| Name |
|---|
SDR42E1 Geneshort chain dehydrogenase/reductase family 42E, member 1 Predicted to enable oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor. Predicted to be involved in steroid biosynthetic process. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ACSS3 Geneacyl-CoA synthetase short-chain family member 3 Enables propionate-CoA ligase activity. Predicted to be involved in ketone body biosynthetic process. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Mar 2025] |
ACSS2 Geneacyl-CoA synthetase short-chain family member 2 This gene encodes a cytosolic enzyme that catalyzes the activation of acetate for use in lipid synthesis and energy generation. The protein acts as a monomer and produces acetyl-CoA from acetate in a reaction that requires ATP. Expression of this gene is regulated by sterol regulatory element-binding proteins, transcription factors that activate genes required for the synthesis of cholesterol and unsaturated fatty acids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009] |
ACSS1 Geneacyl-CoA synthetase short-chain family member 1 This gene encodes a mitochondrial acetyl-CoA synthetase enzyme. A similar protein in mice plays an important role in the tricarboxylic acid cycle by catalyzing the conversion of acetate to acetyl CoA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
SDR42E2 Geneshort chain dehydrogenase/reductase family 42E, member 2 Predicted to enable oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor. Predicted to be involved in steroid biosynthetic process. [provided by Alliance of Genome Resources, Mar 2025] |
ACADSB Geneacyl-CoA dehydrogenase, short/branched chain Short/branched chain acyl-CoA dehydrogenase(ACADSB) is a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. Substrate specificity is the primary characteristic used to define members of this gene family. The ACADSB gene product has the greatest activity towards the short branched chain acyl-CoA derivative, (S)-2-methylbutyryl-CoA, but also reacts significantly with other 2-methyl branched chain substrates and with short straight chain acyl-CoAs. The cDNA encodes for a mitochondrial precursor protein which is cleaved upon mitochondrial import and predicted to yield a mature peptide of approximately 43.7-KDa. [provided by RefSeq, Jul 2008] |
SHOX2 Geneshort stature homeobox 2 This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009] |
KIR2DS5 Genekiller cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 5 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] |
KIR2DS2 Genekiller cell immunoglobulin-like receptor, two domains, short 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 represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014] |
SCOCP1 Geneshort coiled-coil protein pseudogene 1 |
SHOX Geneshort stature homeobox This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008] |
LOC100132571 Geneshort coiled-coil protein pseudogene |
KIR2DS4 Genekiller cell immunoglobulin-like receptor, two domains, short 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. [provided by RefSeq, Jul 2008] |
KIR2DS3 Genekiller cell immunoglobulin-like receptor, two domains, short 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] |
KIR2DS1 Genekiller cell immunoglobulin-like receptor, two domains, short 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] |
SDR16C6P Geneshort chain dehydrogenase/reductase family 16C, member 6, pseudogene |
OPN1SW Geneopsin 1 (cone pigments), short-wave-sensitive This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008] |
ACADS Geneacyl-CoA dehydrogenase, C-2 to C-3 short chain This gene encodes a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with short-chain acyl-CoA dehydrogenase (SCAD) deficiency. Alternative splicing results in two variants which encode different isoforms. [provided by RefSeq, Oct 2014] |
ECHS1 Geneenoyl CoA hydratase, short chain, 1, mitochondrial The protein encoded by this gene functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. The gene product is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. [provided by RefSeq, Jul 2008] |
LOC100422348 Geneshort chain dehydrogenase/reductase family 42E, member 1 pseudogene |
LOC100422346 Geneshort chain dehydrogenase/reductase family 42E, member 1 pseudogene |
LOC100422347 Geneshort chain dehydrogenase/reductase family 42E, member 1 pseudogene |
KIR3DS1 Genekiller cell immunoglobulin-like receptor, three domains, short 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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
SDR42E1P1 Geneshort chain dehydrogenase/reductase family 42E, member 1 pseudogene 1 |
SEMA5B Genesema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B This gene encodes a member of the semaphorin protein family which regulates axon growth during development of the nervous system. The encoded protein has a characteristic Sema domain near the N-terminus, through which semaphorins bind to plexin, and five thrombospondin type 1 repeats in the C-terminal region of the protein. The protein product may be cleaved and exist as a secreted molecule (PMID: 19463192). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012] |
SEMA5A Genesema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010] |
SCOC Geneshort coiled-coil protein This gene encodes a short coiled-coiled domain-containing protein that localizes to the Golgi apparatus. The encoded protein interacts with ADP-ribosylation factor-like proteins. Pseudogenes of this gene are found on chromosomes 1 and 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009] |
SDR9C7 Geneshort chain dehydrogenase/reductase family 9C, member 7 This gene encodes a protein with similarity to the short-chain dehydrogenase/reductase (SDR) family but has not been shown to have retinoid or dehydrogenase activities. [provided by RefSeq, Apr 2010] |
HSCR7 GeneHirschsprung disease, short-segment, 3 |
HSCR6 GeneHirschsprung disease, short-segment, 2 |
MRSS GeneMental retardation, X-linked, with short stature |
SEMA3A Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A This gene is a member of the semaphorin family and encodes a protein with an Ig-like C2-type (immunoglobulin-like) domain, a PSI domain and a Sema domain. This secreted protein can function as either a chemorepulsive agent, inhibiting axonal outgrowth, or as a chemoattractive agent, stimulating the growth of apical dendrites. In both cases, the protein is vital for normal neuronal pattern development. Increased expression of this protein is associated with schizophrenia and is seen in a variety of human tumor cell lines. Also, aberrant release of this protein is associated with the progression of Alzheimer's disease. [provided by RefSeq, Jul 2008] |
SEMA3C Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017] |
SEMA3B Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B The protein encoded by this gene belongs to the class-3 semaphorin/collapsin family, whose members function in growth cone guidance during neuronal development. This family member inhibits axonal extension and has been shown to act as a tumor suppressor by inducing apoptosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
SEMA3E Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. This gene encodes a class 4 semaphorin. This gene encodes a class 3 semaphorin. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010] |
SEMA3D Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin like domain and a C-terminal basic domain. The protein encoded by this gene binds neuropilin and plays an important role in cardiovascular development. [provided by RefSeq, Aug 2016] |
SEMA3G Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G The transcription of this gene is activated by PPAR-gamma, and the resulting protein product plays a role in endothelial cell migration. Expression of this gene also inhibits tumor cell migration and invasion. [provided by RefSeq, Jul 2016] |
SEMA3F Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin loop and a C-terminal basic domain. This gene is expressed by the endothelial cells where it was found to act in an autocrine fashion to induce apoptosis, inhibit cell proliferation and survival, and function as an anti-tumorigenic agent. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
LOC100422339 Geneshort chain dehydrogenase/reductase family 42E, member 1 pseudogene |
SDR16C5 Geneshort chain dehydrogenase/reductase family 16C, member 5 This gene encodes a member of the short-chain alcohol dehydrogenase/reductase superfamily of proteins and is involved in the oxidation of retinol to retinaldehyde. The encoded protein is associated with the endoplasmic reticulum and is predicted to contain three transmembrane helices, suggesting that it is an integral membrane protein. It recognizes all-trans-retinol and all-trans-retinaldehyde as substrates and exhibits a strong preference for NAD(+)/NADH as cofactors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
LOC100422730 Genesema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A pseudogene |
SEMA4A Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010] |
SEMA4B Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B Predicted to enable chemorepellent activity; neuropilin binding activity; and semaphorin receptor binding activity. Predicted to be involved in several processes, including axon guidance; neural crest cell migration; and semaphorin-plexin signaling pathway. Predicted to be located in membrane and synapse. Predicted to be active in glutamatergic synapse and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4C Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C Predicted to enable chemorepellent activity; neuropilin binding activity; and semaphorin receptor binding activity. Involved in muscle cell differentiation and positive regulation of stress-activated MAPK cascade. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4D Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D Enables identical protein binding activity; semaphorin receptor binding activity; and transmembrane signaling receptor activity. Involved in several processes, including ossification involved in bone maturation; positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and regulation of neuron projection development. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4F Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F This gene encodes a transmembrane class IV semaphorin family protein, which plays a role in neural development. This gene may be involved in neurogenesis in prostate cancer, the development of neurofibromas, and breast cancer tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
SEMA4G Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011] |
SDR39U1 Geneshort chain dehydrogenase/reductase family 39U, member 1 This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) superfamily, which includes both classical and extended types. The encoded protein represents an extended type, with similarity to epimerases. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Mar 2014] |
LOC105371187 Geneputative short-chain dehydrogenase/reductase family 42E member 2 |
STMP1 Geneshort transmembrane mitochondrial protein 1 Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrion. Is active in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC124901069 Geneshort transmembrane mitochondrial protein 1-like |
LINC01221 Genelong intergenic non-protein coding RNA 1221 |
LINC01227 Genelong intergenic non-protein coding RNA 1227 |
LINC01091 Genelong intergenic non-protein coding RNA 1091 |
LINC01090 Genelong intergenic non-protein coding RNA 1090 |
LINC01093 Genelong intergenic non-protein coding RNA 1093 |
LINC01095 Genelong intergenic non-protein coding RNA 1095 |
LINC01094 Genelong intergenic non-protein coding RNA 1094 |
LINC01097 Genelong intergenic non-protein coding RNA 1097 |
LINC01096 Genelong intergenic non-protein coding RNA 1096 |
LINC01098 Genelong intergenic non-protein coding RNA 1098 |
LINC00320 Genelong intergenic non-protein coding RNA 320 |
LINC00323 Genelong intergenic non-protein coding RNA 323 |
LINC00324 Genelong intergenic non-protein coding RNA 324 |
LINC00326 Genelong intergenic non-protein coding RNA 326 |
LINC00327 Genelong intergenic non-protein coding RNA 327 |
LINC00328 Genelong intergenic non-protein coding RNA 328 |
LINC01215 Genelong intergenic non-protein coding RNA 1215 |
LINC01214 Genelong intergenic non-protein coding RNA 1214 |
LINC00847 Genelong intergenic non-protein coding RNA 847 |
LINC00849 Genelong intergenic non-protein coding RNA 849 |
LINC01251 Genelong intergenic non-protein coding RNA 1251 |
LINC01250 Genelong intergenic non-protein coding RNA 1250 |
LINC01257 Genelong intergenic non-protein coding RNA 1257 |
CCDC26 GeneCCDC26 long non-coding RNA Implicated in brain cancer and high grade glioma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01255 Genelong intergenic non-protein coding RNA 1255 |
LINC01491 Genelong intergenic non-protein coding RNA 1491 |
LINC01490 Genelong intergenic non-protein coding RNA 1490 |
LINC01198 Genelong intergenic non-protein coding RNA 1198 Biomarker of malignant astrocytoma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01194 Genelong intergenic non-protein coding RNA 1194 |
LINC01195 Genelong intergenic non-protein coding RNA 1195 |
LINC01197 Genelong intergenic non-protein coding RNA 1197 |
LINC01191 Genelong intergenic non-protein coding RNA 1191 |
LINC01192 Genelong intergenic non-protein coding RNA 1192 |
LINC01193 Genelong intergenic non-protein coding RNA 1193 |
LINC01360 Genelong intergenic non-protein coding RNA 1360 |
HEIH Genehepatocellular carcinoma up-regulated EZH2-associated long non-coding RNA Biomarker of esophagus squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01365 Genelong intergenic non-protein coding RNA 1365 |
LINC01547 Genelong intergenic non-protein coding RNA 1547 Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01546 Genelong intergenic non-protein coding RNA 1546 |
LINC01545 Genelong intergenic non-protein coding RNA 1545 |
LINC01549 Genelong intergenic non-protein coding RNA 1549 |
LINC01548 Genelong intergenic non-protein coding RNA 1548 |
LINC00633 Genelong intergenic non-protein coding RNA 633 |
LINC00630 Genelong intergenic non-protein coding RNA 630 |
LINC00636 Genelong intergenic non-protein coding RNA 636 |
LINC00637 Genelong intergenic non-protein coding RNA 637 |
LINC00635 Genelong intergenic non-protein coding RNA 635 |
LINC00638 Genelong intergenic non-protein coding RNA 638 |
LINC00639 Genelong intergenic non-protein coding RNA 639 |
LINC01348 Genelong intergenic non-protein coding RNA 1348 |
LINC01550 Genelong intergenic non-protein coding RNA 1550 |
LINC01551 Genelong intergenic non-protein coding RNA 1551 |
LINC01552 Genelong intergenic non-protein coding RNA 1552 |
LINC00879 Genelong intergenic non-protein coding RNA 879 |
LINC00877 Genelong intergenic non-protein coding RNA 877 |
LINC00870 Genelong intergenic non-protein coding RNA 870 |
LINC00871 Genelong intergenic non-protein coding RNA 871 |
LINC00265-3P Genelong intergenic non-protein coding RNA 265-3, pseudogene |
LINC00969 Genelong intergenic non-protein coding RNA 969 |
LINC00404 Genelong intergenic non-protein coding RNA 404 |
LINC00400 Genelong intergenic non-protein coding RNA 400 |
LINC00403 Genelong intergenic non-protein coding RNA 403 |
LINC00402 Genelong intergenic non-protein coding RNA 402 |
LINC00408 Genelong intergenic non-protein coding RNA 408 |
LINC01510 Genelong intergenic non-protein coding RNA 1510 This gene encodes a natural antisense transcript highly expressed in papillary thyroid carcinomas harboring BRAF V600E mutation or RET gene rearrangements. This lncRNA induces the downstream MAPK pathway and is part of a co-expression network including different oncogenes belonging to the MAPK and PI3H/AKT pathways. In thyroid carcinomas, this gene has oncogenic properties associated with increased proliferation and drug resistance. [provided by RefSeq, Jan 2020] |
LINC01114 Genelong intergenic non-protein coding RNA 1114 |
LINC01115 Genelong intergenic non-protein coding RNA 1115 |
LINC01116 Genelong intergenic non-protein coding RNA 1116 |
LINC01117 Genelong intergenic non-protein coding RNA 1117 |
LINC01111 Genelong intergenic non-protein coding RNA 1111 |
LINC01118 Genelong intergenic non-protein coding RNA 1118 |
LINC01514 Genelong intergenic non-protein coding RNA 1514 |
LINC00244 Genelong intergenic non-protein coding RNA 244 |
LINC00243 Genelong intergenic non-protein coding RNA 243 |
LINC00242 Genelong intergenic non-protein coding RNA 242 |
LINC00240 Genelong intergenic non-protein coding RNA 240 |
LINC00939 Genelong intergenic non-protein coding RNA 939 |
LINC00938 Genelong intergenic non-protein coding RNA 938 |
LINC00930 Genelong intergenic non-protein coding RNA 930 |
LINC00933 Genelong intergenic non-protein coding RNA 933 |
LINC00935 Genelong intergenic non-protein coding RNA 935 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and sperm flagellum. Predicted to be active in axonemal A tubule inner sheath. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00934 Genelong intergenic non-protein coding RNA 934 |
LINC00937 Genelong intergenic non-protein coding RNA 937 |
LINC00443 Genelong intergenic non-protein coding RNA 443 |
LINC01099 Genelong intergenic non-protein coding RNA 1099 |
LINC00322 Genelong intergenic non-protein coding RNA 322 |
LINC01327 Genelong intergenic non-protein coding RNA 1327 |
LINC01324 Genelong intergenic non-protein coding RNA 1324 |
LINC01322 Genelong intergenic non-protein coding RNA 1322 |
LINC01320 Genelong intergenic non-protein coding RNA 1320 |
LINC00433 Genelong intergenic non-protein coding RNA 433 |
LINC01424 Genelong intergenic non-protein coding RNA 1424 |
LINC01425 Genelong intergenic non-protein coding RNA 1425 |
LINC01426 Genelong intergenic non-protein coding RNA 1426 |
LINC01427 Genelong intergenic non-protein coding RNA 1427 |
LINC01420 Genelong intergenic non-protein coding RNA 1420 Involved in negative regulation of cytoplasmic mRNA processing body assembly and nuclear-transcribed mRNA catabolic process. Located in P-body. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01422 Genelong intergenic non-protein coding RNA 1422 |
LINC01423 Genelong intergenic non-protein coding RNA 1423 |
LINC01428 Genelong intergenic non-protein coding RNA 1428 |
LINC01280 Genelong intergenic non-protein coding RNA 1280 |
LINC01281 Genelong intergenic non-protein coding RNA 1281 |
LINC01282 Genelong intergenic non-protein coding RNA 1282 |
LINC01284 Genelong intergenic non-protein coding RNA 1284 |
LINC01285 Genelong intergenic non-protein coding RNA 1285 |
LINC01287 Genelong intergenic non-protein coding RNA 1287 |
LINC01288 Genelong intergenic non-protein coding RNA 1288 |
LINC01289 Genelong intergenic non-protein coding RNA 1289 |
LINC00488 Genelong intergenic non-protein coding RNA 488 |
LINC00484 Genelong intergenic non-protein coding RNA 484 |
LINC00487 Genelong intergenic non-protein coding RNA 487 |
LINC00486 Genelong intergenic non-protein coding RNA 486 |
LINC00483 Genelong intergenic non-protein coding RNA 483 |
LINC00482 Genelong intergenic non-protein coding RNA 482 |
SHFLD3 GeneSplit-hand/foot malformation with long bone deficiency 3 |
SPTLC1P1 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 1 |
SPTLC1P2 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 2 |
SPTLC1P5 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 5 |
SPTLC1P4 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 4 |
LINC00266-4P Genelong intergenic non-protein coding RNA 266-4, pseudogene |
LLPH GeneLLP homolog, long-term synaptic facilitation (Aplysia) Enables RNA binding activity. Predicted to be involved in dendrite extension and positive regulation of dendritic spine development. Located in chromosome and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01363 Genelong intergenic non-protein coding RNA 1363 |
LINC00526 Genelong intergenic non-protein coding RNA 526 |
LINC00527 Genelong intergenic non-protein coding RNA 527 |
LINC00524 Genelong intergenic non-protein coding RNA 524 |
LINC00525 Genelong intergenic non-protein coding RNA 525 |
LINC00523 Genelong intergenic non-protein coding RNA 523 |
LINC00520 Genelong intergenic non-protein coding RNA 520 |
LINC00521 Genelong intergenic non-protein coding RNA 521 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00528 Genelong intergenic non-protein coding RNA 528 |
LINC00529 Genelong intergenic non-protein coding RNA 529 |
LINC01499 Genelong intergenic non-protein coding RNA 1499 |
OLMALINC Geneoligodendrocyte maturation-associated long intergenic non-coding RNA |
LINC00200 Genelong intergenic non-protein coding RNA 200 |
LINC00207 Genelong intergenic non-protein coding RNA 207 |
LINC00052 Genelong intergenic non-protein coding RNA 52 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00165 Genelong intergenic non-protein coding RNA 165 |
LINC01252 Genelong intergenic non-protein coding RNA 1252 |
LINC01256 Genelong intergenic non-protein coding RNA 1256 |
LINC01254 Genelong intergenic non-protein coding RNA 1254 |
LINC01258 Genelong intergenic non-protein coding RNA 1258 |
LINC01590 Genelong intergenic non-protein coding RNA 1590 |
LINC01591 Genelong intergenic non-protein coding RNA 1591 |
LINC01592 Genelong intergenic non-protein coding RNA 1592 |
LINC01594 Genelong intergenic non-protein coding RNA 1594 |
LINC01599 Genelong intergenic non-protein coding RNA 1599 |
LINC01046 Genelong intergenic non-protein coding RNA 1046 |
LINC01047 Genelong intergenic non-protein coding RNA 1047 |
LINC01044 Genelong intergenic non-protein coding RNA 1044 |
LINC01043 Genelong intergenic non-protein coding RNA 1043 |
LINC01040 Genelong intergenic non-protein coding RNA 1040 |
LINC01049 Genelong intergenic non-protein coding RNA 1049 |
LINC00311 Genelong intergenic non-protein coding RNA 311 |
LINC00310 Genelong intergenic non-protein coding RNA 310 |
LINC00313 Genelong intergenic non-protein coding RNA 313 |
LINC00312 Genelong intergenic non-protein coding RNA 312 This gene produces an intronless transcript that is thought to function as a tumor suppressor. This transcript is downregulated in nasopharyngeal carcinoma and is a negative regulator of estrogen receptor signaling. A common polymorphism in this transcript allows the production of a 94 aa open reading frame in some individuals, which may interact directly with estrogen receptor 1 (PMID:15474036). This open reading frame does not exist on the reference genome haplotype, which is hypothesized to function through a non-coding RNA product. [provided by RefSeq, Mar 2017] |
LINC00315 Genelong intergenic non-protein coding RNA 315 |
LINC00314 Genelong intergenic non-protein coding RNA 314 |
LINC00316 Genelong intergenic non-protein coding RNA 316 |
LINCMD1 Genelong intergenic non-protein coding RNA, muscle differentiation 1 |
LINC-ROR Genelong intergenic non-protein coding RNA, regulator of reprogramming This gene produces a long non-coding RNA that regulates the reprogramming of pluripotent stem cells. This RNA suppresses induction of tumor protein p53 after DNA damage. It is thought to act as a sponge for microRNAs that regulate stem cell factors POU class 5 homeobox 1, Nanog, and SRY-box 2. This RNA may also have a extracellular role in modulating response to hypoxia in hepatocellular cancer cells. Expression of this transcript is associated with tumor progression and epithelial to mesenchymal transition and metastasis. [provided by RefSeq, Dec 2017] |
LINC00571 Genelong intergenic non-protein coding RNA 571 |
LINC01209 Genelong intergenic non-protein coding RNA 1209 |
LINC01201 Genelong intergenic non-protein coding RNA 1201 |
LINC01202 Genelong intergenic non-protein coding RNA 1202 |
LINC01203 Genelong intergenic non-protein coding RNA 1203 |
LINC01204 Genelong intergenic non-protein coding RNA 1204 |
LINC01205 Genelong intergenic non-protein coding RNA 1205 |
LINC01206 Genelong intergenic non-protein coding RNA 1206 |
LINC01207 Genelong intergenic non-protein coding RNA 1207 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01452 Genelong intergenic non-protein coding RNA 1452 |
LINC01166 Genelong intergenic non-protein coding RNA 1166 |
LINC00415 Genelong intergenic non-protein coding RNA 415 |
LINC00411 Genelong intergenic non-protein coding RNA 411 |
LINC01088 Genelong intergenic non-protein coding RNA 1088 |
LINC01518 Genelong intergenic non-protein coding RNA 1518 |
LINC01519 Genelong intergenic non-protein coding RNA 1519 |
LINC01516 Genelong intergenic non-protein coding RNA 1516 |
LINC00391 Genelong intergenic non-protein coding RNA 391 |
LINC00393 Genelong intergenic non-protein coding RNA 393 |
LINC00392 Genelong intergenic non-protein coding RNA 392 |
LINC00395 Genelong intergenic non-protein coding RNA 395 |
LINC00396 Genelong intergenic non-protein coding RNA 396 |
LINC00399 Genelong intergenic non-protein coding RNA 399 |
LINC00398 Genelong intergenic non-protein coding RNA 398 |
LINC00152 Genelong intergenic non-protein coding RNA 152 This gene produces a long non-coding RNA that is overexpressed in cancer cells and promotes cell proliferation and epithelial-mesenchymal transition. This RNA may bind enhancer of zeste homolog 2 and participate in the transcriptional silencing of tumor suppressor genes. It may act as a sponge for microRNAs. Alternatively spliced variants have been observed. [provided by RefSeq, Dec 2017] |
LINC00159 Genelong intergenic non-protein coding RNA 159 |
LINC00158 Genelong intergenic non-protein coding RNA 158 |
LINC00845 Genelong intergenic non-protein coding RNA 845 |
LINC00844 Genelong intergenic non-protein coding RNA 844 |
LINC00841 Genelong intergenic non-protein coding RNA 841 |
LINC00840 Genelong intergenic non-protein coding RNA 840 |
LINC00843 Genelong intergenic non-protein coding RNA 843 |
LINC00842 Genelong intergenic non-protein coding RNA 842 |
LINC01495 Genelong intergenic non-protein coding RNA 1495 |
LINC01494 Genelong intergenic non-protein coding RNA 1494 |
LINC01497 Genelong intergenic non-protein coding RNA 1497 |
LINC01496 Genelong intergenic non-protein coding RNA 1496 |
LINC01493 Genelong intergenic non-protein coding RNA 1493 |
LINC01492 Genelong intergenic non-protein coding RNA 1492 |
LINC01498 Genelong intergenic non-protein coding RNA 1498 |
LINC00458 Genelong intergenic non-protein coding RNA 458 |
LINC00459 Genelong intergenic non-protein coding RNA 459 |
LINC00452 Genelong intergenic non-protein coding RNA 452 |
LINC00456 Genelong intergenic non-protein coding RNA 456 |
LINC00457 Genelong intergenic non-protein coding RNA 457 |
LINC00454 Genelong intergenic non-protein coding RNA 454 |
LINC00954 Genelong intergenic non-protein coding RNA 954 |
LINC01128 Genelong intergenic non-protein coding RNA 1128 |
LINC01125 Genelong intergenic non-protein coding RNA 1125 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01124 Genelong intergenic non-protein coding RNA 1124 |
LINC01126 Genelong intergenic non-protein coding RNA 1126 |
LINC01121 Genelong intergenic non-protein coding RNA 1121 |
LINC01120 Genelong intergenic non-protein coding RNA 1120 |
LINC01123 Genelong intergenic non-protein coding RNA 1123 |
LINC01122 Genelong intergenic non-protein coding RNA 1122 |
LINC00298 Genelong intergenic non-protein coding RNA 298 |
LINC00299 Genelong intergenic non-protein coding RNA 299 |
LINC00294 Genelong intergenic non-protein coding RNA 294 |
LINC00297 Genelong intergenic non-protein coding RNA 297 |
LINC00293 Genelong intergenic non-protein coding RNA 293 |
LINC00364 Genelong intergenic non-protein coding RNA 364 |
LINC01402 Genelong intergenic non-protein coding RNA 1402 |
LINC01024 Genelong intergenic non-protein coding RNA 1024 |
LINC00643 Genelong intergenic non-protein coding RNA 643 |
LINC00642 Genelong intergenic non-protein coding RNA 642 |
LINC00641 Genelong intergenic non-protein coding RNA 641 |
LINC00640 Genelong intergenic non-protein coding RNA 640 |
LINC00645 Genelong intergenic non-protein coding RNA 645 |
LINC00644 Genelong intergenic non-protein coding RNA 644 |
LINC00649 Genelong intergenic non-protein coding RNA 649 |
LINC00648 Genelong intergenic non-protein coding RNA 648 |
LINC00251 Genelong intergenic non-protein coding RNA 251 |
LINC00929 Genelong intergenic non-protein coding RNA 929 |
LINC00603 Genelong intergenic non-protein coding RNA 603 |
LINC01419 Genelong intergenic non-protein coding RNA 1419 |
LINC01415 Genelong intergenic non-protein coding RNA 1415 |
LINC01416 Genelong intergenic non-protein coding RNA 1416 |
LINC01411 Genelong intergenic non-protein coding RNA 1411 |
LINC01413 Genelong intergenic non-protein coding RNA 1413 |
LINC01412 Genelong intergenic non-protein coding RNA 1412 |
LINC00504 Genelong intergenic non-protein coding RNA 504 |
LINC00505 Genelong intergenic non-protein coding RNA 505 |
LINC00506 Genelong intergenic non-protein coding RNA 506 |
LINC00507 Genelong intergenic non-protein coding RNA 507 |
LINC00501 Genelong intergenic non-protein coding RNA 501 |
LINC00216 Genelong intergenic non-protein coding RNA 216 |
LINC00210 Genelong intergenic non-protein coding RNA 210 |
LINC00211 Genelong intergenic non-protein coding RNA 211 |
LINC00967 Genelong intergenic non-protein coding RNA 967 |
LINC00964 Genelong intergenic non-protein coding RNA 964 |
LINC00965 Genelong intergenic non-protein coding RNA 965 |
LINC00963 Genelong intergenic non-protein coding RNA 963 |
LINC00960 Genelong intergenic non-protein coding RNA 960 |
LINC00961 Genelong intergenic non-protein coding RNA 961 Involved in cellular response to amino acid stimulus and negative regulation of TORC1 signaling. Located in late endosome membrane and lysosomal proton-transporting V-type ATPase complex. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01608 Genelong intergenic non-protein coding RNA 1608 |
LINC01609 Genelong intergenic non-protein coding RNA 1609 |
LINC01604 Genelong intergenic non-protein coding RNA 1604 |
LINC01605 Genelong intergenic non-protein coding RNA 1605 |
LINC01606 Genelong intergenic non-protein coding RNA 1606 |
LINC01607 Genelong intergenic non-protein coding RNA 1607 |
LINC01600 Genelong intergenic non-protein coding RNA 1600 |
LINC01601 Genelong intergenic non-protein coding RNA 1601 |
LINC01602 Genelong intergenic non-protein coding RNA 1602 |
LINC01603 Genelong intergenic non-protein coding RNA 1603 |
LINC00559 Genelong intergenic non-protein coding RNA 559 |
LINC00558 Genelong intergenic non-protein coding RNA 558 |
LINC00557 Genelong intergenic non-protein coding RNA 557 |
LINC00556 Genelong intergenic non-protein coding RNA 556 |
LINC00555 Genelong intergenic non-protein coding RNA 555 |
LINC00552 Genelong intergenic non-protein coding RNA 552 |
LINC00551 Genelong intergenic non-protein coding RNA 551 |
LINC00550 Genelong intergenic non-protein coding RNA 550 |
LINC01337 Genelong intergenic non-protein coding RNA 1337 |
LINC01375 Genelong intergenic non-protein coding RNA 1375 |
LINC01376 Genelong intergenic non-protein coding RNA 1376 |
LINC01377 Genelong intergenic non-protein coding RNA 1377 |
LINC01370 Genelong intergenic non-protein coding RNA 1370 |
LINC01378 Genelong intergenic non-protein coding RNA 1378 |
PARTICL Genepromoter of MAT2A antisense radiation-induced circulating long non-coding RNA Enables dsDNA-RNA triple helix-forming chromatin adaptor activity and mRNA binding activity. Involved in cellular response to ionizing radiation and regulatory ncRNA-mediated heterochromatin formation. Is active in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01484 Genelong intergenic non-protein coding RNA 1484 |
LINC00028 Genelong intergenic non-protein coding RNA 28 |
LINC01483 Genelong intergenic non-protein coding RNA 1483 |
LINC00160 Genelong intergenic non-protein coding RNA 160 |
LINC01039 Genelong intergenic non-protein coding RNA 1039 |
LINC01038 Genelong intergenic non-protein coding RNA 1038 |
LINC01036 Genelong intergenic non-protein coding RNA 1036 |
LINC01033 Genelong intergenic non-protein coding RNA 1033 |
LINC01032 Genelong intergenic non-protein coding RNA 1032 |
LINC01031 Genelong intergenic non-protein coding RNA 1031 |
LINC01030 Genelong intergenic non-protein coding RNA 1030 |
LINC01410 Genelong intergenic non-protein coding RNA 1410 |
LINC01231 Genelong intergenic non-protein coding RNA 1231 |
LINC01230 Genelong intergenic non-protein coding RNA 1230 |
LINC01233 Genelong intergenic non-protein coding RNA 1233 |
LINC01237 Genelong intergenic non-protein coding RNA 1237 |
LINC00184 Genelong intergenic non-protein coding RNA 184 |
LINC00189 Genelong intergenic non-protein coding RNA 189 |
LINC00448 Genelong intergenic non-protein coding RNA 448 |
LSINCT5 Genelong stress-induced non-coding transcript 5 |
LINC01179 Genelong intergenic non-protein coding RNA 1179 |
LINC00441 Genelong intergenic non-protein coding RNA 441 |
LINC00440 Genelong intergenic non-protein coding RNA 440 |
LINC00442 Genelong intergenic non-protein coding RNA 442 |
LINC00445 Genelong intergenic non-protein coding RNA 445 |
LINC00444 Genelong intergenic non-protein coding RNA 444 |
LINC00446 Genelong intergenic non-protein coding RNA 446 |
LINC01234 Genelong intergenic non-protein coding RNA 1234 |
LINC01239 Genelong intergenic non-protein coding RNA 1239 |
LINC01521 Genelong intergenic non-protein coding RNA 1521 |
LINC01520 Genelong intergenic non-protein coding RNA 1520 |
LINC01525 Genelong intergenic non-protein coding RNA 1525 |
LINC01524 Genelong intergenic non-protein coding RNA 1524 |
LINC01527 Genelong intergenic non-protein coding RNA 1527 |
LINC01529 Genelong intergenic non-protein coding RNA 1529 |
LINC00691 Genelong intergenic non-protein coding RNA 691 |
LINC00692 Genelong intergenic non-protein coding RNA 692 |
LINC00693 Genelong intergenic non-protein coding RNA 693 |
LINC00698 Genelong intergenic non-protein coding RNA 698 |
LINC00346 Genelong intergenic non-protein coding RNA 346 |
LINC00347 Genelong intergenic non-protein coding RNA 347 |
LINC00345 Genelong intergenic non-protein coding RNA 345 |
LINC00342 Genelong intergenic non-protein coding RNA 342 Biomarker of Huntington's disease. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00343 Genelong intergenic non-protein coding RNA 343 |
LINC00341 Genelong intergenic non-protein coding RNA 341 |
LINC00348 Genelong intergenic non-protein coding RNA 348 |
LINC01543 Genelong intergenic non-protein coding RNA 1543 |
LINC01541 Genelong intergenic non-protein coding RNA 1541 |
LINC01544 Genelong intergenic non-protein coding RNA 1544 |
LINC00102 Genelong intergenic non-protein coding RNA 102 |
LINC00290 Genelong intergenic non-protein coding RNA 290 |
LINC00266-3 Genelong intergenic non-protein coding RNA 266-3 |
LINC00266-1 Genelong intergenic non-protein coding RNA 266-1 |
LINC00632 Genelong intergenic non-protein coding RNA 632 |
LINC00634 Genelong intergenic non-protein coding RNA 634 Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ACADVL Geneacyl-CoA dehydrogenase, very long chain The protein encoded by this gene is targeted to the inner mitochondrial membrane where it catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. This acyl-Coenzyme A dehydrogenase is specific to long-chain and very-long-chain fatty acids. A deficiency in this gene product reduces myocardial fatty acid beta-oxidation and is associated with cardiomyopathy. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
KIR3DL1 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR3DL2 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011] |
KIR3DL3 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. [provided by RefSeq, Jul 2008] |
LINC01176 Genelong intergenic non-protein coding RNA 1176 |
LINC01177 Genelong intergenic non-protein coding RNA 1177 |
LINC01069 Genelong intergenic non-protein coding RNA 1069 |
LINC01065 Genelong intergenic non-protein coding RNA 1065 |
LINC00862 Genelong intergenic non-protein coding RNA 862 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00333 Genelong intergenic non-protein coding RNA 333 |
LINC00331 Genelong intergenic non-protein coding RNA 331 |
LINC01468 Genelong intergenic non-protein coding RNA 1468 |
LINC01003 Genelong intergenic non-protein coding RNA 1003 |
LINC00618 Genelong intergenic non-protein coding RNA 618 |
LINC00619 Genelong intergenic non-protein coding RNA 619 |
LINC00610 Genelong intergenic non-protein coding RNA 610 |
LINC00612 Genelong intergenic non-protein coding RNA 612 |
LINC00613 Genelong intergenic non-protein coding RNA 613 |
LINC00614 Genelong intergenic non-protein coding RNA 614 |
LINC00615 Genelong intergenic non-protein coding RNA 615 |
LINC00616 Genelong intergenic non-protein coding RNA 616 |
LINC01435 Genelong intergenic non-protein coding RNA 1435 |
LINC01151 Genelong intergenic non-protein coding RNA 1151 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00968 Genelong intergenic non-protein coding RNA 968 |
LINC01005 Genelong intergenic non-protein coding RNA 1005 |
LINC00892 Genelong intergenic non-protein coding RNA 892 |
LINC00893 Genelong intergenic non-protein coding RNA 893 |
LINC00890 Genelong intergenic non-protein coding RNA 890 Predicted to be located in membrane. Predicted to be active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00891 Genelong intergenic non-protein coding RNA 891 |
LINC00896 Genelong intergenic non-protein coding RNA 896 |
LINC00894 Genelong intergenic non-protein coding RNA 894 |
LINC00895 Genelong intergenic non-protein coding RNA 895 |
LINC00898 Genelong intergenic non-protein coding RNA 898 |
LINC00899 Genelong intergenic non-protein coding RNA 899 |
LINC01442 Genelong intergenic non-protein coding RNA 1442 |
LINC01443 Genelong intergenic non-protein coding RNA 1443 |
LINC01440 Genelong intergenic non-protein coding RNA 1440 |
LINC01446 Genelong intergenic non-protein coding RNA 1446 |
LINC01447 Genelong intergenic non-protein coding RNA 1447 |
LINC01444 Genelong intergenic non-protein coding RNA 1444 |
LINC01445 Genelong intergenic non-protein coding RNA 1445 |
LINC01448 Genelong intergenic non-protein coding RNA 1448 |
LINC01449 Genelong intergenic non-protein coding RNA 1449 |
LINC00229 Genelong intergenic non-protein coding RNA 229 |
LINC00226 Genelong intergenic non-protein coding RNA 226 |
LINC00221 Genelong intergenic non-protein coding RNA 221 |
LINC00222 Genelong intergenic non-protein coding RNA 222 |
ABALON Geneapoptotic BCL2L1-antisense long non-coding RNA |
LINC00917 Genelong intergenic non-protein coding RNA 917 |
LINC00911 Genelong intergenic non-protein coding RNA 911 |
LINC00910 Genelong intergenic non-protein coding RNA 910 |
LINC01515 Genelong intergenic non-protein coding RNA 1515 |
LINC01349 Genelong intergenic non-protein coding RNA 1349 |
LINC01344 Genelong intergenic non-protein coding RNA 1344 |
LINC01347 Genelong intergenic non-protein coding RNA 1347 |
LINC01346 Genelong intergenic non-protein coding RNA 1346 |
LINC01341 Genelong intergenic non-protein coding RNA 1341 |
LINC01340 Genelong intergenic non-protein coding RNA 1340 |
LINC01343 Genelong intergenic non-protein coding RNA 1343 |
LINC01342 Genelong intergenic non-protein coding RNA 1342 |
LINC01264 Genelong intergenic non-protein coding RNA 1264 |
LINC00710 Genelong intergenic non-protein coding RNA 710 |
LINC00498 Genelong intergenic non-protein coding RNA 498 |
LINC00499 Genelong intergenic non-protein coding RNA 499 |
LINC00997 Genelong intergenic non-protein coding RNA 997 |
LINC00994 Genelong intergenic non-protein coding RNA 994 |
LINC00993 Genelong intergenic non-protein coding RNA 993 |
LINC00992 Genelong intergenic non-protein coding RNA 992 |
LINC00999 Genelong intergenic non-protein coding RNA 999 |
LINC00998 Genelong intergenic non-protein coding RNA 998 Involved in negative regulation of type I interferon-mediated signaling pathway. Located in endoplasmic reticulum membrane and mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00508 Genelong intergenic non-protein coding RNA 508 |
LINC00502 Genelong intergenic non-protein coding RNA 502 |
LINC00696 Genelong intergenic non-protein coding RNA 696 |
SPTLC2 Geneserine palmitoyltransferase, long chain base subunit 2 This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011] |
SPTLC3 Geneserine palmitoyltransferase, long chain base subunit 3 This gene encodes a subunit of the serine palmitoyltransferase complex which catalyzes the rate-limiting step in sphingolipid biosynthesis. This subunit metabolizes lauroyl- and myristoyl-CoA and generates C14 and C16-sphingoid bases. [provided by RefSeq, Mar 2017] |
SPTLC1 Geneserine palmitoyltransferase, long chain base subunit 1 This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013] |
LINC00317 Genelong intergenic non-protein coding RNA 317 |
LINC01372 Genelong intergenic non-protein coding RNA 1372 |
LINC01068 Genelong intergenic non-protein coding RNA 1068 |
LINC01060 Genelong intergenic non-protein coding RNA 1060 |
LINC01061 Genelong intergenic non-protein coding RNA 1061 |
LINC01063 Genelong intergenic non-protein coding RNA 1063 |
LINC00339 Genelong intergenic non-protein coding RNA 339 |
LINC00337 Genelong intergenic non-protein coding RNA 337 |
LINC00336 Genelong intergenic non-protein coding RNA 336 |
LINC00334 Genelong intergenic non-protein coding RNA 334 |
LINC00330 Genelong intergenic non-protein coding RNA 330 |
LINC01220 Genelong intergenic non-protein coding RNA 1220 |
LINC00029 Genelong intergenic non-protein coding RNA 29 |
LINC00674 Genelong intergenic non-protein coding RNA 674 |
LINC01268 Genelong intergenic non-protein coding RNA 1268 |
LINC01266 Genelong intergenic non-protein coding RNA 1266 |
LINC01267 Genelong intergenic non-protein coding RNA 1267 |
LINC01265 Genelong intergenic non-protein coding RNA 1265 |
LINC01260 Genelong intergenic non-protein coding RNA 1260 |
LINC01232 Genelong intergenic non-protein coding RNA 1232 |
LINC00094 Genelong intergenic non-protein coding RNA 94 |
LINC01384 Genelong intergenic non-protein coding RNA 1384 |
LINC00587 Genelong intergenic non-protein coding RNA 587 |
LINC00581 Genelong intergenic non-protein coding RNA 581 |
LINC00582 Genelong intergenic non-protein coding RNA 582 |
LINC00583 Genelong intergenic non-protein coding RNA 583 |
LINC00588 Genelong intergenic non-protein coding RNA 588 |
LINC00589 Genelong intergenic non-protein coding RNA 589 |
LINC01189 Genelong intergenic non-protein coding RNA 1189 |
LINC01183 Genelong intergenic non-protein coding RNA 1183 |
LINC01182 Genelong intergenic non-protein coding RNA 1182 |
LINC01181 Genelong intergenic non-protein coding RNA 1181 |
LINC01187 Genelong intergenic non-protein coding RNA 1187 |
LINC01186 Genelong intergenic non-protein coding RNA 1186 |
LINC01185 Genelong intergenic non-protein coding RNA 1185 |
LINC-PINT Genelong intergenic non-protein coding RNA, p53 induced transcript Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00378 Genelong intergenic non-protein coding RNA 378 |
OPN1LW Geneopsin 1 (cone pigments), long-wave-sensitive This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of partial, protanopic colorblindness. [provided by RefSeq, Jul 2008] |
LINC01119 Genelong intergenic non-protein coding RNA 1119 |
LINC01578 Genelong intergenic non-protein coding RNA 1578 Predicted to be involved in several processes, including adipose tissue development; regulation of gene expression; and thymus development. Predicted to be active in chromatin and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01579 Genelong intergenic non-protein coding RNA 1579 |
LINC01574 Genelong intergenic non-protein coding RNA 1574 |
LINC01572 Genelong intergenic non-protein coding RNA 1572 |
LINC01573 Genelong intergenic non-protein coding RNA 1573 |
LINC01570 Genelong intergenic non-protein coding RNA 1570 |
LINC01571 Genelong intergenic non-protein coding RNA 1571 |
LINC01398 Genelong intergenic non-protein coding RNA 1398 |
LINC01399 Genelong intergenic non-protein coding RNA 1399 |
LINC01392 Genelong intergenic non-protein coding RNA 1392 |
LINC01393 Genelong intergenic non-protein coding RNA 1393 |
LINC01391 Genelong intergenic non-protein coding RNA 1391 |
LINC01396 Genelong intergenic non-protein coding RNA 1396 |
LINC01397 Genelong intergenic non-protein coding RNA 1397 |
LINC01395 Genelong intergenic non-protein coding RNA 1395 |
LINC00621 Genelong intergenic non-protein coding RNA 621 |
LINC00620 Genelong intergenic non-protein coding RNA 620 |
LINC00623 Genelong intergenic non-protein coding RNA 623 |
LINC00624 Genelong intergenic non-protein coding RNA 624 |
LINC00626 Genelong intergenic non-protein coding RNA 626 |
LINC00629 Genelong intergenic non-protein coding RNA 629 |
LINC00628 Genelong intergenic non-protein coding RNA 628 |
SHFLD2 GeneSplit-hand/foot malformation with long deficiency 2 |
LINC00265-2P Genelong intergenic non-protein coding RNA 265-2, pseudogene |
LINC00869 Genelong intergenic non-protein coding RNA 869 |
LINC00868 Genelong intergenic non-protein coding RNA 868 |
LINC00867 Genelong intergenic non-protein coding RNA 867 |
LINC00866 Genelong intergenic non-protein coding RNA 866 |
LINC01180 Genelong intergenic non-protein coding RNA 1180 |
LINC01184 Genelong intergenic non-protein coding RNA 1184 |
LINC00936 Genelong intergenic non-protein coding RNA 936 |
LINC00470 Genelong intergenic non-protein coding RNA 470 |
LINC00472 Genelong intergenic non-protein coding RNA 472 |
LINC00473 Genelong intergenic non-protein coding RNA 473 Involved in DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00474 Genelong intergenic non-protein coding RNA 474 |
LINC00475 Genelong intergenic non-protein coding RNA 475 |
LINC00476 Genelong intergenic non-protein coding RNA 476 |
LINC00477 Genelong intergenic non-protein coding RNA 477 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00479 Genelong intergenic non-protein coding RNA 479 |
LINC01103 Genelong intergenic non-protein coding RNA 1103 |
LINC01102 Genelong intergenic non-protein coding RNA 1102 |
LINC01101 Genelong intergenic non-protein coding RNA 1101 |
LINC01100 Genelong intergenic non-protein coding RNA 1100 |
LINC01107 Genelong intergenic non-protein coding RNA 1107 |
LINC01106 Genelong intergenic non-protein coding RNA 1106 |
LINC01105 Genelong intergenic non-protein coding RNA 1105 |
LINC01104 Genelong intergenic non-protein coding RNA 1104 |
LINC01109 Genelong intergenic non-protein coding RNA 1109 |
LINC01108 Genelong intergenic non-protein coding RNA 1108 |
LINC00278 Genelong intergenic non-protein coding RNA 278 |
LINC00279 Genelong intergenic non-protein coding RNA 279 |
LINC00708 Genelong intergenic non-protein coding RNA 708 |
LINC00709 Genelong intergenic non-protein coding RNA 709 |
LINC00702 Genelong intergenic non-protein coding RNA 702 |
ACADL Geneacyl-CoA dehydrogenase, long chain The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008] |
LINC01312 Genelong intergenic non-protein coding RNA 1312 |
LINC01310 Genelong intergenic non-protein coding RNA 1310 |
LINC01311 Genelong intergenic non-protein coding RNA 1311 |
LINC01314 Genelong intergenic non-protein coding RNA 1314 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01315 Genelong intergenic non-protein coding RNA 1315 |
LINC01235 Genelong intergenic non-protein coding RNA 1235 |
LINC01433 Genelong intergenic non-protein coding RNA 1433 |
LINC01432 Genelong intergenic non-protein coding RNA 1432 |
LINC01431 Genelong intergenic non-protein coding RNA 1431 |
LINC01430 Genelong intergenic non-protein coding RNA 1430 |
LINC01299 Genelong intergenic non-protein coding RNA 1299 |
LINC01293 Genelong intergenic non-protein coding RNA 1293 |
LINC01291 Genelong intergenic non-protein coding RNA 1291 |
LINC01165 Genelong intergenic non-protein coding RNA 1165 |
LINC00944 Genelong intergenic non-protein coding RNA 944 |
LINC00945 Genelong intergenic non-protein coding RNA 945 |
LINC00941 Genelong intergenic non-protein coding RNA 941 Enables promoter-enhancer loop anchoring activity. Involved in chromatin looping and positive regulation of transcription by RNA polymerase II. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00942 Genelong intergenic non-protein coding RNA 942 |
LINC00943 Genelong intergenic non-protein coding RNA 943 |
OVAAL Geneovarian adenocarcinoma amplified long non-coding RNA Predicted to enable pre-mRNA branch point binding activity. Predicted to be involved in mRNA branch site recognition. Predicted to be part of U2 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00535 Genelong intergenic non-protein coding RNA 535 |
LINC00534 Genelong intergenic non-protein coding RNA 534 |
LINC00537 Genelong intergenic non-protein coding RNA 537 Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00536 Genelong intergenic non-protein coding RNA 536 |
LINC00533 Genelong intergenic non-protein coding RNA 533 |
LINC00539 Genelong intergenic non-protein coding RNA 539 |
LINC00538 Genelong intergenic non-protein coding RNA 538 |
LINC01588 Genelong intergenic non-protein coding RNA 1588 |
LINC01585 Genelong intergenic non-protein coding RNA 1585 |
LINC01583 Genelong intergenic non-protein coding RNA 1583 |
LINC01582 Genelong intergenic non-protein coding RNA 1582 |
LINC01581 Genelong intergenic non-protein coding RNA 1581 |
LINC01580 Genelong intergenic non-protein coding RNA 1580 |
LINC01055 Genelong intergenic non-protein coding RNA 1055 |
LINC01057 Genelong intergenic non-protein coding RNA 1057 |
LINC01056 Genelong intergenic non-protein coding RNA 1056 |
LINC01050 Genelong intergenic non-protein coding RNA 1050 |
LINC01053 Genelong intergenic non-protein coding RNA 1053 |
LINC01059 Genelong intergenic non-protein coding RNA 1059 |
LINC01217 Genelong intergenic non-protein coding RNA 1217 |
LINC01216 Genelong intergenic non-protein coding RNA 1216 |
LINC01210 Genelong intergenic non-protein coding RNA 1210 |
LINC01219 Genelong intergenic non-protein coding RNA 1219 |
LINC01218 Genelong intergenic non-protein coding RNA 1218 |
LINC01213 Genelong intergenic non-protein coding RNA 1213 |
LINC00328-2P Genelong intergenic non-protein coding RNA 328-2, pseudogene |
LINC01298 Genelong intergenic non-protein coding RNA 1298 |
LINC01296 Genelong intergenic non-protein coding RNA 1296 |
LINC01507 Genelong intergenic non-protein coding RNA 1507 |
LINC01506 Genelong intergenic non-protein coding RNA 1506 |
LINC01505 Genelong intergenic non-protein coding RNA 1505 |
LINC01503 Genelong intergenic non-protein coding RNA 1503 |
LINC01502 Genelong intergenic non-protein coding RNA 1502 |
LINC01501 Genelong intergenic non-protein coding RNA 1501 |
LINC01500 Genelong intergenic non-protein coding RNA 1500 |
LINC01509 Genelong intergenic non-protein coding RNA 1509 |
LINC01508 Genelong intergenic non-protein coding RNA 1508 |
LINC00368 Genelong intergenic non-protein coding RNA 368 |
LINC00365 Genelong intergenic non-protein coding RNA 365 |
LINC00366 Genelong intergenic non-protein coding RNA 366 |
LINC00367 Genelong intergenic non-protein coding RNA 367 |
LINC00362 Genelong intergenic non-protein coding RNA 362 |
LINC00363 Genelong intergenic non-protein coding RNA 363 |
LINC01144 Genelong intergenic non-protein coding RNA 1144 |
LINC01140 Genelong intergenic non-protein coding RNA 1140 |
MT-LIPCAR Genemitochondrially encoded long non-coding cardiac associated RNA |
LINC00167 Genelong intergenic non-protein coding RNA 167 |
LINC00162 Genelong intergenic non-protein coding RNA 162 |
LINC00163 Genelong intergenic non-protein coding RNA 163 |
LINC00161 Genelong intergenic non-protein coding RNA 161 |
LINC00836 Genelong intergenic non-protein coding RNA 836 |
LINC00837 Genelong intergenic non-protein coding RNA 837 |
LINC00838 Genelong intergenic non-protein coding RNA 838 |
LINC00839 Genelong intergenic non-protein coding RNA 839 |
LOC100422263 Geneserine palmitoyltransferase, long chain base subunit 2 pseudogene |
LINC01158 Genelong intergenic non-protein coding RNA 1158 Predicted to act upstream of or within regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01159 Genelong intergenic non-protein coding RNA 1159 Predicted to act upstream of or within cerebellar cortex structural organization; homeostasis of number of cells within a tissue; and regulation of gene expression. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01150 Genelong intergenic non-protein coding RNA 1150 |
LINC01152 Genelong intergenic non-protein coding RNA 1152 |
LINC01153 Genelong intergenic non-protein coding RNA 1153 |
SPTLC1P3 Geneserine palmitoyltransferase, long chain base subunit 1 pseudogene 3 |
LINC00283 Genelong intergenic non-protein coding RNA 283 |
LINC00282 Genelong intergenic non-protein coding RNA 282 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00280 Genelong intergenic non-protein coding RNA 280 |
LINC00284 Genelong intergenic non-protein coding RNA 284 |
LINC00678 Genelong intergenic non-protein coding RNA 678 |
LINC00676 Genelong intergenic non-protein coding RNA 676 |
LINC00677 Genelong intergenic non-protein coding RNA 677 |
LINC00675 Genelong intergenic non-protein coding RNA 675 Involved in intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00672 Genelong intergenic non-protein coding RNA 672 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00673 Genelong intergenic non-protein coding RNA 673 This gene produces a long non-protein coding RNA that is involved in the regulation of gene expression during tumor progression. This transcript can promote cell proliferation in gastric cancer through interaction with enhancer of zeste 2 and other epigenetic suppressors of gene expression, thereby downregulating target genes including Kruppel like factors 2 and 4. This transcript may also act as a tumor suppressor by promoting interaction between protein tyrosine phosphatase, non-receptor type 11 (Ptpn11) and ubiquitin ligase, resulting in degradation of Ptpn11 and lowered oncogenic signalling. Naturally-occurring variation at this locus results in the formation of a binding site for miR-1231, which negatively regulates activity of this transcript. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2017] |
LINC00670 Genelong intergenic non-protein coding RNA 670 |
LINC00671 Genelong intergenic non-protein coding RNA 671 |
LINC00092 Genelong intergenic non-protein coding RNA 92 |
LINC01276 Genelong intergenic non-protein coding RNA 1276 |
NKILA GeneNF-kappaB interacting long non-coding RNA |
LINC00863 Genelong intergenic non-protein coding RNA 863 |
LINC00861 Genelong intergenic non-protein coding RNA 861 |
LINC00865 Genelong intergenic non-protein coding RNA 865 |
LINC00864 Genelong intergenic non-protein coding RNA 864 |
PNKY Genelong intergenic non-protein coding RNA PNKY |
GAPLINC Genegastric adenocarcinoma associated, positive CD44 regulator, long intergenic non-coding RNA |
LINC01460 Genelong intergenic non-protein coding RNA 1460 |
LINC01461 Genelong intergenic non-protein coding RNA 1461 |
LINC01465 Genelong intergenic non-protein coding RNA 1465 |
LINC01467 Genelong intergenic non-protein coding RNA 1467 |
LINC00924 Genelong intergenic non-protein coding RNA 924 |
LINC00485 Genelong intergenic non-protein coding RNA 485 |
SHFL1 GeneSplit-hand/foot malformation with long bone deficiency 1 |
LINC00208 Genelong intergenic non-protein coding RNA 208 |
LINC01450 Genelong intergenic non-protein coding RNA 1450 |
LINC00974 Genelong intergenic non-protein coding RNA 974 |
LINC00977 Genelong intergenic non-protein coding RNA 977 |
LINC00971 Genelong intergenic non-protein coding RNA 971 |
LINC00970 Genelong intergenic non-protein coding RNA 970 |
LINC00973 Genelong intergenic non-protein coding RNA 973 |
LINC00972 Genelong intergenic non-protein coding RNA 972 |
LINC00562 Genelong intergenic non-protein coding RNA 562 |
LINC00563 Genelong intergenic non-protein coding RNA 563 |
LINC00560 Genelong intergenic non-protein coding RNA 560 |
LINC00561 Genelong intergenic non-protein coding RNA 561 |
LINC00566 Genelong intergenic non-protein coding RNA 566 |
LINC00567 Genelong intergenic non-protein coding RNA 567 |
LINC00564 Genelong intergenic non-protein coding RNA 564 |
LINC00565 Genelong intergenic non-protein coding RNA 565 |
LINC00471 Genelong intergenic non-protein coding RNA 471 |
KIR2DL5B Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL5A Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
LINC01362 Genelong intergenic non-protein coding RNA 1362 |
LINC01361 Genelong intergenic non-protein coding RNA 1361 |
LINC01366 Genelong intergenic non-protein coding RNA 1366 |
LINC01364 Genelong intergenic non-protein coding RNA 1364 |
LINC01002 Genelong intergenic non-protein coding RNA 1002 |
LINC01000 Genelong intergenic non-protein coding RNA 1000 |
LINC01006 Genelong intergenic non-protein coding RNA 1006 Predicted to be located in cytoplasm and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01007 Genelong intergenic non-protein coding RNA 1007 |
LINC01004 Genelong intergenic non-protein coding RNA 1004 Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01212 Genelong intergenic non-protein coding RNA 1212 |
HELLPAR GeneHELLP associated long non-coding RNA |
LINC01523 Genelong intergenic non-protein coding RNA 1523 |
LINC01522 Genelong intergenic non-protein coding RNA 1522 |
LINC01526 Genelong intergenic non-protein coding RNA 1526 |
LINC01208 Genelong intergenic non-protein coding RNA 1208 |
LINC00202-1 Genelong intergenic non-protein coding RNA 202-1 |
LINC00202-2 Genelong intergenic non-protein coding RNA 202-2 |
LINC00690 Genelong intergenic non-protein coding RNA 690 |
LINC00694 Genelong intergenic non-protein coding RNA 694 |
LINC00349 Genelong intergenic non-protein coding RNA 349 |
SALRNA3 Genesenescence associated long non-coding RNA 3 |
LINC01001 Genelong intergenic non-protein coding RNA 1001 |
LINC01082 Genelong intergenic non-protein coding RNA 1082 |
LINC01080 Genelong intergenic non-protein coding RNA 1080 |
LINC01081 Genelong intergenic non-protein coding RNA 1081 |
LINC01087 Genelong intergenic non-protein coding RNA 1087 |
LINC01085 Genelong intergenic non-protein coding RNA 1085 |
LINC01089 Genelong intergenic non-protein coding RNA 1089 |
LINC00689 Genelong intergenic non-protein coding RNA 689 Implicated in colorectal cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00687 Genelong intergenic non-protein coding RNA 687 |
LINC00686 Genelong intergenic non-protein coding RNA 686 |
LINC00685 Genelong intergenic non-protein coding RNA 685 |
LINC00684 Genelong intergenic non-protein coding RNA 684 |
LINC00682 Genelong intergenic non-protein coding RNA 682 |
LINC00681 Genelong intergenic non-protein coding RNA 681 |
LINC00355 Genelong intergenic non-protein coding RNA 355 |
LINC00354 Genelong intergenic non-protein coding RNA 354 |
LINC00351 Genelong intergenic non-protein coding RNA 351 |
LINC00350 Genelong intergenic non-protein coding RNA 350 |
LINC00353 Genelong intergenic non-protein coding RNA 353 |
LINC00352 Genelong intergenic non-protein coding RNA 352 |
LINC00359 Genelong intergenic non-protein coding RNA 359 |
LINC00358 Genelong intergenic non-protein coding RNA 358 |
LINC00272 Genelong intergenic non-protein coding RNA 272 |
LINC00273 Genelong intergenic non-protein coding RNA 273 |
LINC00271 Genelong intergenic non-protein coding RNA 271 |
LINC00276 Genelong intergenic non-protein coding RNA 276 |
SALRNA1 Genesenescence associated long non-coding RNA 1 |
LINC01246 Genelong intergenic non-protein coding RNA 1246 |
LINC01241 Genelong intergenic non-protein coding RNA 1241 |
LINC01248 Genelong intergenic non-protein coding RNA 1248 |
LINC01249 Genelong intergenic non-protein coding RNA 1249 |
LINC00599 Genelong intergenic non-protein coding RNA 599 Predicted to act upstream of or within several processes, including long-term synaptic potentiation; miRNA-mediated post-transcriptional gene silencing; and sensory perception of sound. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00598 Genelong intergenic non-protein coding RNA 598 |
LINC00116 Genelong intergenic non-protein coding RNA 116 Involved in several processes, including positive regulation of mitochondrial membrane potential; positive regulation of sequestering of calcium ion; and triglyceride homeostasis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00115 Genelong intergenic non-protein coding RNA 115 |
LINC00114 Genelong intergenic non-protein coding RNA 114 |
LINC00113 Genelong intergenic non-protein coding RNA 113 |
LINC00112 Genelong intergenic non-protein coding RNA 112 |
LINC00111 Genelong intergenic non-protein coding RNA 111 |
LINC00996 Genelong intergenic non-protein coding RNA 996 |
HULC Genehepatocellular carcinoma up-regulated long non-coding RNA This gene produces a long RNA that was discovered as upregulated in hepatocellular carcinoma and is associated with cancer progression. Expression of this transcript is regulated by microRNAs and at the transcriptional level by Sp1 family factors. The transcript may regulate gene expression by functioning as a competing RNA for microRNAs. [provided by RefSeq, Dec 2017] |
LINC01160 Genelong intergenic non-protein coding RNA 1160 |
LINC01163 Genelong intergenic non-protein coding RNA 1163 |
LINC01164 Genelong intergenic non-protein coding RNA 1164 |
LINC01167 Genelong intergenic non-protein coding RNA 1167 |
LINC01169 Genelong intergenic non-protein coding RNA 1169 |
LINC01168 Genelong intergenic non-protein coding RNA 1168 |
LINC01554 Genelong intergenic non-protein coding RNA 1554 |
LINC01555 Genelong intergenic non-protein coding RNA 1555 |
LINC01556 Genelong intergenic non-protein coding RNA 1556 |
LINC01553 Genelong intergenic non-protein coding RNA 1553 |
LINC01558 Genelong intergenic non-protein coding RNA 1558 |
LINC01559 Genelong intergenic non-protein coding RNA 1559 |
LINC00607 Genelong intergenic non-protein coding RNA 607 |
LINC00606 Genelong intergenic non-protein coding RNA 606 |
LINC00605 Genelong intergenic non-protein coding RNA 605 |
LINC00602 Genelong intergenic non-protein coding RNA 602 |
LINC00601 Genelong intergenic non-protein coding RNA 601 |
LINC00609 Genelong intergenic non-protein coding RNA 609 |
LINC00608 Genelong intergenic non-protein coding RNA 608 |
LINC00106 Genelong intergenic non-protein coding RNA 106 |
LINC00881 Genelong intergenic non-protein coding RNA 881 |
LINC00880 Genelong intergenic non-protein coding RNA 880 |
LINC00883 Genelong intergenic non-protein coding RNA 883 Predicted to act upstream of or within several processes, including generation of neurons; negative regulation of macromolecule biosynthetic process; and protein stabilization. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00882 Genelong intergenic non-protein coding RNA 882 |
LINC00885 Genelong intergenic non-protein coding RNA 885 Implicated in cervical cancer. Biomarker of cervical cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00884 Genelong intergenic non-protein coding RNA 884 |
LINC00887 Genelong intergenic non-protein coding RNA 887 |
LINC00886 Genelong intergenic non-protein coding RNA 886 |
LINC00889 Genelong intergenic non-protein coding RNA 889 |
LINC00489 Genelong intergenic non-protein coding RNA 489 |
LINC01451 Genelong intergenic non-protein coding RNA 1451 |
LINC01455 Genelong intergenic non-protein coding RNA 1455 |
LINC01473 Genelong intergenic non-protein coding RNA 1473 |
LINC00417 Genelong intergenic non-protein coding RNA 417 |
LINC00412 Genelong intergenic non-protein coding RNA 412 |
LINC00410 Genelong intergenic non-protein coding RNA 410 |
FALEC Genefocally amplified long non-coding RNA in epithelial cancer |
LOC100132304 Genelong intergenic non-protein coding RNA 684 |
LINC00268-2P Genelong intergenic non-protein coding RNA 268-2, pseudogene |
DALIR GeneDNMT1-associated long intergenic non-coding RNA |
LINC00554 Genelong intergenic non-protein coding RNA 554 |
LINC00254 Genelong intergenic non-protein coding RNA 254 |
LINC00437 Genelong intergenic non-protein coding RNA 437 |
SALRNA2 Genesenescence associated long non-coding RNA 2 |
LINC00928 Genelong intergenic non-protein coding RNA 928 |
LINC00922 Genelong intergenic non-protein coding RNA 922 |
LINC00923 Genelong intergenic non-protein coding RNA 923 |
LINC00921 Genelong intergenic non-protein coding RNA 921 |
LINC00926 Genelong intergenic non-protein coding RNA 926 |
LINC00927 Genelong intergenic non-protein coding RNA 927 |
LINC00925 Genelong intergenic non-protein coding RNA 925 |
HAGLR GeneHOXD antisense growth-associated long non-coding RNA |
PTX3 Genepentraxin 3, long This gene encodes a member of the pentraxin protein family. The expression of this protein is induced by inflammatory cytokines in response to inflammatory stimuli in several mesenchymal and epithelial cell types, particularly endothelial cells and mononuclear phagocytes. The protein promotes fibrocyte differentiation and is involved in regulating inflammation and complement activation. It also plays a role in angiogenesis and tissue remodeling. The protein serves as a biomarker for several inflammatory conditions. [provided by RefSeq, Jun 2016] |
PTX4 Genepentraxin 4, long This gene belongs to the pentraxin superfamily, whose members encode highly conserved multifunctional proteins. The encoded protein, like other members of this family, contains a conserved pentraxin domain at the C-terminus. The highest levels of expression of the protein were observed in bone marrow, small intestine and testes. [provided by RefSeq, Jun 2016] |
LINC01338 Genelong intergenic non-protein coding RNA 1338 |
LINC01339 Genelong intergenic non-protein coding RNA 1339 |
LINC01330 Genelong intergenic non-protein coding RNA 1330 |
LINC01331 Genelong intergenic non-protein coding RNA 1331 |
LINC01335 Genelong intergenic non-protein coding RNA 1335 |
LINC01336 Genelong intergenic non-protein coding RNA 1336 |
LINC00051 Genelong intergenic non-protein coding RNA 51 |
LOC100421637 Geneacyl-CoA synthetase long-chain family member 3 pseudogene |
LINC00332 Genelong intergenic non-protein coding RNA 332 |
LINC01317 Genelong intergenic non-protein coding RNA 1317 |
LINC01048 Genelong intergenic non-protein coding RNA 1048 |
LINC00494 Genelong intergenic non-protein coding RNA 494 |
LINC00492 Genelong intergenic non-protein coding RNA 492 |
LINC00493 Genelong intergenic non-protein coding RNA 493 Enables protein kinase binding activity and transmembrane transporter binding activity. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00491 Genelong intergenic non-protein coding RNA 491 |
LINC00920 Genelong intergenic non-protein coding RNA 920 |
LINC01479 Genelong intergenic non-protein coding RNA 1479 |
LINC01387 Genelong intergenic non-protein coding RNA 1387 |
LINC00519 Genelong intergenic non-protein coding RNA 519 |
LINC00518 Genelong intergenic non-protein coding RNA 518 |
LINC00511 Genelong intergenic non-protein coding RNA 511 |
LINC00517 Genelong intergenic non-protein coding RNA 517 |
LINC00515 Genelong intergenic non-protein coding RNA 515 |
LINC00514 Genelong intergenic non-protein coding RNA 514 |
LINC01597 Genelong intergenic non-protein coding RNA 1597 |
THRIL GeneTNF and HNRNPL related immunoregulatory long non-coding RNA |
LINC01333 Genelong intergenic non-protein coding RNA 1333 |
LINC00319 Genelong intergenic non-protein coding RNA 319 |
LINC00237 Genelong intergenic non-protein coding RNA 237 |
LINC01072 Genelong intergenic non-protein coding RNA 1072 |
LINC01070 Genelong intergenic non-protein coding RNA 1070 |
LINC01075 Genelong intergenic non-protein coding RNA 1075 |
LINC00308 Genelong intergenic non-protein coding RNA 308 |
LINC00309 Genelong intergenic non-protein coding RNA 309 |
LINC00302 Genelong intergenic non-protein coding RNA 302 |
LINC00303 Genelong intergenic non-protein coding RNA 303 |
LINC00301 Genelong intergenic non-protein coding RNA 301 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00307 Genelong intergenic non-protein coding RNA 307 |
LINC00304 Genelong intergenic non-protein coding RNA 304 |
LINC00305 Genelong intergenic non-protein coding RNA 305 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01429 Genelong intergenic non-protein coding RNA 1429 |
LINC01170 Genelong intergenic non-protein coding RNA 1170 |
LINC01279 Genelong intergenic non-protein coding RNA 1279 |
LINC01278 Genelong intergenic non-protein coding RNA 1278 |
LINC01277 Genelong intergenic non-protein coding RNA 1277 |
LINC01271 Genelong intergenic non-protein coding RNA 1271 |
LINC01270 Genelong intergenic non-protein coding RNA 1270 |
LINC01273 Genelong intergenic non-protein coding RNA 1273 |
LINC00593 Genelong intergenic non-protein coding RNA 593 |
LINC00592 Genelong intergenic non-protein coding RNA 592 |
LINC00597 Genelong intergenic non-protein coding RNA 597 |
LINC00596 Genelong intergenic non-protein coding RNA 596 |
LINC00595 Genelong intergenic non-protein coding RNA 595 |
LINC00594 Genelong intergenic non-protein coding RNA 594 |
LINC00578 Genelong intergenic non-protein coding RNA 578 |
LINC00570 Genelong intergenic non-protein coding RNA 570 |
LINC01569 Genelong intergenic non-protein coding RNA 1569 |
LINC01568 Genelong intergenic non-protein coding RNA 1568 |
LINC01565 Genelong intergenic non-protein coding RNA 1565 |
LINC01564 Genelong intergenic non-protein coding RNA 1564 |
LINC01567 Genelong intergenic non-protein coding RNA 1567 |
LINC01566 Genelong intergenic non-protein coding RNA 1566 |
LINC01561 Genelong intergenic non-protein coding RNA 1561 |
LINC01560 Genelong intergenic non-protein coding RNA 1560 |
LINC01563 Genelong intergenic non-protein coding RNA 1563 |
LINC01562 Genelong intergenic non-protein coding RNA 1562 |
LINC01389 Genelong intergenic non-protein coding RNA 1389 |
LINC01386 Genelong intergenic non-protein coding RNA 1386 |
LINC00382 Genelong intergenic non-protein coding RNA 382 |
LINC00383 Genelong intergenic non-protein coding RNA 383 |
LINC00380 Genelong intergenic non-protein coding RNA 380 |
LINC00381 Genelong intergenic non-protein coding RNA 381 |
LINC00387 Genelong intergenic non-protein coding RNA 387 |
LINC00384 Genelong intergenic non-protein coding RNA 384 |
LINC00388 Genelong intergenic non-protein coding RNA 388 |
LINC00854 Genelong intergenic non-protein coding RNA 854 |
LINC01436 Genelong intergenic non-protein coding RNA 1436 |
LINC00856 Genelong intergenic non-protein coding RNA 856 |
LINC00857 Genelong intergenic non-protein coding RNA 857 |
LINC00852 Genelong intergenic non-protein coding RNA 852 |
LINC00853 Genelong intergenic non-protein coding RNA 853 |
LINC00850 Genelong intergenic non-protein coding RNA 850 |
LINC00851 Genelong intergenic non-protein coding RNA 851 |
LINC00858 Genelong intergenic non-protein coding RNA 858 |
LINC01486 Genelong intergenic non-protein coding RNA 1486 |
LINC01481 Genelong intergenic non-protein coding RNA 1481 |
LINC01488 Genelong intergenic non-protein coding RNA 1488 |
LINC00469 Genelong intergenic non-protein coding RNA 469 |
LINC00467 Genelong intergenic non-protein coding RNA 467 |
LINC00463 Genelong intergenic non-protein coding RNA 463 |
LINC00462 Genelong intergenic non-protein coding RNA 462 |
LINC00461 Genelong intergenic non-protein coding RNA 461 This is an evolutionarily conserved gene that produces alternatively spliced long non-coding RNAs that may be expressed predominantly in the brain and visual cortex. These transcripts may be involved in tumorigenesis, as depletion by siRNA suppressed glioma cell division. Transcripts may also bind to and regulate the activity of miR-411-5p and argonaut 2, thereby altering the expression of genes involved in tumor growth. [provided by RefSeq, Nov 2017] |
LINC00460 Genelong intergenic non-protein coding RNA 460 |
LINC01127 Genelong intergenic non-protein coding RNA 1127 |
LINC01487 Genelong intergenic non-protein coding RNA 1487 |
LINC01485 Genelong intergenic non-protein coding RNA 1485 |
LINC01482 Genelong intergenic non-protein coding RNA 1482 |
LINC01480 Genelong intergenic non-protein coding RNA 1480 |
LINC01138 Genelong intergenic non-protein coding RNA 1138 |
LINC01139 Genelong intergenic non-protein coding RNA 1139 |
LINC01136 Genelong intergenic non-protein coding RNA 1136 |
LINC01137 Genelong intergenic non-protein coding RNA 1137 |
LINC01134 Genelong intergenic non-protein coding RNA 1134 |
LINC01135 Genelong intergenic non-protein coding RNA 1135 |
LINC01132 Genelong intergenic non-protein coding RNA 1132 |
LINC01133 Genelong intergenic non-protein coding RNA 1133 |
LINC01489 Genelong intergenic non-protein coding RNA 1489 |
LINC00261 Genelong intergenic non-protein coding RNA 261 This gene produces a long non-coding RNA that acts as a negative regulator of cell growth. This transcript may promote differentiation and apoptosis. [provided by RefSeq, Dec 2017] |
LINC00260 Genelong intergenic non-protein coding RNA 260 |
LINC00265 Genelong intergenic non-protein coding RNA 265 |
LINC00264 Genelong intergenic non-protein coding RNA 264 |
LINC00269 Genelong intergenic non-protein coding RNA 269 |
LINC00268 Genelong intergenic non-protein coding RNA 268 |
LINC00466 Genelong intergenic non-protein coding RNA 466 |
LINC00909 Genelong intergenic non-protein coding RNA 909 |
LINC01272 Genelong intergenic non-protein coding RNA 1272 |
LINC00205 Genelong intergenic non-protein coding RNA 205 |
LINC00654 Genelong intergenic non-protein coding RNA 654 |
LINC00656 Genelong intergenic non-protein coding RNA 656 |
LINC00652 Genelong intergenic non-protein coding RNA 652 |
LINC00658 Genelong intergenic non-protein coding RNA 658 |
LINC00659 Genelong intergenic non-protein coding RNA 659 |
LINC01300 Genelong intergenic non-protein coding RNA 1300 |
LINC01304 Genelong intergenic non-protein coding RNA 1304 |
LINC01309 Genelong intergenic non-protein coding RNA 1309 |
LINC01358 Genelong intergenic non-protein coding RNA 1358 |
LINC01356 Genelong intergenic non-protein coding RNA 1356 |
LINC01353 Genelong intergenic non-protein coding RNA 1353 |
LINC01351 Genelong intergenic non-protein coding RNA 1351 |
LINC01478 Genelong intergenic non-protein coding RNA 1478 |
LINC01405 Genelong intergenic non-protein coding RNA 1405 |
LOC646644 GeneLLP homolog, long-term synaptic facilitation (Aplysia) pseudogene |
LINC00959 Genelong intergenic non-protein coding RNA 959 |
LINC00958 Genelong intergenic non-protein coding RNA 958 |
LINC00951 Genelong intergenic non-protein coding RNA 951 |
LINC00950 Genelong intergenic non-protein coding RNA 950 |
LINC00957 Genelong intergenic non-protein coding RNA 957 |
LINC00955 Genelong intergenic non-protein coding RNA 955 |
LINC00540 Genelong intergenic non-protein coding RNA 540 |
LINC00543 Genelong intergenic non-protein coding RNA 543 |
LINC00544 Genelong intergenic non-protein coding RNA 544 |
LINC00545 Genelong intergenic non-protein coding RNA 545 |
LINC00547 Genelong intergenic non-protein coding RNA 547 |
LINC00548 Genelong intergenic non-protein coding RNA 548 |
LINC00683 Genelong intergenic non-protein coding RNA 683 |
LINC00032 Genelong intergenic non-protein coding RNA 32 |
LINC01011 Genelong intergenic non-protein coding RNA 1011 |
LINC01010 Genelong intergenic non-protein coding RNA 1010 |
LINC00940 Genelong intergenic non-protein coding RNA 940 |
LINC01269 Genelong intergenic non-protein coding RNA 1269 |
LINC01020 Genelong intergenic non-protein coding RNA 1020 |
LINC01021 Genelong intergenic non-protein coding RNA 1021 |
LINC01023 Genelong intergenic non-protein coding RNA 1023 |
LINC01028 Genelong intergenic non-protein coding RNA 1028 |
LINC01029 Genelong intergenic non-protein coding RNA 1029 |
LINC01262 Genelong intergenic non-protein coding RNA 1262 |
LINC01222 Genelong intergenic non-protein coding RNA 1222 |
LINC01226 Genelong intergenic non-protein coding RNA 1226 |
LINC01224 Genelong intergenic non-protein coding RNA 1224 |
LINC01225 Genelong intergenic non-protein coding RNA 1225 |
LINC01228 Genelong intergenic non-protein coding RNA 1228 |
LINC01229 Genelong intergenic non-protein coding RNA 1229 |
LINC00266-2P Genelong intergenic non-protein coding RNA 266-2, pseudogene |
LINC01589 Genelong intergenic non-protein coding RNA 1589 |
SENCR Genesmooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA |
LINC01017 Genelong intergenic non-protein coding RNA 1017 |
LINC01247 Genelong intergenic non-protein coding RNA 1247 |
LINC01242 Genelong intergenic non-protein coding RNA 1242 |
LINC01243 Genelong intergenic non-protein coding RNA 1243 |
LINC01532 Genelong intergenic non-protein coding RNA 1532 |
LINC01533 Genelong intergenic non-protein coding RNA 1533 |
LINC01530 Genelong intergenic non-protein coding RNA 1530 |
LINC01531 Genelong intergenic non-protein coding RNA 1531 |
LINC01537 Genelong intergenic non-protein coding RNA 1537 |
LINC01534 Genelong intergenic non-protein coding RNA 1534 |
LINC01535 Genelong intergenic non-protein coding RNA 1535 |
LINC01538 Genelong intergenic non-protein coding RNA 1538 |
LINC01539 Genelong intergenic non-protein coding RNA 1539 |
LINC00379 Genelong intergenic non-protein coding RNA 379 |
LINC00371 Genelong intergenic non-protein coding RNA 371 |
LINC00370 Genelong intergenic non-protein coding RNA 370 |
LINC00377 Genelong intergenic non-protein coding RNA 377 |
LINC00376 Genelong intergenic non-protein coding RNA 376 |
LINC00375 Genelong intergenic non-protein coding RNA 375 |
LINC00707 Genelong intergenic non-protein coding RNA 707 |
LINC00704 Genelong intergenic non-protein coding RNA 704 |
LINC00703 Genelong intergenic non-protein coding RNA 703 |
LINC00174 Genelong intergenic non-protein coding RNA 174 |
LINC00176 Genelong intergenic non-protein coding RNA 176 |
LINC00173 Genelong intergenic non-protein coding RNA 173 |
LINC00824 Genelong intergenic non-protein coding RNA 824 |
TRERNA1 Genetranslation regulatory long non-coding RNA 1 |
LINC01441 Genelong intergenic non-protein coding RNA 1441 |
LINC00706 Genelong intergenic non-protein coding RNA 706 |
LINC01146 Genelong intergenic non-protein coding RNA 1146 |
LINC01143 Genelong intergenic non-protein coding RNA 1143 |
LINC01142 Genelong intergenic non-protein coding RNA 1142 |
LINC01141 Genelong intergenic non-protein coding RNA 1141 |
LINC01149 Genelong intergenic non-protein coding RNA 1149 |
LINC00423 Genelong intergenic non-protein coding RNA 423 |
LINC00421 Genelong intergenic non-protein coding RNA 421 |
LINC00427 Genelong intergenic non-protein coding RNA 427 |
LINC00426 Genelong intergenic non-protein coding RNA 426 |
LINC00424 Genelong intergenic non-protein coding RNA 424 |
LINC00669 Genelong intergenic non-protein coding RNA 669 |
LINC00668 Genelong intergenic non-protein coding RNA 668 |
LINC00665 Genelong intergenic non-protein coding RNA 665 |
LINC00664 Genelong intergenic non-protein coding RNA 664 |
LINC00667 Genelong intergenic non-protein coding RNA 667 |
LINC00661 Genelong intergenic non-protein coding RNA 661 |
LINC00663 Genelong intergenic non-protein coding RNA 663 |
LINC00662 Genelong intergenic non-protein coding RNA 662 |
LINC00083 Genelong intergenic non-protein coding RNA 83 Predicted to enable carbohydrate binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LINC00657 Genelong intergenic non-protein coding RNA 657 Predicted to enable protein sequestering activity. Predicted to be involved in several processes, including determination of adult lifespan; hair follicle development; and skeletal muscle fiber development. Predicted to be active in cytoplasm. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
ELDR GeneEGFR long non-coding downstream RNA Predicted to act upstream of or within regulation of gene expression and response to wounding. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01301 Genelong intergenic non-protein coding RNA 1301 |
LINC01305 Genelong intergenic non-protein coding RNA 1305 |
LINC01307 Genelong intergenic non-protein coding RNA 1307 |
LINC01477 Genelong intergenic non-protein coding RNA 1477 |
LINC01476 Genelong intergenic non-protein coding RNA 1476 |
LINC01475 Genelong intergenic non-protein coding RNA 1475 |
LINC01474 Genelong intergenic non-protein coding RNA 1474 |
LINC01471 Genelong intergenic non-protein coding RNA 1471 |
LINC01470 Genelong intergenic non-protein coding RNA 1470 |
LINC00434 Genelong intergenic non-protein coding RNA 434 |
ACSL3 Geneacyl-CoA synthetase long-chain family member 3 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in brain, and preferentially utilizes myristate, arachidonate, and eicosapentaenoate as substrates. The amino acid sequence of this isozyme is 92% identical to that of rat homolog. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
ACSL1 Geneacyl-CoA synthetase long-chain family member 1 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
ACSL6 Geneacyl-CoA synthetase long-chain family member 6 The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2011] |
LINC00431 Genelong intergenic non-protein coding RNA 431 |
ACSL4 Geneacyl-CoA synthetase long-chain family member 4 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016] |
ACSL5 Geneacyl-CoA synthetase long-chain family member 5 The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in uterus and spleen, and in trace amounts in normal brain, but has markedly increased levels in malignant gliomas. This gene functions in mediating fatty acid-induced glioma cell growth. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LINC01511 Genelong intergenic non-protein coding RNA 1511 |
LINC01512 Genelong intergenic non-protein coding RNA 1512 |
LINC01517 Genelong intergenic non-protein coding RNA 1517 |
LINC01504 Genelong intergenic non-protein coding RNA 1504 |
LINC00238 Genelong intergenic non-protein coding RNA 238 |
LINC00239 Genelong intergenic non-protein coding RNA 239 |
LINC00235 Genelong intergenic non-protein coding RNA 235 |
LINC00900 Genelong intergenic non-protein coding RNA 900 |
LINC00901 Genelong intergenic non-protein coding RNA 901 |
LINC00903 Genelong intergenic non-protein coding RNA 903 |
LINC00904 Genelong intergenic non-protein coding RNA 904 |
LINC00905 Genelong intergenic non-protein coding RNA 905 |
LINC00906 Genelong intergenic non-protein coding RNA 906 |
LINC00907 Genelong intergenic non-protein coding RNA 907 |
LINC00908 Genelong intergenic non-protein coding RNA 908 |
LINC00397 Genelong intergenic non-protein coding RNA 397 |
LINC00572 Genelong intergenic non-protein coding RNA 572 |
LINC00575 Genelong intergenic non-protein coding RNA 575 |
LINC00574 Genelong intergenic non-protein coding RNA 574 |
LINC00577 Genelong intergenic non-protein coding RNA 577 |
LINC01587 Genelong intergenic non-protein coding RNA 1587 This gene is expressed in neuroblastoma; however, the function of this gene is not yet determined. [provided by RefSeq, Jul 2008] |
LINC01584 Genelong intergenic non-protein coding RNA 1584 |
LINC00622 Genelong intergenic non-protein coding RNA 622 |
LINC01054 Genelong intergenic non-protein coding RNA 1054 |
LINC01058 Genelong intergenic non-protein coding RNA 1058 |
KIR2DL3 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL2 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL1 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL4 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016] |
LINC00428 Genelong intergenic non-protein coding RNA 428 |
LINC01354 Genelong intergenic non-protein coding RNA 1354 |
LINC01355 Genelong intergenic non-protein coding RNA 1355 |
LINC01350 Genelong intergenic non-protein coding RNA 1350 |
LINC01019 Genelong intergenic non-protein coding RNA 1019 |
LINC01018 Genelong intergenic non-protein coding RNA 1018 |
LINC01013 Genelong intergenic non-protein coding RNA 1013 |
LINC01012 Genelong intergenic non-protein coding RNA 1012 |
LINC01015 Genelong intergenic non-protein coding RNA 1015 |
LINC01014 Genelong intergenic non-protein coding RNA 1014 |
LINC01016 Genelong intergenic non-protein coding RNA 1016 |
LINC00888 Genelong intergenic non-protein coding RNA 888 |
LINC01162 Genelong intergenic non-protein coding RNA 1162 |
LINC00919 Genelong intergenic non-protein coding RNA 919 |
LINC00914 Genelong intergenic non-protein coding RNA 914 |
LINC00705 Genelong intergenic non-protein coding RNA 705 |
LINC00700 Genelong intergenic non-protein coding RNA 700 |
LINC00701 Genelong intergenic non-protein coding RNA 701 |
LINC01359 Genelong intergenic non-protein coding RNA 1359 |
LINC01352 Genelong intergenic non-protein coding RNA 1352 |
LINC01586 Genelong intergenic non-protein coding RNA 1586 |
LINC00989 Genelong intergenic non-protein coding RNA 989 |
LINC00982 Genelong intergenic non-protein coding RNA 982 |
LINC00987 Genelong intergenic non-protein coding RNA 987 |
HAO2 Genehydroxyacid oxidase 2 (long chain) This gene is one of three related genes that have 2-hydroxyacid oxidase activity. The encoded protein localizes to the peroxisome has the highest activity toward the substrate 2-hydroxypalmitate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
LINC02618 Genelong intergenic non-protein coding RNA 2618 |
LINC02249 Genelong intergenic non-protein coding RNA 2249 |
LINC01963 Genelong intergenic non-protein coding RNA 1963 |
LNCTAM34A Genelong non coding transcriptional activator of miR34a |
LINC01833 Genelong intergenic non-protein coding RNA 1833 Predicted to be involved in regulation of gene expression. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01806 Genelong intergenic non-protein coding RNA 1806 |
LINC01788 Genelong intergenic non-protein coding RNA 1788 |
LINC01843 Genelong intergenic non-protein coding RNA 1843 |
LINC03040 Genelong intergenic non-protein coding RNA 3040 |
LINC01719 Genelong intergenic non-protein coding RNA 1719 |
LINC01772 Genelong intergenic non-protein coding RNA 1772 |
LINC02035 Genelong intergenic non-protein coding RNA 2035 |
LINC01781 Genelong intergenic non-protein coding RNA 1781 |
LINC02044 Genelong intergenic non-protein coding RNA 2044 |
LINC01852 Genelong intergenic non-protein coding RNA 1852 |
LINC01914 Genelong intergenic non-protein coding RNA 1914 |
LINC02102 Genelong intergenic non-protein coding RNA 2102 |
LINC01933 Genelong intergenic non-protein coding RNA 1933 |
LINC02904 Genelong intergenic non-protein coding RNA 2904 |
LINC02910 Genelong intergenic non-protein coding RNA 2910 |
LINC01814 Genelong intergenic non-protein coding RNA 1814 |
LINC02908 Genelong intergenic non-protein coding RNA 2908 |
LINC01829 Genelong intergenic non-protein coding RNA 1829 |
LINC00680 Genelong intergenic non-protein coding RNA 680 |
LINC02019 Genelong intergenic non-protein coding RNA 2019 |
LINC02094 Genelong intergenic non-protein coding RNA 2094 |
LINC02147 Genelong intergenic non-protein coding RNA 2147 |
LINC02012 Genelong intergenic non-protein coding RNA 2012 |
LINC01896 Genelong intergenic non-protein coding RNA 1896 |
LINC02185 Genelong intergenic non-protein coding RNA 2185 |
LINC01828 Genelong intergenic non-protein coding RNA 1828 |
LINC01619 Genelong intergenic non-protein coding RNA 1619 |
LINC01679 Genelong intergenic non-protein coding RNA 1679 |
PRECSIT Genep53 regulated carcinoma associated Stat3 activating long intergenic non-protein coding transcript |
LINC02208 Genelong intergenic non-protein coding RNA 2208 |
LINC02210 Genelong intergenic non-protein coding RNA 2210 |
LINC03011 Genelong intergenic non-protein coding RNA 3011 |
LINC01702 Genelong intergenic non-protein coding RNA 1702 |
LINC02037 Genelong intergenic non-protein coding RNA 2037 |
LINC02197 Genelong intergenic non-protein coding RNA 2197 |
LINC01595 Genelong intergenic non-protein coding RNA 1595 Implicated in prostate cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LINC02898 Genelong intergenic non-protein coding RNA 2898 |
LINC02716 Genelong intergenic non-protein coding RNA 2716 |
LINC02116 Genelong intergenic non-protein coding RNA 2116 |
LINC01713 Genelong intergenic non-protein coding RNA 1713 |
LINC02174 Genelong intergenic non-protein coding RNA 2174 |
LINC02052 Genelong intergenic non-protein coding RNA 2052 |
LINC00449 Genelong intergenic non-protein coding RNA 449 |
LINC02084 Genelong intergenic non-protein coding RNA 2084 |
LINC01980 Genelong intergenic non-protein coding RNA 1980 |
LINC01876 Genelong intergenic non-protein coding RNA 1876 |
LINC02167 Genelong intergenic non-protein coding RNA 2167 |
LINC02212 Genelong intergenic non-protein coding RNA 2212 |
LINC02145 Genelong intergenic non-protein coding RNA 2145 |
LINC02905 Genelong intergenic non-protein coding RNA 2905 |
LINC02693 Genelong intergenic non-protein coding RNA 2693 |
LINC01978 Genelong intergenic non-protein coding RNA 1978 |
LINC01979 Genelong intergenic non-protein coding RNA 1979 |
LINC02015 Genelong intergenic non-protein coding RNA 2015 |
LINC01625 Genelong intergenic non-protein coding RNA 1625 |
LINC02202 Genelong intergenic non-protein coding RNA 2202 |
LINC01786 Genelong intergenic non-protein coding RNA 1786 |
LINC01714 Genelong intergenic non-protein coding RNA 1714 |
LINC02028 Genelong intergenic non-protein coding RNA 2028 |
HISLA GeneHIF1A stabilizing long noncoding RNA |
LINC01836 Genelong intergenic non-protein coding RNA 1836 |
LINC01977 Genelong intergenic non-protein coding RNA 1977 |
LINC01907 Genelong intergenic non-protein coding RNA 1907 |
LINC01748 Genelong intergenic non-protein coding RNA 1748 |
ARLNC1 Geneandrogen receptor regulated long noncoding RNA 1 |
LINC01754 Genelong intergenic non-protein coding RNA 1754 |
LINC01770 Genelong intergenic non-protein coding RNA 1770 |
MINCR GeneMYC-induced long non-coding RNA |
LINC02086 Genelong intergenic non-protein coding RNA 2086 |
LINC02193 Genelong intergenic non-protein coding RNA 2193 |
LINC01819 Genelong intergenic non-protein coding RNA 1819 |
LINC02018 Genelong intergenic non-protein coding RNA 2018 |
LINC01869 Genelong intergenic non-protein coding RNA 1869 |
MALINC1 Genemitosis associated long intergenic non-coding RNA 1 |
LINC02106 Genelong intergenic non-protein coding RNA 2106 |
LINC02076 Genelong intergenic non-protein coding RNA 2076 |
LINC02021 Genelong intergenic non-protein coding RNA 2021 |
LINC01915 Genelong intergenic non-protein coding RNA 1915 |
LINC01881 Genelong intergenic non-protein coding RNA 1881 |
LINC01801 Genelong intergenic non-protein coding RNA 1801 |
LINC01750 Genelong intergenic non-protein coding RNA 1750 |
LINC02175 Genelong intergenic non-protein coding RNA 2175 |
LINC02188 Genelong intergenic non-protein coding RNA 2188 |
LINC02913 Genelong intergenic non-protein coding RNA 2913 |
LINC02897 Genelong intergenic non-protein coding RNA 2897 |
LINC02875 Genelong intergenic non-protein coding RNA 2875 |
LINC01238 Genelong intergenic non-protein coding RNA 1238 |
LINC01943 Genelong intergenic non-protein coding RNA 1943 |
LINC02881 Genelong intergenic non-protein coding RNA 2881 |
LINC01345 Genelong intergenic non-protein coding RNA 1345 |
LINC02692 Genelong intergenic non-protein coding RNA 2692 |
LINC02107 Genelong intergenic non-protein coding RNA 2107 |
LINC01874 Genelong intergenic non-protein coding RNA 1874 |
LINC01707 Genelong intergenic non-protein coding RNA 1707 |
LINC01697 Genelong intergenic non-protein coding RNA 1697 |
LINC01684 Genelong intergenic non-protein coding RNA 1684 |
LINC01816 Genelong intergenic non-protein coding RNA 1816 |
LINC01626 Genelong intergenic non-protein coding RNA 1626 |
LINC01623 Genelong intergenic non-protein coding RNA 1623 |
LINC01612 Genelong intergenic non-protein coding RNA 1612 |
LINC01643 Genelong intergenic non-protein coding RNA 1643 |
LINC01647 Genelong intergenic non-protein coding RNA 1647 |
LINC01655 Genelong intergenic non-protein coding RNA 1655 |
LINC01667 Genelong intergenic non-protein coding RNA 1667 |
LINC01749 Genelong intergenic non-protein coding RNA 1749 |
LINC01747 Genelong intergenic non-protein coding RNA 1747 |
LINC01744 Genelong intergenic non-protein coding RNA 1744 |
LINC01743 Genelong intergenic non-protein coding RNA 1743 |
LINC01739 Genelong intergenic non-protein coding RNA 1739 |
LINC01728 Genelong intergenic non-protein coding RNA 1728 |
LINC01723 Genelong intergenic non-protein coding RNA 1723 |
LINC01718 Genelong intergenic non-protein coding RNA 1718 |
LINC01712 Genelong intergenic non-protein coding RNA 1712 |
LINC01704 Genelong intergenic non-protein coding RNA 1704 |
LINC01677 Genelong intergenic non-protein coding RNA 1677 |
LINC01676 Genelong intergenic non-protein coding RNA 1676 |
LINC01673 Genelong intergenic non-protein coding RNA 1673 |
LINC01672 Genelong intergenic non-protein coding RNA 1672 |
LINC01374 Genelong intergenic non-protein coding RNA 1374 |
LINC01297 Genelong intergenic non-protein coding RNA 1297 |
LINC01755 Genelong intergenic non-protein coding RNA 1755 |
LINC01760 Genelong intergenic non-protein coding RNA 1760 |
LINC01763 Genelong intergenic non-protein coding RNA 1763 |
LINC01764 Genelong intergenic non-protein coding RNA 1764 |
LINC02046 Genelong intergenic non-protein coding RNA 2046 |
LINC02045 Genelong intergenic non-protein coding RNA 2045 |
LINC02040 Genelong intergenic non-protein coding RNA 2040 |
LINC02039 Genelong intergenic non-protein coding RNA 2039 |
LINC02034 Genelong intergenic non-protein coding RNA 2034 |
LINC02032 Genelong intergenic non-protein coding RNA 2032 |
LINC02025 Genelong intergenic non-protein coding RNA 2025 |
LINC02022 Genelong intergenic non-protein coding RNA 2022 |
LINC02020 Genelong intergenic non-protein coding RNA 2020 |
LINC02013 Genelong intergenic non-protein coding RNA 2013 |
LINC01999 Genelong intergenic non-protein coding RNA 1999 |
LINC01995 Genelong intergenic non-protein coding RNA 1995 |
LINC01988 Genelong intergenic non-protein coding RNA 1988 |
LINC01986 Genelong intergenic non-protein coding RNA 1986 |
LINC02056 Genelong intergenic non-protein coding RNA 2056 |
LINC02064 Genelong intergenic non-protein coding RNA 2064 |
LINC02166 Genelong intergenic non-protein coding RNA 2166 |
LINC02165 Genelong intergenic non-protein coding RNA 2165 |
LINC02156 Genelong intergenic non-protein coding RNA 2156 |
LINC02152 Genelong intergenic non-protein coding RNA 2152 |
LINC02117 Genelong intergenic non-protein coding RNA 2117 |
LINC02114 Genelong intergenic non-protein coding RNA 2114 |
LINC02113 Genelong intergenic non-protein coding RNA 2113 |
LINC02110 Genelong intergenic non-protein coding RNA 2110 |
LINC02103 Genelong intergenic non-protein coding RNA 2103 |
LINC02096 Genelong intergenic non-protein coding RNA 2096 |
LINC02089 Genelong intergenic non-protein coding RNA 2089 |
LINC02087 Genelong intergenic non-protein coding RNA 2087 |
LINC02079 Genelong intergenic non-protein coding RNA 2079 |
LINC02072 Genelong intergenic non-protein coding RNA 2072 |
LINC02069 Genelong intergenic non-protein coding RNA 2069 |
LINC02059 Genelong intergenic non-protein coding RNA 2059 |
LINC01976 Genelong intergenic non-protein coding RNA 1976 |
LINC01944 Genelong intergenic non-protein coding RNA 1944 |
LINC01855 Genelong intergenic non-protein coding RNA 1855 |
LINC01851 Genelong intergenic non-protein coding RNA 1851 |
LINC01849 Genelong intergenic non-protein coding RNA 1849 |
LINC01846 Genelong intergenic non-protein coding RNA 1846 |
LINC01844 Genelong intergenic non-protein coding RNA 1844 |
LINC01837 Genelong intergenic non-protein coding RNA 1837 |
LINC01818 Genelong intergenic non-protein coding RNA 1818 |
LINC01815 Genelong intergenic non-protein coding RNA 1815 |
LINC01803 Genelong intergenic non-protein coding RNA 1803 |
LINC01799 Genelong intergenic non-protein coding RNA 1799 |
LINC01783 Genelong intergenic non-protein coding RNA 1783 Predicted to enable triplet codon-amino acid adaptor activity. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Mar 2025] |
LINC01778 Genelong intergenic non-protein coding RNA 1778 |
LINC01766 Genelong intergenic non-protein coding RNA 1766 |
LINC01872 Genelong intergenic non-protein coding RNA 1872 |
LINC01962 Genelong intergenic non-protein coding RNA 1962 |
LINC01878 Genelong intergenic non-protein coding RNA 1878 |
LINC01888 Genelong intergenic non-protein coding RNA 1888 |
LINC01938 Genelong intergenic non-protein coding RNA 1938 |
LINC01937 Genelong intergenic non-protein coding RNA 1937 |
LINC01931 Genelong intergenic non-protein coding RNA 1931 |
LINC01927 Genelong intergenic non-protein coding RNA 1927 |
LINC01925 Genelong intergenic non-protein coding RNA 1925 |
LINC01923 Genelong intergenic non-protein coding RNA 1923 |
LINC01919 Genelong intergenic non-protein coding RNA 1919 |
LINC01917 Genelong intergenic non-protein coding RNA 1917 |
LINC01913 Genelong intergenic non-protein coding RNA 1913 |
LINC01912 Genelong intergenic non-protein coding RNA 1912 |
LINC01911 Genelong intergenic non-protein coding RNA 1911 |
LINC01909 Genelong intergenic non-protein coding RNA 1909 |
LINC01905 Genelong intergenic non-protein coding RNA 1905 |
LINC01899 Genelong intergenic non-protein coding RNA 1899 |
LINC01890 Genelong intergenic non-protein coding RNA 1890 |
LINC01884 Genelong intergenic non-protein coding RNA 1884 |
LINC00390 Genelong intergenic non-protein coding RNA 390 |
LINC01052 Genelong intergenic non-protein coding RNA 1052 |
LINC01066 Genelong intergenic non-protein coding RNA 1066 |
LINC02016 Genelong intergenic non-protein coding RNA 2016 |
LINC01694 Genelong intergenic non-protein coding RNA 1694 |
LINC02587 Genelong intergenic non-protein coding RNA 2587 |
LINC02204 Genelong intergenic non-protein coding RNA 2204 |
LINC01785 Genelong intergenic non-protein coding RNA 1785 |
LINC02207 Genelong intergenic non-protein coding RNA 2207 |
LINC02446 Genelong intergenic non-protein coding RNA 2446 |
LINC01857 Genelong intergenic non-protein coding RNA 1857 |
LINC01871 Genelong intergenic non-protein coding RNA 1871 |
GRASLND Geneglycosaminoglycan regulatory associated long non-coding RNA |
LINC01762 Genelong intergenic non-protein coding RNA 1762 |
LINC02027 Genelong intergenic non-protein coding RNA 2027 |
LINC01924 Genelong intergenic non-protein coding RNA 1924 |
LINC01934 Genelong intergenic non-protein coding RNA 1934 |
LINC02251 Genelong intergenic non-protein coding RNA 2251 |
LINC02397 Genelong intergenic non-protein coding RNA 2397 |
LINC01967 Genelong intergenic non-protein coding RNA 1967 |
LINC01357 Genelong intergenic non-protein coding RNA 1357 |
LINC02593 Genelong intergenic non-protein coding RNA 2593 |
LINC02362 Genelong intergenic non-protein coding RNA 2362 |
LINC02523 Genelong intergenic non-protein coding RNA 2523 |
LINC01717 Genelong intergenic non-protein coding RNA 1717 |
LINC02009 Genelong intergenic non-protein coding RNA 2009 |
LINC01724 Genelong intergenic non-protein coding RNA 1724 |
LINC02437 Genelong intergenic non-protein coding RNA 2437 |
LINC01965 Genelong intergenic non-protein coding RNA 1965 |
LINC02836 Genelong intergenic non-protein coding RNA 2836 |
LINC02785 Genelong intergenic non-protein coding RNA 2785 |
LINC01831 Genelong intergenic non-protein coding RNA 1831 |
LINC02053 Genelong intergenic non-protein coding RNA 2053 |
LINC02768 Genelong intergenic non-protein coding RNA 2768 |
LINC02360 Genelong intergenic non-protein coding RNA 2360 |
LINC02237 Genelong intergenic non-protein coding RNA 2237 |
LINC02511 Genelong intergenic non-protein coding RNA 2511 |
LINC01695 Genelong intergenic non-protein coding RNA 1695 |
LINC02901 Genelong intergenic non-protein coding RNA 2901 |
LINC02888 Genelong intergenic non-protein coding RNA 2888 |
LINC02903 Genelong intergenic non-protein coding RNA 2903 |
LINC02899 Genelong intergenic non-protein coding RNA 2899 |
C3ORF86P Genelong intergenic non-protein coding RNA 694 |
LINC02694 Genelong intergenic non-protein coding RNA 2694 |
LINC02902 Genelong intergenic non-protein coding RNA 2902 |
LINC02798 Genelong intergenic non-protein coding RNA 2798 |
LINC02615 Genelong intergenic non-protein coding RNA 2615 |
LINC02696 Genelong intergenic non-protein coding RNA 2696 |
LINC02614 Genelong intergenic non-protein coding RNA 2614 |
LINC02609 Genelong intergenic non-protein coding RNA 2609 |
LINC02981 Genelong intergenic non-protein coding RNA 2981 |
LINC02731 Genelong intergenic non-protein coding RNA 2731 |
LINC02987 Genelong intergenic non-protein coding RNA 2987 |
LINC02544 Genelong intergenic non-protein coding RNA 2544 |
LINC02649 Genelong intergenic non-protein coding RNA 2649 |
LINC02728 Genelong intergenic non-protein coding RNA 2728 |
LINC02803 Genelong intergenic non-protein coding RNA 2803 |
LINC02349 Genelong intergenic non-protein coding RNA 2349 |
LINC02539 Genelong intergenic non-protein coding RNA 2539 |
LINC03002 Genelong intergenic non-protein coding RNA 3002 |
LINC02381 Genelong intergenic non-protein coding RNA 2381 |
LINC02232 Genelong intergenic non-protein coding RNA 2232 |
LINC03100 Genelong intergenic non-protein coding RNA 3100 |
LINC02894 Genelong intergenic non-protein coding RNA 2894 |
LINC02328 Genelong intergenic non-protein coding RNA 2328 |
LINC01779 Genelong intergenic non-protein coding RNA 1779 |
LINC03135 Genelong intergenic non-protein coding RNA 3135 |
LINC02965 Genelong intergenic non-protein coding RNA 2965 |
LINC03052 Genelong intergenic non-protein coding RNA 3052 |
LINC02235 Genelong intergenic non-protein coding RNA 2235 |
LINC02576 Genelong intergenic non-protein coding RNA 2576 |
LINC02560 Genelong intergenic non-protein coding RNA 2560 |
LINC02762 Genelong intergenic non-protein coding RNA 2762 |
LINC02610 Genelong intergenic non-protein coding RNA 2610 |
LINC02854 Genelong intergenic non-protein coding RNA 2854 |
LINC02983 Genelong intergenic non-protein coding RNA 2983 |
LINC02268 Genelong intergenic non-protein coding RNA 2268 |
LINC02893 Genelong intergenic non-protein coding RNA 2893 |
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. |
Short Long Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Long Chain/Very Long Chain Acyl Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain/Very Long Chain Acyl Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
childhood-onset short-trunk short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neonatal short-trunk short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the neonatal short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
disproportionate short-trunk short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the disproportionate short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
disproportionate short-limb short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the disproportionate short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lethal short-limbed short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the lethal short-limbed short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
childhood onset short-limb short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neonatal short-limb short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Lethal Short-Limbed Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lethal Short-Limbed Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood-Onset Short-Trunk Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disproportionate Short-Limb Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Disproportionate Short-Trunk Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neonatal Short-Limb Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neonatal Short-Trunk Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Childhood Onset Short-Limb Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Infancy Onset Short-Trunk Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infancy Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset. |
Split-hand/foot malformation with long bone deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset. |
long 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. |
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. |
split-hand/foot malformation with long bone deficiency 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
split-hand/foot malformation with long bone deficiency 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
long 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. |
Split-Hand-Foot Malformation With Long Bone Deficiency 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Long Bone Deficiency 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Thickening Of Long Bone Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Thickening Of Long Bone Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
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. |
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. |
short nasal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short frontal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short squamosal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short squamosal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short zygomatic bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short zygomatic bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short presphenoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short presphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short zygomatic bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short zygomatic bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short frontal bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short frontal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short nasal bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short nasal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short facial bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short facial bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short temporal bone squamous part Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short temporal bone squamous part phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short presphenoid bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short presphenoid bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short parietal bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short parietal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Short stature and advanced bone age Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature and advanced bone age 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. |
long insular gyri, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in long insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
long insular gyri, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in long insular gyri, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
the prc2 complex sets long-term gene silencing through modification of histone tails Gene SetFrom Biocarta Pathways proteins participating in the the prc2 complex sets long-term gene silencing through modification of histone tails pathway from the Biocarta Pathways dataset. |
Long QT syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acquired long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LONG QT SYNDROME 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LONG QT SYNDROME 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long QT syndrome 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Long Qt Syndrome 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Long Qt Syndrome 9 from the curated CTD Gene-Disease Associations dataset. |
LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
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 chain 3 hydroxyacyl coa dehydrogenase deficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the long chain 3 hydroxyacyl coa dehydrogenase deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the long upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long-segment aganglionic megacolon Gene SetFrom HPO Gene-Disease Associations genes associated with the long-segment aganglionic megacolon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
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. |
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 2, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome, acquired, reduced susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
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. |
Long Chain Acyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain Acyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Very Long Chain Acyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Very Long Chain Acyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Narrow Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Narrow Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long-Chain Dicarboxylic Aciduria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long-Chain Dicarboxylic Aciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
short insular gyri, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in short insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
short insular gyri, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in short insular gyri, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
Short stature, idiopathic, autosomal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib-polydactyly syndrome, Majewski type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia/short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, idiopathic, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-sleeper Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-sleeper phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-rib thoracic dysplasia 11 with or without polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
short QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, short stature, and impaired glucose metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital short bowel syndrome, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib polydactyly syndrome 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short rib polydactyly syndrome 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-rib thoracic dysplasia 10 with or without polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
SHORT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the SHORT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brachyrachia (short spine dysplasia) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short-rib thoracic dysplasia 3 with or without polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Yakut short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Yakut short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spondylometaepiphyseal dysplasia short limb-hand type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
short-chain collagen trimer Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
short-chain collagen trimer Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, X-Linked, with Short Stature Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset. |
Short QT Syndrome 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short QT Syndrome 1 from the curated CTD Gene-Disease Associations dataset. |
Short QT Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short QT Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Short QT Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short QT Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Short Stature, Idiopathic, Autosomal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset. |
Short Stature, Idiopathic, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset. |
Short Rib-Polydactyly Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short Rib-Polydactyly Syndrome from the curated CTD Gene-Disease Associations dataset. |
Short chain Acyl CoA dehydrogenase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset. |
SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset. |
Memory, Short-Term Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Memory, Short-Term in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
short bowel syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease short bowel syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
memory, short-term Gene SetFrom GAD Gene-Disease Associations genes associated with the disease memory, short-term in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
short stature Gene SetFrom GAD Gene-Disease Associations genes associated with the disease short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
idiopathic short stature Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; short bowel syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
short-term response to haloperidol treatment Gene SetFrom GAD Gene-Disease Associations genes associated with the disease short-term response to haloperidol treatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
short Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term short in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
16478745-SuppTable1-short Gene SetFrom GeneSigDB Published Gene Signatures genes in signature reported in the publication with PubMedID 16478745-SuppTable1-short from the GeneSigDB Published Gene Signatures dataset. |
short-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of short-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2015 dataset. |
short-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
short-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
short-chain fatty acid import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid import biological process from the curated GO Biological Process Annotations 2015 dataset. |
short-term memory Gene SetFrom GO Biological Process Annotations 2015 genes participating in the short-term memory biological process from the curated GO Biological Process Annotations 2015 dataset. |
short-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
short-chain collagen trimer Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the short-chain collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
short-chain fatty acid uptake transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the short-chain fatty acid uptake transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
short-chain carboxylesterase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
short-chain fatty acid transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the short-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Hypertension risk in short sleep duration Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
short attention span Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the short attention span phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
short distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
moderately short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the moderately short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short nasal bridge Gene SetFrom HPO Gene-Disease Associations genes associated with the short nasal bridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short chordae tendineae of the tricuspid valve Gene SetFrom HPO Gene-Disease Associations genes associated with the short chordae tendineae of the tricuspid valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short nose Gene SetFrom HPO Gene-Disease Associations genes associated with the short nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 5th toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short 5th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 4th toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short 4th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short diaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the short diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short metacarpals with rounded proximal ends Gene SetFrom HPO Gene-Disease Associations genes associated with the short metacarpals with rounded proximal ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the short 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the short femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short digit Gene SetFrom HPO Gene-Disease Associations genes associated with the short digit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
relatively short spine Gene SetFrom HPO Gene-Disease Associations genes associated with the relatively short spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short sacroiliac notch Gene SetFrom HPO Gene-Disease Associations genes associated with the short sacroiliac notch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short chordae tendineae of the mitral valve Gene SetFrom HPO Gene-Disease Associations genes associated with the short chordae tendineae of the mitral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short columella Gene SetFrom HPO Gene-Disease Associations genes associated with the short columella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short nail Gene SetFrom HPO Gene-Disease Associations genes associated with the short nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short fourth metatarsal Gene SetFrom HPO Gene-Disease Associations genes associated with the short fourth metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short humerus Gene SetFrom HPO Gene-Disease Associations genes associated with the short humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mesomelic short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the mesomelic short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the short philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short metatarsal Gene SetFrom HPO Gene-Disease Associations genes associated with the short metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short umbilical cord Gene SetFrom HPO Gene-Disease Associations genes associated with the short umbilical cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the short upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the short palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short femur Gene SetFrom HPO Gene-Disease Associations genes associated with the short femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short attention span Gene SetFrom HPO Gene-Disease Associations genes associated with the short attention span phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 5th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the short 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short chin Gene SetFrom HPO Gene-Disease Associations genes associated with the short chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the short thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short mandibular rami Gene SetFrom HPO Gene-Disease Associations genes associated with the short mandibular rami phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short lingual frenulum Gene SetFrom HPO Gene-Disease Associations genes associated with the short lingual frenulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
disproportionate short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the disproportionate short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 3rd metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the short 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short palm Gene SetFrom HPO Gene-Disease Associations genes associated with the short palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short mandibular condyles Gene SetFrom HPO Gene-Disease Associations genes associated with the short mandibular condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 2nd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short 2nd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short proximal phalanx of thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mild short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the mild short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short neck Gene SetFrom HPO Gene-Disease Associations genes associated with the short neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe short-limb dwarfism Gene SetFrom HPO Gene-Disease Associations genes associated with the severe short-limb dwarfism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short foot Gene SetFrom HPO Gene-Disease Associations genes associated with the short foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short ribs Gene SetFrom HPO Gene-Disease Associations genes associated with the short ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short proximal phalanx of hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the short proximal phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short ear Gene SetFrom HPO Gene-Disease Associations genes associated with the short ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proportionate short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the proportionate short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short iliac bones Gene SetFrom HPO Gene-Disease Associations genes associated with the short iliac bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the short lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short phalanx of hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the short phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short hard palate Gene SetFrom HPO Gene-Disease Associations genes associated with the short hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the short nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the short metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short sternum Gene SetFrom HPO Gene-Disease Associations genes associated with the short sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short stepped shuffling gait Gene SetFrom HPO Gene-Disease Associations genes associated with the short stepped shuffling gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short tibia Gene SetFrom HPO Gene-Disease Associations genes associated with the short tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 4th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the short 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe short stature Gene SetFrom HPO Gene-Disease Associations genes associated with the severe short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short tubular bones (hand) Gene SetFrom HPO Gene-Disease Associations genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short clavicles Gene SetFrom HPO Gene-Disease Associations genes associated with the short clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short first metatarsal Gene SetFrom HPO Gene-Disease Associations genes associated with the short first metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the short hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Short Bowel Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Short Bowel Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Memory, Short-Term Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Memory, Short-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Short hematopoietin receptor, family 1, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Short hematopoietin receptor, family 1, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Short hematopoietin receptor, family 2, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Short hematopoietin receptor, family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Short-chain dehydrogenase/reductase, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Short-chain dehydrogenase/reductase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Short-chain dehydrogenase/reductase SDR Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Short-chain dehydrogenase/reductase SDR protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
short perineum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short perineum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short tail Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short photoreceptor inner segment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short malleus manubrium Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short malleus manubrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short metestrus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short metestrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short metatarsal bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short metatarsal bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short diestrus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short diestrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short photoreceptor outer segment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short vertebral body Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short fibula Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short palate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short premaxilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short premaxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short excitatory postsynaptic current decay time Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short excitatory postsynaptic current decay time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short proestrus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short proestrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short ureter Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short ureter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short humerus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short humerus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short uterine horn Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short uterine horn phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal short term object recognition memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal short term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short tibia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short tibia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short radius Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short ulna Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short stride length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short stride length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short vibrissae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short umbilical cord Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short umbilical cord phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short malleus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short malleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short lumbar vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short lumbar vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short estrous cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short mandible Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short mandible phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short rostral-caudal axis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short cochlear hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short maxilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short maxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short kidney papilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short kidney papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short outer hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short oviduct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short oviduct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short ribs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short snout Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short snout phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short vertebral column Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short vertebral column phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short nails Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short cochlear outer hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short gestation period Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short gestation period phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short sternum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short sternum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal short term spatial reference memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal short term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short neck Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short neck phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short femur Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short sperm flagellum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short sperm flagellum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short limbs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short limbs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short metacarpal bones Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short metacarpal bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short incisors Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short scapula Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short scapula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short scala media Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short scala media phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short trachea Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short trachea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short estrus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short estrus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the short syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 10 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 4 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
[short sleeper] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [short sleeper] phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia/short stature syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 6 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 7 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
spondylometaepiphyseal dysplasia, short limb-hand type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 11 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital short bowel syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
short qt syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the short qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
short qt syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the short qt syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
short qt syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the short qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
mental retardation, x-linked, with short stature Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 9 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
acyl-coa dehydrogenase, short-chain, deficiency of Gene SetFrom OMIM Gene-Disease Associations genes associated with the acyl-coa dehydrogenase, short-chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, short stature, and impaired glucose metabolism Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, short stature, and impaired glucose metabolism phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 3 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene SetFrom OMIM Gene-Disease Associations genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 8 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature with microcephaly and distinctive facies Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature with microcephaly and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 2 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, idiopathic familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset. |
short-rib thoracic dysplasia 5 with or without polydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset. |
Ear, Patella, Short Stature Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ear, Patella, Short Stature Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Segment Hirschsprung'S Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Segment Hirschsprung'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Corpus Callosum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short-Term Memory Impairment Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short-Term Memory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Sleeper Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Sleeper Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Stature Homeobox Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Stature Homeobox Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Distal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 2Nd Toe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 2Nd Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Rib-Polydactyly Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Rib-Polydactyly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short-Rib Thoracic Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short-Rib Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Hard Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Hard Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spondyloperipheral Dysplasia Short Ulna Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spondyloperipheral Dysplasia Short Ulna in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pituitary Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pituitary Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Bowel Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Bowel Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Rib Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Rib Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Middle Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Chordae Tendineae Of The Mitral Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Chordae Tendineae Of The Mitral Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Chordae Tendineae Of The Tricuspid Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Chordae Tendineae Of The Tricuspid Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Short-Limb Dwarfism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Short-Limb Dwarfism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Bowel Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Bowel in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Digit Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Digit in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Stature, Idiopathic, Autosomal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Stature, Idiopathic, Autosomal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Fifth Metatarsal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Fifth Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Joint Laxity, Short Stature, And Myopia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Joint Laxity, Short Stature, And Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Diaphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Diaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Facial Dysmorphism, Immunodeficiency, Livedo, And Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Facial Dysmorphism, Immunodeficiency, Livedo, And Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Poor Short-Term Memory Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Poor Short-Term Memory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Shox-Related Short Stature Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Shox-Related Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 5Th Toe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 5Th Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Relatively Short Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Relatively Short Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Stature, Ctcae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stature, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Distal Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Lower Third Of Face Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Lower Third Of Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Disproportionate Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proportionate Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proportionate Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Thorax Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Thorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Columella Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Columella in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Neck (In Some Patients) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Neck (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Upturned Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Upturned Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 1St Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 1St Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Toe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Extremities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Philtrum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Philtrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Foot Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Metacarpals With Rounded Proximal Ends Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metacarpals With Rounded Proximal Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Palm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Palm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Memory, Short-Term Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory, Short-Term in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Stepped Shuffling Gait Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stepped Shuffling Gait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Humerus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Humerus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Ribs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Ribs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Tibia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Tibia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mild Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Leg Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Leg in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Palpebral Fissure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Palpebral Fissure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Upper Lip Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Sternum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Sternum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Nasal Septum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Nasal Septum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Telomere Length Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Telomere Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Clavicle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Clavicle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Iliac Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Iliac Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Frenulum Of Tongue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Frenulum Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Metatarsal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 2Nd Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 2Nd Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 5Th Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 5Th Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Middle Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Proximal Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Ear Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Sperm Flagella Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Sperm Flagella in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Moderately Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Moderately Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Tubular Bones Of The Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Tubular Bones Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 4Th Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 4Th Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Fourth Metatarsal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Fourth Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Sacroiliac Notch Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Sacroiliac Notch in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 3Rd Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 3Rd Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Face Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deficit In Phonologic Short-Term Memory Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deficit In Phonologic Short-Term Memory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Third Metatarsal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Third Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short First Metatarsal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short First Metatarsal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Stature, Postnatal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Stature, Postnatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short-Rib Thoracic Dysplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short-Rib Thoracic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Mandibular Rami Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Mandibular Rami in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Cord Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Nasal Bridge Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Nasal Bridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dorsolateral Bowed, Short Radii Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dorsolateral Bowed, Short Radii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mesomelic Short Stature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mesomelic Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Forearm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Forearm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Uvula Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 4Th Toe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 4Th Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Dental Roots Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Dental Roots in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Fetal Femur Length Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Fetal Femur Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Bowed Radii Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Bowed Radii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of short-term neuronal synaptic plasticity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-term memory Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-term memory biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-chain fatty acid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-chain fatty acid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-chain fatty acid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of short-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-chain fatty acid transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-chain fatty acid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of short-term synaptic potentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of short-term synaptic potentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
short-chain fatty acid transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the short-chain fatty acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
short-chain-acyl-CoA dehydrogenase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the short-chain-acyl-CoA dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
short-chain carboxylesterase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
short tibia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short tibia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short humerus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short humerus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short radius Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short radius phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short ulna Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short ulna phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short mandible Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short mandible phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short maxilla Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short maxilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short ribs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short ribs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short femur Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short femur phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short rostral-caudal axis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short metacarpal bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short metacarpal bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short metatarsal bones Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short metatarsal bones phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short vertebral body Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short tail Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short tail phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short premaxilla Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short premaxilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short Meckel's cartilage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short Meckel's cartilage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short lower incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short lower incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short nasal septum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short nasal septum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short vertebral column Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short vertebral column phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short snout Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short snout phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short limbs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short limbs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short fibula Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short fibula phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short oviduct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short oviduct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short photoreceptor outer segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short vibrissae Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short vibrissae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short sternum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short sternum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short photoreceptor inner segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short malleus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short malleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short stride length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short stride length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short ears Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short ears phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short scapula Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short scapula phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short lumbar vertebrae Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short lumbar vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short face Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short face phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short basicranium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short basicranium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short trachea Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short trachea phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short endolymphatic duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short cochlear outer hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short estrous cycle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short estrous cycle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short diestrus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short diestrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short estrus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short estrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal incus short process morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal incus short process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short sperm flagellum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short sperm flagellum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short nails Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short nails phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short excitatory postsynaptic current decay time Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short excitatory postsynaptic current decay time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short outer hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short scala media Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short scala media phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short soft palate Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short soft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short ureter Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short ureter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short proestrus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short proestrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short styloid process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short styloid process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short cochlear hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short tongue Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short tongue phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short neck Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short neck phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short perineum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short perineum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent incus short process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent incus short process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal short-term spatial reference memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal short-term spatial reference memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short philtrum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short philtrum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short malleus manubrium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short malleus manubrium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short umbilical cord Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short umbilical cord phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short Tomes' process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short Tomes' process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short gestation period Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short gestation period phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short uterine horn Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short uterine horn phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short femur neck Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short femur neck phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short chin Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short chin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal short-term object recognition memory Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal short-term object recognition memory phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short ilium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short ilium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short tooth root Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short tooth root phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short nasal bridge Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short nasal bridge phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short vestibular hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short vestibular hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short metestrus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short metestrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short forehead Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short forehead phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short kidney papilla Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short kidney papilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short mandibular coronoid process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short mandibular coronoid process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short excitatory postsynaptic current rise time Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short excitatory postsynaptic current rise time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short tibia Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the short tibia phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Tonsil - L2 - Short lived IgM+ PC Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Short lived IgM+ PC cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Short Loop Descending Limb cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Short Loop Descending Limb cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Short-lived effector cell (SLEC)_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Short-lived effector cell (SLEC)_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 Gene Setproteins participating in the Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 pathway from the Reactome Pathways 2024 dataset. |