| Name |
|---|
CMAP Signatures of Differentially Expressed Genes for Small Molecules DatasetFrom Connectivity Map mRNA expression profiles for cell lines following chemical perturbation |
GEO Signatures of Differentially Expressed Genes for Small Molecules DatasetmRNA expression profiles for cell lines or tissues following small molecule perturbation |
LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules Dataset (Archived)From LINCS L1000 Connectivity Map mRNA expression profiles for cell lines following small molecule perturbation |
RHDNS1 GeneRenal hypodysplasia, nonsyndromic, 1 |
PTCPRN GenePapillary thyroid carcinoma with papillary renal neoplasia |
AABT GeneBeta-amino acids, renal transport of |
RFH1 GeneRenal failure, progressive, with hypertension |
GLYS1 Geneglycosuria 1, renal |
PRCC Genepapillary renal cell carcinoma (translocation-associated) This gene encodes a protein that may play a role in pre-mRNA splicing. Chromosomal translocations (X;1)(p11;q21) that result in fusion of this gene to TFE3 (GeneID 7030) have been associated with papillary renal cell carcinoma. A PRCC-TFE3 fusion protein is expressed in affected carcinomas and is likely associated with altered gene transactivation. This fusion protein has also been associated with disruption of the cell cycle.[provided by RefSeq, Aug 2010] |
DIRC1 Genedisrupted in renal carcinoma 1 Disruption of DIRC1 by translocation is associated with familial clear cell renal cancer. Overexpression of DIRC1 is associated with tumor progression and poor prognosis in gastric cancer. [provided by RefSeq, Mar 2019] |
DIRC3 Genedisrupted in renal carcinoma 3 |
DIRC2 Genedisrupted in renal carcinoma 2 This gene encodes a membrane-bound protein from the major facilitator superfamily of transporters. Disruption of this gene by translocation has been associated with haplo-insufficiency and renal cell carcinomas. Alternatively spliced transcript variants have been described, but their biological validity has not yet been determined. [provided by RefSeq, Jul 2008] |
DPEP1 Genedipeptidase 1 (renal) The protein encoded by this gene is a kidney membrane enzyme involved in the metabolism of glutathione and other similar proteins by dipeptide hydrolysis. The encoded protein is known to regulate leukotriene activity by catalyzing the conversion of leukotriene D4 to leukotriene E4. This protein uses zinc as a cofactor and acts as a disulfide-linked homodimer. [provided by RefSeq, Dec 2020] |
PRR5 Geneproline rich 5 (renal) This gene encodes a protein with a proline-rich domain. This gene is located in a region of chromosome 22 reported to contain a tumor suppressor gene that may be involved in breast and colorectal tumorigenesis. The protein is a component of the mammalian target of rapamycin complex 2 (mTORC2), and it regulates platelet-derived growth factor (PDGF) receptor beta expression and PDGF signaling to Akt and S6K1. Alternative splicing and the use of alternative promoters results in transcripts encoding different isoforms. Read-through transcripts from this gene into the downstream Rho GTPase activating protein 8 (ARHGAP8) gene also exist, which led to the original description of PRR5 and ARHGAP8 being a single gene. [provided by RefSeq, Nov 2010] |
TKCR Genetorticollis, keloids, cryptorchidism and renal dysplasia |
MS Genemultiple sclerosis |
SHANK3 GeneSH3 and multiple ankyrin repeat domains 3 This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012] |
SHANK2 GeneSH3 and multiple ankyrin repeat domains 2 This gene encodes a protein that is a member of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses. Shank proteins contain multiple domains for protein-protein interaction, including ankyrin repeats, and an SH3 domain. This particular family member contains a PDZ domain, a consensus sequence for cortactin SH3 domain-binding peptides and a sterile alpha motif. The alternative splicing demonstrated in Shank genes has been suggested as a mechanism for regulating the molecular structure of Shank and the spectrum of Shank-interacting proteins in the postsynaptic densities of the adult and developing brain. Alterations in the encoded protein may be associated with susceptibility to autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
SHANK1 GeneSH3 and multiple ankyrin repeat domains 1 This gene encodes a member of the SHANK (SH3 domain and ankyrin repeat containing) family of proteins. Members of this family act as scaffold proteins that are required for the development and function of neuronal synapses. Deletions in this gene may be associated with autism spectrum disorder in males. [provided by RefSeq, Apr 2016] |
EXT3 Geneexostoses (multiple) 3 |
MMDFS GeneMultiple mitochondrial dysfunctions syndrome |
MEN1 Genemultiple endocrine neoplasia I This gene encodes menin, a tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. Menin is a scaffold protein that functions in histone modification and epigenetic gene regulation. It is thought to regulate several pathways and processes by altering chromatin structure through the modification of histones. [provided by RefSeq, May 2019] |
MCTP1 Genemultiple C2 domains, transmembrane 1 Enables calcium ion binding activity. Predicted to be involved in several processes, including modulation of chemical synaptic transmission; negative regulation of endocytosis; and negative regulation of response to oxidative stress. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MCTP2 Genemultiple C2 domains, transmembrane 2 Enables calcium ion binding activity. Predicted to be involved in regulation of neurotransmitter secretion. Located in cytosol; membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
MMEDF GeneMacrocephaly with multiple epiphyseal dysplasia and distinctive facies |
MEGF8 Genemultiple EGF-like-domains 8 The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012] |
CNC2 GeneCarney complex type 2, multiple neoplasia and lentiginosis |
RBPMS2 GeneRNA binding protein with multiple splicing 2 The protein encoded by this gene is a member of the RNA recognition motif (RRM)-containing protein family and is involved in the development and dedifferentiation of digestive smooth muscle cells. The encoded protein functions as a homodimer and indirectly inhibits the bone morphogenetic protein pathway. [provided by RefSeq, Aug 2016] |
MCFD2P1 Genemultiple coagulation factor deficiency 2 pseudogene 1 |
MINPP1 Genemultiple inositol-polyphosphate phosphatase 1 This gene encodes multiple inositol polyphosphate phosphatase; an enzyme that removes 3-phosphate from inositol phosphate substrates. It is the only enzyme known to hydrolzye inositol pentakisphosphate and inositol hexakisphosphate. This enzyme also converts 2,3 bisphosphoglycerate (2,3-BPG) to 2-phosphoglycerate; an activity formerly thought to be exclusive to 2,3-BPG synthase/2-phosphatase (BPGM) in the Rapoport-Luebering shunt of the glycolytic pathway.[provided by RefSeq, Sep 2009] |
RBPMSLP GeneRNA binding protein with multiple splicing-like pseudogene |
MS4 GeneMultiple sclerosis, susceptiblity to, 4 |
MS3 GeneMultiple sclerosis, susceptibility to, 3 |
MS2 GeneMultiple sclerosis, susceptibility to, 2 |
CSMD2 GeneCUB and Sushi multiple domains 2 The protein encoded by this gene is thought to be involved in the control of complement cascade of the immune system. Defects in this gene have been associated with schizophrenia. This gene may act as a tumor suppressor for colorectal cancer. [provided by RefSeq, Jan 2020] |
CSMD3 GeneCUB and Sushi multiple domains 3 Predicted to be involved in regulation of dendrite development. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CSMD1 GeneCUB and Sushi multiple domains 1 Predicted to act upstream of or within several processes, including learning or memory; mammary gland branching involved in pregnancy; and reproductive structure development. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105373985 Genemultiple epidermal growth factor-like domains protein 6 |
MFT2 GeneTrichoepithelioma, multiple familial, 2 |
EGFL7 GeneEGF-like-domain, multiple 7 This gene encodes a secreted endothelial cell protein that contains two epidermal growth factor-like domains. The encoded protein may play a role in regulating vasculogenesis. This protein may be involved in the growth and proliferation of tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
EGFL6 GeneEGF-like-domain, multiple 6 This gene encodes a member of the epidermal growth factor (EGF) repeat superfamily. Members of this superfamily are characterized by the presence of EGF-like repeats and are often involved in the regulation of cell cycle, proliferation, and developmental processes. The gene product contains a signal peptide, suggesting that it is secreted; an EGF repeat region consisting of 4 complete EGF-like repeats and 1 partial EGF-like repeat, 3 of which have a calcium-binding consensus sequence; an arg-gly-asp integrin association motif; and a MAM domain, which is believed to have an adhesive function. This gene is expressed early during development, and its expression has been detected in lung and meningioma tumors. [provided by RefSeq, Jul 2008] |
EGFL8 GeneEGF-like-domain, multiple 8 Predicted to enable signaling receptor binding activity. Predicted to be involved in vasculogenesis. Predicted to be active in cell surface and extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
MEGF9 Genemultiple EGF-like-domains 9 Predicted to enable small GTPase binding activity. Predicted to be involved in regulation of actin filament polymerization. Predicted to be located in basement membrane and membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
MEGF6 Genemultiple EGF-like-domains 6 Predicted to enable calcium ion binding activity and scavenger receptor activity. Predicted to be involved in vesicle-mediated transport. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
CHDT3 GeneCongenital heart defects, multiple types, 3 |
EXTL2P1 Geneexostoses (multiple)-like 2 pseudogene 1 |
ODPF GeneOsseous dysplasia, digital, with facial pigmentary defects and multiple frenula |
MPDZ Genemultiple PDZ domain protein The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015] |
RBPMS GeneRNA binding protein with multiple splicing This gene encodes a member of the RNA recognition motif family of RNA-binding proteins. The RNA recognition motif is between 80-100 amino acids in length and family members contain one to four copies of the motif. The RNA recognition motif consists of two short stretches of conserved sequence, as well as a few highly conserved hydrophobic residues. The encoded protein has a single, putative RNA recognition motif in its N-terminus. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013] |
MCFD2 Genemultiple coagulation factor deficiency 2 This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D); a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2016] |
MEGF10 Genemultiple EGF-like-domains 10 This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012] |
MEGF11 Genemultiple EGF-like-domains 11 Predicted to be involved in homotypic cell-cell adhesion and retina layer formation. Predicted to be located in basolateral plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5B-1 GeneRNA, U5B small nuclear 1 Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPCP6 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 6 |
LOC101928952 Geneserine palmitoyltransferase small subunit A pseudogene |
RNU6-67P GeneRNA, U6 small nuclear 67, pseudogene |
RNU7-36P GeneRNA, U7 small nuclear 36 pseudogene |
SNORA81 Genesmall nucleolar RNA, H/ACA box 81 Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA81, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
SNORA84 Genesmall nucleolar RNA, H/ACA box 84 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SGSM3 Genesmall G protein signaling modulator 3 Enables GTPase activator activity and small GTPase binding activity. Involved in several processes, including Rap protein signal transduction; positive regulation of GTPase activity; and regulation of Rab protein signal transduction. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-14 Genesmall nucleolar RNA, C/D box 115-14 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-16 Genesmall nucleolar RNA, C/D box 115-16 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-17 Genesmall nucleolar RNA, C/D box 115-17 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-10 Genesmall nucleolar RNA, C/D box 115-10 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-16P GeneRNA, U1 small nuclear 16, pseudogene |
KRR1 GeneKRR1, small subunit (SSU) processome component, homolog (yeast) Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in chromosome; intercellular bridge; and nuclear lumen. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-53P GeneRNA, U7 small nuclear 53 pseudogene |
RNU5A-5P GeneRNA, U5A small nuclear 5, pseudogene |
SNORD48 Genesmall nucleolar RNA, C/D box 48 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD90 Genesmall nucleolar RNA, C/D box 90 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD41 Genesmall nucleolar RNA, C/D box 41 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD47 Genesmall nucleolar RNA, C/D box 47 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD44 Genesmall nucleolar RNA, C/D box 44 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD93 Genesmall nucleolar RNA, C/D box 93 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD4B Genesmall nucleolar RNA, C/D box 4B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD4A Genesmall nucleolar RNA, C/D box 4A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100133102 Generas-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) pseudogene |
LOC100422227 Genesmall ubiquitin-like modifier 1 pseudogene |
U2AF1L4 GeneU2 small nuclear RNA auxiliary factor 1-like 4 Predicted to enable pre-mRNA 3'-splice site binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be part of U2AF complex and spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNU2-6P GeneRNA, U2 small nuclear 6, pseudogene |
SNORD91B Genesmall nucleolar RNA, C/D box 91B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD91A Genesmall nucleolar RNA, C/D box 91A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC402230 Genesmall nuclear ribonucleoprotein 27kDa (U4/U6.U5) pseudogene |
SNORD115-6 Genesmall nucleolar RNA, C/D box 115-6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-7 Genesmall nucleolar RNA, C/D box 115-7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-4 Genesmall nucleolar RNA, C/D box 115-4 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-1 Genesmall nucleolar RNA, C/D box 115-1 This gene encodes a small nucleolar RNA (snoRNA) that is found clustered with dozens of other similar snoRNAs on chromosome 15. These genes are found mostly within introns of the IC-SNURF-SNRPN transcript, which is paternally imprinted and from the Prader-Willi/Angelman syndrome (PWS) region. This gene has been designated as copy 1 of the cluster and may be involved in the regulation of RNA editing and/or alternative splicing of the serotonin receptor 2C (HTR2C) transcript. This gene is not thought to play a major role in PWS. [provided by RefSeq, Jul 2008] |
LOC100131425 GeneLSM5 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
LOC100820733 GeneLSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
RNU7-1 GeneRNA, U7 small nuclear 1 Implicated in Aicardi-Goutieres syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-46P GeneRNA, U6 small nuclear 46, pseudogene |
SERF2 Genesmall EDRK-rich factor 2 Involved in protein destabilization. Predicted to be located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD45A Genesmall nucleolar RNA, C/D box 45A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929101 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
SNORD111B Genesmall nucleolar RNA, C/D box 111B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100631265 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
LOC100631267 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
LOC100631266 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
LOC100631268 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU5E-6P GeneRNA, U5E small nuclear 6, pseudogene |
RNU7-24P GeneRNA, U7 small nuclear 24 pseudogene |
SNRPD3 Genesmall nuclear ribonucleoprotein D3 polypeptide 18kDa This gene encodes a core component of the spliceosome, which is a nuclear ribonucleoprotein complex that functions in pre-mRNA splicing. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
SNRPD2 Genesmall nuclear ribonucleoprotein D2 polypeptide 16.5kDa The protein encoded by this gene belongs to the small nuclear ribonucleoprotein core protein family. It is required for pre-mRNA splicing and small nuclear ribonucleoprotein biogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009] |
SNRPD1 Genesmall nuclear ribonucleoprotein D1 polypeptide 16kDa This gene encodes a small nuclear ribonucleoprotein that belongs to the SNRNP core protein family. The protein may act as a charged protein scaffold to promote SNRNP assembly or strengthen SNRNP-SNRNP interactions through nonspecific electrostatic contacts with RNA. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014] |
MPHOSPH10 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) This gene encodes a protein that is phosphorylated during mitosis. The protein localizes to the nucleolus during interphase and to the chromosomes during M phase. The protein associates with the U3 small nucleolar ribonucleoprotein 60-80S complexes and may be involved in pre-rRNA processing. [provided by RefSeq, Dec 2010] |
LOC100131877 Genesmall EDRK-rich factor 2 pseudogene |
RNU1-28P GeneRNA, U1 small nuclear 28, pseudogene |
RNU1-13P GeneRNA, U1 small nuclear 13, pseudogene |
RNU7-5P GeneRNA, U7 small nuclear 5 pseudogene |
SPRR4 Genesmall proline-rich protein 4 Predicted to be involved in keratinization. Predicted to be located in cell cortex. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR3 Genesmall proline-rich protein 3 Predicted to enable structural molecule activity. Predicted to be involved in keratinocyte differentiation and wound healing. Located in Golgi apparatus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6ATAC5P GeneRNA, U6atac small nuclear 5, pseudogene |
LSM8 GeneLSM8 homolog, U6 small nuclear RNA associated (S. cerevisiae) This gene encodes a member of the like-Sm family of proteins. The encoded protein consists of a closed barrel shape, made up of five anti-parallel beta strands and an alpha helix. This protein partners with six paralogs to form a heteroheptameric ring which transiently binds U6 small nuclear RNAs and is involved in the general maturation of RNA in the nucleus. [provided by RefSeq, Jan 2010] |
LSM4 GeneLSM4 homolog, U6 small nuclear RNA associated (S. cerevisiae) This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
LSM5 GeneLSM5 homolog, U6 small nuclear RNA associated (S. cerevisiae) Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004] |
LSM6 GeneLSM6 homolog, U6 small nuclear RNA associated (S. cerevisiae) Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004] |
SNRPGP9 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 9 |
SNRPGP7 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 7 |
SNRPGP6 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 6 |
SNRPGP5 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 5 |
SNRPGP4 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 4 |
SNRPGP1 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 1 |
LOC100129534 Genesmall nuclear ribonucleoprotein polypeptide N pseudogene |
LOC101927923 Genesmall integral membrane protein 12-like |
LOC100131747 Genesmall EDRK-rich factor 2 pseudogene |
SNORD12C Genesmall nucleolar RNA, C/D box 12C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD12B Genesmall nucleolar RNA, C/D box 12B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD123 Genesmall nucleolar RNA, C/D box 123 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD127 Genesmall nucleolar RNA, C/D box 127 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD124 Genesmall nucleolar RNA, C/D box 124 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-62P GeneRNA, U7 small nuclear 62 pseudogene |
RNU6-79P GeneRNA, U6 small nuclear 79, pseudogene |
RNU4-7P GeneRNA, U4 small nuclear 7, pseudogene |
RNU6-8 GeneRNA, U6 small nuclear 8 Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-9 GeneRNA, U6 small nuclear 9 Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-7 GeneRNA, U6 small nuclear 7 Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-1 GeneRNA, U6 small nuclear 1 Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-2 GeneRNA, U6 small nuclear 2 Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-69P GeneRNA, U6 small nuclear 69, pseudogene |
SNORA9 Genesmall nucleolar RNA, H/ACA box 9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA8 Genesmall nucleolar RNA, H/ACA box 8 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA1 Genesmall nucleolar RNA, H/ACA box 1 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA4 Genesmall nucleolar RNA, H/ACA box 4 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA6 Genesmall nucleolar RNA, H/ACA box 6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-20P GeneRNA, U1 small nuclear 20, pseudogene |
LOC100421121 Genesmall G protein signaling modulator 1 pseudogene |
RRP9 Generibosomal RNA processing 9, small subunit (SSU) processome component, homolog (yeast) This gene encodes a member of the WD-repeat protein family. The encoded protein is a component of the nucleolar small nuclear ribonucleoprotein particle (snoRNP) and is essential for 18s rRNA processing during ribosome synthesis. It contains seven WD domains required for nucleolar localization and specific interaction with the U3 small nucleolar RNA (U3 snoRNA). [provided by RefSeq, Oct 2012] |
SMIM13 Genesmall integral membrane protein 13 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM12 Genesmall integral membrane protein 12 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM11 Genesmall integral membrane protein 11 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM10 Genesmall integral membrane protein 10 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM17 Genesmall integral membrane protein 17 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM15 Genesmall integral membrane protein 15 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM14 Genesmall integral membrane protein 14 Predicted to act upstream of or within blastocyst hatching. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM19 Genesmall integral membrane protein 19 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM18 Genesmall integral membrane protein 18 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-47P GeneRNA, U7 small nuclear 47 pseudogene |
RNU7-86P GeneRNA, U7 small nuclear 86 pseudogene |
SNORD121B Genesmall nucleolar RNA, C/D box 121B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD121A Genesmall nucleolar RNA, C/D box 121A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-13P GeneRNA, U7 small nuclear 13 pseudogene |
RNU6-36P GeneRNA, U6 small nuclear 36, pseudogene |
RNU4ATAC2P GeneRNA, U4atac small nuclear 2, pseudogene |
RNU6-64P GeneRNA, U6 small nuclear 64, pseudogene |
SNRNP200 Genesmall nuclear ribonucleoprotein 200kDa (U5) Pre-mRNA splicing is catalyzed by the spliceosome, a complex of specialized RNA and protein subunits that removes introns from a transcribed pre-mRNA segment. The spliceosome consists of small nuclear RNA proteins (snRNPs) U1, U2, U4, U5 and U6, together with approximately 80 conserved proteins. U5 snRNP contains nine specific proteins. This gene encodes one of the U5 snRNP-specific proteins. This protein belongs to the DEXH-box family of putative RNA helicases. It is a core component of U4/U6-U5 snRNPs and appears to catalyze an ATP-dependent unwinding of U4/U6 RNA duplices. Mutations in this gene cause autosomal-dominant retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined. [provided by RefSeq, Mar 2010] |
RNU5B-5P GeneRNA, U5B small nuclear 5, pseudogene |
RNU6-63P GeneRNA, U6 small nuclear 63, pseudogene |
SNORA74A Genesmall nucleolar RNA, H/ACA box 74A Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA74B Genesmall nucleolar RNA, H/ACA box 74B Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA74B, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
RNU7-54P GeneRNA, U7 small nuclear 54 pseudogene |
RNU5A-2P GeneRNA, U5A small nuclear 2, pseudogene |
SNORD115-43 Genesmall nucleolar RNA, C/D box 115-43 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-41 Genesmall nucleolar RNA, C/D box 115-41 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-47 Genesmall nucleolar RNA, C/D box 115-47 |
SNORD1A Genesmall nucleolar RNA, C/D box 1A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD1B Genesmall nucleolar RNA, C/D box 1B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD1C Genesmall nucleolar RNA, C/D box 1C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD16 Genesmall nucleolar RNA, C/D box 16 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD10 Genesmall nucleolar RNA, C/D box 10 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD11 Genesmall nucleolar RNA, C/D box 11 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD19 Genesmall nucleolar RNA, C/D box 19 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-32P GeneRNA, U7 small nuclear 32 pseudogene |
SNORD43 Genesmall nucleolar RNA, C/D box 43 Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD43, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD43, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008] |
SNORD46 Genesmall nucleolar RNA, C/D box 46 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-6 Genesmall nucleolar RNA, C/D box 116-6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-F Genesmall ILF3/NF90-associated RNA F |
SNAR-E Genesmall ILF3/NF90-associated RNA E Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-D Genesmall ILF3/NF90-associated RNA D |
KCNN4 Genepotassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4 The protein encoded by this gene is part of a potentially heterotetrameric voltage-independent potassium channel that is activated by intracellular calcium. Activation is followed by membrane hyperpolarization, which promotes calcium influx. The encoded protein may be part of the predominant calcium-activated potassium channel in T-lymphocytes. This gene is similar to other KCNN family potassium channel genes, but it differs enough to possibly be considered as part of a new subfamily. [provided by RefSeq, Jul 2008] |
KCNN3 Genepotassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3 Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. This gene belongs to the KCNN family of potassium channels. It encodes an integral membrane protein that forms a voltage-independent calcium-activated channel, which is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene contains two CAG repeat regions in the coding sequence. It was thought that expansion of one or both of these repeats could lead to an increased susceptibility to schizophrenia or bipolar disorder, but studies indicate that this is probably not the case. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011] |
KCNN2 Genepotassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2 Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene is a member of the KCNN family of potassium channel genes. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. Alternate splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013] |
KCNN1 Genepotassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 1 Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. This gene is a member of the KCNN family of potassium channel genes. [provided by RefSeq, Jul 2008] |
RNU7-33P GeneRNA, U7 small nuclear 33 pseudogene |
RNU5D-2P GeneRNA, U5D small nuclear 2, pseudogene |
SNORA33 Genesmall nucleolar RNA, H/ACA box 33 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA32 Genesmall nucleolar RNA, H/ACA box 32 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA31 Genesmall nucleolar RNA, H/ACA box 31 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. Implicated in brain disease. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA30 Genesmall nucleolar RNA, H/ACA box 30 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA35 Genesmall nucleolar RNA, H/ACA box 35 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA34 Genesmall nucleolar RNA, H/ACA box 34 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA38 Genesmall nucleolar RNA, H/ACA box 38 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-76P GeneRNA, U6 small nuclear 76, pseudogene |
RNU7-27P GeneRNA, U7 small nuclear 27 pseudogene |
SNRPCP9 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 9 |
SNRPCP8 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 8 |
SNRPCP3 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 3 |
SNRPCP2 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 2 |
SNRPCP7 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 7 |
SNRPCP4 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 4 |
SNAPC3 Genesmall nuclear RNA activating complex, polypeptide 3, 50kDa Predicted to enable RNA polymerase III type 3 promoter sequence-specific DNA binding activity and bent DNA binding activity. Predicted to contribute to RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and core promoter sequence-specific DNA binding activity. Predicted to be involved in snRNA transcription by RNA polymerase II and snRNA transcription by RNA polymerase III. Located in nuclear body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAPC2 Genesmall nuclear RNA activating complex, polypeptide 2, 45kDa This gene encodes a subunit of the snRNA-activating protein complex which is associated with the TATA box-binding protein. The encoded protein is necessary for RNA polymerase II and III dependent small-nuclear RNA gene transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009] |
SNAPC1 Genesmall nuclear RNA activating complex, polypeptide 1, 43kDa Predicted to enable sequence-specific DNA binding activity. Predicted to be involved in snRNA transcription by RNA polymerase II and snRNA transcription by RNA polymerase III. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SNAPC5 Genesmall nuclear RNA activating complex, polypeptide 5, 19kDa This gene encodes a subunit of the small nuclear RNA (snRNA)-activating protein complex that plays a role in the transcription of snRNA genes. This complex binds to the promoters of snRNA genes transcribed by either RNA polymerase II or III and recruits other regulatory factors to activate snRNA gene transcription. The encoded protein may play a role in stabilizing this complex. A pseudogene of this gene has been identified on chromosome 6. [provided by RefSeq, Jul 2016] |
SNAPC4 Genesmall nuclear RNA activating complex, polypeptide 4, 190kDa This gene encodes the largest subunit of the small nuclear RNA-activating protein (SNAP) complex. The encoded protein contains a Myb DNA-binding domain, and is essential for RNA polymerase II and III polymerase transcription from small nuclear RNA promoters. A mutation in this gene is associated with ankylosing spondylitis. [provided by RefSeq, Jul 2016] |
SNORD98 Genesmall nucleolar RNA, C/D box 98 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD99 Genesmall nucleolar RNA, C/D box 99 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD94 Genesmall nucleolar RNA, C/D box 94 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD95 Genesmall nucleolar RNA, C/D box 95 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD97 Genesmall nucleolar RNA, C/D box 97 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD92 Genesmall nucleolar RNA, C/D box 92 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-21P GeneRNA, U6 small nuclear 21, pseudogene |
UTP14A GeneUTP14, U3 small nucleolar ribonucleoprotein, homolog A (yeast) This gene encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the encoded protein is involved in ribosome biogenesis and 18S rRNA synthesis. An autosomal retrotransposed copy of this X-linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009] |
UTP14C GeneUTP14, U3 small nucleolar ribonucleoprotein, homolog C (yeast) Predicted to be involved in several processes, including meiotic cell cycle; rRNA processing; and spermatogenesis. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU2-3P GeneRNA, U2 small nuclear 3, pseudogene |
RNU7-75P GeneRNA, U7 small nuclear 75 pseudogene |
RNU7-4P GeneRNA, U7 small nuclear 4 pseudogene |
RN7SKP1 GeneRNA, 7SK small nuclear pseudogene 1 |
LOC102724525 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
RNU5A-8P GeneRNA, U5A small nuclear 8, pseudogene |
RNU6-53P GeneRNA, U6 small nuclear 53, pseudogene |
RNU6-39P GeneRNA, U6 small nuclear 39, pseudogene |
RNU5F-6P GeneRNA, U5F small nuclear 6, pseudogene |
SNAR-A8 Genesmall ILF3/NF90-associated RNA A8 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU4-4P GeneRNA, U4 small nuclear 4, pseudogene |
SNAR-G1 Genesmall ILF3/NF90-associated RNA G1 |
SNAR-G2 Genesmall ILF3/NF90-associated RNA G2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-83P GeneRNA, U6 small nuclear 83, pseudogene |
RNU1-27P GeneRNA, U1 small nuclear 27, pseudogene |
RNU6-48P GeneRNA, U6 small nuclear 48, pseudogene |
RNU1-18P GeneRNA, U1 small nuclear 18, pseudogene |
SMIM23 Genesmall integral membrane protein 23 Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM20 Genesmall integral membrane protein 20 Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM21 Genesmall integral membrane protein 21 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM24 Genesmall integral membrane protein 24 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU2-1 GeneRNA, U2 small nuclear 1 The spliceosome is a multicomponent ribonucleoprotein complex that catalyzes the removal of introns from nuclear mRNA precursors. The spliceosome is composed of four small ribonucleoprotein particles (the U1, U2, and U4/U6 snRNPs) and numerous additional proteins. The U2 small nuclear RNA (snRNA) is a RNA component of the U2 snRNP that interacts with the 3' region of the intron at the branch site. Several sites in the human genome express U2 snRNAs. This locus represents an array of U2 snRNA genes located at 17q21-22 that undergoes concerted evolution to homogenize repeat units within the array. Each repeat in this array is approximately 6.1 kb long and contains a single copy of the U2 snRNA. Arrays of six to more than 30 repeats have been reported. [provided by RefSeq, Mar 2009] |
RNU7-42P GeneRNA, U7 small nuclear 42 pseudogene |
SNORD32A Genesmall nucleolar RNA, C/D box 32A Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD32B Genesmall nucleolar RNA, C/D box 32B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-85P GeneRNA, U7 small nuclear 85 pseudogene |
SCLC1 Genesmall cell cancer of the lung |
SNORD17 Genesmall nucleolar RNA, C/D box 17 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG5 Genesmall nucleolar RNA host gene 5 This gene represent a snoRNA host gene and produces a long non-coding RNA. This RNA may regulate gene expression by acting as a sponge for microRNAs. This transcript may also stabilize mRNAs by blocking degradation by staufen double-stranded RNA binding protein 1. [provided by RefSeq, Dec 2017] |
SNHG4 Genesmall nucleolar RNA host gene 4 |
SNHG7 Genesmall nucleolar RNA host gene 7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG6 Genesmall nucleolar RNA host gene 6 |
SNHG1 Genesmall nucleolar RNA host gene 1 This locus represents a small nucleolar RNA host gene that produces multiple alternatively spliced long non-coding RNAs. This gene is upregulated in cancers and is thought to act as promoter of cell proliferation. This transcript negatively regulates tumor suppressor genes such as tumor protein p53. Expression of this locus may be a marker of tumor progression. [provided by RefSeq, Dec 2017] |
SNHG8 Genesmall nucleolar RNA host gene 8 |
RNU7-28P GeneRNA, U7 small nuclear 28 pseudogene |
RNU7-65P GeneRNA, U7 small nuclear 65 pseudogene |
RNU7-38P GeneRNA, U7 small nuclear 38 pseudogene |
SNORD15B Genesmall nucleolar RNA, C/D box 15B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD15A Genesmall nucleolar RNA, C/D box 15A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD3B-1 Genesmall nucleolar RNA, C/D box 3B-1 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD3B-2 Genesmall nucleolar RNA, C/D box 3B-2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421673 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
LOC100421672 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
LOC101929749 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
TSKU Genetsukushi, small leucine rich proteoglycan Predicted to enable transforming growth factor beta binding activity. Predicted to be involved in several processes, including cholesterol efflux; cholesterol homeostasis; and nervous system development. Predicted to act upstream of or within several processes, including ciliary body morphogenesis; negative regulation of Wnt signaling pathway; and telencephalon development. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LOC643802 Geneu3 small nucleolar ribonucleoprotein protein MPP10-like |
SNORD83A Genesmall nucleolar RNA, C/D box 83A Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD83A, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD83A, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008] |
SNORD83B Genesmall nucleolar RNA, C/D box 83B Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD83B, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD83B, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008] |
SNORA71C Genesmall nucleolar RNA, H/ACA box 71C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA71B Genesmall nucleolar RNA, H/ACA box 71B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA71A Genesmall nucleolar RNA, H/ACA box 71A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA71E Genesmall nucleolar RNA, H/ACA box 71E Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-66P GeneRNA, U6 small nuclear 66, pseudogene |
SNORD85 Genesmall nucleolar RNA, C/D box 85 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
UTP3 GeneUTP3, small subunit (SSU) processome component, homolog (S. cerevisiae) Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-8P GeneRNA, U7 small nuclear 8 pseudogene |
SNORD114-31 Genesmall nucleolar RNA, C/D box 114-31 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-30 Genesmall nucleolar RNA, C/D box 114-30 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMKR1 Genesmall lysine-rich protein 1 |
LOC100820734 GeneLSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
RNU7-14P GeneRNA, U7 small nuclear 14 pseudogene |
LOC729200 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
RNVU1-17 GeneRNA, variant U1 small nuclear 17 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-14 GeneRNA, variant U1 small nuclear 14 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-15 GeneRNA, variant U1 small nuclear 15 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-11 GeneRNA, variant U1 small nuclear 11 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-18 GeneRNA, variant U1 small nuclear 18 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-19 GeneRNA, variant U1 small nuclear 19 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD12 Genesmall nucleolar RNA, C/D box 12 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-30P GeneRNA, U7 small nuclear 30 pseudogene |
SNORD13 Genesmall nucleolar RNA, C/D box 13 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM11P1 Genesmall integral membrane protein 11 pseudogene 1 |
SNORA68 Genesmall nucleolar RNA, H/ACA box 68 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA64 Genesmall nucleolar RNA, H/ACA box 64 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA65 Genesmall nucleolar RNA, H/ACA box 65 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA66 Genesmall nucleolar RNA, H/ACA box 66 This gene encodes a non-coding RNA that functions in the biogenesis of other small nuclear RNAs. This RNA is found in the nucleolus, where it may be involved in the pseudouridylation of 18S ribosomal RNA. This RNA is found associated with the GAR1 protein. [provided by RefSeq, Apr 2009] |
SNORA67 Genesmall nucleolar RNA, H/ACA box 67 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA60 Genesmall nucleolar RNA, H/ACA box 60 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA61 Genesmall nucleolar RNA, H/ACA box 61 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA62 Genesmall nucleolar RNA, H/ACA box 62 Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA63 Genesmall nucleolar RNA, H/ACA box 63 Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116@ Genesmall nucleolar RNA, C/D box 116 cluster |
SNAPC5P1 Genesmall nuclear RNA activating complex, polypeptide 5, 19kDa pseudogene 1 |
SNRPGP13 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 13 |
SNRPGP12 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 12 |
SNRPGP11 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 11 |
SNRPGP14 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 14 |
SNORD116-25 Genesmall nucleolar RNA, C/D box 116-25 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-27 Genesmall nucleolar RNA, C/D box 116-27 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-21 Genesmall nucleolar RNA, C/D box 116-21 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5E-8P GeneRNA, U5E small nuclear 8, pseudogene |
RNU7-51P GeneRNA, U7 small nuclear 51 pseudogene |
SNORD65 Genesmall nucleolar RNA, C/D box 65 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD64 Genesmall nucleolar RNA, C/D box 64 This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010] |
SNORD67 Genesmall nucleolar RNA, C/D box 67 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD66 Genesmall nucleolar RNA, C/D box 66 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD61 Genesmall nucleolar RNA, C/D box 61 Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in an intron of the RNA binding motif protein, X-linked gene (RBMX). [provided by RefSeq, Sep 2009] |
SNORD60 Genesmall nucleolar RNA, C/D box 60 Predicted to be involved in RNA processing. Predicted to act upstream of or within intracellular cholesterol transport. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD63 Genesmall nucleolar RNA, C/D box 63 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD69 Genesmall nucleolar RNA, C/D box 69 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD68 Genesmall nucleolar RNA, C/D box 68 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-15P GeneRNA, U6 small nuclear 15, pseudogene |
RNU2-4P GeneRNA, U2 small nuclear 4, pseudogene |
RNU1-15P GeneRNA, U1 small nuclear 15, pseudogene |
RNU5F-4P GeneRNA, U5F small nuclear 4, pseudogene |
RNU6ATAC3P GeneRNA, U6atac small nuclear 3, pseudogene |
SVIP Genesmall VCP/p97-interacting protein Endoplasmic reticulum-associated degradation (ERAD) is the pathway by which misfolded proteins in the endoplasmic reticulum are targeted to the proteasome for degradation. Multiple specialized proteins interact with one another during ERAD to complete this process. The protein encoded by this gene is an inhibitor of ERAD, functioning to disrupt the interaction of these protein components. This downregulation of ERAD may be needed to protect the cell from overactive protein degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016] |
SMIM22 Genesmall integral membrane protein 22 Involved in several processes, including lipid droplet formation; positive regulation of cell migration; and regulation of actin cytoskeleton organization. Predicted to be located in late endosome and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-72P GeneRNA, U7 small nuclear 72 pseudogene |
RNU6-56P GeneRNA, U6 small nuclear 56, pseudogene |
SNORD114-20 Genesmall nucleolar RNA, C/D box 114-20 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPGP8 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 8 |
SNORD115-21 Genesmall nucleolar RNA, C/D box 115-21 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-20 Genesmall nucleolar RNA, C/D box 115-20 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-23 Genesmall nucleolar RNA, C/D box 115-23 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-22 Genesmall nucleolar RNA, C/D box 115-22 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-25 Genesmall nucleolar RNA, C/D box 115-25 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-24 Genesmall nucleolar RNA, C/D box 115-24 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-27 Genesmall nucleolar RNA, C/D box 115-27 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-26 Genesmall nucleolar RNA, C/D box 115-26 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-29 Genesmall nucleolar RNA, C/D box 115-29 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-28 Genesmall nucleolar RNA, C/D box 115-28 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131448 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene |
RNU3P2 GeneRNA, U3 small nucleolar pseudogene 2 |
RNU3P3 GeneRNA, U3 small nucleolar pseudogene 3 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU3P1 GeneRNA, U3 small nucleolar pseudogene 1 |
RNU3P4 GeneRNA, U3 small nucleolar pseudogene 4 |
SNHG15 Genesmall nucleolar RNA host gene 15 This gene represents a snoRNA host gene that produces a short-lived long non-coding RNA. This non-coding RNA is upregulated in tumor cells and may contribute to cell proliferation by acting as a sponge for microRNAs. [provided by RefSeq, Dec 2017] |
SNHG14 Genesmall nucleolar RNA host gene 14 This gene is located within the Prader-Willi critical region and produces a long, spliced paternally-imprinted RNA that initiates within a common upstream promoter region shared by the SNRPN (small nuclear ribonucleoprotein polypeptide N) and SNURF genes. This transcript serves as a host RNA for the small nucleolar RNA, C/D box 115 and 116 clusters. This RNA extends in antisense into the region of the ubiquitin protein ligase E3A gene (UBE3A), and is thought to regulate imprinted expression of UBE3A in the brain. This transcript undergoes extensive alternative splicing, and may initiate and terminate at multiple locations within this genomic region. The full-length structure of all splice forms is not determined. [provided by RefSeq, Mar 2017] |
SNHG17 Genesmall nucleolar RNA host gene 17 |
SNHG16 Genesmall nucleolar RNA host gene 16 |
SNHG11 Genesmall nucleolar RNA host gene 11 This gene is a member of the non-protein-coding multiple snoRNA host gene family. Two snoRNAs are derived from the introns of this host gene. Although many alternative splice variants have been observed, the gene is thought to have no protein-coding potential. [provided by RefSeq, Jul 2008] |
SNHG12 Genesmall nucleolar RNA host gene 12 This gene produces a long RNA that is overexpressed in tumor cells. This RNA may promote tumorigenesis by acting as a sponge for microRNAs. [provided by RefSeq, Dec 2017] |
SNHG19 Genesmall nucleolar RNA host gene 19 |
SNHG18 Genesmall nucleolar RNA host gene 18 |
SNORA80E Genesmall nucleolar RNA, H/ACA box 80E Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA80B Genesmall nucleolar RNA, H/ACA box 80B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA80A Genesmall nucleolar RNA, H/ACA box 80A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU4-9P GeneRNA, U4 small nuclear 9, pseudogene |
RNU6-71P GeneRNA, U6 small nuclear 71, pseudogene |
SNORA45A Genesmall nucleolar RNA, H/ACA box 45A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-22P GeneRNA, U7 small nuclear 22 pseudogene |
SNRPB2 Genesmall nuclear ribonucleoprotein polypeptide B The protein encoded by this gene associates with stem loop IV of U2 small nuclear ribonucleoprotein (U2 snRNP) in the presence of snRNP-A'. The encoded protein may play a role in pre-mRNA splicing. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
ASH2LP1 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene 1 |
RNU7-59P GeneRNA, U7 small nuclear 59 pseudogene |
SNORD88A Genesmall nucleolar RNA, C/D box 88A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD88B Genesmall nucleolar RNA, C/D box 88B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD88C Genesmall nucleolar RNA, C/D box 88C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-26P GeneRNA, U6 small nuclear 26, pseudogene |
UTP11L GeneUTP11-like, U3 small nucleolar ribonucleoprotein (yeast) Enables RNA binding activity. Involved in nervous system development; positive regulation of apoptotic process; and ribosomal small subunit biogenesis. Located in cytoplasm; extracellular space; and nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-10P GeneRNA, U6 small nuclear 10, pseudogene |
SNORD114-1 Genesmall nucleolar RNA, C/D box 114-1 Small nucleolar RNAs (snoRNAs), like SNORD114-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD114-1 is 1 of 31 tandem SNORD114 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010] |
SNORD114-6 Genesmall nucleolar RNA, C/D box 114-6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-5 Genesmall nucleolar RNA, C/D box 114-5 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-4 Genesmall nucleolar RNA, C/D box 114-4 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ASH1L Geneash1 (absent, small, or homeotic)-like (Drosophila) This gene encodes a member of the trithorax group of transcriptional activators. The protein contains four AT hooks, a SET domain, a PHD-finger motif, and a bromodomain. It is localized to many small speckles in the nucleus, and also to cell-cell tight junctions. [provided by RefSeq, Jul 2008] |
LOC100422490 GeneUTP6, small subunit (SSU) processome component, homolog (yeast) pseudogene |
LOC100422497 GeneUTP18, small subunit (SSU) processome component, homolog (yeast) pseudogene |
RNU7-41P GeneRNA, U7 small nuclear 41 pseudogene |
SCARNA27 Genesmall Cajal body-specific RNA 27 |
SCARNA22 Genesmall Cajal body-specific RNA 22 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA23 Genesmall Cajal body-specific RNA 23 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA20 Genesmall Cajal body-specific RNA 20 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA21 Genesmall Cajal body-specific RNA 21 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6ATAC4P GeneRNA, U6atac small nuclear 4, pseudogene |
RNU1-3 GeneRNA, U1 small nuclear 3 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-2 GeneRNA, U1 small nuclear 2 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-31P GeneRNA, U6 small nuclear 31, pseudogene |
SNORD115-5 Genesmall nucleolar RNA, C/D box 115-5 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-2 Genesmall nucleolar RNA, C/D box 115-2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-3 Genesmall nucleolar RNA, C/D box 115-3 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-8 Genesmall nucleolar RNA, C/D box 115-8 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-9 Genesmall nucleolar RNA, C/D box 115-9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD101 Genesmall nucleolar RNA, C/D box 101 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD100 Genesmall nucleolar RNA, C/D box 100 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD102 Genesmall nucleolar RNA, C/D box 102 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD105 Genesmall nucleolar RNA, C/D box 105 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD104 Genesmall nucleolar RNA, C/D box 104 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD107 Genesmall nucleolar RNA, C/D box 107 Small nucleolar RNAs (snoRNAs) are small non-coding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in a cluster of genes including the SNURF-SNRPN gene, which serves as a host for multiple snoRNAs. [provided by RefSeq, Oct 2011] |
SNORD108 Genesmall nucleolar RNA, C/D box 108 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-60P GeneRNA, U7 small nuclear 60 pseudogene |
LOC441722 GeneU2 small nuclear RNA auxiliary factor 1-like 4 pseudogene |
SNORD23 Genesmall nucleolar RNA, C/D box 23 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-B2 Genesmall ILF3/NF90-associated RNA B2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-B1 Genesmall ILF3/NF90-associated RNA B1 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5B-3P GeneRNA, U5B small nuclear 3, pseudogene |
LOC100631374 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
SNRNP40 Genesmall nuclear ribonucleoprotein 40kDa (U5) This gene encodes a component of the U5 small nuclear ribonucleoprotein (snRNP) particle. The U5 snRNP is part of the spliceosome, a multiprotein complex that catalyzes the removal of introns from pre-messenger RNAs. [provided by RefSeq, Jul 2008] |
SNRNP48 Genesmall nuclear ribonucleoprotein 48kDa (U11/U12) Predicted to enable metal ion binding activity. Predicted to be involved in RNA splicing. Located in cytosol and nucleoplasm. Part of U12-type spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
CDC42SE2 GeneCDC42 small effector 2 Enables signaling adaptor activity. Involved in regulation of signal transduction. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CDC42SE1 GeneCDC42 small effector 1 Predicted to enable GTPase inhibitor activity. Predicted to be involved in signal transduction. Located in cell junction. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-22P GeneRNA, U1 small nuclear 22, pseudogene |
SCARNA5 Genesmall Cajal body-specific RNA 5 Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA4 Genesmall Cajal body-specific RNA 4 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMAGP Genesmall cell adhesion glycoprotein Located in cell junction; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RN7SKP8 GeneRNA, 7SK small nuclear pseudogene 8 |
RN7SKP9 GeneRNA, 7SK small nuclear pseudogene 9 |
RN7SKP6 GeneRNA, 7SK small nuclear pseudogene 6 |
RN7SKP7 GeneRNA, 7SK small nuclear pseudogene 7 |
RN7SKP4 GeneRNA, 7SK small nuclear pseudogene 4 |
RN7SKP5 GeneRNA, 7SK small nuclear pseudogene 5 |
RN7SKP2 GeneRNA, 7SK small nuclear pseudogene 2 |
RN7SKP3 GeneRNA, 7SK small nuclear pseudogene 3 |
SCARNA2 Genesmall Cajal body-specific RNA 2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG3 Genesmall nucleolar RNA host gene 3 Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM2 Genesmall integral membrane protein 2 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM1 Genesmall integral membrane protein 1 (Vel blood group) This gene encodes a small, conserved protein that participates in red blood cell formation. The encoded protein is localized to the cell membrane and is the antigen for the Vel blood group. Alternative splicing results in different transcript variants that encode the same protein. [provided by RefSeq, Dec 2013] |
SNHG9 Genesmall nucleolar RNA host gene 9 |
RNU7-80P GeneRNA, U7 small nuclear 80 pseudogene |
RNU7-11P GeneRNA, U7 small nuclear 11 pseudogene |
LOC643605 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene |
RNU7-35P GeneRNA, U7 small nuclear 35 pseudogene |
SNORD45C Genesmall nucleolar RNA, C/D box 45C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD45B Genesmall nucleolar RNA, C/D box 45B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-68P GeneRNA, U7 small nuclear 68 pseudogene |
SNORD18A Genesmall nucleolar RNA, C/D box 18A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD18C Genesmall nucleolar RNA, C/D box 18C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD18B Genesmall nucleolar RNA, C/D box 18B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA53 Genesmall nucleolar RNA, H/ACA box 53 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM10L1 Genesmall integral membrane protein 10 like 1 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA76C Genesmall nucleolar RNA, H/ACA box 76C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA76A Genesmall nucleolar RNA, H/ACA box 76A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-52P GeneRNA, U7 small nuclear 52 pseudogene |
RNU5A-4P GeneRNA, U5A small nuclear 4, pseudogene |
SNORD3D Genesmall nucleolar RNA, C/D box 3D Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD3@ Genesmall nucleolar RNA, C/D box 3 cluster |
SNORD3A Genesmall nucleolar RNA, C/D box 3A U3 RNA, an abundant small nucleolar RNA (snoRNA), is thought to play a role in the processing of ribosomal RNA precursors (Bernstein et al., 1983 [PubMed 6186397]).[supplied by OMIM, Jun 2009] |
SNORD37 Genesmall nucleolar RNA, C/D box 37 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD34 Genesmall nucleolar RNA, C/D box 34 Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD33 Genesmall nucleolar RNA, C/D box 33 Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD30 Genesmall nucleolar RNA, C/D box 30 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD31 Genesmall nucleolar RNA, C/D box 31 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-45P GeneRNA, U6 small nuclear 45, pseudogene |
RNU6-34P GeneRNA, U6 small nuclear 34, pseudogene |
LSM1P1 GeneLSM1, U6 small nuclear RNA associated pseudogene 1 |
LOC102724677 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
RNU6-55P GeneRNA, U6 small nuclear 55, pseudogene |
SNORA19 Genesmall nucleolar RNA, H/ACA box 19 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA18 Genesmall nucleolar RNA, H/ACA box 18 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA15 Genesmall nucleolar RNA, H/ACA box 15 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA17 Genesmall nucleolar RNA, H/ACA box 17 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA12 Genesmall nucleolar RNA, H/ACA box 12 Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA12, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
RNU5F-7P GeneRNA, U5F small nuclear 7, pseudogene Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-19P GeneRNA, U7 small nuclear 19 pseudogene |
RNU7-78P GeneRNA, U7 small nuclear 78 pseudogene |
RNU4ATAC GeneRNA, U4atac small nuclear (U12-dependent splicing) The small nuclear RNA (snRNA) encoded by this gene is part of the U12-dependent minor spliceosome complex. In addition to the encoded RNA, this ribonucleoprotein complex consists of U11, U12, U5, and U6atac snRNAs. The U12-dependent spliceosome acts on approximately 700 specific introns in the human genome. Defects in this gene are a cause of microcephalic osteodysplastic primordial dwarfism type 1 (MOPD). [provided by RefSeq, Jul 2011] |
RNU7-25P GeneRNA, U7 small nuclear 25 pseudogene |
RNU7-81P GeneRNA, U7 small nuclear 81 pseudogene |
SNAR-C3 Genesmall ILF3/NF90-associated RNA C3 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-23P GeneRNA, U6 small nuclear 23, pseudogene |
RNU7-10P GeneRNA, U7 small nuclear 10 pseudogene |
CTDSP1 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 1 This gene encodes a member of the small C-terminal domain phosphatase (SCP) family of nuclear phosphatases. These proteins play a role in transcriptional regulation through specific dephosphorylation of phosphoserine 5 within tandem heptapeptide repeats of the C-terminal domain of RNA polymerase II. The encoded protein plays a role in neuronal gene silencing in non-neuronal cells, and may also inhibit osteoblast differentiation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011] |
CTDSP2 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 Enables RNA polymerase II CTD heptapeptide repeat phosphatase activity. Involved in protein dephosphorylation. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CTDSPL GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like Predicted to enable RNA polymerase II CTD heptapeptide repeat phosphatase activity. Predicted to be involved in chromatin remodeling and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of G1/S transition of mitotic cell cycle and negative regulation of protein phosphorylation. Located in extracellular exosome. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-20P GeneRNA, U7 small nuclear 20 pseudogene |
SNORD116-10 Genesmall nucleolar RNA, C/D box 116-10 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-12 Genesmall nucleolar RNA, C/D box 116-12 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-6P GeneRNA, U7 small nuclear 6 pseudogene |
RNU7-77P GeneRNA, U7 small nuclear 77 pseudogene |
RN7SK GeneRNA, 7SK small nuclear Predicted to be involved in negative regulation of transcription elongation by RNA polymerase II. Part of 7SK snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
UTP18 GeneUTP18 small subunit (SSU) processome component homolog (yeast) Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in nuclear membrane; nucleolus; and nucleoplasm. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA36A Genesmall nucleolar RNA, H/ACA box 36A Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residues U105 and U1244 of 18S rRNA. [provided by RefSeq, Feb 2009] |
SNAR-A14 Genesmall ILF3/NF90-associated RNA A14 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A11 Genesmall ILF3/NF90-associated RNA A11 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A10 Genesmall ILF3/NF90-associated RNA A10 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD3C Genesmall nucleolar RNA, C/D box 3C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD105B Genesmall nucleolar RNA, C/D box 105B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5D-1 GeneRNA, U5D small nuclear 1 Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU4-6P GeneRNA, U4 small nuclear 6, pseudogene |
SNORA71D Genesmall nucleolar RNA, H/ACA box 71D Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100303749 GeneLSM3 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
SNAR-A3 Genesmall ILF3/NF90-associated RNA A3 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A2 Genesmall ILF3/NF90-associated RNA A2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A7 Genesmall ILF3/NF90-associated RNA A7 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A6 Genesmall ILF3/NF90-associated RNA A6 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A5 Genesmall ILF3/NF90-associated RNA A5 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A4 Genesmall ILF3/NF90-associated RNA A4 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA16A Genesmall nucleolar RNA, H/ACA box 16A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
CMSS1 Genecms1 ribosomal small subunit homolog (yeast) Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
SNRNP70 Genesmall nuclear ribonucleoprotein 70kDa (U1) Enables U1 snRNA binding activity. Involved in mRNA splicing, via spliceosome and regulation of RNA splicing. Located in nucleoplasm. Part of U1 snRNP and spliceosomal complex. Implicated in disease of mental health and systemic lupus erythematosus. Biomarker of Alzheimer's disease. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-49P GeneRNA, U7 small nuclear 49 pseudogene |
RNU5E-1 GeneRNA, U5E small nuclear 1 Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD70 Genesmall nucleolar RNA, C/D box 70 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-21P GeneRNA, U1 small nuclear 21, pseudogene |
LOC100421863 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
RNU7-44P GeneRNA, U7 small nuclear 44 pseudogene |
SNORD116-5 Genesmall nucleolar RNA, C/D box 116-5 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-7 Genesmall nucleolar RNA, C/D box 116-7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-87P GeneRNA, U7 small nuclear 87 pseudogene |
RNU7-12P GeneRNA, U7 small nuclear 12 pseudogene |
RNU6ATAC GeneRNA, U6atac small nuclear (U12-dependent splicing) Predicted to enable U4atac snRNA binding activity and pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition and spliceosomal tri-snRNP complex assembly. Predicted to be part of U6atac snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD62B Genesmall nucleolar RNA, C/D box 62B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM12P1 Genesmall integral membrane protein 12 pseudogene 1 |
SPTSSA Geneserine palmitoyltransferase, small subunit A Serine palmitoyltransferase (SPT; EC 2.3.1.50) catalyzes the first committed and rate-limiting step in sphingolipid biosynthesis. SSSPTA is a small SPT subunit that stimulates SPT activity and confers acyl-CoA preference to the SPT catalytic heterodimer of SPTLC1 (MIM 605712) and either SPTLC2 (MIM 605713) or SPTLC3 (MIM 611120) (Han et al., 2009 [PubMed 19416851]).[supplied by OMIM, Nov 2010] |
SPTSSB Geneserine palmitoyltransferase, small subunit B Serine palmitoyltransferase (SPT; EC 2.3.1.50) catalyzes the first committed and rate-limiting step in sphingolipid biosynthesis. SSSPTB is a small SPT subunit that stimulates SPT activity and confers acyl-CoA preference to the SPT catalytic heterodimer of SPTLC1 (MIM 605712) and either SPTLC2 (MIM 605713) or SPTLC3 (MIM 611120) (Han et al., 2009 [PubMed 19416851]).[supplied by OMIM, Nov 2010] |
SNORA11 Genesmall nucleolar RNA, H/ACA box 11 Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
SNORA10 Genesmall nucleolar RNA, H/ACA box 10 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA13 Genesmall nucleolar RNA, H/ACA box 13 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102724822 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
UTP6 GeneUTP6, small subunit (SSU) processome component, homolog (yeast) Predicted to enable snoRNA binding activity. Involved in ribosomal small subunit biogenesis. Located in chromosome and nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD126 Genesmall nucleolar RNA, C/D box 126 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD125 Genesmall nucleolar RNA, C/D box 125 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105377886 Genesmall EDRK-rich factor 2 pseudogene |
RSG1 GeneREM2 and RAB-like small GTPase 1 Predicted to enable GTP binding activity. Predicted to be involved in cilium assembly; protein localization; and regulation of vesicle-mediated transport. Predicted to act upstream of or within several processes, including axoneme assembly; endocardial cushion fusion; and regulation of smoothened signaling pathway. Located in centriole; ciliary basal body; and ciliary transition zone. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5B-6P GeneRNA, U5B small nuclear 6, pseudogene |
SNORA73A Genesmall nucleolar RNA, H/ACA box 73A Predicted to be involved in RNA processing. Located in nucleus. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA73B Genesmall nucleolar RNA, H/ACA box 73B |
RNU7-57P GeneRNA, U7 small nuclear 57 pseudogene |
RNU6-52P GeneRNA, U6 small nuclear 52, pseudogene |
RAC2 Generas-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) This gene encodes a member of the Ras superfamily of small guanosine triphosphate (GTP)-metabolizing proteins. The encoded protein localizes to the plasma membrane, where it regulates diverse processes, such as secretion, phagocytosis, and cell polarization. Activity of this protein is also involved in the generation of reactive oxygen species. Mutations in this gene are associated with neutrophil immunodeficiency syndrome. There is a pseudogene for this gene on chromosome 6. [provided by RefSeq, Jul 2013] |
RAC3 Generas-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3) The protein encoded by this gene is a GTPase which belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015] |
RAC1 Generas-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1) The protein encoded by this gene is a GTPase which belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009] |
SNAR-A12 Genesmall ILF3/NF90-associated RNA A12 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-88P GeneRNA, U7 small nuclear 88 pseudogene |
RN7SKP10 GeneRNA, 7SK small nuclear pseudogene 10 |
BA395L14.12 Genesmall nuclear ribonucleoprotein polypeptide A' pseudogene |
RNU6-58P GeneRNA, U6 small nuclear 58, pseudogene |
RNU5E-9P GeneRNA, U5E small nuclear 9, pseudogene |
SNORD113-1 Genesmall nucleolar RNA, C/D box 113-1 Small nucleolar RNAs (snoRNAs), like SNORD113-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD113-1 is 1 of 9 tandem SNORD113 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010] |
SNORD113-3 Genesmall nucleolar RNA, C/D box 113-3 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-42 Genesmall nucleolar RNA, C/D box 115-42 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-40 Genesmall nucleolar RNA, C/D box 115-40 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-46 Genesmall nucleolar RNA, C/D box 115-46 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-45 Genesmall nucleolar RNA, C/D box 115-45 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-44 Genesmall nucleolar RNA, C/D box 115-44 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-48 Genesmall nucleolar RNA, C/D box 115-48 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD42B Genesmall nucleolar RNA, C/D box 42B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD42A Genesmall nucleolar RNA, C/D box 42A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA46 Genesmall nucleolar RNA, H/ACA box 46 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA47 Genesmall nucleolar RNA, H/ACA box 47 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA44 Genesmall nucleolar RNA, H/ACA box 44 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA43 Genesmall nucleolar RNA, H/ACA box 43 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA40 Genesmall nucleolar RNA, H/ACA box 40 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA41 Genesmall nucleolar RNA, H/ACA box 41 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA48 Genesmall nucleolar RNA, H/ACA box 48 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA49 Genesmall nucleolar RNA, H/ACA box 49 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114@ Genesmall nucleolar RNA, C/D box 114 cluster |
RNU7-73P GeneRNA, U7 small nuclear 73 pseudogene |
RNU6V GeneRNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence |
SNORD58A Genesmall nucleolar RNA, C/D box 58A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD58C Genesmall nucleolar RNA, C/D box 58C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD58B Genesmall nucleolar RNA, C/D box 58B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD89 Genesmall nucleolar RNA, C/D box 89 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD87 Genesmall nucleolar RNA, C/D box 87 Small nucleolar RNAs (snoRNAs) of the C/D class, such as SNORD87, are involved in 2-prime-methylation of preribosomal RNA precursors (Gogolevskaya et al., 2002 [PubMed 12119114]).[supplied by OMIM, Aug 2008] |
SNORD86 Genesmall nucleolar RNA, C/D box 86 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD84 Genesmall nucleolar RNA, C/D box 84 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD82 Genesmall nucleolar RNA, C/D box 82 The majority of small nucleolar RNAs (snoRNAs) function as guide RNAs in the nucleotide modification of preribosomal RNA (pre-rRNA). C/D box snoRNAs, like SNORD82, are involved in site-specific 2-prime-O-ribose methylation of pre-rRNA (Rebane and Metspalu, 1999 [PubMed 10524220]).[supplied by OMIM, Mar 2008] |
SNORD81 Genesmall nucleolar RNA, C/D box 81 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD80 Genesmall nucleolar RNA, C/D box 80 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5E-5P GeneRNA, U5E small nuclear 5, pseudogene |
SGTB Genesmall glutamine-rich tetratricopeptide repeat (TPR)-containing, beta Predicted to enable molecular adaptor activity. Predicted to be involved in post-translational protein targeting to endoplasmic reticulum membrane. Predicted to be part of TRC complex. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SGTA Genesmall glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha This gene encodes a protein which is capable of interacting with the major nonstructural protein of parvovirus H-1 and 70-kDa heat shock cognate protein; however, its function is not known. Since this transcript is expressed ubiquitously in various tissues, this protein may serve a housekeeping function. [provided by RefSeq, Jul 2008] |
SNRPGP10 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 10 |
SNRPGP15 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 15 Predicted to contribute to RNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleus. Predicted to be part of SMN-Sm protein complex and nucleus. Predicted to be active in P granule. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-17P GeneRNA, U1 small nuclear 17, pseudogene |
RNU2-2P GeneRNA, U2 small nuclear 2, pseudogene |
RNU5F-2P GeneRNA, U5F small nuclear 2, pseudogene |
RNU7-74P GeneRNA, U7 small nuclear 74 pseudogene |
RNU6-50P GeneRNA, U6 small nuclear 50, pseudogene |
SMIM3 Genesmall integral membrane protein 3 Enables identical protein binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM7 Genesmall integral membrane protein 7 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM6 Genesmall integral membrane protein 6 Predicted to act upstream of or within negative regulation of ATPase-coupled calcium transmembrane transporter activity. Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM5 Genesmall integral membrane protein 5 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM4 Genesmall integral membrane protein 4 Enables mitochondrial ribosome binding activity. Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrion. Is active in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM9 Genesmall integral membrane protein 9 Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM8 Genesmall integral membrane protein 8 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-36 Genesmall nucleolar RNA, C/D box 115-36 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-37 Genesmall nucleolar RNA, C/D box 115-37 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-33 Genesmall nucleolar RNA, C/D box 115-33 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-30 Genesmall nucleolar RNA, C/D box 115-30 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-31 Genesmall nucleolar RNA, C/D box 115-31 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5E-2P GeneRNA, U5E small nuclear 2, pseudogene |
SNORD50A Genesmall nucleolar RNA, C/D box 50A SNORD50A belongs to the C/D box class of small nucleolar RNAs (snoRNAs), which are thought to function as guide RNAs in the site-specific ribose methylation of preribosomal RNA (Kiss-Laszlo et al., 1996 [PubMed 8674114]).[supplied by OMIM, Nov 2009] |
SNORD50B Genesmall nucleolar RNA, C/D box 50B SNORD50B is a C/D box-type small nucleolar RNA (snoRNA) that is predicted to function as a guide RNA in 2-prime O-methylation of 28S ribosomal RNA (Tanaka et al., 2000 [PubMed 10792466]).[supplied by OMIM, Feb 2010] |
SNORA16B Genesmall nucleolar RNA, H/ACA box 16B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRNP25 Genesmall nuclear ribonucleoprotein 25kDa (U11/U12) Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes and removes U12-type introns, which are rare and have distinct splice consensus signals. The U12-type spliceosome consists of several small nuclear RNAs and associated proteins. This gene encodes a 25K protein that is a component of the U12-type spliceosome. [provided by RefSeq, Apr 2010] |
SNRNP27 Genesmall nuclear ribonucleoprotein 27kDa (U4/U6.U5) This gene encodes a serine/arginine-rich (SR) protein. SR proteins play important roles in pre-mRNA splicing by facilitating the recognition and selection of splice sites. The encoded protein associates with the 25S U4/U6.U5 tri-snRNP, a major component of the U2-type spiceosome. The expression of this gene may be altered in cells infected with the human T-cell lymphotropic virus type 1 (HTLV-1) retrovirus. A pseudogene of this gene is located on the long arm of chromosome 5. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011] |
RNU6-82P GeneRNA, U6 small nuclear 82, pseudogene |
RNU1-24P GeneRNA, U1 small nuclear 24, pseudogene |
RNU7-43P GeneRNA, U7 small nuclear 43 pseudogene |
SNORA11E Genesmall nucleolar RNA, H/ACA box 11E Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR1A Genesmall proline-rich protein 1A A structural constituent of skin epidermis. Involved in keratinocyte differentiation and peptide cross-linking. Located in cornified envelope. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR1B Genesmall proline-rich protein 1B The protein encoded by this gene is an envelope protein of keratinocytes. The encoded protein is crosslinked to membrane proteins by transglutaminase, forming an insoluble layer under the plasma membrane. This protein is proline-rich and contains several tandem amino acid repeats. [provided by RefSeq, Nov 2015] |
SERF1A Genesmall EDRK-rich factor 1A (telomeric) This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The duplication region includes both a telomeric and a centromeric copy of this gene. Deletions of this gene, the telomeric copy, often accompany deletions of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients, and so it is thought that this gene may be a modifier of the SMA phenotype. The function of this protein is not known; however, it bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. [provided by RefSeq, Jul 2008] |
SERF1B Genesmall EDRK-rich factor 1B (centromeric) This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is the centromeric copy which is identical to the telomeric copy. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. The gene encodes a protein of unknown function which bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. [provided by RefSeq, Jul 2008] |
RNU7-66P GeneRNA, U7 small nuclear 66 pseudogene |
RNU6-19P GeneRNA, U6 small nuclear 19, pseudogene |
LOC100736412 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
SNORA69 Genesmall nucleolar RNA, H/ACA box 69 This gene encodes a member of the family of box ACA small nucleolar RNAs, characterized by a consensus ACA motif positioned 3 nucleotides from the 3' end of the RNAs and a double-hairpin structure. The box ACA small nucleolar RNAs may play a role in rRNA maturation. This gene is co-transcribed with the ribosomal protein L39 gene. [provided by RefSeq, Oct 2009] |
RNU4-3P GeneRNA, U4 small nuclear 3, pseudogene |
RNU6-16P GeneRNA, U6 small nuclear 16, pseudogene |
IMP3 GeneIMP3, U3 small nucleolar ribonucleoprotein This gene encodes the human homolog of the yeast Imp3 protein. The protein localizes to the nucleoli and interacts with the U3 snoRNP complex. The protein contains an S4 domain. [provided by RefSeq, Jul 2008] |
IMP4 GeneIMP4, U3 small nucleolar ribonucleoprotein The protein encoded by this gene, along with IMP3 and MPP10, is part of the 60-80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) complex. This complex is necessary for the early cleavage steps of pre-18S ribosomal RNA processing. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016] |
SNORA70B Genesmall nucleolar RNA, H/ACA box 70B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA70D Genesmall nucleolar RNA, H/ACA box 70D Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA70E Genesmall nucleolar RNA, H/ACA box 70E Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA70F Genesmall nucleolar RNA, H/ACA box 70F Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA70G Genesmall nucleolar RNA, H/ACA box 70G Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-9P GeneRNA, U7 small nuclear 9 pseudogene |
RNU7-82P GeneRNA, U7 small nuclear 82 pseudogene |
RNU7-17P GeneRNA, U7 small nuclear 17 pseudogene |
RNU105B GeneRNA, U105B small nucleolar Predicted to be involved in RNA processing. Predicted to act upstream of or within response to bacterium. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC401703 GeneU2 small nuclear RNA auxiliary factor 1-like 4 pseudogene |
RNU6-6P GeneRNA, U6 small nuclear 6, pseudogene Predicted to be located in nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM10L2B Genesmall integral membrane protein 10 like 2B |
RNVU1-20 GeneRNA, variant U1 small nuclear 20 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100736411 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
RNU4-1 GeneRNA, U4 small nuclear 1 Predicted to enable U6 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4 snRNP and U4/U6 x U5 tri-snRNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-37P GeneRNA, U7 small nuclear 37 pseudogene |
SNORA7B Genesmall nucleolar RNA, H/ACA box 7B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA7A Genesmall nucleolar RNA, H/ACA box 7A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA79 Genesmall nucleolar RNA, H/ACA box 79 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA78 Genesmall nucleolar RNA, H/ACA box 78 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA77 Genesmall nucleolar RNA, H/ACA box 77 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA75 Genesmall nucleolar RNA, H/ACA box 75 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA72 Genesmall nucleolar RNA, H/ACA box 72 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA70 Genesmall nucleolar RNA, H/ACA box 70 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD49B Genesmall nucleolar RNA, C/D box 49B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130001 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
SNORD116-30 Genesmall nucleolar RNA, C/D box 116-30 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-18P GeneRNA, U7 small nuclear 18 pseudogene |
RNU86 GeneRNA, U86 small nucleolar Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like U86, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like U86, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008] |
HSPB11 Geneheat shock protein family B (small), member 11 Predicted to enable metal ion binding activity. Predicted to be involved in kidney development; smoothened signaling pathway; and spermatogenesis. Predicted to act upstream of or within several processes, including left/right axis specification; lung development; and skeletal system development. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD51 Genesmall nucleolar RNA, C/D box 51 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD52 Genesmall nucleolar RNA, C/D box 52 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD53 Genesmall nucleolar RNA, C/D box 53 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD54 Genesmall nucleolar RNA, C/D box 54 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD55 Genesmall nucleolar RNA, C/D box 55 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD57 Genesmall nucleolar RNA, C/D box 57 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-24 Genesmall nucleolar RNA, C/D box 116-24 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-26 Genesmall nucleolar RNA, C/D box 116-26 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-22 Genesmall nucleolar RNA, C/D box 116-22 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-23 Genesmall nucleolar RNA, C/D box 116-23 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
KRR1P1 GeneKRR1, small subunit (SSU) processome component, homolog (yeast) pseudogene 1 |
RNU1-14P GeneRNA, U1 small nuclear 14, pseudogene |
SNORD116-28 Genesmall nucleolar RNA, C/D box 116-28 |
LOC150417 Genesmall nuclear ribonucleoprotein polypeptide A' pseudogene |
RNU6ATAC2P GeneRNA, U6atac small nuclear 2, pseudogene |
RNU5F-5P GeneRNA, U5F small nuclear 5, pseudogene |
SNRPA1 Genesmall nuclear ribonucleoprotein polypeptide A' Enables RNA binding activity. Involved in mRNA splicing, via spliceosome and spermatogenesis. Located in nuclear speck. Part of U2-type catalytic step 2 spliceosome and U2-type precatalytic spliceosome. Implicated in connective tissue disease. [provided by Alliance of Genome Resources, Mar 2025] |
UTP15 GeneUTP15, U3 small nucleolar ribonucleoprotein, homolog (S. cerevisiae) Enables RNA binding activity. Involved in positive regulation of rRNA processing; positive regulation of transcription by RNA polymerase I; and ribosomal small subunit biogenesis. Located in endoplasmic reticulum and fibrillar center. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA9L Genesmall Cajal body-specific RNA 9-like Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-71P GeneRNA, U7 small nuclear 71 pseudogene |
SNORA36B Genesmall nucleolar RNA, H/ACA box 36B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA36C Genesmall nucleolar RNA, H/ACA box 36C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-3 GeneRNA, variant U1 small nuclear 3 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-68P GeneRNA, U6 small nuclear 68, pseudogene |
RNU6-57P GeneRNA, U6 small nuclear 57, pseudogene |
SNORD115-18 Genesmall nucleolar RNA, C/D box 115-18 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-19 Genesmall nucleolar RNA, C/D box 115-19 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-15 Genesmall nucleolar RNA, C/D box 115-15 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-11 Genesmall nucleolar RNA, C/D box 115-11 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-12 Genesmall nucleolar RNA, C/D box 115-12 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-13 Genesmall nucleolar RNA, C/D box 115-13 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-14 Genesmall nucleolar RNA, C/D box 114-14 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
CAPNS1 Genecalpain, small subunit 1 This gene is a member of the calpain small subunit family. Calpains are calcium-dependent cysteine proteinases that are widely distributed in mammalian cells. Calpains operate as heterodimers, comprising a specific large catalytic subunit (calpain 1 subunit in Calpain I, and calpain 2 subunit in Calpain II), and a common small regulatory subunit encoded by this gene. This encoded protein is essential for the stability and function of both calpain heterodimers, whose proteolytic activities influence various cellular functions including apoptosis, proliferation, migration, adhesion, and autophagy. Calpains have been implicated in neurodegenerative processes, such as myotonic dystrophy. A pseudogene of this gene has been defined on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014] |
CAPNS2 Genecalpain, small subunit 2 Enables calcium-dependent cysteine-type endopeptidase activity. Predicted to be located in cytosol and plasma membrane. Predicted to be part of calpain complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD73B Genesmall nucleolar RNA, C/D box U73B (pseudogene) Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD73A Genesmall nucleolar RNA, C/D box 73A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-I Genesmall ILF3/NF90-associated RNA I |
LSM7 GeneLSM7 homolog, U6 small nuclear RNA associated (S. cerevisiae) Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004] |
LSM1 GeneLSM1, U6 small nuclear RNA associated This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Increased expression of this gene may play a role in cellular transformation and the progression of several malignancies including lung cancer, mesothelioma and breast cancer. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Nov 2011] |
LSM2 GeneLSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011] |
RNU6-72P GeneRNA, U6 small nuclear 72, pseudogene |
RNU5E-7P GeneRNA, U5E small nuclear 7, pseudogene |
RNU12 GeneRNA, U12 small nuclear Predicted to enable pre-mRNA branch point binding activity. Predicted to be involved in negative regulation of neuron apoptotic process. Predicted to act upstream of or within RNA splicing. Predicted to be part of U12 snRNP. Implicated in autosomal recessive spinocerebellar ataxia 33. [provided by Alliance of Genome Resources, Mar 2025] |
RNU11 GeneRNA, U11 small nuclear Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to act upstream of or within RNA splicing. Predicted to be part of U11 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU4-8P GeneRNA, U4 small nuclear 8, pseudogene |
RNU7-58P GeneRNA, U7 small nuclear 58 pseudogene |
RNU5A-7P GeneRNA, U5A small nuclear 7, pseudogene |
RNU7-23P GeneRNA, U7 small nuclear 23 pseudogene |
SNORD109A Genesmall nucleolar RNA, C/D box 109A This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010] |
SNORD109B Genesmall nucleolar RNA, C/D box 109B This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010] |
SNORA70C Genesmall nucleolar RNA, H/ACA box 70C This gene produces a small nucleolar RNA (snoRNA) that plays a role in post-transcriptional modification. This snoRNA is a type-3 retrotransposed snoRNA, where the ribosomal protein L10 gene on chromosome X is its parental gene, and this, together with part of the parental gene, was subsequently mobilized into an intron of the astrotactin 2 host gene on chromosome 9. This snoRNA contains a H/ACA box, which serves as a guide for the pseudouridylation of selected bases of ribosomal RNA by forming short duplexes with the 18S rRNA U1692, the target for this snoRNA. This gene is specific to human, chimp and orangutan, and is not found in the genomes of rhesus or marmoset. [provided by RefSeq, Jun 2010] |
SNRPEP9 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 9 |
SNRPEP8 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 8 |
SNRPEP5 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 5 |
SNRPEP4 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 4 |
SNRPEP7 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 7 |
SNRPEP6 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 6 |
SNRPEP1 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 1 |
SNRPEP3 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 3 |
SNRPEP2 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 2 |
SNORA51 Genesmall nucleolar RNA, H/ACA box 51 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA11D Genesmall nucleolar RNA, H/ACA box 11D Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPCP1 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 1 |
SCARNA13 Genesmall Cajal body-specific RNA 13 Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA12 Genesmall Cajal body-specific RNA 12 This gene produces a small nuclear RNA that localizes specifically to Cajal bodies, which are conserved subnuclear organelles that are present in the nucleoplasm. This RNA is processed from an intron of the prohibitin 2 host gene. It includes both an H/ACA box and a C/D box, and is thought to guide the pseudouridylation of residue U46 in the U5 small nuclear RNA. [provided by RefSeq, Jun 2010] |
SCARNA11 Genesmall Cajal body-specific RNA 11 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA10 Genesmall Cajal body-specific RNA 10 Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA17 Genesmall Cajal body-specific RNA 17 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA16 Genesmall Cajal body-specific RNA 16 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA15 Genesmall Cajal body-specific RNA 15 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA14 Genesmall Cajal body-specific RNA 14 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA18 Genesmall Cajal body-specific RNA 18 Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
SMAP1 Genesmall ArfGAP 1 The protein encoded by this gene is similar to the mouse stromal membrane-associated protein-1. This similarity suggests that this human gene product is also a type II membrane glycoprotein involved in the erythropoietic stimulatory activity of stromal cells. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
SMAP2 Genesmall ArfGAP2 Predicted to enable GTPase activator activity. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-89P GeneRNA, U7 small nuclear 89 pseudogene |
LOC101929087 Genesmall ubiquitin-related modifier 2-like |
SNORA45B Genesmall nucleolar RNA, H/ACA box 45B Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA45, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
SNORA21 Genesmall nucleolar RNA, H/ACA box 21 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA24 Genesmall nucleolar RNA, H/ACA box 24 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA28 Genesmall nucleolar RNA, H/ACA box 28 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA29 Genesmall nucleolar RNA, H/ACA box 29 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD118 Genesmall nucleolar RNA, C/D box 118 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD119 Genesmall nucleolar RNA, C/D box 119 |
SNORD117 Genesmall nucleolar RNA, C/D box 117 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD112 Genesmall nucleolar RNA, C/D box 112 Small nucleolar RNAs (snoRNAs), like SNORD112, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010] |
SNORD110 Genesmall nucleolar RNA, C/D box 110 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD111 Genesmall nucleolar RNA, C/D box 111 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-61P GeneRNA, U7 small nuclear 61 pseudogene |
SNORD11B Genesmall nucleolar RNA, C/D box 11B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-63P GeneRNA, U7 small nuclear 63 pseudogene |
SNRPGP2 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 2 |
SNAR-C5 Genesmall ILF3/NF90-associated RNA C5 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-C4 Genesmall ILF3/NF90-associated RNA C4 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-C1 Genesmall ILF3/NF90-associated RNA C1 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-C2 Genesmall ILF3/NF90-associated RNA C2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU12-2P GeneRNA, U12 small nuclear 2, pseudogene |
SCARNA9 Genesmall Cajal body-specific RNA 9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA8 Genesmall Cajal body-specific RNA 8 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA7 Genesmall Cajal body-specific RNA 7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA3 Genesmall Cajal body-specific RNA 3 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA1 Genesmall Cajal body-specific RNA 1 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPEP10 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 10 |
RNU7-46P GeneRNA, U7 small nuclear 46 pseudogene |
SNORD36A Genesmall nucleolar RNA, C/D box 36A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD36C Genesmall nucleolar RNA, C/D box 36C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD36B Genesmall nucleolar RNA, C/D box 36B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5A-1 GeneRNA, U5A small nuclear 1 Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA38B Genesmall nucleolar RNA, H/ACA box 38B Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-35P GeneRNA, U6 small nuclear 35, pseudogene |
SNRPD2P2 Genesmall nuclear ribonucleoprotein D2 pseudogene 2 |
SNRPD2P1 Genesmall nuclear ribonucleoprotein D2 pseudogene 1 |
SNORD116-9 Genesmall nucleolar RNA, C/D box 116-9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-8 Genesmall nucleolar RNA, C/D box 116-8 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-4 Genesmall nucleolar RNA, C/D box 116-4 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-1 Genesmall nucleolar RNA, C/D box 116-1 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-3 Genesmall nucleolar RNA, C/D box 116-3 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-2 Genesmall nucleolar RNA, C/D box 116-2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-40P GeneRNA, U7 small nuclear 40 pseudogene |
RNU7-69P GeneRNA, U7 small nuclear 69 pseudogene |
RNU7-34P GeneRNA, U7 small nuclear 34 pseudogene |
SNORD19B Genesmall nucleolar RNA, C/D box 19B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5B-4P GeneRNA, U5B small nuclear 4, pseudogene |
RNU7-55P GeneRNA, U7 small nuclear 55 pseudogene |
RNU5A-3P GeneRNA, U5A small nuclear 3, pseudogene |
SNORD21 Genesmall nucleolar RNA, C/D box 21 This gene encodes a small nucleolar RNA (snoRNA) that may be involved in biogenesis of the large (28S) ribosomal subunit. This gene is found within an intron of the RPL5 gene. [provided by RefSeq, Mar 2009] |
SNORD20 Genesmall nucleolar RNA, C/D box 20 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD22 Genesmall nucleolar RNA, C/D box 22 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD25 Genesmall nucleolar RNA, C/D box 25 |
SNORD24 Genesmall nucleolar RNA, C/D box 24 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD27 Genesmall nucleolar RNA, C/D box 27 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD26 Genesmall nucleolar RNA, C/D box 26 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD29 Genesmall nucleolar RNA, C/D box 29 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD28 Genesmall nucleolar RNA, C/D box 28 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU105C GeneRNA, U105C small nucleolar Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100422088 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
SNAR-A9 Genesmall ILF3/NF90-associated RNA A9 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-26P GeneRNA, U7 small nuclear 26 pseudogene |
SNAR-A1 Genesmall ILF3/NF90-associated RNA A1 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPN Genesmall nuclear ribonucleoprotein polypeptide N This gene is located within the Prader-Willi Syndrome critical region on chromosome 15 and is imprinted and expressed from the paternal allele. It encodes a component of the small nuclear ribonucleoprotein complex, which functions in pre-mRNA processing and may contribute to tissue-specific alternative splicing. Alternative promoter use and alternative splicing result in a multitude of transcript variants encoding the same protein. Transcript variants that initiate at the CpG island-associated imprinting center may be bicistronic and also encode the SNRPN upstream reading frame protein (SNURF) from an upstream open reading frame. In addition, long spliced transcripts for small nucleolar RNA host gene 14 (SNHG14) may originate from the promoters at this locus and share exons with this gene. Alterations in this region are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017] |
SNRPB Genesmall nuclear ribonucleoprotein polypeptides B and B1 The protein encoded by this gene is one of several nuclear proteins that are found in common among U1, U2, U4/U6, and U5 small ribonucleoprotein particles (snRNPs). These snRNPs are involved in pre-mRNA splicing, and the encoded protein may also play a role in pre-mRNA splicing or snRNP structure. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding different isoforms (B and B') have been found for this gene. [provided by RefSeq, Jul 2008] |
SNRPC Genesmall nuclear ribonucleoprotein polypeptide C This gene encodes one of the specific protein components of the U1 small nuclear ribonucleoprotein (snRNP) particle required for the formation of the spliceosome. The encoded protein participates in the processing of nuclear precursor messenger RNA splicing. snRNP particles are attacked by autoantibodies frequently produced by patients with connective tissue diseases. The genome contains several pseudogenes of this functional gene. Alternative splicing results in a non-coding transcript variant.[provided by RefSeq, Oct 2009] |
SNRPA Genesmall nuclear ribonucleoprotein polypeptide A The protein encoded by this gene associates with stem loop II of the U1 small nuclear ribonucleoprotein, which binds the 5' splice site of precursor mRNAs and is required for splicing. The encoded protein autoregulates itself by polyadenylation inhibition of its own pre-mRNA via dimerization and has been implicated in the coupling of splicing and polyadenylation. [provided by RefSeq, Oct 2010] |
SNRPF Genesmall nuclear ribonucleoprotein polypeptide F Enables RNA binding activity. Involved in spliceosomal snRNP assembly. Located in cytosol and nucleus. Part of several cellular components, including methylosome; nucleus; and pICln-Sm protein complex. Biomarker of nasopharynx carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPG Genesmall nuclear ribonucleoprotein polypeptide G The protein encoded by this gene is a component of the U1, U2, U4, and U5 small nuclear ribonucleoprotein complexes, precursors of the spliceosome. The encoded protein may also be a part of the U7 small nuclear ribonucleoprotein complex, which participates in the processing of the 3' end of histone transcripts. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
SNRPE Genesmall nuclear ribonucleoprotein polypeptide E The protein encoded by this gene is a core component of U small nuclear ribonucleoproteins, which are key components of the pre-mRNA processing spliceosome. The encoded protein plays a role in the 3' end processing of histone transcripts. This protein is one of the targets in the autoimmune disease systemic lupus erythematosus, and mutations in this gene have been associated with hypotrichosis. Several pseudogenes of this gene have been identified. [provided by RefSeq, Jun 2016] |
CAPNS1P1 Genecalpain, small subunit 1 pseudogene 1 |
RNVU1-8 GeneRNA, variant U1 small nuclear 8 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-4 GeneRNA, variant U1 small nuclear 4 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-6 GeneRNA, variant U1 small nuclear 6 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be located in nucleus. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-7 GeneRNA, variant U1 small nuclear 7 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNVU1-1 GeneRNA, variant U1 small nuclear 1 |
SNORA20 Genesmall nucleolar RNA, H/ACA box 20 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA22 Genesmall nucleolar RNA, H/ACA box 22 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA23 Genesmall nucleolar RNA, H/ACA box 23 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA25 Genesmall nucleolar RNA, H/ACA box 25 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA26 Genesmall nucleolar RNA, H/ACA box 26 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA27 Genesmall nucleolar RNA, H/ACA box 27 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA2A Genesmall nucleolar RNA, H/ACA box 2A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA2B Genesmall nucleolar RNA, H/ACA box 2B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SERF1AP1 Genesmall EDRK-rich factor 1A (telomeric) pseudogene 1 |
U2AF1 GeneU2 small nuclear RNA auxiliary factor 1 This gene belongs to the splicing factor SR family of genes. U2 auxiliary factor, comprising a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the small subunit which plays a critical role in both constitutive and enhancer-dependent RNA splicing by directly mediating interactions between the large subunit and proteins bound to the enhancers. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
U2AF2 GeneU2 small nuclear RNA auxiliary factor 2 U2 auxiliary factor (U2AF), comprised of a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the U2AF large subunit which contains a sequence-specific RNA-binding region with 3 RNA recognition motifs and an Arg/Ser-rich domain necessary for splicing. The large subunit binds to the polypyrimidine tract of introns early during spliceosome assembly. Multiple transcript variants have been detected for this gene, but the full-length natures of only two have been determined to date. [provided by RefSeq, Jul 2008] |
RNU6-75P GeneRNA, U6 small nuclear 75, pseudogene |
SNORD56B Genesmall nucleolar RNA, C/D box 56B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5E-4P GeneRNA, U5E small nuclear 4, pseudogene |
SNRPCP19 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 19 |
SNRPCP18 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 18 |
SNRPCP15 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 15 |
SNRPCP14 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 14 |
SNRPCP12 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 12 |
SNRPCP11 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 11 |
SNORD116-20 Genesmall nucleolar RNA, C/D box 116-20 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-29 Genesmall nucleolar RNA, C/D box 116-29 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-11P GeneRNA, U1 small nuclear 11, pseudogene |
RNU7-7P GeneRNA, U7 small nuclear 7 pseudogene |
LOC100130842 Genesmall integral membrane protein 7 pseudogene |
RNU6-81P GeneRNA, U6 small nuclear 81, pseudogene |
RNU7-76P GeneRNA, U7 small nuclear 76 pseudogene |
UTP23 GeneUTP23, small subunit (SSU) processome component, homolog (yeast) Enables mRNA 3'-UTR binding activity and mRNA 5'-UTR binding activity. Predicted to be involved in rRNA processing. Predicted to act upstream of or within endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Predicted to be located in nucleus. Predicted to be part of small-subunit processome. Predicted to be active in nucleolus. Implicated in colorectal adenocarcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
UTP20 GeneUTP20, small subunit (SSU) processome component, homolog (yeast) UTP20 is a component of the U3 small nucleolar RNA (snoRNA) (SNORD3A; MIM 180710) protein complex (U3 snoRNP) and is involved in 18S rRNA processing (Wang et al., 2007 [PubMed 17498821]).[supplied by OMIM, Jun 2009] |
RNU4-2 GeneRNA, U4 small nuclear 2 Predicted to enable U6 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4 snRNP and U4/U6 x U5 tri-snRNP complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPFP4 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 4 |
SNRPFP2 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 2 |
SNRPFP1 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 1 |
SNHG10 Genesmall nucleolar RNA host gene 10 This gene is small nucleolar RNA host gene 10 and represents a non-protein coding RNA. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013] |
SUMO1 Genesmall ubiquitin-like modifier 1 This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last four amino acids of the carboxy-terminus have been cleaved off. Several pseudogenes have been reported for this gene. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Jul 2008] |
SUMO2 Genesmall ubiquitin-like modifier 2 This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last two amino acids of the carboxy-terminus have been cleaved off. Numerous pseudogenes have been reported for this gene. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
SUMO4 Genesmall ubiquitin-like modifier 4 This gene is a member of the SUMO gene family. This family of genes encode small ubiquitin-related modifiers that are attached to proteins and control the target proteins' subcellular localization, stability, or activity. The protein described in this record is located in the cytoplasm and specifically modifies IKBA, leading to negative regulation of NF-kappa-B-dependent transcription of the IL12B gene. A specific polymorphism in this SUMO gene, which leads to the M55V substitution, has been associated with type I diabetes. The RefSeq contains this polymorphism. [provided by RefSeq, Jul 2008] |
LOC100652840 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU4-5P GeneRNA, U4 small nuclear 5, pseudogene |
SNRPGP3 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 3 |
LOC100129492 Genesmall nuclear ribonucleoprotein Sm D1 pseudogene |
SGSM2 Genesmall G protein signaling modulator 2 The protein encoded by this gene is a GTPase activator with activity towards RAB32 and RAB33B, which are regulators of membrane trafficking. The encoded protein inactivates RAB32 and can bind RAB9A-GTP, a protein required for RAB32 activation. [provided by RefSeq, Oct 2016] |
SGSM1 Genesmall G protein signaling modulator 1 Enables GTPase activator activity and small GTPase binding activity. Predicted to act upstream of or within positive regulation of transcription by RNA polymerase II. Located in cytoplasmic vesicle membrane and cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA14B Genesmall nucleolar RNA, H/ACA box 14B Small nucleolar RNAs (snoRNAs) are 60-150 nt long non-coding RNAs, and include two groups: C/D box snoRNAs and H/ACA box snoRNAs. The C/D box snoRNAs are guides for the 2'-O-ribose methylation of rRNAs or snRNAs. The H/ACA box snoRNAs are guides for the isomerization of uridine residues into pseudouridine. This gene belongs to the group of the H/ACA box snoRNAs, and functions in 18S rRNA pseudouridylation at position U966. The gene duplication generates a 91% identical copy on chromosome 7. [provided by RefSeq, Oct 2008] |
SNORA14A Genesmall nucleolar RNA, H/ACA box 14A Small nucleolar RNAs (snoRNAs) are 60-150 nt long non-coding RNAs, and include two groups: C/D box snoRNAs and H/ACA box snoRNAs. The C/D box snoRNAs are guides for the 2'-O-ribose methylation of rRNAs or snRNAs. The H/ACA box snoRNAs are guides for the isomerization of uridine residues into pseudouridine. This gene belongs to the group of the H/ACA box snoRNAs, and functions in 18S rRNA pseudouridylation at position U966. The gene duplication generates a 91% identical copy on chromosome 1. [provided by RefSeq, Oct 2008] |
RNU4-10P GeneRNA, U4 small nuclear 10, pseudogene |
LOC101929240 GeneU5 small nuclear ribonucleoprotein 200 kDa helicase pseudogene |
RNU1-19P GeneRNA, U1 small nuclear 19, pseudogene |
RNU6-14P GeneRNA, U6 small nuclear 14, pseudogene |
RNU5F-8P GeneRNA, U5F small nuclear 8, pseudogene |
SNORD35A Genesmall nucleolar RNA, C/D box 35A Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD35B Genesmall nucleolar RNA, C/D box 35B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM10L2A Genesmall integral membrane protein 10 like 2A This gene encodes a highly conserved small protein that contains a conserved motif (DUF4560) and may function as an integral membrane protein. This transcript was also shown to associate with enhancer chromatin and therefore may also function as an RNA to regulate enhancers. [provided by RefSeq, Jan 2017] |
RNU7-45P GeneRNA, U7 small nuclear 45 pseudogene |
RNU7-84P GeneRNA, U7 small nuclear 84 pseudogene |
RNU6-30P GeneRNA, U6 small nuclear 30, pseudogene |
SNORD13P1 Genesmall nucleolar RNA, C/D box 13 pseudogene 1 |
SNORD13P3 Genesmall nucleolar RNA, C/D box 13 pseudogene 3 |
SNORD13P2 Genesmall nucleolar RNA, C/D box 13 pseudogene 2 |
RNU6-78P GeneRNA, U6 small nuclear 78, pseudogene |
LOC100422645 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene |
RNU7-39P GeneRNA, U7 small nuclear 39 pseudogene |
SNORD14E Genesmall nucleolar RNA, C/D box 14E |
SNORD14D Genesmall nucleolar RNA, C/D box 14D Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD14A Genesmall nucleolar RNA, C/D box 14A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD14C Genesmall nucleolar RNA, C/D box 14C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD14B Genesmall nucleolar RNA, C/D box 14B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD49A Genesmall nucleolar RNA, C/D box 49A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-64P GeneRNA, U7 small nuclear 64 pseudogene |
LOC100533850 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU7-70P GeneRNA, U7 small nuclear 70 pseudogene |
SNORA37 Genesmall nucleolar RNA, H/ACA box 37 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-56P GeneRNA, U7 small nuclear 56 pseudogene |
RNU5F-1 GeneRNA, U5F small nuclear 1 Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD62A Genesmall nucleolar RNA, C/D box 62A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-22 Genesmall nucleolar RNA, C/D box 114-22 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-23 Genesmall nucleolar RNA, C/D box 114-23 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-21 Genesmall nucleolar RNA, C/D box 114-21 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-26 Genesmall nucleolar RNA, C/D box 114-26 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-27 Genesmall nucleolar RNA, C/D box 114-27 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-24 Genesmall nucleolar RNA, C/D box 114-24 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-25 Genesmall nucleolar RNA, C/D box 114-25 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-28 Genesmall nucleolar RNA, C/D box 114-28 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-29 Genesmall nucleolar RNA, C/D box 114-29 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-15P GeneRNA, U7 small nuclear 15 pseudogene |
RNU1-1 GeneRNA, U1 small nuclear 1 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
RNU1-4 GeneRNA, U1 small nuclear 4 Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-H Genesmall ILF3/NF90-associated RNA H |
LOC100631375 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU6-59P GeneRNA, U6 small nuclear 59, pseudogene |
RNU7-31P GeneRNA, U7 small nuclear 31 pseudogene |
LOC105379766 Genesmall nuclear ribonucleoprotein-associated protein N-like |
SNORA5A Genesmall nucleolar RNA, H/ACA box 5A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA5C Genesmall nucleolar RNA, H/ACA box 5C Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA5C, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
SNORA5B Genesmall nucleolar RNA, H/ACA box 5B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA58 Genesmall nucleolar RNA, H/ACA box 58 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA52 Genesmall nucleolar RNA, H/ACA box 52 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA55 Genesmall nucleolar RNA, H/ACA box 55 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA54 Genesmall nucleolar RNA, H/ACA box 54 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA57 Genesmall nucleolar RNA, H/ACA box 57 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA56 Genesmall nucleolar RNA, H/ACA box 56 Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residue U1664 of 28S rRNA. [provided by RefSeq, Feb 2009] |
RNU5B-2P GeneRNA, U5B small nuclear 2, pseudogene |
RNU5E-3P GeneRNA, U5E small nuclear 3, pseudogene |
RNU7-50P GeneRNA, U7 small nuclear 50 pseudogene |
RNU5A-6P GeneRNA, U5A small nuclear 6, pseudogene |
SCARNA6 Genesmall Cajal body-specific RNA 6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5E-10P GeneRNA, U5E small nuclear 10, pseudogene |
SNORD116-19 Genesmall nucleolar RNA, C/D box 116-19 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-18 Genesmall nucleolar RNA, C/D box 116-18 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-11 Genesmall nucleolar RNA, C/D box 116-11 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-13 Genesmall nucleolar RNA, C/D box 116-13 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-15 Genesmall nucleolar RNA, C/D box 116-15 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-14 Genesmall nucleolar RNA, C/D box 116-14 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-17 Genesmall nucleolar RNA, C/D box 116-17 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD116-16 Genesmall nucleolar RNA, C/D box 116-16 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-29P GeneRNA, U7 small nuclear 29 pseudogene |
SNORD59B Genesmall nucleolar RNA, C/D box 59B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD59A Genesmall nucleolar RNA, C/D box 59A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPBP1 Genesmall nuclear ribonucleoprotein polypeptides B and B1 pseudogene 1 |
LOC100128056 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene |
SNORD72 Genesmall nucleolar RNA, C/D box 72 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD77 Genesmall nucleolar RNA, C/D box 77 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD74 Genesmall nucleolar RNA, C/D box 74 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD75 Genesmall nucleolar RNA, C/D box 75 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD78 Genesmall nucleolar RNA, C/D box 78 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD79 Genesmall nucleolar RNA, C/D box 79 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-79P GeneRNA, U7 small nuclear 79 pseudogene |
RNU6-28P GeneRNA, U6 small nuclear 28, pseudogene |
SNRPFP3 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 3 |
RNU2-5P GeneRNA, U2 small nuclear 5, pseudogene |
SNORD56 Genesmall nucleolar RNA, C/D box 56 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-8 Genesmall nucleolar RNA, C/D box 113-8 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-9 Genesmall nucleolar RNA, C/D box 113-9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-4 Genesmall nucleolar RNA, C/D box 113-4 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-5 Genesmall nucleolar RNA, C/D box 113-5 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-6 Genesmall nucleolar RNA, C/D box 113-6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-7 Genesmall nucleolar RNA, C/D box 113-7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD113-2 Genesmall nucleolar RNA, C/D box 113-2 |
SNORD96B Genesmall nucleolar RNA, C/D box 96B |
SNORD96A Genesmall nucleolar RNA, C/D box 96A |
RNU5F-3P GeneRNA, U5F small nuclear 3, pseudogene |
SNORD38B Genesmall nucleolar RNA, C/D box 38B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD38A Genesmall nucleolar RNA, C/D box 38A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LSM10 GeneLSM10, U7 small nuclear RNA associated Enables U7 snRNA binding activity. Involved in positive regulation of G1/S transition of mitotic cell cycle. Located in Cajal body. Part of U7 snRNP. [provided by Alliance of Genome Resources, Mar 2025] |
LSM11 GeneLSM11, U7 small nuclear RNA associated Enables U7 snRNA binding activity. Involved in mRNA 3'-end processing by stem-loop binding activity and cleavage; positive regulation of G1/S transition of mitotic cell cycle; and regulation of chromatin organization. Located in nuclear body. Part of U7 snRNP and telomerase holoenzyme complex. Implicated in Aicardi-Goutieres syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-48P GeneRNA, U7 small nuclear 48 pseudogene |
SNORD115-34 Genesmall nucleolar RNA, C/D box 115-34 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-35 Genesmall nucleolar RNA, C/D box 115-35 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-32 Genesmall nucleolar RNA, C/D box 115-32 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-38 Genesmall nucleolar RNA, C/D box 115-38 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-39 Genesmall nucleolar RNA, C/D box 115-39 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG20 Genesmall nucleolar RNA host gene 20 Predicted to be involved in several processes, including cellular response to fatty acid; macrophage activation; and tyrosine phosphorylation of STAT protein. Implicated in lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG21 Genesmall nucleolar RNA host gene 21 |
SNHG22 Genesmall nucleolar RNA host gene 22 |
SNHG23 Genesmall nucleolar RNA host gene 23 |
SNHG24 Genesmall nucleolar RNA host gene 24 |
RNU6-42P GeneRNA, U6 small nuclear 42, pseudogene |
SNORD115@ Genesmall nucleolar RNA, C/D box 115 cluster |
SNORA59A Genesmall nucleolar RNA, H/ACA box 59A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA59B Genesmall nucleolar RNA, H/ACA box 59B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC728825 Genesmall ubiquitin-like modifier 2 |
RNU7-21P GeneRNA, U7 small nuclear 21 pseudogene |
SNORD71 Genesmall nucleolar RNA, C/D box 71 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD76 Genesmall nucleolar RNA, C/D box 76 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA11C Genesmall nucleolar RNA, H/ACA box 11C Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA11B Genesmall nucleolar RNA, H/ACA box 11B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRNP35 Genesmall nuclear ribonucleoprotein 35kDa (U11/U12) The protein encoded by this gene is a homolog of the U1-snRNP binding protein. The N-terminal half contains a RNA recognition motif and the C-terminal half is rich in Arg/Asp and Arg/Glu dipeptides, which is a characteristic of a variety of splicing factors. This protein is a component of the U11/U12 small nuclear ribonucleoproteins (snRNP) that form part of the U12-type spliceosome. Alternative splicing results in multiple transcript variants encoding two distinct isoforms and representing a non-protein coding variant. [provided by RefSeq, Aug 2013] |
SMPX Genesmall muscle protein, X-linked This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011] |
RNU7-3P GeneRNA, U7 small nuclear 3 pseudogene |
SNORD6 Genesmall nucleolar RNA, C/D box 6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD7 Genesmall nucleolar RNA, C/D box 7 This gene encodes a spliceosomal small nuclear RNA that has orthologs in S. pombe and D. melanogaster. In S. pombe, this gene is required for site-specific 2'-O-methylation of U6 snRNA at position A41. While this is not an essential gene for S. pombe growth, loss of this gene's function may result in a slight decrease in mRNA splicing efficiency. [provided by RefSeq, Oct 2008] |
SNORD5 Genesmall nucleolar RNA, C/D box 5 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD2 Genesmall nucleolar RNA, C/D box 2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD8 Genesmall nucleolar RNA, C/D box 8 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD9 Genesmall nucleolar RNA, C/D box 9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ASH2L Geneash2 (absent, small, or homeotic)-like (Drosophila) Enables beta-catenin binding activity and transcription cis-regulatory region binding activity. Involved in positive regulation of cell population proliferation; response to estrogen; and transcription initiation-coupled chromatin remodeling. Acts upstream of or within DNA damage response. Located in nucleus. Part of MLL1 complex; MLL3/4 complex; and Set1C/COMPASS complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-2P GeneRNA, U7 small nuclear 2 pseudogene |
RNU2-7P GeneRNA, U2 small nuclear 7, pseudogene |
SMLR1 Genesmall leucine-rich protein 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-8 Genesmall nucleolar RNA, C/D box 114-8 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR2E Genesmall proline-rich protein 2E This gene encodes a member of a family of small proline-rich proteins clustered in the epidermal differentiation complex on chromosome 1q21. The encoded protein, along with other family members, is a component of the cornified cell envelope that forms beneath the plasma membrane in terminally differentiated stratified squamous epithelia. This envelope serves as a barrier against extracellular and environmental factors. The seven SPRR2 genes (A-G) appear to have been homogenized by gene conversion compared to others in the cluster that exhibit greater differences in protein structure. [provided by RefSeq, Feb 2014] |
SPRR2D Genesmall proline-rich protein 2D Predicted to be involved in female gonad development. Predicted to act upstream of or within response to estradiol. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR2G Genesmall proline-rich protein 2G Predicted to be involved in keratinocyte differentiation. Predicted to act upstream of or within response to estradiol. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR2F Genesmall proline-rich protein 2F Predicted to be involved in keratinocyte differentiation. Predicted to act upstream of or within response to estradiol. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR2A Genesmall proline-rich protein 2A Enables lipid binding activity. Involved in antibacterial humoral response and defense response to Gram-positive bacterium. Located in cytoplasm. Is active in extracellular region and secretory granule. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR2C Genesmall proline-rich protein 2C (pseudogene) |
SPRR2B Genesmall proline-rich protein 2B Predicted to be involved in keratinocyte differentiation. Predicted to act upstream of or within response to estradiol. Predicted to be located in cornified envelope and cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-33P GeneRNA, U6 small nuclear 33, pseudogene |
LSM3 GeneLSM3 homolog, U6 small nuclear RNA associated (S. cerevisiae) Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004] |
SUMO3 Genesmall ubiquitin-like modifier 3 This gene encodes a member of the small ubiquitin-related modifier (SUMO) family of eukaryotic proteins. The encoded protein is covalently conjugated to other proteins via a post-translation modification known as sumoylation. Sumoylation may play a role in a wide variety of cellular processes, including nuclear transport, DNA replication and repair, mitosis, transcriptional regulation, and signal transduction. Alternatively spliced transcript variants encoding distinct proteins have been described. [provided by RefSeq, Feb 2014] |
RNU7-67P GeneRNA, U7 small nuclear 67 pseudogene |
CTDSPL2 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 Enables RNA polymerase II CTD heptapeptide repeat phosphatase activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of BMP signaling pathway; positive regulation of protein export from nucleus; and protein dephosphorylation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD103B Genesmall nucleolar RNA, C/D box 103B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD103A Genesmall nucleolar RNA, C/D box 103A Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-9 Genesmall nucleolar RNA, C/D box 114-9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-3 Genesmall nucleolar RNA, C/D box 114-3 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-2 Genesmall nucleolar RNA, C/D box 114-2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-7 Genesmall nucleolar RNA, C/D box 114-7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-19 Genesmall nucleolar RNA, C/D box 114-19 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-18 Genesmall nucleolar RNA, C/D box 114-18 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-13 Genesmall nucleolar RNA, C/D box 114-13 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-12 Genesmall nucleolar RNA, C/D box 114-12 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-11 Genesmall nucleolar RNA, C/D box 114-11 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-10 Genesmall nucleolar RNA, C/D box 114-10 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-17 Genesmall nucleolar RNA, C/D box 114-17 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-16 Genesmall nucleolar RNA, C/D box 114-16 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-15 Genesmall nucleolar RNA, C/D box 114-15 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-83P GeneRNA, U7 small nuclear 83 pseudogene |
SNAR-A13 Genesmall ILF3/NF90-associated RNA A13 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-16P GeneRNA, U7 small nuclear 16 pseudogene |
UTP4 GeneUTP4 small subunit processome component This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016] |
SNU13 Genesmall nuclear ribonucleoprotein 13 Originally named because of its sequence similarity to the Saccharomyces cerevisiae NHP2 (non-histone protein 2), this protein appears to be a highly conserved nuclear protein that is a component of the [U4/U6.U5] tri-snRNP. It binds to the 5' stem-loop of U4 snRNA. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
UTP11 GeneUTP11 small subunit processome component Enables RNA binding activity. Involved in nervous system development; positive regulation of apoptotic process; and ribosomal small subunit biogenesis. Located in cytoplasm; extracellular space; and nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
UTP25 GeneUTP25 small subunit processome component Enables RNA binding activity. Involved in several processes, including protein catabolic process; protein destabilization; and protein localization to nucleolus. Located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM26 Genesmall integral membrane protein 26 Enables protein kinase binding activity and transmembrane transporter binding activity. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SVBP Genesmall vasohibin binding protein Enables microtubule binding activity and peptidase activator activity. Involved in axon development; proteolysis; and regulation of metallopeptidase activity. Acts upstream of or within negative regulation of endothelial cell migration; negative regulation of protein ubiquitination; and protein secretion. Located in apical part of cell. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM41 Genesmall integral membrane protein 41 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SCYGR4 Genesmall cysteine and glycine repeat containing 4 Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM36 Genesmall integral membrane protein 36 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM33 Genesmall integral membrane protein 33 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM40 Genesmall integral membrane protein 40 Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM38 Genesmall integral membrane protein 38 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG32 Genesmall nucleolar RNA host gene 32 Predicted to enable double-stranded RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM27 Genesmall integral membrane protein 27 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM29 Genesmall integral membrane protein 29 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM31 Genesmall integral membrane protein 31 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM35 Genesmall integral membrane protein 35 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM43 Genesmall integral membrane protein 43 Enables transmembrane transporter binding activity. Predicted to be involved in mesendoderm development. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SPAAR Genesmall regulatory polypeptide of amino acid response 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] |
SMIM45 Genesmall integral membrane protein 45 Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM30 Genesmall integral membrane protein 30 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] |
SNHG25 Genesmall nucleolar RNA host gene 25 |
SNHG28 Genesmall nucleolar RNA host gene 28 Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG29 Genesmall nucleolar RNA host gene 29 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG30 Genesmall nucleolar RNA host gene 30 |
RNU6-645P GeneRNA, U6 small nuclear 645, pseudogene |
SNORA17B Genesmall nucleolar RNA, H/ACA box 17B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM44 Genesmall integral membrane protein 44 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA63B Genesmall nucleolar RNA, H/ACA box 63B Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG26 Genesmall nucleolar RNA host gene 26 |
SPRR5 Genesmall proline rich protein 5 |
STRIT1 Genesmall transmembrane regulator of ion transport 1 Predicted to enable enzyme activator activity. Predicted to be involved in regulation of calcium ion transport and regulation of striated muscle contraction. Predicted to act upstream of or within positive regulation of ATPase-coupled calcium transmembrane transporter activity and positive regulation of calcium ion import. Predicted to be located in sarcoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SCYGR6 Genesmall cysteine and glycine repeat containing 6 Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM42 Genesmall integral membrane protein 42 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM47 Genesmall integral membrane protein 47 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM32 Genesmall integral membrane protein 32 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SCYGR10 Genesmall cysteine and glycine repeat containing 10 (gene/pseudogene) This gene is a member of a large gene family that encodes keratin associated proteins (KRTAP) that play a role in hair formation. This gene belongs to a subfamily of the KRTAP family termed small cysteine and glycine repeat containing (SCYGR) genes and it resides in a cluster of SCYGR genes on chromosome 2q36.3. Allelic polymorphisms in this gene result in both coding and non-coding transcripts; the reference genome represents the non-coding allele. [provided by RefSeq, Jan 2024] |
FSAF1 Gene40S small subunit processome assembly factor 1 Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in chromosome. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
SCYGR1 Genesmall cysteine and glycine repeat containing 1 |
SCYGR7 Genesmall cysteine and glycine repeat containing 7 |
SCYGR8 Genesmall cysteine and glycine repeat containing 8 |
SCYGR3 Genesmall cysteine and glycine repeat containing 3 |
SCYGR2 Genesmall cysteine and glycine repeat containing 2 |
SCYGR5 Genesmall cysteine and glycine repeat containing 5 |
LOC107983987 Genesmall integral membrane protein 34B |
SMIM39 Genesmall integral membrane protein 39 |
SMIM10L3 Genesmall integral membrane protein 10 like 3 |
SMIM46 Genesmall integral membrane protein 46 |
multiple small medullary renal cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Multiple Small Medullary Renal Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Small Medullary Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
multiple renal cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Multiple Renal Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple renal cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple renal cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Medullary Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Medullary Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
carcinoma, medullary; lymphatic metastasis; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; lymphatic metastasis; medullary carcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma, oxyphilic; carcinoma, medullary; carcinoma, papillary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma, oxyphilic; carcinoma, medullary; carcinoma, papillary; medullary carcinoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple glomerular cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple glomerular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Multiple Lung Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lung Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Glomerular Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Glomerular Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Renal cysts and diabetes syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset. |
renal corticomedullary cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the renal corticomedullary cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal glomerulus cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal cysts and diabetes syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal cysts and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
Renal Corticomedullary Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Corticomedullary Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Cysts And Diabetes Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Cysts And Diabetes Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Cortical Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Cortical Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Renal cysts and diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal cysts and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Renal cortical cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal cortical cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
small inner medullary pyramid Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small inner medullary pyramid Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Renal Medullary Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Medullary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
SMARCB1-deficient renal medullary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease SMARCB1-deficient renal medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; multiple trauma; sepsis; systemic infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; multiple trauma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Multiple synapse bouton, contacting multiple dendrites Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton, contacting multiple dendrites cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
multiple small vertebral fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[<small>Dsmall>-Phe2]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Phe2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[<small>Dsmall>-Bpa5 Ile13]motilin (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Bpa5 Ile13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[His5 <small>Dsmall>-Tyr6]GnRH Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [His5 <small>Dsmall>-Tyr6]GnRH ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[<small>Lsmall>-Bpa5 Ile13]motilin (human) Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Lsmall>-Bpa5 Ile13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d[<small>Dsmall>-Pal2]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d[<small>Dsmall>-Pal2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[<small>Dsmall>-Lys1 des-Arg10]kallidin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [<small>Dsmall>-Lys1 des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
<small>Dsmall>-Lys0-[des-Arg10]kallidin Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the <small>Dsmall>-Lys0-[des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
[125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the [125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts 2a Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephalic leukoencephalopathy with subcortical cysts 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephalic leukoencephalopathy with subcortical cysts 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebroretinal microangiopathy with calcifications and cysts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone Cysts, Aneurysmal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Cysts, Aneurysmal from the curated CTD Gene-Disease Associations dataset. |
Cysts Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cysts from the curated CTD Gene-Disease Associations dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Megalencephalic leukoencephalopathy with subcortical cysts from the curated CTD Gene-Disease Associations dataset. |
Ovarian Cysts Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ovarian Cysts from the curated CTD Gene-Disease Associations dataset. |
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset. |
cysts; epilepsy; tuberous sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cysts; epilepsy; tuberous sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asymptomatic diseases; cyst; cysts; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asymptomatic diseases; cyst; cysts; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cysts; pneumothorax; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cysts; pneumothorax; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cysts Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term cysts in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
pancreatic cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the pancreatic cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
subependymal cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the subependymal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
periventricular cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the periventricular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
basal ganglia cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the basal ganglia cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Ovarian Cysts Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ovarian Cysts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cysts Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Cysts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Odontogenic Cysts Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Odontogenic Cysts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
kidney medulla cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney medulla cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterus cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterus cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inner ear cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inner ear cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney corticomedullary cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney corticomedullary cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
liver cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
gastric cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the gastric cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
urinary bladder cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the urinary bladder cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
atrium cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrium cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
prostate gland cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the prostate gland cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lung cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lung cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney cortex cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney cortex cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epithelioid cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the epithelioid cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dermal cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dermal cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
megalencephalic leukoencephalopathy with subcortical cysts 2a Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2a phenotype from the curated OMIM Gene-Disease Associations dataset. |
aneurysmal bone cysts Gene SetFrom OMIM Gene-Disease Associations genes associated with the aneurysmal bone cysts phenotype from the curated OMIM Gene-Disease Associations dataset. |
cerebroretinal microangiopathy with calcifications and cysts Gene SetFrom OMIM Gene-Disease Associations genes associated with the cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated OMIM Gene-Disease Associations dataset. |
megalencephalic leukoencephalopathy with subcortical cysts Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts phenotype from the curated OMIM Gene-Disease Associations dataset. |
megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset. |
Bone Cysts, Aneurysmal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bone Cysts, Aneurysmal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arachnoid Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arachnoid Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Basal Ganglia Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Basal Ganglia Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bone Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bone Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ovarian Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Odontogenic Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Odontogenic Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rathke Cleft Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rathke Cleft Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracranial Arachnoid Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Arachnoid Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subchondral Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subchondral Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Jaw Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Jaw Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pilar And Trichilemmal Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pilar And Trichilemmal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colloid Cysts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colloid Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periventricular Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periventricular Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Subependymal Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subependymal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Interhemispheric Cysts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Interhemispheric Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Megalencephalic leukoencephalopathy with subcortical cysts from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Blessig's cysts Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blessig's cysts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts 2B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Megalencephalic leukoencephalopathy with subcortical cysts 2A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megalencephalic leukoencephalopathy with subcortical cysts 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pancreatic cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancreatic cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatic cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatic cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Periventricular cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Periventricular cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
central medullary reticular group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral medullary reticular group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral medullary reticular group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central medullary reticular group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
medullary hindbrain (medulla) Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in medullary hindbrain (medulla) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Medullary reticular nucleus, dorsal part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medullary reticular nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Medullary reticular nucleus, ventral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medullary reticular nucleus, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Medullary reticular nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medullary reticular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Familial medullary thyroid carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Histiocytic medullary reticulosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Histiocytic medullary reticulosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Medullary cystic kidney disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lateral Medullary Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lateral Medullary Syndrome from the curated CTD Gene-Disease Associations dataset. |
Thyroid cancer, medullary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid cancer, medullary from the curated CTD Gene-Disease Associations dataset. |
Familial medullary thyroid carcinoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset. |
Medullary Cystic Kidney Disease 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, Medullary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Medullary from the curated CTD Gene-Disease Associations dataset. |
Medullary cystic kidney disease 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Medullary cystic kidney disease 1 from the curated CTD Gene-Disease Associations dataset. |
breast medullary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thyroid medullary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thyroid medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lateral medullary syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lateral medullary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial medullary thyroid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary medullary thyroid carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary medullary thyroid carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thyroid cancer; thyroid carcinoma, sporadic medullary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thyroid cancer; thyroid carcinoma, sporadic medullary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; carcinoma, papillary; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; carcinoma, papillary; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
medullary sponge kidney disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease medullary sponge kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; neoplasm metastasis; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; neoplasm metastasis; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; hyperplasia; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; hyperplasia; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, medullary; neoplasm recurrence, local; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, medullary; neoplasm recurrence, local; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
medullary Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term medullary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
outer medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
medullary reticular formation development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the medullary reticular formation development biological process from the curated GO Biological Process Annotations 2015 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. |
medullary thyroid carcinoma Gene SetFrom HPO Gene-Disease Associations genes associated with the medullary thyroid carcinoma 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. |
adrenal medullary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenal medullary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Carcinoma, Medullary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Medullary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neoplasms, Ductal, Lobular, and Medullary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Ductal, Lobular, and Medullary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
dilated lymph node medullary sinus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated lymph node medullary sinus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node medullary sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node medullary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medullary septa cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lymph node medullary cord hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lymph node medullary cord hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney medullary ray morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney medullary ray morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node medullary cord morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node medullary cord morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
diaphyseal medullary stenosis with malignant fibrous histiocytoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the diaphyseal medullary stenosis with malignant fibrous histiocytoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
medullary thyroid carcinoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
medullary thyroid carcinoma, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
medullary cystic kidney disease 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the medullary cystic kidney disease 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
medullary cystic kidney disease 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the medullary cystic kidney disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
inner medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
thymic medullary epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thymic medullary epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary thyroid carcinoma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary thyroid carcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary thyroid carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary thyroid carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
thymic medullary epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thymic medullary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary thyroid carcinoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease medullary thyroid carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Thymus-medullary thymic epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Thymus-medullary thymic epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Medullary Carcinoma With Lymphoid Stroma Of Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Carcinoma With Lymphoid Stroma Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Neoplasms Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Neoplasms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Non-Medullary Thyroid Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Medullary Thyroid Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Medullary Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Sponge Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Sponge Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Medullary Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Medullary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyroid Carcinoma, Sporadic Medullary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Carcinoma, Sporadic Medullary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mixed Medullary-Follicular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mixed Medullary-Follicular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Nephrocalcinosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Nephrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lateral Medullary Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lateral Medullary Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Sponge Kidney Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Sponge Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Cystic Kidney Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Cystic Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Cystic Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Cystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diaphyseal Medullary Stenosis With Bone Malignancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diaphyseal Medullary Stenosis With Bone Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medullary Thyroid Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease 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. |
Expanded Metacarpals With Widened Medullary Cavities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expanded Metacarpals With Widened Medullary Cavities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Expanded Metatarsals With Widened Medullary Cavities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expanded Metatarsals With Widened Medullary Cavities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Expanded Phalanges With Widened Medullary Cavities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Expanded Phalanges With Widened Medullary Cavities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Adrenal Medullary Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adrenal Medullary Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Narrowing Of Medullary Canal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrowing Of Medullary Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
outer medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal lymph node medullary cord morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymph node medullary cord morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lymph node medullary cord hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lymph node medullary cord hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair medullary septa cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney medullary ray morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney medullary ray morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated lymph node medullary sinus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated lymph node medullary sinus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Kidney - L2 - Inner Medullary Collecting Duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Medullary Fibroblast Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Medullary Fibroblast cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Medullary Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Medullary Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Outer Medullary Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Outer Medullary Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Outer Medullary Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Outer Medullary Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Inner Medullary Collecting Duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Medullary Fibroblast Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Medullary Fibroblast cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Medullary Thick Ascending Limb Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Medullary Thick Ascending Limb cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Outer Medullary Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Outer Medullary Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Outer Medullary Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Outer Medullary Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Medullary cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medullary cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Interstitial Cell (Medullary)_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Interstitial Cell (Medullary)_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner Medullary Collecting Ductal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner Medullary Collecting Ductal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medullary thick ascending limb limb cell (MTAL limb cell)_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medullary thick ascending limb limb cell (MTAL limb cell)_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner Medullary Collecting Ductal cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner Medullary Collecting Ductal cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medullary thymus epithelial cell_Thymus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medullary thymus epithelial cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mature medullary thymic epithelial cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Mature medullary thymic epithelial cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Immature medullary thymic epithelial cell_Thymus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Immature medullary thymic epithelial cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medullary cell_Thymus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medullary cell_Thymus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medullary reticular cell (MedRCs)_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medullary reticular cell (MedRCs)_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Thoracic thymus_CT1_myo-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_myo-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Thoracic thymus_CT1_neuro-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Thoracic thymus_CT1_neuro-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Inner Medullary Collecting Duct Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Inner Medullary Collecting Duct Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Inner Medullary Collecting Duct Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Inner Medullary Collecting Duct Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_myo-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_myo-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Thoracic thymus_CT1_neuro-medullary thymic epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Thoracic thymus_CT1_neuro-medullary thymic epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
outer medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
Thyroid gland medullary carcinoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thyroid gland medullary carcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Thyroid gland medullary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thyroid gland medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Breast medullary carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast medullary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial medullary thyroid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lateral medullary syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lateral medullary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Medullary colon carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medullary colon carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diaphyseal medullary stenosis with malignant fibrous histiocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diaphyseal medullary stenosis with malignant fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thymic medullary epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thymic medullary epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Thymic medullary epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Thymic medullary epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary thyroid carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary thyroid carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary thyroid carcinoma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary thyroid carcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary breast carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary breast carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Histiocytic medullary reticulosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Histiocytic medullary reticulosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial medullary thyroid carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant medullary cystic kidney disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant medullary cystic kidney disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Medullary thyroid carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Invasive medullary breast carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Invasive medullary breast carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diaphyseal medullary stenosis-bone malignancy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Diaphyseal medullary stenosis-bone malignancy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
diabetes, post-renal transplant; post-renal transplant diabetes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, post-renal transplant; post-renal transplant diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
renal involvement and renal sequelae Gene SetFrom GAD Gene-Disease Associations genes associated with the disease renal involvement and renal sequelae in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene SetFrom Biocarta Pathways proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset. |
CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Multiple synostoses syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, 3, with myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene 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. |
Cataract 15, multiple types Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, autosomal dominant, multiple types, with microcornea Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal multiple pterygium syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Cutaneous and Mucosal Venous Malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spondyloepimetaphyseal dysplasia with multiple dislocations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple endocrine neoplasia, type 2b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple fibrofolliculomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple fibrofolliculomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple sulfatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple synostoses syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple pterygium syndrome Escobar type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital heart disease, multiple types, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital heart defects, multiple types, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple gastrointestinal atresias Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple exostoses type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple exostoses type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple endocrine neoplasia, type 2a Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple mitochondrial dysfunctions syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple mitochondrial dysfunctions syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial multiple polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple endocrine neoplasia, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple endocrine neoplasia, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple congenital exostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple epiphyseal dysplasia 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple epiphyseal dysplasia 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple epiphyseal dysplasia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple fibroadenomas of the breast Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple fibroadenomas of the breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LIPOMATOSIS, MULTIPLE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LIPOMATOSIS, MULTIPLE from the curated CTD Gene-Disease Associations dataset. |
Multiple Endocrine Neoplasia Type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset. |
Cafe au lait spots, multiple Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cafe au lait spots, multiple from the curated CTD Gene-Disease Associations dataset. |
Multiple Organ Failure Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Organ Failure from the curated CTD Gene-Disease Associations dataset. |
EXOSTOSES, MULTIPLE, TYPE II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE II from the curated CTD Gene-Disease Associations dataset. |
Multiple Endocrine Neoplasia Type 2a Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2a from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset. |
Multiple Myeloma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Myeloma from the curated CTD Gene-Disease Associations dataset. |
Venous Malformations, Multiple Cutaneous and Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset. |
MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset. |
Multiple Synostoses Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Synostoses Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
CATARACT 32, MULTIPLE TYPES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset. |
Exostoses, Multiple Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hamartoma Syndrome, Multiple Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hamartoma Syndrome, Multiple from the curated CTD Gene-Disease Associations dataset. |
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset. |
CATARACT 6, MULTIPLE TYPES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset. |
Multiple Endocrine Neoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia from the curated CTD Gene-Disease Associations dataset. |
Exostoses, Multiple, Type III Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple, Type III from the curated CTD Gene-Disease Associations dataset. |
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset. |
Multiple Sclerosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sclerosis from the curated CTD Gene-Disease Associations dataset. |
Multiple Chemical Sensitivity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Chemical Sensitivity from the curated CTD Gene-Disease Associations dataset. |
Multiple synostoses syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple synostoses syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Multiple Sclerosis, Relapsing-Remitting Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sclerosis, Relapsing-Remitting from the curated CTD Gene-Disease Associations dataset. |
Multiple Endocrine Neoplasia Type 2b Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2b from the curated CTD Gene-Disease Associations dataset. |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset. |
Cataract, Autosomal Dominant, Multiple Types 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset. |
Trichoepithelioma multiple familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset. |
Multiple pterygium syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple pterygium syndrome from the curated CTD Gene-Disease Associations dataset. |
Abnormalities, Multiple Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abnormalities, Multiple from the curated CTD Gene-Disease Associations dataset. |
Multiple Endocrine Neoplasia, Type IV Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Endocrine Neoplasia, Type IV from the curated CTD Gene-Disease Associations dataset. |
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset. |
CATARACT 3, MULTIPLE TYPES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset. |
EXOSTOSES, MULTIPLE, TYPE I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE I from the curated CTD Gene-Disease Associations dataset. |
CATARACT 4, MULTIPLE TYPES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset. |
Multiple Sulfatase Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
MULTIPLE SYNOSTOSES SYNDROME 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MULTIPLE SYNOSTOSES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset. |
Trichoepithelioma, Multiple Familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal dysplasia, multiple, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal dysplasia, multiple, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal dysplasia, multiple, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal dysplasia, multiple, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal dysplasia, multiple, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset. |
Multiple Sclerosis Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Multiple Sclerosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Multiple Myeloma Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Multiple Myeloma in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
multiple system atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary multiple exostoses Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary multiple exostoses from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple epiphyseal dysplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple sclerosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple sclerosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple carboxylase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple myeloma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
multiple sclerosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease multiple sclerosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
multiple intestinal atresia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple myeloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary multiple exostoses Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple mucosal neuroma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple chemical sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple symmetrical lipomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple symmetrical lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple epiphyseal dysplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple carboxylase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple symmetric lipomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple cranial nerve palsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple personality disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
relapsing-remitting multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; optic neuritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; optic neuritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; craniofacial abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; sepsis; shock, septic; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; sepsis; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple epiphyseal dysplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
burns; multiple organ failure; shock Gene SetFrom GAD Gene-Disease Associations genes associated with the disease burns; multiple organ failure; shock in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis (age of onset) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; diabetes, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; multiple sclerosis; hiv Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; multiple sclerosis; hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; respiratory distress syndrome, adult; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
susceptibility to multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease susceptibility to multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic predisposition to disease; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic predisposition to disease; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
learning disorders; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease learning disorders; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hamartoma syndrome, multiple Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hamartoma syndrome, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
jaw diseases; multiple myeloma; osteonecrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease jaw diseases; multiple myeloma; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple epiphyseal dysplasia; pseudoachondroplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis(ppmultiple sclerosis) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis(ppmultiple sclerosis) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
head and neck neoplasms; neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple familial trichoepithelioma and familial cylindromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
encephalomyelitis, autoimmune, experimental; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease encephalomyelitis, autoimmune, experimental; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; sepsis; systemic infection; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple autoimmune diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; neuromyelitis optica Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; neuromyelitis optica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis, relapsing-remitting; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; plasmacytoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; plasmacytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
normalized brain volume, multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease normalized brain volume, multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus, systemic; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple chemical sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple chemical sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pseudoachondroplasia and multiple epiphyseal dysplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melanoma; neoplasms, multiple primary; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; pneumonia; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; short bowel syndrome Gene 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. |
adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
churg-strauss syndrome; multiple sclerosis; wegener granulomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease churg-strauss syndrome; multiple sclerosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tic; combined vocal and multiple motor; tourette syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
juvenile multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease juvenile multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia type 2b Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia type 2a Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leiomyoma; neoplasms, multiple primary; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leiomyoma; neoplasms, multiple primary; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis, chronic progressive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 1; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infection; multiple myeloma; sepsis; systemic infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloma, multiple Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloma, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; multiple sclerosis, relapsing-remitting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis (severity) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis (severity) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple oesophageal dysplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
epstein-barr virus infections; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease epstein-barr virus infections; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary multiple exostoses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary multiple exostoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; pneumonia; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; pneumonia; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis, relapsing-remitting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infection; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone diseases; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone diseases; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoproliferative disorders; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malaria, falciparum; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple endocrine neoplasia type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple endocrine neoplasia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early onset of multiple sclerosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft vs host disease; leukemia; multiple myeloma; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft vs host disease; leukemia; multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple myeloma; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple myeloma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonic disorders; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple system atophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple system atophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; carcinoma; multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term multiple in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Multiple sclerosis--Brain Glutamate Levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple myeloma Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple sclerosis or amyotrophic lateral sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple myeloma (IgH translocation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple sclerosis (severity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (severity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple myeloma (hyperdiploidy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple myeloma (hyperdiploidy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple sclerosis (OCB status) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (OCB status) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple sclerosis (age of onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
multiple myeloma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
multiple sclerosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
multiple mitochondrial dna deletions Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
multiple myeloma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the multiple myeloma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
multiple exostoses Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple epiphyseal dysplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple gastric polyps Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple gastric polyps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple cutaneous leiomyomas Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple cutaneous leiomyomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple impacted teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple impacted teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple enchondromatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple enchondromatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple prenatal fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple prenatal fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple joint contractures Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple joint contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple rows of eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple rows of eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple myeloma Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple myeloma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple plantar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple plantar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ventricular preexcitation with multiple accessory pathways Gene SetFrom HPO Gene-Disease Associations genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple digital exostoses Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple digital exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bowing of limbs due to multiple fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple suture craniosynostosis Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple suture craniosynostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple lipomas Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple lipomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of multiple cell lineages in the bone marrow Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple carpal ossification centers Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple mitochondrial dna deletions Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple pterygia Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple pterygia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple cafe-au-lait spots Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple cafe-au-lait spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple rib fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple rib fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple lentigines Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple lentigines phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple skeletal anomalies Gene SetFrom HPO Gene-Disease Associations genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Multiple Trauma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Trauma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Organ Failure Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Organ Failure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Sclerosis, Chronic Progressive Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Endocrine Neoplasia Type 2b Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 2b phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Endocrine Neoplasia Type 2a Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 2a phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Myeloma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Myeloma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Sclerosis, Relapsing-Remitting Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Relapsing-Remitting phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Exostoses, Multiple Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Exostoses, Multiple Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Abnormalities, Multiple Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abnormalities, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hamartoma Syndrome, Multiple Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hamartoma Syndrome, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Endocrine Neoplasia Type 1 Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia Type 1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Endocrine Neoplasia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Endocrine Neoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple System Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Sclerosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple Chemical Sensitivity Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Chemical Sensitivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neoplasms, Multiple Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Multiple Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
multiple major aortopulmonary collateral arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
intestinal atresia, multiple Gene SetFrom OMIM Gene-Disease Associations genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset. |
?epiphyseal dysplasia, multiple, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 5, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
adenomas, multiple colorectal Gene SetFrom OMIM Gene-Disease Associations genes associated with the adenomas, multiple colorectal phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 9, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple endocrine neoplasia iib Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple endocrine neoplasia iia Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia iia phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple pterygium syndrome, lethal type Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 3, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple myeloma, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple myeloma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 1, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple sclerosis, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple system atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple sclerosis, susceptibility to, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
orolaryngeal cancer, multiple, Gene SetFrom OMIM Gene-Disease Associations genes associated with the orolaryngeal cancer, multiple, phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple fibroadenomas of the breast Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple fibroadenomas of the breast phenotype from the curated OMIM Gene-Disease Associations dataset. |
{vitiligo-associated multiple autoimmune disease susceptiblity 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {vitiligo-associated multiple autoimmune disease susceptiblity 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, with myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 20, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene SetFrom OMIM Gene-Disease Associations genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple mitochondrial dysfunctions syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple mitochondrial dysfunctions syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital heart defects, multiple types, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital heart defects, multiple types, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 14, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
venous malformations, multiple cutaneous and mucosal Gene SetFrom OMIM Gene-Disease Associations genes associated with the venous malformations, multiple cutaneous and mucosal phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 12, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 39, multiple types, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, with myopia and deafness Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple sclerosis, disease progression, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, disease progression, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple endocrine neoplasia, type iv Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia, type iv phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple endocrine neoplasia 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple endocrine neoplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{vitiligo-associated multiple autoimmune disease susceptibility 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {vitiligo-associated multiple autoimmune disease susceptibility 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 34, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 11, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 6, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 2, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple myeloma, resistance to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple myeloma, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 16, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 15, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple sulfatase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple sulfatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
?multiple synostoses syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?multiple synostoses syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple synostoses syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple synostoses syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple synostoses syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple synostoses syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple sclerosis, susceptibility to, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple sclerosis, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple sclerosis, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple sclerosis, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epiphyseal dysplasia, multiple, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
exostoses, multiple, type 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
exostoses, multiple, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
exostoses, multiple, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the exostoses, multiple, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 17, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 4, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene 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. |
cataract 31, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract 10, multiple types Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset. |
?multiple mitochondrial dysfunctions syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
trichoepithelioma, multiple familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
trichoepithelioma, multiple familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple self-healing squamous epithelioma, susceptiblity to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple self-healing squamous epithelioma, susceptiblity to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Setproteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways dataset. |
Defective HLCS causes multiple carboxylase deficiency Gene Setproteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset. |
multiple myeloma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
multiple myeloma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Multiple Chronic Conditions Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Chronic Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Myeloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis, Relapsing-Remitting Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Relapsing-Remitting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipomatosis, Multiple Symmetrical Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipomatosis, Multiple Symmetrical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vitiligo-Associated Multiple Autoimmune Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vitiligo-Associated Multiple Autoimmune Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Lipomata Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lipomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Adenomatous Polyps Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Adenomatous Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Endocrine Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Endocrine Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Multiple Exostoses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Epiphyseal Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Epiphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Pterygium Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple System Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Gastrointestinal Atresias (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Gastrointestinal Atresias (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Trichoepitheliomata Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis, Primary Progressive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Polyps Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Meningiomas, Multiple Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Meningiomas, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Myeloma Progression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Myeloma Progression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Lacunar Infarcts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lacunar Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Atypical Multiple Mole-Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis, Acute Fulminating Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Acute Fulminating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis, Acute Relapsing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Acute Relapsing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Multiple Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis In Children Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Opticospinal Multiple Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Opticospinal Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sulfatase Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sulfatase Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Carboxylase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Carboxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Joint Dislocations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Multiple Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis Relapse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis Relapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Mitochondrial Dysfunctions Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Mitochondrial Dysfunctions Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Lentigines Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lentigines in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Nevi Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Nevi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple System Atrophy, Cerebellar Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis, Secondary Progressive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Fibrofolliculomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Fibrofolliculomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Asymptomatic Multiple Myeloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Asymptomatic Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis, Chronic Progressive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Self-Healing Squamous Epithelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Self-Healing Squamous Epithelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Biliary Hamartomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Biliary Hamartomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Pterygium Syndrome, Lethal Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Lethal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, With Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Linear Skin Defects With Multiple Congenital Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Linear Skin Defects With Multiple Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Factor Deficiency Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Abscesses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Abscesses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Lipomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Trichoepitheliomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Trichoepitheliomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Synostoses Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Synostoses Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Allergies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Allergies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Of Lung - Multiple Primary Sites Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Lung - Multiple Primary Sites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Basal Cell Papillomata Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Basal Cell Papillomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Exostoses, Multiple, Type Ii Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Exostoses, Multiple, Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Multiple Osteochondromas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Osteochondromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple 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. |
Multiple Evanescent White Dot Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Evanescent White Dot Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Trichodiscomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Multiple Cell Lineages In The Bone Marrow Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Multiple Cell Lineages In The Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nevi Flammei, Familial Multiple Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Non-Ossifying Fibromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Non-Ossifying Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Hemangioblastomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Hemangioblastomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Milia, Multiple Eruptive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Milia, Multiple Eruptive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Disability Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Coagulation Factor Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Pancreatic Beta-Cell Adenomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pancreatic Beta-Cell Adenomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Exacerbation Of Multiple Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indolent Multiple Myeloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indolent Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Pterygium Syndrome, Autosomal Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Pterygium Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cranial Neuropathies, Multiple Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cranial Neuropathies, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Fibroadenomas Of The Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Fibroadenomas Of The Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Digital Exostoses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Digital Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Lentigines/Leopard Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lentigines/Leopard Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Lineage Myelodysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lineage Myelodysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Cranial Nerve Palsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Cranial Nerve Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Aneurysms Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Aneurysms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple, Subcutaneous Nodules Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple, Subcutaneous Nodules in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Venous Malformations, Multiple Cutaneous And Mucosal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Venous Malformations, Multiple Cutaneous And Mucosal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Sclerosis Lesion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Self-Healing Epithelioma Of Ferguson-Smith Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Self-Healing Epithelioma Of Ferguson-Smith in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Myeloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Ventricular Septal Defects Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Ventricular Septal Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Tumors Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Tumors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Prenatal Fractures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Prenatal Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Malignancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Organ Failure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Organ Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Unerupted Teeth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Unerupted Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple System Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Suture Craniosynostosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Suture Craniosynostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Skeletal Anomalies Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Skeletal Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Palmar Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Palmar Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Plantar Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Plantar Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Joint Dislocations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Chemical Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Chemical Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Myeloma, T(11;14) Type, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Myeloma, T(11;14) Type, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Impacted Teeth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Impacted Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cancer Of Multiple Types, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cancer Of Multiple Types, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Pterygia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Pterygia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Contractures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Carpal Ossification Centers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Carpal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bowing Of Limbs Due To Multiple Fractures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bowing Of Limbs Due To Multiple Fractures 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. |
Facial Dysmorphism With Multiple Malformations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Dysmorphism With Multiple Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neoplasms, Multiple Primary Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neoplasms, Multiple Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anti-Multiple Nuclear Dots Antibody Positivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Multiple Nuclear Dots Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Mitochondrial Dna Deletions Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ventricular Preexcitation With Multiple Accessory Pathways Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Preexcitation With Multiple Accessory Pathways in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Self-Healing Squamous Epithelioma, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Self-Healing Squamous Epithelioma, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multiple Rows Of Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Rows Of Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
multiple spine synapse organization, single dendrite Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2023 dataset. |
multiple spine synapse organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
CUX1-19635798-MULTIPLE-CANCER-TYPES-HUMAN Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the CUX1-19635798-MULTIPLE-CANCER-TYPES-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
multiple major aortopulmonary collateral arteries Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
multiple persisting craniopharyngeal ducts Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the multiple persisting craniopharyngeal ducts phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Multiple pluripotent progenitor cell_Bone marrow_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Multiple pluripotent progenitor cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Multiple myeloma(MM) cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Multiple myeloma(MM) cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Multiple ductal cell_Pancreatic duct_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Multiple ductal cell_Pancreatic duct_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Multiple epiphyseal dysplasia and pseudoachondroplasia genes Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Multiple epiphyseal dysplasia and pseudoachondroplasia genes pathway from the WikiPathways Pathways 2024 dataset. |
Defective HLCS causes multiple carboxylase deficiency Gene Setproteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways 2024 dataset. |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models Gene Setproteins participating in the Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models pathway from the Reactome Pathways 2024 dataset. |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Setproteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways 2024 dataset. |
multiple spine synapse organization, single dendrite Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2025 dataset. |
multiple spine synapse organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
Multiple endocrine neoplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple endocrine neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple endocrine neoplasia type 2A Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple endocrine neoplasia type 2A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary multiple exostoses Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary multiple exostoses from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple myeloma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple myeloma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Noonan syndrome with multiple lentigines Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Noonan syndrome with multiple lentigines from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple mitochondrial dysfunctions syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple carboxylase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple sclerosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple sclerosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple system atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple system atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple acyl-CoA dehydrogenase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple acyl-CoA dehydrogenase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple cutaneous and mucosal venous malformations Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple cutaneous and mucosal venous malformations from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Linear skin defects with multiple congenital anomalies 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Linear skin defects with multiple congenital anomalies 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Multiple myeloma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple myeloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple synostoses syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple acyl-CoA dehydrogenase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple acyl-CoA dehydrogenase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary multiple exostoses Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary progressive multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Secondary progressive multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
relapsing-remitting multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple endocrine neoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple endocrine neoplasia type 2B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple personality disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple intestinal atresia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple carboxylase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary arterial and articular multiple calcification syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary arterial and articular multiple calcification syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple endocrine neoplasia type 2A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple synostoses syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 9 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 9 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome with multiple lentigines Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple synostoses syndrome 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple system atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial multiple lipomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial multiple lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple symmetric lipomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple chemical sensitivity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple endocrine neoplasia type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Progressive relapsing multiple sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive relapsing multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple cranial nerve palsy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 8 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 8 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Linear skin defects with multiple congenital anomalies 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 6 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 6 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple synostoses syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple synostoses syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial multiple nevi flammei Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial multiple nevi flammei in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple endocrine neoplasia type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple endocrine neoplasia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple cutaneous and mucosal venous malformations Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple cutaneous and mucosal venous malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 1 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 1 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome with multiple lentigines 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 32 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 32 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome with multiple lentigines 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple benign circumferential skin creases on limbs Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple benign circumferential skin creases on limbs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 4 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 4 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 11 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 11 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 10 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 10 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 3 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 3 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 21 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 21 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mucosal neuroma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 31 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 31 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 14 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 14 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cataract 34 multiple types Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 34 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Linear skin defects with multiple congenital anomalies 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Linear skin defects with multiple congenital anomalies 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome with multiple lentigines 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome with multiple lentigines 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia with myopia and deafness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia with myopia and deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple myeloma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Multiple myeloma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Multiple synapse bouton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Multiple synapse bouton, contacting single dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multiple synapse bouton, contacting single dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Familial multiple polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple system atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple symmetric lipomatosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple symmetric lipomatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple congenital exostosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple acyl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple sulfatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple epiphyseal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple epiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Vitiligo-associated multiple autoimmune disease susceptibility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vitiligo-associated multiple autoimmune disease susceptibility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial multiple trichoepitheliomata Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple trichoepitheliomata phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 12 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 12 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple myeloma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple myeloma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple synostoses syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple synostoses syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 1 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 1 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple cutaneous and mucosal venous malformations Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple cutaneous and mucosal venous malformations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple sclerosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple self-healing squamous epithelioma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple self-healing squamous epithelioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MULTIPLE MYEL Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE MYEL phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple endocrine neoplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple endocrine neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MULTIPLE ENDOCRINE NEOPLA Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE ENDOCRINE NEOPLA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 4 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 4 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 3 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 3 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 9 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 9 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive multiple pterygium syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lethal multiple pterygium syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary arterial and articular multiple calcification syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary arterial and articular multiple calcification syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple congenital anomalies-hypotonia-seizures syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
MULTIPLE JOINT DISLOCATI Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE JOINT DISLOCATI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple joint dislocations Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple mitochondrial dysfunctions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 16 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 16 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 39 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 39 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
KAT6B-related multiple congenital anomalies syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the KAT6B-related multiple congenital anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple gastrointestinal atresias Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial multiple nevi flammei Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple nevi flammei phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 14 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 14 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 15 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 15 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 10 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 10 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple benign circumferential skin creases on limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple benign circumferential skin creases on limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fatal multiple mitochondrial dysfunctions syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal multiple mitochondrial dysfunctions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 34 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 34 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 11 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 11 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 6 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 6 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 5 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 5 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 21 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 21 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 22 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 22 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple congenital anomalies/dysmorphic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies/dysmorphic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary Multiple Osteochondromatosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary Multiple Osteochondromatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 19 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 19 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 17 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 17 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe dermatitis-multiple allergies-metabolic wasting syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe dermatitis-multiple allergies-metabolic wasting syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary progressive multiple sclerosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple joint contractures Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple joint contractures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple mitochondrial dysfunctions syndrome 9b Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple mitochondrial dysfunctions syndrome 9b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 20 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 20 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract 31 multiple Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 31 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple congenital anomalies-neurodevelopmental syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple congenital anomalies-neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple fibroadenoma of the breast Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple fibroadenoma of the breast phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple myeloma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple myeloma (survival) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma (survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to interferon beta in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to interferon beta in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple myeloma and monoclonal gammopathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma and monoclonal gammopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple system atrophy (pathologically confirmed) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy (pathologically confirmed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple system atrophy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bortezomib-induced peripheral neuropathy in multiple myeloma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bortezomib-induced peripheral neuropathy in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
B-cell malignancies (chronic lymphocytic leukemia, Hodgkin lymphoma or multiple myeloma) (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the B-cell malignancies (chronic lymphocytic leukemia, Hodgkin lymphoma or multiple myeloma) (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Decreased low contrast letter acuity in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Decreased low contrast letter acuity in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Drug-induced liver injury in interferon-beta-treated multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Drug-induced liver injury in interferon-beta-treated multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in multiple sclerosis (pre-diagnosis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis (pre-diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in multiple sclerosis (post-diagnosis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis (post-diagnosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Relapse in treatment-naive multiple sclerosis (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relapse in treatment-naive multiple sclerosis (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis or amyotrophic lateral sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Oligoclonal band status in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Oligoclonal band status in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin G index levels in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin G index levels in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Uterine fibroid number (single vs multiple) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Uterine fibroid number (single vs multiple) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis (severity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (severity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis (age of onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis--Brain Glutamate Levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis (OCB status) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis (OCB status) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple myeloma (IgH translocation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Clostridium difficile infection in multiple myeloma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Clostridium difficile infection in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Relapse in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relapse in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and systolic blood pressure (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and systolic blood pressure (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and body mass index (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and body mass index (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and waist-to-hip-ratio (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and waist-to-hip-ratio (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and type 2 diabetes (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and type 2 diabetes (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and C-reactive protein levels (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and C-reactive protein levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and triglyceride levels (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and triglyceride levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and LDL levels (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and LDL levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and HDL levels (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and HDL levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple keratinocyte cancers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple keratinocyte cancers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic lymphocytic leukemia or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic lymphocytic leukemia or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diffuse large B-cell lymphoma or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diffuse large B-cell lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Follicular lymphoma or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Follicular lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Marginal zone lymphoma or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Marginal zone lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hippo signaling pathway - multiple species Gene SetFrom KEGG Pathways 2026 proteins participating in the Hippo signaling pathway - multiple species pathway from the KEGG Pathways 2026 dataset. |
Apoptosis - multiple species Gene SetFrom KEGG Pathways 2026 proteins participating in the Apoptosis - multiple species pathway from the KEGG Pathways 2026 dataset. |
Longevity regulating pathway - multiple species Gene SetFrom KEGG Pathways 2026 proteins participating in the Longevity regulating pathway - multiple species pathway from the KEGG Pathways 2026 dataset. |
Pathways of neurodegeneration - multiple diseases Gene SetFrom KEGG Pathways 2026 proteins participating in the Pathways of neurodegeneration - multiple diseases pathway from the KEGG Pathways 2026 dataset. |
Non-small cell lung cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brain small vessel disease with hemorrhage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mitochondrial small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
preribosome, small subunit precursor Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the preribosome, small subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nuclear ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |