| Name |
|---|
SHFLD3 GeneSplit-hand/foot malformation with long bone deficiency 3 |
SHFL1 GeneSplit-hand/foot malformation with long bone deficiency 1 |
SHFLD2 GeneSplit-hand/foot malformation with long deficiency 2 |
CCM2 Genecerebral cavernous malformation 2 This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009] |
CCM2L Genecerebral cavernous malformation 2-like Predicted to be involved in heart morphogenesis. Predicted to act upstream of or within several processes, including heart development; negative regulation of homotypic cell-cell adhesion; and positive regulation of fibroblast growth factor production. [provided by Alliance of Genome Resources, Mar 2025] |
SHFM1P1 Genesplit hand/foot malformation (ectrodactyly) type 1 pseudogene 1 |
SHFM3 GeneSplit-hand/foot malformation 3 |
SHFM2 Genesplit hand/foot malformation (ectrodactyly) type 2 |
SHFM1 Genesplit hand/foot malformation (ectrodactyly) type 1 The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008] |
SHFM5 Genesplit hand/foot malformation (ectrodactyly) type 5 |
AES Geneamino-terminal enhancer of split The protein encoded by this gene is similar in sequence to the amino terminus of Drosophila enhancer of split groucho, a protein involved in neurogenesis during embryonic development. The encoded protein, which belongs to the groucho/TLE family of proteins, can function as a homooligomer or as a heteroologimer with other family members to dominantly repress the expression of other family member genes. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
TLE1P1 Genetransducin-like enhancer of split 1 pseudogene 1 |
TLE3 Genetransducin-like enhancer of split 3 This gene encodes a transcriptional co-repressor protein that belongs to the transducin-like enhancer family of proteins. The members of this family function in the Notch signaling pathway that regulates determination of cell fate during development. Expression of this gene has been associated with a favorable outcome to chemotherapy with taxanes for ovarian carcinoma. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Sep 2013] |
TLE2 Genetransducin-like enhancer of split 2 Enables transcription corepressor activity. Involved in negative regulation of DNA-templated transcription and negative regulation of canonical Wnt signaling pathway. Located in focal adhesion and nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
TLE1 Genetransducin-like enhancer of split 1 (E(sp1) homolog, Drosophila) Enables DNA-binding transcription factor binding activity; identical protein binding activity; and transcription corepressor activity. Involved in negative regulation of anoikis; negative regulation of signal transduction; and regulation of gene expression. Located in cytosol and nucleoplasm. Part of beta-catenin-TCF complex. [provided by Alliance of Genome Resources, Mar 2025] |
TLE6 Genetransducin-like enhancer of split 6 This gene encodes a member of the Groucho/ transducin-like Enhancer of split family of transcriptional co-repressors. The encoded protein is a component of the mammalian subcortical maternal complex, which is required for preimplantation development. In mouse, knock out of this gene results in cleavage-stage embryonic arrest resulting from defective cytoplasmic F-actin meshwork formation and asymmetric cell division. In human, an allelic variant in this gene is associated with preimplantation embryonic lethality. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
TLE4 Genetransducin-like enhancer of split 4 Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of canonical Wnt signaling pathway and negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within Wnt signaling pathway; cellular response to leukemia inhibitory factor; and negative regulation of DNA-templated transcription. Located in nucleoplasm. Part of beta-catenin-TCF complex. [provided by Alliance of Genome Resources, Mar 2025] |
MMAA Genemethylmalonic aciduria (cobalamin deficiency) cblA type The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008] |
MMAB Genemethylmalonic aciduria (cobalamin deficiency) cblB type This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011] |
GCCD2 GeneGlucocorticoid deficiency 2 |
GCCD3 Geneglucocorticoid deficiency 3 |
IGAD1 Geneimmunoglobulin A (IgA) deficiency susceptibility 1 |
MMACHC Genemethylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria The exact function of the protein encoded by this gene is not known, however, its C-terminal region shows similarity to TonB, a bacterial protein involved in energy transduction for cobalamin (vitamin B12) uptake. Hence, it is postulated that this protein may have a role in the binding and intracellular trafficking of cobalamin. Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC. [provided by RefSeq, Oct 2009] |
MMADHC Genemethylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008] |
AGMX2 Geneagammaglobulinemia, X-linked 2 (with growth hormone deficiency) |
RRDX GeneRadial ray deficiency |
MCFD2P1 Genemultiple coagulation factor deficiency 2 pseudogene 1 |
LOC100216356 Genemethylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria pseudogene |
LOC100216355 Genemethylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria pseudogene |
CANDN1 Genecandidiasis, nail 1 (with ICAM1 deficiency) |
MCFD2 Genemultiple 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] |
NKCD GeneNatural killer cell deficiency, familial isolated |
ALPL Genealkaline phosphatase, liver/bone/kidney This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015] |
ANBC GeneAneurysmal bone cysts |
BMND8 Genebone mineral density quantiative trait locus 8 |
BMND9 GeneBone mineral density QTL 9 |
BMND6 GeneBone mineral density QTL 6 |
BMND5 GeneBone mineral density variation QTL 5 |
BMND2 GeneBone mineral density variation 2 |
BMND3 GeneBone mineral density variability 3 |
BSZQTL GeneBone size QTL |
BRKS1 GeneTelopeptide lysyl hydroxylase, bone-specific |
PDB6 GenePaget disease of bone 6 |
PDB4 GenePaget disease of bone 4 |
PDB5 GenePaget disease of bone 5 |
PDB1 GenePaget disease of bone 1 |
PRG2 Geneproteoglycan 2, bone marrow (natural killer cell activator, eosinophil granule major basic protein) The protein encoded by this gene is the predominant constituent of the crystalline core of the eosinophil granule. High levels of the proform of this protein are also present in placenta and pregnancy serum, where it exists as a complex with several other proteins including pregnancy-associated plasma protein A (PAPPA), angiotensinogen (AGT), and C3dg. This protein may be involved in antiparasitic defense mechanisms as a cytotoxin and helminthotoxin, and in immune hypersensitivity reactions. The encoded protein contains a peptide that displays potent antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, and fungi. It is directly implicated in epithelial cell damage, exfoliation, and bronchospasm in allergic diseases. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014] |
BMP7 Genebone morphogenetic protein 7 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer, which plays a role in bone, kidney and brown adipose tissue development. Additionally, this protein induces ectopic bone formation and may promote fracture healing in human patients. [provided by RefSeq, Jul 2016] |
BMP6 Genebone morphogenetic protein 6 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates a wide range of biological processes including iron homeostasis, fat and bone development, and ovulation. Differential expression of this gene may be associated with progression of breast and prostate cancer. Mutations in this gene may be associated with iron overload in human patients. [provided by RefSeq, Jul 2016] |
BMP5 Genebone morphogenetic protein 5 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer, which plays a role in bone and cartilage development. Polymorphisms in this gene may be associated with osteoarthritis in human patients. This gene is differentially regulated in multiple human cancers. This gene encodes distinct protein isoforms that may be similarly proteolytically processed. [provided by RefSeq, Jul 2016] |
BMP4 Genebone morphogenetic protein 4 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates heart development and adipogenesis. Mutations in this gene are associated with orofacial cleft and microphthalmia in human patients. The encoded protein may also be involved in the pathology of multiple cardiovascular diseases and human cancers. [provided by RefSeq, Jul 2016] |
BMP3 Genebone morphogenetic protein 3 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein suppresses osteoblast differentiation, and negatively regulates bone density, by modulating TGF-beta receptor availability to other ligands. [provided by RefSeq, Jul 2016] |
BMP2 Genebone morphogenetic protein 2 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer, which plays a role in bone and cartilage development. Duplication of a regulatory region downstream of this gene causes a form of brachydactyly characterized by a malformed index finger and second toe in human patients. [provided by RefSeq, Jul 2016] |
BMP1 Genebone morphogenetic protein 1 This gene encodes a protein that is capable of inducing formation of cartilage in vivo. Although other bone morphogenetic proteins are members of the TGF-beta superfamily, this gene encodes a protein that is not closely related to other known growth factors. This gene is expressed as alternatively spliced variants that share an N-terminal protease domain but differ in their C-terminal region. [provided by RefSeq, Aug 2008] |
BRINP3 Genebone morphogenetic protein/retinoic acid inducible neural-specific 3 This gene is overexpressed in pituitary tumors but is underexpressed in tongue squamous cell carcinomas, ulcerative colitis, and peri-implantitis. Polymorphisms that increase expression of this gene have been shown to increase vascular inflammation, and an association of this gene with myocardial infarction has been demonstrated. Finally, hypermethylation of this gene may find usefulness as a biomarker for gastric cancer. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
BRINP2 Genebone morphogenetic protein/retinoic acid inducible neural-specific 2 Predicted to be involved in cellular response to retinoic acid; central nervous system neuron differentiation; and negative regulation of mitotic cell cycle. Predicted to act upstream of or within locomotion and nervous system development. Predicted to be located in extracellular region. Predicted to be active in cytoplasm; dendrite; and neuronal cell body. Implicated in oral squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
BRINP1 Genebone morphogenetic protein/retinoic acid inducible neural-specific 1 This gene is located within a chromosomal region that shows loss of heterozygosity in some bladder cancers. It contains a 5' CpG island that may be a frequent target of hypermethylation, and it may undergo hypermethylation-based silencing in some bladder cancers. [provided by RefSeq, Jul 2008] |
BMND10 GeneBone mineral density QTL 10 |
BMND11 GeneBone mineral density QTL 11 |
BMND13 GeneBone mineral density QTL 13 |
BMND14 GeneBone mineral density QTL 14 |
BSZQTL3 GeneBone size quantitative trait locus 3 |
BSZQTL2 GeneBone size QTL |
BMP8A Genebone morphogenetic protein 8a This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein may play a role in development of the reproductive system. This gene may have arose from a gene duplication event and its gene duplicate is also present on chromosome 1. [provided by RefSeq, Jul 2016] |
BMP8B Genebone morphogenetic protein 8b This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. The encoded protein stimulates thermogenesis in brown adipose tissue. Expression of this gene may be downregulated in pancreatic cancer. This gene may have arose from a gene duplication event and its gene duplicate is also present on chromosome 1. [provided by RefSeq, Jul 2016] |
BGLAP Genebone gamma-carboxyglutamate (gla) protein This gene encodes a highly abundant bone protein secreted by osteoblasts that regulates bone remodeling and energy metabolism. The encoded protein contains a Gla (gamma carboxyglutamate) domain, which functions in binding to calcium and hydroxyapatite, the mineral component of bone. Serum osteocalcin levels may be negatively correlated with metabolic syndrome. Read-through transcription exists between this gene and the neighboring upstream gene, PMF1 (polyamine-modulated factor 1), but the encoded protein only shows sequence identity with the upstream gene product. [provided by RefSeq, Jun 2015] |
BMND7 Genebone mineral density quantiative trait locus 7 |
BMND4 GeneBone mineral density variation QTL 4 |
BMPR1APS1 Genebone morphogenetic protein receptor, type IA pseudogene 1 |
BMPR1APS2 Genebone morphogenetic protein receptor, type IA pseudogene 2 |
BMPR2 Genebone morphogenetic protein receptor, type II (serine/threonine kinase) This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Mutations in this gene have been associated with primary pulmonary hypertension, both familial and fenfluramine-associated, and with pulmonary venoocclusive disease. [provided by RefSeq, May 2020] |
BST1 Genebone marrow stromal cell antigen 1 Bone marrow stromal cell antigen-1 is a stromal cell line-derived glycosylphosphatidylinositol-anchored molecule that facilitates pre-B-cell growth. The deduced amino acid sequence exhibits 33% similarity with CD38. BST1 expression is enhanced in bone marrow stromal cell lines derived from patients with rheumatoid arthritis. The polyclonal B-cell abnormalities in rheumatoid arthritis may be, at least in part, attributed to BST1 overexpression in the stromal cell population. [provided by RefSeq, Jul 2008] |
BST2 Genebone marrow stromal cell antigen 2 Bone marrow stromal cells are involved in the growth and development of B-cells. The specific function of the protein encoded by the bone marrow stromal cell antigen 2 is undetermined; however, this protein may play a role in pre-B-cell growth and in rheumatoid arthritis. [provided by RefSeq, Jul 2008] |
BMP10 Genebone morphogenetic protein 10 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which binds to the activin receptor-like kinase 1 (ALK1) and plays important roles in cardiovascular development including cardiomyocyte proliferation and regulation of heart size, closure of the ductus arteriosus, angiogenesis and ventricular trabeculation. [provided by RefSeq, Aug 2016] |
BMP15 Genebone morphogenetic protein 15 This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate subunits of a disulfide-linked homodimer, or alternatively, a heterodimer, with the related protein, growth differentiation factor 9 (GDF9). This protein plays a role in oocyte maturation and follicular development, through activation of granulosa cells. Defects in this gene are the cause of ovarian dysgenesis and are associated with premature ovarian failure. [provided by RefSeq, Aug 2016] |
BMP6P1 Genebone morphogenetic protein 6 pseudogene 1 |
BMPR1A Genebone morphogenetic protein receptor, type IA The bone morphogenetic protein (BMP) receptors are a family of transmembrane serine/threonine kinases that include the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. These receptors are also closely related to the activin receptors, ACVR1 and ACVR2. The ligands of these receptors are members of the TGF-beta superfamily. TGF-betas and activins transduce their signals through the formation of heteromeric complexes with 2 different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. [provided by RefSeq, Jul 2008] |
BMPR1B Genebone morphogenetic protein receptor, type IB This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of 2 different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2012] |
BMNCR Genebone marrow associated non-coding RNA |
LINC01221 Genelong intergenic non-protein coding RNA 1221 |
LINC01227 Genelong intergenic non-protein coding RNA 1227 |
LINC01091 Genelong intergenic non-protein coding RNA 1091 |
LINC01090 Genelong intergenic non-protein coding RNA 1090 |
LINC01093 Genelong intergenic non-protein coding RNA 1093 |
LINC01095 Genelong intergenic non-protein coding RNA 1095 |
LINC01094 Genelong intergenic non-protein coding RNA 1094 |
LINC01097 Genelong intergenic non-protein coding RNA 1097 |
LINC01096 Genelong intergenic non-protein coding RNA 1096 |
LINC01098 Genelong intergenic non-protein coding RNA 1098 |
LINC00320 Genelong intergenic non-protein coding RNA 320 |
LINC00323 Genelong intergenic non-protein coding RNA 323 |
LINC00324 Genelong intergenic non-protein coding RNA 324 |
LINC00326 Genelong intergenic non-protein coding RNA 326 |
LINC00327 Genelong intergenic non-protein coding RNA 327 |
LINC00328 Genelong intergenic non-protein coding RNA 328 |
LINC01215 Genelong intergenic non-protein coding RNA 1215 |
LINC01214 Genelong intergenic non-protein coding RNA 1214 |
LINC00847 Genelong intergenic non-protein coding RNA 847 |
LINC00849 Genelong intergenic non-protein coding RNA 849 |
LINC01251 Genelong intergenic non-protein coding RNA 1251 |
LINC01250 Genelong intergenic non-protein coding RNA 1250 |
LINC01257 Genelong intergenic non-protein coding RNA 1257 |
CCDC26 GeneCCDC26 long non-coding RNA Implicated in brain cancer and high grade glioma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01255 Genelong intergenic non-protein coding RNA 1255 |
LINC01491 Genelong intergenic non-protein coding RNA 1491 |
LINC01490 Genelong intergenic non-protein coding RNA 1490 |
LINC01198 Genelong intergenic non-protein coding RNA 1198 Biomarker of malignant astrocytoma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01194 Genelong intergenic non-protein coding RNA 1194 |
LINC01195 Genelong intergenic non-protein coding RNA 1195 |
LINC01197 Genelong intergenic non-protein coding RNA 1197 |
LINC01191 Genelong intergenic non-protein coding RNA 1191 |
LINC01192 Genelong intergenic non-protein coding RNA 1192 |
LINC01193 Genelong intergenic non-protein coding RNA 1193 |
LINC01360 Genelong intergenic non-protein coding RNA 1360 |
HEIH Genehepatocellular carcinoma up-regulated EZH2-associated long non-coding RNA Biomarker of esophagus squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01365 Genelong intergenic non-protein coding RNA 1365 |
LINC01547 Genelong intergenic non-protein coding RNA 1547 Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01546 Genelong intergenic non-protein coding RNA 1546 |
LINC01545 Genelong intergenic non-protein coding RNA 1545 |
LINC01549 Genelong intergenic non-protein coding RNA 1549 |
LINC01548 Genelong intergenic non-protein coding RNA 1548 |
LINC00633 Genelong intergenic non-protein coding RNA 633 |
LINC00630 Genelong intergenic non-protein coding RNA 630 |
LINC00636 Genelong intergenic non-protein coding RNA 636 |
LINC00637 Genelong intergenic non-protein coding RNA 637 |
LINC00635 Genelong intergenic non-protein coding RNA 635 |
LINC00638 Genelong intergenic non-protein coding RNA 638 |
LINC00639 Genelong intergenic non-protein coding RNA 639 |
LINC01348 Genelong intergenic non-protein coding RNA 1348 |
LINC01550 Genelong intergenic non-protein coding RNA 1550 |
LINC01551 Genelong intergenic non-protein coding RNA 1551 |
LINC01552 Genelong intergenic non-protein coding RNA 1552 |
LINC00879 Genelong intergenic non-protein coding RNA 879 |
LINC00877 Genelong intergenic non-protein coding RNA 877 |
LINC00870 Genelong intergenic non-protein coding RNA 870 |
LINC00871 Genelong intergenic non-protein coding RNA 871 |
LINC00265-3P Genelong intergenic non-protein coding RNA 265-3, pseudogene |
LINC00969 Genelong intergenic non-protein coding RNA 969 |
LINC00404 Genelong intergenic non-protein coding RNA 404 |
LINC00400 Genelong intergenic non-protein coding RNA 400 |
LINC00403 Genelong intergenic non-protein coding RNA 403 |
LINC00402 Genelong intergenic non-protein coding RNA 402 |
LINC00408 Genelong intergenic non-protein coding RNA 408 |
LINC01510 Genelong intergenic non-protein coding RNA 1510 This gene encodes a natural antisense transcript highly expressed in papillary thyroid carcinomas harboring BRAF V600E mutation or RET gene rearrangements. This lncRNA induces the downstream MAPK pathway and is part of a co-expression network including different oncogenes belonging to the MAPK and PI3H/AKT pathways. In thyroid carcinomas, this gene has oncogenic properties associated with increased proliferation and drug resistance. [provided by RefSeq, Jan 2020] |
LINC01114 Genelong intergenic non-protein coding RNA 1114 |
LINC01115 Genelong intergenic non-protein coding RNA 1115 |
LINC01116 Genelong intergenic non-protein coding RNA 1116 |
LINC01117 Genelong intergenic non-protein coding RNA 1117 |
LINC01111 Genelong intergenic non-protein coding RNA 1111 |
LINC01118 Genelong intergenic non-protein coding RNA 1118 |
LINC01514 Genelong intergenic non-protein coding RNA 1514 |
LINC00244 Genelong intergenic non-protein coding RNA 244 |
LINC00243 Genelong intergenic non-protein coding RNA 243 |
LINC00242 Genelong intergenic non-protein coding RNA 242 |
LINC00240 Genelong intergenic non-protein coding RNA 240 |
LINC00939 Genelong intergenic non-protein coding RNA 939 |
LINC00938 Genelong intergenic non-protein coding RNA 938 |
LINC00930 Genelong intergenic non-protein coding RNA 930 |
LINC00933 Genelong intergenic non-protein coding RNA 933 |
LINC00935 Genelong intergenic non-protein coding RNA 935 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and sperm flagellum. Predicted to be active in axonemal A tubule inner sheath. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00934 Genelong intergenic non-protein coding RNA 934 |
LINC00937 Genelong intergenic non-protein coding RNA 937 |
LINC00443 Genelong intergenic non-protein coding RNA 443 |
LINC01099 Genelong intergenic non-protein coding RNA 1099 |
LINC00322 Genelong intergenic non-protein coding RNA 322 |
LINC01327 Genelong intergenic non-protein coding RNA 1327 |
LINC01324 Genelong intergenic non-protein coding RNA 1324 |
LINC01322 Genelong intergenic non-protein coding RNA 1322 |
LINC01320 Genelong intergenic non-protein coding RNA 1320 |
LINC00433 Genelong intergenic non-protein coding RNA 433 |
LINC01424 Genelong intergenic non-protein coding RNA 1424 |
LINC01425 Genelong intergenic non-protein coding RNA 1425 |
LINC01426 Genelong intergenic non-protein coding RNA 1426 |
LINC01427 Genelong intergenic non-protein coding RNA 1427 |
LINC01420 Genelong intergenic non-protein coding RNA 1420 Involved in negative regulation of cytoplasmic mRNA processing body assembly and nuclear-transcribed mRNA catabolic process. Located in P-body. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01422 Genelong intergenic non-protein coding RNA 1422 |
LINC01423 Genelong intergenic non-protein coding RNA 1423 |
LINC01428 Genelong intergenic non-protein coding RNA 1428 |
LINC01280 Genelong intergenic non-protein coding RNA 1280 |
LINC01281 Genelong intergenic non-protein coding RNA 1281 |
LINC01282 Genelong intergenic non-protein coding RNA 1282 |
LINC01284 Genelong intergenic non-protein coding RNA 1284 |
LINC01285 Genelong intergenic non-protein coding RNA 1285 |
LINC01287 Genelong intergenic non-protein coding RNA 1287 |
LINC01288 Genelong intergenic non-protein coding RNA 1288 |
LINC01289 Genelong intergenic non-protein coding RNA 1289 |
LINC00488 Genelong intergenic non-protein coding RNA 488 |
LINC00484 Genelong intergenic non-protein coding RNA 484 |
LINC00487 Genelong intergenic non-protein coding RNA 487 |
LINC00486 Genelong intergenic non-protein coding RNA 486 |
LINC00483 Genelong intergenic non-protein coding RNA 483 |
LINC00482 Genelong intergenic non-protein coding RNA 482 |
SPTLC1P1 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 1 |
SPTLC1P2 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 2 |
SPTLC1P5 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 5 |
SPTLC1P4 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 4 |
LINC00266-4P Genelong intergenic non-protein coding RNA 266-4, pseudogene |
LLPH GeneLLP homolog, long-term synaptic facilitation (Aplysia) Enables RNA binding activity. Predicted to be involved in dendrite extension and positive regulation of dendritic spine development. Located in chromosome and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01363 Genelong intergenic non-protein coding RNA 1363 |
LINC00526 Genelong intergenic non-protein coding RNA 526 |
LINC00527 Genelong intergenic non-protein coding RNA 527 |
LINC00524 Genelong intergenic non-protein coding RNA 524 |
LINC00525 Genelong intergenic non-protein coding RNA 525 |
LINC00523 Genelong intergenic non-protein coding RNA 523 |
LINC00520 Genelong intergenic non-protein coding RNA 520 |
LINC00521 Genelong intergenic non-protein coding RNA 521 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00528 Genelong intergenic non-protein coding RNA 528 |
LINC00529 Genelong intergenic non-protein coding RNA 529 |
LINC01499 Genelong intergenic non-protein coding RNA 1499 |
OLMALINC Geneoligodendrocyte maturation-associated long intergenic non-coding RNA |
LINC00200 Genelong intergenic non-protein coding RNA 200 |
LINC00207 Genelong intergenic non-protein coding RNA 207 |
LINC00052 Genelong intergenic non-protein coding RNA 52 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00165 Genelong intergenic non-protein coding RNA 165 |
LINC01252 Genelong intergenic non-protein coding RNA 1252 |
LINC01256 Genelong intergenic non-protein coding RNA 1256 |
LINC01254 Genelong intergenic non-protein coding RNA 1254 |
LINC01258 Genelong intergenic non-protein coding RNA 1258 |
LINC01590 Genelong intergenic non-protein coding RNA 1590 |
LINC01591 Genelong intergenic non-protein coding RNA 1591 |
LINC01592 Genelong intergenic non-protein coding RNA 1592 |
LINC01594 Genelong intergenic non-protein coding RNA 1594 |
LINC01599 Genelong intergenic non-protein coding RNA 1599 |
LINC01046 Genelong intergenic non-protein coding RNA 1046 |
LINC01047 Genelong intergenic non-protein coding RNA 1047 |
LINC01044 Genelong intergenic non-protein coding RNA 1044 |
LINC01043 Genelong intergenic non-protein coding RNA 1043 |
LINC01040 Genelong intergenic non-protein coding RNA 1040 |
LINC01049 Genelong intergenic non-protein coding RNA 1049 |
LINC00311 Genelong intergenic non-protein coding RNA 311 |
LINC00310 Genelong intergenic non-protein coding RNA 310 |
LINC00313 Genelong intergenic non-protein coding RNA 313 |
LINC00312 Genelong intergenic non-protein coding RNA 312 This gene produces an intronless transcript that is thought to function as a tumor suppressor. This transcript is downregulated in nasopharyngeal carcinoma and is a negative regulator of estrogen receptor signaling. A common polymorphism in this transcript allows the production of a 94 aa open reading frame in some individuals, which may interact directly with estrogen receptor 1 (PMID:15474036). This open reading frame does not exist on the reference genome haplotype, which is hypothesized to function through a non-coding RNA product. [provided by RefSeq, Mar 2017] |
LINC00315 Genelong intergenic non-protein coding RNA 315 |
LINC00314 Genelong intergenic non-protein coding RNA 314 |
LINC00316 Genelong intergenic non-protein coding RNA 316 |
LINCMD1 Genelong intergenic non-protein coding RNA, muscle differentiation 1 |
LINC-ROR Genelong intergenic non-protein coding RNA, regulator of reprogramming This gene produces a long non-coding RNA that regulates the reprogramming of pluripotent stem cells. This RNA suppresses induction of tumor protein p53 after DNA damage. It is thought to act as a sponge for microRNAs that regulate stem cell factors POU class 5 homeobox 1, Nanog, and SRY-box 2. This RNA may also have a extracellular role in modulating response to hypoxia in hepatocellular cancer cells. Expression of this transcript is associated with tumor progression and epithelial to mesenchymal transition and metastasis. [provided by RefSeq, Dec 2017] |
LINC00571 Genelong intergenic non-protein coding RNA 571 |
LINC01209 Genelong intergenic non-protein coding RNA 1209 |
LINC01201 Genelong intergenic non-protein coding RNA 1201 |
LINC01202 Genelong intergenic non-protein coding RNA 1202 |
LINC01203 Genelong intergenic non-protein coding RNA 1203 |
LINC01204 Genelong intergenic non-protein coding RNA 1204 |
LINC01205 Genelong intergenic non-protein coding RNA 1205 |
LINC01206 Genelong intergenic non-protein coding RNA 1206 |
LINC01207 Genelong intergenic non-protein coding RNA 1207 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01452 Genelong intergenic non-protein coding RNA 1452 |
LINC01166 Genelong intergenic non-protein coding RNA 1166 |
LINC00415 Genelong intergenic non-protein coding RNA 415 |
LINC00411 Genelong intergenic non-protein coding RNA 411 |
LINC01088 Genelong intergenic non-protein coding RNA 1088 |
LINC01518 Genelong intergenic non-protein coding RNA 1518 |
LINC01519 Genelong intergenic non-protein coding RNA 1519 |
LINC01516 Genelong intergenic non-protein coding RNA 1516 |
LINC00391 Genelong intergenic non-protein coding RNA 391 |
LINC00393 Genelong intergenic non-protein coding RNA 393 |
LINC00392 Genelong intergenic non-protein coding RNA 392 |
LINC00395 Genelong intergenic non-protein coding RNA 395 |
LINC00396 Genelong intergenic non-protein coding RNA 396 |
LINC00399 Genelong intergenic non-protein coding RNA 399 |
LINC00398 Genelong intergenic non-protein coding RNA 398 |
LINC00152 Genelong intergenic non-protein coding RNA 152 This gene produces a long non-coding RNA that is overexpressed in cancer cells and promotes cell proliferation and epithelial-mesenchymal transition. This RNA may bind enhancer of zeste homolog 2 and participate in the transcriptional silencing of tumor suppressor genes. It may act as a sponge for microRNAs. Alternatively spliced variants have been observed. [provided by RefSeq, Dec 2017] |
LINC00159 Genelong intergenic non-protein coding RNA 159 |
LINC00158 Genelong intergenic non-protein coding RNA 158 |
LINC00845 Genelong intergenic non-protein coding RNA 845 |
LINC00844 Genelong intergenic non-protein coding RNA 844 |
LINC00841 Genelong intergenic non-protein coding RNA 841 |
LINC00840 Genelong intergenic non-protein coding RNA 840 |
LINC00843 Genelong intergenic non-protein coding RNA 843 |
LINC00842 Genelong intergenic non-protein coding RNA 842 |
LINC01495 Genelong intergenic non-protein coding RNA 1495 |
LINC01494 Genelong intergenic non-protein coding RNA 1494 |
LINC01497 Genelong intergenic non-protein coding RNA 1497 |
LINC01496 Genelong intergenic non-protein coding RNA 1496 |
LINC01493 Genelong intergenic non-protein coding RNA 1493 |
LINC01492 Genelong intergenic non-protein coding RNA 1492 |
LINC01498 Genelong intergenic non-protein coding RNA 1498 |
LINC00458 Genelong intergenic non-protein coding RNA 458 |
LINC00459 Genelong intergenic non-protein coding RNA 459 |
LINC00452 Genelong intergenic non-protein coding RNA 452 |
LINC00456 Genelong intergenic non-protein coding RNA 456 |
LINC00457 Genelong intergenic non-protein coding RNA 457 |
LINC00454 Genelong intergenic non-protein coding RNA 454 |
LINC00954 Genelong intergenic non-protein coding RNA 954 |
LINC01128 Genelong intergenic non-protein coding RNA 1128 |
LINC01125 Genelong intergenic non-protein coding RNA 1125 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01124 Genelong intergenic non-protein coding RNA 1124 |
LINC01126 Genelong intergenic non-protein coding RNA 1126 |
LINC01121 Genelong intergenic non-protein coding RNA 1121 |
LINC01120 Genelong intergenic non-protein coding RNA 1120 |
LINC01123 Genelong intergenic non-protein coding RNA 1123 |
LINC01122 Genelong intergenic non-protein coding RNA 1122 |
LINC00298 Genelong intergenic non-protein coding RNA 298 |
LINC00299 Genelong intergenic non-protein coding RNA 299 |
LINC00294 Genelong intergenic non-protein coding RNA 294 |
LINC00297 Genelong intergenic non-protein coding RNA 297 |
LINC00293 Genelong intergenic non-protein coding RNA 293 |
LINC00364 Genelong intergenic non-protein coding RNA 364 |
LINC01402 Genelong intergenic non-protein coding RNA 1402 |
LINC01024 Genelong intergenic non-protein coding RNA 1024 |
LINC00643 Genelong intergenic non-protein coding RNA 643 |
LINC00642 Genelong intergenic non-protein coding RNA 642 |
LINC00641 Genelong intergenic non-protein coding RNA 641 |
LINC00640 Genelong intergenic non-protein coding RNA 640 |
LINC00645 Genelong intergenic non-protein coding RNA 645 |
LINC00644 Genelong intergenic non-protein coding RNA 644 |
LINC00649 Genelong intergenic non-protein coding RNA 649 |
LINC00648 Genelong intergenic non-protein coding RNA 648 |
LINC00251 Genelong intergenic non-protein coding RNA 251 |
LINC00929 Genelong intergenic non-protein coding RNA 929 |
LINC00603 Genelong intergenic non-protein coding RNA 603 |
LINC01419 Genelong intergenic non-protein coding RNA 1419 |
LINC01415 Genelong intergenic non-protein coding RNA 1415 |
LINC01416 Genelong intergenic non-protein coding RNA 1416 |
LINC01411 Genelong intergenic non-protein coding RNA 1411 |
LINC01413 Genelong intergenic non-protein coding RNA 1413 |
LINC01412 Genelong intergenic non-protein coding RNA 1412 |
LINC00504 Genelong intergenic non-protein coding RNA 504 |
LINC00505 Genelong intergenic non-protein coding RNA 505 |
LINC00506 Genelong intergenic non-protein coding RNA 506 |
LINC00507 Genelong intergenic non-protein coding RNA 507 |
LINC00501 Genelong intergenic non-protein coding RNA 501 |
LINC00216 Genelong intergenic non-protein coding RNA 216 |
LINC00210 Genelong intergenic non-protein coding RNA 210 |
LINC00211 Genelong intergenic non-protein coding RNA 211 |
LINC00967 Genelong intergenic non-protein coding RNA 967 |
LINC00964 Genelong intergenic non-protein coding RNA 964 |
LINC00965 Genelong intergenic non-protein coding RNA 965 |
LINC00963 Genelong intergenic non-protein coding RNA 963 |
LINC00960 Genelong intergenic non-protein coding RNA 960 |
LINC00961 Genelong intergenic non-protein coding RNA 961 Involved in cellular response to amino acid stimulus and negative regulation of TORC1 signaling. Located in late endosome membrane and lysosomal proton-transporting V-type ATPase complex. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01608 Genelong intergenic non-protein coding RNA 1608 |
LINC01609 Genelong intergenic non-protein coding RNA 1609 |
LINC01604 Genelong intergenic non-protein coding RNA 1604 |
LINC01605 Genelong intergenic non-protein coding RNA 1605 |
LINC01606 Genelong intergenic non-protein coding RNA 1606 |
LINC01607 Genelong intergenic non-protein coding RNA 1607 |
LINC01600 Genelong intergenic non-protein coding RNA 1600 |
LINC01601 Genelong intergenic non-protein coding RNA 1601 |
LINC01602 Genelong intergenic non-protein coding RNA 1602 |
LINC01603 Genelong intergenic non-protein coding RNA 1603 |
LINC00559 Genelong intergenic non-protein coding RNA 559 |
LINC00558 Genelong intergenic non-protein coding RNA 558 |
LINC00557 Genelong intergenic non-protein coding RNA 557 |
LINC00556 Genelong intergenic non-protein coding RNA 556 |
LINC00555 Genelong intergenic non-protein coding RNA 555 |
LINC00552 Genelong intergenic non-protein coding RNA 552 |
LINC00551 Genelong intergenic non-protein coding RNA 551 |
LINC00550 Genelong intergenic non-protein coding RNA 550 |
LINC01337 Genelong intergenic non-protein coding RNA 1337 |
LINC01375 Genelong intergenic non-protein coding RNA 1375 |
LINC01376 Genelong intergenic non-protein coding RNA 1376 |
LINC01377 Genelong intergenic non-protein coding RNA 1377 |
LINC01370 Genelong intergenic non-protein coding RNA 1370 |
LINC01378 Genelong intergenic non-protein coding RNA 1378 |
PARTICL Genepromoter of MAT2A antisense radiation-induced circulating long non-coding RNA Enables dsDNA-RNA triple helix-forming chromatin adaptor activity and mRNA binding activity. Involved in cellular response to ionizing radiation and regulatory ncRNA-mediated heterochromatin formation. Is active in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01484 Genelong intergenic non-protein coding RNA 1484 |
LINC00028 Genelong intergenic non-protein coding RNA 28 |
LINC01483 Genelong intergenic non-protein coding RNA 1483 |
LINC00160 Genelong intergenic non-protein coding RNA 160 |
LINC01039 Genelong intergenic non-protein coding RNA 1039 |
LINC01038 Genelong intergenic non-protein coding RNA 1038 |
LINC01036 Genelong intergenic non-protein coding RNA 1036 |
LINC01033 Genelong intergenic non-protein coding RNA 1033 |
LINC01032 Genelong intergenic non-protein coding RNA 1032 |
LINC01031 Genelong intergenic non-protein coding RNA 1031 |
LINC01030 Genelong intergenic non-protein coding RNA 1030 |
LINC01410 Genelong intergenic non-protein coding RNA 1410 |
LINC01231 Genelong intergenic non-protein coding RNA 1231 |
LINC01230 Genelong intergenic non-protein coding RNA 1230 |
LINC01233 Genelong intergenic non-protein coding RNA 1233 |
LINC01237 Genelong intergenic non-protein coding RNA 1237 |
LINC00184 Genelong intergenic non-protein coding RNA 184 |
LINC00189 Genelong intergenic non-protein coding RNA 189 |
LINC00448 Genelong intergenic non-protein coding RNA 448 |
LSINCT5 Genelong stress-induced non-coding transcript 5 |
LINC01179 Genelong intergenic non-protein coding RNA 1179 |
LINC00441 Genelong intergenic non-protein coding RNA 441 |
LINC00440 Genelong intergenic non-protein coding RNA 440 |
LINC00442 Genelong intergenic non-protein coding RNA 442 |
LINC00445 Genelong intergenic non-protein coding RNA 445 |
LINC00444 Genelong intergenic non-protein coding RNA 444 |
LINC00446 Genelong intergenic non-protein coding RNA 446 |
LINC01234 Genelong intergenic non-protein coding RNA 1234 |
LINC01239 Genelong intergenic non-protein coding RNA 1239 |
LINC01521 Genelong intergenic non-protein coding RNA 1521 |
LINC01520 Genelong intergenic non-protein coding RNA 1520 |
LINC01525 Genelong intergenic non-protein coding RNA 1525 |
LINC01524 Genelong intergenic non-protein coding RNA 1524 |
LINC01527 Genelong intergenic non-protein coding RNA 1527 |
LINC01529 Genelong intergenic non-protein coding RNA 1529 |
LINC00691 Genelong intergenic non-protein coding RNA 691 |
LINC00692 Genelong intergenic non-protein coding RNA 692 |
LINC00693 Genelong intergenic non-protein coding RNA 693 |
LINC00698 Genelong intergenic non-protein coding RNA 698 |
LINC00346 Genelong intergenic non-protein coding RNA 346 |
LINC00347 Genelong intergenic non-protein coding RNA 347 |
LINC00345 Genelong intergenic non-protein coding RNA 345 |
LINC00342 Genelong intergenic non-protein coding RNA 342 Biomarker of Huntington's disease. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00343 Genelong intergenic non-protein coding RNA 343 |
LINC00341 Genelong intergenic non-protein coding RNA 341 |
LINC00348 Genelong intergenic non-protein coding RNA 348 |
LINC01543 Genelong intergenic non-protein coding RNA 1543 |
LINC01541 Genelong intergenic non-protein coding RNA 1541 |
LINC01544 Genelong intergenic non-protein coding RNA 1544 |
LINC00102 Genelong intergenic non-protein coding RNA 102 |
LINC00290 Genelong intergenic non-protein coding RNA 290 |
LINC00266-3 Genelong intergenic non-protein coding RNA 266-3 |
LINC00266-1 Genelong intergenic non-protein coding RNA 266-1 |
LINC00632 Genelong intergenic non-protein coding RNA 632 |
LINC00634 Genelong intergenic non-protein coding RNA 634 Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ACADVL Geneacyl-CoA dehydrogenase, very long chain The protein encoded by this gene is targeted to the inner mitochondrial membrane where it catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. This acyl-Coenzyme A dehydrogenase is specific to long-chain and very-long-chain fatty acids. A deficiency in this gene product reduces myocardial fatty acid beta-oxidation and is associated with cardiomyopathy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
KIR3DL1 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR3DL2 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011] |
KIR3DL3 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. [provided by RefSeq, Jul 2008] |
LINC01176 Genelong intergenic non-protein coding RNA 1176 |
LINC01177 Genelong intergenic non-protein coding RNA 1177 |
LINC01069 Genelong intergenic non-protein coding RNA 1069 |
LINC01065 Genelong intergenic non-protein coding RNA 1065 |
LINC00862 Genelong intergenic non-protein coding RNA 862 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00333 Genelong intergenic non-protein coding RNA 333 |
LINC00331 Genelong intergenic non-protein coding RNA 331 |
LINC01468 Genelong intergenic non-protein coding RNA 1468 |
LINC01003 Genelong intergenic non-protein coding RNA 1003 |
LINC00618 Genelong intergenic non-protein coding RNA 618 |
LINC00619 Genelong intergenic non-protein coding RNA 619 |
LINC00610 Genelong intergenic non-protein coding RNA 610 |
LINC00612 Genelong intergenic non-protein coding RNA 612 |
LINC00613 Genelong intergenic non-protein coding RNA 613 |
LINC00614 Genelong intergenic non-protein coding RNA 614 |
LINC00615 Genelong intergenic non-protein coding RNA 615 |
LINC00616 Genelong intergenic non-protein coding RNA 616 |
LINC01435 Genelong intergenic non-protein coding RNA 1435 |
LINC01151 Genelong intergenic non-protein coding RNA 1151 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00968 Genelong intergenic non-protein coding RNA 968 |
LINC01005 Genelong intergenic non-protein coding RNA 1005 |
LINC00892 Genelong intergenic non-protein coding RNA 892 |
LINC00893 Genelong intergenic non-protein coding RNA 893 |
LINC00890 Genelong intergenic non-protein coding RNA 890 Predicted to be located in membrane. Predicted to be active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00891 Genelong intergenic non-protein coding RNA 891 |
LINC00896 Genelong intergenic non-protein coding RNA 896 |
LINC00894 Genelong intergenic non-protein coding RNA 894 |
LINC00895 Genelong intergenic non-protein coding RNA 895 |
LINC00898 Genelong intergenic non-protein coding RNA 898 |
LINC00899 Genelong intergenic non-protein coding RNA 899 |
LINC01442 Genelong intergenic non-protein coding RNA 1442 |
LINC01443 Genelong intergenic non-protein coding RNA 1443 |
LINC01440 Genelong intergenic non-protein coding RNA 1440 |
LINC01446 Genelong intergenic non-protein coding RNA 1446 |
LINC01447 Genelong intergenic non-protein coding RNA 1447 |
LINC01444 Genelong intergenic non-protein coding RNA 1444 |
LINC01445 Genelong intergenic non-protein coding RNA 1445 |
LINC01448 Genelong intergenic non-protein coding RNA 1448 |
LINC01449 Genelong intergenic non-protein coding RNA 1449 |
LINC00229 Genelong intergenic non-protein coding RNA 229 |
LINC00226 Genelong intergenic non-protein coding RNA 226 |
LINC00221 Genelong intergenic non-protein coding RNA 221 |
LINC00222 Genelong intergenic non-protein coding RNA 222 |
ABALON Geneapoptotic BCL2L1-antisense long non-coding RNA |
LINC00917 Genelong intergenic non-protein coding RNA 917 |
LINC00911 Genelong intergenic non-protein coding RNA 911 |
LINC00910 Genelong intergenic non-protein coding RNA 910 |
LINC01515 Genelong intergenic non-protein coding RNA 1515 |
LINC01349 Genelong intergenic non-protein coding RNA 1349 |
LINC01344 Genelong intergenic non-protein coding RNA 1344 |
LINC01347 Genelong intergenic non-protein coding RNA 1347 |
LINC01346 Genelong intergenic non-protein coding RNA 1346 |
LINC01341 Genelong intergenic non-protein coding RNA 1341 |
LINC01340 Genelong intergenic non-protein coding RNA 1340 |
LINC01343 Genelong intergenic non-protein coding RNA 1343 |
LINC01342 Genelong intergenic non-protein coding RNA 1342 |
LINC01264 Genelong intergenic non-protein coding RNA 1264 |
LINC00710 Genelong intergenic non-protein coding RNA 710 |
LINC00498 Genelong intergenic non-protein coding RNA 498 |
LINC00499 Genelong intergenic non-protein coding RNA 499 |
LINC00997 Genelong intergenic non-protein coding RNA 997 |
LINC00994 Genelong intergenic non-protein coding RNA 994 |
LINC00993 Genelong intergenic non-protein coding RNA 993 |
LINC00992 Genelong intergenic non-protein coding RNA 992 |
LINC00999 Genelong intergenic non-protein coding RNA 999 |
LINC00998 Genelong intergenic non-protein coding RNA 998 Involved in negative regulation of type I interferon-mediated signaling pathway. Located in endoplasmic reticulum membrane and mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00508 Genelong intergenic non-protein coding RNA 508 |
LINC00502 Genelong intergenic non-protein coding RNA 502 |
LINC00696 Genelong intergenic non-protein coding RNA 696 |
SPTLC2 Geneserine palmitoyltransferase, long chain base subunit 2 This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011] |
SPTLC3 Geneserine palmitoyltransferase, long chain base subunit 3 This gene encodes a subunit of the serine palmitoyltransferase complex which catalyzes the rate-limiting step in sphingolipid biosynthesis. This subunit metabolizes lauroyl- and myristoyl-CoA and generates C14 and C16-sphingoid bases. [provided by RefSeq, Mar 2017] |
SPTLC1 Geneserine palmitoyltransferase, long chain base subunit 1 This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013] |
LINC00317 Genelong intergenic non-protein coding RNA 317 |
LINC01372 Genelong intergenic non-protein coding RNA 1372 |
LINC01068 Genelong intergenic non-protein coding RNA 1068 |
LINC01060 Genelong intergenic non-protein coding RNA 1060 |
LINC01061 Genelong intergenic non-protein coding RNA 1061 |
LINC01063 Genelong intergenic non-protein coding RNA 1063 |
LINC00339 Genelong intergenic non-protein coding RNA 339 |
LINC00337 Genelong intergenic non-protein coding RNA 337 |
LINC00336 Genelong intergenic non-protein coding RNA 336 |
LINC00334 Genelong intergenic non-protein coding RNA 334 |
LINC00330 Genelong intergenic non-protein coding RNA 330 |
LINC01220 Genelong intergenic non-protein coding RNA 1220 |
LINC00029 Genelong intergenic non-protein coding RNA 29 |
LINC00674 Genelong intergenic non-protein coding RNA 674 |
LINC01268 Genelong intergenic non-protein coding RNA 1268 |
LINC01266 Genelong intergenic non-protein coding RNA 1266 |
LINC01267 Genelong intergenic non-protein coding RNA 1267 |
LINC01265 Genelong intergenic non-protein coding RNA 1265 |
LINC01260 Genelong intergenic non-protein coding RNA 1260 |
LINC01232 Genelong intergenic non-protein coding RNA 1232 |
LINC00094 Genelong intergenic non-protein coding RNA 94 |
LINC01384 Genelong intergenic non-protein coding RNA 1384 |
LINC00587 Genelong intergenic non-protein coding RNA 587 |
LINC00581 Genelong intergenic non-protein coding RNA 581 |
LINC00582 Genelong intergenic non-protein coding RNA 582 |
LINC00583 Genelong intergenic non-protein coding RNA 583 |
LINC00588 Genelong intergenic non-protein coding RNA 588 |
LINC00589 Genelong intergenic non-protein coding RNA 589 |
LINC01189 Genelong intergenic non-protein coding RNA 1189 |
LINC01183 Genelong intergenic non-protein coding RNA 1183 |
LINC01182 Genelong intergenic non-protein coding RNA 1182 |
LINC01181 Genelong intergenic non-protein coding RNA 1181 |
LINC01187 Genelong intergenic non-protein coding RNA 1187 |
LINC01186 Genelong intergenic non-protein coding RNA 1186 |
LINC01185 Genelong intergenic non-protein coding RNA 1185 |
LINC-PINT Genelong intergenic non-protein coding RNA, p53 induced transcript Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00378 Genelong intergenic non-protein coding RNA 378 |
OPN1LW Geneopsin 1 (cone pigments), long-wave-sensitive This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of partial, protanopic colorblindness. [provided by RefSeq, Jul 2008] |
LINC01119 Genelong intergenic non-protein coding RNA 1119 |
LINC01578 Genelong intergenic non-protein coding RNA 1578 Predicted to be involved in several processes, including adipose tissue development; regulation of gene expression; and thymus development. Predicted to be active in chromatin and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01579 Genelong intergenic non-protein coding RNA 1579 |
LINC01574 Genelong intergenic non-protein coding RNA 1574 |
LINC01572 Genelong intergenic non-protein coding RNA 1572 |
LINC01573 Genelong intergenic non-protein coding RNA 1573 |
LINC01570 Genelong intergenic non-protein coding RNA 1570 |
LINC01571 Genelong intergenic non-protein coding RNA 1571 |
LINC01398 Genelong intergenic non-protein coding RNA 1398 |
LINC01399 Genelong intergenic non-protein coding RNA 1399 |
LINC01392 Genelong intergenic non-protein coding RNA 1392 |
LINC01393 Genelong intergenic non-protein coding RNA 1393 |
LINC01391 Genelong intergenic non-protein coding RNA 1391 |
LINC01396 Genelong intergenic non-protein coding RNA 1396 |
LINC01397 Genelong intergenic non-protein coding RNA 1397 |
LINC01395 Genelong intergenic non-protein coding RNA 1395 |
LINC00621 Genelong intergenic non-protein coding RNA 621 |
LINC00620 Genelong intergenic non-protein coding RNA 620 |
LINC00623 Genelong intergenic non-protein coding RNA 623 |
LINC00624 Genelong intergenic non-protein coding RNA 624 |
LINC00626 Genelong intergenic non-protein coding RNA 626 |
LINC00629 Genelong intergenic non-protein coding RNA 629 |
LINC00628 Genelong intergenic non-protein coding RNA 628 |
LINC00265-2P Genelong intergenic non-protein coding RNA 265-2, pseudogene |
LINC00869 Genelong intergenic non-protein coding RNA 869 |
LINC00868 Genelong intergenic non-protein coding RNA 868 |
LINC00867 Genelong intergenic non-protein coding RNA 867 |
LINC00866 Genelong intergenic non-protein coding RNA 866 |
LINC01180 Genelong intergenic non-protein coding RNA 1180 |
LINC01184 Genelong intergenic non-protein coding RNA 1184 |
LINC00936 Genelong intergenic non-protein coding RNA 936 |
LINC00470 Genelong intergenic non-protein coding RNA 470 |
LINC00472 Genelong intergenic non-protein coding RNA 472 |
LINC00473 Genelong intergenic non-protein coding RNA 473 Involved in DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00474 Genelong intergenic non-protein coding RNA 474 |
LINC00475 Genelong intergenic non-protein coding RNA 475 |
LINC00476 Genelong intergenic non-protein coding RNA 476 |
LINC00477 Genelong intergenic non-protein coding RNA 477 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00479 Genelong intergenic non-protein coding RNA 479 |
LINC01103 Genelong intergenic non-protein coding RNA 1103 |
LINC01102 Genelong intergenic non-protein coding RNA 1102 |
LINC01101 Genelong intergenic non-protein coding RNA 1101 |
LINC01100 Genelong intergenic non-protein coding RNA 1100 |
LINC01107 Genelong intergenic non-protein coding RNA 1107 |
LINC01106 Genelong intergenic non-protein coding RNA 1106 |
LINC01105 Genelong intergenic non-protein coding RNA 1105 |
LINC01104 Genelong intergenic non-protein coding RNA 1104 |
LINC01109 Genelong intergenic non-protein coding RNA 1109 |
LINC01108 Genelong intergenic non-protein coding RNA 1108 |
LINC00278 Genelong intergenic non-protein coding RNA 278 |
LINC00279 Genelong intergenic non-protein coding RNA 279 |
LINC00708 Genelong intergenic non-protein coding RNA 708 |
LINC00709 Genelong intergenic non-protein coding RNA 709 |
LINC00702 Genelong intergenic non-protein coding RNA 702 |
ACADL Geneacyl-CoA dehydrogenase, long chain The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008] |
LINC01312 Genelong intergenic non-protein coding RNA 1312 |
LINC01310 Genelong intergenic non-protein coding RNA 1310 |
LINC01311 Genelong intergenic non-protein coding RNA 1311 |
LINC01314 Genelong intergenic non-protein coding RNA 1314 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01315 Genelong intergenic non-protein coding RNA 1315 |
LINC01235 Genelong intergenic non-protein coding RNA 1235 |
LINC01433 Genelong intergenic non-protein coding RNA 1433 |
LINC01432 Genelong intergenic non-protein coding RNA 1432 |
LINC01431 Genelong intergenic non-protein coding RNA 1431 |
LINC01430 Genelong intergenic non-protein coding RNA 1430 |
LINC01299 Genelong intergenic non-protein coding RNA 1299 |
LINC01293 Genelong intergenic non-protein coding RNA 1293 |
LINC01291 Genelong intergenic non-protein coding RNA 1291 |
LINC01165 Genelong intergenic non-protein coding RNA 1165 |
LINC00944 Genelong intergenic non-protein coding RNA 944 |
LINC00945 Genelong intergenic non-protein coding RNA 945 |
LINC00941 Genelong intergenic non-protein coding RNA 941 Enables promoter-enhancer loop anchoring activity. Involved in chromatin looping and positive regulation of transcription by RNA polymerase II. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00942 Genelong intergenic non-protein coding RNA 942 |
LINC00943 Genelong intergenic non-protein coding RNA 943 |
OVAAL Geneovarian adenocarcinoma amplified long non-coding RNA Predicted to enable pre-mRNA branch point binding activity. Predicted to be involved in mRNA branch site recognition. Predicted to be part of U2 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00535 Genelong intergenic non-protein coding RNA 535 |
LINC00534 Genelong intergenic non-protein coding RNA 534 |
LINC00537 Genelong intergenic non-protein coding RNA 537 Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00536 Genelong intergenic non-protein coding RNA 536 |
LINC00533 Genelong intergenic non-protein coding RNA 533 |
LINC00539 Genelong intergenic non-protein coding RNA 539 |
LINC00538 Genelong intergenic non-protein coding RNA 538 |
LINC01588 Genelong intergenic non-protein coding RNA 1588 |
LINC01585 Genelong intergenic non-protein coding RNA 1585 |
LINC01583 Genelong intergenic non-protein coding RNA 1583 |
LINC01582 Genelong intergenic non-protein coding RNA 1582 |
LINC01581 Genelong intergenic non-protein coding RNA 1581 |
LINC01580 Genelong intergenic non-protein coding RNA 1580 |
LINC01055 Genelong intergenic non-protein coding RNA 1055 |
LINC01057 Genelong intergenic non-protein coding RNA 1057 |
LINC01056 Genelong intergenic non-protein coding RNA 1056 |
LINC01050 Genelong intergenic non-protein coding RNA 1050 |
LINC01053 Genelong intergenic non-protein coding RNA 1053 |
LINC01059 Genelong intergenic non-protein coding RNA 1059 |
LINC01217 Genelong intergenic non-protein coding RNA 1217 |
LINC01216 Genelong intergenic non-protein coding RNA 1216 |
LINC01210 Genelong intergenic non-protein coding RNA 1210 |
LINC01219 Genelong intergenic non-protein coding RNA 1219 |
LINC01218 Genelong intergenic non-protein coding RNA 1218 |
LINC01213 Genelong intergenic non-protein coding RNA 1213 |
LINC00328-2P Genelong intergenic non-protein coding RNA 328-2, pseudogene |
LINC01298 Genelong intergenic non-protein coding RNA 1298 |
LINC01296 Genelong intergenic non-protein coding RNA 1296 |
LINC01507 Genelong intergenic non-protein coding RNA 1507 |
LINC01506 Genelong intergenic non-protein coding RNA 1506 |
LINC01505 Genelong intergenic non-protein coding RNA 1505 |
LINC01503 Genelong intergenic non-protein coding RNA 1503 |
LINC01502 Genelong intergenic non-protein coding RNA 1502 |
LINC01501 Genelong intergenic non-protein coding RNA 1501 |
LINC01500 Genelong intergenic non-protein coding RNA 1500 |
LINC01509 Genelong intergenic non-protein coding RNA 1509 |
LINC01508 Genelong intergenic non-protein coding RNA 1508 |
LINC00368 Genelong intergenic non-protein coding RNA 368 |
LINC00365 Genelong intergenic non-protein coding RNA 365 |
LINC00366 Genelong intergenic non-protein coding RNA 366 |
LINC00367 Genelong intergenic non-protein coding RNA 367 |
LINC00362 Genelong intergenic non-protein coding RNA 362 |
LINC00363 Genelong intergenic non-protein coding RNA 363 |
LINC01144 Genelong intergenic non-protein coding RNA 1144 |
LINC01140 Genelong intergenic non-protein coding RNA 1140 |
MT-LIPCAR Genemitochondrially encoded long non-coding cardiac associated RNA |
LINC00167 Genelong intergenic non-protein coding RNA 167 |
LINC00162 Genelong intergenic non-protein coding RNA 162 |
LINC00163 Genelong intergenic non-protein coding RNA 163 |
LINC00161 Genelong intergenic non-protein coding RNA 161 |
LINC00836 Genelong intergenic non-protein coding RNA 836 |
LINC00837 Genelong intergenic non-protein coding RNA 837 |
LINC00838 Genelong intergenic non-protein coding RNA 838 |
LINC00839 Genelong intergenic non-protein coding RNA 839 |
LOC100422263 Geneserine palmitoyltransferase, long chain base subunit 2 pseudogene |
LINC01158 Genelong intergenic non-protein coding RNA 1158 Predicted to act upstream of or within regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01159 Genelong intergenic non-protein coding RNA 1159 Predicted to act upstream of or within cerebellar cortex structural organization; homeostasis of number of cells within a tissue; and regulation of gene expression. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01150 Genelong intergenic non-protein coding RNA 1150 |
LINC01152 Genelong intergenic non-protein coding RNA 1152 |
LINC01153 Genelong intergenic non-protein coding RNA 1153 |
SPTLC1P3 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 3 |
LINC00283 Genelong intergenic non-protein coding RNA 283 |
LINC00282 Genelong intergenic non-protein coding RNA 282 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00280 Genelong intergenic non-protein coding RNA 280 |
LINC00284 Genelong intergenic non-protein coding RNA 284 |
LINC00678 Genelong intergenic non-protein coding RNA 678 |
LINC00676 Genelong intergenic non-protein coding RNA 676 |
LINC00677 Genelong intergenic non-protein coding RNA 677 |
LINC00675 Genelong intergenic non-protein coding RNA 675 Involved in intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00672 Genelong intergenic non-protein coding RNA 672 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00673 Genelong intergenic non-protein coding RNA 673 This gene produces a long non-protein coding RNA that is involved in the regulation of gene expression during tumor progression. This transcript can promote cell proliferation in gastric cancer through interaction with enhancer of zeste 2 and other epigenetic suppressors of gene expression, thereby downregulating target genes including Kruppel like factors 2 and 4. This transcript may also act as a tumor suppressor by promoting interaction between protein tyrosine phosphatase, non-receptor type 11 (Ptpn11) and ubiquitin ligase, resulting in degradation of Ptpn11 and lowered oncogenic signalling. Naturally-occurring variation at this locus results in the formation of a binding site for miR-1231, which negatively regulates activity of this transcript. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2017] |
LINC00670 Genelong intergenic non-protein coding RNA 670 |
LINC00671 Genelong intergenic non-protein coding RNA 671 |
LINC00092 Genelong intergenic non-protein coding RNA 92 |
LINC01276 Genelong intergenic non-protein coding RNA 1276 |
NKILA GeneNF-kappaB interacting long non-coding RNA |
LINC00863 Genelong intergenic non-protein coding RNA 863 |
LINC00861 Genelong intergenic non-protein coding RNA 861 |
LINC00865 Genelong intergenic non-protein coding RNA 865 |
LINC00864 Genelong intergenic non-protein coding RNA 864 |
PNKY Genelong intergenic non-protein coding RNA PNKY |
GAPLINC Genegastric adenocarcinoma associated, positive CD44 regulator, long intergenic non-coding RNA |
LINC01460 Genelong intergenic non-protein coding RNA 1460 |
LINC01461 Genelong intergenic non-protein coding RNA 1461 |
LINC01465 Genelong intergenic non-protein coding RNA 1465 |
LINC01467 Genelong intergenic non-protein coding RNA 1467 |
LINC00924 Genelong intergenic non-protein coding RNA 924 |
LINC00485 Genelong intergenic non-protein coding RNA 485 |
LINC00208 Genelong intergenic non-protein coding RNA 208 |
LINC01450 Genelong intergenic non-protein coding RNA 1450 |
LINC00974 Genelong intergenic non-protein coding RNA 974 |
LINC00977 Genelong intergenic non-protein coding RNA 977 |
LINC00971 Genelong intergenic non-protein coding RNA 971 |
LINC00970 Genelong intergenic non-protein coding RNA 970 |
LINC00973 Genelong intergenic non-protein coding RNA 973 |
LINC00972 Genelong intergenic non-protein coding RNA 972 |
LINC00562 Genelong intergenic non-protein coding RNA 562 |
LINC00563 Genelong intergenic non-protein coding RNA 563 |
LINC00560 Genelong intergenic non-protein coding RNA 560 |
LINC00561 Genelong intergenic non-protein coding RNA 561 |
LINC00566 Genelong intergenic non-protein coding RNA 566 |
LINC00567 Genelong intergenic non-protein coding RNA 567 |
LINC00564 Genelong intergenic non-protein coding RNA 564 |
LINC00565 Genelong intergenic non-protein coding RNA 565 |
LINC00471 Genelong intergenic non-protein coding RNA 471 |
KIR2DL5B Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL5A Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
LINC01362 Genelong intergenic non-protein coding RNA 1362 |
LINC01361 Genelong intergenic non-protein coding RNA 1361 |
LINC01366 Genelong intergenic non-protein coding RNA 1366 |
LINC01364 Genelong intergenic non-protein coding RNA 1364 |
LINC01002 Genelong intergenic non-protein coding RNA 1002 |
LINC01000 Genelong intergenic non-protein coding RNA 1000 |
LINC01006 Genelong intergenic non-protein coding RNA 1006 Predicted to be located in cytoplasm and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01007 Genelong intergenic non-protein coding RNA 1007 |
LINC01004 Genelong intergenic non-protein coding RNA 1004 Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01212 Genelong intergenic non-protein coding RNA 1212 |
HELLPAR GeneHELLP associated long non-coding RNA |
LINC01523 Genelong intergenic non-protein coding RNA 1523 |
LINC01522 Genelong intergenic non-protein coding RNA 1522 |
LINC01526 Genelong intergenic non-protein coding RNA 1526 |
LINC01208 Genelong intergenic non-protein coding RNA 1208 |
LINC00202-1 Genelong intergenic non-protein coding RNA 202-1 |
LINC00202-2 Genelong intergenic non-protein coding RNA 202-2 |
LINC00690 Genelong intergenic non-protein coding RNA 690 |
LINC00694 Genelong intergenic non-protein coding RNA 694 |
LINC00349 Genelong intergenic non-protein coding RNA 349 |
SALRNA3 Genesenescence associated long non-coding RNA 3 |
LINC01001 Genelong intergenic non-protein coding RNA 1001 |
LINC01082 Genelong intergenic non-protein coding RNA 1082 |
LINC01080 Genelong intergenic non-protein coding RNA 1080 |
LINC01081 Genelong intergenic non-protein coding RNA 1081 |
LINC01087 Genelong intergenic non-protein coding RNA 1087 |
LINC01085 Genelong intergenic non-protein coding RNA 1085 |
LINC01089 Genelong intergenic non-protein coding RNA 1089 |
LINC00689 Genelong intergenic non-protein coding RNA 689 Implicated in colorectal cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00687 Genelong intergenic non-protein coding RNA 687 |
LINC00686 Genelong intergenic non-protein coding RNA 686 |
LINC00685 Genelong intergenic non-protein coding RNA 685 |
LINC00684 Genelong intergenic non-protein coding RNA 684 |
LINC00682 Genelong intergenic non-protein coding RNA 682 |
LINC00681 Genelong intergenic non-protein coding RNA 681 |
LINC00355 Genelong intergenic non-protein coding RNA 355 |
LINC00354 Genelong intergenic non-protein coding RNA 354 |
LINC00351 Genelong intergenic non-protein coding RNA 351 |
LINC00350 Genelong intergenic non-protein coding RNA 350 |
LINC00353 Genelong intergenic non-protein coding RNA 353 |
LINC00352 Genelong intergenic non-protein coding RNA 352 |
LINC00359 Genelong intergenic non-protein coding RNA 359 |
LINC00358 Genelong intergenic non-protein coding RNA 358 |
LINC00272 Genelong intergenic non-protein coding RNA 272 |
LINC00273 Genelong intergenic non-protein coding RNA 273 |
LINC00271 Genelong intergenic non-protein coding RNA 271 |
LINC00276 Genelong intergenic non-protein coding RNA 276 |
SALRNA1 Genesenescence associated long non-coding RNA 1 |
LINC01246 Genelong intergenic non-protein coding RNA 1246 |
LINC01241 Genelong intergenic non-protein coding RNA 1241 |
LINC01248 Genelong intergenic non-protein coding RNA 1248 |
LINC01249 Genelong intergenic non-protein coding RNA 1249 |
LINC00599 Genelong intergenic non-protein coding RNA 599 Predicted to act upstream of or within several processes, including long-term synaptic potentiation; miRNA-mediated post-transcriptional gene silencing; and sensory perception of sound. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00598 Genelong intergenic non-protein coding RNA 598 |
LINC00116 Genelong intergenic non-protein coding RNA 116 Involved in several processes, including positive regulation of mitochondrial membrane potential; positive regulation of sequestering of calcium ion; and triglyceride homeostasis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00115 Genelong intergenic non-protein coding RNA 115 |
LINC00114 Genelong intergenic non-protein coding RNA 114 |
LINC00113 Genelong intergenic non-protein coding RNA 113 |
LINC00112 Genelong intergenic non-protein coding RNA 112 |
LINC00111 Genelong intergenic non-protein coding RNA 111 |
LINC00996 Genelong intergenic non-protein coding RNA 996 |
HULC Genehepatocellular carcinoma up-regulated long non-coding RNA This gene produces a long RNA that was discovered as upregulated in hepatocellular carcinoma and is associated with cancer progression. Expression of this transcript is regulated by microRNAs and at the transcriptional level by Sp1 family factors. The transcript may regulate gene expression by functioning as a competing RNA for microRNAs. [provided by RefSeq, Dec 2017] |
LINC01160 Genelong intergenic non-protein coding RNA 1160 |
LINC01163 Genelong intergenic non-protein coding RNA 1163 |
LINC01164 Genelong intergenic non-protein coding RNA 1164 |
LINC01167 Genelong intergenic non-protein coding RNA 1167 |
LINC01169 Genelong intergenic non-protein coding RNA 1169 |
LINC01168 Genelong intergenic non-protein coding RNA 1168 |
LINC01554 Genelong intergenic non-protein coding RNA 1554 |
LINC01555 Genelong intergenic non-protein coding RNA 1555 |
LINC01556 Genelong intergenic non-protein coding RNA 1556 |
LINC01553 Genelong intergenic non-protein coding RNA 1553 |
LINC01558 Genelong intergenic non-protein coding RNA 1558 |
LINC01559 Genelong intergenic non-protein coding RNA 1559 |
LINC00607 Genelong intergenic non-protein coding RNA 607 |
LINC00606 Genelong intergenic non-protein coding RNA 606 |
LINC00605 Genelong intergenic non-protein coding RNA 605 |
LINC00602 Genelong intergenic non-protein coding RNA 602 |
LINC00601 Genelong intergenic non-protein coding RNA 601 |
LINC00609 Genelong intergenic non-protein coding RNA 609 |
LINC00608 Genelong intergenic non-protein coding RNA 608 |
LINC00106 Genelong intergenic non-protein coding RNA 106 |
LINC00881 Genelong intergenic non-protein coding RNA 881 |
LINC00880 Genelong intergenic non-protein coding RNA 880 |
LINC00883 Genelong intergenic non-protein coding RNA 883 Predicted to act upstream of or within several processes, including generation of neurons; negative regulation of macromolecule biosynthetic process; and protein stabilization. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00882 Genelong intergenic non-protein coding RNA 882 |
LINC00885 Genelong intergenic non-protein coding RNA 885 Implicated in cervical cancer. Biomarker of cervical cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00884 Genelong intergenic non-protein coding RNA 884 |
LINC00887 Genelong intergenic non-protein coding RNA 887 |
LINC00886 Genelong intergenic non-protein coding RNA 886 |
LINC00889 Genelong intergenic non-protein coding RNA 889 |
LINC00489 Genelong intergenic non-protein coding RNA 489 |
LINC01451 Genelong intergenic non-protein coding RNA 1451 |
LINC01455 Genelong intergenic non-protein coding RNA 1455 |
LINC01473 Genelong intergenic non-protein coding RNA 1473 |
LINC00417 Genelong intergenic non-protein coding RNA 417 |
LINC00412 Genelong intergenic non-protein coding RNA 412 |
LINC00410 Genelong intergenic non-protein coding RNA 410 |
FALEC Genefocally amplified long non-coding RNA in epithelial cancer |
LOC100132304 Genelong intergenic non-protein coding RNA 684 |
LINC00268-2P Genelong intergenic non-protein coding RNA 268-2, pseudogene |
DALIR GeneDNMT1-associated long intergenic non-coding RNA |
LINC00554 Genelong intergenic non-protein coding RNA 554 |
LINC00254 Genelong intergenic non-protein coding RNA 254 |
LINC00437 Genelong intergenic non-protein coding RNA 437 |
SALRNA2 Genesenescence associated long non-coding RNA 2 |
LINC00928 Genelong intergenic non-protein coding RNA 928 |
LINC00922 Genelong intergenic non-protein coding RNA 922 |
LINC00923 Genelong intergenic non-protein coding RNA 923 |
LINC00921 Genelong intergenic non-protein coding RNA 921 |
LINC00926 Genelong intergenic non-protein coding RNA 926 |
LINC00927 Genelong intergenic non-protein coding RNA 927 |
LINC00925 Genelong intergenic non-protein coding RNA 925 |
HAGLR GeneHOXD antisense growth-associated long non-coding RNA |
PTX3 Genepentraxin 3, long This gene encodes a member of the pentraxin protein family. The expression of this protein is induced by inflammatory cytokines in response to inflammatory stimuli in several mesenchymal and epithelial cell types, particularly endothelial cells and mononuclear phagocytes. The protein promotes fibrocyte differentiation and is involved in regulating inflammation and complement activation. It also plays a role in angiogenesis and tissue remodeling. The protein serves as a biomarker for several inflammatory conditions. [provided by RefSeq, Jun 2016] |
PTX4 Genepentraxin 4, long This gene belongs to the pentraxin superfamily, whose members encode highly conserved multifunctional proteins. The encoded protein, like other members of this family, contains a conserved pentraxin domain at the C-terminus. The highest levels of expression of the protein were observed in bone marrow, small intestine and testes. [provided by RefSeq, Jun 2016] |
LINC01338 Genelong intergenic non-protein coding RNA 1338 |
LINC01339 Genelong intergenic non-protein coding RNA 1339 |
LINC01330 Genelong intergenic non-protein coding RNA 1330 |
LINC01331 Genelong intergenic non-protein coding RNA 1331 |
LINC01335 Genelong intergenic non-protein coding RNA 1335 |
LINC01336 Genelong intergenic non-protein coding RNA 1336 |
LINC00051 Genelong intergenic non-protein coding RNA 51 |
LOC100421637 Geneacyl-CoA synthetase long-chain family member 3 pseudogene |
LINC00332 Genelong intergenic non-protein coding RNA 332 |
LINC01317 Genelong intergenic non-protein coding RNA 1317 |
LINC01048 Genelong intergenic non-protein coding RNA 1048 |
LINC00494 Genelong intergenic non-protein coding RNA 494 |
LINC00492 Genelong intergenic non-protein coding RNA 492 |
LINC00493 Genelong intergenic non-protein coding RNA 493 Enables protein kinase binding activity and transmembrane transporter binding activity. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00491 Genelong intergenic non-protein coding RNA 491 |
LINC00920 Genelong intergenic non-protein coding RNA 920 |
LINC01479 Genelong intergenic non-protein coding RNA 1479 |
LINC01387 Genelong intergenic non-protein coding RNA 1387 |
LINC00519 Genelong intergenic non-protein coding RNA 519 |
LINC00518 Genelong intergenic non-protein coding RNA 518 |
LINC00511 Genelong intergenic non-protein coding RNA 511 |
LINC00517 Genelong intergenic non-protein coding RNA 517 |
LINC00515 Genelong intergenic non-protein coding RNA 515 |
LINC00514 Genelong intergenic non-protein coding RNA 514 |
LINC01597 Genelong intergenic non-protein coding RNA 1597 |
THRIL GeneTNF and HNRNPL related immunoregulatory long non-coding RNA |
LINC01333 Genelong intergenic non-protein coding RNA 1333 |
LINC00319 Genelong intergenic non-protein coding RNA 319 |
LINC00237 Genelong intergenic non-protein coding RNA 237 |
LINC01072 Genelong intergenic non-protein coding RNA 1072 |
LINC01070 Genelong intergenic non-protein coding RNA 1070 |
LINC01075 Genelong intergenic non-protein coding RNA 1075 |
LINC00308 Genelong intergenic non-protein coding RNA 308 |
LINC00309 Genelong intergenic non-protein coding RNA 309 |
LINC00302 Genelong intergenic non-protein coding RNA 302 |
LINC00303 Genelong intergenic non-protein coding RNA 303 |
LINC00301 Genelong intergenic non-protein coding RNA 301 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00307 Genelong intergenic non-protein coding RNA 307 |
LINC00304 Genelong intergenic non-protein coding RNA 304 |
LINC00305 Genelong intergenic non-protein coding RNA 305 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01429 Genelong intergenic non-protein coding RNA 1429 |
LINC01170 Genelong intergenic non-protein coding RNA 1170 |
LINC01279 Genelong intergenic non-protein coding RNA 1279 |
LINC01278 Genelong intergenic non-protein coding RNA 1278 |
LINC01277 Genelong intergenic non-protein coding RNA 1277 |
LINC01271 Genelong intergenic non-protein coding RNA 1271 |
LINC01270 Genelong intergenic non-protein coding RNA 1270 |
LINC01273 Genelong intergenic non-protein coding RNA 1273 |
LINC00593 Genelong intergenic non-protein coding RNA 593 |
LINC00592 Genelong intergenic non-protein coding RNA 592 |
LINC00597 Genelong intergenic non-protein coding RNA 597 |
LINC00596 Genelong intergenic non-protein coding RNA 596 |
LINC00595 Genelong intergenic non-protein coding RNA 595 |
LINC00594 Genelong intergenic non-protein coding RNA 594 |
LINC00578 Genelong intergenic non-protein coding RNA 578 |
LINC00570 Genelong intergenic non-protein coding RNA 570 |
LINC01569 Genelong intergenic non-protein coding RNA 1569 |
LINC01568 Genelong intergenic non-protein coding RNA 1568 |
LINC01565 Genelong intergenic non-protein coding RNA 1565 |
LINC01564 Genelong intergenic non-protein coding RNA 1564 |
LINC01567 Genelong intergenic non-protein coding RNA 1567 |
LINC01566 Genelong intergenic non-protein coding RNA 1566 |
LINC01561 Genelong intergenic non-protein coding RNA 1561 |
LINC01560 Genelong intergenic non-protein coding RNA 1560 |
LINC01563 Genelong intergenic non-protein coding RNA 1563 |
LINC01562 Genelong intergenic non-protein coding RNA 1562 |
LINC01389 Genelong intergenic non-protein coding RNA 1389 |
LINC01386 Genelong intergenic non-protein coding RNA 1386 |
LINC00382 Genelong intergenic non-protein coding RNA 382 |
LINC00383 Genelong intergenic non-protein coding RNA 383 |
LINC00380 Genelong intergenic non-protein coding RNA 380 |
LINC00381 Genelong intergenic non-protein coding RNA 381 |
LINC00387 Genelong intergenic non-protein coding RNA 387 |
LINC00384 Genelong intergenic non-protein coding RNA 384 |
LINC00388 Genelong intergenic non-protein coding RNA 388 |
LINC00854 Genelong intergenic non-protein coding RNA 854 |
LINC01436 Genelong intergenic non-protein coding RNA 1436 |
LINC00856 Genelong intergenic non-protein coding RNA 856 |
LINC00857 Genelong intergenic non-protein coding RNA 857 |
LINC00852 Genelong intergenic non-protein coding RNA 852 |
LINC00853 Genelong intergenic non-protein coding RNA 853 |
LINC00850 Genelong intergenic non-protein coding RNA 850 |
LINC00851 Genelong intergenic non-protein coding RNA 851 |
LINC00858 Genelong intergenic non-protein coding RNA 858 |
LINC01486 Genelong intergenic non-protein coding RNA 1486 |
LINC01481 Genelong intergenic non-protein coding RNA 1481 |
LINC01488 Genelong intergenic non-protein coding RNA 1488 |
LINC00469 Genelong intergenic non-protein coding RNA 469 |
LINC00467 Genelong intergenic non-protein coding RNA 467 |
LINC00463 Genelong intergenic non-protein coding RNA 463 |
LINC00462 Genelong intergenic non-protein coding RNA 462 |
LINC00461 Genelong intergenic non-protein coding RNA 461 This is an evolutionarily conserved gene that produces alternatively spliced long non-coding RNAs that may be expressed predominantly in the brain and visual cortex. These transcripts may be involved in tumorigenesis, as depletion by siRNA suppressed glioma cell division. Transcripts may also bind to and regulate the activity of miR-411-5p and argonaut 2, thereby altering the expression of genes involved in tumor growth. [provided by RefSeq, Nov 2017] |
LINC00460 Genelong intergenic non-protein coding RNA 460 |
LINC01127 Genelong intergenic non-protein coding RNA 1127 |
LINC01487 Genelong intergenic non-protein coding RNA 1487 |
LINC01485 Genelong intergenic non-protein coding RNA 1485 |
LINC01482 Genelong intergenic non-protein coding RNA 1482 |
LINC01480 Genelong intergenic non-protein coding RNA 1480 |
LINC01138 Genelong intergenic non-protein coding RNA 1138 |
LINC01139 Genelong intergenic non-protein coding RNA 1139 |
LINC01136 Genelong intergenic non-protein coding RNA 1136 |
LINC01137 Genelong intergenic non-protein coding RNA 1137 |
LINC01134 Genelong intergenic non-protein coding RNA 1134 |
LINC01135 Genelong intergenic non-protein coding RNA 1135 |
LINC01132 Genelong intergenic non-protein coding RNA 1132 |
LINC01133 Genelong intergenic non-protein coding RNA 1133 |
LINC01489 Genelong intergenic non-protein coding RNA 1489 |
LINC00261 Genelong intergenic non-protein coding RNA 261 This gene produces a long non-coding RNA that acts as a negative regulator of cell growth. This transcript may promote differentiation and apoptosis. [provided by RefSeq, Dec 2017] |
LINC00260 Genelong intergenic non-protein coding RNA 260 |
LINC00265 Genelong intergenic non-protein coding RNA 265 |
LINC00264 Genelong intergenic non-protein coding RNA 264 |
LINC00269 Genelong intergenic non-protein coding RNA 269 |
LINC00268 Genelong intergenic non-protein coding RNA 268 |
LINC00466 Genelong intergenic non-protein coding RNA 466 |
LINC00909 Genelong intergenic non-protein coding RNA 909 |
LINC01272 Genelong intergenic non-protein coding RNA 1272 |
LINC00205 Genelong intergenic non-protein coding RNA 205 |
LINC00654 Genelong intergenic non-protein coding RNA 654 |
LINC00656 Genelong intergenic non-protein coding RNA 656 |
LINC00652 Genelong intergenic non-protein coding RNA 652 |
LINC00658 Genelong intergenic non-protein coding RNA 658 |
LINC00659 Genelong intergenic non-protein coding RNA 659 |
LINC01300 Genelong intergenic non-protein coding RNA 1300 |
LINC01304 Genelong intergenic non-protein coding RNA 1304 |
LINC01309 Genelong intergenic non-protein coding RNA 1309 |
LINC01358 Genelong intergenic non-protein coding RNA 1358 |
LINC01356 Genelong intergenic non-protein coding RNA 1356 |
LINC01353 Genelong intergenic non-protein coding RNA 1353 |
LINC01351 Genelong intergenic non-protein coding RNA 1351 |
LINC01478 Genelong intergenic non-protein coding RNA 1478 |
LINC01405 Genelong intergenic non-protein coding RNA 1405 |
LOC646644 GeneLLP homolog, long-term synaptic facilitation (Aplysia) pseudogene |
LINC00959 Genelong intergenic non-protein coding RNA 959 |
LINC00958 Genelong intergenic non-protein coding RNA 958 |
LINC00951 Genelong intergenic non-protein coding RNA 951 |
LINC00950 Genelong intergenic non-protein coding RNA 950 |
LINC00957 Genelong intergenic non-protein coding RNA 957 |
LINC00955 Genelong intergenic non-protein coding RNA 955 |
LINC00540 Genelong intergenic non-protein coding RNA 540 |
LINC00543 Genelong intergenic non-protein coding RNA 543 |
LINC00544 Genelong intergenic non-protein coding RNA 544 |
LINC00545 Genelong intergenic non-protein coding RNA 545 |
LINC00547 Genelong intergenic non-protein coding RNA 547 |
LINC00548 Genelong intergenic non-protein coding RNA 548 |
LINC00683 Genelong intergenic non-protein coding RNA 683 |
LINC00032 Genelong intergenic non-protein coding RNA 32 |
LINC01011 Genelong intergenic non-protein coding RNA 1011 |
LINC01010 Genelong intergenic non-protein coding RNA 1010 |
LINC00940 Genelong intergenic non-protein coding RNA 940 |
LINC01269 Genelong intergenic non-protein coding RNA 1269 |
LINC01020 Genelong intergenic non-protein coding RNA 1020 |
LINC01021 Genelong intergenic non-protein coding RNA 1021 |
LINC01023 Genelong intergenic non-protein coding RNA 1023 |
LINC01028 Genelong intergenic non-protein coding RNA 1028 |
LINC01029 Genelong intergenic non-protein coding RNA 1029 |
LINC01262 Genelong intergenic non-protein coding RNA 1262 |
LINC01222 Genelong intergenic non-protein coding RNA 1222 |
LINC01226 Genelong intergenic non-protein coding RNA 1226 |
LINC01224 Genelong intergenic non-protein coding RNA 1224 |
LINC01225 Genelong intergenic non-protein coding RNA 1225 |
LINC01228 Genelong intergenic non-protein coding RNA 1228 |
LINC01229 Genelong intergenic non-protein coding RNA 1229 |
LINC00266-2P Genelong intergenic non-protein coding RNA 266-2, pseudogene |
LINC01589 Genelong intergenic non-protein coding RNA 1589 |
SENCR Genesmooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA |
LINC01017 Genelong intergenic non-protein coding RNA 1017 |
LINC01247 Genelong intergenic non-protein coding RNA 1247 |
LINC01242 Genelong intergenic non-protein coding RNA 1242 |
LINC01243 Genelong intergenic non-protein coding RNA 1243 |
LINC01532 Genelong intergenic non-protein coding RNA 1532 |
LINC01533 Genelong intergenic non-protein coding RNA 1533 |
LINC01530 Genelong intergenic non-protein coding RNA 1530 |
LINC01531 Genelong intergenic non-protein coding RNA 1531 |
LINC01537 Genelong intergenic non-protein coding RNA 1537 |
LINC01534 Genelong intergenic non-protein coding RNA 1534 |
LINC01535 Genelong intergenic non-protein coding RNA 1535 |
LINC01538 Genelong intergenic non-protein coding RNA 1538 |
LINC01539 Genelong intergenic non-protein coding RNA 1539 |
LINC00379 Genelong intergenic non-protein coding RNA 379 |
LINC00371 Genelong intergenic non-protein coding RNA 371 |
LINC00370 Genelong intergenic non-protein coding RNA 370 |
LINC00377 Genelong intergenic non-protein coding RNA 377 |
LINC00376 Genelong intergenic non-protein coding RNA 376 |
LINC00375 Genelong intergenic non-protein coding RNA 375 |
LINC00707 Genelong intergenic non-protein coding RNA 707 |
LINC00704 Genelong intergenic non-protein coding RNA 704 |
LINC00703 Genelong intergenic non-protein coding RNA 703 |
LINC00174 Genelong intergenic non-protein coding RNA 174 |
LINC00176 Genelong intergenic non-protein coding RNA 176 |
LINC00173 Genelong intergenic non-protein coding RNA 173 |
LINC00824 Genelong intergenic non-protein coding RNA 824 |
TRERNA1 Genetranslation regulatory long non-coding RNA 1 |
LINC01441 Genelong intergenic non-protein coding RNA 1441 |
LINC00706 Genelong intergenic non-protein coding RNA 706 |
LINC01146 Genelong intergenic non-protein coding RNA 1146 |
LINC01143 Genelong intergenic non-protein coding RNA 1143 |
LINC01142 Genelong intergenic non-protein coding RNA 1142 |
LINC01141 Genelong intergenic non-protein coding RNA 1141 |
LINC01149 Genelong intergenic non-protein coding RNA 1149 |
LINC00423 Genelong intergenic non-protein coding RNA 423 |
LINC00421 Genelong intergenic non-protein coding RNA 421 |
LINC00427 Genelong intergenic non-protein coding RNA 427 |
LINC00426 Genelong intergenic non-protein coding RNA 426 |
LINC00424 Genelong intergenic non-protein coding RNA 424 |
LINC00669 Genelong intergenic non-protein coding RNA 669 |
LINC00668 Genelong intergenic non-protein coding RNA 668 |
LINC00665 Genelong intergenic non-protein coding RNA 665 |
LINC00664 Genelong intergenic non-protein coding RNA 664 |
LINC00667 Genelong intergenic non-protein coding RNA 667 |
LINC00661 Genelong intergenic non-protein coding RNA 661 |
LINC00663 Genelong intergenic non-protein coding RNA 663 |
LINC00662 Genelong intergenic non-protein coding RNA 662 |
LINC00083 Genelong intergenic non-protein coding RNA 83 Predicted to enable carbohydrate binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00657 Genelong intergenic non-protein coding RNA 657 Predicted to enable protein sequestering activity. Predicted to be involved in several processes, including determination of adult lifespan; hair follicle development; and skeletal muscle fiber development. Predicted to be active in cytoplasm. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
ELDR GeneEGFR long non-coding downstream RNA Predicted to act upstream of or within regulation of gene expression and response to wounding. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01301 Genelong intergenic non-protein coding RNA 1301 |
LINC01305 Genelong intergenic non-protein coding RNA 1305 |
LINC01307 Genelong intergenic non-protein coding RNA 1307 |
LINC01477 Genelong intergenic non-protein coding RNA 1477 |
LINC01476 Genelong intergenic non-protein coding RNA 1476 |
LINC01475 Genelong intergenic non-protein coding RNA 1475 |
LINC01474 Genelong intergenic non-protein coding RNA 1474 |
LINC01471 Genelong intergenic non-protein coding RNA 1471 |
LINC01470 Genelong intergenic non-protein coding RNA 1470 |
LINC00434 Genelong intergenic non-protein coding RNA 434 |
ACSL3 Geneacyl-CoA synthetase long-chain family member 3 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in brain, and preferentially utilizes myristate, arachidonate, and eicosapentaenoate as substrates. The amino acid sequence of this isozyme is 92% identical to that of rat homolog. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
ACSL1 Geneacyl-CoA synthetase long-chain family member 1 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
ACSL6 Geneacyl-CoA synthetase long-chain family member 6 The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2011] |
LINC00431 Genelong intergenic non-protein coding RNA 431 |
ACSL4 Geneacyl-CoA synthetase long-chain family member 4 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016] |
ACSL5 Geneacyl-CoA synthetase long-chain family member 5 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in uterus and spleen, and in trace amounts in normal brain, but has markedly increased levels in malignant gliomas. This gene functions in mediating fatty acid-induced glioma cell growth. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LINC01511 Genelong intergenic non-protein coding RNA 1511 |
LINC01512 Genelong intergenic non-protein coding RNA 1512 |
LINC01517 Genelong intergenic non-protein coding RNA 1517 |
LINC01504 Genelong intergenic non-protein coding RNA 1504 |
LINC00238 Genelong intergenic non-protein coding RNA 238 |
LINC00239 Genelong intergenic non-protein coding RNA 239 |
LINC00235 Genelong intergenic non-protein coding RNA 235 |
LINC00900 Genelong intergenic non-protein coding RNA 900 |
LINC00901 Genelong intergenic non-protein coding RNA 901 |
LINC00903 Genelong intergenic non-protein coding RNA 903 |
LINC00904 Genelong intergenic non-protein coding RNA 904 |
LINC00905 Genelong intergenic non-protein coding RNA 905 |
LINC00906 Genelong intergenic non-protein coding RNA 906 |
LINC00907 Genelong intergenic non-protein coding RNA 907 |
LINC00908 Genelong intergenic non-protein coding RNA 908 |
LINC00397 Genelong intergenic non-protein coding RNA 397 |
LINC00572 Genelong intergenic non-protein coding RNA 572 |
LINC00575 Genelong intergenic non-protein coding RNA 575 |
LINC00574 Genelong intergenic non-protein coding RNA 574 |
LINC00577 Genelong intergenic non-protein coding RNA 577 |
LINC01587 Genelong intergenic non-protein coding RNA 1587 This gene is expressed in neuroblastoma; however, the function of this gene is not yet determined. [provided by RefSeq, Jul 2008] |
LINC01584 Genelong intergenic non-protein coding RNA 1584 |
LINC00622 Genelong intergenic non-protein coding RNA 622 |
LINC01054 Genelong intergenic non-protein coding RNA 1054 |
LINC01058 Genelong intergenic non-protein coding RNA 1058 |
KIR2DL3 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL2 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL1 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL4 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016] |
LINC00428 Genelong intergenic non-protein coding RNA 428 |
LINC01354 Genelong intergenic non-protein coding RNA 1354 |
LINC01355 Genelong intergenic non-protein coding RNA 1355 |
LINC01350 Genelong intergenic non-protein coding RNA 1350 |
LINC01019 Genelong intergenic non-protein coding RNA 1019 |
LINC01018 Genelong intergenic non-protein coding RNA 1018 |
LINC01013 Genelong intergenic non-protein coding RNA 1013 |
LINC01012 Genelong intergenic non-protein coding RNA 1012 |
LINC01015 Genelong intergenic non-protein coding RNA 1015 |
LINC01014 Genelong intergenic non-protein coding RNA 1014 |
LINC01016 Genelong intergenic non-protein coding RNA 1016 |
LINC00888 Genelong intergenic non-protein coding RNA 888 |
LINC01162 Genelong intergenic non-protein coding RNA 1162 |
LINC00919 Genelong intergenic non-protein coding RNA 919 |
LINC00914 Genelong intergenic non-protein coding RNA 914 |
LINC00705 Genelong intergenic non-protein coding RNA 705 |
LINC00700 Genelong intergenic non-protein coding RNA 700 |
LINC00701 Genelong intergenic non-protein coding RNA 701 |
LINC01359 Genelong intergenic non-protein coding RNA 1359 |
LINC01352 Genelong intergenic non-protein coding RNA 1352 |
LINC01586 Genelong intergenic non-protein coding RNA 1586 |
LINC00989 Genelong intergenic non-protein coding RNA 989 |
LINC00982 Genelong intergenic non-protein coding RNA 982 |
LINC00987 Genelong intergenic non-protein coding RNA 987 |
HAO2 Genehydroxyacid oxidase 2 (long chain) This gene is one of three related genes that have 2-hydroxyacid oxidase activity. The encoded protein localizes to the peroxisome has the highest activity toward the substrate 2-hydroxypalmitate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
LINC02618 Genelong intergenic non-protein coding RNA 2618 |
LINC02249 Genelong intergenic non-protein coding RNA 2249 |
LINC01963 Genelong intergenic non-protein coding RNA 1963 |
LNCTAM34A Genelong non coding transcriptional activator of miR34a |
LINC01833 Genelong intergenic non-protein coding RNA 1833 Predicted to be involved in regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01806 Genelong intergenic non-protein coding RNA 1806 |
LINC01788 Genelong intergenic non-protein coding RNA 1788 |
LINC01843 Genelong intergenic non-protein coding RNA 1843 |
LINC03040 Genelong intergenic non-protein coding RNA 3040 |
LINC01719 Genelong intergenic non-protein coding RNA 1719 |
LINC01772 Genelong intergenic non-protein coding RNA 1772 |
LINC02035 Genelong intergenic non-protein coding RNA 2035 |
LINC01781 Genelong intergenic non-protein coding RNA 1781 |
LINC02044 Genelong intergenic non-protein coding RNA 2044 |
LINC01852 Genelong intergenic non-protein coding RNA 1852 |
LINC01914 Genelong intergenic non-protein coding RNA 1914 |
LINC02102 Genelong intergenic non-protein coding RNA 2102 |
LINC01933 Genelong intergenic non-protein coding RNA 1933 |
LINC02904 Genelong intergenic non-protein coding RNA 2904 |
LINC02910 Genelong intergenic non-protein coding RNA 2910 |
LINC01814 Genelong intergenic non-protein coding RNA 1814 |
LINC02908 Genelong intergenic non-protein coding RNA 2908 |
LINC01829 Genelong intergenic non-protein coding RNA 1829 |
LINC00680 Genelong intergenic non-protein coding RNA 680 |
LINC02019 Genelong intergenic non-protein coding RNA 2019 |
LINC02094 Genelong intergenic non-protein coding RNA 2094 |
LINC02147 Genelong intergenic non-protein coding RNA 2147 |
LINC02012 Genelong intergenic non-protein coding RNA 2012 |
LINC01896 Genelong intergenic non-protein coding RNA 1896 |
LINC02185 Genelong intergenic non-protein coding RNA 2185 |
LINC01828 Genelong intergenic non-protein coding RNA 1828 |
LINC01619 Genelong intergenic non-protein coding RNA 1619 |
LINC01679 Genelong intergenic non-protein coding RNA 1679 |
PRECSIT Genep53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcript |
LINC02208 Genelong intergenic non-protein coding RNA 2208 |
LINC02210 Genelong intergenic non-protein coding RNA 2210 |
LINC03011 Genelong intergenic non-protein coding RNA 3011 |
LINC01702 Genelong intergenic non-protein coding RNA 1702 |
LINC02037 Genelong intergenic non-protein coding RNA 2037 |
LINC02197 Genelong intergenic non-protein coding RNA 2197 |
LINC01595 Genelong intergenic non-protein coding RNA 1595 Implicated in prostate cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC02898 Genelong intergenic non-protein coding RNA 2898 |
LINC02716 Genelong intergenic non-protein coding RNA 2716 |
LINC02116 Genelong intergenic non-protein coding RNA 2116 |
LINC01713 Genelong intergenic non-protein coding RNA 1713 |
LINC02174 Genelong intergenic non-protein coding RNA 2174 |
LINC02052 Genelong intergenic non-protein coding RNA 2052 |
LINC00449 Genelong intergenic non-protein coding RNA 449 |
LINC02084 Genelong intergenic non-protein coding RNA 2084 |
LINC01980 Genelong intergenic non-protein coding RNA 1980 |
LINC01876 Genelong intergenic non-protein coding RNA 1876 |
LINC02167 Genelong intergenic non-protein coding RNA 2167 |
LINC02212 Genelong intergenic non-protein coding RNA 2212 |
LINC02145 Genelong intergenic non-protein coding RNA 2145 |
LINC02905 Genelong intergenic non-protein coding RNA 2905 |
LINC02693 Genelong intergenic non-protein coding RNA 2693 |
LINC01978 Genelong intergenic non-protein coding RNA 1978 |
LINC01979 Genelong intergenic non-protein coding RNA 1979 |
LINC02015 Genelong intergenic non-protein coding RNA 2015 |
LINC01625 Genelong intergenic non-protein coding RNA 1625 |
LINC02202 Genelong intergenic non-protein coding RNA 2202 |
LINC01786 Genelong intergenic non-protein coding RNA 1786 |
LINC01714 Genelong intergenic non-protein coding RNA 1714 |
LINC02028 Genelong intergenic non-protein coding RNA 2028 |
HISLA GeneHIF1A stabilizing long noncoding RNA |
LINC01836 Genelong intergenic non-protein coding RNA 1836 |
LINC01977 Genelong intergenic non-protein coding RNA 1977 |
LINC01907 Genelong intergenic non-protein coding RNA 1907 |
LINC01748 Genelong intergenic non-protein coding RNA 1748 |
ARLNC1 Geneandrogen receptor regulated long noncoding RNA 1 |
LINC01754 Genelong intergenic non-protein coding RNA 1754 |
LINC01770 Genelong intergenic non-protein coding RNA 1770 |
MINCR GeneMYC-induced long non-coding RNA |
LINC02086 Genelong intergenic non-protein coding RNA 2086 |
LINC02193 Genelong intergenic non-protein coding RNA 2193 |
LINC01819 Genelong intergenic non-protein coding RNA 1819 |
LINC02018 Genelong intergenic non-protein coding RNA 2018 |
LINC01869 Genelong intergenic non-protein coding RNA 1869 |
MALINC1 Genemitosis associated long intergenic non-coding RNA 1 |
LINC02106 Genelong intergenic non-protein coding RNA 2106 |
LINC02076 Genelong intergenic non-protein coding RNA 2076 |
LINC02021 Genelong intergenic non-protein coding RNA 2021 |
LINC01915 Genelong intergenic non-protein coding RNA 1915 |
LINC01881 Genelong intergenic non-protein coding RNA 1881 |
LINC01801 Genelong intergenic non-protein coding RNA 1801 |
LINC01750 Genelong intergenic non-protein coding RNA 1750 |
LINC02175 Genelong intergenic non-protein coding RNA 2175 |
LINC02188 Genelong intergenic non-protein coding RNA 2188 |
LINC02913 Genelong intergenic non-protein coding RNA 2913 |
LINC02897 Genelong intergenic non-protein coding RNA 2897 |
LINC02875 Genelong intergenic non-protein coding RNA 2875 |
LINC01238 Genelong intergenic non-protein coding RNA 1238 |
LINC01943 Genelong intergenic non-protein coding RNA 1943 |
LINC02881 Genelong intergenic non-protein coding RNA 2881 |
LINC01345 Genelong intergenic non-protein coding RNA 1345 |
LINC02692 Genelong intergenic non-protein coding RNA 2692 |
LINC02107 Genelong intergenic non-protein coding RNA 2107 |
LINC01874 Genelong intergenic non-protein coding RNA 1874 |
LINC01707 Genelong intergenic non-protein coding RNA 1707 |
LINC01697 Genelong intergenic non-protein coding RNA 1697 |
LINC01684 Genelong intergenic non-protein coding RNA 1684 |
LINC01816 Genelong intergenic non-protein coding RNA 1816 |
LINC01626 Genelong intergenic non-protein coding RNA 1626 |
LINC01623 Genelong intergenic non-protein coding RNA 1623 |
LINC01612 Genelong intergenic non-protein coding RNA 1612 |
LINC01643 Genelong intergenic non-protein coding RNA 1643 |
LINC01647 Genelong intergenic non-protein coding RNA 1647 |
LINC01655 Genelong intergenic non-protein coding RNA 1655 |
LINC01667 Genelong intergenic non-protein coding RNA 1667 |
LINC01749 Genelong intergenic non-protein coding RNA 1749 |
LINC01747 Genelong intergenic non-protein coding RNA 1747 |
LINC01744 Genelong intergenic non-protein coding RNA 1744 |
LINC01743 Genelong intergenic non-protein coding RNA 1743 |
LINC01739 Genelong intergenic non-protein coding RNA 1739 |
LINC01728 Genelong intergenic non-protein coding RNA 1728 |
LINC01723 Genelong intergenic non-protein coding RNA 1723 |
LINC01718 Genelong intergenic non-protein coding RNA 1718 |
LINC01712 Genelong intergenic non-protein coding RNA 1712 |
LINC01704 Genelong intergenic non-protein coding RNA 1704 |
LINC01677 Genelong intergenic non-protein coding RNA 1677 |
LINC01676 Genelong intergenic non-protein coding RNA 1676 |
LINC01673 Genelong intergenic non-protein coding RNA 1673 |
LINC01672 Genelong intergenic non-protein coding RNA 1672 |
LINC01374 Genelong intergenic non-protein coding RNA 1374 |
LINC01297 Genelong intergenic non-protein coding RNA 1297 |
LINC01755 Genelong intergenic non-protein coding RNA 1755 |
LINC01760 Genelong intergenic non-protein coding RNA 1760 |
LINC01763 Genelong intergenic non-protein coding RNA 1763 |
LINC01764 Genelong intergenic non-protein coding RNA 1764 |
LINC02046 Genelong intergenic non-protein coding RNA 2046 |
LINC02045 Genelong intergenic non-protein coding RNA 2045 |
LINC02040 Genelong intergenic non-protein coding RNA 2040 |
LINC02039 Genelong intergenic non-protein coding RNA 2039 |
LINC02034 Genelong intergenic non-protein coding RNA 2034 |
LINC02032 Genelong intergenic non-protein coding RNA 2032 |
LINC02025 Genelong intergenic non-protein coding RNA 2025 |
LINC02022 Genelong intergenic non-protein coding RNA 2022 |
LINC02020 Genelong intergenic non-protein coding RNA 2020 |
LINC02013 Genelong intergenic non-protein coding RNA 2013 |
LINC01999 Genelong intergenic non-protein coding RNA 1999 |
LINC01995 Genelong intergenic non-protein coding RNA 1995 |
LINC01988 Genelong intergenic non-protein coding RNA 1988 |
LINC01986 Genelong intergenic non-protein coding RNA 1986 |
LINC02056 Genelong intergenic non-protein coding RNA 2056 |
LINC02064 Genelong intergenic non-protein coding RNA 2064 |
LINC02166 Genelong intergenic non-protein coding RNA 2166 |
LINC02165 Genelong intergenic non-protein coding RNA 2165 |
LINC02156 Genelong intergenic non-protein coding RNA 2156 |
LINC02152 Genelong intergenic non-protein coding RNA 2152 |
LINC02117 Genelong intergenic non-protein coding RNA 2117 |
LINC02114 Genelong intergenic non-protein coding RNA 2114 |
LINC02113 Genelong intergenic non-protein coding RNA 2113 |
LINC02110 Genelong intergenic non-protein coding RNA 2110 |
LINC02103 Genelong intergenic non-protein coding RNA 2103 |
LINC02096 Genelong intergenic non-protein coding RNA 2096 |
LINC02089 Genelong intergenic non-protein coding RNA 2089 |
LINC02087 Genelong intergenic non-protein coding RNA 2087 |
LINC02079 Genelong intergenic non-protein coding RNA 2079 |
LINC02072 Genelong intergenic non-protein coding RNA 2072 |
LINC02069 Genelong intergenic non-protein coding RNA 2069 |
LINC02059 Genelong intergenic non-protein coding RNA 2059 |
LINC01976 Genelong intergenic non-protein coding RNA 1976 |
LINC01944 Genelong intergenic non-protein coding RNA 1944 |
LINC01855 Genelong intergenic non-protein coding RNA 1855 |
LINC01851 Genelong intergenic non-protein coding RNA 1851 |
LINC01849 Genelong intergenic non-protein coding RNA 1849 |
LINC01846 Genelong intergenic non-protein coding RNA 1846 |
LINC01844 Genelong intergenic non-protein coding RNA 1844 |
LINC01837 Genelong intergenic non-protein coding RNA 1837 |
LINC01818 Genelong intergenic non-protein coding RNA 1818 |
LINC01815 Genelong intergenic non-protein coding RNA 1815 |
LINC01803 Genelong intergenic non-protein coding RNA 1803 |
LINC01799 Genelong intergenic non-protein coding RNA 1799 |
LINC01783 Genelong intergenic non-protein coding RNA 1783 Predicted to enable triplet codon-amino acid adaptor activity. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01778 Genelong intergenic non-protein coding RNA 1778 |
LINC01766 Genelong intergenic non-protein coding RNA 1766 |
LINC01872 Genelong intergenic non-protein coding RNA 1872 |
LINC01962 Genelong intergenic non-protein coding RNA 1962 |
LINC01878 Genelong intergenic non-protein coding RNA 1878 |
LINC01888 Genelong intergenic non-protein coding RNA 1888 |
LINC01938 Genelong intergenic non-protein coding RNA 1938 |
LINC01937 Genelong intergenic non-protein coding RNA 1937 |
LINC01931 Genelong intergenic non-protein coding RNA 1931 |
LINC01927 Genelong intergenic non-protein coding RNA 1927 |
LINC01925 Genelong intergenic non-protein coding RNA 1925 |
LINC01923 Genelong intergenic non-protein coding RNA 1923 |
LINC01919 Genelong intergenic non-protein coding RNA 1919 |
LINC01917 Genelong intergenic non-protein coding RNA 1917 |
LINC01913 Genelong intergenic non-protein coding RNA 1913 |
LINC01912 Genelong intergenic non-protein coding RNA 1912 |
LINC01911 Genelong intergenic non-protein coding RNA 1911 |
LINC01909 Genelong intergenic non-protein coding RNA 1909 |
LINC01905 Genelong intergenic non-protein coding RNA 1905 |
LINC01899 Genelong intergenic non-protein coding RNA 1899 |
LINC01890 Genelong intergenic non-protein coding RNA 1890 |
LINC01884 Genelong intergenic non-protein coding RNA 1884 |
LINC00390 Genelong intergenic non-protein coding RNA 390 |
LINC01052 Genelong intergenic non-protein coding RNA 1052 |
LINC01066 Genelong intergenic non-protein coding RNA 1066 |
LINC02016 Genelong intergenic non-protein coding RNA 2016 |
LINC01694 Genelong intergenic non-protein coding RNA 1694 |
LINC02587 Genelong intergenic non-protein coding RNA 2587 |
LINC02204 Genelong intergenic non-protein coding RNA 2204 |
LINC01785 Genelong intergenic non-protein coding RNA 1785 |
LINC02207 Genelong intergenic non-protein coding RNA 2207 |
LINC02446 Genelong intergenic non-protein coding RNA 2446 |
LINC01857 Genelong intergenic non-protein coding RNA 1857 |
LINC01871 Genelong intergenic non-protein coding RNA 1871 |
GRASLND Geneglycosaminoglycan regulatory associated long non-coding RNA |
LINC01762 Genelong intergenic non-protein coding RNA 1762 |
LINC02027 Genelong intergenic non-protein coding RNA 2027 |
LINC01924 Genelong intergenic non-protein coding RNA 1924 |
LINC01934 Genelong intergenic non-protein coding RNA 1934 |
LINC02251 Genelong intergenic non-protein coding RNA 2251 |
LINC02397 Genelong intergenic non-protein coding RNA 2397 |
LINC01967 Genelong intergenic non-protein coding RNA 1967 |
LINC01357 Genelong intergenic non-protein coding RNA 1357 |
LINC02593 Genelong intergenic non-protein coding RNA 2593 |
LINC02362 Genelong intergenic non-protein coding RNA 2362 |
LINC02523 Genelong intergenic non-protein coding RNA 2523 |
LINC01717 Genelong intergenic non-protein coding RNA 1717 |
LINC02009 Genelong intergenic non-protein coding RNA 2009 |
LINC01724 Genelong intergenic non-protein coding RNA 1724 |
LINC02437 Genelong intergenic non-protein coding RNA 2437 |
LINC01965 Genelong intergenic non-protein coding RNA 1965 |
LINC02836 Genelong intergenic non-protein coding RNA 2836 |
LINC02785 Genelong intergenic non-protein coding RNA 2785 |
LINC01831 Genelong intergenic non-protein coding RNA 1831 |
LINC02053 Genelong intergenic non-protein coding RNA 2053 |
LINC02768 Genelong intergenic non-protein coding RNA 2768 |
LINC02360 Genelong intergenic non-protein coding RNA 2360 |
LINC02237 Genelong intergenic non-protein coding RNA 2237 |
LINC02511 Genelong intergenic non-protein coding RNA 2511 |
LINC01695 Genelong intergenic non-protein coding RNA 1695 |
LINC02901 Genelong intergenic non-protein coding RNA 2901 |
LINC02888 Genelong intergenic non-protein coding RNA 2888 |
LINC02903 Genelong intergenic non-protein coding RNA 2903 |
LINC02899 Genelong intergenic non-protein coding RNA 2899 |
C3ORF86P Genelong intergenic non-protein coding RNA 694 |
LINC02694 Genelong intergenic non-protein coding RNA 2694 |
LINC02902 Genelong intergenic non-protein coding RNA 2902 |
LINC02798 Genelong intergenic non-protein coding RNA 2798 |
LINC02615 Genelong intergenic non-protein coding RNA 2615 |
LINC02696 Genelong intergenic non-protein coding RNA 2696 |
LINC02614 Genelong intergenic non-protein coding RNA 2614 |
LINC02609 Genelong intergenic non-protein coding RNA 2609 |
LINC02981 Genelong intergenic non-protein coding RNA 2981 |
LINC02731 Genelong intergenic non-protein coding RNA 2731 |
LINC02987 Genelong intergenic non-protein coding RNA 2987 |
LINC02544 Genelong intergenic non-protein coding RNA 2544 |
LINC02649 Genelong intergenic non-protein coding RNA 2649 |
LINC02728 Genelong intergenic non-protein coding RNA 2728 |
LINC02803 Genelong intergenic non-protein coding RNA 2803 |
LINC02349 Genelong intergenic non-protein coding RNA 2349 |
LINC02539 Genelong intergenic non-protein coding RNA 2539 |
LINC03002 Genelong intergenic non-protein coding RNA 3002 |
LINC02381 Genelong intergenic non-protein coding RNA 2381 |
LINC02232 Genelong intergenic non-protein coding RNA 2232 |
LINC03100 Genelong intergenic non-protein coding RNA 3100 |
LINC02894 Genelong intergenic non-protein coding RNA 2894 |
LINC02328 Genelong intergenic non-protein coding RNA 2328 |
LINC01779 Genelong intergenic non-protein coding RNA 1779 |
LINC03135 Genelong intergenic non-protein coding RNA 3135 |
LINC02965 Genelong intergenic non-protein coding RNA 2965 |
LINC03052 Genelong intergenic non-protein coding RNA 3052 |
LINC02235 Genelong intergenic non-protein coding RNA 2235 |
LINC02576 Genelong intergenic non-protein coding RNA 2576 |
LINC02560 Genelong intergenic non-protein coding RNA 2560 |
LINC02762 Genelong intergenic non-protein coding RNA 2762 |
LINC02610 Genelong intergenic non-protein coding RNA 2610 |
LINC02854 Genelong intergenic non-protein coding RNA 2854 |
LINC02983 Genelong intergenic non-protein coding RNA 2983 |
LINC02268 Genelong intergenic non-protein coding RNA 2268 |
LINC02893 Genelong intergenic non-protein coding RNA 2893 |
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset. |
Split-hand/foot malformation with long bone deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Split-Hand-Foot Malformation With Long Bone Deficiency 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Long Bone Deficiency 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary malformation without arteriovenous malformation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Capillary malformation-arteriovenous malformation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Capillary malformation-arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Capillary Malformation-Arteriovenous Malformation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Capillary Malformation-Arteriovenous Malformation from the curated CTD Gene-Disease Associations dataset. |
capillary malformation-arteriovenous malformation Gene SetFrom OMIM Gene-Disease Associations genes associated with the capillary malformation-arteriovenous malformation phenotype from the curated OMIM Gene-Disease Associations dataset. |
Capillary Malformation Without Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Capillary Malformation Without Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary malformation-arteriovenous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Capillary malformation-arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Capillary malformation-arteriovenous malformation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Capillary malformation-arteriovenous malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Long Chain/Very Long Chain Acyl Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain/Very Long Chain Acyl Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long bone adamantinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease long bone adamantinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
dumbbell-shaped long bone Gene SetFrom HPO Gene-Disease Associations genes associated with the dumbbell-shaped long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortical thickening of long bone diaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the cortical thickening of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of long bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of long bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skin dimple over apex of long bone angulation Gene SetFrom HPO Gene-Disease Associations genes associated with the skin dimple over apex of long bone angulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased density of long bone diaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the increased density of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender long bone Gene SetFrom HPO Gene-Disease Associations genes associated with the slender long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short long bone Gene SetFrom HPO Gene-Disease Associations genes associated with the short long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone diaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone diaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased long bone epiphyseal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphyseal plate proliferative zone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal plate proliferative zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone hypertrophic chondrocyte zone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone hypertrophic chondrocyte zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased long bone epiphyseal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal limb long bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal limb long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphyseal ossification zone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphyseal plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thickened long bone epiphysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
disorganized long bone epiphyseal plate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long bone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue long bone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Broad Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Thickening Of Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Thickening Of Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Osteochondroma Of Long Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Osteochondroma Of Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skin Dimple Over Apex Of Long Bone Angulation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skin Dimple Over Apex Of Long Bone Angulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dumbbell-Shaped Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dumbbell-Shaped Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Long-Bone Exostoses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Long-Bone Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thin Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thin Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Density Of Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Density Of Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Long Bone Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Long Bone Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal long bone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphyseal plate morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal plate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphyseal ossification zone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone diaphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone diaphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased long bone epiphyseal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone hypertrophic chondrocyte zone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone hypertrophic chondrocyte zone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphyseal plate proliferative zone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal plate proliferative zone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized long bone epiphyseal plate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased long bone epiphyseal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thickened long bone epiphysis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal limb long bone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal limb long bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone internal diameter Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone internal diameter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Long bone adamantinoma Gene SetFrom 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 SetFrom 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. |
split Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term split in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Sensory disturbances after bilateral sagittal split ramus osteotomy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Sensory disturbances after bilateral sagittal split ramus osteotomy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
junctional split Gene SetFrom HPO Gene-Disease Associations genes associated with the junctional split phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
split nail Gene SetFrom HPO Gene-Disease Associations genes associated with the split nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
TUP1-like enhancer of split Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TUP1-like enhancer of split protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FMN-binding split barrel Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FMN-binding split barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
split cervical atlas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split cervical atlas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
split notochord Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split notochord phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
split sternal manubrium Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split sternal manubrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
split vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
split cervical axis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split cervical axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
split sternum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split sternum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
split xiphoid process Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the split xiphoid process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Split Ends Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Junctional Split Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Junctional Split in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Longitudinal Split Nail Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Longitudinal Split Nail in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
split xiphoid process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split xiphoid process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
split sternum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split sternum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
split sternal manubrium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split sternal manubrium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
split notochord Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split notochord phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
split cervical atlas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split cervical atlas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
split cervical axis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split cervical axis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
split vertebrae Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the split vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Split septin rings Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Split septin rings cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Sensory disturbances after bilateral sagittal split ramus osteotomy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sensory disturbances after bilateral sagittal split ramus osteotomy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
INFLUENZA A VIRUS, SPLIT VIRION Gene Setinteracting proteins for the INFLUENZA A VIRUS, SPLIT VIRION drug from theDGIdb Drug Targets 2026 dataset. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
long chain 3 hydroxyacyl coa dehydrogenase deficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the long chain 3 hydroxyacyl coa dehydrogenase deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
Long Chain Acyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain Acyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Very Long Chain Acyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Very Long Chain Acyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom 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. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom 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. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom 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 chain 3-hydroxyacyl-CoA dehydrogenase deficiency Gene SetFrom 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. |
bone resorption; fractures, bone Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Dandy-Walker like malformation with atrioventricular septal defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Malformation of the heart Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Malformation of the heart phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Split-hand/foot malformation 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Split-hand/foot malformation 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Split-hand/foot malformation 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Split-hand/foot malformation 1 with sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly-capillary malformation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly-capillary malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Split-Hand/Foot Malformation 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation 6 from the curated CTD Gene-Disease Associations dataset. |
Arnold-Chiari Malformation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arnold-Chiari Malformation from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation 4 from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation 5 from the curated CTD Gene-Disease Associations dataset. |
SPLIT-HAND/FOOT MALFORMATION 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SPLIT-HAND/FOOT MALFORMATION 2 from the curated CTD Gene-Disease Associations dataset. |
arteriovenous malformation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease arteriovenous malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chiari type i malformation and syringomyelia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chiari type i malformation and syringomyelia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriovenous malformations; congenital arteriovenous malformation; hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intracranial arteriovenous malformation; intracranial arteriovenous malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intracranial arteriovenous malformation; intracranial arteriovenous malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wilms' tumor and congenital male genitourinary malformation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; intracranial arteriovenous malformation; intracranial arteriovenous malformations; intracranial hemorrhages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; intracranial arteriovenous malformation; intracranial arteriovenous malformations; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic nerve malformation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic nerve malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malformation Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term malformation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Congenital heart malformation Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Congenital heart malformation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
thyroid malformation Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease thyroid malformation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
malformation of the heart and great vessels Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the malformation of the heart and great vessels phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
malformation of the heart and great vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the malformation of the heart and great vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
external ear malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the external ear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gastrointestinal arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the gastrointestinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arnold-chiari malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the arnold-chiari malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital malformation of the great arteries Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital malformation of the great arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cochlear malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the cochlear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal vascular malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal vascular malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arnold-chiari type i malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the arnold-chiari type i malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malformation of the hepatic ductal plate Gene SetFrom HPO Gene-Disease Associations genes associated with the malformation of the hepatic ductal plate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
venous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the venous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dandy-walker malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the dandy-walker malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital malformation of the right heart Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital malformation of the right heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital malformation of the left heart Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital malformation of the left heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Arnold-Chiari Malformation Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Arnold-Chiari Malformation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
cerebral arteriovenous malformation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cerebral arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary arteriovenous malformation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
arteriovenous malformation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
microcephaly-capillary malformation syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly-capillary malformation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
split hand/foot malformation 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split hand/foot malformation 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split hand/foot malformation 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split hand/foot malformation 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?split-hand/foot malformation 1 with sensorineural hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation 3, gene duplication syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 3, gene duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
megalencephaly-capillary malformation-polymicrogyria syndrome, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephaly-capillary malformation-polymicrogyria syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Cerebellar Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Venous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Venous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malformation Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arteriovenous Malformation Of Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arteriovenous Malformation Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary Malformation-Arteriovenous Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Capillary Malformation-Arteriovenous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Pulmonary Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Pulmonary Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracranial Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinal Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinal Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rieger Eye Malformation Sequence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rieger Eye Malformation Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skeletal Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skeletal Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary Malformation (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Capillary Malformation (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arnold Chiari Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arnold Chiari Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malformation Of Corpus Callosum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Vascular Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Vascular Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malformation Of The Left Heart Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Of The Left Heart in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand/Foot Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Malformation With Mental Retardation, Basal Ganglia Disease, And Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chiari Malformation Type Ii Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chiari Malformation Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Parachute Malformation Of Mitral Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Parachute Malformation Of Mitral Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Congenital Malformation Syndromes, Not Elsewhere Classified In Icd10Cm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Congenital Malformation Syndromes, Not Elsewhere Classified In Icd10Cm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Split-Hand-Foot Malformation With Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malformation Of Cerebral Vessels Nos Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Of Cerebral Vessels Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cerebral Cavernous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Cavernous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Atresia With Splenic Malformation Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Atresia With Splenic Malformation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corpus Callosum Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corpus Callosum Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Adenomatoid Malformation Of Lung, Congenital Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Adenomatoid Malformation Of Lung, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vascular Malformation, Primary Intraosseous Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vascular Malformation, Primary Intraosseous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Capillary Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Capillary Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lymphatic Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lymphatic Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Vascular Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Vascular Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Malformation Syndromes With Other Skeletal Changes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformation Syndromes With Other Skeletal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracranial Arteriovenous Malformation, Ruptured Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Arteriovenous Malformation, Ruptured in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malformation Of Cornea Nos Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Of Cornea Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary-Venous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Capillary-Venous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Scoliosis Due To Bony Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Scoliosis Due To Bony Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malformation Of Cardiac Chambers And Connections, Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malformation Of Cardiac Chambers And Connections, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Split-Foot Malformation With Mesoaxial Polydactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Foot Malformation With Mesoaxial Polydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Malformation, Cleft Lip-Palate, Microcephaly And Digital Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Malformation, Cleft Lip-Palate, Microcephaly And Digital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Anorectal Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Anorectal Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ductal Plate Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ductal Plate Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retinal Arteriovenous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retinal Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Segmental Outgrowth, Lipomatosis, Arteriovenous Malformation, Epidermal Nevus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Segmental Outgrowth, Lipomatosis, Arteriovenous Malformation, Epidermal Nevus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heart And Brain Malformation Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heart And Brain Malformation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Lymphatic Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Lymphatic Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cochlear Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cochlear Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Arterial Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Arterial Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Inner Ear Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inner Ear Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Malformation Of The Hepatic Ductal Plate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malformation Of The Hepatic Ductal Plate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retinal Vascular Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Vascular Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Laryngeal Cartilage Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Laryngeal Cartilage Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dieulafoy'S Vascular Malformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dieulafoy'S Vascular Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
arteriovenous malformation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the arteriovenous malformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary arteriovenous malformation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary arteriovenous malformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cerebral arteriovenous malformation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral arteriovenous malformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Ebstein's malformation of tricuspid valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the Ebstein's malformation of tricuspid valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Cerebral cavernous malformation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral cavernous malformation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Cerebral cavernous malformation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral cavernous malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Arteriovenous malformation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arteriovenous malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lissencephaly 9 with complex brainstem malformation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lissencephaly 9 with complex brainstem malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 1 with sensorineural hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 1 with sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thyroid malformation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thyroid malformation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
CSF1R-related brain malformation and osteopetrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease CSF1R-related brain malformation and osteopetrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ear malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ear malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebral cavernous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cavernous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Split hand-foot malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Split hand-foot malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glomuvenous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glomuvenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebral arteriovenous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Vascular malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vascular malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Megalencephaly-capillary malformation-polymicrogyria syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Megalencephaly-capillary malformation-polymicrogyria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Rare venous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare venous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Rare combined vascular malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare combined vascular malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Capillary malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Capillary malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Microcephaly-capillary malformation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephaly-capillary malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lymphatic malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lymphatic malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malformation of the heart and great vessels Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malformation of the heart and great vessels phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cardiac malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiac malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Extracranial arteriovenous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Extracranial arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Brain malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Brain malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Venous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Venous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Split-foot malformation-mesoaxial polydactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Split-foot malformation-mesoaxial polydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary intraosseous venous malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary intraosseous venous malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heart and brain malformation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Heart and brain malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genitourinary and/or brain malformation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genitourinary and/or brain malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-syndromic renal or urinary tract malformation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-syndromic renal or urinary tract malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Anorectal malformation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anorectal malformation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Congenital heart malformation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Congenital heart malformation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
bone resorption; vitamin k deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone resorption; vitamin k deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Neuraminidase deficiency with beta-galactosidase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset. |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset. |
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choline deficiency; dna damage; folic acid deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Setproteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset. |
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Setproteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset. |
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Setproteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset. |
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Setproteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset. |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
long insular gyri, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in long insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
long insular gyri, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in long insular gyri, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
the prc2 complex sets long-term gene silencing through modification of histone tails Gene SetFrom Biocarta Pathways proteins participating in the the prc2 complex sets long-term gene silencing through modification of histone tails pathway from the Biocarta Pathways dataset. |
Long QT syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acquired long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LONG QT SYNDROME 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LONG QT SYNDROME 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long Qt Syndrome 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 9 from the curated CTD Gene-Disease Associations dataset. |
Long QT Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long QT Syndrome from the curated CTD Gene-Disease Associations dataset. |
Long QT syndrome type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long QT syndrome type 3 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 5 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 6 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 10 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 11 from the curated CTD Gene-Disease Associations dataset. |
Long Qt Syndrome 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 12 from the curated CTD Gene-Disease Associations dataset. |
LONG QT SYNDROME 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LONG QT SYNDROME 13 from the curated CTD Gene-Disease Associations dataset. |
Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset. |
long qt syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease long qt syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
long qt syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease long qt syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
long qt syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease long qt syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
human long-term memory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease human long-term memory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inherited cardiac arrhythmia long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inherited cardiac arrhythmia long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
drug-induced long-qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease drug-induced long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome; torsades de pointes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long-qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; heart arrest; long qt syndrome; syncope Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; heart arrest; long qt syndrome; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disease models, animal; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delayed graft function acute rejection episodes and long-term graft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arrhythmias, cardiac; death, sudden; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long qt syndrome; sinus tachycardia; tachycardia, sinus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long qt syndrome; sinus tachycardia; tachycardia, sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression ; long qt syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression ; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long-term kidney allograft survival Gene SetFrom GAD Gene-Disease Associations genes associated with the disease long-term kidney allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
long Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term long in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty-acyl-coa biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty-acyl-coa biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty-acyl-coa metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty-acyl-coa metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty-acyl-coa metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty-acyl-coa metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-term memory Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-term memory biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty-acyl-coa catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty-acyl-coa catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset. |
long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of long term synaptic depression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset. |
peroxisomal long-chain fatty acid import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peroxisomal long-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of plasma membrane long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
very long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the very long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
long-chain-enoyl-coa hydratase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-enoyl-coa hydratase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain acyl-coa hydrolase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acid-coa ligase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acid-coa ligase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very-long-chain-(s)-2-hydroxy-acid oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very-long-chain-(s)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acid binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acid binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol o-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol o-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-fatty-acyl-coa reductase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-fatty-acyl-coa reductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very long chain acyl-coa hydrolase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very long chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very-long-chain-acyl-coa dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very-long-chain-acyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-3-hydroxyacyl-coa dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-3-hydroxyacyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acyl-coa binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acyl-coa binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
very long-chain fatty acid-coa ligase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the very long-chain fatty acid-coa ligase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-acyl-coa dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-acyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain fatty acid transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long qt syndrome Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease long qt syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
increased density of long bones Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased density of long bones phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thickened cortex of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the thickened cortex of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long face Gene SetFrom HPO Gene-Disease Associations genes associated with the long face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fractures of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the fractures of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cortically dense long tubular bones Gene SetFrom HPO Gene-Disease Associations genes associated with the cortically dense long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long neck Gene SetFrom HPO Gene-Disease Associations genes associated with the long neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long foot Gene SetFrom HPO Gene-Disease Associations genes associated with the long foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the long metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the long fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long coccyx Gene SetFrom HPO Gene-Disease Associations genes associated with the long coccyx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
periosteal thickening of long tubular bones Gene SetFrom HPO Gene-Disease Associations genes associated with the periosteal thickening of long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long fibula Gene SetFrom HPO Gene-Disease Associations genes associated with the long fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long penis Gene SetFrom HPO Gene-Disease Associations genes associated with the long penis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long palm Gene SetFrom HPO Gene-Disease Associations genes associated with the long palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the long hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased density of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the increased density of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
crumpled long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the crumpled long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long second metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the long second metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the broad long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
very long chain fatty acid accumulation Gene SetFrom HPO Gene-Disease Associations genes associated with the very long chain fatty acid accumulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
stenosis of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the stenosis of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long clavicles Gene SetFrom HPO Gene-Disease Associations genes associated with the long clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness of long finger extensor muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of long finger extensor muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bowing of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the bowing of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the long upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-segment aganglionic megacolon Gene SetFrom HPO Gene-Disease Associations genes associated with the long-segment aganglionic megacolon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated long chain fatty acids Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated long chain fatty acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long nose Gene SetFrom HPO Gene-Disease Associations genes associated with the long nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long toe Gene SetFrom HPO Gene-Disease Associations genes associated with the long toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the long thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-tract signs Gene SetFrom HPO Gene-Disease Associations genes associated with the long-tract signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the long palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior bowing of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior bowing of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of long-chain fatty-acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of long-chain fatty-acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
overtubulated long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the overtubulated long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long ear Gene SetFrom HPO Gene-Disease Associations genes associated with the long ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
protuberances at ends of long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the protuberances at ends of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the long philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-chain dicarboxylic aciduria Gene SetFrom HPO Gene-Disease Associations genes associated with the long-chain dicarboxylic aciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long eyelashes in irregular rows Gene SetFrom HPO Gene-Disease Associations genes associated with the long eyelashes in irregular rows phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the long eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long eyebrows Gene SetFrom HPO Gene-Disease Associations genes associated with the long eyebrows phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Memory, Long-Term Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Memory, Long-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Long QT Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Long QT Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Long hematopoietin receptor, single chain, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Long hematopoietin receptor, single chain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Long hematopoietin receptor, Gp130 family 2, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Long hematopoietin receptor, Gp130 family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Long hematopoietin receptor, soluble alpha chain, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Long hematopoietin receptor, soluble alpha chain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PLUNC, long form Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PLUNC, long form protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peroxysomal long chain fatty acyl transporter Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peroxysomal long chain fatty acyl transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acyl-CoA thioesterase, long chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA thioesterase, long chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Anaphase-promoting complex subunit 4 long domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Anaphase-promoting complex subunit 4 long domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
long term depression Gene SetFrom KEGG Pathways proteins participating in the long term depression pathway from the KEGG Pathways dataset. |
long term potentiation Gene SetFrom KEGG Pathways proteins participating in the long term potentiation pathway from the KEGG Pathways dataset. |
long hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enhanced long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enhanced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long nails Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased length of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long snout Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long snout phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased diameter of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long fibula Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased length of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long gestation period Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long gestation period phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term object recognition memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased diameter of long bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long radius Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long ribs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long lived plasma cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long lived plasma cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long tibia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long tibia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term potentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long mandible Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long mandible phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long tail Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long femur Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long stride length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long stride length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term spatial reference memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long ulna Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long humerus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long humerus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long limbs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long limbs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long term depression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long incisors Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long toenails Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long toenails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long qt syndrome 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 1, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 1, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome-11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome-11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome-10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome-10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 2, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome, acquired, reduced susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
long qt syndrome-3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the long qt syndrome-3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Beta-oxidation of very long chain fatty acids Gene Setproteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways dataset. |
Repair synthesis of patch ~27-30 bases long by DNA polymerase Gene Setproteins participating in the Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway from the Reactome Pathways dataset. |
Synthesis of very long-chain fatty acyl-CoAs Gene Setproteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways dataset. |
Acquired Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Narrow Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Narrow Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Chain Dicarboxylic Aciduria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long-Chain Dicarboxylic Aciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Deletion Of Long Arm Of Chromosome 18 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Deletion Of Long Arm Of Chromosome 18 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Proximal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Segment Aganglionic Megacolon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long-Segment Aganglionic Megacolon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Tract Signs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long-Tract Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Philtrum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Philtrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Very Long Chain Fatty Acid Accumulation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Very Long Chain Fatty Acid Accumulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Palpebral Fissure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Palpebral Fissure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Face Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Foot Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Long Finger Extensor Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Long Finger Extensor Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bowing Of The Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bowing Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thickened Cortex Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thickened Cortex Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Toe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Upper Lip Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Long Bones With Narrow Diaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Long Bones With Narrow Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Overtubulated Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Overtubulated Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Thorax Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Thorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Fibula Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Fibula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Ulna Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Ulna in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Sleeper Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Sleeper Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Clavicle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Clavicle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fractures Of The Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fractures Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Crumpled Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Crumpled Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Periosteal Thickening Of Long Tubular Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periosteal Thickening Of Long Tubular Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Ear Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Protuberances At Ends Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Protuberances At Ends Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Medullary Cavity Of The Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Medullary Cavity Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Bowing Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Bowing Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Eyelashes In Irregular Rows Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Eyelashes In Irregular Rows in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Palm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Palm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Qt Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Eyebrows Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Eyebrows in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Curly Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Curly Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long, Smooth Philtrum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long, Smooth Philtrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Second Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Second Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Density Of Long Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Density Of Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cortically Dense Long Tubular Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cortically Dense Long Tubular Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Coccyx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Coccyx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
long-chain fatty-acyl-CoA biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty-acyl-CoA biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term memory Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term memory biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty-acyl-CoA catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty-acyl-CoA metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty-acyl-CoA metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid import into peroxisome Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid import into peroxisome biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty-acyl-CoA catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty-acyl-CoA metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty-acyl-CoA metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-term synaptic depression Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-term synaptic depression biological process from the curated GO Biological Process Annotations 2023 dataset. |
very long-chain fatty acid beta-oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the very long-chain fatty acid beta-oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of long-chain fatty acid import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of long-chain fatty acid import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of long-chain fatty acid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
long-chain fatty acyl-CoA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acyl-CoA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain acyl-CoA hydrolase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain fatty acid omega-hydroxylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acid omega-hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain fatty acid omega-1 hydroxylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acid omega-1 hydroxylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain fatty acid binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain fatty acid binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-acyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
very-long-chain-acyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the very-long-chain-acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-aldehyde dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-aldehyde dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
N-(long-chain-acyl)ethanolamine deacylase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the N-(long-chain-acyl)ethanolamine deacylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-3-hydroxyacyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-3-hydroxyacyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
very long chain acyl-CoA hydrolase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the very long chain acyl-CoA hydrolase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-fatty-acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-fatty-acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol O-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
very-long-chain enoyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the very-long-chain enoyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
decreased length of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased diameter of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased diameter of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long nails Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long nails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term object recognition memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term object recognition memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced long-term potentiation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced long-term potentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long gestation period Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long gestation period phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased diameter of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term spatial reference memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term spatial reference memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long tail Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long tail phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long ribs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long ribs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long toenails Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long toenails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long-term depression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long-term depression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal incus long process morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal incus long process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long fibula Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long fibula phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long tibia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long tibia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long stride length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long stride length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long femur Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long femur phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long lower incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long lower incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long humerus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long humerus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased length of long bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased length of long bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long mandible Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long mandible phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long snout Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long snout phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long ulna Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long ulna phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long radius Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long radius phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long limbs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long limbs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long lived plasma cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long lived plasma cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long photoreceptor outer segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long photoreceptor outer segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long tibia Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the long tibia phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Long-term hematopoietic stem cell_Bone marrow_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Long-term hematopoietic stem cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Long-projecting GABAergic cell_Brain_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Long-projecting GABAergic cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Long Descending Limb (Outer Medulla) cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Long Descending Limb (Outer Medulla) cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mitochondrial long chain fatty acid beta oxidation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mitochondrial long chain fatty acid beta oxidation pathway from the WikiPathways Pathways 2024 dataset. |
Beta-oxidation of very long chain fatty acids Gene Setproteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways 2024 dataset. |
Long-term potentiation Gene Setproteins participating in the Long-term potentiation pathway from the Reactome Pathways 2024 dataset. |
PCNA-Dependent Long Patch Base Excision Repair Gene Setproteins participating in the PCNA-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
POLB-Dependent Long Patch Base Excision Repair Gene Setproteins participating in the POLB-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset. |
Synthesis of very long-chain fatty acyl-CoAs Gene Setproteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways 2024 dataset. |
long-chain fatty-acyl-CoA biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-chain fatty-acyl-CoA biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
very long-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of long-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
long-term memory Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-term memory biological process from the curated GO Biological Process Annotations 2025 dataset. |
long-chain fatty-acyl-CoA catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the long-chain fatty-acyl-CoA catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
long-chain fatty acid import into cell Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Long COVID Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Long QT syndrome 3 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Long QT syndrome Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Long QT syndrome 1/ phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Long QT syndrome 3/ Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom KEGG Pathways 2026 proteins participating in the Long-term potentiation pathway from the KEGG Pathways 2026 dataset. |
Long-term depression Gene SetFrom KEGG Pathways 2026 proteins participating in the Long-term depression pathway from the KEGG Pathways 2026 dataset. |
regulators of bone mineralization Gene SetFrom Biocarta Pathways proteins participating in the regulators of bone mineralization pathway from the Biocarta Pathways dataset. |
bone remodeling Gene SetFrom Biocarta Pathways proteins participating in the bone remodeling pathway from the Biocarta Pathways dataset. |
bone Gene SetFrom BioGPS Mouse Cell Type and Tissue Gene Expression Profiles genes with high or low expression in bone relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset. |
Autosomal recessive hypophosphatemic bone disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gracile bone dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gracile bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasemia with bone disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bent bone dysplasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bent bone dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Osteogenesis imperfecta type 2, thin-bone Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Osteogenesis imperfecta type 2, thin-bone phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
High bone mass Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone Marrow Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Marrow Neoplasms from the curated CTD Gene-Disease Associations dataset. |
Bone Marrow Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Marrow Diseases from the curated CTD Gene-Disease Associations dataset. |
Bone Diseases, Metabolic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Metabolic from the curated CTD Gene-Disease Associations dataset. |
Bone Diseases, Developmental Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Developmental from the curated CTD Gene-Disease Associations dataset. |
Bone Cysts, Aneurysmal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Cysts, Aneurysmal from the curated CTD Gene-Disease Associations dataset. |
Giant Cell Tumor of Bone Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Giant Cell Tumor of Bone from the curated CTD Gene-Disease Associations dataset. |
Bone Diseases, Endocrine Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases, Endocrine from the curated CTD Gene-Disease Associations dataset. |
Fractures, Bone Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fractures, Bone from the curated CTD Gene-Disease Associations dataset. |
Bone Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Diseases from the curated CTD Gene-Disease Associations dataset. |
Bone Resorption Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Resorption from the curated CTD Gene-Disease Associations dataset. |
Paget Disease Of Bone 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Paget Disease Of Bone 4 from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Bone Tissue Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Bone Tissue from the curated CTD Gene-Disease Associations dataset. |
Fibrous Dysplasia of Bone Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrous Dysplasia of Bone from the curated CTD Gene-Disease Associations dataset. |
Bone Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Neoplasms from the curated CTD Gene-Disease Associations dataset. |
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 from the curated CTD Gene-Disease Associations dataset. |
Bone Marrow failure syndromes Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Marrow failure syndromes from the curated CTD Gene-Disease Associations dataset. |
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset. |
Alveolar Bone Loss Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alveolar Bone Loss from the curated CTD Gene-Disease Associations dataset. |
Bone Density Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Bone Density in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
bone remodeling disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone remodeling disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone marrow disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone marrow disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone marrow cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone marrow cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone development disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone development disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
sost-related sclerosing bone dysplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
paget's disease of bone Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease paget's disease of bone from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
ischemic bone disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ischemic bone disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone resorption disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone resorption disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone inflammation disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone inflammation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone marrow cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone marrow cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
paget's disease of bone Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease paget's disease of bone in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone remodeling disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone remodeling disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
ischemic bone disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease ischemic bone disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone resorption disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone resorption disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone structure disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone structure disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone inflammation disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone inflammation disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bone cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bone osteosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone marrow cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone marrow cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone deterioration disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone deterioration disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ischemic bone disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ischemic bone disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone resorption disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone resorption disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone giant cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone inflammation disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone inflammation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone remodeling disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone remodeling disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone marrow disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone marrow disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone ewing's sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone ewing's sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone development disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone development disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone epithelioid hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone epithelioid hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone structure disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone structure disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sost-related sclerosing bone dysplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant fibrous histiocytoma of bone Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant fibrous histiocytoma of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
paget's disease of bone Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paget's disease of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone giant cell sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone giant cell sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fibrosarcoma of bone Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fibrosarcoma of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; bone necrosis; femur head necrosis; osteonecrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; bone necrosis; femur head necrosis; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow diseases; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hip bone loss and fracture Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hip bone loss and fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow diseases; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow diseases; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; hearing loss; osteosarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; hearing loss; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
calcium homeostasis and peripheral bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcium homeostasis and peripheral bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early postmenopausal bone loss at the spine. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontitis; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal bone mineral density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; rett syndrome; scoliosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; rett syndrome; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; fractures, vertebral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; fractures, vertebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, metabolic; scoliosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; muscle strength Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; muscle strength in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; osteopenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; osteopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene SetFrom 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. |
anemia, sickle cell; bone diseases; sickle cell anemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; bone diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow diseases; dyskeratosis congenita; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow diseases; dyskeratosis congenita; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone necrosis; osteonecrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone necrosis; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
paget's disease of bone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease paget's disease of bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
osteoporosis, postmenopausal; bone density; hormone disturbance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease osteoporosis, postmenopausal; bone density; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; fractures, bone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; osteoporosis, postmenopausal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; chronic periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineralization Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineralization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early marginal bone loss around endosseous dental implants. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; rett syndrome; seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density but not spondylosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density but not spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; bone mineral density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary bone lymphomas. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary bone lymphomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone necrosis; femur head necrosis; osteonecrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone necrosis; femur head necrosis; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone resorption; calcinosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone resorption; calcinosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft-versus-host disease; bone marrow transplantation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft-versus-host disease; bone marrow transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral density (bmd) / quantitative ultra sound (qus) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density (bmd) / quantitative ultra sound (qus) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; fracture risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; bone necrosis; liver cirrhosis; osteonecrosis; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; bone necrosis; liver cirrhosis; osteonecrosis; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone necrosis; lupus erythematosus, systemic; osteonecrosis; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone necrosis; lupus erythematosus, systemic; osteonecrosis; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; osteoarthritis; osteoarthritis, knee Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoarthritis; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, developmental; osteoarthritis, hip Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases, developmental; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow diseases; dyskeratosis congenita Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow diseases; dyskeratosis congenita in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
combined bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease combined bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; osteoporosis; spinal fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone cancer; soft tissue sarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone cancer; soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone phenotypes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; sarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; osteoporosis; osteoporosis, postmenopausal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoporosis; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral density (spine) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density (spine) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow transplant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow transplant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone resorption; osteoporosis, postmenopausal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone resorption; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, metabolic; osteoporosis; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; osteoporosis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; osteosarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, metabolic; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; neoplasm invasiveness; osteosarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; neoplasm invasiveness; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyotrophic lateral sclerosis; bone resorption; lead poisoning Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; bone resorption; lead poisoning in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; spondylosis, lumbar Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; spondylosis, lumbar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone remodeling Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone resorption; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone resorption; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral density (bmd) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density (bmd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
very low bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease very low bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone necrosis; osteonecrosis; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone necrosis; osteonecrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early marginal bone loss around endosseous implants. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density and spondylosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density and spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases; degenerative arthropathy ; osteoarthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases; degenerative arthropathy ; osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone necrosis; jaw diseases; neuralgia; osteonecrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone necrosis; jaw diseases; neuralgia; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; fractures; osteocalcin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; fractures; osteocalcin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; calcium; fractures, nonvertebral; milk intolerance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; calcium; fractures, nonvertebral; milk intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density dehydroepiandrosterone sulphate osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density dehydroepiandrosterone sulphate osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cushing syndrome; fractures, bone; spinal fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cushing syndrome; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone resorption Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone resorption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow transplantation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; height Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; fractures, closed; humeral fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; fractures, closed; humeral fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; gram-negative bacterial infections; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; gram-negative bacterial infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, metabolic; osteoporosis, postmenopausal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased bone mass in patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased bone mass in patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; bone diseases, metabolic; osteoporosis; thalassemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; bone diseases, metabolic; osteoporosis; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; dental fistula; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; dental fistula; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
paget disease of bone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease paget disease of bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mass; osteoporotic fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mass; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone metastases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone metastases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; bone resorption; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; bone resorption; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammatory bowel disease; bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammatory bowel disease; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases; multiple myeloma Gene SetFrom 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. |
bone density; coronary calcification Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; coronary calcification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; hip fractures; osteoporosis; spinal injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; tricho-dento-osseous syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; tricho-dento-osseous syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral density (hip) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density (hip) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
testosterone; bone density; stature Gene SetFrom GAD Gene-Disease Associations genes associated with the disease testosterone; bone density; stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral density ; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density ; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone marrow diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone marrow diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
osteoporosis, postmenopausal; bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease osteoporosis, postmenopausal; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone characteristics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone characteristics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peak bone mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peak bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hip bone size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hip bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone mineral mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone mineral mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; osteoporotic fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; height; pth; pyridinoline, urinary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; height; pth; pyridinoline, urinary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; fractures, bone; spinal fractures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, bone; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia ; bone mineral density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia ; bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term bone in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
TET2_KO_GDS4287_429_mouse_LSK - bone marrow progenitor population Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the TET2_KO_GDS4287_429_mouse_LSK - bone marrow progenitor population gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
RUNX2_NULL MUTATION_GDS2184_719_mouse_Embryonal bone (MG-U74A) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the RUNX2_NULL MUTATION_GDS2184_719_mouse_Embryonal bone (MG-U74A) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
TET2_KO_GDS4287_430_mouse_CMP - bone marrow progenitor population Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the TET2_KO_GDS4287_430_mouse_CMP - bone marrow progenitor population gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
TET2_KO_GDS4287_431_mouse_GMP - bone marrow progenitor population Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the TET2_KO_GDS4287_431_mouse_GMP - bone marrow progenitor population gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
negative regulation of bone remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
ossification involved in bone remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ossification involved in bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of bone resorption Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of bone resorption biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell proliferation in bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
hematopoietic stem cell migration to bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hematopoietic stem cell migration to bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
semaphorin-plexin signaling pathway involved in bone trabecula morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the semaphorin-plexin signaling pathway involved in bone trabecula morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of apoptotic process in bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
fibroblast growth factor receptor signaling pathway involved in negative regulation of apoptotic process in bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fibroblast growth factor receptor signaling pathway involved in negative regulation of apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
chondrocyte morphogenesis involved in endochondral bone morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the chondrocyte morphogenesis involved in endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
endochondral bone growth Gene SetFrom GO Biological Process Annotations 2015 genes participating in the endochondral bone growth biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of bone development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of bone development biological process from the curated GO Biological Process Annotations 2015 dataset. |
fibroblast growth factor receptor signaling pathway involved in positive regulation of cell proliferation in bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fibroblast growth factor receptor signaling pathway involved in positive regulation of cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of bone mineralization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of bone mineralization biological process from the curated GO Biological Process Annotations 2015 dataset. |
chondrocyte development involved in endochondral bone morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the chondrocyte development involved in endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone mineralization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone mineralization biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of bone development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of bone development biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone trabecula morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone trabecula morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of apoptotic process in bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of bone mineralization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of bone mineralization biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of bone remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of bone resorption Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of bone resorption biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of bone trabecula formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of bone trabecula formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of bone remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone development biological process from the curated GO Biological Process Annotations 2015 dataset. |
apoptotic process in bone marrow Gene SetFrom GO Biological Process Annotations 2015 genes participating in the apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone resorption Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone resorption biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of bone trabecula formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of bone trabecula formation biological process from the curated GO Biological Process Annotations 2015 dataset. |