| Name |
|---|
LARGE Genelike-glycosyltransferase This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018] |
LARGE-AS1 GeneLARGE antisense RNA 1 |
LARGE-IT1 GeneLARGE intronic transcript 1 |
DLGAP2 Genediscs, large (Drosophila) homolog-associated protein 2 The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014] |
DLGAP3 Genediscs, large (Drosophila) homolog-associated protein 3 Predicted to enable PDZ domain binding activity; molecular adaptor activity; and scaffold protein binding activity. Predicted to be involved in modulation of chemical synaptic transmission and protein-containing complex assembly. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including cholinergic synapse; glutamatergic synapse; and neuromuscular junction. [provided by Alliance of Genome Resources, Mar 2025] |
DLGAP1 Genediscs, large (Drosophila) homolog-associated protein 1 Predicted to enable molecular adaptor activity. Predicted to be a structural constituent of postsynaptic density. Predicted to be involved in several processes, including aggresome assembly; protein localization to synapse; and regulation of proteasomal protein catabolic process. Predicted to be located in plasma membrane. Predicted to be active in glutamatergic synapse and postsynaptic density, intracellular component. [provided by Alliance of Genome Resources, Mar 2025] |
DLGAP4 Genediscs, large (Drosophila) homolog-associated protein 4 The product of this gene is a membrane-associated guanylate kinase found at the postsynaptic density in neuronal cells. It is a signaling molecule that can interact with potassium channels and receptors, as well as other signaling molecules. The protein encoded by this gene can interact with PSD-95 through its guanylate kinase domain and may be involved in clustering PSD-95 in the postsynaptic density region. The encoded protein is one of at least four similar proteins that have been found. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
DLGAP5 Genediscs, large (Drosophila) homolog-associated protein 5 Predicted to enable microtubule binding activity. Predicted to be involved in several processes, including centrosome localization; kinetochore assembly; and mitotic spindle organization. Located in cytosol; nucleus; and spindle. [provided by Alliance of Genome Resources, Mar 2025] |
RPLP2P2 Generibosomal protein, large, P2 pseudogene 2 |
RPLP0P10 Generibosomal protein, large, P0 pseudogene 10 |
LOC390860 Generibosomal protein, large, P0 pseudogene |
RPLP1P12 Generibosomal protein, large, P1 pseudogene 12 |
RPLP1P13 Generibosomal protein, large, P1 pseudogene 13 |
RPLP1P10 Generibosomal protein, large, P1 pseudogene 10 |
RPLP1P11 Generibosomal protein, large, P1 pseudogene 11 |
RPLP0P11 Generibosomal protein, large, P0 pseudogene 11 |
KCNMA1 Genepotassium channel, calcium activated large conductance subfamily M alpha, member 1 This gene encodes the alpha subunit of calcium-activated BK channel. The encoded protein is involved in several physiological processes including smooth muscle contraction, neurotransmitter release and neuronal excitability. Mutations in this gene are associated with a spectrum of neurological disorders including Paroxysmal Nonkinesigenic Dyskinesia 3, Idiopathic Generalized Epilepsy 16 and Liang-Wang syndrome. [provided by RefSeq, Aug 2022] |
LOC101930420 GeneDNA primase large subunit-like |
RPLP1P1 Generibosomal protein, large, P1 pseudogene 1 |
RPLP1P3 Generibosomal protein, large, P1 pseudogene 3 |
RPLP1P4 Generibosomal protein, large, P1 pseudogene 4 |
RPLP1P5 Generibosomal protein, large, P1 pseudogene 5 |
RPLP1P7 Generibosomal protein, large, P1 pseudogene 7 |
RPLP1P8 Generibosomal protein, large, P1 pseudogene 8 |
RPLP1P9 Generibosomal protein, large, P1 pseudogene 9 |
DLG3 Genediscs, large homolog 3 (Drosophila) This gene encodes a member of the membrane-associated guanylate kinase protein family. The encoded protein may play a role in clustering of NMDA receptors at excitatory synapses. It may also negatively regulate cell proliferation through interaction with the C-terminal region of the adenomatosis polyposis coli tumor suppressor protein. Mutations in this gene have been associated with X-linked cognitive disability. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009] |
DLG2 Genediscs, large homolog 2 (Drosophila) This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. The encoded protein forms a heterodimer with a related family member that may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described, but their full-length nature is not known. [provided by RefSeq, Dec 2008] |
DLG5 Genediscs, large homolog 5 (Drosophila) This gene encodes a member of the family of discs large (DLG) homologs, a subset of the membrane-associated guanylate kinase (MAGUK) superfamily. The MAGUK proteins are composed of a catalytically inactive guanylate kinase domain, in addition to PDZ and SH3 domains, and are thought to function as scaffolding molecules at sites of cell-cell contact. The protein encoded by this gene localizes to the plasma membrane and cytoplasm, and interacts with components of adherens junctions and the cytoskeleton. It is proposed to function in the transmission of extracellular signals to the cytoskeleton and in the maintenance of epithelial cell structure. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008] |
DLG1 Genediscs, large homolog 1 (Drosophila) This gene encodes a multi-domain scaffolding protein that is required for normal development. This protein may have a role in septate junction formation, signal transduction, cell proliferation, synaptogenesis and lymphocyte activation. A multitude of transcript variants deriving from alternative splicing and the use of multiple alternate promoter have been observed, including some splice variants that may be specific to brain and other tissues. An upstream uORF may regulate translation at some splice variants of this gene. [provided by RefSeq, Sep 2018] |
DLG4 Genediscs, large homolog 4 (Drosophila) This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. It heteromultimerizes with another MAGUK protein, DLG2, and is recruited into NMDA receptor and potassium channel clusters. These two MAGUK proteins may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
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] |
RPLP0P9 Generibosomal protein, large, P0 pseudogene |
RPLP0P8 Generibosomal protein, large, P0 pseudogene 8 |
RPLP0P1 Generibosomal protein, large, P0 pseudogene 1 |
RPLP0P3 Generibosomal protein, large, P0 pseudogene 3 |
RPLP0P2 Generibosomal protein, large, P0 pseudogene 2 |
RPLP0P5 Generibosomal protein, large, P0 pseudogene 5 |
RPLP0P4 Generibosomal protein, large, P0 pseudogene 4 |
RPLP0P7 Generibosomal protein, large, P0 pseudogene 7 |
RPLP0P6 Generibosomal protein, large, P0 pseudogene 6 Predicted to enable large ribosomal subunit rRNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in cytoplasmic translation. Predicted to be located in ribosome. Predicted to be part of cytosolic large ribosomal subunit. [provided by Alliance of Genome Resources, Mar 2025] |
RPLP2 Generibosomal protein, large, P2 Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P1. The P2 protein can interact with P0 and P1 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008] |
RPLP1 Generibosomal protein, large, P1 Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal phosphoprotein that is a component of the 60S subunit. The protein, which is a functional equivalent of the E. coli L7/L12 ribosomal protein, belongs to the L12P family of ribosomal proteins. It plays an important role in the elongation step of protein synthesis. Unlike most ribosomal proteins, which are basic, the encoded protein is acidic. Its C-terminal end is nearly identical to the C-terminal ends of the ribosomal phosphoproteins P0 and P2. The P1 protein can interact with P0 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Two alternatively spliced transcript variants that encode different proteins have been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008] |
RPLP0 Generibosomal protein, large, P0 Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein, which is the functional equivalent of the E. coli L10 ribosomal protein, belongs to the L10P family of ribosomal proteins. It is a neutral phosphoprotein with a C-terminal end that is nearly identical to the C-terminal ends of the acidic ribosomal phosphoproteins P1 and P2. The P0 protein can interact with P1 and P2 to form a pentameric complex consisting of P1 and P2 dimers, and a P0 monomer. The protein is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008] |
MALSU1 Genemitochondrial assembly of ribosomal large subunit 1 Enables mitochondrial large ribosomal subunit binding activity. Involved in negative regulation of mitochondrial translation and ribosomal large subunit biogenesis. Located in cytosol and mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
DLGAP5P1 Genediscs, large (Drosophila) homolog-associated protein 5 pseudogene 1 |
LSG1 Genelarge 60S subunit nuclear export GTPase 1 This gene encodes a protein related to the yeast large subunit GTPase 1. The encoded protein is necessary for cell viability and may localize in the endoplasmic reticulum, nucleus and cytoplasm.[provided by RefSeq, Feb 2009] |
GVINP1 GeneGTPase, very large interferon inducible pseudogene 1 Predicted to enable GTP binding activity. Predicted to be located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
GVINP2 GeneGTPase, very large interferon inducible pseudogene 2 |
RPLP2P3 Generibosomal protein, large, P2 pseudogene 3 |
RPLP2P1 Generibosomal protein, large P2, pseudogene 1 |
RPLP2P5 Generibosomal protein, large, P2 pseudogene 5 |
RPLP2P4 Generibosomal protein, large, P2 pseudogene 4 |
CAPN2 Genecalpain 2, (m/II) large subunit The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 2. Multiple heterogeneous transcriptional start sites in the 5' UTR have been reported. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009] |
CAPN1 Genecalpain 1, (mu/I) large subunit The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes the large subunit of the ubiquitous enzyme, calpain 1. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010] |
RPLP1P2 Generibosomal protein, large, P1 pseudogene 2 |
RPLP1P6 Generibosomal protein, large, P1 pseudogene 6 |
LARGE2 GeneLARGE xylosyl- and glucuronyltransferase 2 Predicted to enable dystroglycan binding activity; glucuronosyltransferase activity; and xylosyltransferase activity. Involved in protein O-linked mannosylation. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
LARGE1 GeneLARGE xylosyl- and glucuronyltransferase 1 This gene encodes a member of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, and may carry out the synthesis of glycoprotein and glycosphingolipid sugar chains. It may also be involved in the addition of a repeated disaccharide unit. The protein encoded by this gene is the glycotransferase that adds the final xylose and glucuronic acid to alpha-dystroglycan and thereby allows alpha-dystroglycan to bind ligands including laminin 211 and neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized by cognitive disability and abnormal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2018] |
RLTPR GeneRGD motif, leucine rich repeats, tropomodulin domain and proline-rich containing This gene encodes a member of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with and negatively regulates the heterodimeric capping protein and promotes cell migration. Reduced expression of this gene has been observed in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized by smooth muscle tumors and impaired T-cell function. [provided by RefSeq, May 2017] |
PRELP Geneproline/arginine-rich end leucine-rich repeat protein The protein encoded by this gene is a leucine-rich repeat protein present in connective tissue extracellular matrix. This protein functions as a molecule anchoring basement membranes to the underlying connective tissue. This protein has been shown to bind type I collagen to basement membranes and type II collagen to cartilage. It also binds the basement membrane heparan sulfate proteoglycan perlecan. This protein is suggested to be involved in the pathogenesis of Hutchinson-Gilford progeria (HGP), which is reported to lack the binding of collagen in basement membranes and cartilage. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008] |
LOC100631309 Geneproline rich 21 pseudogene |
FBXL14 GeneF-box and leucine-rich repeat protein 14 Members of the F-box protein family, such as FBXL14, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008] |
FBXL19 GeneF-box and leucine-rich repeat protein 19 This gene encodes a member of the Skp1-Cullin-F-box family of E3 ubiquitin ligases. The encoded protein is reported to bind to the transmembrane receptor interleukin 1 receptor-like 1 and regulate its ubiquitination and degradation. This protein has been linked to the regulation of pulmonary inflammation and psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
DMRTB1 GeneDMRT-like family B with proline-rich C-terminal, 1 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in germ cell development; regulation of transcription by RNA polymerase II; and sex differentiation. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC37A10P Geneleucine rich repeat containing 37, member A10, pseudogene |
LOC105378957 Genebasic salivary proline-rich protein 2-like |
LRRC27 Geneleucine rich repeat containing 27 Predicted to enable actin binding activity. Predicted to be involved in cardiac muscle cell development. Predicted to be active in cytoskeleton and sarcomere. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC26 Geneleucine rich repeat containing 26 Enables potassium channel activator activity; transmembrane transporter binding activity; and voltage-gated potassium channel activity. Involved in positive regulation of voltage-gated potassium channel activity and potassium ion transmembrane transport. Located in plasma membrane. Part of voltage-gated potassium channel complex. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC24 Geneleucine rich repeat containing 24 Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in external side of plasma membrane; extracellular matrix; and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC23 Geneleucine rich repeat containing 23 Involved in flagellated sperm motility and radial spoke assembly. Located in sperm flagellum. Implicated in spermatogenic failure 92. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC20 Geneleucine rich repeat containing 20 |
LRRC29 Geneleucine rich repeat containing 29 This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains 9 tandem leucine-rich repeats. Two transcript variants encoding the same protein have been found for this gene. Other variants may occur, but their full-length natures have not been characterized. [provided by RefSeq, Jul 2008] |
LRRC28 Geneleucine rich repeat containing 28 Predicted to be involved in intracellular signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
LRRN4 Geneleucine rich repeat neuronal 4 Predicted to be involved in long-term memory. Predicted to act upstream of or within visual learning. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
LRRN1 Geneleucine rich repeat neuronal 1 Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in extracellular matrix and extracellular space. Biomarker of stomach cancer. [provided by Alliance of Genome Resources, Mar 2025] |
SRSF9P1 Geneserine/arginine-rich splicing factor 9 pseudogene 1 |
RSRC1 Genearginine/serine-rich coiled-coil 1 This gene encodes a member of the serine and arginine rich-related protein family. The encoded protein is involved in both constitutive and alternative mRNA splicing. This gene may be associated with schizophrenia. A pseudogene of this gene is located on chromosome 9. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012] |
RSRC2 Genearginine/serine-rich coiled-coil 2 Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420832 Genecysteine and glycine-rich protein 2 pseudogene |
CITED1 GeneCbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1 This gene encodes a member of the CREB-binding protein/p300-interacting transactivator with Asp/Glu-rich C-terminal domain (CITED) family of proteins. The encoded protein, also known as melanocyte-specific gene 1, may function as a transcriptional coactivator and may play a role in pigmentation of melanocytes. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009] |
CITED4 GeneCbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4 The protein encoded by this intronless gene belongs to the CITED family of transcriptional coactivators that bind to several proteins, including CREB-binding protein (CBP) and p300, via a conserved 32 aa C-terminal motif, and regulate gene transcription. This protein also interacts with transcription factor AP2 (TFAP2), and thus may function as a co-activator for TFAP2. Hypermethylation and transcriptional downregulation of this gene has been observed in oligodendroglial tumors with deletions of chromosomal arms 1p and 19q, and associated with longer recurrence-free and overall survival of patients with oligodendroglial tumors. [provided by RefSeq, Aug 2011] |
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] |
LOC100130639 Geneleucine rich repeat containing 3C pseudogene |
PHGR1 Geneproline/histidine/glycine-rich 1 |
LOC100131877 Genesmall EDRK-rich factor 2 pseudogene |
LRRC25 Geneleucine rich repeat containing 25 Located in cytosol; endoplasmic reticulum; and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
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] |
FLRT1 Genefibronectin leucine rich transmembrane protein 1 This gene encodes a member of the fibronectin leucine rich transmembrane protein (FLRT) family. The family members may function in cell adhesion and/or receptor signalling. Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix. The encoded protein shares sequence similarity with two other family members, FLRT2 and FLRT3. This gene is expressed in kidney and brain. [provided by RefSeq, Jul 2008] |
FLRT3 Genefibronectin leucine rich transmembrane protein 3 This gene encodes a member of the fibronectin leucine rich transmembrane protein (FLRT) family. FLRTs may function in cell adhesion and/or receptor signalling. Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix. This gene is expressed in many tissues. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2010] |
FLRT2 Genefibronectin leucine rich transmembrane protein 2 This gene encodes a member of the fibronectin leucine rich transmembrane (FLRT) family of cell adhesion molecules, which regulate early embryonic vascular and neural development. The encoded type I transmembrane protein has an extracellular region consisting of an N-terminal leucine-rich repeat domain and a type 3 fibronectin domain, followed by a transmembrane domain and a short C-terminal cytoplasmic tail domain. It functions as both a homophilic cell adhesion molecule and a heterophilic chemorepellent through its interaction with members of the uncoordinated-5 receptor family. Proteolytic removal of the extracellular region controls the migration of neurons in the developing cortex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
LOC105378176 Geneproline-rich receptor-like protein kinase PERK2 |
PRR13P3 Geneproline rich 13 pseudogene 3 |
PRR13P1 Geneproline rich 13 pseudogene 1 |
LRRC37A2 Geneleucine rich repeat containing 37, member A2 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC37A3 Geneleucine rich repeat containing 37, member A3 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PRR13P5 Geneproline rich 13 pseudogene 5 |
PRR13P4 Geneproline rich 13 pseudogene 4 |
BCL2L12 GeneBCL2-like 12 (proline rich) This gene encodes a member of a family of proteins containing a Bcl-2 homology domain 2 (BH2). The encoded protein is an anti-apoptotic factor that acts as an inhibitor of caspases 3 and 7 in the cytoplasm. In the nucleus, it binds to the p53 tumor suppressor protein, preventing its association with target genes. Overexpression of this gene has been detected in a number of different cancers. There is a pseudogene for this gene on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
CHIC2 Genecysteine-rich hydrophobic domain 2 This gene encodes a member of the CHIC family of proteins. The encoded protein contains a cysteine-rich hydrophobic (CHIC) motif, and is localized to vesicular structures and the plasma membrane. This gene is associated with some cases of acute myeloid leukemia. [provided by RefSeq, Jul 2008] |
CHIC1 Genecysteine-rich hydrophobic domain 1 This gene encodes a cysteine-rich hydrophobic (CHIC) domain-containing protein, and is one of the few protein-coding genes found near the X-inactivation center. Studies in mouse indicate that the mouse ortholog of this gene is subject to X-inactivation in mouse. Experiments with other CHIC domain-containing family members show that the cysteine residues are palmitoylated post-translationally, resulting in membrane association. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017] |
LOC105377133 Genebasic proline-rich protein-like |
SREK1 Genesplicing regulatory glutamine/lysine-rich protein 1 This gene encodes a member of a family of serine/arginine-rich (SR) splicing proteins containing RNA recognition motif (RRM) domains. The encoded protein interacts with other SR proteins to modulate splice site selection. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
LOC100131747 Genesmall EDRK-rich factor 2 pseudogene |
CDPF1 Genecysteine-rich, DPF motif domain containing 1 |
JARID2 Genejumonji, AT rich interactive domain 2 This gene encodes a Jumonji- and AT-rich interaction domain (ARID)-domain-containing protein. The encoded protein is a DNA-binding protein that functions as a transcriptional repressor. This protein interacts with the Polycomb repressive complex 2 (PRC2) which plays an essential role in regulating gene expression during embryonic development. This protein facilitates the recruitment of the PRC2 complex to target genes. Alternate splicing results in multiple transcript variants. Mutations in this gene are associated with chronic myeloid malignancies. [provided by RefSeq, May 2012] |
PRH2 Geneproline-rich protein HaeIII subfamily 2 This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. In western population this locus is commonly biallelic and encodes proline-rich protein (PRP) isoforms, PRP-1 and PRP-2. The reference genome encodes the PRP-1 allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Oct 2015] |
PRH1 Geneproline-rich protein HaeIII subfamily 1 This gene encodes a member of the heterogeneous family of proline-rich salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid and submandibular/sublingual glands. Multiple distinct alleles of this locus including the parotid isoelectric-focusing variant slow (PIF-s), the parotid acidic protein (Pa), and the double band slow (Db-s) isoforms have been characterized. The reference genome encodes the Db-s allele. Certain alleles of this gene are associated with susceptibility to dental caries. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Co-transcription of this gene with adjacent genes has been observed. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015] |
LOC105371804 Geneleucine-rich repeat-containing protein 37A3 pseudogene |
LOC105372013 Genebasic salivary proline-rich protein 2-like |
LRRC9 Geneleucine rich repeat containing 9 Predicted to enable U2 snRNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC4 Geneleucine rich repeat containing 4 Predicted to be involved in modulation of chemical synaptic transmission and synapse organization. Predicted to act upstream of or within synapse organization. Predicted to be located in dendritic spine; excitatory synapse; and postsynaptic membrane. Predicted to be active in Schaffer collateral - CA1 synapse; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC6 Geneleucine rich repeat containing 6 The protein encoded by this gene contains several leucine-rich repeat domains and appears to be involved in the motility of cilia. Defects in this gene are a cause of primary ciliary dyskinesia-19 (CILD19). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4, 11 and 22. [provided by RefSeq, Apr 2016] |
LRRC7 Geneleucine rich repeat containing 7 Predicted to enable protein kinase binding activity. Predicted to be involved in several processes, including establishment or maintenance of epithelial cell apical/basal polarity; protein localization to postsynapse; and receptor clustering. Located in several cellular components, including centrosome; cytosol; and nucleoplasm. Implicated in cocaine dependence. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC1 Geneleucine rich repeat containing 1 Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC3 Geneleucine rich repeat containing 3 Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LSMEM1 Geneleucine-rich single-pass membrane protein 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LSMEM2 Geneleucine-rich single-pass membrane protein 2 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SRSF11 Geneserine/arginine-rich splicing factor 11 This gene encodes 54-kD nuclear protein that contains an arginine/serine-rich region similar to segments found in pre-mRNA splicing factors. Although the function of this protein is not yet known, structure and immunolocalization data suggest that it may play a role in pre-mRNA processing. Alternative splicing results in multiple transcript variants encoding different proteins. In addition, a pseudogene of this gene has been found on chromosome 12.[provided by RefSeq, Sep 2010] |
SRSF10 Geneserine/arginine-rich splicing factor 10 This gene product is a member of the serine-arginine (SR) family of proteins, which are involved in constitutive and regulated RNA splicing. Members of this family are characterized by N-terminal RNP1 and RNP2 motifs, which are required for binding to RNA, and multiple C-terminal SR/RS repeats, which are important in mediating association with other cellular proteins. This protein interacts with the oncoprotein TLS, and abrogates the influence of TLS on adenovirus E1A pre-mRNA splicing. This gene has pseudogenes on chromosomes 4, 9, 14, 18, and 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
SRSF12 Geneserine/arginine-rich splicing factor 12 Enables RNA binding activity. Involved in mRNA 5'-splice site recognition and regulation of alternative mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be active in nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
HNRNPDP1 Geneheterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) pseudogene 1 |
PRR30 Geneproline rich 30 |
PRR31 Geneproline rich 31 |
PRR32 Geneproline rich 32 |
PRR33 Geneproline rich 33 Predicted to act upstream of or within response to wounding. [provided by Alliance of Genome Resources, Mar 2025] |
PRR34 Geneproline rich 34 |
PRR35 Geneproline rich 35 |
PRR36 Geneproline rich 36 This gene encodes a large protein of unknown function that contains internal regions of low complexity sequence. Alternative splicing results in multiple transcript variants. The transcript structure of the protein-coding variant at this locus is conserved between human and mouse. [provided by RefSeq, Oct 2013] |
LOC642515 Geneproline-rich transmembrane protein 1-like Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC18 Geneleucine rich repeat containing 18 Predicted to enable protein serine/threonine phosphatase activity. Predicted to be involved in intracellular signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC19 Geneleucine rich repeat containing 19 Predicted to enable signaling receptor activity. Acts upstream of or within positive regulation of non-canonical NF-kappaB signal transduction. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC17 Geneleucine rich repeat containing 17 Predicted to be involved in bone marrow development and negative regulation of osteoclast differentiation. Predicted to be located in extracellular region. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC14 Geneleucine rich repeat containing 14 This gene encodes a leucine-rich repeat-containing protein. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
LRRC15 Geneleucine rich repeat containing 15 Enables several functions, including fibronectin binding activity; laminin binding activity; and protein sequestering activity. Involved in several processes, including negative regulation of protein localization to plasma membrane; negative regulation of viral entry into host cell; and receptor-mediated virion attachment to host cell. Located in collagen-containing extracellular matrix and plasma membrane. Is active in apical plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC10 Geneleucine rich repeat containing 10 Predicted to enable actin binding activity. Predicted to be involved in cardiac muscle cell development. Predicted to be located in mitochondrion; myofibril; and nucleus. Predicted to be active in cytoskeleton and sarcomere. [provided by Alliance of Genome Resources, Mar 2025] |
AARD Genealanine and arginine rich domain containing protein Predicted to act upstream of or within response to testosterone. [provided by Alliance of Genome Resources, Mar 2025] |
CRISPLD2 Genecysteine-rich secretory protein LCCL domain containing 2 Predicted to enable glycosaminoglycan binding activity. Involved in face morphogenesis. Located in transport vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
CRISPLD1 Genecysteine-rich secretory protein LCCL domain containing 1 Involved in face morphogenesis. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
FBXL20 GeneF-box and leucine-rich repeat protein 20 Members of the F-box protein family, such as FBXL20, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008] |
FBXL21 GeneF-box and leucine-rich repeat protein 21 (gene/pseudogene) This locus represents a transcribed pseudogene that is related to genes encoding members of the F-box family of proteins. [provided by RefSeq, Nov 2017] |
FBXL22 GeneF-box and leucine-rich repeat protein 22 This gene encodes a member of the F-box protein family. This F-box protein interacts with S-phase kinase-associated protein 1A and cullin in order to form SCF complexes which function as ubiquitin ligases.[provided by RefSeq, Sep 2010] |
LOC105378101 Genebasic proline-rich protein-like |
CYYR1-AS1 Genecysteine/tyrosine-rich 1 antisense RNA 1 |
LRRK1 Geneleucine-rich repeat kinase 1 This gene encodes a multi-domain protein that is a leucine-rich repeat kinase and a GDP/GTP binding protein. The encoded protein is thought to play a role in the regulation of bone mass. Mice lacking a similar gene showed severe osteopetrosis, increased bone mineralization and decreased bone resorption. [provided by RefSeq, Jan 2017] |
LRRK2 Geneleucine-rich repeat kinase 2 This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a RAS domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8. [provided by RefSeq, Jul 2008] |
PHLPP1 GenePH domain and leucine rich repeat protein phosphatase 1 This gene encodes a member of the serine/threonine phosphatase family. The encoded protein promotes apoptosis by dephosphorylating and inactivating the serine/threonine kinase Akt, and functions as a tumor suppressor in multiple types of cancer. Increased expression of this gene may also play a role in obesity and type 2 diabetes by interfering with Akt-mediated insulin signaling. [provided by RefSeq, Dec 2011] |
HRCT1 Genehistidine rich carboxyl terminus 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SSC5D Genescavenger receptor cysteine rich family, 5 domains Predicted to enable fibronectin binding activity; laminin binding activity; and scavenger receptor activity. Predicted to be involved in defense response; detection of bacterial lipoprotein; and negative regulation of interleukin-8 production. Predicted to act upstream of or within regulation of interleukin-8 production. Predicted to be located in collagen-containing extracellular matrix. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
ISLR Geneimmunoglobulin superfamily containing leucine-rich repeat Predicted to be involved in cell adhesion. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
CYHR1 Genecysteine/histidine-rich 1 Predicted to enable zinc ion binding activity. Predicted to be located in nuclear envelope and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANP32BP2 Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member B pseudogene 2 |
ANP32F Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member F |
ANP32D Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member D Phosphoprotein 32 (PP32) is a tumor suppressor that can inhibit several types of cancers, including prostate and breast cancers. The protein encoded by this gene is one of at least two proteins that are similar in amino acid sequence to PP32 and are part of the same acidic nuclear phosphoprotein gene family. However, unlike PP32, the encoded protein is tumorigenic. The tumor suppressor function of PP32 has been localized to a 25 amino acid region that is absent in the protein encoded by this gene. This gene does not contain introns. [provided by RefSeq, Jul 2008] |
ANP32E Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member E Enables histone binding activity; histone chaperone activity; and protein folding chaperone. Predicted to be involved in regulation of apoptotic process. Located in nucleus. Part of Swr1 complex. [provided by Alliance of Genome Resources, Mar 2025] |
ANP32B Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member B Enables RNA polymerase binding activity and histone binding activity. Involved in several processes, including nucleosome assembly; positive regulation of cysteine-type endopeptidase activity; and positive regulation of protein export from nucleus. Located in cytoplasm; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANP32C Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member C Predicted to enable histone binding activity. Predicted to be involved in nucleocytoplasmic transport and regulation of apoptotic process. Predicted to be active in nucleus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANP32A Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member A Enables RNA binding activity. Involved in nucleocytoplasmic transport. Located in endoplasmic reticulum; nucleus; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PRR23A Geneproline rich 23A |
PRR23B Geneproline rich 23B |
LRRN3 Geneleucine rich repeat neuronal 3 Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LRRN2 Geneleucine rich repeat neuronal 2 The protein encoded by this gene belongs to the leucine-rich repeat superfamily. This gene was found to be amplified and overexpressed in malignant gliomas. The encoded protein has homology with other proteins that function as cell-adhesion molecules or as signal transduction receptors and is a candidate for the target gene in the 1q32.1 amplicon in malignant gliomas. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008] |
CSRNP1 Genecysteine-serine-rich nuclear protein 1 This gene encodes a protein that localizes to the nucleus and expression of this gene is induced in response to elevated levels of axin. The Wnt signalling pathway, which is negatively regulated by axin, is important in axis formation in early development and impaired regulation of this signalling pathway is often involved in tumors. A decreased level of expression of this gene in tumors compared to the level of expression in their corresponding normal tissues suggests that this gene product has a tumor suppressor function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
CSRNP2 Genecysteine-serine-rich nuclear protein 2 The protein encoded by this gene belongs to the CSRNP family of nuclear proteins that share conserved regions, including cysteine- and serine- rich regions, a basic domain, a transcriptional activation domain, and bind the sequence 'AGAGTG', thus have the hallmark of transcription factors. Studies in mice suggest that these genes may have redundant functions. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011] |
CSRNP3 Genecysteine-serine-rich nuclear protein 3 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Predicted to be involved in positive regulation of apoptotic process and positive regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100631255 Genearginine/serine-rich coiled-coil 2 pseudogene |
LOC105376335 Genebasic proline-rich protein-like |
PROSER1 Geneproline and serine rich 1 This gene encodes a conserved protein containing proline and serine rich regions. These regions may be important in protein-protein interactions. [provided by RefSeq, Aug 2012] |
PROSER2 Geneproline and serine rich 2 |
PROSER3 Geneproline and serine rich 3 Located in centrosome. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105371788 Geneleucine-rich repeat-containing protein 37B-like |
PRR9 Geneproline rich 9 |
CLASRP GeneCLK4-associating serine/arginine rich protein Predicted to be involved in RNA splicing and mRNA processing. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
HNRNPD Geneheterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are nucleic acid binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two repeats of quasi-RRM domains that bind to RNAs. It localizes to both the nucleus and the cytoplasm. This protein is implicated in the regulation of mRNA stability. Alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008] |
SH3BGRL GeneSH3 domain binding glutamate-rich protein like Enables protein-RNA adaptor activity and ubiquitin-like ligase-substrate adaptor activity. Involved in positive regulation of cytoplasmic translational initiation and proteasome-mediated ubiquitin-dependent protein catabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379194 Genebasic salivary proline-rich protein 4-like |
ANP32BP1 Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member B pseudogene 1 |
ERICH6B Geneglutamate-rich 6B |
LRRC37A4P Geneleucine rich repeat containing 37, member A4, pseudogene |
LRRIQ3 Geneleucine-rich repeats and IQ motif containing 3 |
LOC100996699 Geneproline-rich protein 2-like |
GPBP1 GeneGC-rich promoter binding protein 1 This gene was originally isolated by subtractive hybridization of cDNAs expressed in atherosclerotic plaques with a thrombus, and was found to be expressed only in vascular smooth muscle cells. However, a shorter splice variant was found to be more ubiquitously expressed. This protein is suggested to play a role in the development of atherosclerosis. Studies in mice suggest that it may also function as a GC-rich promoter-specific trans-activating transcription factor. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011] |
LOC102725115 Geneproline-rich protein 23D1-like |
LOC392439 Geneserine/arginine-rich splicing factor 2 pseudogene |
LOC100129391 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 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] |
LRTM2 Geneleucine-rich repeats and transmembrane domains 2 Predicted to enable Roundabout binding activity and heparin binding activity. Predicted to be involved in axon guidance and negative chemotaxis. Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC727896 Genecysteine and histidine-rich domain (CHORD) containing 1 pseudogene |
LOC105371752 Geneproline-rich protein 36-like |
ERICH6 Geneglutamate-rich 6 |
ERICH5 Geneglutamate-rich 5 |
ERICH4 Geneglutamate-rich 4 |
ERICH3 Geneglutamate-rich 3 Involved in cilium assembly. Located in cytoplasm and non-motile cilium. [provided by Alliance of Genome Resources, Mar 2025] |
ERICH2 Geneglutamate-rich 2 |
ERICH1 Geneglutamate-rich 1 |
SMKR1 Genesmall lysine-rich protein 1 |
LOC101930132 Genepollen-specific leucine-rich repeat extensin-like protein 1 |
PAGR1 GenePAXIP1 associated glutamate-rich protein 1 Enables nuclear estrogen receptor binding activity. Involved in positive regulation of cell cycle G1/S phase transition; positive regulation of intracellular estrogen receptor signaling pathway; and positive regulation of transcription by RNA polymerase II. Located in nucleus. Part of MLL3/4 complex. Biomarker of esophagus squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420765 Geneleucine-rich pentatricopeptide repeat containing pseudogene |
SH3BGR GeneSH3 domain binding glutamate-rich protein Predicted to enable SH3 domain binding activity. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC41 Geneleucine rich repeat containing 41 Predicted to enable identical protein binding activity. Predicted to be involved in protein ubiquitination. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC40 Geneleucine rich repeat containing 40 Predicted to be involved in intracellular signal transduction. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC43 Geneleucine rich repeat containing 43 Predicted to enable dynein complex binding activity. Predicted to be involved in axoneme assembly. Predicted to be active in axoneme. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC42 Geneleucine rich repeat containing 42 |
LRRC45 Geneleucine rich repeat containing 45 Located in several cellular components, including centrosome; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC47 Geneleucine rich repeat containing 47 Enables RNA binding activity. Predicted to be involved in phenylalanyl-tRNA aminoacylation. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC46 Geneleucine rich repeat containing 46 |
LRRC49 Geneleucine rich repeat containing 49 Located in centriolar satellite. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC48 Geneleucine rich repeat containing 48 Located in axoneme. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC4C Geneleucine rich repeat containing 4C NGL1 is a specific binding partner for netrin G1 (NTNG1; MIM 608818), which is a member of the netrin family of axon guidance molecules (Lin et al., 2003 [PubMed 14595443]).[supplied by OMIM, Mar 2008] |
LRRC4B Geneleucine rich repeat containing 4B Predicted to enable signaling receptor binding activity. Predicted to be involved in regulation of synapse assembly and synaptic membrane adhesion. Predicted to be located in cerebellar mossy fiber and presynaptic membrane. Predicted to be active in glutamatergic synapse and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CITED2 GeneCbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 The protein encoded by this gene inhibits transactivation of HIF1A-induced genes by competing with binding of hypoxia-inducible factor 1-alpha to p300-CH1. Mutations in this gene are a cause of cardiac septal defects. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012] |
MARCKS Genemyristoylated alanine-rich protein kinase C substrate The protein encoded by this gene is a substrate for protein kinase C. It is localized to the plasma membrane and is an actin filament crosslinking protein. Phosphorylation by protein kinase C or binding to calcium-calmodulin inhibits its association with actin and with the plasma membrane, leading to its presence in the cytoplasm. The protein is thought to be involved in cell motility, phagocytosis, membrane trafficking and mitogenesis. [provided by RefSeq, Jul 2008] |
LRRC37BP1 Geneleucine rich repeat containing 37B pseudogene 1 |
RECK Genereversion-inducing-cysteine-rich protein with kazal motifs The protein encoded by this gene is a cysteine-rich, extracellular protein with protease inhibitor-like domains whose expression is suppressed strongly in many tumors and cells transformed by various kinds of oncogenes. In normal cells, this membrane-anchored glycoprotein may serve as a negative regulator for matrix metalloproteinase-9, a key enzyme involved in tumor invasion and metastasis. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015] |
LRCOL1 Geneleucine rich colipase-like 1 Predicted to enable enzyme activator activity. Predicted to be involved in digestion and lipid catabolic process. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
ANP32AP1 Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member A pseudogene 1 |
SFPQP1 Genesplicing factor proline/glutamine-rich (polypyrimidine tract binding protein associated) pseudogene 1 |
LRRC32 Geneleucine rich repeat containing 32 This gene encodes a type I membrane protein which contains 20 leucine-rich repeats. Alterations in the chromosomal region 11q13-11q14 are involved in several pathologies. [provided by RefSeq, Jul 2008] |
LRRC36 Geneleucine rich repeat containing 36 |
FBXL3 GeneF-box and leucine-rich repeat protein 3 This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains several tandem leucine-rich repeats and is localized in the nucleus. [provided by RefSeq, Jul 2008] |
FBXL5 GeneF-box and leucine-rich repeat protein 5 This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains several tandem leucine-rich repeats. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2010] |
SPATS2L Genespermatogenesis associated, serine-rich 2-like Enables RNA binding activity. Located in cytosol; nucleolus; and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNPS1P1 GeneRNA binding protein S1, serine-rich domain pseudogene 1 |
LOC105376685 Genebasic proline-rich protein-like |
LOC643118 Geneserine/arginine-rich splicing factor 2 pseudogene |
LRRC37A9P Geneleucine rich repeat containing 37, member A9, pseudogene |
LOC644158 Geneleucine rich repeat containing 2 pseudogene |
PCS GeneParotid proline-rich salivary protein Pc |
PRR15L Geneproline rich 15-like |
LOC100419917 Genelysine-rich coiled-coil 1 pseudogene |
LRRFIP1 Geneleucine rich repeat (in FLII) interacting protein 1 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and protein homodimerization activity. Involved in negative regulation of transcription by RNA polymerase II. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRFIP2 Geneleucine rich repeat (in FLII) interacting protein 2 The protein encoded by this gene, along with MYD88, binds to the cytosolic tail of toll-like receptor 4 (TLR4), which results in activation of nuclear factor kappa B signaling. The ubiquitin-like protein FAT10 prevents the interaction of the encoded protein and TLR4, thereby inactivating the nuclear factor kappa B signaling pathway. In addition, this protein can downregulate the NLRP3 inflammasome by recruiting the caspase-1 inhibitor Flightless-I to the inflammasome complex. [provided by RefSeq, Jan 2017] |
CHORDC2P Genecysteine and histidine-rich domain (CHORD) containing 2 pseudogene |
PRR5L Geneproline rich 5 like Enables ubiquitin protein ligase binding activity. Involved in several processes, including TORC2 signaling; regulation of fibroblast migration; and regulation of primary metabolic process. Part of TORC2 complex. [provided by Alliance of Genome Resources, Mar 2025] |
QSER1 Geneglutamine and serine rich 1 Predicted to be located in chromosome. [provided by Alliance of Genome Resources, Mar 2025] |
PURB Genepurine-rich element binding protein B This gene product is a sequence-specific, single-stranded DNA-binding protein. It binds preferentially to the single strand of the purine-rich element termed PUR, which is present at origins of replication and in gene flanking regions in a variety of eukaryotes from yeasts through humans. Thus, it is implicated in the control of both DNA replication and transcription. Deletion of this gene has been associated with myelodysplastic syndrome and acute myelogenous leukemia. [provided by RefSeq, Jul 2008] |
PURA Genepurine-rich element binding protein A This gene product is a sequence-specific, single-stranded DNA-binding protein. It binds preferentially to the single strand of the purine-rich element termed PUR, which is present at origins of replication and in gene flanking regions in a variety of eukaryotes from yeasts through humans. Thus, it is implicated in the control of both DNA replication and transcription. Deletion of this gene has been associated with myelodysplastic syndrome and acute myelogenous leukemia. [provided by RefSeq, Jul 2008] |
PURG Genepurine-rich element binding protein G The exact function of this gene is not known, however, its encoded product is highly similar to purine-rich element binding protein A. The latter is a DNA-binding protein which binds preferentially to the single strand of the purine-rich element termed PUR, and has been implicated in the control of both DNA replication and transcription. This gene lies in close proximity to the Werner syndrome gene, but on the opposite strand, on chromosome 8p11. [provided by RefSeq, Apr 2016] |
LOC105374567 Geneproline-rich protein 2-like |
LOC101927997 Geneproline-rich protein 23D1-like |
LRRC74A Geneleucine rich repeat containing 74A |
LRRC74B Geneleucine rich repeat containing 74B |
PRORY Geneproline rich, Y-linked |
LOC105379534 Geneproline-rich receptor-like protein kinase PERK2 |
PRAP1 Geneproline-rich acidic protein 1 Predicted to enable triglyceride binding activity. Involved in DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest; deactivation of mitotic spindle assembly checkpoint; and negative regulation of apoptotic process. Predicted to be located in endoplasmic reticulum and extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929013 Geneproline-rich protein 23D1-like |
LRRC37A11P Geneleucine rich repeat containing 37, member A11, pseudogene |
LRRC3B Geneleucine rich repeat containing 3B The protein encoded by this gene is a tumor suppressor, with lowered expression levels found in gastric, renal, colorectal, lung, and breast cancer tissues. The promoter of this gene is frequently hypermethylated in these cancer tissues, although the hypermethylation does not appear to be the cause of the reduced expression of this gene. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2015] |
PRIMA1 Geneproline rich membrane anchor 1 The product of this gene functions to organize acetylcholinesterase (AChE) into tetramers, and to anchor AChE at neural cell membranes. [provided by RefSeq, Nov 2008] |
LRRC38 Geneleucine rich repeat containing 38 Enables potassium channel activator activity and transmembrane transporter binding activity. Involved in positive regulation of voltage-gated potassium channel activity and potassium ion transmembrane transport. Part of voltage-gated potassium channel complex. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC39 Geneleucine rich repeat containing 39 Predicted to be involved in intracellular signal transduction. Predicted to be located in M band. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC30 Geneleucine rich repeat containing 30 Predicted to be involved in intracellular signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC31 Geneleucine rich repeat containing 31 |
LRRC34 Geneleucine rich repeat containing 34 Predicted to be involved in cell differentiation. Predicted to be located in cytoplasm and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LRIG3 Geneleucine-rich repeats and immunoglobulin-like domains 3 Predicted to act upstream of or within otolith morphogenesis. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LRIG2 Geneleucine-rich repeats and immunoglobulin-like domains 2 This gene encodes a transmembrane protein containing leucine-rich repeats and immunoglobulin-like domains. The encoded protein promotes epidermal growth factor signalling, resulting in increased proliferation. Its expression in the cytoplasm of glioma cells is correlated with poor survival. Mutations in this gene can cause urofacial syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
LRIG1 Geneleucine-rich repeats and immunoglobulin-like domains 1 Predicted to act upstream of or within several processes, including innervation; otolith morphogenesis; and sensory perception of sound. Predicted to be located in plasma membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
GRWD1 Geneglutamate-rich WD repeat containing 1 This gene encodes a glutamate-rich protein that contains five WD-repeat motifs. The encoded protein may play a critical role in ribosome biogenesis and may also play a role in histone methylation through interactions with CUL4-DDB1 ubiquitin E3 ligase. [provided by RefSeq, Feb 2012] |
GRSF1 GeneG-rich RNA sequence binding factor 1 The protein encoded by this gene is a cellular protein that binds RNAs containing the G-rich element. The protein is localized in the cytoplasm, and has been shown to stimulate translation of viral mRNAs in vitro. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
OSER1 Geneoxidative stress responsive serine-rich 1 Predicted to be involved in cellular response to hydrogen peroxide. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MARCKSP1 Genemyristoylated alanine-rich protein kinase C substrate pseudogene 1 |
WRB Genetryptophan rich basic protein This gene is located in the candidate region for congenital heart disease (CHD) in Down syndrome (DS). It encodes a basic protein that functions as a receptor that promotes insertion of tail-anchored proteins in the endoplasmic reticulum membrane. This gene is located at a maternally-methylated differentially methylated region (DMR); however, its transcription may be biallelic, not imprinted. Alternative splicing results in different transcript variants. A pseudogene has been defined on chromosome 4. [provided by RefSeq, Apr 2017] |
LOC101927402 Geneuncharacterized proline-rich protein-like |
LMCD1 GeneLIM and cysteine-rich domains 1 This gene encodes a member of the LIM-domain family of zinc finger proteins. The encoded protein contains an N-terminal cysteine-rich domain and two C-terminal LIM domains. The presence of LIM domains suggests involvement in protein-protein interactions. The protein may act as a co-regulator of transcription along with other transcription factors. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013] |
CRELD2 Genecysteine-rich with EGF-like domains 2 Predicted to enable calcium ion binding activity and protein disulfide isomerase activity. Predicted to be located in Golgi apparatus; endoplasmic reticulum; and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
CRELD1 Genecysteine-rich with EGF-like domains 1 This gene encodes a member of a subfamily of epidermal growth factor-related proteins. The encoded protein is characterized by a cysteine-rich with epidermal growth factor-like domain. This protein may function as a cell adhesion molecule. Mutations in this gene are the cause of atrioventricular septal defect. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010] |
LOC100128772 Geneproline-rich protein 3 pseudogene |
LOC100418956 Geneproline rich 11 pseudogene |
PRR13P7 Geneproline rich 13 pseudogene 7 |
SPARC Genesecreted protein, acidic, cysteine-rich (osteonectin) This gene encodes a cysteine-rich acidic matrix-associated protein. The encoded protein is required for the collagen in bone to become calcified but is also involved in extracellular matrix synthesis and promotion of changes to cell shape. The gene product has been associated with tumor suppression but has also been correlated with metastasis based on changes to cell shape which can promote tumor cell invasion. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2015] |
LOC102723665 Genebasic proline-rich protein-like |
ISLR2 Geneimmunoglobulin superfamily containing leucine-rich repeat 2 Predicted to be involved in positive regulation of axon extension. Predicted to be located in plasma membrane. Predicted to be active in cell surface. [provided by Alliance of Genome Resources, Mar 2025] |
TOPORS Genetopoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase This gene encodes a nuclear protein which is serine and arginine rich, and contains a RING-type zinc finger domain. It is highly expressed in the testis, and functions as an ubiquitin-protein E3 ligase. Mutations in this gene are associated with retinitis pigmentosa type 31. Alternatively spliced transcript variants, encoding different isoforms, have been observed for this locus. [provided by RefSeq, Sep 2010] |
LOC402076 GeneF-box and leucine-rich repeat protein 12 pseudogene |
KNOP1P5 Genelysine-rich nucleolar protein 1 pseudogene 5 |
KNOP1P2 Genelysine-rich nucleolar protein 1 pseudogene 2 |
HRG Genehistidine-rich glycoprotein This histidine-rich glycoprotein contains two cystatin-like domains and is located in plasma and platelets. The physiological function has not been determined but it is known that the protein binds heme, dyes and divalent metal ions. The encoded protein also has a peptide that displays antimicrobial activity against C. albicans, E. coli, S. aureus, P. aeruginosa, and E. faecalis. It can inhibit rosette formation and interacts with heparin, thrombospondin and plasminogen. Two of the protein's effects, the inhibition of fibrinolysis and the reduction of inhibition of coagulation, indicate a potential prothrombotic effect. Mutations in this gene lead to thrombophilia due to abnormal histidine-rich glycoprotein levels. [provided by RefSeq, Nov 2014] |
HRC Genehistidine rich calcium binding protein This gene encodes a luminal sarcoplasmic reticulum protein identified by its ability to bind low-density lipoprotein with high affinity. The protein interacts with the cytoplasmic domain of triadin, the main transmembrane protein of the junctional sarcoplasmic reticulum (SR) of skeletal muscle. The protein functions in the regulation of releasable calcium into the SR. [provided by RefSeq, Sep 2008] |
LRTM1 Geneleucine-rich repeats and transmembrane domains 1 Predicted to enable Roundabout binding activity and heparin binding activity. Predicted to be involved in axon guidance and negative chemotaxis. Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CYSRT1 Genecysteine-rich tail protein 1 Enables identical protein binding activity. Involved in biological process involved in interaction with symbiont and establishment of skin barrier. Located in cornified envelope. [provided by Alliance of Genome Resources, Mar 2025] |
PSRC1 Geneproline/serine-rich coiled-coil 1 This gene encodes a proline-rich protein that is a target for regulation by the tumor suppressor protein p53. The encoded protein plays an important role in mitosis by recruiting and regulating microtubule depolymerases that destabalize microtubules. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Apr 2014] |
LOC105377805 Genebasic salivary proline-rich protein 3-like |
LOC100418986 Geneproline rich 21 pseudogene |
FBXL4 GeneF-box and leucine-rich repeat protein 4 This gene encodes a member of the F-box protein family, which are characterized by an approximately 40 amino acid motif, the F-box. F-box proteins constitute one subunit of modular E3 ubiquitin ligase complexes, called SCF complexes, which function in phosphorylation-dependent ubiquitination. The F-box domain mediates protein-protein interactions and binds directly to S-phase kinase-associated protein 1. In addition to an F-box domain, the encoded protein contains at least 9 tandem leucine-rich repeats. The ubiquitin ligase complex containing the encoded protein may function in cell-cycle control by regulating levels of lysine-specific demethylase 4A. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
LOC100533663 Genehistidine-rich glycoprotein pseudogene |
LOC100418989 Geneproline rich 21 pseudogene |
TOPORSLP Genetopoisomerase I binding, arginine/serine-rich like, pseudogene |
LOC101929254 Geneleucine-rich repeat-containing protein 37B-like |
ARID5B GeneAT rich interactive domain 5B (MRF1-like) This gene encodes a member of the AT-rich interaction domain (ARID) family of DNA binding proteins. The encoded protein forms a histone H3K9Me2 demethylase complex with PHD finger protein 2 and regulates the transcription of target genes involved in adipogenesis and liver development. This gene also plays a role in cell growth and differentiation of B-lymphocyte progenitors, and single nucleotide polymorphisms in this gene are associated with acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011] |
ARID5A GeneAT rich interactive domain 5A (MRF1-like) Members of the ARID protein family, including ARID5A, have diverse functions but all appear to play important roles in development, tissue-specific gene expression, and regulation of cell growth (Patsialou et al., 2005 [PubMed 15640446]).[supplied by OMIM, Mar 2008] |
LOC100131261 Geneproline-rich nuclear receptor coactivator 2 pseudogene |
LOC644422 Genesplicing factor, arginine/serine-rich 6 pseudogene |
SRSF10P2 Geneserine/arginine-rich splicing factor 10 pseudogene 2 |
SERTM1 Geneserine-rich and transmembrane domain containing 1 Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
PRR29 Geneproline rich 29 |
PRR27 Geneproline rich 27 Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
PRR26 Geneproline rich 26 |
PRR25 Geneproline rich 25 |
PRR22 Geneproline rich 22 |
PRR21 Geneproline rich 21 |
ZRSR1 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 1 Predicted to enable pre-mRNA 3'-splice site binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleus. Predicted to be part of U2AF complex and spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105377886 Genesmall EDRK-rich factor 2 pseudogene |
LOC646555 GeneAT rich interactive domain 3B pseudogene |
FBXL13 GeneF-box and leucine-rich repeat protein 13 Members of the F-box protein family, such as FBXL13, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008] |
FBXL12 GeneF-box and leucine-rich repeat protein 12 Members of the F-box protein family, such as FBXL12, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008] |
FBXL15 GeneF-box and leucine-rich repeat protein 15 Involved in several processes, including G2/M transition of mitotic cell cycle; SCF-dependent proteasomal ubiquitin-dependent protein catabolic process; and positive regulation of BMP signaling pathway. Located in cytoplasm. Part of SCF ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
FBXL17 GeneF-box and leucine-rich repeat protein 17 Members of the F-box protein family, such as FBXL17, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008] |
FBXL16 GeneF-box and leucine-rich repeat protein 16 Members of the F-box protein family, such as FBXL16, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008] |
FBXL18 GeneF-box and leucine-rich repeat protein 18 The protein encoded by this gene is a member of a family of proteins that contain an approximately 40-amino acid F-box motif. This motif is important for interaction with SKP1 and for targeting some proteins for degradation. The encoded protein has been shown to control the cellular level of FBXL7, a protein that induces mitotic arrest, by targeting it for polyubiquitylation and proteasomal degradation. Members of the F-box protein family, such as FBXL18, are characterized by an approximately 40-amino acid F-box motif. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains. [provided by RefSeq, Mar 2016] |
LOC100128027 Genecysteine-rich, DPF motif domain containing 1 pseudogene |
LOC100506569 Geneserine/arginine-rich splicing factor 3 pseudogene |
LRRC34P2 Geneleucine rich repeat containing 34 pseudogene 2 |
LRRC34P1 Geneleucine rich repeat containing 34 pseudogene 1 |
CSRP2P Genecysteine and glycine-rich protein 2 pseudogene |
LOC100421293 Geneserine/arginine-rich splicing factor 10 pseudogene |
CYSTM1 Genecysteine-rich transmembrane module containing 1 Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
LOC401777 Geneserine/arginine-rich splicing factor 10 pseudogene |
LOC724105 Genecysteine-rich transmembrane module containing 1 pseudogene |
LOC724104 GeneSH3 domain binding glutamate-rich protein like 3 pseudogene |
LOC100418987 Geneproline rich 21 pseudogene |
SMDT1 Genesingle-pass membrane protein with aspartate-rich tail 1 This gene encodes a core regulatory component of a calcium channel in the mitochondrial inner membrane. [provided by RefSeq, Apr 2017] |
LRRC69 Geneleucine rich repeat containing 69 Predicted to be involved in intracellular signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC63 Geneleucine rich repeat containing 63 Predicted to be involved in intracellular signal transduction. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC61 Geneleucine rich repeat containing 61 Predicted to enable alpha-tubulin binding activity and dynein heavy chain binding activity. Predicted to be involved in outer dynein arm assembly. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC66 Geneleucine rich repeat containing 66 This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. [provided by RefSeq, Apr 2017] |
LGR5 Geneleucine-rich repeat containing G protein-coupled receptor 5 The protein encoded by this gene is a leucine-rich repeat-containing receptor (LGR) and member of the G protein-coupled, 7-transmembrane receptor (GPCR) superfamily. The encoded protein is a receptor for R-spondins and is involved in the canonical Wnt signaling pathway. This protein plays a role in the formation and maintenance of adult intestinal stem cells during postembryonic development. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2015] |
LGR4 Geneleucine-rich repeat containing G protein-coupled receptor 4 The protein encoded by this gene is a G-protein coupled receptor that binds R-spondins and activates the Wnt signaling pathway. This Wnt signaling pathway activation is necessary for proper development of many organs of the body. [provided by RefSeq, Oct 2016] |
LGR6 Geneleucine-rich repeat containing G protein-coupled receptor 6 This gene encodes a member of the leucine-rich repeat-containing subgroup of the G protein-coupled 7-transmembrane protein superfamily. The encoded protein is a glycoprotein hormone receptor with a large N-terminal extracellular domain that contains leucine-rich repeats important for the formation of a horseshoe-shaped interaction motif for ligand binding. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008] |
PELP1 Geneproline, glutamate and leucine rich protein 1 This gene encodes a transcription factor which coactivates transcription of estrogen receptor responsive genes and corepresses genes activated by other hormone receptors or sequence-specific transcription factors. Expression of this gene is regulated by both members of the estrogen receptor family. This gene may be involved in the progression of several types of cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013] |
LRRIQ1 Geneleucine-rich repeats and IQ motif containing 1 Predicted to be involved in regulation of signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
LRRIQ4 Geneleucine-rich repeats and IQ motif containing 4 Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100418988 Geneproline rich 21 pseudogene |
LGI4 Geneleucine-rich repeat LGI family, member 4 Involved in regulation of myelination. Predicted to be located in extracellular region. Predicted to be active in extracellular space. Implicated in arthrogryposis multiplex congenita-1 and childhood absence epilepsy. [provided by Alliance of Genome Resources, Mar 2025] |
LGI1 Geneleucine-rich, glioma inactivated 1 This gene encodes a member of the secreted leucine-rich repeat (LRR) superfamily and shares homology with members of the SLIT protein family. The encoded protein may regulate the activity of voltage-gated potassium channels and may be involved in neuronal growth regulation and cell survival. This gene is rearranged as a result of translocations in glioblastoma cell lines, and it is frequently down-regulated or rearranged in malignant gliomas. Mutations in this gene result in autosomal dominant lateral temporal epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
LGI2 Geneleucine-rich repeat LGI family, member 2 Predicted to be involved in inhibitory synapse assembly. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LGI3 Geneleucine-rich repeat LGI family, member 3 Predicted to be involved in regulation of exocytosis. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LRSAM1 Geneleucine rich repeat and sterile alpha motif containing 1 This gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways and cell adhesion, mediation of self-ubiquitylation, and involvement in cargo sorting during receptor endocytosis. Mutations in this gene have been associated with Charcot-Marie-Tooth disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jan 2012] |
PROL1 Geneproline rich, lacrimal 1 This gene encodes a member of the proline-rich protein family. The encoded protein has multiple proposed functions, including roles in pain suppression, penile erection, and protection of the eye surface. The QRFSR pentapeptide, known as opiorphin, is derived from the N-terminal of this protein. Opiorphin inhibits the enkephalin-inactivating peptidases neprilysin and aminopeptidase N, and this activity is thought to reduce sensitivity to painful stimuli by effecting enkephalin-related activation of opioid-dependent pathways. Opiorphin may also act as an anti-depressant. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014] |
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] |
CRIPT Genecysteine-rich PDZ-binding protein This gene encodes a protein that binds to the PDZ3 peptide recognition domain. The encoded protein may modulates protein interactions with the cytoskeleton. A mutation in this gene resulted in short stature with microcephaly and distinctive facies. [provided by RefSeq, Jun 2014] |
CRIP1 Genecysteine-rich protein 1 (intestinal) Cysteine-rich intestinal protein (CRIP) belongs to the LIM/double zinc finger protein family, members of which include cysteine- and glycine-rich protein-1 (CSRP1; MIM 123876), rhombotin-1 (RBTN1; MIM 186921), rhombotin-2 (RBTN2; MIM 180385), and rhombotin-3 (RBTN3; MIM 180386). CRIP may be involved in intestinal zinc transport (Hempe and Cousins, 1991 [PubMed 1946385]).[supplied by OMIM, Mar 2008] |
CRIP3 Genecysteine-rich protein 3 Predicted to enable metal ion binding activity. Predicted to act upstream of or within T cell proliferation. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CRIP2 Genecysteine-rich protein 2 This gene encodes a putative transcription factor with two LIM zinc-binding domains. The encoded protein may participate in the differentiation of smooth muscle tissue. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012] |
LOC100131114 Geneserine/arginine-rich splicing factor 3 pseudogene |
LOC100500773 Geneserine/arginine-rich splicing factor 3 pseudogene |
LRRC10B Geneleucine rich repeat containing 10B |
PNRC1 Geneproline-rich nuclear receptor coactivator 1 Predicted to be involved in nuclear-transcribed mRNA catabolic process, nonsense-mediated decay. Predicted to be active in P-body and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PNRC2 Geneproline-rich nuclear receptor coactivator 2 Involved in nuclear-transcribed mRNA catabolic process, nonsense-mediated decay. Located in Golgi apparatus; P-body; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC6P1 Geneleucine rich repeat containing 6 pseudogene 1 |
MGARP Genemitochondria-localized glutamic acid-rich protein Predicted to be involved in several processes, including axonal transport; cellular response to gonadotropin-releasing hormone; and nervous system development. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC37A7P Geneleucine rich repeat containing 37, member A7, pseudogene |
CRIM1 Genecysteine rich transmembrane BMP regulator 1 (chordin-like) This gene encodes a transmembrane protein containing six cysteine-rich repeat domains and an insulin-like growth factor-binding domain. The encoded protein may play a role in tissue development though interactions with members of the transforming growth factor beta family, such as bone morphogenetic proteins. [provided by RefSeq, Nov 2010] |
LOC100128442 Geneserine/arginine-rich splicing factor 6 pseudogene |
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] |
LOC642554 Geneleucine rich repeat containing 59 pseudogene |
LRRC37A Geneleucine rich repeat containing 37A Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CRCT1 Genecysteine-rich C-terminal 1 |
LOC100421775 Geneleucine rich repeat containing 8 family, member B pseudogene |
LRRC2 Geneleucine rich repeat containing 2 This gene encodes a member of the leucine-rich repeat-containing family of proteins, which function in diverse biological pathways. This family member may possibly be a nuclear protein. Similarity to the RAS suppressor protein, as well as expression down-regulation observed in tumor cells, suggests that it may function as a tumor suppressor. The gene is located in the chromosome 3 common eliminated region 1 (C3CER1), a 1.4 Mb region that is commonly deleted in diverse tumors. A related pseudogene has been identified on chromosome 2. [provided by RefSeq, Sep 2011] |
CCSER1 Genecoiled-coil serine-rich protein 1 Implicated in cocaine dependence. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100133244 Geneleucine rich repeat containing 37, member A3 pseudogene |
SH3BGRL3 GeneSH3 domain binding glutamate-rich protein like 3 Involved in cytoskeleton organization. Located in cytosol; nuclear body; and ruffle membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SH3BGRL2 GeneSH3 domain binding glutamate-rich protein like 2 Predicted to enable SH3 domain binding activity. Located in nuclear membrane and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRPPRC Geneleucine-rich pentatricopeptide repeat containing This gene encodes a leucine-rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization, vesicular transport, or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N-terminal mitochondrial targeting sequence. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome. [provided by RefSeq, Mar 2012] |
LRG1 Geneleucine-rich alpha-2-glycoprotein 1 The leucine-rich repeat (LRR) family of proteins, including LRG1, have been shown to be involved in protein-protein interaction, signal transduction, and cell adhesion and development. LRG1 is expressed during granulocyte differentiation (O'Donnell et al., 2002 [PubMed 12223515]).[supplied by OMIM, Mar 2008] |
PNISR GenePNN-interacting serine/arginine-rich protein Enables RNA binding activity. Located in cytosol; nuclear speck; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SSMEM1 Geneserine-rich single-pass membrane protein 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PR@ Geneproline-rich protein gene cluster |
TRIL GeneTLR4 interactor with leucine-rich repeats TRIL is a component of the TLR4 (MIM 603030) complex and is induced in a number of cell types by lipopolysaccharide (LPS) (Carpenter et al., 2009 [PubMed 19710467]).[supplied by OMIM, Apr 2010] |
LOC105373984 Geneanther-specific proline-rich protein APG-like |
LRCH4 Geneleucine-rich repeats and calponin homology (CH) domain containing 4 This gene encodes a protein that contains leucine-rich repeats (LRR) at its amino terminus and that is known to be involved in ligand binding. The carboxyl terminus may act as a membrane anchor. Identified structural elements suggest that the encoded protein resembles a receptor. [provided by RefSeq, Jul 2008] |
LRCH1 Geneleucine-rich repeats and calponin homology (CH) domain containing 1 This gene encodes a protein with a leucine-rich repeat and a calponin homology domain. Polymorphism in this gene may be associated with susceptibililty to knee osteoarthritis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2010] |
LRCH2 Geneleucine-rich repeats and calponin homology (CH) domain containing 2 This gene encodes a member of the leucine-rich repeat and calponin homology domain-containing protein family. These family members contain multiple N-terminal leucine-rich repeats, in addition to a C-terminal calponin homology domain, a type of domain that mediates interactions with actin filaments. These proteins are conserved across animal species, and studies of a similar Drosophila protein indicate a function as a cytoskeletal scaffolding protein. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2011] |
LRCH3 Geneleucine-rich repeats and calponin homology (CH) domain containing 3 Involved in septin cytoskeleton organization. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC37B Geneleucine rich repeat containing 37B Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC52 Geneleucine rich repeat containing 52 Enables potassium channel activator activity; transmembrane transporter binding activity; and voltage-gated potassium channel activity. Involved in positive regulation of voltage-gated potassium channel activity and potassium ion transmembrane transport. Part of voltage-gated potassium channel complex. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC53 Geneleucine rich repeat containing 53 |
LRRC56 Geneleucine rich repeat containing 56 Predicted to be involved in cell projection organization. Predicted to be located in cilium. Implicated in primary ciliary dyskinesia 39. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC57 Geneleucine rich repeat containing 57 Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC55 Geneleucine rich repeat containing 55 Enables potassium channel activator activity; transmembrane transporter binding activity; and voltage-gated potassium channel activity. Involved in positive regulation of voltage-gated potassium channel activity and potassium ion transmembrane transport. Part of voltage-gated potassium channel complex. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC58 Geneleucine rich repeat containing 58 Predicted to be involved in intracellular signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC59 Geneleucine rich repeat containing 59 Enables RNA binding activity and cadherin binding activity. Predicted to be involved in intracellular signal transduction. Located in endoplasmic reticulum and mitochondrial nucleoid. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105373780 Geneproline-rich protein 18-like |
PROB1 Geneproline-rich basic protein 1 Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100533934 Geneleucine rich repeat containing 37A pseudogene |
LOC100533933 Geneleucine rich repeat containing 37A pseudogene |
LOC100419016 Geneproline rich 21 pseudogene |
KRCC1 Genelysine-rich coiled-coil 1 |
LRRC14B Geneleucine rich repeat containing 14B The protein encoded by this gene is a leucine-rich repeat containing protein that is a member of the PRAME family. [provided by RefSeq, Apr 2017] |
DRICH1 Geneaspartate-rich 1 |
CRISP1 Genecysteine-rich secretory protein 1 Fertilization consists of a sequence of specific cell-cell interactions culminating in the fusion of the sperm and egg plasma membranes. Recognition, binding, and fusion occur through the interaction of complementary molecules that are localized to specific domains of the sperm and egg plasma membranes. In the sperm, the postacrosomal region or equatorial segment is involved in sperm-egg plasma membrane fusion. The protein encoded by this gene is a member of the cysteine-rich secretory protein (CRISP) family. It is expressed in the epididymis, is secreted into the epididymal lumen, and binds to the postacrosomal region of the sperm head, where it plays a role in sperm-egg fusion. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011] |
CRISP3 Genecysteine-rich secretory protein 3 This gene encodes a member of the cysteine-rich secretory protein (CRISP) family within the CRISP, antigen 5 and pathogenesis-related 1 proteins superfamily. The encoded protein has an N-terminal CRISP, antigen 5 and pathogenesis-related 1 proteins domain, a hinge region, and a C-terminal ion channel regulator domain. This protein contains cysteine residues, located in both the N- and C-terminal domains, that form eight disulfide bonds, a distinguishing characteristic of this family. This gene is expressed in the male reproductive tract where it plays a role in sperm function and fertilization, and the female reproductive tract where it plays a role in endometrial receptivity for embryo implantation. This gene is upregulated in certain types of prostate cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016] |
CRISP2 Genecysteine-rich secretory protein 2 Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105374299 Geneproline-rich protein 36-like |
RNPS1 GeneRNA binding protein S1, serine-rich domain This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein binds to the mRNA and remains bound after nuclear export, acting as a nucleocytoplasmic shuttling protein. This protein contains many serine residues. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
LOC105371937 Genebasic proline-rich protein-like |
GRXCR2 Geneglutaredoxin, cysteine rich 2 This gene encodes a protein containing a glutaredoxin domain, which functions in protein S-glutathionylation. A mutation in this gene was found in a family with autoosomal recessive nonsyndromic sensorineural deafness-101. [provided by RefSeq, Jun 2014] |
PRRC2CP1 Geneproline-rich coiled-coil 2C pseudogene 1 |
LOC100129099 Geneproline-rich nuclear receptor coactivator 2 pseudogene |
LOC100128048 Genecysteine and histidine-rich domain (CHORD) containing 1 pseudogene |
LRTOMT Geneleucine rich transmembrane and O-methyltransferase domain containing This locus represents naturally occurring readthrough transcription between the neighboring LRRC51 (leucine-rich repeat containing 51) and TOMT (transmembrane O-methyltransferase) genes on chromosome 11. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. Multiple reports implicate mutations in this gene in nonsyndromic deafness.[provided by RefSeq, Feb 2021] |
LRRC37A6P Geneleucine rich repeat containing 37, member A6, pseudogene |
LOC100418992 Geneproline rich 21 pseudogene |
LRRC37A8P Geneleucine rich repeat containing 37, member A8, pseudogene |
LOC105375620 Genebasic salivary proline-rich protein 2-like |
LOC105376849 Genebasic proline-rich protein-like |
PRR23C Geneproline rich 23C |
LRRTM4 Geneleucine rich repeat transmembrane neuronal 4 Predicted to enable heparan sulfate proteoglycan binding activity. Predicted to be involved in regulation of synapse assembly. Predicted to act upstream of or within AMPA glutamate receptor clustering; positive regulation of synapse assembly; and regulation of presynaptic membrane organization. Predicted to be located in postsynaptic membrane. Predicted to be part of AMPA glutamate receptor complex. Predicted to be active in several cellular components, including GABA-ergic synapse; photoreceptor ribbon synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRTM1 Geneleucine rich repeat transmembrane neuronal 1 Predicted to be involved in regulation of postsynaptic density assembly and regulation of presynapse assembly. Predicted to act upstream of or within several processes, including long-term synaptic potentiation; negative regulation of receptor internalization; and positive regulation of synapse assembly. Located in endoplasmic reticulum and growth cone. Is active in GABA-ergic synapse and postsynaptic specialization membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRTM3 Geneleucine rich repeat transmembrane neuronal 3 Involved in regulation of presynapse assembly. Acts upstream of or within positive regulation of amyloid-beta formation. Is active in glutamatergic synapse. [provided by Alliance of Genome Resources, Mar 2025] |
LRRTM2 Geneleucine rich repeat transmembrane neuronal 2 Predicted to enable neurexin family protein binding activity. Predicted to be involved in regulation of postsynaptic density assembly. Predicted to act upstream of or within several processes, including long-term synaptic potentiation; negative regulation of receptor internalization; and positive regulation of synapse assembly. Is active in GABA-ergic synapse and postsynaptic specialization membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SRSF1P1 Geneserine/arginine-rich splicing factor 1 pseudogene 1 |
FBXL8 GeneF-box and leucine-rich repeat protein 8 This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class. It shares 78% sequence identity with the mouse protein. [provided by RefSeq, Jul 2008] |
FBXL2 GeneF-box and leucine-rich repeat protein 2 This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains 12 tandem leucine-rich repeats. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010] |
FBXL7 GeneF-box and leucine-rich repeat protein 7 This gene encodes a member of the F-box protein family which is characterized by a 42-48 amino acid motif, the F-box, which binds to the S-phase kinase-associated protein 1 (Skp1) protein. The F-box proteins constitute one of the four subunits of E3 ubiquitin protein ligases called SCFs (SKP1-Cul1-F-box), which play a role in phosphorylation-dependent ubiquitination of proteins. The F-box proteins are divided into 3 subfamilies based on the other domain in the protein: F-box proteins that also have a WD-40 domain (Fbws subfamily), F-box proteins that also have leucine-rich repeats (Fbls subfamily) and F-box proteins that contain other motifs or lack known protein-interaction domains (Fbxs subfamily). The protein encoded by this gene belongs to the Fbls subfamily. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013] |
FBXL6 GeneF-box and leucine-rich repeat protein 6 This gene encodes a member of a family of proteins that are characterized by an F-box motif. The encoded protein also contains leucine-rich repeats. F-box-containing proteins comprise one of the subunits of the SCF (SKP1-cullin-F-box) complex, which functions in phosphorylation-dependent ubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
LOC105375131 Genebasic proline-rich protein-like |
LRRC8E Geneleucine rich repeat containing 8 family, member E This gene encodes a member of a small, conserved family of proteins with similar structure, including a string of extracellular leucine-rich repeats. A related protein was shown to be involved in B-cell development. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2012] |
LRRC8D Geneleucine rich repeat containing 8 family, member D Enables volume-sensitive anion channel activity. Involved in several processes, including monoatomic anion transmembrane transport; organic acid transmembrane transport; and protein hexamerization. Located in cytoplasm and plasma membrane. Part of monoatomic ion channel complex. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC8A Geneleucine rich repeat containing 8 family, member A This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008] |
LRRC8B Geneleucine rich repeat containing 8 family, member B Contributes to volume-sensitive anion channel activity. Involved in monoatomic anion transmembrane transport. Located in cytoplasm and plasma membrane. Part of monoatomic ion channel complex. [provided by Alliance of Genome Resources, Mar 2025] |
BCL2L12P1 GeneBCL2-like 12 (proline rich) pseudogene 1 |
PRR20A Geneproline rich 20A This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008] |
QRICH2 Geneglutamine rich 2 Involved in cell projection assembly; flagellated sperm motility; and negative regulation of ubiquitin-dependent protein catabolic process. Located in sperm flagellum. Implicated in spermatogenic failure 35. [provided by Alliance of Genome Resources, Mar 2025] |
QRICH1 Geneglutamine-rich 1 Enables DNA binding activity. Involved in intracellular signal transduction; positive regulation of DNA-templated transcription; and positive regulation of apoptotic process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC37A17P Geneleucine rich repeat containing 37, member A17, pseudogene |
CCSER2 Genecoiled-coil serine-rich protein 2 Predicted to enable microtubule binding activity. Predicted to be involved in microtubule bundle formation. Predicted to be located in cytoplasm and cytoskeleton. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105377064 Geneaspartate, glycine, lysine and serine-rich protein-like |
ARID3A GeneAT rich interactive domain 3A (BRIGHT-like) This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA binding proteins. It was found by homology to the Drosophila dead ringer gene, which is important for normal embryogenesis. Other ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation, and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008] |
ARID3C GeneAT rich interactive domain 3C (BRIGHT-like) This gene is a member of the ARID (AT-rich interaction domain) family of proteins. The ARID domain is a helix-turn-helix motif-based DNA-binding domain. ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008] |
ARID3B GeneAT rich interactive domain 3B (BRIGHT-like) This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA-binding proteins. The encoded protein is homologous with two proteins that bind to the retinoblastoma gene product, and also with the mouse Bright and Drosophila dead ringer proteins. A pseudogene on chromosome 1p31 exists for this gene. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008] |
LOC101927509 Genebasic proline-rich protein-like |
LRRD1 Geneleucine-rich repeats and death domain containing 1 Predicted to be involved in signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
AKT1S1 GeneAKT1 substrate 1 (proline-rich) AKT1S1 is a proline-rich substrate of AKT (MIM 164730) that binds 14-3-3 protein (see YWHAH, MIM 113508) when phosphorylated (Kovacina et al., 2003 [PubMed 12524439]).[supplied by OMIM, Mar 2008] |
LOC105376719 Genebasic proline-rich protein-like |
SRSF11P1 Geneserine/arginine-rich splicing factor 11 pseudogene 1 |
CSRP1 Genecysteine and glycine-rich protein 1 This gene encodes a member of the cysteine-rich protein (CSRP) family. This gene family includes a group of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this gene product occurs in proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2010] |
CSRP3 Genecysteine and glycine-rich protein 3 (cardiac LIM protein) This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008] |
CSRP2 Genecysteine and glycine-rich protein 2 CSRP2 is a member of the CSRP family of genes, encoding a group of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. CRP2 contains two copies of the cysteine-rich amino acid sequence motif (LIM) with putative zinc-binding activity, and may be involved in regulating ordered cell growth. Other genes in the family include CSRP1 and CSRP3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
LURAP1L Geneleucine rich adaptor protein 1-like Predicted to be involved in regulation of signal transduction. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105378577 Genebasic proline-rich protein-like |
ZRSR2 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 This gene encodes an essential splicing factor. The encoded protein associates with the U2 auxiliary factor heterodimer, which is required for the recognition of a functional 3' splice site in pre-mRNA splicing, and may play a role in network interactions during spliceosome assembly. [provided by RefSeq, Jul 2008] |
LRRC37A16P Geneleucine rich repeat containing 37, member A16, pseudogene |
LRGUK Geneleucine-rich repeats and guanylate kinase domain containing Predicted to enable guanylate kinase activity. Predicted to be involved in axoneme assembly and spermatogenesis. Predicted to be located in acrosomal vesicle and manchette. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
LURAP1 Geneleucine rich adaptor protein 1 Involved in positive regulation of canonical NF-kappaB signal transduction and positive regulation of cytokine production. Located in cytosol and intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
LRFN5 Geneleucine rich repeat and fibronectin type III domain containing 5 This gene encodes a protein that belongs to the leucine-rich repeat and fibronectin type III domain-containing family of proteins. A similar protein in mouse, a glycosylated transmembrane protein, is thought to function in presynaptic differentiation. [provided by RefSeq, Sep 2016] |
SRSF5 Geneserine/arginine-rich splicing factor 5 The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
SRSF4 Geneserine/arginine-rich splicing factor 4 Enables RNA binding activity. Involved in negative regulation of mRNA splicing, via spliceosome. Located in nuclear speck. Biomarker of Down syndrome; acute myeloid leukemia; clear cell renal cell carcinoma; and colon adenocarcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
SRSF7 Geneserine/arginine-rich splicing factor 7 The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an N-terminal RNA recognition motif (RRM) for binding RNA and a C-terminal RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018] |
SRSF6 Geneserine/arginine-rich splicing factor 6 The protein encoded by this gene is involved in mRNA splicing and may play a role in the determination of alternative splicing. The encoded nuclear protein belongs to the splicing factor SR family and has been shown to bind with and modulate another member of the family, SFRS12. Alternative splicing results in multiple transcript variants. In addition, two pseudogenes, one on chromosome 17 and the other on the X chromosome, have been found for this gene.[provided by RefSeq, Sep 2010] |
SRSF1 Geneserine/arginine-rich splicing factor 1 This gene encodes a member of the arginine/serine-rich splicing factor protein family. The encoded protein can either activate or repress splicing, depending on its phosphorylation state and its interaction partners. Multiple transcript variants have been found for this gene. There is a pseudogene of this gene on chromosome 13. [provided by RefSeq, Jun 2014] |
SRSF3 Geneserine/arginine-rich splicing factor 3 The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Two transcript variants, one protein-coding and the other non-coding, have been found for this gene. [provided by RefSeq, Sep 2010] |
SRSF2 Geneserine/arginine-rich splicing factor 2 The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Two transcript variants encoding the same protein and one non-coding transcript variant have been found for this gene. In addition, a pseudogene of this gene has been found on chromosome 11. [provided by RefSeq, Sep 2010] |
SRSF9 Geneserine/arginine-rich splicing factor 9 The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an RNA recognition motif (RRM) for binding RNA and an RS domain for binding other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Two pseudogenes, one on chromosome 15 and the other on chromosome 21, have been found for this gene. [provided by RefSeq, Sep 2010] |
SRSF8 Geneserine/arginine-rich splicing factor 8 This gene encodes a member of a family of proteins containing a ribonucleoprotein (RNP)-type RNA binding motif and a carboxyl-terminal arginine-serine-rich (RS) domain. The encoded protein functions as a pre-mRNA splicing factor. There is a pseudogene for this gene on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013] |
LOC100131038 GeneGC-rich promoter binding protein 1 pseudogene |
LRRFIP1P1 Geneleucine rich repeat (in FLII) interacting protein 1 pseudogene 1 |
PRB1 Geneproline-rich protein BstNI subfamily 1 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
SSC4D Genescavenger receptor cysteine rich family, 4 domains The scavenger receptor cysteine-rich (SRCR) superfamily is an ancient and highly conserved group of cell surface and/or secreted proteins, some of which are involved in the development of the immune system and the regulation of both innate and adaptive immune responses. Group B SRCR domains usually contain 8 regularly spaced cysteines that give rise to a well-defined intradomain disulfide-bond pattern.[supplied by OMIM, Apr 2004] |
LOC105370298 Geneproline-rich protein 20A |
GRXCR1 Geneglutaredoxin, cysteine rich 1 This gene is one of 60 loci associated with autosomal-recessive nonsyndromic hearing impairment. This gene encodes a protein which contains GRX-like domains; these domains play a role in the S-glutathionylation of proteins and may be involved in actin organization in hair cells. [provided by RefSeq, Sep 2010] |
SERF1AP1 Genesmall EDRK-rich factor 1A (telomeric) pseudogene 1 |
PRR20B Geneproline rich 20B This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008] |
PRR20C Geneproline rich 20C This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008] |
PRR20D Geneproline rich 20D This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008] |
PRR20E Geneproline rich 20E This gene is one of five identical loci in a cluster on chromosome 13q21.1. The predicted protein is proline-rich and contains several dopamine D4 receptor signatures and PRINTS domains. [provided by RefSeq, Oct 2008] |
CHORDC1 Genecysteine and histidine-rich domain (CHORD) containing 1 Enables Hsp90 protein binding activity. Predicted to be involved in several processes, including centrosome duplication; chaperone-mediated protein folding; and negative regulation of Rho-dependent protein serine/threonine kinase activity. [provided by Alliance of Genome Resources, Mar 2025] |
LRFN3 Geneleucine rich repeat and fibronectin type III domain containing 3 Predicted to be involved in regulation of presynapse assembly; regulation of synaptic membrane adhesion; and synaptic membrane adhesion. Predicted to be located in plasma membrane. Predicted to be active in cell surface; glutamatergic synapse; and synaptic membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRFN2 Geneleucine rich repeat and fibronectin type III domain containing 2 Predicted to be involved in modulation of chemical synaptic transmission and regulation of postsynapse organization. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including Schaffer collateral - CA1 synapse; cell surface; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRFN1 Geneleucine rich repeat and fibronectin type III domain containing 1 Predicted to be involved in regulation of postsynaptic density assembly. Predicted to be located in plasma membrane. Predicted to be active in cell surface; postsynaptic density membrane; and presynaptic active zone membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRFN4 Geneleucine rich repeat and fibronectin type III domain containing 4 Predicted to be involved in regulation of postsynaptic density assembly; regulation of presynapse assembly; and synaptic membrane adhesion. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including GABA-ergic synapse; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PRB2 Geneproline-rich protein BstNI subfamily 2 This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature isoforms before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats, polymorphic cleavage sites and polymorphic stop codons have been identified. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, May 2023] |
PRB3 Geneproline-rich protein BstNI subfamily 3 This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the `Long` allele. The protein isoforms encoded by this gene are recognized as the `first line of oral defense` against the detrimental effects of polyphenols in the diet and pathogen infections. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. [provided by RefSeq, Nov 2015] |
PRB4 Geneproline-rich protein BstNI subfamily 4 This gene encodes a member of the heterogeneous family of basic, proline-rich, human salivary glycoproteins. The encoded preproprotein undergoes proteolytic processing to generate one or more mature peptides before secretion from the parotid glands. Multiple alleles of this gene exhibiting variations in the length of the tandem repeats have been identified. The reference genome encodes the `Small` allele. This gene is located in a cluster of closely related salivary proline-rich proteins on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Nov 2015] |
LOC100631310 Geneproline rich 21 pseudogene |
LRWD1 Geneleucine-rich repeats and WD repeat domain containing 1 The protein encoded by this gene interacts with components of the origin recognition complex (ORC) and regulates the formation of the prereplicative complex. The encoded protein stabilizes the ORC and therefore aids in DNA replication. This protein is required for the G1/S phase transition of the cell cycle. In addition, the encoded protein binds to trimethylated histone H3 in heterochromatin and recruits the ORC and lysine methyltransferases, which help maintain the repressive heterochromatic state. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015] |
STAC GeneSH3 and cysteine rich domain Predicted to enable transmembrane transporter binding activity. Predicted to be involved in positive regulation of protein localization to plasma membrane; positive regulation of voltage-gated calcium channel activity; and skeletal muscle contraction. Predicted to act upstream of or within cellular response to heat; muscle contraction; and regulation of voltage-gated calcium channel activity. Predicted to be located in cytoplasmic side of plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102725118 Geneproline-rich protein 23D1-like |
LOC105370939 Geneproline-rich protein HaeIII subfamily 1-like |
LOC100421235 Geneserine/arginine-rich splicing factor 9 pseudogene |
LOC100128297 Geneserine/arginine-rich splicing factor 10 pseudogene |
LOC647145 Geneserine/arginine-rich splicing factor 8 pseudogene |
PRRG4 Geneproline rich Gla (G-carboxyglutamic acid) 4 (transmembrane) Enables WW domain binding activity. Predicted to be involved in blood coagulation. Located in plasma membrane. Biomarker of cholangiocarcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
PRRG1 Geneproline rich Gla (G-carboxyglutamic acid) 1 This gene encodes a vitamin K-dependent, gamma-carboxyglutamic acid (Gla)-containing, single-pass transmembrane protein. This protein contains a Gla domain at the N-terminus, preceded by a propeptide sequence required for post-translational gamma-carboxylation of specific glutamic acid residues by a vitamin K-dependent gamma-carboxylase. The C-terminus is proline-rich containing PPXY and PXXP motifs found in a variety of signaling and cytoskeletal proteins. This gene is highly expressed in the spinal cord. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010] |
PRRG2 Geneproline rich Gla (G-carboxyglutamic acid) 2 The protein encoded by this gene is a single-pass transmembrane protein containing an N-terminal gamma-carboxyglutamic acid (Gla) domain and tandem Pro/Leu-Pro-Xaa-Tyr (PY) motifs at its C-terminal end. The Gla domain is exposed on the cell surface while the PY motifs are cytoplasmic. The PY motifs of the encoded protein have been shown to interact with YAP1, a WW domain-containing protein. Therefore, it is thought that the encoded protein may be part of a signal transduction pathway. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015] |
PRRG3 Geneproline rich Gla (G-carboxyglutamic acid) 3 (transmembrane) This gene encodes a protein which contains a vitamin K-dependent carboxylation/gamma-carboxyglutamic domain. The encoded protein is a member of a family of vitamin K-dependent transmembrane proteins which contain a glutamate-rich extracellular domain. [provided by RefSeq, Aug 2011] |
LOC105378804 Geneleucine-rich repeat-containing protein 53 |
LOC105378803 Geneleucine-rich repeat-containing protein 53-like Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420850 Geneleucine rich repeat containing 37B pseudogene |
LOC105371179 Geneproline-rich receptor-like protein kinase PERK2 |
LOC105373442 Genebasic proline-rich protein-like |
ARID2 GeneAT rich interactive domain 2 (ARID, RFX-like) This gene encodes a member of the AT-rich interactive domain (ARID)-containing family of DNA-binding proteins. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and chromatin structure modification. This protein functions as a subunit of the polybromo- and BRG1-associated factor or PBAF (SWI/SNF-B) chromatin remodeling complex which facilitates ligand-dependent transcriptional activation by nuclear receptors. Mutations in this gene are associated with hepatocellular carcinomas. A pseudogene of this gene is found on chromosome1. [provided by RefSeq, Dec 2016] |
ARGLU1 Genearginine and glutamate rich 1 Enables nuclear receptor coactivator activity and pre-mRNA binding activity. Involved in regulation of alternative mRNA splicing, via spliceosome. Located in cytosol; mitochondrion; and nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
LOC391048 Genecysteine and histidine-rich domain (CHORD) containing 1 pseudogene |
LRRC8C Geneleucine rich repeat containing 8 family, member C Enables volume-sensitive anion channel activity. Involved in cyclic-GMP-AMP transmembrane import across plasma membrane and monoatomic anion transmembrane transport. Located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRIT2 Geneleucine-rich repeat, immunoglobulin-like and transmembrane domains 2 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRIT3 Geneleucine-rich repeat, immunoglobulin-like and transmembrane domains 3 This gene encodes a protein that has a fibronectin type III domain and a C-terminal transmembrane domain, as well as a leucine-rich repeat domain and immunoglobulin-like domain near the N-terminus. The encoded protein may regulate fibroblast growth factor receptors and affect the modification of these receptors, which are glycosylated differently in the Golgi and endoplasmic reticulum. Mutations in this gene are associated with congenital stationary night blindness, type 1F. [provided by RefSeq, May 2013] |
LRIT1 Geneleucine-rich repeat, immunoglobulin-like and transmembrane domains 1 Predicted to be involved in visual perception. Predicted to be located in dendrite; endoplasmic reticulum; and membrane. Predicted to be active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105378949 Genebasic salivary proline-rich protein 2-like |
LOC105378947 Geneproline-rich extensin-like protein EPR1 |
PHLPP2 GenePH domain and leucine rich repeat protein phosphatase 2 Predicted to enable protein serine/threonine phosphatase activity. Predicted to be involved in intracellular signal transduction. Located in several cellular components, including intercellular bridge; mitotic spindle; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC37A5P Geneleucine rich repeat containing 37, member A5, pseudogene |
ARID4A GeneAT rich interactive domain 4A (RBP1-like) The protein encoded by this gene is a ubiquitously expressed nuclear protein. It binds directly, with several other proteins, to retinoblastoma protein (pRB) which regulates cell proliferation. pRB represses transcription by recruiting the encoded protein. This protein, in turn, serves as a bridging molecule to recruit HDACs and, in addition, provides a second HDAC-independent repression function. The encoded protein possesses transcriptional repression activity. Multiple alternatively spliced transcripts have been observed for this gene, although not all transcript variants have been fully described. [provided by RefSeq, Jul 2008] |
ARID4B GeneAT rich interactive domain 4B (RBP1-like) This gene encodes a protein with sequence similarity to retinoblastoma-binding protein-1. The encoded protein is a subunit of the histone deacetylase-dependant SIN3A transcriptional corepressor complex, which functions in diverse cellular processes including proliferation, differentiation, apoptosis, oncogenesis, and cell fate determination. The gene product is recognized by IgG antibody isolated from a breast cancer patient and appears to be a molecular marker associated with a broad range of human malignancies. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Jul 2008] |
KNOP1P4 Genelysine-rich nucleolar protein 1 pseudogene 4 |
PRRT4 Geneproline-rich transmembrane protein 4 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PRRT1 Geneproline-rich transmembrane protein 1 Enables identical protein binding activity. Predicted to be involved in several processes, including long-term synaptic depression; protein localization to cell surface; and regulation of AMPA receptor activity. Predicted to act upstream of or within several processes, including learning or memory; long-term synaptic potentiation; and synapse organization. Predicted to be located in plasma membrane and synaptic vesicle membrane. Predicted to be active in glutamatergic synapse and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PRRT3 Geneproline-rich transmembrane protein 3 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PRRT2 Geneproline-rich transmembrane protein 2 This gene encodes a transmembrane protein containing a proline-rich domain in its N-terminal half. Studies in mice suggest that it is predominantly expressed in brain and spinal cord in embryonic and postnatal stages. Mutations in this gene are associated with episodic kinesigenic dyskinesia-1. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012] |
WRBP1 Genetryptophan rich basic protein pseudogene 1 |
RSRP1 Genearginine/serine-rich protein 1 Involved in spliceosomal complex assembly. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SRSF10P1 Geneserine/arginine-rich splicing factor 10 pseudogene 1 |
PRR12 Geneproline rich 12 This gene encodes a proline-rich protein that contains two A-T hook DNA binding domains. A chromosomal translocation and gene fusion between this gene and zinc finger, MIZ-type containing 1 (Gene ID: 57178) may underlie intellectual disability and neuropsychiatric problems in a human patient. Enriched expression of this gene in embryonic mouse brain suggests that this gene may play a role in nervous system development. [provided by RefSeq, Jul 2016] |
PRR13 Geneproline rich 13 Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PRR11 Geneproline rich 11 Involved in regulation of cell cycle. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PRR16 Geneproline rich 16 Involved in positive regulation of cell size and positive regulation of translation. [provided by Alliance of Genome Resources, Mar 2025] |
PRR14 Geneproline rich 14 The protein encoded by this gene tethers heterochromatin to the nuclear laminar scaffold by binding heterochromatin protein 1 (HP1) and the nuclear lamina. The tether is broken during mitosis and reforms quickly after mitosis, with the encoded protein first binding HP1 and then attaching to the nuclear lamina. This protein also has been shown to promote MyoD activity and skeletal myogenesis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2016] |
PRR15 Geneproline rich 15 |
PRR18 Geneproline rich 18 |
PRR19 Geneproline rich 19 Predicted to be involved in meiotic cell cycle. Predicted to be located in chromosome and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LRR1 Geneleucine rich repeat protein 1 The protein encoded by this gene contains a leucine-rich repeat (LRR). It specifically interacts with TNFRSF9/4-1BB, a member of the tumor necrosis factor receptor (TNFR) superfamily. Overexpression of this gene suppresses the activation of NF-kappa B induced by TNFRSF9 or TNF receptor-associated factor 2 (TRAF2), which suggests that this protein is a negative regulator of TNFRSF9-mediated signaling cascades. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011] |
LRRCC1 Geneleucine rich repeat and coiled-coil centrosomal protein 1 This gene encodes a centrosomal protein that maintains the structural integrity of the centrosome and plays a key role in mitotic spindle formation. The encoded protein contains an N-terminal leucine-rich repeat domain and a C-terminal coiled-coil domain. It associates with the centrosome throughout the cell cycle and accumulates on the mitotic centrosome. [provided by RefSeq, Mar 2017] |
PRR3 Geneproline rich 3 Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
PRR4 Geneproline rich 4 (lacrimal) This gene encodes a member of the proline-rich protein family that lacks a conserved repetitive domain. This protein may play a role in protective functions in the eye. Alternative splicing result in multiple transcript variants. Read-through transcription also exists between this gene and the upstream PRH1 (proline-rich protein HaeIII subfamily 1) gene. [provided by RefSeq, Feb 2011] |
PRR5 Geneproline rich 5 (renal) This gene encodes a protein with a proline-rich domain. This gene is located in a region of chromosome 22 reported to contain a tumor suppressor gene that may be involved in breast and colorectal tumorigenesis. The protein is a component of the mammalian target of rapamycin complex 2 (mTORC2), and it regulates platelet-derived growth factor (PDGF) receptor beta expression and PDGF signaling to Akt and S6K1. Alternative splicing and the use of alternative promoters results in transcripts encoding different isoforms. Read-through transcripts from this gene into the downstream Rho GTPase activating protein 8 (ARHGAP8) gene also exist, which led to the original description of PRR5 and ARHGAP8 being a single gene. [provided by RefSeq, Nov 2010] |
PRR7 Geneproline rich 7 (synaptic) Enables long-chain fatty acid binding activity; protein tyrosine kinase binding activity; and ubiquitin-like protein ligase binding activity. Involved in positive regulation of apoptotic process; positive regulation of cysteine-type endopeptidase activity; and regulation of transcription by RNA polymerase I. Located in several cellular components, including cytosol; nucleoplasm; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CRIPAK Genecysteine-rich PAK1 inhibitor CRIPAK is a negative regulator of PAK1 (MIM 602590) that is upregulated by estrogen (Talukder et al., 2006 [PubMed 16278681]).[supplied by OMIM, Mar 2008] |
LOC100133261 Genecysteine and histidine-rich domain (CHORD) containing 1 pseudogene |
CYYR1 Genecysteine/tyrosine-rich 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC3C Geneleucine rich repeat containing 3C Predicted to be located in membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929527 Geneserine/arginine-rich splicing factor 3 pseudogene |
LOC100129202 Genearginine/serine-rich coiled-coil 1 pseudogene |
KPRP Genekeratinocyte proline-rich protein This gene encodes a proline-rich skin protein possibly involved in keratinocyte differentiation. [provided by RefSeq, Jul 2016] |
GCFC2 GeneGC-rich sequence DNA-binding factor 2 The first mRNA transcript isolated for this gene was part of an artificial chimera derived from two distinct gene transcripts and a primer used in the cloning process (see Genbank accession M29204). A positively charged amino terminus present only in the chimera was determined to bind GC-rich DNA, thus mistakenly thought to identify a transcription factor gene. [provided by RefSeq, Jul 2008] |
CRIP1P4 Genecysteine-rich protein 1 (intestinal) pseudogene 4 |
CRIP1P2 Genecysteine-rich protein 1 (intestinal) pseudogene 2 |
STPG2 Genesperm-tail PG-rich repeat containing 2 |
STPG1 Genesperm-tail PG-rich repeat containing 1 Involved in positive regulation of apoptotic process and positive regulation of mitochondrial membrane permeability involved in apoptotic process. Predicted to be located in mitochondrion and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC70 Geneleucine rich repeat containing 70 Involved in positive regulation of response to cytokine stimulus. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC71 Geneleucine rich repeat containing 71 |
LRRC72 Geneleucine rich repeat containing 72 |
LRRC73 Geneleucine rich repeat containing 73 |
SFPQ Genesplicing factor proline/glutamine-rich Enables DNA binding activity; histone deacetylase binding activity; and protein homodimerization activity. Involved in several processes, including alternative mRNA splicing, via spliceosome; positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway; and regulation of transcription by RNA polymerase II. Acts upstream of or within double-strand break repair via homologous recombination. Located in chromatin; nuclear matrix; and paraspeckles. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420575 Geneleucine rich repeat containing 57 pseudogene |
LOC646030 Geneleucine-rich repeat-containing protein 37A2-like |
LOC100533935 Geneleucine rich repeat containing 37, member A2 pseudogene |
SMCP Genesperm mitochondria-associated cysteine-rich protein Sperm mitochondria differ in morphology and subcellular localization from those of somatic cells. They are elongated, flattened, and arranged circumferentially to form a helical coiled sheath in the midpiece of the sperm flagellum. The protein encoded by this gene localizes to the capsule associated with the mitochondrial outer membranes and is thought to function in the organization and stabilization of the helical structure of the sperm's mitochondrial sheath. [provided by RefSeq, Jul 2008] |
KNOP1P1 Genelysine-rich nucleolar protein 1 pseudogene 1 |
KNOP1P3 Genelysine-rich nucleolar protein 1 pseudogene 3 |
LOC101060825 Geneserine/arginine-rich splicing factor 11-like |
LOC100128738 Geneleucine rich repeat (in FLII) interacting protein 2 pseudogene |
LRRC16A Geneleucine rich repeat containing 16A Involved in several processes, including actin filament network formation; plasma membrane bounded cell projection organization; and positive regulation of cellular component organization. Located in several cellular components, including lamellipodium; macropinosome; and nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC16B Geneleucine rich repeat containing 16B Predicted to be involved in cell migration and regulation of Arp2/3 complex-mediated actin nucleation. Located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
STAC2 GeneSH3 and cysteine rich domain 2 This gene encodes a protein containing an SH3 domain and a zinc finger domain. The encoded protein has been shown to regulate calcium channel inactivation in a human cell line. Reduced expression of this gene has been observed in human heart failure. [provided by RefSeq, May 2017] |
STAC3 GeneSH3 and cysteine rich domain 3 The protein encoded by this gene is a component of the excitation-contraction coupling machinery of muscles. This protein is a member of the Stac gene family and contains an N-terminal cysteine-rich domain and two SH3 domains. Mutations in this gene are a cause of Native American myopathy. [provided by RefSeq, Nov 2013] |
LOC100131126 Geneleucine rich repeat containing 59 pseudogene |
LEKR1 Geneleucine, glutamate and lysine rich 1 |
CYR61 Genecysteine-rich, angiogenic inducer, 61 The secreted protein encoded by this gene is growth factor-inducible and promotes the adhesion of endothelial cells. The encoded protein interacts with several integrins and with heparan sulfate proteoglycan. This protein also plays a role in cell proliferation, differentiation, angiogenesis, apoptosis, and extracellular matrix formation. [provided by RefSeq, Sep 2011] |
LOC100128964 Geneserine/arginine-rich splicing factor 3 pseudogene |
GPBP1L1 GeneGC-rich promoter binding protein 1-like 1 Predicted to enable DNA binding activity and RNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ANP32BP3 Geneacidic (leucine-rich) nuclear phosphoprotein 32 family, member B pseudogene 3 |
LOC100127962 Genecoiled-coil serine-rich protein 2 pseudogene |
LOC100418997 Geneproline rich 21 pseudogene |
LOC100418990 Geneproline rich 21 pseudogene |
LOC100418991 Geneproline rich 21 pseudogene |
LOC100418993 Geneproline rich 21 pseudogene |
LOC100499471 Geneleucine rich repeat containing 14 pseudogene |
LOC105375604 Geneuncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like |
LELP1 Genelate cornified envelope-like proline-rich 1 |
SMLR1 Genesmall leucine-rich protein 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PRR23D2 Geneproline rich 23 domain containing 2 |
PRR23D1 Geneproline rich 23 domain containing 1 |
PRR14L Geneproline rich 14-like |
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] |
LOC102724064 Geneproline-rich receptor-like protein kinase PERK13 |
CCER1 Genecoiled-coil glutamate-rich protein 1 |
CCER2 Genecoiled-coil glutamate-rich protein 2 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105378158 Genebasic proline-rich protein-like |
PRRC2C Geneproline-rich coiled-coil 2C Enables RNA binding activity. Involved in stress granule assembly. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
PRRC2B Geneproline-rich coiled-coil 2B Enables RNA binding activity. Predicted to be involved in cell differentiation. Predicted to act upstream of or within in utero embryonic development. [provided by Alliance of Genome Resources, Mar 2025] |
PRRC2A Geneproline-rich coiled-coil 2A A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010] |
PRRC1 Geneproline-rich coiled-coil 1 Predicted to enable protein kinase A regulatory subunit binding activity. Predicted to be involved in epithelial structure maintenance. Predicted to be located in Golgi apparatus. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419008 Geneproline rich 20B pseudogene |
LOC101929211 Geneproline-rich protein 2-like |
ARID1B GeneAT rich interactive domain 1B (SWI1-like) This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016] |
ARID1A GeneAT rich interactive domain 1A (SWI-like) This gene encodes a member of the SWI/SNF family, whose members have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. It possesses at least two conserved domains that could be important for its function. First, it has a DNA-binding domain that can specifically bind an AT-rich DNA sequence known to be recognized by a SNF/SWI complex at the beta-globin locus. Second, the C-terminus of the protein can stimulate glucocorticoid receptor-dependent transcriptional activation. It is thought that the protein encoded by this gene confers specificity to the SNF/SWI complex and may recruit the complex to its targets through either protein-DNA or protein-protein interactions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LRRC75B Geneleucine rich repeat containing 75B |
LRRC75A Geneleucine rich repeat containing 75A Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be part of Cul2-RING ubiquitin ligase complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LINGO4 Geneleucine rich repeat and Ig domain containing 4 Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LINGO3 Geneleucine rich repeat and Ig domain containing 3 Predicted to be located in membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LINGO2 Geneleucine rich repeat and Ig domain containing 2 Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in several cellular components, including extracellular space; glutamatergic synapse; and synaptic membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LINGO1 Geneleucine rich repeat and Ig domain containing 1 Predicted to enable epidermal growth factor receptor binding activity. Predicted to act upstream of or within negative regulation of oligodendrocyte differentiation; negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and neuron development. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including extracellular space; glutamatergic synapse; and presynapse. Implicated in autosomal recessive intellectual developmental disorder 64 and glaucoma. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105370297 Geneserine/arginine-rich splicing factor SR45-like |
KNOP1 Genelysine-rich nucleolar protein 1 The protein encoded by this gene is a nucleolar protein that interacts with zinc finger 106 protein. The encoded protein has several of the same characteristics as nucleostemin and may be involved in testis development. [provided by RefSeq, Feb 2017] |
ELFN1 Geneextracellular leucine-rich repeat and fibronectin type III domain containing 1 Predicted to enable protein phosphatase inhibitor activity. Predicted to be involved in synapse organization. Predicted to act upstream of or within several processes, including chemical synaptic transmission; synapse assembly; and visual perception. Predicted to be located in dendrite and excitatory synapse. Predicted to be active in several cellular components, including axon terminus; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ELFN2 Geneextracellular leucine-rich repeat and fibronectin type III domain containing 2 Predicted to enable protein phosphatase inhibitor activity. Predicted to be involved in synaptic membrane adhesion. Predicted to act upstream of or within chemical synaptic transmission; establishment of protein localization; and gene expression. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
SPATS1 Genespermatogenesis associated, serine-rich 1 |
SPATS2 Genespermatogenesis associated, serine-rich 2 Enables RNA binding activity. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
DERPC GeneDERPC proline and glycine rich nuclear protein Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LRRC51 Geneleucine rich repeat containing 51 This gene belongs to the leucine-rich repeat containing family. The encoded protein contains a transmembrane domain and two leucine-rich repeat domains. Unlike in mouse and other mammals, readthrough transcription is observed in primates between this gene and the adjacent transmembrane O-methyltransferase (Tomt) gene. Previously, this locus was annotated as a single gene representing the readthrough transcripts as well as the two different transcript species that encoded different proteins. It has since been split into three genes, including the two stand-alone genes and a third gene representing the readthrough transcription. [provided by RefSeq, Feb 2022] |
FBXL9P GeneF-box and leucine rich repeat protein, pseudogene This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class and, in addition to an F-box, contains 9 tandem leucine-rich repeats. Two transcript variants encoding the same protein have been found for this gene. Other variants may occur, but their full-length natures have not been characterized. [provided by RefSeq, Jul 2008] |
STPG4 Genesperm-tail PG-rich repeat containing 4 Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in epigenetic programing of male pronucleus. Predicted to act upstream of or within pyrimidine-containing compound catabolic process. Predicted to be located in cytoplasm and nucleus. Predicted to be active in female pronucleus; germinal vesicle; and male pronucleus. [provided by Alliance of Genome Resources, Mar 2025] |
FBXL21P GeneF-box and leucine rich repeat protein 21, pseudogene This locus represents a transcribed pseudogene that is related to genes encoding members of the F-box family of proteins. [provided by RefSeq, Nov 2017] |
LRMDA Geneleucine rich melanocyte differentiation associated This gene encodes a leucine-rich repeat protein. The encoded protein is thought to play a role in melanocyte differentiation. Mutations in this gene have been associated with autosomal recessive oculocutaneous albinism 7 (OCA7). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015] |
STPG3 Genesperm-tail PG-rich repeat containing 3 Predicted to be active in cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
SERTM2 Geneserine rich and transmembrane domain containing 2 Predicted to be located in membrane. Predicted to be active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
GREP1 Geneglycine rich extracellular protein 1 |
LRRC77P Geneleucine rich repeat containing 77, pseudogene |
LOC122455342 Genetestis-specific serine/proline-rich protein |
PRRT1B Geneproline rich transmembrane protein 1B Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SPRR5 Genesmall proline rich protein 5 |
PRR20G Geneproline rich 20G |
SCPPPQ1 Genesecretory calcium-binding phosphoprotein proline-glutamine rich 1 |
LRTM3 Geneleucine rich repeat transmembrane protein 3 |
T-Cell/Histiocyte Rich Large B-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease T-Cell/Histiocyte Rich Large B-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
burkitt lymphoma; hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoproliferative disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease burkitt lymphoma; hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brill-symmers disease; lymphoma, follicular; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
LARGE PROLINE-RICH PROTEIN BAG6 Gene Setinteracting proteins for the LARGE PROLINE-RICH PROTEIN BAG6 drug from theDGIdb Drug Targets 2026 dataset. |
Lymphocyte Rich Classical Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lymphocyte Rich Classical Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Lymphocyte-Rich Classical Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Lymphocyte-Rich Classical Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
lymphoma; non-hodgkin's lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, non-hodgkin; lymphoma, non-hodgkin's; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, non-hodgkin; lymphoma, non-hodgkin's; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin disease; lymphoma; lymphoma, non-hodgkin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin disease; lymphoma; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Thrombophilia, histidine-rich glycoprotein-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, histidine-rich glycoprotein-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
triglyceride-rich lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the triglyceride-rich lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
triglyceride-rich lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the triglyceride-rich lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset. |
lymphoplasmacyte-rich meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lymphoplasmacyte-rich meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lipid-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rich Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term rich in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
triglyceride-rich lipoprotein particle clearance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the triglyceride-rich lipoprotein particle clearance biological process from the curated GO Biological Process Annotations 2015 dataset. |
triglyceride-rich lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
triglyceride-rich lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the triglyceride-rich lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
proline-rich region binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the proline-rich region binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
au-rich element binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the au-rich element binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mrna 3'-utr au-rich region binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mrna 3'-utr au-rich region binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
purine-rich negative regulatory element binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the purine-rich negative regulatory element binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
pre-mrna intronic pyrimidine-rich binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the pre-mrna intronic pyrimidine-rich binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Pleiotrophin/Midkine disulphide-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pleiotrophin/Midkine disulphide-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich protein PRCC Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich protein PRCC protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine/arginine-rich splicing factor 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine/arginine-rich splicing factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine/arginine-rich splicing factor 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine/arginine-rich splicing factor 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine/histidine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine/histidine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich acidic protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich acidic protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich nuclear receptor coactivator 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich nuclear receptor coactivator 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ADAM, cysteine-rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the ADAM, cysteine-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat flightless-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat flightless-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline/serine-rich coiled-coil protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline/serine-rich coiled-coil protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich secretory protein, allergen V5/Tpx-1-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich secretory protein, allergen V5/Tpx-1-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Purine-rich element binding protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Purine-rich element binding protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein/late cornified envelope protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat, ribonuclease inhibitor subtype Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat, ribonuclease inhibitor subtype protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FAST kinase leucine-rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FAST kinase leucine-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich Golgi apparatus protein 1 repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich Golgi apparatus protein 1 repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine rich repeat 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine rich repeat 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SH3-binding, glutamic acid-rich protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SH3-binding, glutamic acid-rich protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Arginine/serine-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Arginine/serine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histidine-rich calcium-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histidine-rich calcium-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 16C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 16C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histidine-rich calcium-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histidine-rich calcium-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myristoylated alanine-rich C-kinase substrate MARCKS Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myristoylated alanine-rich C-kinase substrate MARCKS protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spermatogenesis-associated serine-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated serine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine/serine-rich nuclear protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine/serine-rich nuclear protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AT-rich interactive domain-containing protein 5B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AT-rich interactive domain-containing protein 5B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutamate-rich protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutamate-rich protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 37A/B like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 37A/B like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TNFR/NGFR cysteine-rich region Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TNFR/NGFR cysteine-rich region protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich flanking region, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich flanking region, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 4B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 4B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 4C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 4C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich secretory protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich secretory protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
BRCA1, serine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the BRCA1, serine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Centromere protein Cenp-F, leucine-rich repeat-containing domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Centromere protein Cenp-F, leucine-rich repeat-containing domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat and fibronectin type-III domain-containing protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat and fibronectin type-III domain-containing protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histone deacetylase, glutamine rich N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histone deacetylase, glutamine rich N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coiled-coil domain-containing glutamate-rich protein family 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coiled-coil domain-containing glutamate-rich protein family 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine and tyrosine-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine and tyrosine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich Golgi apparatus protein 1 repeat, eukaryote Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich Golgi apparatus protein 1 repeat, eukaryote protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Trypsin Inhibitor-like, cysteine rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Trypsin Inhibitor-like, cysteine rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Groucho/TLE, N-terminal Q-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Groucho/TLE, N-terminal Q-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GC-rich sequence DNA-binding factor domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GC-rich sequence DNA-binding factor domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sperm-tail PG-rich repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sperm-tail PG-rich repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich domain, DPF-motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich domain, DPF-motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Furin-like cysteine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Furin-like cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Late cornified envelope-like proline-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Late cornified envelope-like proline-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 16B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 16B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PSP, proline-rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PSP, proline-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutamine synthetase, glycine-rich site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutamine synthetase, glycine-rich site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutamate-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutamate-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine-rich coiled-coil domain-containing protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine-rich coiled-coil domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CAP Gly-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CAP Gly-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing 41 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing 41 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 8, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 8, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich nuclear receptor coactivator 1/2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich nuclear receptor coactivator 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised protein family Cys-rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised protein family Cys-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GC-rich sequence DNA-binding factor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GC-rich sequence DNA-binding factor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich protein 15 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich protein 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised domain, cysteine-rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised domain, cysteine-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat, typical subtype Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat, typical subtype protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich glioma-inactivated , EPTP repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich glioma-inactivated , EPTP repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich membrane anchor 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich membrane anchor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FY-rich, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FY-rich, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Gamma-carboxyglutamic acid-rich (GLA) domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Gamma-carboxyglutamic acid-rich (GLA) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AP-3 complex subunit beta 1, serine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AP-3 complex subunit beta 1, serine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing protein 16A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing protein 16A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heat shock protein DnaJ, cysteine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Heat shock protein DnaJ, cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AT-rich interactive domain-containing protein 4B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AT-rich interactive domain-containing protein 4B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TACI, cysteine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TACI, cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myxococcus cysteine-rich repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myxococcus cysteine-rich repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine-rich transmembrane CYSTM domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine-rich transmembrane CYSTM domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat, cysteine-containing subtype Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat, cysteine-containing subtype protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine rich repeat 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine rich repeat 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Insulin-like growth factor binding protein, N-terminal, Cys-rich conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Insulin-like growth factor binding protein, N-terminal, Cys-rich conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Gap junction protein, cysteine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Gap junction protein, cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine-rich coiled-coil domain-containing protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine-rich coiled-coil domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine-rich coiled-coil domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine-rich coiled-coil domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat-containing N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat-containing N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine rich protein interaction Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine rich protein interaction protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lysine-rich nucleolar protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysine-rich nucleolar protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosome receptor lysine/proline rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosome receptor lysine/proline rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli protein, cysteine-rich repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli protein, cysteine-rich repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-rich protein 19 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-rich protein 19 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dickkopf, N-terminal cysteine-rich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dickkopf, N-terminal cysteine-rich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PRAME family/Leucine-rich repeat-containing protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PRAME family/Leucine-rich repeat-containing protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FY-rich, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FY-rich, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
proline-rich Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term proline-rich in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways Gene Setproteins participating in the Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways pathway from the Reactome Pathways dataset. |
Regulation of mRNA stability by proteins that bind AU-rich elements Gene Setproteins participating in the Regulation of mRNA stability by proteins that bind AU-rich elements pathway from the Reactome Pathways dataset. |
Hamman-Rich Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hamman-Rich Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Osteoclast-Rich Osteopetrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Osteoclast-Rich Osteopetrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid-Rich Breast Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid-Rich Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid-Rich Carcinoma Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lipid-Rich Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
triglyceride-rich lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2023 dataset. |
nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
ficolin-1-rich granule lumen Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the ficolin-1-rich granule lumen cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
ficolin-1-rich granule membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the ficolin-1-rich granule membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
ficolin-1-rich granule Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the ficolin-1-rich granule cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the triglyceride-rich plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
mRNA 3'-UTR AU-rich region binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the mRNA 3'-UTR AU-rich region binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
G-rich strand telomeric DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the G-rich strand telomeric DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
minor groove of adenine-thymine-rich DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the minor groove of adenine-thymine-rich DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
pre-mRNA intronic pyrimidine-rich binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the pre-mRNA intronic pyrimidine-rich binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
purine-rich negative regulatory element binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the purine-rich negative regulatory element binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
C-rich strand telomeric DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the C-rich strand telomeric DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
G-rich single-stranded DNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the G-rich single-stranded DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways Gene Setproteins participating in the Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways pathway from the Reactome Pathways 2024 dataset. |
Regulation of mRNA stability by proteins that bind AU-rich elements Gene Setproteins participating in the Regulation of mRNA stability by proteins that bind AU-rich elements pathway from the Reactome Pathways 2024 dataset. |
nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
triglyceride-rich lipoprotein particle remodeling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
ficolin-1-rich granule lumen Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the ficolin-1-rich granule lumen cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
ficolin-1-rich granule membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the ficolin-1-rich granule membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
ficolin-1-rich granule Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the ficolin-1-rich granule cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the triglyceride-rich plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
mRNA 3'-UTR AU-rich region binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the mRNA 3'-UTR AU-rich region binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
G-rich strand telomeric DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the G-rich strand telomeric DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
minor groove of adenine-thymine-rich DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the minor groove of adenine-thymine-rich DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
pre-mRNA intronic pyrimidine-rich binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the pre-mRNA intronic pyrimidine-rich binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
purine-rich negative regulatory element binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the purine-rich negative regulatory element binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
C-rich strand telomeric DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the C-rich strand telomeric DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
G-rich single-stranded DNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the G-rich single-stranded DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
lymphoplasmacyte-rich meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease lymphoplasmacyte-rich meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
lipid-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease lipid-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
glycogen-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease glycogen-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Breast lipid-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast lipid-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the triglyceride-rich plasma lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
ficolin-1-rich granule membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the ficolin-1-rich granule membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
ficolin-1-rich granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the ficolin-1-rich granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
ficolin-1-rich granule lumen Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the ficolin-1-rich granule lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
triglyceride-rich plasma lipoprotein particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the triglyceride-rich plasma lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
ficolin-1-rich granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the ficolin-1-rich granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
ficolin-1-rich granule lumen Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the ficolin-1-rich granule lumen cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
ficolin-1-rich granule membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the ficolin-1-rich granule membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Hereditary thrombophilia due to congenital histidine-rich Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital histidine-rich phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
organellar large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the organellar large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytosolic large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytosolic large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
gamma-tubulin large complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the gamma-tubulin large complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
preribosome, large subunit precursor Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the preribosome, large subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytosolic large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytosolic large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
chloroplast large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chloroplast large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
organellar large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the organellar large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
gamma-tubulin large complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the gamma-tubulin large complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
large latent transforming growth factor-beta complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the large latent transforming growth factor-beta complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
plastid large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plastid large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Large Drosha complex Gene Setproteins in the Large Drosha complex protein complex from the CORUM Protein Complexes dataset. |
Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa from the curated CTD Gene-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. |
adipocyte size, large subcutaneous abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipocyte size, large subcutaneous abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, large granular lymphocytic; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, large granular lymphocytic; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; felty's syndrome; large granular lymphocyte syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
large Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term large 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. |
LGLL - Large granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during LGLL - Large granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 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. |
ribosomal large subunit biogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal large subunit biogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
rna polymerase i transcriptional preinitiation complex assembly at the promoter for the nuclear large rrna transcript Gene SetFrom GO Biological Process Annotations 2015 genes participating in the rna polymerase i transcriptional preinitiation complex assembly at the promoter for the nuclear large rrna transcript biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal large subunit assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal large subunit assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of large conductance calcium-activated potassium channel activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of transcription of nuclear large rrna transcript from rna polymerase i promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription of nuclear large rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of transcription of nuclear large rrna transcript from rna polymerase i promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription of nuclear large rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
transcription of nuclear large rrna transcript from rna polymerase i promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the transcription of nuclear large rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription of nuclear large rrna transcript from rna polymerase i promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription of nuclear large rrna transcript from rna polymerase i promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of large conductance calcium-activated potassium channel activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal large subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal large subunit export from nucleus biological process from the curated GO Biological Process Annotations 2015 dataset. |
organellar large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the organellar large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
mitochondrial large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
gamma-tubulin large complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the gamma-tubulin large complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
preribosome, large subunit precursor Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the preribosome, large subunit precursor cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cytosolic large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cytosolic large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
large conductance calcium-activated potassium channel activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the large conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ribosomal large subunit binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ribosomal large subunit binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Large artery stroke Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Coronary artery disease or large artery stroke Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Coronary artery disease or large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 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. |
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. |
large sella turcica Gene SetFrom HPO Gene-Disease Associations genes associated with the large sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large earlobe Gene SetFrom HPO Gene-Disease Associations genes associated with the large earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large placenta Gene SetFrom HPO Gene-Disease Associations genes associated with the large placenta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large hands Gene SetFrom HPO Gene-Disease Associations genes associated with the large hands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large iliac wings Gene SetFrom HPO Gene-Disease Associations genes associated with the large iliac wings phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large artery calcification Gene SetFrom HPO Gene-Disease Associations genes associated with the large artery calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
contractures of the large joints Gene SetFrom HPO Gene-Disease Associations genes associated with the contractures of the large joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large hyperpigmented retinal spots Gene SetFrom HPO Gene-Disease Associations genes associated with the large hyperpigmented retinal spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large vessel vasculitis Gene SetFrom HPO Gene-Disease Associations genes associated with the large vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
medial calcification of large arteries Gene SetFrom HPO Gene-Disease Associations genes associated with the medial calcification of large arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased number of large peripheral myelinated nerve fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large face Gene SetFrom HPO Gene-Disease Associations genes associated with the large face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large joint dislocations Gene SetFrom HPO Gene-Disease Associations genes associated with the large joint dislocations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large cafe-au-lait macules with irregular margins Gene SetFrom HPO Gene-Disease Associations genes associated with the large cafe-au-lait macules with irregular margins phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large sternal ossification centers Gene SetFrom HPO Gene-Disease Associations genes associated with the large sternal ossification centers 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. |
large beaked nose Gene SetFrom HPO Gene-Disease Associations genes associated with the large beaked nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large posterior fontanelle Gene SetFrom HPO Gene-Disease Associations genes associated with the large posterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large fontanelles Gene SetFrom HPO Gene-Disease Associations genes associated with the large fontanelles 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. |
large fleshy ears Gene SetFrom HPO Gene-Disease Associations genes associated with the large fleshy ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large intestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the large intestinal polyposis 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. |
large tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the large tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large clumps of pigment irregularly distributed along hair shaft Gene SetFrom HPO Gene-Disease Associations genes associated with the large clumps of pigment irregularly distributed along hair shaft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large eyes Gene SetFrom HPO Gene-Disease Associations genes associated with the large eyes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large foramen magnum Gene SetFrom HPO Gene-Disease Associations genes associated with the large foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large forehead Gene SetFrom HPO Gene-Disease Associations genes associated with the large forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large for gestational age Gene SetFrom HPO Gene-Disease Associations genes associated with the large for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the large basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large central visual field defect Gene SetFrom HPO Gene-Disease Associations genes associated with the large central visual field defect 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. |
Leukemia, Large Granular Lymphocytic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Leukemia, Large Granular Lymphocytic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carbamoyl-phosphate synthase, large subunit, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, large subunit, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA large subunit methyltransferase E Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA large subunit methyltransferase E protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Large neutral amino acids transporter small subunit 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Large neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase C2, calpain, large subunit, domain III Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase C2, calpain, large subunit, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA large subunit methyltransferase F-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA large subunit methyltransferase F-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 1/3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 1/3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Citrate synthase-like, large alpha subdomain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Citrate synthase-like, large alpha subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA primase large subunit, eukaryotic/archaeal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase large subunit, eukaryotic/archaeal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Very large inducible GTPASE (VLIG)-type guanine nucleotide-binding (G) domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Very large inducible GTPASE (VLIG)-type guanine nucleotide-binding (G) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribonucleotide reductase large subunit, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribonucleotide reductase large subunit, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthetase large subunit-like, ATP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthetase large subunit-like, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CD81 antigen, large extracellular loop domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CD81 antigen, large extracellular loop domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthase, large subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, large subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron hydrogenase, large subunit, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase, large subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA primase, large subunit, eukaryotic Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, large subunit, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Disks large 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Disks large 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthetase, large subunit oligomerisation domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthetase, large subunit oligomerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthase large subunit, CPSase domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase large subunit, CPSase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U2 snRNP auxilliary factor, large subunit, splicing factor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U2 snRNP auxilliary factor, large subunit, splicing factor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribonucleotide reductase large subunit, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribonucleotide reductase large subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations 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. |
large lymphoid organs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the large lymphoid organs 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. |
large intestinal inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the large intestinal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
large penis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the large penis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
large anterior fontanelle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the large anterior fontanelle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal large intestinal transit time Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal large intestinal transit time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
large orbits Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the large orbits 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 ureter Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the large ureter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
LARGE Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for LARGE from the Pathway Commons Protein-Protein Interactions 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. |
large granular lymphocyte Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue large granular lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
large granular lymphocyte Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue large granular lymphocyte in proteomics datasets from the TISSUES Experimental 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. |
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. |
large granular lymphocyte Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue large granular lymphocyte 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-Artery Atherosclerosis (Embolus/Thrombosis) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Large-Artery Atherosclerosis (Embolus/Thrombosis) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Crohn'S Disease Of Large Bowel Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Crohn'S Disease Of Large Bowel in GWAS and other genetic association datasets from the DisGeNET 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. |
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. |
Large Beaked Nose Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Large Beaked Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vasculitis Of Large Artery Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vasculitis Of Large Artery 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. |
Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Large Hyperpigmented Retinal Spots Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Large Hyperpigmented Retinal Spots 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. |
Large Intestinal Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Large Intestinal Polyposis 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. |
Medial Calcification Of Large Arteries Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Medial Calcification Of Large Arteries in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Fleshy Ears Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Fleshy Ears in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large For Gestational Age Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large For Gestational Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Head (Disorder) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Head (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Sella Turcica Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Sella Turcica in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Iliac Wings Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Iliac Wings in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Fontanelle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Fontanelle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large, Squared Nose Tip Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large, Squared Nose Tip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Face Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Face in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Knee Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Knee in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Basal Ganglia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Tonsils (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Tonsils (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormally Large Globe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormally Large Globe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Forehead Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Forehead in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Number Of Large Peripheral Myelinated Nerve Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Number Of Large Peripheral Myelinated Nerve Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Earlobe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Earlobe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Tarsal Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Tarsal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Foramen Magnum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Foramen Magnum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Elbow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Elbow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Cafe-Au-Lait Macules With Irregular Margins Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Cafe-Au-Lait Macules With Irregular Margins 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. |
Large Posterior Fontanelle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Posterior Fontanelle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Central Visual Field Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Nostrils Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Nostrils in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Adenoids Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Adenoids in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Placenta Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Placenta in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Clumps Of Pigment Irregularly Distributed Along Hair Shaft Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Clumps Of Pigment Irregularly Distributed Along Hair Shaft in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Sternal Ossification Centers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Sternal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
ribosomal large subunit biogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ribosomal large subunit biogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
ribosomal large subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ribosomal large subunit export from nucleus biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of large conductance calcium-activated potassium channel activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of transcription of nucleolar large rRNA by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of transcription of nucleolar large rRNA by RNA polymerase I biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of transcription of nucleolar large rRNA by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of transcription of nucleolar large rRNA by RNA polymerase I biological process from the curated GO Biological Process Annotations 2023 dataset. |
ribosomal large subunit assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ribosomal large subunit assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
large intestinal transit Gene SetFrom GO Biological Process Annotations 2023 genes participating in the large intestinal transit biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitochondrial large ribosomal subunit assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitochondrial large ribosomal subunit assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
nucleolar large rRNA transcription by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nucleolar large rRNA transcription by RNA polymerase I biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of transcription of nucleolar large rRNA by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of transcription of nucleolar large rRNA by RNA polymerase I biological process from the curated GO Biological Process Annotations 2023 dataset. |
assembly of large subunit precursor of preribosome Gene SetFrom GO Biological Process Annotations 2023 genes participating in the assembly of large subunit precursor of preribosome biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of large conductance calcium-activated potassium channel activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
preribosome, large subunit precursor Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the preribosome, large subunit precursor cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
cytosolic large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cytosolic large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
mitochondrial large ribosomal subunit binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the mitochondrial large ribosomal subunit binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
ribosomal large subunit binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ribosomal large subunit binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
large conductance calcium-activated potassium channel activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the large conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
mitochondrial ribosomal large subunit rRNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the mitochondrial ribosomal large subunit rRNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
large ribosomal subunit rRNA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the large ribosomal subunit rRNA binding molecular function from the curated GO Molecular Function Annotations 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. |
large anterior fontanelle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large anterior fontanelle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large intestinal inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large intestinal inflammation 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. |
large ureter Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large ureter 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. |
large fontanelles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large fontanelles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large nasal septum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large nasal septum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large cranial foramen ovale Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large cranial foramen ovale phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large foramen rotundum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large foramen rotundum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large lymphoid organs Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large lymphoid organs phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal large intestinal transit time Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal large intestinal transit time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large femur head Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large femur head phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large posterior fontanelle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large posterior fontanelle 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. |
large penis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large penis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large orbits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large orbits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large mandible Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large mandible phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large face Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large face phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Large granular lymphocyte_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Large granular lymphocyte_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Large vessel cell_Blood vessel_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Large vessel cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Defective LARGE causes MDDGA6 and MDDGB6 Gene Setproteins participating in the Defective LARGE causes MDDGA6 and MDDGB6 pathway from the Reactome Pathways 2024 dataset. |
Large intestine_CT1_absorptive Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_absorptive cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_goblet Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_goblet cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_Paneth Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_Paneth cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_neuroendocrine Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_neuroendocrine cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alph beta positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph beta positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD4+ lymphocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD4+ lymphocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/beta Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/beta cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_eosinophil Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_eosinophil cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_capillary endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_capillary endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_lymphatic endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_lymphatic endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_pericyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_pericyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_macrophage Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_macrophage cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_ILF lymphatic endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_ILF lymphatic endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_ILV high endothelial venule endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_ILV high endothelial venule endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_neutrophil Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_neutrophil cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_nerve Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_nerve cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_adipocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_adipocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_arteriole endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_arteriole endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_venule endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_venule endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alpha beta positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha beta positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_squamou Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_squamou cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_melanocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_melanocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_keratinocyte Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_keratinocyte cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_T helper Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_T helper cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_T killer Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_T killer cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_T reg Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_T reg cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_venous endothelium Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_venous endothelium cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_skeletal muscle Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Large intestine_CT1_skeletal muscle cell type from the HuBMAP ASCT+B dataset. |
Large intestine_CT1_ILF lymphatic endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_ILF lymphatic endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_ILV high endothelial venule endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_ILV high endothelial venule endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_Paneth Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_Paneth cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_T helper Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_T helper cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_T killer Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_T killer cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_T reg Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_T reg cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_absorptive Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_absorptive cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_adipocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_adipocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_arteriole endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_arteriole endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_capillary endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_capillary endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_eosinophil Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_eosinophil cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_goblet Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_goblet cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_keratinocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_keratinocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_lymphatic endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_lymphatic endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_macrophage Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_macrophage cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_melanocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_melanocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_nerve Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_nerve cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_neuroendocrine Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_neuroendocrine cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_neutrophil Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_neutrophil cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_pericyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_pericyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_skeletal muscle Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_skeletal muscle cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_squamou Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_squamou cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD4+ lymphocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD4+ lymphocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/beta Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/beta cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alph beta positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph beta positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD8+ alpha beta positive alpha/beta lymphocyte Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha beta positive alpha/beta lymphocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_venous endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_venous endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Large intestine_CT1_venule endothelium Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Large intestine_CT1_venule endothelium cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
mitochondrial large ribosomal subunit assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondrial large ribosomal subunit assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
ribosomal large subunit biogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ribosomal large subunit biogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
ribosomal large subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ribosomal large subunit export from nucleus biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of large conductance calcium-activated potassium channel activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of transcription of nucleolar large rRNA by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of transcription of nucleolar large rRNA by RNA polymerase I biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of ribosomal large subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of ribosomal large subunit export from nucleus biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of transcription of nucleolar large rRNA by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of transcription of nucleolar large rRNA by RNA polymerase I biological process from the curated GO Biological Process Annotations 2025 dataset. |
ribosomal large subunit assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ribosomal large subunit assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
large intestinal transit Gene SetFrom GO Biological Process Annotations 2025 genes participating in the large intestinal transit biological process from the curated GO Biological Process Annotations 2025 dataset. |
nucleolar large rRNA transcription by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nucleolar large rRNA transcription by RNA polymerase I biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of transcription of nucleolar large rRNA by RNA polymerase I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of transcription of nucleolar large rRNA by RNA polymerase I biological process from the curated GO Biological Process Annotations 2025 dataset. |
assembly of large subunit precursor of preribosome Gene SetFrom GO Biological Process Annotations 2025 genes participating in the assembly of large subunit precursor of preribosome biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of ribosomal large subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of ribosomal large subunit export from nucleus biological process from the curated GO Biological Process Annotations 2025 dataset. |
preribosome, large subunit precursor Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the preribosome, large subunit precursor cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
cytosolic large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cytosolic large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
large ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the large ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
mitochondrial large ribosomal subunit binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the mitochondrial large ribosomal subunit binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ribosomal large subunit binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ribosomal large subunit binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
large conductance calcium-activated potassium channel activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the large conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
mitochondrial ribosomal large subunit rRNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the mitochondrial ribosomal large subunit rRNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
large ribosomal subunit rRNA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the large ribosomal subunit rRNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Large congenital melanocytic nevus Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Large congenital melanocytic nevus from the DISEASES Curated Gene-Disease Association Evidence Scores 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. |
Large congenital melanocytic nevus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Large congenital melanocytic nevus 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. |
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 granular lymphocyte Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Large granular lymphocyte 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. |
Large granular lymphocyte Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Large granular lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Large granular lymphocyte Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Large granular lymphocyte 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. |
Organellar large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Organellar large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Mitochondrial large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
gamma-tubulin large complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the gamma-tubulin large complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cytosolic large ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cytosolic large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
preribosome, large subunit precursor Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the preribosome, large subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
gamma-tubulin large complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the gamma-tubulin large complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Large latent transforming growth factor-beta complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Large latent transforming growth factor-beta complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Organellar large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Organellar large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cytosolic large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytosolic large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
preribosome, large subunit precursor Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the preribosome, large subunit precursor cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Chloroplast large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Chloroplast large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Plastid large ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Plastid large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Large congenital melanocytic nevus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Large congenital melanocytic nevus phenotype from the curated ClinVar Gene-Phenotype Associations 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. |
Mitochondrial large ribosomal subunit - 2 Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial large ribosomal subunit - 2 assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Large ribosomal subunit Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Large ribosomal subunit assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Mitochondrial large ribosomal subunit Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial large ribosomal subunit assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Ischemic stroke (large artery atherosclerosis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ischemic stroke (large artery atherosclerosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large artery stroke (CCSp classification)j Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (CCSp classification)j phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large artery stroke (TOAST classification) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large artery stroke (CCS and TOAST classification) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (CCS and TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large artery stroke (CCS or TOAST classification) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (CCS or TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large artery stroke Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Coronary artery disease or large artery stroke Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease or large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Phospholipid levels in large VLDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Phospholipid levels in large VLDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Triglyceride levels in large VLDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels in large VLDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Phospholipid levels in large HDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Phospholipid levels in large HDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Total cholesterol levels in large HDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Total cholesterol levels in large HDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cholesterol ester levels in very large HDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholesterol ester levels in very large HDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Free cholesterol levels in large HDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Free cholesterol levels in large HDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Free cholesterol levels in large LDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Free cholesterol levels in large LDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large HDL particle concentration Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large HDL particle concentration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Total cholesterol levels in large LDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Total cholesterol levels in large LDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cholesterol ester levels in large LDL Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholesterol ester levels in large LDL phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Large LDL particle concentration Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large LDL particle concentration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Very large VLDL particle concentration Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Very large VLDL particle concentration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LARGE NEUROMEDIN N Gene Setinteracting proteins for the LARGE NEUROMEDIN N drug from theDGIdb Drug Targets 2026 dataset. |
LARGE NEUROTENSIN Gene Setinteracting proteins for the LARGE NEUROTENSIN drug from theDGIdb Drug Targets 2026 dataset. |
Hodgkin lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hodgkin lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Burkitt lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Burkitt lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphoma, Follicular Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoma, Follicular from the curated CTD Gene-Disease Associations dataset. |
Lymphoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoma from the curated CTD Gene-Disease Associations dataset. |
Lymphoma, AIDS-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoma, AIDS-Related from the curated CTD Gene-Disease Associations dataset. |
Lymphoma, Non-Hodgkin Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoma, Non-Hodgkin from the curated CTD Gene-Disease Associations dataset. |
Burkitt Lymphoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Burkitt Lymphoma from the curated CTD Gene-Disease Associations dataset. |
hodgkin's lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease hodgkin's lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
non-hodgkin lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease non-hodgkin lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
central nervous system lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
prostate lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prostate lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pediatric lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pediatric lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hodgkin's lymphoma, lymphocytic-histiocytic predominance Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hodgkin's lymphoma, lymphocytic-histiocytic predominance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrointestinal lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrointestinal lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
orbit lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease orbit lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gallbladder lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gallbladder lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chest wall lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chest wall lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hodgkin's lymphoma, lymphocytic depletion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hodgkin's lymphoma, lymphocytic depletion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastric lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
precursor b lymphoblastic lymphoma/leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease precursor b lymphoblastic lymphoma/leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pancreas lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pancreas lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
testicular lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease testicular lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
paranasal sinus lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paranasal sinus lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
nasal cavity lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nasal cavity lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
heart lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease heart lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
composite lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease composite lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thyroid lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thyroid lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lymphoplasmacytic lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lymphoplasmacytic lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
retina lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retina lymphoma 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. |
liver lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease liver lymphoma 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. |
hodgkin's lymphoma, mixed cellularity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hodgkin's lymphoma, mixed cellularity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intraocular lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intraocular lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
splenic marginal zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease splenic marginal zone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gray zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gray zone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
non-hodgkin lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-hodgkin lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adult lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bladder lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bladder lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
precursor t-lymphoblastic lymphoma/leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease precursor t-lymphoblastic lymphoma/leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tracheal lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tracheal lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spinal cord lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hodgkin's lymphoma, nodular sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hodgkin's lymphoma, nodular sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
burkitt lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease burkitt lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hodgkin's lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hodgkin's lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cerebral lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mediastinal gray zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mediastinal gray zone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
precursor lymphoblastic lymphoma/leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease precursor lymphoblastic lymphoma/leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chromosomal instability; lymphoma; neoplasms; nijmegen breakage syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosomal instability; lymphoma; neoplasms; nijmegen breakage syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mucosa-associated lymphoid tissue lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mucosa-associated lymphoid tissue lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cryoglobulinemia; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cryoglobulinemia; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cancer; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cancer; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system neoplasms; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-hodgkin lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-hodgkin lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pediatric lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pediatric lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; breast neoplasms; lymphoma, non-hodgkin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; breast neoplasms; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brill-symmers disease; chromosome deletion; lymphoma, follicular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; chromosome deletion; lymphoma, follicular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, lymphoid; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, lymphoid; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cachexia; gastrointestinal neoplasms; leukemia; lymphoma; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cachexia; gastrointestinal neoplasms; leukemia; lymphoma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; liver neoplasms; lymphoma, non-hodgkin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; liver neoplasms; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-hodgkin's lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
follicular lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease follicular lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; lymphoma; lymphoproliferative disorders; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; lymphoma; lymphoproliferative disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brill-symmers disease; lymphoma, follicular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; lymphoma, follicular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system neoplasms; central nervous system tumors; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; lymphoma, non-hodgkin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
waldenstrom macroglobulinaemia; hodgkin lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease waldenstrom macroglobulinaemia; hodgkin lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma; hodgkin's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; hodgkin's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; lymphoma; mammary neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; lymphoma; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; colonic neoplasms; lymphoma; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; colonic neoplasms; lymphoma; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma; obesity, localized Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; obesity, localized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosomal instability; immunologic deficiency syndromes; lymphoma, non-hodgkin; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosomal instability; immunologic deficiency syndromes; lymphoma, non-hodgkin; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, follicular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, follicular 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. |
central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, non-hodgkin; neoplasm invasiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, non-hodgkin; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin disease; lymphoma, non-hodgkin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin disease; lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma; splenic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; splenic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune lymphoproliferative syndrome; lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune lymphoproliferative syndrome; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, follicle center Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, follicle center in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin's disease; non-hodgkin's lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin's disease; non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma, non-hodgkin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, non-hodgkin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
follicle center lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease follicle center lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphocytic lymphoma of intermediate differentiation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphocytic lymphoma of intermediate differentiation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoma Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term lymphoma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
CBFA2T3_KD_GDS4045_458_human_Non-Hodgkin's lymphoma Reh cells Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the CBFA2T3_KD_GDS4045_458_human_Non-Hodgkin's lymphoma Reh cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
Follicular lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Follicular lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hodgkin's lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hodgkin's lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
hodgkin's lymphoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease hodgkin's lymphoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
non-hodgkin lymphoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease non-hodgkin lymphoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lymphoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease lymphoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lymphoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the lymphoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
non-hodgkin lymphoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the non-hodgkin lymphoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hodgkin lymphoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hodgkin lymphoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
non-hodgkin lymphoma Gene SetFrom HPO Gene-Disease Associations genes associated with the non-hodgkin lymphoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hodgkin lymphoma Gene SetFrom HPO Gene-Disease Associations genes associated with the hodgkin lymphoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lymphoma Gene SetFrom HPO Gene-Disease Associations genes associated with the lymphoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Lymphoma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lymphoma, AIDS-Related Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, AIDS-Related phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lymphoma, Mucosa-Associated Lymphoid Tissue Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, Mucosa-Associated Lymphoid Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lymphoma, Non-Hodgkin Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, Non-Hodgkin phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lymphoma, Follicular Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, Follicular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lymphoma, Lymphoblastic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, Lymphoblastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Burkitt Lymphoma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Burkitt Lymphoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
increased lymphoblastic lymphoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lymphoblastic lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lymphoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased follicular lymphoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased follicular lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased small lymphocytic lymphoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased small lymphocytic lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased splenic marginal zone lymphoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased splenic marginal zone lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased lymphoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{hodgkin lymphoma, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hodgkin lymphoma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphoma, non-hodgkin, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphoma, non-hodgkin, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
{follicular lymphoma, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {follicular lymphoma, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
burkitt lymphoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the burkitt lymphoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
{lymphoma, follicular, somatic} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {lymphoma, follicular, somatic} phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphoma, non-hodgkin Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphoma, non-hodgkin phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphoma, malt, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphoma, malt, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
non-hodgkin lymphoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the non-hodgkin lymphoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphoma Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term lymphoma in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
daltons lymphoma ascites Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue daltons lymphoma ascites in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
lymphoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease lymphoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Hodgkin's lymphoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Hodgkin's lymphoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Burkitt's lymphoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Burkitt's lymphoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
AIDS-related lymphoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease AIDS-related lymphoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Intraocular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intraocular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
African Burkitt'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease African Burkitt'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Classical Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Classical Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Classical Hodgkin'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Classical Hodgkin'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indolent Adult Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indolent Adult Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indolent Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indolent Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Plasmablastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Plasmablastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Central Nervous System Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Central Nervous System Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Double-Hit Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Double-Hit Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Primary Gastric Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Gastric Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nodular Sclerosis Classical Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nodular Sclerosis Classical Hodgkin Lymphoma 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. |
Primary Effusion Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Effusion Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B Lymphoblastic Leukemia Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B Lymphoblastic Leukemia Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thymic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thymic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Extracavitary Primary Effusion Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Extracavitary Primary Effusion Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastric Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastric Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Lymphocytic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Lymphocytic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aggressive Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aggressive Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade Lymphoma (Neoplasm) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade Lymphoma (Neoplasm) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hydroa Vacciniforme-Like Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydroa Vacciniforme-Like Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Cutaneous Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Cutaneous Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Extranodal Marginal Zone Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Extranodal Marginal Zone Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hodgkin'S Lymphoma Transformed Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Transformed Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Feline Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Feline Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult T Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult T Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood T Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aggressive Adult Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aggressive Adult Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastric Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastric Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hodgkin'S Lymphoma Of Central Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Of Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sporadic Burkitt'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Burkitt'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Childhood Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Immunoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Immunoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Immunoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Immunoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pyothorax-Associated Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pyothorax-Associated Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hodgkin Lymphoma, Nodular Lymphocyte Predominance Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hodgkin Lymphoma, Nodular Lymphocyte Predominance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Lymphoma (Neoplasm) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Lymphoma (Neoplasm) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ocular Adnexal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ocular Adnexal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult B Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Burkitt'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Burkitt'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Centrocytic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Centrocytic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood B Lymphoblastic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Composite Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Composite Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Double Expressor Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Double Expressor Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Extranodal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Extranodal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
In Situ Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease In Situ Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pediatric Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pediatric Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Cerebral Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Cerebral Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Cutaneous Follicle Center Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Cutaneous Follicle Center Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyroid Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triple Hit Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triple Hit Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lymphoepithelioid Lymphoma (Clinical) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lymphoepithelioid Lymphoma (Clinical) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hodgkin'S And Non-Hodgkin'S Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hodgkin'S And Non-Hodgkin'S Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Digestive System Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Digestive System Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Lung Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Lung Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Marginal Zone Lymphoma Refractory Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Marginal Zone Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Refractory Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Intestinal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Intestinal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mantle Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mantle Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hodgkin'S Lymphoma Refractory Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Refractory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Orbital Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Orbital Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hodgkin Lymphoma, Lymphocyte Depletion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hodgkin Lymphoma, Lymphocyte Depletion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mixed Cellularity Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mixed Cellularity Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mediastinal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mediastinal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chicken Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chicken Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Nodular Sclerosis Classical Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Nodular Sclerosis Classical Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Nodular Sclerosis Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Sclerosis Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prostate Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prostate Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Follicle Center Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Follicle Center Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ebv-Related Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ebv-Related Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Lymphocytic Lymphoma With Plasmacytoid Differentiation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Lymphocytic Lymphoma With Plasmacytoid Differentiation 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. |
Ebv-Related Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ebv-Related Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Duodenal-Type Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Duodenal-Type Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pediatric Nodal Marginal Zone Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pediatric Nodal Marginal Zone Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lymphoma, Somatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lymphoma, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Classical Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Classical Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastric Burkitt Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastric Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Transformed Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Transformed Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatosplenic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatosplenic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Immunoblastic Lymphoma (Kiel Classification) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Immunoblastic Lymphoma (Kiel Classification) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retroperitoneal Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retroperitoneal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mediastinal Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mediastinal Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Bone Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Bone Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
HNF1A-27111144-CD8+TCELLS-MOUSE-BLOOD-LYMPHOMA Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the HNF1A-27111144-CD8+TCELLS-MOUSE-BLOOD-LYMPHOMA transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
BRD4-28847988-BCBL1-HUMAN-BLOOD-LYMPHOMA Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the BRD4-28847988-BCBL1-HUMAN-BLOOD-LYMPHOMA transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
ARID1A-32646524-H9-HUMAN-BONEMARROW-LYMPHOMA Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the ARID1A-32646524-H9-HUMAN-BONEMARROW-LYMPHOMA transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
GTF3C2-35216376-H9-HUMAN-BONEMARROW-LYMPHOMA Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the GTF3C2-35216376-H9-HUMAN-BONEMARROW-LYMPHOMA transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
increased lymphoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased lymphoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased lymphoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased lymphoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased follicular lymphoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased follicular lymphoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased small lymphocytic lymphoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased small lymphocytic lymphoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased lymphoblastic lymphoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased lymphoblastic lymphoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased splenic marginal zone lymphoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased splenic marginal zone lymphoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
non-Hodgkin lymphoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease non-Hodgkin lymphoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Lymphoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lymphoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Lymphoplasmacytic lymphoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lymphoplasmacytic lymphoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Hodgkin's lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
non-Hodgkin lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease non-Hodgkin lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Marginal zone lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Marginal zone lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lymphoplasmacytic lymphoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Lymphoplasmacytic lymphoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma, nodular sclerosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Hodgkin's lymphoma, nodular sclerosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
non-Hodgkin lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-Hodgkin lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hodgkin's lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lymphoblastic lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lymphoblastic lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Burkitt lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Burkitt lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Plasmablastic lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Plasmablastic lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Follicular lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Follicular lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Marginal zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Marginal zone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Testicular lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Testicular lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adult lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lymphoplasmacytic lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lymphoplasmacytic lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nodal marginal zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nodal marginal zone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chronic lymphocytic leukemia/small lymphocytic lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic lymphocytic leukemia/small lymphocytic lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intraocular lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intraocular lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gastric lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastric lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cerebral lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Composite lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Composite lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gastrointestinal lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gastrointestinal lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Childhood lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lung lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lung lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Breast lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Splenic marginal zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Splenic marginal zone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma, nodular sclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hodgkin's lymphoma, nodular sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gray zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gray zone lymphoma 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. |
Thyroid lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thyroid lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma, lymphocytic-histiocytic predominance Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hodgkin's lymphoma, lymphocytic-histiocytic predominance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mediastinal gray zone lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mediastinal gray zone lymphoma 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. |
Spinal cord lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thymus lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thymus lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Retina lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retina lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Orbit lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Orbit lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma, mixed cellularity Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hodgkin's lymphoma, mixed cellularity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma with iAMP21 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma with iAMP21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma with hypodiploidy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma with hypodiploidy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovarian lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bladder lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bladder lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma MLL rearranged Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma MLL rearranged in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma with BCR-ABL1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma with BCR-ABL1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Retroperitoneal lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retroperitoneal lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Liver lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Liver lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma with hyperdiploidy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma with hyperdiploidy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Rectum lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rectum lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chest wall lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chest wall lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hodgkin's lymphoma, lymphocytic depletion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hodgkin's lymphoma, lymphocytic depletion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pancreas lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pancreas lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Prostate lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Prostate lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nasal cavity lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nasal cavity lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma with TCF3-PBX1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma with TCF3-PBX1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sternum lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sternum lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gallbladder lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gallbladder lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Paranasal sinus lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Paranasal sinus lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Appendix lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Appendix lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Heart lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Heart lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ureteral lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ureteral lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Tracheal lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tracheal lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cecum lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cecum lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophagus lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophagus lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Refractory T lymphoblastic leukemia/lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Refractory T lymphoblastic leukemia/lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Daltons lymphoma ascites Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Daltons lymphoma ascites in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
B lymphoblastic leukemia lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the B lymphoblastic leukemia lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 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. |
Lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-Hodgkin lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-Hodgkin lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Burkitt lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Burkitt lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
B Lymphoblastic Leukemia/Lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the B Lymphoblastic Leukemia/Lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
B-lymphoblastic leukemia/lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the B-lymphoblastic leukemia/lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mucosa-associated lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mucosa-associated lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Classic Hodgkin lymphoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Classic Hodgkin lymphoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Nodular sclerosis Hodgkin lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nodular sclerosis Hodgkin lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mixed cellularity Hodgkin lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mixed cellularity Hodgkin lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hodgkin's lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hodgkin's lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Follicular lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Follicular lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Marginal zone lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Marginal zone lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waldenstrom macroglobulinemia / lymphoplasmacytic lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waldenstrom macroglobulinemia / lymphoplasmacytic lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Primary central nervous system lymphoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary central nervous system lymphoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Follicular lymphoma or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Follicular lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Marginal zone lymphoma or multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Marginal zone lymphoma or multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Follicular lymphoma or rheumatoid arthritis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Follicular lymphoma or rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Marginal zone lymphoma or rheumatoid arthritis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Marginal zone lymphoma or rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Marginal zone lymphoma or systemic lupus erythematosus Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Marginal zone lymphoma or systemic lupus erythematosus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |