skin dimple over apex of long bone angulation Gene Set From 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.
increased density of long bone diaphyses Gene Set From 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 Set From 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.
short long bone Gene Set From 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.
abnormal long bone metaphysis morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long bone epiphysis morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long bone diaphysis morphology Gene Set From 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 Set From 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.
abnormal long bone morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long bone epiphyseal plate proliferative zone Gene Set From 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 bone hypertrophic chondrocyte zone Gene Set From 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.
increased long bone epiphyseal plate size Gene Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal limb long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long bone epiphyseal ossification zone morphology Gene Set From 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 bone epiphyseal plate morphology Gene Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
split-hand/foot malformation with long bone deficiency 3 Gene Set From 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 Set From 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 Set From 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 bone Gene Set From 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.
Broad Long Bone Diaphyses Gene Set From 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 Set From 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 Set From 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.
Short Long Bone Gene Set From 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.
Skin Dimple Over Apex Of Long Bone Angulation Gene Set From 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.
Slender Long Bone Gene Set From 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.
Dumbbell-Shaped Long Bone Gene Set From 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.
Thin Long Bone Diaphyses Gene Set From 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.
Increased Density Of Long Bone Diaphyses Gene Set From 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.
Abnormality Of Long Bone Morphology Gene Set From 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.
abnormal long bone morphology Gene Set From 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 Set From 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.
abnormal long bone epiphyseal ossification zone morphology Gene Set From 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.
abnormal long bone diaphysis morphology Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
abnormal long bone epiphysis morphology Gene Set From 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.
disorganized long bone epiphyseal plate Gene Set From 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.
decreased long bone epiphyseal plate size Gene Set From 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.
thickened long bone epiphysis Gene Set From 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 limb long bone morphology Gene Set From 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 long bone internal diameter Gene Set From 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.
Long bone adamantinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long bone adamantinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long bone Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Long bone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone diseases; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease bone diseases; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormality of multiple cell lineages in the bone marrow Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Abnormality Of Multiple Cell Lineages In The Bone Marrow Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Multiple Cell Lineages In The Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
bone resorption; fractures, bone Gene Set From GAD Gene-Disease Associations genes associated with the disease bone resorption; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone density; bone responsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease bone density; bone responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
low bone-mineral density and rapid postmenopausal bone loss Gene Set From GAD Gene-Disease Associations genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal bone mineralization involved in bone maturation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone mineralization involved in bone maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
negative regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of bone mineralization involved in bone maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
long insular gyri, right Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Long QT Syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
long qt syndrome Gene Set From 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 Set From 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 Set From 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.
human long-term memory Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 the medullary cavity of the long bones Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
long neck Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
long fibula Gene Set From 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 proximal phalanx of finger Gene Set From 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 penis Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
long phalanx of finger Gene Set From 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.
broad long bones Gene Set From 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.
very long chain fatty acid accumulation Gene Set From 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 Set From 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 Set From 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.
weakness of long finger extensor muscles Gene Set From 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.
bowing of the long bones Gene Set From 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 Set From 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 Set From 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 Set From 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.
elevated long chain fatty acids Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 distal phalanx of finger Gene Set From 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 ear Gene Set From 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 Set From 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.
long philtrum Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From KEGG Pathways proteins participating in the long term depression pathway from the KEGG Pathways dataset.
long term potentiation Gene Set From KEGG Pathways proteins participating in the long term potentiation pathway from the KEGG Pathways dataset.
long hair Gene Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enhanced long term potentiation Gene Set From 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 Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the reduced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
long snout Gene Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the long fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased length of long bones Gene Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the long gestation period phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long term object recognition memory Gene Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the long radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
long ribs Gene Set From 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 Set From 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.
long tibia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the long tibia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long term potentiation Gene Set From 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 Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the long tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
long femur Gene Set From 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 Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the long ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
long humerus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the long humerus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
long limbs Gene Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the long incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
long toenails Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
long qt syndrome-3 Gene Set From 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways dataset.
Acquired Long Qt Syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Long-Chain Dicarboxylic Aciduria Gene Set From 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 Set From 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.
Long Phalanx Of Finger Gene Set From 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.
Deletion Of Long Arm Of Chromosome 18 Gene Set From 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 Distal Phalanx Of Finger Gene Set From 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 Set From 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.
Long-Segment Aganglionic Megacolon Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Long Foot Gene Set From 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.
Weakness Of Long Finger Extensor Muscles Gene Set From 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.
Long Fingers Gene Set From 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.
Bowing Of The Long Bones Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Bones With Narrow Diaphyses Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Crumpled Long Bones Gene Set From 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 Set From 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 Set From 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.
Protuberances At Ends Of Long Bones Gene Set From 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 Set From 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.
Long Hallux Gene Set From 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.
Long Metacarpals Gene Set From 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.
Anterior Bowing Of Long Bones Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
decreased length of long bones Gene Set From 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.
reduced long-term potentiation Gene Set From 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.
increased diameter of long bones Gene Set From 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 Set From 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 Set From 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-term object recognition memory Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the long incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
long gestation period Gene Set From 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 diameter of long bones Gene Set From 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.
abnormal long-term spatial reference memory Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 incus long process morphology Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 lived plasma cell morphology Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Reactome Pathways 2024 proteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways 2024 dataset.
Long-term potentiation Gene Set From Reactome Pathways 2024 proteins participating in the Long-term potentiation pathway from the Reactome Pathways 2024 dataset.
PCNA-Dependent Long Patch Base Excision Repair Gene Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
long-chain fatty acid import into cell Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of long-term synaptic depression Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset.
long-term synaptic potentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of long-term synaptic potentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty acid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty-acyl-CoA metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty-acyl-CoA metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of long-term neuronal synaptic plasticity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of long-term synaptic depression Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty acid transport Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of long-chain fatty acid import into cell Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of long-chain fatty acid import into cell Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of long-chain fatty acid import across plasma membrane Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset.
very long-chain fatty acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the very long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty acid import across plasma membrane Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty acid import into peroxisome Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid import into peroxisome biological process from the curated GO Biological Process Annotations 2025 dataset.
very long-chain fatty acid catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the very long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of long-chain fatty acid import across plasma membrane Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset.
very long-chain fatty-acyl-CoA catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the very long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
long-chain fatty acid catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of long-term synaptic potentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
very long-chain fatty-acyl-CoA metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the very long-chain fatty-acyl-CoA metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
long-term synaptic depression Gene Set From GO Biological Process Annotations 2025 genes participating in the long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of long-term synaptic depression Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2025 dataset.
very long-chain fatty acid beta-oxidation Gene Set From GO Biological Process Annotations 2025 genes participating in the very long-chain fatty acid beta-oxidation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of long-chain fatty acid import across plasma membrane Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of long-chain fatty acid import into cell Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2025 dataset.
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acyl-CoA binding Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acyl-CoA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acyl-CoA hydrolase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acid-CoA ligase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acid-CoA ligase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
very long-chain fatty acid-CoA ligase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very long-chain fatty acid-CoA ligase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acid omega-hydroxylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acid omega-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acid omega-1 hydroxylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acid omega-1 hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acid binding Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acid binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty acyl-CoA dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
very-long-chain fatty acyl-CoA dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very-long-chain fatty acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain-alcohol oxidase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain fatty aldehyde dehydrogenase (NAD+) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain fatty aldehyde dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
N-(long-chain-acyl)ethanolamine deacylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the N-(long-chain-acyl)ethanolamine deacylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain-3-hydroxyacyl-CoA dehydrogenase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain-3-hydroxyacyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
very long-chain fatty acid omega-hydroxylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very long-chain fatty acid omega-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
very long-chain fatty acyl-CoA hydrolase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very long-chain fatty acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
very-long-chain 3-oxoacyl-CoA reductase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very-long-chain 3-oxoacyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
long-chain-alcohol O-fatty-acyltransferase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
alcohol-forming long-chain fatty acyl-CoA reductase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the alcohol-forming long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
very-long-chain enoyl-CoA reductase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the very-long-chain enoyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Long QT syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Long QT syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Very long chain acyl-CoA dehydrogenase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Very long chain acyl-CoA dehydrogenase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Long COVID Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long COVID in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Very long chain acyl-CoA dehydrogenase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Very long chain acyl-CoA dehydrogenase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Long QT syndrome 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Long QT syndrome 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Very long chain acyl-CoA dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long QT syndrome 1/ Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long QT syndrome 1/ phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long QT syndrome 3/ Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long QT syndrome 3/ phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long QT syndrome 2/ Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long QT syndrome 2/ phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long fingers Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long fingers phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long telomere syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Long telomere syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Very long chain fatty acid accumulation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Very long chain fatty acid accumulation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Long QT syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Long QT syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
First fracture in long-term childhood cancer survivors (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the First fracture in long-term childhood cancer survivors (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Systolic blood pressure (long-term average) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diastolic blood pressure (long-term average) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mean arterial pressure (long-term average) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Triglyceride levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x long total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x long total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
LDL cholesterol levels x long total sleep time interaction (1df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x long total sleep time interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HDL cholesterol levels x long total sleep time interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x long total sleep time interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to long-chain n-3 polyunsaturated fatty acid supplementation (change in triglyceride levels) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to long-chain n-3 polyunsaturated fatty acid supplementation (change in triglyceride levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hallucinations in long-term cannabis use Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hallucinations in long-term cannabis use phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Long-term memory (delayed word recall task) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Long-term memory (delayed word recall task) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma exacerbations in long-acting beta2-agonist treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma exacerbations in long-acting beta2-agonist treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Very long-chain saturated fatty acid levels (fatty acid 20:0) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Very long-chain saturated fatty acid levels (fatty acid 20:0) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Very long-chain saturated fatty acid levels (fatty acid 22:0) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Very long-chain saturated fatty acid levels (fatty acid 22:0) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Very long-chain saturated fatty acid levels (fatty acid 24:0) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Very long-chain saturated fatty acid levels (fatty acid 24:0) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sleep duration (long sleep) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sleep duration (long sleep) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Worry too long after an embarrassing experience Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Worry too long after an embarrassing experience phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parental longevity (at least one long-lived parent) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parental longevity (at least one long-lived parent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Number of alcoholic drinks required to feel an effect (long-term average) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Number of alcoholic drinks required to feel an effect (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fasting glucose change (long-term) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting glucose change (long-term) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Long-term potentiation Gene Set From KEGG Pathways 2026 proteins participating in the Long-term potentiation pathway from the KEGG Pathways 2026 dataset.
Long-term depression Gene Set From KEGG Pathways 2026 proteins participating in the Long-term depression pathway from the KEGG Pathways 2026 dataset.
multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set From Biocarta Pathways proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset.
CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Multiple synostoses syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 15, multiple types Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant, multiple types, with microcornea Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal multiple pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple endocrine neoplasia, type 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple fibrofolliculomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple fibrofolliculomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple sulfatase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple pterygium syndrome Escobar type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart defects, multiple types, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple gastrointestinal atresias Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple exostoses type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple exostoses type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple endocrine neoplasia, type 2a Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple mitochondrial dysfunctions syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple mitochondrial dysfunctions syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple endocrine neoplasia, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital exostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple epiphyseal dysplasia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple fibroadenomas of the breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple fibroadenomas of the breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOMATOSIS, MULTIPLE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LIPOMATOSIS, MULTIPLE from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.
Cafe au lait spots, multiple Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cafe au lait spots, multiple from the curated CTD Gene-Disease Associations dataset.
Multiple Organ Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Organ Failure from the curated CTD Gene-Disease Associations dataset.
EXOSTOSES, MULTIPLE, TYPE II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE II from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Type 2a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2a from the curated CTD Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.
Multiple Myeloma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Myeloma from the curated CTD Gene-Disease Associations dataset.
Venous Malformations, Multiple Cutaneous and Mucosal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.
MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.
Multiple Synostoses Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Synostoses Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
CATARACT 32, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Exostoses, Multiple Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset.
Hamartoma Syndrome, Multiple Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hamartoma Syndrome, Multiple from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
CATARACT 6, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia from the curated CTD Gene-Disease Associations dataset.
Exostoses, Multiple, Type III Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple, Type III from the curated CTD Gene-Disease Associations dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.
Multiple Sclerosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sclerosis from the curated CTD Gene-Disease Associations dataset.
Multiple Chemical Sensitivity Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Chemical Sensitivity from the curated CTD Gene-Disease Associations dataset.
Multiple synostoses syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple synostoses syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Multiple Sclerosis, Relapsing-Remitting Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sclerosis, Relapsing-Remitting from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Type 2b Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2b from the curated CTD Gene-Disease Associations dataset.
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant, Multiple Types 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma multiple familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.
Multiple pterygium syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple pterygium syndrome from the curated CTD Gene-Disease Associations dataset.
Abnormalities, Multiple Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Abnormalities, Multiple from the curated CTD Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia, Type IV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia, Type IV from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.
CATARACT 3, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.
EXOSTOSES, MULTIPLE, TYPE I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE I from the curated CTD Gene-Disease Associations dataset.
CATARACT 4, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
MULTIPLE SYNOSTOSES SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE SYNOSTOSES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma, Multiple Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.
Epiphyseal dysplasia, multiple, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.
Multiple Sclerosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Multiple Sclerosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Multiple Myeloma Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Multiple Myeloma in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
hereditary multiple exostoses Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary multiple exostoses from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple epiphyseal dysplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple sclerosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple carboxylase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple myeloma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease multiple sclerosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
multiple intestinal atresia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple myeloma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary multiple exostoses Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple mucosal neuroma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple chemical sensitivity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple symmetrical lipomatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple symmetrical lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple epiphyseal dysplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple carboxylase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple symmetric lipomatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
relapsing-remitting multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set From GAD Gene-Disease Associations genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; optic neuritis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; optic neuritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; shock, septic; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple epiphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burns; multiple organ failure; shock Gene Set From GAD Gene-Disease Associations genes associated with the disease burns; multiple organ failure; shock in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis (age of onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; diabetes, type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; multiple sclerosis; hiv Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; multiple sclerosis; hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; respiratory distress syndrome, adult; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
susceptibility to multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease susceptibility to multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genetic predisposition to disease; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disorders; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease learning disorders; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hamartoma syndrome, multiple Gene Set From GAD Gene-Disease Associations genes associated with the disease hamartoma syndrome, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaw diseases; multiple myeloma; osteonecrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease jaw diseases; multiple myeloma; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis(ppmultiple sclerosis) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis(ppmultiple sclerosis) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
encephalomyelitis, autoimmune, experimental; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease encephalomyelitis, autoimmune, experimental; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple autoimmune diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; neuromyelitis optica Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; neuromyelitis optica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; plasmacytoma Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; plasmacytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
normalized brain volume, multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease normalized brain volume, multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, systemic; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple chemical sensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple chemical sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasms, multiple primary; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; pneumonia; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; short bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis; iga nephropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
churg-strauss syndrome; multiple sclerosis; wegener granulomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease churg-strauss syndrome; multiple sclerosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tic; combined vocal and multiple motor; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
juvenile multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease juvenile multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 2b Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 2a Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leiomyoma; neoplasms, multiple primary; uterine neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease leiomyoma; neoplasms, multiple primary; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 1; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; multiple myeloma; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloma, multiple Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloma, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c, chronic; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis (severity) Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (severity) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple oesophageal dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epstein-barr virus infections; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease epstein-barr virus infections; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary multiple exostoses Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary multiple exostoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; pneumonia; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; pneumonia; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple endocrine neoplasia type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset of multiple sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft vs host disease; leukemia; multiple myeloma; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease graft vs host disease; leukemia; multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple myeloma; neoplasm recurrence, local Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple myeloma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; carcinoma; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term multiple in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Multiple sclerosis--Brain Glutamate Levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis or amyotrophic lateral sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple myeloma (IgH translocation) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (severity) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (severity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple myeloma (hyperdiploidy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma (hyperdiploidy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (OCB status) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (OCB status) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Multiple sclerosis (age of onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
multiple myeloma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
multiple sclerosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
multiple mitochondrial dna deletions Gene Set From GWASdb SNP-Phenotype Associations genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
multiple myeloma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the multiple myeloma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
multiple exostoses Gene Set From HPO Gene-Disease Associations genes associated with the multiple exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple epiphyseal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the multiple epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple gastric polyps Gene Set From HPO Gene-Disease Associations genes associated with the multiple gastric polyps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple cutaneous leiomyomas Gene Set From HPO Gene-Disease Associations genes associated with the multiple cutaneous leiomyomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple impacted teeth Gene Set From HPO Gene-Disease Associations genes associated with the multiple impacted teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple enchondromatosis Gene Set From HPO Gene-Disease Associations genes associated with the multiple enchondromatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple prenatal fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple prenatal fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple joint contractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple joint contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple rows of eyelashes Gene Set From HPO Gene-Disease Associations genes associated with the multiple rows of eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple myeloma Gene Set From HPO Gene-Disease Associations genes associated with the multiple myeloma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple plantar creases Gene Set From HPO Gene-Disease Associations genes associated with the multiple plantar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple small vertebral fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular preexcitation with multiple accessory pathways Gene Set From HPO Gene-Disease Associations genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple digital exostoses Gene Set From HPO Gene-Disease Associations genes associated with the multiple digital exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bowing of limbs due to multiple fractures Gene Set From HPO Gene-Disease Associations genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple glomerular cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple glomerular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple suture craniosynostosis Gene Set From HPO Gene-Disease Associations genes associated with the multiple suture craniosynostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple lipomas Gene Set From HPO Gene-Disease Associations genes associated with the multiple lipomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple carpal ossification centers Gene Set From HPO Gene-Disease Associations genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple mitochondrial dna deletions Gene Set From HPO Gene-Disease Associations genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple pterygia Gene Set From HPO Gene-Disease Associations genes associated with the multiple pterygia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple small medullary renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple cafe-au-lait spots Gene Set From HPO Gene-Disease Associations genes associated with the multiple cafe-au-lait spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple palmar creases Gene Set From HPO Gene-Disease Associations genes associated with the multiple palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple rib fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple rib fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple lentigines Gene Set From HPO Gene-Disease Associations genes associated with the multiple lentigines phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple skeletal anomalies Gene Set From HPO Gene-Disease Associations genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Trauma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Trauma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Organ Failure Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Organ Failure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Type 2b Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 2b phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Type 2a Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 2a phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Myeloma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Myeloma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Sclerosis, Relapsing-Remitting Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Relapsing-Remitting phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Exostoses, Multiple Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Exostoses, Multiple Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Abnormalities, Multiple Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Abnormalities, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hamartoma Syndrome, Multiple Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hamartoma Syndrome, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Type 1 Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Endocrine Neoplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Sclerosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple Chemical Sensitivity Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Chemical Sensitivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neoplasms, Multiple Primary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Multiple Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
multiple major aortopulmonary collateral arteries Gene Set From MPO Gene-Phenotype Associations gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intestinal atresia, multiple Gene Set From OMIM Gene-Disease Associations genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset.
?epiphyseal dysplasia, multiple, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 5, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
adenomas, multiple colorectal Gene Set From OMIM Gene-Disease Associations genes associated with the adenomas, multiple colorectal phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 9, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia iib Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia iib phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia iia Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia iia phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple pterygium syndrome, lethal type Gene Set From OMIM Gene-Disease Associations genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 3, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple myeloma, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple myeloma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 1, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple system atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
orolaryngeal cancer, multiple, Gene Set From OMIM Gene-Disease Associations genes associated with the orolaryngeal cancer, multiple, phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple fibroadenomas of the breast Gene Set From OMIM Gene-Disease Associations genes associated with the multiple fibroadenomas of the breast phenotype from the curated OMIM Gene-Disease Associations dataset.
{vitiligo-associated multiple autoimmune disease susceptiblity 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {vitiligo-associated multiple autoimmune disease susceptiblity 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 20, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set From OMIM Gene-Disease Associations genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple mitochondrial dysfunctions syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple mitochondrial dysfunctions syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital heart defects, multiple types, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital heart defects, multiple types, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 14, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
venous malformations, multiple cutaneous and mucosal Gene Set From OMIM Gene-Disease Associations genes associated with the venous malformations, multiple cutaneous and mucosal phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 12, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 39, multiple types, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopia and deafness Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, disease progression, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, disease progression, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple endocrine neoplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{vitiligo-associated multiple autoimmune disease susceptibility 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {vitiligo-associated multiple autoimmune disease susceptibility 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 34, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 11, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 6, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 2, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple myeloma, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple myeloma, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 16, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 15, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple sulfatase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the multiple sulfatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple synostoses syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple synostoses syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple synostoses syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple synostoses syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple synostoses syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple synostoses syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple sclerosis, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
exostoses, multiple, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
exostoses, multiple, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
exostoses, multiple, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 17, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 4, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From OMIM Gene-Disease Associations genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 31, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 10, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
?multiple mitochondrial dysfunctions syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple self-healing squamous epithelioma, susceptiblity to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple self-healing squamous epithelioma, susceptiblity to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Set From Reactome Pathways 2014 proteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways dataset.
Defective HLCS causes multiple carboxylase deficiency Gene Set From Reactome Pathways 2014 proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset.
multiple myeloma cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
multiple myeloma cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Multiple Chronic Conditions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Chronic Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Relapsing-Remitting Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Relapsing-Remitting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lipomatosis, Multiple Symmetrical Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lipomatosis, Multiple Symmetrical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitiligo-Associated Multiple Autoimmune Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitiligo-Associated Multiple Autoimmune Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lipomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lipomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Adenomatous Polyps Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Adenomatous Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Endocrine Neoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Endocrine Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Multiple Exostoses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Epiphyseal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Epiphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Gastrointestinal Atresias (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Gastrointestinal Atresias (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichoepitheliomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Primary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Polyps Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meningiomas, Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meningiomas, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Myeloma Progression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Myeloma Progression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lacunar Infarcts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lacunar Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Multiple Mole-Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Renal Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Acute Fulminating Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Acute Fulminating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Acute Relapsing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Acute Relapsing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis In Children Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Opticospinal Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Opticospinal Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sulfatase Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Carboxylase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Carboxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Joint Dislocations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis Relapse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis Relapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Mitochondrial Dysfunctions Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Mitochondrial Dysfunctions Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lentigines Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lentigines in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Nevi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Nevi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Small Medullary Renal Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Small Medullary Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Secondary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Fibrofolliculomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Fibrofolliculomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymptomatic Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymptomatic Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Self-Healing Squamous Epithelioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Self-Healing Squamous Epithelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Biliary Hamartomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Biliary Hamartomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome, Lethal Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Lethal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, With Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Linear Skin Defects With Multiple Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Linear Skin Defects With Multiple Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Factor Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Abscesses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Abscesses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Lipomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Trichoepitheliomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Trichoepitheliomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Synostoses Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Synostoses Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Allergies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Allergies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Neoplasm Of Lung - Multiple Primary Sites Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Lung - Multiple Primary Sites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Basal Cell Papillomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Basal Cell Papillomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exostoses, Multiple, Type Ii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exostoses, Multiple, Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Multiple Osteochondromas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Osteochondromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Evanescent White Dot Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Evanescent White Dot Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichodiscomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Lung Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lung Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nevi Flammei, Familial Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Non-Ossifying Fibromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Non-Ossifying Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Hemangioblastomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Hemangioblastomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Cysts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Milia, Multiple Eruptive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Milia, Multiple Eruptive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pancreatic Beta-Cell Adenomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pancreatic Beta-Cell Adenomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indolent Multiple Myeloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indolent Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Pterygium Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Harmonizome 3.0

MS Gene

SHANK3 Gene

SHANK2 Gene

SHANK1 Gene

EXT3 Gene

MMDFS Gene

MEN1 Gene

MCTP1 Gene

MCTP2 Gene

MMEDF Gene

MEGF8 Gene

CNC2 Gene

RBPMS2 Gene

MCFD2P1 Gene

MINPP1 Gene

RBPMSLP Gene

MS4 Gene

MS3 Gene

MS2 Gene

CSMD2 Gene

CSMD3 Gene

CSMD1 Gene

LOC105373985 Gene

MFT2 Gene

EGFL7 Gene

EGFL6 Gene

EGFL8 Gene

MEGF9 Gene

MEGF6 Gene

CHDT3 Gene

EXTL2P1 Gene

ODPF Gene

MPDZ Gene

RBPMS Gene

MCFD2 Gene

MEGF10 Gene

MEGF11 Gene

LINC01221 Gene

LINC01227 Gene

LINC01091 Gene

LINC01090 Gene

LINC01093 Gene

LINC01095 Gene

LINC01094 Gene

LINC01097 Gene

LINC01096 Gene

LINC01098 Gene

LINC00320 Gene

LINC00323 Gene

LINC00324 Gene

LINC00326 Gene

LINC00327 Gene

LINC00328 Gene

LINC01215 Gene

LINC01214 Gene

LINC00847 Gene

LINC00849 Gene

LINC01251 Gene

LINC01250 Gene

LINC01257 Gene

CCDC26 Gene

LINC01255 Gene

LINC01491 Gene

LINC01490 Gene

LINC01198 Gene

LINC01194 Gene

LINC01195 Gene

LINC01197 Gene

LINC01191 Gene

LINC01192 Gene

LINC01193 Gene

LINC01360 Gene

HEIH Gene

LINC01365 Gene

LINC01547 Gene

LINC01546 Gene

LINC01545 Gene

LINC01549 Gene

LINC01548 Gene