| 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 |
CMM Genecutaneous malignant melanoma/dysplastic nevus Malignant melanoma is a malignant neoplasm of melanocytes, arising de novo or from a pre-existing benign nevus, which occurs most often in the skin but also may involve other sites.[supplied by OMIM, Jul 2002] |
MCTS1 Genemalignant T cell amplified sequence 1 Enables RNA cap binding activity; ribosomal small subunit binding activity; and translation factor activity, non-nucleic acid binding. Involved in IRES-dependent viral translational initiation; cytoplasmic translational initiation; and ribosome disassembly. Is active in cytoplasm. Implicated in primary immunodeficiency disease. [provided by Alliance of Genome Resources, Mar 2025] |
MFHAS1 Genemalignant fibrous histiocytoma amplified sequence 1 Identified in a human 8p amplicon, this gene is a potential oncogene whose expression is enhanced in some malignant fibrous histiocytomas (MFH). The primary structure of its product includes an ATP/GTP-binding site, three leucine zipper domains, and a leucine-rich tandem repeat, which are structural or functional elements for interactions among proteins related to the cell cycle, and which suggest that overexpression might be oncogenic with respect to MFH. [provided by RefSeq, Jul 2008] |
DMBT1 Genedeleted in malignant brain tumors 1 Loss of sequences from human chromosome 10q has been associated with the progression of human cancers. This gene was originally isolated based on its deletion in a medulloblastoma cell line. This gene is expressed with transcripts of 6.0, 7.5, and 8.0 kb in fetal lung and with one transcript of 8.0 kb in adult lung, although the 7.5 kb transcript has not been characterized. The encoded protein precursor is a glycoprotein containing multiple scavenger receptor cysteine-rich (SRCR) domains separated by SRCR-interspersed domains (SID). Transcript variant 2 (8.0 kb) has been shown to bind surfactant protein D independently of carbohydrate recognition. This indicates that DMBT1 may not be a classical tumor suppressor gene, but rather play a role in the interaction of tumor cells and the immune system. [provided by RefSeq, Mar 2016] |
CMM4 GeneMelanoma, cutaneous malignant, 4 |
MCTS2P Genemalignant T cell amplified sequence 2, pseudogene This locus represents a retrogene copy of MCTS1 (GeneID:28985) and contains an ORF similar to that parent gene. This locus is situated in a differentially methylated region (DMR) and transcripts in this region are imprinted. [provided by RefSeq, Nov 2021] |
CMM7 GeneMelanoma, cutaneous malignant, susceptibility to, 7 |
MHS6 Genemalignant hyperthermia susceptibility 6 |
MHS4 Genemalignant hyperthermia susceptibility 4 |
MHS2 Genemalignant hyperthermia susceptibility 2 |
MHS3 GeneMalignant hyperthermia susceptibility 3 |
MMS GeneMalignant mesothelioma, susceptibility to |
DMBT1P1 Genedeleted in malignant brain tumors 1 pseudogene 1 |
DMBT1L1 Genedeleted in malignant brain tumors 1 like 1 (pseudogene) |
MTVR2 Genemouse mammary tumor virus receptor homolog 2 |
LOC101926986 Geneglioma tumor suppressor candidate region gene 1 protein-like |
TP53I3 Genetumor protein p53 inducible protein 3 The protein encoded by this gene is similar to oxidoreductases, which are enzymes involved in cellular responses to oxidative stresses and irradiation. This gene is induced by the tumor suppressor p53 and is thought to be involved in p53-mediated cell death. It contains a p53 consensus binding site in its promoter region and a downstream pentanucleotide microsatellite sequence. P53 has been shown to transcriptionally activate this gene by interacting with the downstream pentanucleotide microsatellite sequence. The microsatellite is polymorphic, with a varying number of pentanucleotide repeats directly correlated with the extent of transcriptional activation by p53. It has been suggested that the microsatellite polymorphism may be associated with differential susceptibility to cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011] |
TUSC2P1 Genetumor suppressor candidate 2 pseudogene 1 |
TPD52L2 Genetumor protein D52-like 2 This gene encodes a member of the tumor protein D52-like family. These proteins are characterized by an N-terminal coiled-coil motif that is used to form homo- and heteromeric complexes with other tumor protein D52-like proteins. Expression of this gene may be a marker for breast cancer and acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 12. [provided by RefSeq, Aug 2011] |
TPD52L3 Genetumor protein D52-like 3 This gene encodes a member of the tumor protein D52-like family of proteins. These proteins are characterized by an N-terminal coiled-coil motif that is used to form homo- and heteromeric complexes with other tumor protein D52-like proteins. The encoded protein may play a role in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
TPD52L1 Genetumor protein D52-like 1 This gene encodes a member of a family of proteins that contain coiled-coil domains and may form hetero- or homomers. The encoded protein is involved in cell proliferation and calcium signaling. It also interacts with the mitogen-activated protein kinase kinase kinase 5 (MAP3K5/ASK1) and positively regulates MAP3K5-induced apoptosis. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2016] |
MLRL GeneMyeloid leukemia-related gene (myeloid tumor suppressor) |
TP63 Genetumor protein p63 This gene encodes a member of the p53 family of transcription factors. The functional domains of p53 family proteins include an N-terminal transactivation domain, a central DNA-binding domain and an oligomerization domain. Alternative splicing of this gene and the use of alternative promoters results in multiple transcript variants encoding different isoforms that vary in their functional properties. These isoforms function during skin development and maintenance, adult stem/progenitor cell regulation, heart development and premature aging. Some isoforms have been found to protect the germline by eliminating oocytes or testicular germ cells that have suffered DNA damage. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrimal-tooth); limb-mammary syndrome; Rap-Hodgkin syndrome (RHS); and orofacial cleft 8. [provided by RefSeq, Aug 2016] |
OVCA2 Geneovarian tumor suppressor candidate 2 Predicted to enable hydrolase activity. Involved in response to retinoic acid. Located in cytoplasm. Biomarker of ovarian cancer. [provided by Alliance of Genome Resources, Mar 2025] |
TNFRSF12A Genetumor necrosis factor receptor superfamily, member 12A Involved in positive regulation of extrinsic apoptotic signaling pathway and regulation of wound healing. Predicted to be located in cell surface and ruffle. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC286059 Genetumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain pseudogene |
RELT GeneRELT tumor necrosis factor receptor The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is especially abundant in hematologic tissues. It has been shown to activate the NF-kappaB pathway and selectively bind TNF receptor-associated factor 1 (TRAF1). This receptor is capable of stimulating T-cell proliferation in the presence of CD3 signaling, which suggests its regulatory role in immune response. Two alternatively spliced transcript variants of this gene encoding the same protein have been reported. [provided by RefSeq, Jul 2008] |
TP53I11 Genetumor protein p53 inducible protein 11 Predicted to be involved in negative regulation of cell population proliferation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MTUS1 Genemicrotubule associated tumor suppressor 1 This gene encodes a protein which contains a C-terminal domain able to interact with the angiotension II (AT2) receptor and a large coiled-coil region allowing dimerization. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. One of the transcript variants has been shown to encode a mitochondrial protein that acts as a tumor suppressor and partcipates in AT2 signaling pathways. Other variants may encode nuclear or transmembrane proteins but it has not been determined whether they also participate in AT2 signaling pathways. [provided by RefSeq, Jul 2008] |
MTUS2 Genemicrotubule associated tumor suppressor candidate 2 Enables microtubule binding activity and protein homodimerization activity. Located in centrosome; cytoplasmic microtubule; and intercellular bridge. Part of nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TNFRSF10A Genetumor necrosis factor receptor superfamily, member 10a The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL), and thus transduces cell death signal and induces cell apoptosis. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. [provided by RefSeq, Jul 2008] |
VHL Genevon Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase This gene encodes a component of a ubiquitination complex. The encoded protein is involved in the ubiquitination and degradation of hypoxia-inducible-factor (HIF), which is a transcription factor that plays a central role in the regulation of gene expression by oxygen. In addition to oxygen-related gene expression, this protein plays a role in many other cellular processes including cilia formation, cytokine signaling, regulation of senescence, and formation of the extracellular matrix. Variants of this gene are associated with von Hippel-Lindau syndrome, pheochromocytoma, erythrocytosis, renal cell carcinoma, and cerebellar hemangioblastoma. [provided by RefSeq, Jun 2022] |
TNFRSF21 Genetumor necrosis factor receptor superfamily, member 21 This gene encodes a member of the tumor necrosis factor receptor superfamily. The encoded protein activates nuclear factor kappa-B and mitogen-activated protein kinase 8 (also called c-Jun N-terminal kinase 1), and induces cell apoptosis. Through its death domain, the encoded receptor interacts with tumor necrosis factor receptor type 1-associated death domain (TRADD) protein, which is known to mediate signal transduction of tumor necrosis factor receptors. Knockout studies in mice suggest that this gene plays a role in T-helper cell activation, and may be involved in inflammation and immune regulation. [provided by RefSeq, Jul 2013] |
TNFRSF25 Genetumor necrosis factor receptor superfamily, member 25 The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is expressed preferentially in the tissues enriched in lymphocytes, and it may play a role in regulating lymphocyte homeostasis. This receptor has been shown to stimulate NF-kappa B activity and regulate cell apoptosis. The signal transduction of this receptor is mediated by various death domain containing adaptor proteins. Knockout studies in mice suggested the role of this gene in the removal of self-reactive T cells in the thymus. Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported, most of which are potentially secreted molecules. The alternative splicing of this gene in B and T cells encounters a programmed change upon T-cell activation, which predominantly produces full-length, membrane bound isoforms, and is thought to be involved in controlling lymphocyte proliferation induced by T-cell activation. [provided by RefSeq, Jul 2008] |
TP53I13 Genetumor protein p53 inducible protein 13 Involved in several processes, including negative regulation of cell cycle; response to UV; and response to xenobiotic stimulus. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
GLTSCR1 Geneglioma tumor suppressor candidate region gene 1 Enables transcription regulator activator activity. Involved in positive regulation of DNA-templated transcription. Located in nucleus. Part of SWI/SNF complex. Implicated in Coffin-Siris syndrome 12. [provided by Alliance of Genome Resources, Mar 2025] |
GLTSCR2 Geneglioma tumor suppressor candidate region gene 2 Enables 5S rRNA binding activity; identical protein binding activity; and p53 binding activity. Involved in several processes, including mitotic G2 DNA damage checkpoint signaling; regulation of intracellular signal transduction; and regulation of primary metabolic process. Located in cytosol; nuclear lumen; and rDNA heterochromatin. [provided by Alliance of Genome Resources, Mar 2025] |
TP53BP1 Genetumor protein p53 binding protein 1 This gene encodes a protein that functions in the DNA double-strand break repair pathway choice, promoting non-homologous end joining (NHEJ) pathways, and limiting homologous recombination. This protein plays multiple roles in the DNA damage response, including promoting checkpoint signaling following DNA damage, acting as a scaffold for recruitment of DNA damage response proteins to damaged chromatin, and promoting NHEJ pathways by limiting end resection following a double-strand break. These roles are also important during V(D)J recombination, class switch recombination and at unprotected telomeres. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017] |
TP53BP2 Genetumor protein p53 binding protein 2 This gene encodes a member of the ASPP (apoptosis-stimulating protein of p53) family of p53 interacting proteins. The protein contains four ankyrin repeats and an SH3 domain involved in protein-protein interactions. It is localized to the perinuclear region of the cytoplasm, and regulates apoptosis and cell growth through interactions with other regulatory molecules including members of the p53 family. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
MGCT Genemale germ cell tumor |
TNF Genetumor necrosis factor This gene encodes a multifunctional proinflammatory cytokine that belongs to the tumor necrosis factor (TNF) superfamily. This cytokine is mainly secreted by macrophages. It can bind to, and thus functions through its receptors TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. This cytokine is involved in the regulation of a wide spectrum of biological processes including cell proliferation, differentiation, apoptosis, lipid metabolism, and coagulation. This cytokine has been implicated in a variety of diseases, including autoimmune diseases, insulin resistance, psoriasis, rheumatoid arthritis ankylosing spondylitis, tuberculosis, autosomal dominant polycystic kidney disease, and cancer. Mutations in this gene affect susceptibility to cerebral malaria, septic shock, and Alzheimer disease. Knockout studies in mice also suggested the neuroprotective function of this cytokine. [provided by RefSeq, Aug 2020] |
TPRG1 Genetumor protein p63 regulated 1 Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PTTG1IP Genepituitary tumor-transforming 1 interacting protein This gene encodes a single-pass type I integral membrane protein, which binds to pituitary tumor-transforming 1 protein (PTTG1), and facilitates translocation of PTTG1 into the nucleus. Coexpression of this protein and PTTG1 induces transcriptional activation of basic fibroblast growth factor. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2013] |
DEL11P13 GeneWilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome |
TP53AIP1 Genetumor protein p53 regulated apoptosis inducing protein 1 This gene is specifically expressed in the thymus, and encodes a protein that is localized to the mitochondrion. The expression of this gene is inducible by p53, and it is thought to play an important role in mediating p53-dependent apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011] |
VHLL Genevon Hippel-Lindau tumor suppressor-like Von Hippel-Lindau (VHL) tumor suppressor protein is a component of an E3 ubiquitin ligase complex that selectively ubiquitinates the alpha subunit of the hypoxia-inducible factor (HIF) transcription factor for proteasome-mediated degradation. Inactivation of VHL causes VHL disease and sporadic kidney cancer. This gene encodes a VHL homolog that lacks one of two key domains necessary for VHL function. This gene may contribute to the regulation of oxygen homeostasis and neovascularization during placenta development. This gene is intronless, and can also be interpreted as a retrotransposed pseudogene of the VHL locus located on chromosome 3. However, the protein is represented in this RefSeq due to evidence in PMID:14757845 that strongly suggests it is translated. The same publication also indicates that this protein binds HIF alpha but fails to recruit the E3 ubiquitin ligase complex, and it therefore functions as a dominant-negative VHL protein and a protector of HIF alpha. [provided by RefSeq, Jan 2010] |
TPT1P14 Genetumor protein, translationally-controlled 1 pseudogene 14 |
TPT1P13 Genetumor protein, translationally-controlled 1 pseudogene 13 |
HOTS GeneH19 Opposite Tumor Suppressor |
PTTG4P Genepituitary tumor-transforming 4 pseudogene |
TNFRSF10C Genetumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008] |
TNFRSF10B Genetumor necrosis factor receptor superfamily, member 10b The protein encoded by this gene is a member of the TNF-receptor superfamily, and contains an intracellular death domain. This receptor can be activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL/APO-2L), and transduces an apoptosis signal. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. Two transcript variants encoding different isoforms and one non-coding transcript have been found for this gene. [provided by RefSeq, Mar 2009] |
TNFRSF10D Genetumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain, a transmembrane domain, and a truncated cytoplamic death domain. This receptor does not induce apoptosis, and has been shown to play an inhibitory role in TRAIL-induced cell apoptosis. [provided by RefSeq, Jul 2008] |
TPT1P12 Genetumor protein, translationally-controlled 1 pseudogene 12 |
TPT1P10 Genetumor protein, translationally-controlled 1 pseudogene 10 |
LOC102723852 Genetranslationally-controlled tumor protein pseudogene |
TP53BP2P1 Genetumor protein p53 binding protein 2 pseudogene 1 |
BTS1 Genebladder tumor susceptibility 1 |
TP53 Genetumor protein p53 This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016] |
TP53INP1 Genetumor protein p53 inducible nuclear protein 1 Predicted to enable antioxidant activity. Involved in autophagic cell death; positive regulation of DNA-templated transcription; and positive regulation of autophagy. Located in autophagosome; cytosol; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TP53INP2 Genetumor protein p53 inducible nuclear protein 2 The protein encoded by this gene promotes autophagy and is essential for proper autophagosome formation and processing. In addition, the encoded protein can enhance rDNA transcription by helping in the assembly of the POLR1/RNA polymerase I preinitiation complex. Finally, this protein serves as a transcriptional activator for some genes. [provided by RefSeq, Jul 2016] |
TPT1P9 Genetumor protein, translationally-controlled 1 pseudogene 9 |
TNFSF9 Genetumor necrosis factor (ligand) superfamily, member 9 The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This transmembrane cytokine is a bidirectional signal transducer that acts as a ligand for TNFRSF9/4-1BB, which is a costimulatory receptor molecule in T lymphocytes. This cytokine and its receptor are involved in the antigen presentation process and in the generation of cytotoxic T cells. The receptor TNFRSF9/4-1BB is absent from resting T lymphocytes but rapidly expressed upon antigenic stimulation. The ligand encoded by this gene, TNFSF9/4-1BBL, has been shown to reactivate anergic T lymphocytes in addition to promoting T lymphocyte proliferation. This cytokine has also been shown to be required for the optimal CD8 responses in CD8 T cells. This cytokine is expressed in carcinoma cell lines, and is thought to be involved in T cell-tumor cell interaction.[provided by RefSeq, Oct 2008] |
TNFSF4 Genetumor necrosis factor (ligand) superfamily, member 4 This gene encodes a cytokine of the tumor necrosis factor (TNF) ligand family. The encoded protein functions in T cell antigen-presenting cell (APC) interactions and mediates adhesion of activated T cells to endothelial cells. Polymorphisms in this gene have been associated with Sjogren's syndrome and systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
TP53COR1 Genetumor protein p53 pathway corepressor 1 (non-protein coding) Predicted to act upstream of or within negative regulation of gene expression. Predicted to be part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Mar 2025] |
PTTG3P Genepituitary tumor-transforming 3, pseudogene Predicted to enable SH3 domain binding activity. Predicted to be involved in homologous chromosome segregation. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TSG11 GeneTumor suppressor gene on chromosome 11 |
TUSC5 Genetumor suppressor candidate 5 Predicted to be involved in endosome to plasma membrane protein transport and glucose import in response to insulin stimulus. Predicted to act upstream of or within establishment of localization in cell and vesicle fusion to plasma membrane. Predicted to be located in cytoplasmic vesicle membrane and plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TUSC7 Genetumor suppressor candidate 7 (non-protein coding) |
TUSC1 Genetumor suppressor candidate 1 This gene is located within the region of chromosome 9p that harbors tumor suppressor genes critical in carcinogenesis. It is an intronless gene which is downregulated in non-small-cell lung cancer and small-cell lung cancer cell lines, suggesting that it may play a role in lung tumorigenesis. [provided by RefSeq, Jul 2008] |
TUSC2 Genetumor suppressor candidate 2 Predicted to be involved in inflammatory response and regulation of mitochondrial membrane potential. Predicted to act upstream of or within several processes, including natural killer cell differentiation; neutrophil-mediated killing of gram-negative bacterium; and regulation of cytokine production. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
TUSC3 Genetumor suppressor candidate 3 This gene encodes a protein that has been associated with several biological functions including cellular magnesium uptake, protein glycosylation and embryonic development. This protein localizes to the endoplasmic reticulum and acts as a component of the oligosaccharyl transferase complex which is responsible for N-linked protein glycosylation. This gene is a candidate tumor suppressor gene. Homozygous mutations in this gene are associated with autosomal recessive nonsyndromic mental retardation-7 and in the proliferation and invasiveness of several cancers including metastatic pancreatic cancer, ovarian cancer and glioblastoma multiform. [provided by RefSeq, Oct 2017] |
TUSC8 Genetumor suppressor candidate 8 (non-protein coding) Enables miRNA inhibitor activity via base-pairing. Involved in lncRNA-mediated post-transcriptional gene silencing. [provided by Alliance of Genome Resources, Mar 2025] |
TTIM1 GeneT-cell tumor invasion and metastasis 1 |
LATS2 Genelarge tumor suppressor kinase 2 This gene encodes a serine/threonine protein kinase belonging to the LATS tumor suppressor family. The protein localizes to centrosomes during interphase, and early and late metaphase. It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis. It also interacts with a negative regulator of p53 and may function in a positive feedback loop with p53 that responds to cytoskeleton damage. Additionally, it can function as a co-repressor of androgen-responsive gene expression. [provided by RefSeq, Jul 2008] |
LATS1 Genelarge tumor suppressor kinase 1 The protein encoded by this gene is a putative serine/threonine kinase that localizes to the mitotic apparatus and complexes with cell cycle controller CDC2 kinase in early mitosis. The protein is phosphorylated in a cell-cycle dependent manner, with late prophase phosphorylation remaining through metaphase. The N-terminal region of the protein binds CDC2 to form a complex showing reduced H1 histone kinase activity, indicating a role as a negative regulator of CDC2/cyclin A. In addition, the C-terminal kinase domain binds to its own N-terminal region, suggesting potential negative regulation through interference with complex formation via intramolecular binding. Biochemical and genetic data suggest a role as a tumor suppressor. This is supported by studies in knockout mice showing development of soft-tissue sarcomas, ovarian stromal cell tumors and a high sensitivity to carcinogenic treatments. [provided by RefSeq, Apr 2017] |
TNFAIP8 Genetumor necrosis factor, alpha-induced protein 8 Enables cysteine-type endopeptidase inhibitor activity involved in apoptotic process. Involved in positive regulation of apoptotic process. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC442087 Geneprostate tumor overexpressed 1 pseudogene |
TNFRSF8 Genetumor necrosis factor receptor superfamily, member 8 The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is expressed by activated, but not by resting, T and B cells. TRAF2 and TRAF5 can interact with this receptor, and mediate the signal transduction that leads to the activation of NF-kappaB. This receptor is a positive regulator of apoptosis, and also has been shown to limit the proliferative potential of autoreactive CD8 effector T cells and protect the body against autoimmunity. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
TNFRSF9 Genetumor necrosis factor receptor superfamily, member 9 The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contributes to the clonal expansion, survival, and development of T cells. It can also induce proliferation in peripheral monocytes, enhance T cell apoptosis induced by TCR/CD3 triggered activation, and regulate CD28 co-stimulation to promote Th1 cell responses. The expression of this receptor is induced by lymphocyte activation. TRAF adaptor proteins have been shown to bind to this receptor and transduce the signals leading to activation of NF-kappaB. [provided by RefSeq, Jul 2008] |
TNFRSF4 Genetumor necrosis factor receptor superfamily, member 4 The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor has been shown to activate NF-kappaB through its interaction with adaptor proteins TRAF2 and TRAF5. Knockout studies in mice suggested that this receptor promotes the expression of apoptosis inhibitors BCL2 and BCL2lL1/BCL2-XL, and thus suppresses apoptosis. The knockout studies also suggested the roles of this receptor in CD4+ T cell response, as well as in T cell-dependent B cell proliferation and differentiation. [provided by RefSeq, Jul 2008] |
LOC100419935 Genetumor protein D52-like 2 pseudogene |
TNFAIP6 Genetumor necrosis factor, alpha-induced protein 6 The protein encoded by this gene is a secretory protein that contains a hyaluronan-binding domain, and thus is a member of the hyaluronan-binding protein family. The hyaluronan-binding domain is known to be involved in extracellular matrix stability and cell migration. This protein has been shown to form a stable complex with inter-alpha-inhibitor (I alpha I), and thus enhance the serine protease inhibitory activity of I alpha I, which is important in the protease network associated with inflammation. This gene can be induced by proinflammatory cytokines such as tumor necrosis factor alpha and interleukin-1. Enhanced levels of this protein are found in the synovial fluid of patients with osteoarthritis and rheumatoid arthritis.[provided by RefSeq, Dec 2010] |
TNFAIP1 Genetumor necrosis factor, alpha-induced protein 1 (endothelial) This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. Studies of a similar gene in mouse suggest that the expression of this gene is developmentally regulated in a tissue-specific manner. [provided by RefSeq, Jul 2008] |
TNFAIP3 Genetumor necrosis factor, alpha-induced protein 3 This gene was identified as a gene whose expression is rapidly induced by the tumor necrosis factor (TNF). The protein encoded by this gene is a zinc finger protein and ubiqitin-editing enzyme, and has been shown to inhibit NF-kappa B activation as well as TNF-mediated apoptosis. The encoded protein, which has both ubiquitin ligase and deubiquitinase activities, is involved in the cytokine-mediated immune and inflammatory responses. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2012] |
TNFAIP2 Genetumor necrosis factor, alpha-induced protein 2 This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. The expression of this gene was shown to be induced by retinoic acid in a cell line expressing a oncogenic version of the retinoic acid receptor alpha fusion protein, which suggested that this gene may be a retinoic acid target gene in acute promyelocytic leukemia. [provided by RefSeq, Jul 2008] |
CYLD Genecylindromatosis (turban tumor syndrome) This gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
TNFSF13 Genetumor necrosis factor (ligand) superfamily, member 13 The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF17/BCMA, a member of the TNF receptor family. This protein and its receptor are both found to be important for B cell development. In vitro experiments suggested that this protein may be able to induce apoptosis through its interaction with other TNF receptor family proteins such as TNFRSF6/FAS and TNFRSF14/HVEM. Alternative splicing results in multiple transcript variants. Some transcripts that skip the last exon of the upstream gene (TNFSF12) and continue into the second exon of this gene have been identified; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010] |
TNFSF12 Genetumor necrosis factor (ligand) superfamily, member 12 The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein is a ligand for the FN14/TWEAKR receptor. This cytokine has overlapping signaling functions with TNF, but displays a much wider tissue distribution. This cytokine, which exists in both membrane-bound and secreted forms, can induce apoptosis via multiple pathways of cell death in a cell type-specific manner. This cytokine is also found to promote proliferation and migration of endothelial cells, and thus acts as a regulator of angiogenesis. Alternative splicing results in multiple transcript variants. Some transcripts skip the last exon of this gene and continue into the second exon of the neighboring TNFSF13 gene; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010] |
TNFSF11 Genetumor necrosis factor (ligand) superfamily, member 11 This gene encodes a member of the tumor necrosis factor (TNF) cytokine family which is a ligand for osteoprotegerin and functions as a key factor for osteoclast differentiation and activation. This protein was shown to be a dentritic cell survival factor and is involved in the regulation of T cell-dependent immune response. T cell activation was reported to induce expression of this gene and lead to an increase of osteoclastogenesis and bone loss. This protein was shown to activate antiapoptotic kinase AKT/PKB through a signaling complex involving SRC kinase and tumor necrosis factor receptor-associated factor (TRAF) 6, which indicated this protein may have a role in the regulation of cell apoptosis. Targeted disruption of the related gene in mice led to severe osteopetrosis and a lack of osteoclasts. The deficient mice exhibited defects in early differentiation of T and B lymphocytes, and failed to form lobulo-alveolar mammary structures during pregnancy. Two alternatively spliced transcript variants have been found. [provided by RefSeq, Jul 2008] |
TNFSF10 Genetumor necrosis factor (ligand) superfamily, member 10 The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein preferentially induces apoptosis in transformed and tumor cells, but does not appear to kill normal cells although it is expressed at a significant level in most normal tissues. This protein binds to several members of TNF receptor superfamily including TNFRSF10A/TRAILR1, TNFRSF10B/TRAILR2, TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and possibly also to TNFRSF11B/OPG. The activity of this protein may be modulated by binding to the decoy receptors TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and TNFRSF11B/OPG that cannot induce apoptosis. The binding of this protein to its receptors has been shown to trigger the activation of MAPK8/JNK, caspase 8, and caspase 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010] |
TNFSF18 Genetumor necrosis factor (ligand) superfamily, member 18 The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for receptor TNFRSF18/AITR/GITR. It has been shown to modulate T lymphocyte survival in peripheral tissues. This cytokine is also found to be expressed in endothelial cells, and is thought to be important for interaction between T lymphocytes and endothelial cells. [provided by RefSeq, Jul 2008] |
JST Genetumor suppressor gene JST |
LOC613206 Genemyeloproliferative disease associated tumor antigen 5 |
WT1 GeneWilms tumor 1 This gene encodes a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue-specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and paternal alleles in different tissues. Multiple transcript variants have been described. In several variants, there is evidence for the use of a non-AUG (CUG) translation initiation codon upstream of, and in-frame with the first AUG. Authors of PMID:7926762 also provide evidence that WT1 mRNA undergoes RNA editing in human and rat, and that this process is tissue-restricted and developmentally regulated. [provided by RefSeq, Mar 2015] |
WT2 GeneWilms tumor 2 |
WT3 GeneWilms tumor-3 |
WT4 GeneWilms tumor-4 |
WTAP GeneWilms tumor 1 associated protein The Wilms tumor suppressor gene WT1 appears to play a role in both transcriptional and posttranscriptional regulation of certain cellular genes. This gene encodes a WT1-associating protein, which is a ubiquitously expressed nuclear protein. Like WT1 protein, this protein is localized throughout the nucleoplasm as well as in speckles and partially colocalizes with splicing factors. Alternative splicing of this gene results in several transcript variants encoding three different isoforms. [provided by RefSeq, Jul 2012] |
TNFSF15 Genetumor necrosis factor (ligand) superfamily, member 15 The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein is abundantly expressed in endothelial cells, but is not expressed in either B or T cells. The expression of this protein is inducible by TNF and IL-1 alpha. This cytokine is a ligand for receptor TNFRSF25 and decoy receptor TNFRSF21/DR6. It can activate NF-kappaB and MAP kinases, and acts as an autocrine factor to induce apoptosis in endothelial cells. This cytokine is also found to inhibit endothelial cell proliferation, and thus may function as an angiogenesis inhibitor. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011] |
TNFSF14 Genetumor necrosis factor (ligand) superfamily, member 14 The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF14, which is a member of the tumor necrosis factor receptor superfamily, and which is also known as a herpesvirus entry mediator (HVEM). This protein may function as a costimulatory factor for the activation of lymphoid cells and as a deterrent to infection by herpesvirus. This protein has been shown to stimulate the proliferation of T cells, and trigger apoptosis of various tumor cells. This protein is also reported to prevent tumor necrosis factor alpha mediated apoptosis in primary hepatocyte. Two alternatively spliced transcript variant encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
TPD52 Genetumor protein D52 Enables calcium ion binding activity and protein homodimerization activity. Involved in B cell differentiation. Located in endoplasmic reticulum and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TSG101 Genetumor susceptibility 101 The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with stathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression. [provided by RefSeq, Jul 2008] |
WTIP GeneWilms tumor 1 interacting protein Predicted to enable transcription corepressor activity. Involved in several processes, including miRNA-mediated gene silencing by inhibition of translation; negative regulation of hippo signaling; and response to hypoxia. Acts upstream of or within miRNA-mediated post-transcriptional gene silencing. Located in P-body. [provided by Alliance of Genome Resources, Mar 2025] |
TNFRSF6B Genetumor necrosis factor receptor superfamily, member 6b, decoy This gene belongs to the tumor necrosis factor receptor superfamily. The encoded protein is postulated to play a regulatory role in suppressing FasL- and LIGHT-mediated cell death. It acts as a decoy receptor that competes with death receptors for ligand binding. Over-expression of this gene has been noted in gastrointestinal tract tumors. Read-through transcription into this gene from the neighboring upstream gene, which encodes regulator of telomere elongation helicase 1 (RTEL1), generates a non-coding transcript. [provided by RefSeq, Feb 2011] |
TP73 Genetumor protein p73 This gene encodes a member of the p53 family of transcription factors involved in cellular responses to stress and development. It maps to a region on chromosome 1p36 that is frequently deleted in neuroblastoma and other tumors, and thought to contain multiple tumor suppressor genes. The demonstration that this gene is monoallelically expressed (likely from the maternal allele), supports the notion that it is a candidate gene for neuroblastoma. Many transcript variants resulting from alternative splicing and/or use of alternate promoters have been found for this gene, but the biological validity and the full-length nature of some variants have not been determined. [provided by RefSeq, Feb 2011] |
TNFRSF13B Genetumor necrosis factor receptor superfamily, member 13B The protein encoded by this gene is a lymphocyte-specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein induces activation of the transcription factors NFAT, AP1, and NF-kappa-B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
TNFRSF13C Genetumor necrosis factor receptor superfamily, member 13C B cell-activating factor (BAFF) enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. Overexpression of Baff in mice results in mature B-cell hyperplasia and symptoms of systemic lupus erythematosus (SLE). Also, some SLE patients have increased levels of BAFF in serum. Therefore, it has been proposed that abnormally high levels of BAFF may contribute to the pathogenesis of autoimmune diseases by enhancing the survival of autoreactive B cells. The protein encoded by this gene is a receptor for BAFF and is a type III transmembrane protein containing a single extracellular cysteine-rich domain. It is thought that this receptor is the principal receptor required for BAFF-mediated mature B-cell survival. [provided by RefSeq, Jul 2008] |
WTAPP1 GeneWilms tumor 1 associated protein pseudogene 1 |
PTOV1 Geneprostate tumor overexpressed 1 This gene encodes a protein that was found to be overexpressed in prostate adenocarcinomas. The encoded protein was found to interact with the lipid raft protein flotillin-1 and shuttle it from the cytoplasm to the nucleus in a cell cycle dependent manner. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015] |
LOC101929989 Genelipopolysaccharide-induced tumor necrosis factor-alpha factor-like Predicted to enable zinc ion binding activity. Predicted to be involved in regulation of cytokine production. Predicted to be located in membrane. Predicted to be active in cytoplasmic side of late endosome membrane; cytoplasmic side of lysosomal membrane; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TGCT1 Genetesticular germ cell tumor susceptibility 1 |
PTTG1 Genepituitary tumor-transforming 1 The encoded protein is a homolog of yeast securin proteins, which prevent separins from promoting sister chromatid separation. It is an anaphase-promoting complex (APC) substrate that associates with a separin until activation of the APC. The gene product has transforming activity in vitro and tumorigenic activity in vivo, and the gene is highly expressed in various tumors. The gene product contains 2 PXXP motifs, which are required for its transforming and tumorigenic activities, as well as for its stimulation of basic fibroblast growth factor expression. It also contains a destruction box (D box) that is required for its degradation by the APC. The acidic C-terminal region of the encoded protein can act as a transactivation domain. The gene product is mainly a cytosolic protein, although it partially localizes in the nucleus. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2013] |
PTTG2 Genepituitary tumor-transforming 2 Predicted to enable SH3 domain binding activity. Predicted to be involved in homologous chromosome segregation. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TSSC4 Genetumor suppressing subtransferable candidate 4 This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is located among several imprinted genes; however, this gene, as well as the pan-hematopoietic expression gene (PHEMX), escapes imprinting. This gene may play a role in malignancies and disease that involve this region. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014] |
TSSC2 Genetumor suppressing subtransferable candidate 2 pseudogene |
TSSC1 Genetumor suppressing subtransferable candidate 1 This gene has been reported in PMID 9403053 as one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. Alignment of this gene to genomic sequence data suggests that this gene resides on chromosome 2 rather than chromosome 11. [provided by RefSeq, Dec 2008] |
TNFSF13B Genetumor necrosis factor (ligand) superfamily, member 13b The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for receptors TNFRSF13B/TACI, TNFRSF17/BCMA, and TNFRSF13C/BAFFR. This cytokine is expressed in B cell lineage cells, and acts as a potent B cell activator. It has been also shown to play an important role in the proliferation and differentiation of B cells. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2011] |
ITS GeneInsulinoma tumor suppressor gene locus |
TNFRSF17 Genetumor necrosis factor receptor superfamily, member 17 The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is preferentially expressed in mature B lymphocytes, and may be important for B cell development and autoimmune response. This receptor has been shown to specifically bind to the tumor necrosis factor (ligand) superfamily, member 13b (TNFSF13B/TALL-1/BAFF), and to lead to NF-kappaB and MAPK8/JNK activation. This receptor also binds to various TRAF family members, and thus may transduce signals for cell survival and proliferation. [provided by RefSeq, Jul 2008] |
TNFRSF14 Genetumor necrosis factor receptor superfamily, member 14 This gene encodes a member of the TNF (tumor necrosis factor) receptor superfamily. The encoded protein functions in signal transduction pathways that activate inflammatory and inhibitory T-cell immune response. It binds herpes simplex virus (HSV) viral envelope glycoprotein D (gD), mediating its entry into cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
TNFRSF18 Genetumor necrosis factor receptor superfamily, member 18 This gene encodes a member of the TNF-receptor superfamily. The encoded receptor has been shown to have increased expression upon T-cell activation, and it is thought to play a key role in dominant immunological self-tolerance maintained by CD25(+)CD4(+) regulatory T cells. Knockout studies in mice also suggest the role of this receptor is in the regulation of CD3-driven T-cell activation and programmed cell death. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Feb 2011] |
TNFRSF19 Genetumor necrosis factor receptor superfamily, member 19 The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is highly expressed during embryonic development. It has been shown to interact with TRAF family members, and to activate JNK signaling pathway when overexpressed in cells. This receptor is capable of inducing apoptosis by a caspase-independent mechanism, and it is thought to play an essential role in embryonic development. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008] |
TNFRSF1B Genetumor necrosis factor receptor superfamily, member 1B The protein encoded by this gene is a member of the TNF-receptor superfamily. This protein and TNF-receptor 1 form a heterocomplex that mediates the recruitment of two anti-apoptotic proteins, c-IAP1 and c-IAP2, which possess E3 ubiquitin ligase activity. The function of IAPs in TNF-receptor signalling is unknown, however, c-IAP1 is thought to potentiate TNF-induced apoptosis by the ubiquitination and degradation of TNF-receptor-associated factor 2, which mediates anti-apoptotic signals. Knockout studies in mice also suggest a role of this protein in protecting neurons from apoptosis by stimulating antioxidative pathways. [provided by RefSeq, Jul 2008] |
TNFRSF1A Genetumor necrosis factor receptor superfamily, member 1A This gene encodes a member of the TNF receptor superfamily of proteins. The encoded receptor is found in membrane-bound and soluble forms that interact with membrane-bound and soluble forms, respectively, of its ligand, tumor necrosis factor alpha. Binding of membrane-bound tumor necrosis factor alpha to the membrane-bound receptor induces receptor trimerization and activation, which plays a role in cell survival, apoptosis, and inflammation. Proteolytic processing of the encoded receptor results in release of the soluble form of the receptor, which can interact with free tumor necrosis factor alpha to inhibit inflammation. Mutations in this gene underlie tumor necrosis factor receptor-associated periodic syndrome (TRAPS), characterized by fever, abdominal pain and other features. Mutations in this gene may also be associated with multiple sclerosis in human patients. [provided by RefSeq, Sep 2016] |
LOC440311 Geneglioma tumor suppressor candidate region gene 2 pseudogene |
LOC100130490 Genetumor protein p63 regulated 1-like pseudogene |
LOC100127954 Genepituitary tumor-transforming 1 pseudogene |
TACSTD2 Genetumor-associated calcium signal transducer 2 This intronless gene encodes a carcinoma-associated antigen. This antigen is a cell surface receptor that transduces calcium signals. Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy.[provided by RefSeq, Dec 2009] |
LOC102724868 Genetranslationally-controlled tumor protein pseudogene |
LZTS2 Geneleucine zipper, putative tumor suppressor 2 The protein encoded by this gene belongs to the leucine zipper tumor suppressor family of proteins, which function in transcription regulation and cell cycle control. This family member can repress beta-catenin-mediated transcriptional activation and is a negative regulator of the Wnt signaling pathway. It negatively regulates microtubule severing at centrosomes, and is necessary for central spindle formation and cytokinesis completion. It is implicated in cancer, where it may inhibit cell proliferation and decrease susceptibility to tumor development. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
LZTS3 Geneleucine zipper, putative tumor suppressor family member 3 Predicted to enable PDZ domain binding activity. Predicted to be involved in protein homooligomerization; regulation of dendritic spine morphogenesis; and regulation of postsynapse assembly. Predicted to be located in postsynaptic density. Predicted to be active in dendritic spine and glutamatergic synapse. [provided by Alliance of Genome Resources, Mar 2025] |
LZTS1 Geneleucine zipper, putative tumor suppressor 1 This gene encodes a tumor suppressor protein that is ubiquitously expressed in normal tissues. In uveal melanomas, expression of this protein is silenced in rapidly metastasizing and metastatic tumor cells but has normal expression in slowly metastasizing or nonmetastasizing tumor cells. This protein may have a role in cell-cycle control by interacting with the Cdk1/cyclinB1 complex. This gene is located on chromosomal region 8p22. Loss of heterozygosity (LOH) in the 8p arm is a common characteristic of many types of cancer. [provided by RefSeq, Nov 2009] |
C1QTNF8 GeneC1q and tumor necrosis factor related protein 8 Involved in positive regulation of cell motility. Predicted to be located in extracellular region. Predicted to be part of collagen trimer. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF9 GeneC1q and tumor necrosis factor related protein 9 Enables identical protein binding activity. Predicted to be involved in signal transduction. Predicted to be located in extracellular region. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF2 GeneC1q and tumor necrosis factor related protein 2 Predicted to enable identical protein binding activity and signaling receptor binding activity. Predicted to be involved in regulation of lipid metabolic process. Predicted to act upstream of or within positive regulation of D-glucose import; positive regulation of MAPK cascade; and positive regulation of small molecule metabolic process. Predicted to be located in extracellular space. Predicted to be part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF3 GeneC1q and tumor necrosis factor related protein 3 Enables identical protein binding activity. Involved in several processes, including intracellular triglyceride homeostasis; negative regulation of non-canonical NF-kappaB signal transduction; and regulation of cytokine production. Acts upstream of or within negative regulation of gluconeogenesis. Located in extracellular exosome and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF1 GeneC1q and tumor necrosis factor related protein 1 Enables collagen binding activity. Involved in several processes, including negative regulation of platelet aggregation; positive regulation of aldosterone secretion; and positive regulation of cytosolic calcium ion concentration. Located in extracellular space and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF6 GeneC1q and tumor necrosis factor related protein 6 Enables identical protein binding activity. Predicted to be located in extracellular region and membrane. Predicted to be part of collagen trimer. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF7 GeneC1q and tumor necrosis factor related protein 7 Predicted to enable identical protein binding activity. Predicted to be located in extracellular space. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF4 GeneC1q and tumor necrosis factor related protein 4 Predicted to enable cytokine activity. Involved in positive regulation of cytokine production and positive regulation of signal transduction. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF5 GeneC1q and tumor necrosis factor related protein 5 This gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late-onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled-related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter. [provided by RefSeq, Jun 2013] |
TSG1 Genetumor suppressor TSG1 |
LOC101928596 Geneprobable tumor suppressor protein MN1 |
TPT1P6 Genetumor protein, translationally-controlled 1 pseudogene 6 |
TNFSF8 Genetumor necrosis factor (ligand) superfamily, member 8 The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for TNFRSF8/CD30, which is a cell surface antigen and a marker for Hodgkin lymphoma and related hematologic malignancies. The engagement of this cytokine expressed on B cell surface plays an inhibitory role in modulating Ig class switch. This cytokine was shown to enhance cell proliferation of some lymphoma cell lines, while to induce cell death and reduce cell proliferation of other lymphoma cell lines. The pleiotropic biologic activities of this cytokine on different CD30+ lymphoma cell lines may play a pathophysiologic role in Hodgkin's and some non-Hodgkin's lymphomas. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011] |
TPRG1L Genetumor protein p63 regulated 1-like Predicted to enable calmodulin binding activity and identical protein binding activity. Predicted to be involved in presynaptic modulation of chemical synaptic transmission; regulation of glutamatergic synaptic transmission; and regulation of synaptic vesicle exocytosis. Predicted to act upstream of or within calcineurin-NFAT signaling cascade; negative regulation of synaptic transmission; and synaptic vesicle docking. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
C1QTNF9B GeneC1q and tumor necrosis factor related protein 9B Predicted to enable hormone activity and identical protein binding activity. Predicted to act upstream of or within several processes, including negative regulation of cell size; positive regulation of cellular response to insulin stimulus; and positive regulation of protein serine/threonine kinase activity. Predicted to be located in extracellular space. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Mar 2025] |
TPT1 Genetumor protein, translationally-controlled 1 This gene encodes a protein that is a regulator of cellular growth and proliferation. Its mRNA is highly structured and contains an oligopyrimidine tract (5'-TOP) in its 5' untranslated region that functions to repress its translation under quiescent conditions. The encoded protein is involved in a variety of cellular pathways, including apoptosis, protein synthesis and cell division. It binds to and stabilizes microtubules, and removal of this protein through phosphorylation is required for progression through mitotic and meiotic cell divisions. This gene is known to play a role in carcinogenesis, and is upregulated in some cancer cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017] |
LOC646517 GeneWilms tumor 1 associated protein pseudogene |
ETAA1 GeneEwing tumor-associated antigen 1 Enables protein serine/threonine kinase activator activity. Involved in several processes, including positive regulation of protein serine/threonine kinase activity; regulation of cell cycle phase transition; and replication fork processing. Located in cytosol; nuclear replication fork; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TPT1P8 Genetumor protein, translationally-controlled 1 pseudogene 8 Predicted to enable calcium ion binding activity. Predicted to be involved in apoptotic process. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TPT1P5 Genetumor protein, translationally-controlled 1 pseudogene 5 |
TPT1P4 Genetumor protein, translationally-controlled 1 pseudogene 4 |
TPT1P3 Genetumor protein, translationally-controlled 1 pseudogene 3 |
TPT1P2 Genetumor protein, translationally-controlled 1 pseudogene 2 |
TPT1P1 Genetumor protein, translationally-controlled 1 pseudogene 1 |
TNFRSF11A Genetumor necrosis factor receptor superfamily, member 11a, NFKB activator The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptors can interact with various TRAF family proteins, through which this receptor induces the activation of NF-kappa B and MAPK8/JNK. This receptor and its ligand are important regulators of the interaction between T cells and dendritic cells. This receptor is also an essential mediator for osteoclast and lymph node development. Mutations at this locus have been associated with familial expansile osteolysis, autosomal recessive osteopetrosis, and Paget disease of bone. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2012] |
TNFRSF11B Genetumor necrosis factor receptor superfamily, member 11b The protein encoded by this gene is a member of the TNF-receptor superfamily. This protein is an osteoblast-secreted decoy receptor that functions as a negative regulator of bone resorption. This protein specifically binds to its ligand, osteoprotegerin ligand, both of which are key extracellular regulators of osteoclast development. Studies of the mouse counterpart also suggest that this protein and its ligand play a role in lymph-node organogenesis and vascular calcification. Alternatively spliced transcript variants of this gene have been reported, but their full length nature has not been determined. [provided by RefSeq, Jul 2008] |
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 |
Malignant Tumor Of Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Small Intestine 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. |
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. |
Secondary Malignant Neoplasm Of Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Stromal Tumor Of Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Stromal Tumor Of Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small intestine neuroendocrine tumor Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Small intestine neuroendocrine tumor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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. |
Malignant Neoplasm Of Large Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carcinoid Tumor Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carcinoid Tumor Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carcinoid tumor of intestine Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Carcinoid tumor of intestine phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
small intestine cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease small intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
small intestine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PDX1_KO_GDS4348_360_mouse_Proximal small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PDX1_KO_GDS4348_360_mouse_Proximal small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
small intestine Gene SetFrom GTEx Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. |
small intestine neoplasm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease small intestine neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
small intestine Gene SetFrom HPA Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. |
small intestine Gene SetFrom HPA Tissue Protein Expression Profiles proteins with high or low expression in small intestine relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. |
neoplasm of the small intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestine carcinoid Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestine carcinoid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the small intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal small intestine crypts of lieberkuhn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased small intestine adenocarcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased small intestine adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine placement Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine placement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small intestine mucosa Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue small intestine mucosa from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
small intestine Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue small intestine from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
small intestine Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue small intestine in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
small intestine cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue small intestine cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
small intestine mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue small intestine mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
small intestine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue small intestine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
small intestine epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue small intestine epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Small_Intestine-enterocyte of epithelium of small intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Small_Intestine-enterocyte of epithelium of small intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Small_Intestine-intestinal crypt stem cell of small intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Small_Intestine-intestinal crypt stem cell of small intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Small_Intestine-paneth cell of epithelium of small intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Small_Intestine-paneth cell of epithelium of small intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Small_Intestine-small intestine goblet cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Small_Intestine-small intestine goblet cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Small_Intestine-transit amplifying cell of small intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Small_Intestine-transit amplifying cell of small intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Small Intestine Carcinoid Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Intestine Carcinoid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Intestine Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Intestine Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Shortened Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Shortened Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neoplasm Of Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neoplasm Of Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyp Of Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyp Of Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Dysmotility Of Small Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Dysmotility Of Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aganglionosis Of The Small Intestine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aganglionosis Of The Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal small intestine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal small intestine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal small intestine crypts of Lieberkuhn morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal small intestine crypts of Lieberkuhn morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal small intestine placement Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal small intestine placement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal small intestine goblet cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal small intestine goblet cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small intestine hemorrhage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small intestine hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased small intestine length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased small intestine length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased small intestine adenocarcinoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased small intestine adenocarcinoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased small intestine length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased small intestine length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Small Intestine - Terminal Ileum Gene SetFrom GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Small Intestine - Terminal Ileum relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. |
Small intestine neuroendocrine neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Small intestine neuroendocrine neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine benign neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Small intestine benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Small intestine leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Small intestine Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Small intestine from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine mucosa Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Small intestine mucosa from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Small intestine in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Small intestine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Small intestine epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Small intestine cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Small intestine mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Small intestine carcinoid Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Small intestine carcinoid phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of prostate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Malignant tumor of prostate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
malignant sertoli cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant sertoli cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant leydig cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant leydig cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant dermis tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant dermis tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ovarian brenner tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ovarian brenner tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant giant cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant glandular tumor of peripheral nerve sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant glandular tumor of peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant triton tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant triton tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
epithelioid malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epithelioid malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant giant cell tumor of soft parts Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant giant cell tumor of soft parts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast malignant phyllodes tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast malignant phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Malignant tumor of pancreas_saliva_GSE14245 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Malignant tumor of pancreas_saliva_GSE14245 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
malignant genitourinary tract tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant genitourinary tract tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased malignant tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased malignant tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
malignant mixed muellerian tumor cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue malignant mixed muellerian tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Malignant Tumor Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Cervix Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Cervix in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastasis From Malignant Tumor Of Prostate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastasis From Malignant Tumor Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Exocrine Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Exocrine Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Testicular Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Peritoneum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Peritoneum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Greater Curve Of Stomach Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Greater Curve Of Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Lesser Curve Of Stomach Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Lesser Curve Of Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Odontogenic Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Odontogenic Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Extrahepatic Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Renal Pelvis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Renal Pelvis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Phyllodes Tumor Of Prostate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Phyllodes Tumor Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epithelioid Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epithelioid Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glomus Tumor Of Uncertain Malignant Potential Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glomus Tumor Of Uncertain Malignant Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glomus Tumor, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glomus Tumor, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor, Fusiform Cell Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor, Fusiform Cell Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Phyllodes Tumor Of Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Phyllodes Tumor Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Parathyroid Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Parathyroid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Granular Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Granular Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Mesenchymal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mesenchymal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Mixed Mesodermal (Mullerian) Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mixed Mesodermal (Mullerian) Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Mixed Salivary Gland Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mixed Salivary Gland Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tenosynovial Giant Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tenosynovial Giant Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Phosphaturic Mesenchymal Tumor, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Phosphaturic Mesenchymal Tumor, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Granulosa Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Granulosa Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Giant Cell Tumor Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Giant Cell Tumor Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Mediastinum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Mediastinum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neuroendocrine Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neuroendocrine Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Genitourinary Tract Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Genitourinary Tract Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microsatellite Instability-High Solid Malignant Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microsatellite Instability-High Solid Malignant Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Epithelial Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Epithelial Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Anterior Wall Of Nasopharynx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Anterior Wall Of Nasopharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Lateral Wall Of Nasopharynx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Lateral Wall Of Nasopharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Posterior Wall Of Nasopharynx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Posterior Wall Of Nasopharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Peripheral Nerve Sheath Tumor With Rhabdomyoblastic Differentiation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Peripheral Nerve Sheath Tumor With Rhabdomyoblastic Differentiation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Basal Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Basal Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Ovarian Sex Cord-Stromal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Ovarian Sex Cord-Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Rhabdoid Tumor, Somatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Rhabdoid Tumor, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Melanotic Malignant Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Melanotic Malignant Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Perivascular Epithelioid Tumor, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Perivascular Epithelioid Tumor, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Proliferating Pilar Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Proliferating Pilar Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor, Giant Cell Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor, Giant Cell Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carcinoid Tumor, Malignant Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Carcinoid Tumor, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Malignant Mixed Tumor Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malignant Mixed Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
increased malignant tumor incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased malignant tumor incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant dermis tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant dermis tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Breast malignant phyllodes tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast malignant phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Epithelioid malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelioid malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic malignant tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic malignant tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant ovarian Brenner tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant ovarian Brenner tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant triton tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant triton tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant giant cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant giant cell tumor of soft parts Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant giant cell tumor of soft parts in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant gastric germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant gastric germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant glandular tumor of peripheral nerve sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant glandular tumor of peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant giant cell tumor of the tendon sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant giant cell tumor of the tendon sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant mixed Muellerian tumor cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Malignant mixed Muellerian tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Malignant tumor of breast Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of breast phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of urinary bladder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of urinary bladder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of pancreas Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of pancreas phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of esophagus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of esophagus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of ascending colon Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of ascending colon phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant germ cell tumor of ovary Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant germ cell tumor of ovary phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of testis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of testis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of thyroid gland Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of thyroid gland phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Uterine Tumor Resembling Ovarian Sex Cord Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uterine Tumor Resembling Ovarian Sex Cord Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pten Hamartoma Tumor Syndrome With Granular Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spindle epithelial tumor with thymus-like differentiation tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spindle epithelial tumor with thymus-like differentiation tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Desmoplastic Small Round Cell Tumor from the curated CTD Gene-Disease Associations dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Desmoplastic Small Round Cell Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Adult Desmoplastic Small Round Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Desmoplastic Small Round Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Intestinal Neuroendocrine Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Intestinal Neuroendocrine Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Desmoplastic small round cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Desmoplastic small round cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
EWSR1-negative small round cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease EWSR1-negative small round cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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. |
large intestine cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease large intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
large intestine cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease large intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
large intestine lipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease large intestine lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acute vascular insufficiency of intestine Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute vascular insufficiency of intestine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intestine Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term intestine in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Crohn's disease_Intestine - Large Intestine - Colon (MMHCC)_GSE6731 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Crohn's disease_Intestine - Large Intestine - Colon (MMHCC)_GSE6731 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Cancer of Colon_Intestine - Large Intestine - Colon (MMHCC)_GSE4107 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Cancer of Colon_Intestine - Large Intestine - Colon (MMHCC)_GSE4107 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
PRKCA_KO_GDS2141_300_mouse_small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PRKCA_KO_GDS2141_300_mouse_small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
KLF9_Deficiency_GDS2703_647_mouse_Jejuna - intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KLF9_Deficiency_GDS2703_647_mouse_Jejuna - intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PPARA_KO_GDS2886_484_mouse_small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PPARA_KO_GDS2886_484_mouse_small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
HNF4alpha_KO_GDS1915_173_mouse_Small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the HNF4alpha_KO_GDS1915_173_mouse_Small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PPARA_Deficiency_GDS2934_632_mouse_Small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PPARA_Deficiency_GDS2934_632_mouse_Small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
intestine smooth muscle contraction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intestine smooth muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset. |
determination of intestine left/right asymmetry Gene SetFrom GO Biological Process Annotations 2015 genes participating in the determination of intestine left/right asymmetry biological process from the curated GO Biological Process Annotations 2015 dataset. |
large intestine cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease large intestine cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammation of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammation of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neoplasm of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the large intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the large intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammation of the large intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammation of the large intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the large intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the large intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased large intestine adenocarcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased large intestine adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased intestine copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal large intestine morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal large intestine morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal large intestine placement Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal large intestine placement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
herniated intestine Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the herniated intestine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
intestine polyps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the intestine polyps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed intestine development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed intestine development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal large intestine crypts of lieberkuhn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal large intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
large intestine Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue large intestine from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
intestine Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue intestine from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
large intestine Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue large intestine in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
intestine Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue intestine in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
large intestine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue large intestine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
intestine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue intestine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
intestine-407 cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue intestine-407 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Large_Intestine-enterocyte of epithelium of large intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Large_Intestine-enterocyte of epithelium of large intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Large_Intestine-intestinal crypt stem cell of large intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Large_Intestine-intestinal crypt stem cell of large intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Large_Intestine-large intestine goblet cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Large_Intestine-large intestine goblet cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Large_Intestine-paneth cell of epithelium of large intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Large_Intestine-paneth cell of epithelium of large intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Large_Intestine-transit amplifying cell of large intestine Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Large_Intestine-transit amplifying cell of large intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Vascular Insufficiency Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vascular Insufficiency Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyp Of Large Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyp Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Malrotation Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Villous Atrophy Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Vascular Insufficiency Of Intestine (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Vascular Insufficiency Of Intestine (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Atresia Of Large Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Neoplasm Of Large Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adhesion Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adhesion Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Ulcer Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Ulcer Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Disorder Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Disorder Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Duplication Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duplication Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Duodenal Obstruction Due To Malrotation Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duodenal Obstruction Due To Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Large Intestine Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Large Intestine Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Simple Diverticular Disease Of Large Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Simple Diverticular Disease Of Large Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Intestine Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Large Intestine Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Large Intestine Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
intestine smooth muscle contraction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intestine smooth muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset. |
determination of intestine left/right asymmetry Gene SetFrom GO Biological Process Annotations 2023 genes participating in the determination of intestine left/right asymmetry biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal intestine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
intestine polyps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the intestine polyps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal large intestine crypts of Lieberkuhn morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal large intestine crypts of Lieberkuhn morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestine physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal large intestine morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal large intestine morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
herniated intestine Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the herniated intestine phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased large intestine adenocarcinoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased large intestine adenocarcinoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed intestine development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed intestine development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired intestine regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired intestine regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal large intestine placement Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal large intestine placement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased intestine copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased intestine length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased intestine length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestine development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestine placement Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine placement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
intraembryonal intestine elongation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the intraembryonal intestine elongation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased intestine length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased intestine length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal large intestine goblet cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal large intestine goblet cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Fetal Development - L2 - Intestine-Stromal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Lymphatic endothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Myeloid cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Vascular endothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Chromaffin cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Erythroblasts Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-ENS glia Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Lymphoid cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Mesothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Smooth muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Intestine-ENS neurons Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
GLP 1 secretion from intestine to portal vein Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 secretion from intestine to portal vein pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
intestine smooth muscle contraction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intestine smooth muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset. |
determination of intestine left/right asymmetry Gene SetFrom GO Biological Process Annotations 2025 genes participating in the determination of intestine left/right asymmetry biological process from the curated GO Biological Process Annotations 2025 dataset. |
Large intestine cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Large intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Large intestine cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Large intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intestine carcinoma in situ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intestine carcinoma in situ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Large intestine adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Large intestine adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Large intestine adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Large intestine adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Large intestine lipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Large intestine lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acute vascular insufficiency of intestine Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute vascular insufficiency of intestine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Angiodysplasia of intestine Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Angiodysplasia of intestine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometriosis of intestine Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometriosis of intestine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intestine Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Intestine from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Large intestine Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Large intestine from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Large intestine Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Large intestine in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Intestine Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Intestine in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Intestine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Intestine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Large intestine Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Large intestine in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
intestine-407 cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue intestine-407 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Neoplasm of the large intestine Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neoplasm of the large intestine phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant hyperthermia susceptibility type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant hyperthermia susceptibility type 2 from the curated CTD Gene-Disease Associations dataset. |
Malignant hyperthermia susceptibility type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant hyperthermia susceptibility type 3 from the curated CTD Gene-Disease Associations dataset. |
Malignant hyperthermia susceptibility type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant hyperthermia susceptibility type 1 from the curated CTD Gene-Disease Associations dataset. |
Malignant hyperthermia susceptibility type 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant hyperthermia susceptibility type 6 from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset. |
Histiocytic Disorders, Malignant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytic Disorders, Malignant from the curated CTD Gene-Disease Associations dataset. |
Malignant Hyperthermia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant Hyperthermia from the curated CTD Gene-Disease Associations dataset. |
Mesothelioma, Malignant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mesothelioma, Malignant from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 from the curated CTD Gene-Disease Associations dataset. |
Malignant hyperthermia susceptibility type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant hyperthermia susceptibility type 4 from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Malignant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Malignant from the curated CTD Gene-Disease Associations dataset. |
Melanoma, Cutaneous Malignant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Melanoma, Cutaneous Malignant from the curated CTD Gene-Disease Associations dataset. |
Malignant hyperthermia susceptibility type 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Malignant hyperthermia susceptibility type 5 from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset. |
Neuroleptic Malignant Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuroleptic Malignant Syndrome from the curated CTD Gene-Disease Associations dataset. |
malignant hyperthermia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease malignant hyperthermia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
malignant glioma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease malignant glioma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
malignant renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant histiocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant histiocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cranial nerve malignant neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranial nerve malignant neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant otitis externa Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant otitis externa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ovarian cyst Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ovarian cyst in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ovarian germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ovarian germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant fibroxanthoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant fibroxanthoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant epithelial mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant epithelial mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant acrospiroma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant acrospiroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant spiradenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant spiradenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant skin fibrous histiocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant skin fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant choroid melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant choroid melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pre-malignant neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pre-malignant neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant conjunctiva melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant conjunctiva melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant iris melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant iris melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant hyperthermia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant hyperthermia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant spindle cell melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant spindle cell melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant struma ovarii Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant struma ovarii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant mesenchymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant mesenchymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant biphasic mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant biphasic mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
invasive malignant thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease invasive malignant thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
balloon cell malignant melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease balloon cell malignant melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
nodular malignant melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nodular malignant melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant granular cell myoblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant granular cell myoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant pineal area germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant pineal area germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mediastinal malignant lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mediastinal malignant lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant pleural mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant pleural mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ovarian surface epithelial-stromal neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ovarian surface epithelial-stromal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
neuroleptic malignant syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuroleptic malignant syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant anus melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant anus melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant fibrous histiocytoma of bone Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant fibrous histiocytoma of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular malignant germ cell cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular malignant germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adult malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant syringoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant syringoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ciliary body melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ciliary body melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
epithelial malignant thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epithelial malignant thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant hyperthermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malignant hyperthermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malignant myeloid disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malignant myeloid disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperthermia, malignant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperthermia, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malignant vascular injury Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malignant vascular injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cutaneous malignant melanoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cutaneous malignant melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malignant melanoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malignant melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cutaneous malignant melanoma. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cutaneous malignant melanoma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ventricular arrhythmia, malignant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ventricular arrhythmia, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuroleptic malignant syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuroleptic malignant syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
extra-adrenal and/or malignant phaeochromocytomas Gene SetFrom GAD Gene-Disease Associations genes associated with the disease extra-adrenal and/or malignant phaeochromocytomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, malignant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malignant cystosarcoma phyllodes and soft tissue sarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malignant cystosarcoma phyllodes and soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malignant Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term malignant in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Malignant mesothelioma of pleura_Pleura_GSE2549 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Malignant mesothelioma of pleura_Pleura_GSE2549 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
malignant glioma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease malignant glioma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
malignant mesothelioma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease malignant mesothelioma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
malignant mesothelioma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the malignant mesothelioma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
malignant gastrointestinal tract tumors Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the malignant gastrointestinal tract tumors phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
malignant neoplasm of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the malignant neoplasm of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
malignant neoplasm of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant neoplasm of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant mesothelioma Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant mesothelioma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant gastrointestinal tract tumors Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant gastrointestinal tract tumors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant hyperthermia Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant hyperthermia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malignant eosinophil proliferation Gene SetFrom HPO Gene-Disease Associations genes associated with the malignant eosinophil proliferation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Malignant Hyperthermia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Malignant Hyperthermia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Malignant Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Malignant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Histiocytoma, Malignant Fibrous Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Histiocytoma, Malignant Fibrous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neuroleptic Malignant Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neuroleptic Malignant Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
susceptible to malignant hyperthermia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the susceptible to malignant hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{malignant hyperthermia susceptibility 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant hyperthermia susceptibility 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malignant hyperthermia susceptibility 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant hyperthermia susceptibility 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
malignant melanoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the malignant melanoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malignant hyperthermia susceptibility 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant hyperthermia susceptibility 2} phenotype from the curated OMIM Gene-Disease 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. |
{melanoma, cutaneous malignant, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, susceptibility to, 10} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, susceptibility to, 10} phenotype from the curated OMIM Gene-Disease Associations dataset. |
melanoma, malignant, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the melanoma, malignant, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 9} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 9} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malignant hyperthermia susceptibility 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant hyperthermia susceptibility 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 7} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 7} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malignant hyperthermia susceptibility 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant hyperthermia susceptibility 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malignant hyperthermia susceptibility 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant hyperthermia susceptibility 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{melanoma, cutaneous malignant, susceptibility to, 8} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {melanoma, cutaneous malignant, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{malignant mesothelioma, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {malignant mesothelioma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
malignant fibrous histiocytoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the malignant fibrous histiocytoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
malignant Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term malignant in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
malignant peripheral nerve sheath cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue malignant peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Malignant Mesothelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mesothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Lymph Node Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Lymph Node in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Lung Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Lung Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Hyperpyrexia Due To Anesthesia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Hyperpyrexia Due To Anesthesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Ascites Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Ascites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Fibrous Histiocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Fibrous Histiocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Head And Neck Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Head And Neck Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Histiocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Squamous Cell Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Squamous Cell Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Liver Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Brain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Bone Marrow Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Colon And/Or Rectum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Colon And/Or Rectum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Pleural Mesothelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Pleural Mesothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Neoplasm To Brain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Neoplasm To Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pleural Effusion, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pleural Effusion, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Resectable Malignant Liver Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Resectable Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Peritoneum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Peritoneum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Of Lateral Wall Of Oropharynx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Lateral Wall Of Oropharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Lateral Wall Of Oropharynx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Lateral Wall Of Oropharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Carcinoid Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Carcinoid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Germ Cell Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Germ Cell Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Omentum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Omentum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Teratoma, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Teratoma, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mesothelioma, Biphasic, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesothelioma, Biphasic, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Locally Recurrent Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Locally Recurrent Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Female Reproductive System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Female Reproductive System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Mesothelioma Of Peritoneum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Mesothelioma Of Peritoneum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Of Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Neoplasm In The Viscera Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Neoplasm In The Viscera in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Adrenal Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Vertebral Column Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Vertebral Column in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Superficial Spreading Malignant Melanoma Of Skin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Superficial Spreading Malignant Melanoma Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Myoepithelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Myoepithelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Neoplasm To The Leptomeninges Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Neoplasm To The Leptomeninges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prostate Stromal Proliferation Of Uncertain Malignant Potential Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prostate Stromal Proliferation Of Uncertain Malignant Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Female Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Spinal Cord Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pleural Mesothelioma Malignant Advanced Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pleural Mesothelioma Malignant Advanced in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Eccrine Spiradenoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Eccrine Spiradenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neuroleptic Malignant Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neuroleptic Malignant Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Ovary And Other Uterine Adnexa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Ovary And Other Uterine Adnexa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Of Head Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Head Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epithelioid Mesothelioma, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epithelioid Mesothelioma, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intratubular Malignant Germ Cells Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intratubular Malignant Germ Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Bone Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Bone Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Skin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Epithelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Epithelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infantile Malignant Osteopetrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infantile Malignant Osteopetrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Malignant Mesothelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Malignant Mesothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Blue Nevus Of Skin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Blue Nevus Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acral Lentiginous Malignant Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acral Lentiginous Malignant Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Desmoplastic Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Desmoplastic Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Uterine Corpus Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Uterine Corpus Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Struma Ovarii, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Struma Ovarii, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Environment-Related Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Environment-Related Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Locally Metastatic Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Locally Metastatic Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Appendix Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Appendix in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Malignant Neoplasm Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Papillary Transitional Cell Neoplasm Of Low Malignant Potential Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Papillary Transitional Cell Neoplasm Of Low Malignant Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Axilla Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Axilla in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Hyperthermia Susceptibility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Hyperthermia Susceptibility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Ameloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Ameloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Ovarian Germ Cell Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Ovarian Germ Cell Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Cystosarcoma Phyllodes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Cystosarcoma Phyllodes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hemangiopericytoma, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hemangiopericytoma, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Hemangiopericytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Hemangiopericytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lymphoepithelial Malignant Thymoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lymphoepithelial Malignant Thymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ebv-Related Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ebv-Related Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Prostate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Solid Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Solid Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Malignant Melanoma Of Skin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Melanoma Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Malignant Melanoma 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Malignant Melanoma 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Insulinoma, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Insulinoma, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Pancreatic Insulinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Pancreatic Insulinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Vaginal Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Vaginal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Rectum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Rectum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Liver Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Malignant Solid Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Catatonia, Malignant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Catatonia, Malignant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Atrophic Papulosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Atrophic Papulosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Mediastinum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Mediastinum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Pleurisy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Pleurisy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mesothelioma Malignant Advanced Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesothelioma Malignant Advanced in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mesothelioma Malignant Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesothelioma Malignant Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Locally Advanced Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Locally Advanced Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Vipoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Vipoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Lipomatous Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Lipomatous Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Neoplasm To The Thyroid Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Neoplasm To The Thyroid 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. |
Secondary Malignant Neoplasm Of Pleura Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Pleura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Paraganglionic Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Paraganglionic Neoplasm 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. |
Inflammatory Malignant Fibrous Histiocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Malignant Fibrous Histiocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Pleural Malignant Mesothelioma Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Pleural Malignant Mesothelioma Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Biliary Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Biliary Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Childhood Central Nervous System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Smooth Muscle Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Smooth Muscle Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Intraocular Non-Hodgkin Malignant Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Intraocular Non-Hodgkin Malignant Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Solid Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Experimental Organism Malignant Hepatocholangiocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Experimental Organism Malignant Hepatocholangiocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Asbestos-Related Malignant Mesothelioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Asbestos-Related Malignant Mesothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Fibrous Histiocytoma Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Fibrous Histiocytoma Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Heart Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Heart in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Storiform-Pleomorphic Malignant Fibrous Histiocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Storiform-Pleomorphic Malignant Fibrous Histiocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Syndrome Nos Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Syndrome Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumour Of Parotid Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumour Of Parotid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Epithelial Neoplasm Of Thyroid Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Epithelial Neoplasm Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Ovarian Thecoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Ovarian Thecoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Placental Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Placental Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Chondroid Syringoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Chondroid Syringoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Adult Brain Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Adult Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Epithelial Neoplasm Of Lung Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Epithelial Neoplasm Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Lymph Nodes Of Neck Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Lymph Nodes Of Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Of Bone Marrow Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Endometrium Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Endometrium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Ovarian Teratoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Ovarian Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Spleen Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Spleen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Transformation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malignant Transformation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Disseminated Malignant Neoplasm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disseminated Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Localized Malignant Neoplasm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Localized Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Malignant Hyperthermia, Susceptibility To, 5 Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malignant Hyperthermia, Susceptibility To, 5 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Malignant Bowel Obstruction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malignant Bowel Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Occupational Malignant Neoplasm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Occupational Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
increased susceptibility to malignant hyperthermia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to malignant hyperthermia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Malignant cell_Bile duct_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant cell_Bile duct_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant cell_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant plasma cell_Bone marrow_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant plasma cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant mesothelioma cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant mesothelioma cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant mesothelioma cell_Pleura_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant mesothelioma cell_Pleura_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant stem cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant stem cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Malignant cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Non-malignant epithelial cell_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Non-malignant epithelial cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Malignant hyperthermia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Malignant hyperthermia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Malignant ovarian surface epithelial-stromal neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Malignant ovarian surface epithelial-stromal neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant exocrine pancreas neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Malignant exocrine pancreas neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant astrocytoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Malignant astrocytoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant astrocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant exocrine pancreas neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant exocrine pancreas neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
pre-malignant neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease pre-malignant neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant ovarian surface epithelial-stromal neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant ovarian surface epithelial-stromal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant ovarian germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant ovarian germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant hyperthermia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant hyperthermia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant pleural mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant pleural mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant cystadenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant cystadenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant choroid melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant choroid melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Testicular malignant germ cell cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Testicular malignant germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant breast melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant breast melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant pheochromocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant pheochromocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant iris melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant iris melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant fibrous histiocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Epithelial malignant thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial malignant thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nodular malignant melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nodular malignant melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Invasive malignant thymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Invasive malignant thymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant spindle cell melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant spindle cell melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cranial nerve malignant neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cranial nerve malignant neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant olfactory nerve neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant olfactory nerve neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mediastinal malignant lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mediastinal malignant lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant conjunctival melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant conjunctival melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant skin fibrous histiocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant skin fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant otitis externa Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant otitis externa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neuroleptic malignant syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuroleptic malignant syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant spiradenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant spiradenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant leptomeningeal neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant leptomeningeal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant syringoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant syringoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant ciliary body melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant ciliary body melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant anus melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant anus melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant pineal area germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant pineal area germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant acrospiroma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant acrospiroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant biphasic mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant biphasic mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant struma ovarii Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant struma ovarii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant epithelial mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant epithelial mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant granular cell myoblastoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant granular cell myoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant fibrous histiocytoma of bone Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant fibrous histiocytoma of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant mesenchymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant mesenchymoma 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. |
Malignant epithelioid hemangioendothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant epithelioid hemangioendothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant ovarian cyst Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant ovarian cyst in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant inflammatory fibrous histiocytoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant inflammatory fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant mediastinal neurogenic neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant mediastinal neurogenic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant adenofibroma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant adenofibroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovarian malignant mesothelioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian malignant mesothelioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adult malignant schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Balloon cell malignant melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Balloon cell malignant melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant histiocytic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant histiocytic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant melanocytic neoplasm of the peripheral nerve sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant melanocytic neoplasm of the peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intermediate malignant teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermediate malignant teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant childhood germ cell neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant childhood germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant gastric teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant gastric teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant cystic nephroma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant cystic nephroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant hypertensive renal disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant hypertensive renal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant peripheral nerve sheath cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Malignant peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Malignant lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant hyperthermia of anesthesia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant hyperthermia of anesthesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant hyperthermia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant hyperthermia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant neoplastic disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant neoplastic disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant hypothermia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant hypothermia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant glioma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant glioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant hyperthermia and exertional rhabdomyolosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant hyperthermia and exertional rhabdomyolosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant hyperthermia equivocal Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant hyperthermia equivocal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant neoplasm of brain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant neoplasm of brain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant migrating partial seizures of infancy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant migrating partial seizures of infancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cutaneous Malignant Melanoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cutaneous Malignant Melanoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant fibrous histiocytoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant fibrous histiocytoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant neoplasm of nervous system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant neoplasm of nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cutaneous malignant melanoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cutaneous malignant melanoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neuroblastoma or malignant cutaneous melanoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuroblastoma or malignant cutaneous melanoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
tumor suppressor arf inhibits ribosomal biogenesis Gene SetFrom Biocarta Pathways proteins participating in the tumor suppressor arf inhibits ribosomal biogenesis pathway from the Biocarta Pathways dataset. |
rb tumor suppressor/checkpoint signaling in response to dna damage Gene SetFrom Biocarta Pathways proteins participating in the rb tumor suppressor/checkpoint signaling in response to dna damage pathway from the Biocarta Pathways dataset. |
WT1-19549856-Wilms tumor-derived CCG99?11-human Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the WT1-19549856-Wilms tumor-derived CCG99?11-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
PTEN hamartoma tumor syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PTEN hamartoma tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Wilms tumor 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Wilms tumor 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rhabdoid tumor predisposition syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rhabdoid tumor predisposition syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rhabdoid tumor predisposition syndrome 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rhabdoid tumor predisposition syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tumor predisposition syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tumor predisposition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
tumor necrosis factor receptor superfamily complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the tumor necrosis factor receptor superfamily complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Tumor necrosis factor receptor 1 signaling complex Gene Setproteins in the Tumor necrosis factor receptor 1 signaling complex protein complex from the CORUM Protein Complexes dataset. |
Mixed Tumor, Mullerian Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mixed Tumor, Mullerian from the curated CTD Gene-Disease Associations dataset. |
Leydig Cell Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leydig Cell Tumor from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, Ehrlich Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Ehrlich Tumor from the curated CTD Gene-Disease Associations dataset. |
Giant Cell Tumor of Bone Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Giant Cell Tumor of Bone from the curated CTD Gene-Disease Associations dataset. |
Phyllodes Tumor of the Prostate Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Phyllodes Tumor of the Prostate from the curated CTD Gene-Disease Associations dataset. |
Testicular Germ Cell Tumor 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Testicular Germ Cell Tumor 1 from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor 4 from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor 3 from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor from the curated CTD Gene-Disease Associations dataset. |
MYELOID TUMOR SUPPRESSOR Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYELOID TUMOR SUPPRESSOR from the curated CTD Gene-Disease Associations dataset. |
Familial Wilms tumor 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset. |
Nonseminomatous germ cell tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nonseminomatous germ cell tumor from the curated CTD Gene-Disease Associations dataset. |
TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 from the curated CTD Gene-Disease Associations dataset. |
Testicular Germ Cell Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Testicular Germ Cell Tumor from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset. |
Tumor Lysis Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tumor Lysis Syndrome from the curated CTD Gene-Disease Associations dataset. |
Rhabdoid Tumor Predisposition Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rhabdoid Tumor Predisposition Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
WILMS TUMOR 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease WILMS TUMOR 5 from the curated CTD Gene-Disease Associations dataset. |
Rhabdoid Tumor Predisposition Syndrome 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rhabdoid Tumor Predisposition Syndrome 1 from the curated CTD Gene-Disease Associations dataset. |
Thymic epithelial tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thymic epithelial tumor from the curated CTD Gene-Disease Associations dataset. |
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor from the curated CTD Gene-Disease Associations dataset. |
Smooth Muscle Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Smooth Muscle Tumor from the curated CTD Gene-Disease Associations dataset. |
Receptors, Tumor Necrosis Factor Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Receptors, Tumor Necrosis Factor in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Carcinoid Tumor Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Carcinoid Tumor in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Receptors, Tumor Necrosis Factor, Type II Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Receptors, Tumor Necrosis Factor, Type II in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Tumor Necrosis Factor-alpha Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Tumor Necrosis Factor-alpha in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
peripheral primitive neuroectodermal tumor Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral primitive neuroectodermal tumor from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
gastrointestinal stromal tumor Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease gastrointestinal stromal tumor from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
seminal vesicle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease seminal vesicle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
islet cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease islet cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cerebral primitive neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
smooth muscle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
benign perivascular tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign perivascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ossifying fibromyxoid tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ossifying fibromyxoid tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
perivascular tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease perivascular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrointestinal neuroendocrine benign tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
askin's tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease askin's tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mixed testicular germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
juvenile type testicular granulosa cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile type testicular granulosa cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tsh producing pituitary tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tsh producing pituitary tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
epidermal appendage tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epidermal appendage tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian primitive germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian primitive germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular yolk sac tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular yolk sac tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intracranial primitive neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intracranial primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone giant cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
granular cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease granular cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intestinal neuroendocrine benign tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atypical teratoid rhabdoid tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atypical teratoid rhabdoid tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
supratentorial primitive neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease supratentorial primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
congenital granular cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital granular cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
giant cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular trophoblastic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular trophoblastic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sex cord-gonadal stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sex cord-gonadal stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
vaginal yolk sac tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vaginal yolk sac tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
vulvar squamous tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar squamous tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian brenner tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian brenner tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atypical lipomatous tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atypical lipomatous tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
perivascular epithelioid cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease perivascular epithelioid cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
prolactin producing pituitary tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prolactin producing pituitary tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pacinian tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pacinian tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
benign breast phyllodes tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign breast phyllodes tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
epithelioid trophoblastic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epithelioid trophoblastic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary wilms' tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary neuroendocrine tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary neuroendocrine tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
megakaryocytic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease megakaryocytic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ehrlich tumor carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ehrlich tumor carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eccrine mixed tumor of skin Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eccrine mixed tumor of skin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hemangiopericytic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hemangiopericytic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dermis tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dermis tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system mesenchymal non-meningothelial tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system mesenchymal non-meningothelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
renal wilms' tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sertoli-leydig cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sertoli-leydig cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pediatric ovarian germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pediatric ovarian germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
non-functioning pancreatic endocrine tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-functioning pancreatic endocrine tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular granulosa cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular granulosa cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrointestinal stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mixed endometrial stromal and smooth muscle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular pure germ cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular pure germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
neuroendocrine tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuroendocrine tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tenosynovial giant cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tenosynovial giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
vulvar glandular tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar glandular tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular leydig cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular leydig cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dysembryoplastic neuroepithelial tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dysembryoplastic neuroepithelial tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adrenal rest tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adrenal rest tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
amyloid tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amyloid tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular germ cell tumor non-seminomatous Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular germ cell tumor non-seminomatous in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pineal parenchymal tumor of intermediate differentiation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pineal parenchymal tumor of intermediate differentiation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
klatskin's tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease klatskin's tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
childhood endodermal sinus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
melanotic neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease melanotic neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pancoast tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pancoast tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
placental site trophoblastic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease placental site trophoblastic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
glomus tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glomus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
epithelial predominant wilms' tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epithelial predominant wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral primitive neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cerebellopontine angle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellopontine angle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adenomatoid tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adenomatoid tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
granulosa cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease granulosa cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tumor of exocrine pancreas Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tumor of exocrine pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sertoli cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sertoli cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
leydig cell tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leydig cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thyroid tumor progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thyroid tumor progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal gland neoplasms; adrenal neoplasm; carney complex; neoplasms, testis; sertoli cell tumor; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carney complex; neoplasms, testis; sertoli cell tumor; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoid tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoid tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rhabdoid tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rhabdoid tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; oropharyngeal neoplasms; papillomavirus infections; squamous cell carcinoma; tumor of oropharynx Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; oropharyngeal neoplasms; papillomavirus infections; squamous cell carcinoma; tumor of oropharynx in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
receptors, tumor necrosis factor, type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease receptors, tumor necrosis factor, type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney neoplasms; nephroblastoma; wilms tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney neoplasms; nephroblastoma; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cancer progression and tumor cell motility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer progression and tumor cell motility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colonic neoplasms; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic neoplasms; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fanconi anemia; fanconi's anemia; kidney neoplasms; nephroblastoma; wilms tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fanconi anemia; fanconi's anemia; kidney neoplasms; nephroblastoma; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor necrosis factor-alpha Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor necrosis factor-alpha in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
papillomavirus infections; skin neoplasms; sunburn; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease papillomavirus infections; skin neoplasms; sunburn; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cytokines; tumor markers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cytokines; tumor markers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor progression of bcr/abl negative chronic myeloproliferative disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor progression of bcr/abl negative chronic myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
testicular germ cell tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease testicular germ cell tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
granulosa cell tumor; neoplasms; ovarian neoplasm; ovarian neoplasms; thecoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease granulosa cell tumor; neoplasms; ovarian neoplasm; ovarian neoplasms; thecoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mucinous ovarian tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mucinous ovarian tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
risk factors and tumor characteristics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease risk factors and tumor characteristics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoid tumor; gastrointestinal neoplasms; neuroendocrine tumors; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoid tumor; gastrointestinal neoplasms; neuroendocrine tumors; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; flushing; oesophageal neoplasm; oropharyngeal neoplasms; squamous cell carcinoma; tumor of oropharynx Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; flushing; oesophageal neoplasm; oropharyngeal neoplasms; squamous cell carcinoma; tumor of oropharynx in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sepsis; serum tumor necrosis factor-alpha levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sepsis; serum tumor necrosis factor-alpha levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney neoplasms; wilms tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney neoplasms; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wilms' tumor and congenital male genitourinary malformation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor proliferation and other prognostic indicators Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor proliferation and other prognostic indicators in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor necrosis factor-alpha responses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor necrosis factor-alpha responses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor necrosis factor receptor-associated periodic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor necrosis factor receptor-associated periodic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
receptors, tumor necrosis factor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease receptors, tumor necrosis factor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cytomegalovirus infections; epstein-barr virus infections; polyomavirus infections; recurrence; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cytomegalovirus infections; epstein-barr virus infections; polyomavirus infections; recurrence; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; oropharyngeal neoplasms; tumor of oropharynx Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; oropharyngeal neoplasms; tumor of oropharynx in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney neoplasms; neoplasms, second primary; wilms tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney neoplasms; neoplasms, second primary; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cell transformation, neoplastic; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; tumor virus infections; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wilm's tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wilm's tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; oropharyngeal neoplasms; squamous cell carcinoma; tumor of oropharynx Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; oropharyngeal neoplasms; squamous cell carcinoma; tumor of oropharynx in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nerve sheath neoplasms; neurofibroma; [m]nerve sheath tumor nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nerve sheath neoplasms; neurofibroma; [m]nerve sheath tumor nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
laryngeal neoplasm; laryngeal neoplasms; neoplasm recurrence, local; papilloma; papillomavirus infections; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasm recurrence, local; papilloma; papillomavirus infections; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wilms tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor progression and patient survival Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor progression and patient survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
defense response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the defense response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to tumor necrosis factor Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to tumor necrosis factor biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of tumor necrosis factor superfamily cytokine production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of tumor necrosis factor superfamily cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset. |
tumor necrosis factor-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the tumor necrosis factor-mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of tumor necrosis factor-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of tumor necrosis factor-mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of natural killer cell mediated immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of natural killer cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of tumor necrosis factor-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of tumor necrosis factor-mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of tumor necrosis factor production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of tumor necrosis factor production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of t cell mediated immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of t cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of tumor necrosis factor biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of tumor necrosis factor biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to tumor necrosis factor Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to tumor necrosis factor biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of tumor necrosis factor superfamily cytokine production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of tumor necrosis factor superfamily cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of natural killer cell mediated cytotoxicity directed against tumor cell target Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of natural killer cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of tumor necrosis factor production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of tumor necrosis factor production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of natural killer cell mediated immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of natural killer cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of tumor necrosis factor biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of tumor necrosis factor biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of tumor necrosis factor (ligand) superfamily member 11 production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of tumor necrosis factor (ligand) superfamily member 11 production biological process from the curated GO Biological Process Annotations 2015 dataset. |
tumor necrosis factor production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the tumor necrosis factor production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of tumor necrosis factor biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of tumor necrosis factor biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
tumor necrosis factor superfamily cytokine production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the tumor necrosis factor superfamily cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of tumor necrosis factor-mediated signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of tumor necrosis factor-mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of tumor necrosis factor superfamily cytokine production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of tumor necrosis factor superfamily cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of t cell mediated immune response to tumor cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of t cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of tumor necrosis factor production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of tumor necrosis factor production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of natural killer cell mediated cytotoxicity directed against tumor cell target Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of natural killer cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2015 dataset. |
tumor necrosis factor receptor superfamily complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the tumor necrosis factor receptor superfamily complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
tumor necrosis factor-activated receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the tumor necrosis factor-activated receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
tumor necrosis factor receptor superfamily binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the tumor necrosis factor receptor superfamily binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
tumor necrosis factor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the tumor necrosis factor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
tumor necrosis factor receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the tumor necrosis factor receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Wilms tumor Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Wilms tumor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Testicular germ cell tumor Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Testicular germ cell tumor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Tumor biomarkers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Tumor biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
peripheral primitive neuroectodermal tumor Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease peripheral primitive neuroectodermal tumor in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
nephroblastoma (wilms tumor) Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the nephroblastoma (wilms tumor) phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
primitive neuroectodermal tumor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the primitive neuroectodermal tumor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vocal cord paralysis (caused by tumor impingement) Gene SetFrom HPO Gene-Disease Associations genes associated with the vocal cord paralysis (caused by tumor impingement) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gastrointestinal stroma tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the gastrointestinal stroma tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
keratocystic odontogenic tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the keratocystic odontogenic tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
glomus jugular tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the glomus jugular tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lipomatous tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the lipomatous tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primitive neuroectodermal tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the primitive neuroectodermal tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
precocious puberty with sertoli cell tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the precocious puberty with sertoli cell tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nephroblastoma (wilms tumor) Gene SetFrom HPO Gene-Disease Associations genes associated with the nephroblastoma (wilms tumor) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hoarse voice (caused by tumor impingement) Gene SetFrom HPO Gene-Disease Associations genes associated with the hoarse voice (caused by tumor impingement) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal cord tumor Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal cord tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Giant Cell Tumor of Bone Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Giant Cell Tumor of Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Tumor Virus Infections Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Tumor Virus Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carcinoid Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoid Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Granulosa Cell Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Granulosa Cell Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Wilms Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Wilms Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Adrenal Rest Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Adrenal Rest Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Sertoli Cell Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sertoli Cell Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Glomus Jugulare Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Glomus Jugulare Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Phyllodes Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Phyllodes Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carotid Body Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carotid Body Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Rhabdoid Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Rhabdoid Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Endodermal Sinus Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Endodermal Sinus Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Glomus Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Glomus Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Smooth Muscle Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Smooth Muscle Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Tumor protein p53-inducible protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor necrosis factor ligand superfamily member 15 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor necrosis factor ligand superfamily member 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor necrosis factor ligand superfamily member 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor necrosis factor ligand superfamily member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
tumor regression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the tumor regression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased gastrointestinal tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased gastrointestinal tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mammary gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mammary gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased kidney tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased kidney tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased thymus tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased thymus tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased liver tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased liver tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased hepatobiliary system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased hepatobiliary system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased organ/body region tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tumor latency Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tumor latency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cardiovascular system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cardiovascular system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased integument system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased integument system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased adrenal gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased adrenal gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pituitary adenohypophysis tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pituitary adenohypophysis tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tumor latency Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tumor latency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased alimentary system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased alimentary system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased granulosa cell tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased granulosa cell tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased organ/body region tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
altered tumor susceptibility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the altered tumor susceptibility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased muscle tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased muscle tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pituitary melanotroph tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pituitary melanotroph tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased reproductive system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased reproductive system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased nervous system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased nervous system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased desmoid tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased desmoid tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased respiratory system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased respiratory system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pituitary gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pituitary gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tumor vascularization Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tumor vascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased urinary system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased urinary system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tumor necrosis factor secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tumor necrosis factor secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tumor growth/size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tumor growth/size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lung tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lung tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal organ/body region tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
altered tumor pathology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the altered tumor pathology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased skeletal tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased skeletal tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brain tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brain tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased leydig cell tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased leydig cell tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal classified tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal classified tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tumor incidence following infection Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tumor incidence following infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased lung tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lung tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased sebaceous gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased sebaceous gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased prostate gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased prostate gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tumor necrosis factor secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tumor necrosis factor secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased thyroid tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased thyroid tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased testis tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased testis tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased adrenal cortical tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased adrenal cortical tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased uterus tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased uterus tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased hepatobiliary system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased hepatobiliary system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased liver tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased liver tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased hemolymphoid system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased hemolymphoid system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased harderian gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased harderian gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased facial tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased facial tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tumor latency Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tumor latency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased skin tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased skin tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased parathyroid gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased parathyroid gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased integument system tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased integument system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased classified tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased classified tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tumor growth/size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tumor growth/size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased salivary gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased salivary gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased classified tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased classified tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased colon tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased colon tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mammary gland tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mammary gland tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased gastrointestinal stromal tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased gastrointestinal stromal tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tumor necrosis factor secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tumor necrosis factor secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
altered tumor morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the altered tumor morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mouth tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mouth tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased stomach tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased stomach tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |