| Name |
|---|
IGAD1 Geneimmunoglobulin A (IgA) deficiency susceptibility 1 |
IGIP GeneIgA-inducing protein Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
IGAN2 GeneIgA nephropathy, susceptibility to, 2 |
FCAR GeneFc fragment of IgA receptor This gene is a member of the immunoglobulin gene superfamily and encodes a receptor for the Fc region of IgA. The receptor is a transmembrane glycoprotein present on the surface of myeloid lineage cells such as neutrophils, monocytes, macrophages, and eosinophils, where it mediates immunologic responses to pathogens. It interacts with IgA-opsonized targets and triggers several immunologic defense processes, including phagocytosis, antibody-dependent cell-mediated cytotoxicity, and stimulation of the release of inflammatory mediators. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] |
JCHAIN Genejoining chain of multimeric IgA and IgM Enables IgA binding activity and protein homodimerization activity. Contributes to several functions, including immunoglobulin receptor binding activity; peptidoglycan binding activity; and phosphatidylcholine binding activity. Involved in several processes, including glomerular filtration; innate immune response; and positive regulation of respiratory burst. Located in extracellular space. Part of monomeric IgA immunoglobulin complex; pentameric IgM immunoglobulin complex; and secretory dimeric IgA immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGAN1 GeneIgA nephropathy |
FCAMR GeneFc receptor, IgA, IgM, high affinity Predicted to enable IgA binding activity; IgM binding activity; and transmembrane signaling receptor activity. Predicted to be involved in signal transduction. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
EIPR1 GeneEARP complex and GARP complex interacting protein 1 This gene has been reported in PMID 9403053 as one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. Alignment of this gene to genomic sequence data suggests that this gene resides on chromosome 2 rather than chromosome 11. [provided by RefSeq, Dec 2008] |
IGLVI-38 Geneimmunoglobulin lambda variable (I)-38 (pseudogene) |
IGKV1OR10-1 Geneimmunoglobulin kappa variable 1/OR10-1 (pseudogene) |
LOC102724971 Geneputative V-set and immunoglobulin domain-containing-like protein IGHV4OR15-8 |
IGHVII-60-1 Geneimmunoglobulin heavy variable (II)-60-1 (pseudogene) |
IGHV1-8 Geneimmunoglobulin heavy variable 1-8 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-3 Geneimmunoglobulin heavy variable 1-3 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-2 Geneimmunoglobulin heavy variable 1-2 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD6-25 Geneimmunoglobulin heavy diversity 6-25 |
IGHV4-4 Geneimmunoglobulin heavy variable 4-4 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-12 Geneimmunoglobulin kappa variable 1-12 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-16 Geneimmunoglobulin kappa variable 1-16 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-17 Geneimmunoglobulin kappa variable 1-17 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF9B Geneimmunoglobulin superfamily, member 9B Predicted to enable kinase binding activity. Predicted to be involved in synaptic membrane adhesion. Predicted to act upstream of or within homophilic cell adhesion via plasma membrane adhesion molecules and positive regulation of inhibitory postsynaptic potential. Predicted to be located in dendrite; inhibitory synapse; and neuronal cell body. Predicted to be active in GABA-ergic synapse; neuron projection; and postsynaptic specialization of symmetric synapse. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV5-78 Geneimmunoglobulin heavy variable 5-78 (pseudogene) |
IGLV1-36 Geneimmunoglobulin lambda variable 1-36 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102725029 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
IGKV2-36 Geneimmunoglobulin kappa variable 2-36 (pseudogene) |
IGKV2-30 Geneimmunoglobulin kappa variable 2-30 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2-38 Geneimmunoglobulin kappa variable 2-38 (pseudogene) |
IGHVIII-26-1 Geneimmunoglobulin heavy variable (III)-26-1 (pseudogene) |
IGHV1-69-2 Geneimmunoglobulin heavy variable 1-69-2 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-45 Geneimmunoglobulin heavy variable 1-45 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKDEL Geneimmunoglobulin kappa deleting element or like |
RBPJL Generecombination signal binding protein for immunoglobulin kappa J region-like This gene encodes a member of the suppressor of hairless protein family. A similar protein in mouse is a transcription factor that binds to DNA sequences almost identical to that bound by the Notch receptor signaling pathway transcription factor recombining binding protein J. The mouse protein has been shown to activate transcription in concert with Epstein-Barr virus nuclear antigen-2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
IGHV1-38-4 Geneimmunoglobulin heavy variable 1-38-4 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929818 Genekiller cell immunoglobulin-like receptor 3DL1 |
IGKV2OR2-8 Geneimmunoglobulin kappa variable 2/OR2-8 (pseudogene) |
IGBP1 Geneimmunoglobulin (CD79A) binding protein 1 The proliferation and differentiation of B cells is dependent upon a B-cell antigen receptor (BCR) complex. Binding of antigens to specific B-cell receptors results in a tyrosine phosphorylation reaction through the BCR complex and leads to multiple signal transduction pathways. [provided by RefSeq, Jul 2008] |
IGSF10 Geneimmunoglobulin superfamily, member 10 Predicted to be involved in regulation of neuron migration. Predicted to act upstream of or within ossification. Located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
KIR3DX1 Genekiller cell immunoglobulin-like receptor, three domains, X1 Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in extracellular region. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2D-14 Geneimmunoglobulin kappa variable 2D-14 (pseudogene) |
IGKV2D-10 Geneimmunoglobulin kappa variable 2D-10 (pseudogene) |
IGKV2D-18 Geneimmunoglobulin kappa variable 2D-18 (pseudogene) |
IGKV2D-19 Geneimmunoglobulin kappa variable 2D-19 (pseudogene) |
LOC100289350 Geneimmunoglobulin superfamily, member 3 pseudogene |
IGHEP2 Geneimmunoglobulin heavy constant epsilon P2 (pseudogene) |
IGHEP1 Geneimmunoglobulin heavy constant epsilon P1 (pseudogene) |
IGLL1 Geneimmunoglobulin lambda-like polypeptide 1 The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
IGLL5 Geneimmunoglobulin lambda-like polypeptide 5 This gene encodes one of the immunoglobulin lambda-like polypeptides. It is located within the immunoglobulin lambda locus but it does not require somatic rearrangement for expression. The first exon of this gene is unrelated to immunoglobulin variable genes; the second and third exons are the immunoglobulin lambda joining 1 and the immunoglobulin lambda constant 1 gene segments. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
IGHD3OR15-3B Geneimmunoglobulin heavy diversity 3/OR15-3B (non-functional) |
IGHD3OR15-3A Geneimmunoglobulin heavy diversity 3/OR15-3A (non-functional) |
IGHV3OR16-7 Geneimmunoglobulin heavy variable 3/OR16-7 (pseudogene) |
IGHV3-69-1 Geneimmunoglobulin heavy variable 3-69-1 (pseudogene) |
IGLV5-45 Geneimmunoglobulin lambda variable 5-45 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV5-48 Geneimmunoglobulin lambda variable 5-48 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102725015 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
LOC102724844 Geneimmunoglobulin superfamily member 3-like |
IGHVII-22-1 Geneimmunoglobulin heavy variable (II)-22-1 (pseudogene) |
IGKV3-11 Geneimmunoglobulin kappa variable 3-11 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV3-15 Geneimmunoglobulin kappa variable 3-15 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF8 Geneimmunoglobulin superfamily, member 8 This gene encodes a member the EWI subfamily of the immunoglobulin protein superfamily. Members of this family contain a single transmembrane domain, an EWI (Glu-Trp-Ile)-motif and a variable number of immunoglobulin domains. This protein interacts with the tetraspanins CD81 and CD9 and may regulate their role in certain cellular functions including cell migration and viral infection. The encoded protein may also function as a tumor suppressor by inhibiting the proliferation of certain cancers. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2011] |
IGSF9 Geneimmunoglobulin superfamily, member 9 Predicted to enable cell-cell adhesion mediator activity. Predicted to be involved in axon guidance; dendrite self-avoidance; and homophilic cell adhesion via plasma membrane adhesion molecules. Predicted to act upstream of or within dendrite development and regulation of synapse organization. Predicted to be located in dendrite and inhibitory synapse. Predicted to be active in axon; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF5 Geneimmunoglobulin superfamily, member 5 Predicted to enable PDZ domain binding activity. Predicted to be involved in cell-cell adhesion. Predicted to be located in apical plasma membrane. Predicted to be active in bicellular tight junction and cell surface. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF6 Geneimmunoglobulin superfamily, member 6 Predicted to enable transmembrane signaling receptor activity. Predicted to be involved in cell surface receptor signaling pathway and immune response. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF1 Geneimmunoglobulin superfamily, member 1 This gene encodes a member of the immunoglobulin-like domain-containing superfamily. Proteins in this superfamily contain varying numbers of immunoglobulin-like domains and are thought to participate in the regulation of interactions between cells. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010] |
IGSF3 Geneimmunoglobulin superfamily, member 3 The protein encoded by this gene is an immunoglobulin-like membrane protein containing several V-type Ig-like domains. A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD). [provided by RefSeq, Jun 2016] |
LOC343052 Geneimmunoglobulin superfamily, DCC subclass, member 3 pseudogene |
IGHV3-37 Geneimmunoglobulin heavy variable 3-37 (pseudogene) |
IGHV3-36 Geneimmunoglobulin heavy variable 3-36 (pseudogene) |
IGHV3-35 Geneimmunoglobulin heavy variable 3-35 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-33 Geneimmunoglobulin heavy variable 3-33 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-32 Geneimmunoglobulin heavy variable 3-32 (pseudogene) |
IGHV3-30 Geneimmunoglobulin heavy variable 3-30 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-38 Geneimmunoglobulin heavy variable 3-38 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-13 Geneimmunoglobulin kappa variable 1-13 (gene/pseudogene) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV3-7 Geneimmunoglobulin kappa variable 3-7 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD6-19 Geneimmunoglobulin heavy diversity 6-19 |
IGHD6-13 Geneimmunoglobulin heavy diversity 6-13 |
IGHJ6 Geneimmunoglobulin heavy joining 6 |
IGHJ5 Geneimmunoglobulin heavy joining 5 |
IGHJ4 Geneimmunoglobulin heavy joining 4 |
IGHJ3 Geneimmunoglobulin heavy joining 3 |
IGHJ2 Geneimmunoglobulin heavy joining 2 |
IGHJ1 Geneimmunoglobulin heavy joining 1 Predicted to be involved in adaptive immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
ILDR2 Geneimmunoglobulin-like domain containing receptor 2 Involved in negative regulation of T cell activation. Predicted to be located in tight junction. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ILDR1 Geneimmunoglobulin-like domain containing receptor 1 This gene encodes a protein that contains an immunoglobulin-like domain. The encoded protein may function as a multimeric receptor at the cell surface. The expression of this gene may be a diagnostic marker for cancer progression. Alternatively spliced transcript variants encoding multiple protein isoforms have been observed for this gene. [provided by RefSeq, Dec 2010] |
IGLV8-61 Geneimmunoglobulin lambda variable 8-61 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100422538 Generecombination signal binding protein for immunoglobulin kappa J region pseudogene |
IGLV2-28 Geneimmunoglobulin lambda variable 2-28 (pseudogene) |
IGLV2-23 Geneimmunoglobulin lambda variable 2-23 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF6-DREV1 Generegion containing immunoglobulin superfamily, member 6 and DREV1 |
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] |
IGHV1-12 Geneimmunoglobulin heavy variable 1-12 (pseudogene) |
IGHV1-14 Geneimmunoglobulin heavy variable 1-14 (pseudogene) |
IGLL4P Geneimmunoglobulin lambda-like polypeptide 4, pseudogene |
IGHV3OR16-13 Geneimmunoglobulin heavy variable 3/OR16-13 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
OSCAR Geneosteoclast associated, immunoglobulin-like receptor Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
IGHV7-34-1 Geneimmunoglobulin heavy variable 7-34-1 (pseudogene) |
IGHV3-30-2 Geneimmunoglobulin heavy variable 3-30-2 (pseudogene) |
IGHV3-30-3 Geneimmunoglobulin heavy variable 3-30-3 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-30-5 Geneimmunoglobulin heavy variable 3-30-5 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVIV-53 Geneimmunoglobulin lambda variable (IV)-53 (pseudogene) |
IGLVIV-59 Geneimmunoglobulin lambda variable (IV)-59 (pseudogene) |
IGLVIVOR22-2 Geneimmunoglobulin lambda variable (IV)/OR22-2 (pseudogene) |
IGLVIVOR22-1 Geneimmunoglobulin lambda variable (IV)/OR22-1 (pseudogene) |
IGHV4-38-2 Geneimmunoglobulin heavy variable 4-38-2 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD2-2 Geneimmunoglobulin heavy diversity 2-2 |
IGHD2-8 Geneimmunoglobulin heavy diversity 2-8 |
IGKV2D-29 Geneimmunoglobulin kappa variable 2D-29 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2D-28 Geneimmunoglobulin kappa variable 2D-28 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2D-24 Geneimmunoglobulin kappa variable 2D-24 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2D-26 Geneimmunoglobulin kappa variable 2D-26 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2D-23 Geneimmunoglobulin kappa variable 2D-23 (pseudogene) |
IGKV1D-8 Geneimmunoglobulin kappa variable 1D-8 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV7-35 Geneimmunoglobulin lambda variable 7-35 (pseudogene) |
IGHVII-49-1 Geneimmunoglobulin heavy variable (II)-49-1 (pseudogene) |
IGHD3-9 Geneimmunoglobulin heavy diversity 3-9 |
IGHD3-3 Geneimmunoglobulin heavy diversity 3-3 IGHD3-3 belongs to a cluster of approximately 25 functional diversity (D) genes in the immunoglobulin (Ig) heavy chain locus on chromosome 14. For background information on the Ig heavy chain and the D gene cluster, see (MIM 146910).[supplied by OMIM, Apr 2008] |
SIGIRR Genesingle immunoglobulin and toll-interleukin 1 receptor (TIR) domain Involved in negative regulation of Toll signaling pathway. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379645 Genekiller cell immunoglobulin-like receptor 2DL2 |
IGHV1OR15-2 Geneimmunoglobulin heavy variable 1/OR15-2 (pseudogene) |
IGHV1OR15-3 Geneimmunoglobulin heavy variable 1/OR15-3 (pseudogene) |
IGHV1OR15-1 Geneimmunoglobulin heavy variable 1/OR15-1 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1OR15-6 Geneimmunoglobulin heavy variable 1/OR15-6 (pseudogene) |
IGHV1OR15-4 Geneimmunoglobulin heavy variable 1/OR15-4 (pseudogene) |
IGHV1OR15-9 Geneimmunoglobulin heavy variable 1/OR15-9 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHJ1P Geneimmunoglobulin heavy joining 1P (pseudogene) |
LAIR1 Geneleukocyte-associated immunoglobulin-like receptor 1 The protein encoded by this gene is an inhibitory receptor found on peripheral mononuclear cells, including natural killer cells, T cells, and B cells. Inhibitory receptors regulate the immune response to prevent lysis of cells recognized as self. The gene is a member of both the immunoglobulin superfamily and the leukocyte-associated inhibitory receptor family. The gene maps to a region of 19q13.4 called the leukocyte receptor cluster, which contains at least 29 genes encoding leukocyte-expressed receptors of the immunoglobulin superfamily. The encoded protein has been identified as an anchor for tyrosine phosphatase SHP-1, and may induce cell death in myeloid leukemias. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] |
LAIR2 Geneleukocyte-associated immunoglobulin-like receptor 2 The protein encoded by this gene is a member of the immunoglobulin superfamily. It was identified by its similarity to leukocyte-associated immunoglobulin-like receptor 1, a membrane-bound receptor that modulates innate immune response. The protein encoded by this locus is a soluble receptor that may play roles in both inhibition of collagen-induced platelet aggregation and vessel formation during placental implantation. This gene maps to a region of 19q13.4, termed the leukocyte receptor cluster, which contains 29 genes in the immunoglobulin superfamily. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2013] |
IGHG4 Geneimmunoglobulin heavy constant gamma 4 (G4m marker) Predicted to enable antigen binding activity and immunoglobulin receptor binding activity. Predicted to be involved in antibacterial humoral response and complement activation, classical pathway. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGHG1 Geneimmunoglobulin heavy constant gamma 1 (G1m marker) Enables Fc-gamma receptor I complex binding activity. Involved in antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity. Located in extracellular space. Part of IgG immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHG2 Geneimmunoglobulin heavy constant gamma 2 (G2m marker) Predicted to enable antigen binding activity and immunoglobulin receptor binding activity. Predicted to be involved in antibacterial humoral response and complement activation, classical pathway. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
IGHG3 Geneimmunoglobulin heavy constant gamma 3 (G3m marker) Predicted to enable antigen binding activity and immunoglobulin receptor binding activity. Predicted to be involved in antibacterial humoral response and complement activation, classical pathway. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGHGP Geneimmunoglobulin heavy constant gamma P (non-functional) |
IGHVII-30-1 Geneimmunoglobulin heavy variable (II)-30-1 (pseudogene) |
IGHV2-70 Geneimmunoglobulin heavy variable 2-70 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1OR2-9 Geneimmunoglobulin kappa variable 1/OR2-9 (pseudogene) |
IGKV1D-22 Geneimmunoglobulin kappa variable 1D-22 (pseudogene) |
IGKV1D-27 Geneimmunoglobulin kappa variable 1D-27 (pseudogene) |
IGLCOR22-1 Geneimmunoglobulin lambda constant/OR22-1 (pseudogene) |
IGLCOR22-2 Geneimmunoglobulin lambda constant/OR22-2 (pseudogene) |
IGHV3-48 Geneimmunoglobulin heavy variable 3-48 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-49 Geneimmunoglobulin heavy variable 3-49 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-47 Geneimmunoglobulin heavy variable 3-47 (pseudogene) |
IGHV3-42 Geneimmunoglobulin heavy variable 3-42 (pseudogene) |
IGHV3-43 Geneimmunoglobulin heavy variable 3-43 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-41 Geneimmunoglobulin heavy variable 3-41 (pseudogene) |
IGLVI-56 Geneimmunoglobulin lambda variable (I)-56 (pseudogene) |
IGHVII-26-2 Geneimmunoglobulin heavy variable (II)-26-2 (pseudogene) |
IGKV2OR2-10 Geneimmunoglobulin kappa variable 2/OR2-10 (pseudogene) |
LOC105379650 Genekiller cell immunoglobulin-like receptor 2DS1 |
IGKV1ORY-1 Geneimmunoglobulin kappa variable 1/ORY-1 (pseudogene) |
IGHV3-43D Geneimmunoglobulin heavy variable 3-43D |
IGHVIII-44 Geneimmunoglobulin heavy variable (III)-44 (pseudogene) |
IGHV3-11 Geneimmunoglobulin heavy variable 3-11 (gene/pseudogene) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV10-54 Geneimmunoglobulin lambda variable 10-54 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVII-31-1 Geneimmunoglobulin heavy variable (II)-31-1 (pseudogene) |
KIR2DS5 Genekiller cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 5 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
1060P11.3 Genekiller cell immunoglobulin-like receptor, three domains, pseudogene |
KIR2DS2 Genekiller cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014] |
LOC100422604 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 2 pseudogene |
IGLV1-51 Geneimmunoglobulin lambda variable 1-51 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV1-50 Geneimmunoglobulin lambda variable 1-50 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV7-40 Geneimmunoglobulin heavy variable 7-40 (pseudogene) |
IGJP1 Geneimmunoglobulin J polypeptide pseudogene 1 |
WFIKKN2 GeneWAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 The WFIKKN1 protein contains a WAP domain, follistatin domain, immunoglobulin domain, two tandem Kunitz domains, and an NTR domain. This gene encodes a WFIKKN1-related protein which has the same domain organization as the WFIKKN1 protein. The WAP-type, follistatin type, Kunitz-type, and NTR-type protease inhibitory domains may control the action of multiple types of proteases. [provided by RefSeq, Jul 2008] |
WFIKKN1 GeneWAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1 This gene encodes a secreted multidomain protein consisting of a signal peptide, a WAP domain, a follistatin domain, an immunoglobulin domain, two tandem Kunitz domains, and an NTR domain. These domains have been implicated frequently in inhibition of various types of proteases, suggesting that the encoded protein may be a multivalent protease inhibitor and may control the action of multiple types of serine proteases as well as metalloproteinases. [provided by RefSeq, Jul 2008] |
KIR3DL1 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR3DL2 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011] |
KIR3DL3 Genekiller cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. [provided by RefSeq, Jul 2008] |
IGHD3-22 Geneimmunoglobulin heavy diversity 3-22 |
LILRP1 Geneleukocyte immunoglobulin-like receptor pseudogene 1 |
LILRP2 Geneleukocyte immunoglobulin-like receptor pseudogene 2 |
IGLV7-46 Geneimmunoglobulin lambda variable 7-46 (gene/pseudogene) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV7-43 Geneimmunoglobulin lambda variable 7-43 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVII-44-2 Geneimmunoglobulin heavy variable (II)-44-2 (pseudogene) |
IGHVIII-2-1 Geneimmunoglobulin heavy variable (III)-2-1 (pseudogene) |
IGHVIII-16-1 Geneimmunoglobulin heavy variable (III)-16-1 (pseudogene) |
IGHV2-70D Geneimmunoglobulin heavy variable 2-70D Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-67 Geneimmunoglobulin heavy variable 1-67 (pseudogene) |
IGHV1-68 Geneimmunoglobulin heavy variable 1-68 (pseudogene) |
IGHV1-69 Geneimmunoglobulin heavy variable 1-69 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV4-39 Geneimmunoglobulin heavy variable 4-39 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV4-31 Geneimmunoglobulin heavy variable 4-31 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102725035 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
IGHJ3P Geneimmunoglobulin heavy joining 3P (pseudogene) |
IGKC Geneimmunoglobulin kappa constant Predicted to enable antigen binding activity. Involved in adaptive immune response. Located in blood microparticle and extracellular exosome. Part of IgG immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGBP1P1 Geneimmunoglobulin (CD79A) binding protein 1 pseudogene 1 |
IGBP1P2 Geneimmunoglobulin (CD79A) binding protein 1 pseudogene 2 Predicted to enable protein phosphatase 2A binding activity. Predicted to be involved in regulation of dephosphorylation. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
IGBP1P3 Geneimmunoglobulin (CD79A) binding protein 1 pseudogene 3 |
IGBP1P4 Geneimmunoglobulin (CD79A) binding protein 1 pseudogene 4 |
IGBP1P5 Geneimmunoglobulin (CD79A) binding protein 1 pseudogene 5 |
IGLJCOR18 Geneimmunoglobulin lambda joining-constant/OR18 (pseudogene) |
IGHD1-14 Geneimmunoglobulin heavy diversity 1-14 (non-functional) |
IGHV2-26 Geneimmunoglobulin heavy variable 2-26 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
TMIGD3 Genetransmembrane and immunoglobulin domain containing 3 This gene encodes a transmembrane and immunoglobulin domain-containing protein. Alternative splicing results in multiple transcript variants, one of which shares its 5' terminal exon with that of the overlapping adenosine A3 receptor gene (GeneID:140), thus resulting in a fusion product. [provided by RefSeq, Nov 2014] |
TMIGD2 Genetransmembrane and immunoglobulin domain containing 2 Enables coreceptor activity. Involved in positive regulation of T cell activation; positive regulation of angiogenesis; and positive regulation of cytokine production. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102725023 Genekiller cell immunoglobulin-like receptor 2DS3 allele 0020101 |
IGKV1OR15-118 Geneimmunoglobulin kappa variable 1/OR15-118 (pseudogene) |
IGHD4-17 Geneimmunoglobulin heavy diversity 4-17 |
IGHD4-11 Geneimmunoglobulin heavy diversity 4-11 (non-functional) |
IGHD2OR15-2B Geneimmunoglobulin heavy diversity 2/OR15-2B (non-functional) |
IGHD2OR15-2A Geneimmunoglobulin heavy diversity 2/OR15-2A (non-functional) |
IGKV3D-7 Geneimmunoglobulin kappa variable 3D-7 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102723407 Geneputative V-set and immunoglobulin domain-containing-like protein IGHV4OR15-8 |
IGKV6D-41 Geneimmunoglobulin kappa variable 6D-41 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV4OR15-8 Geneimmunoglobulin heavy variable 4/OR15-8 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHMBP2 Geneimmunoglobulin mu binding protein 2 This gene encodes a helicase superfamily member that binds a specific DNA sequence from the immunoglobulin mu chain switch region. Mutations in this gene lead to spinal muscle atrophy with respiratory distress type 1. [provided by RefSeq, Jul 2008] |
IGLV3-32 Geneimmunoglobulin lambda variable 3-32 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-31 Geneimmunoglobulin lambda variable 3-31 (pseudogene) |
IGLV3-30 Geneimmunoglobulin lambda variable 3-30 (pseudogene) |
IGSF11 Geneimmunoglobulin superfamily, member 11 IGSF11 is an immunoglobulin (Ig) superfamily member that is preferentially expressed in brain and testis. It shares significant homology with coxsackievirus and adenovirus receptor (CXADR; MIM 602621) and endothelial cell-selective adhesion molecule (ESAM).[supplied by OMIM, Apr 2005] |
VSIG10L GeneV-set and immunoglobulin domain containing 10 like Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV10-67 Geneimmunoglobulin lambda variable 10-67 (pseudogene) |
IGKV2-4 Geneimmunoglobulin kappa variable 2-4 (pseudogene) |
IGKV3-34 Geneimmunoglobulin kappa variable 3-34 (pseudogene) |
IGKV3-31 Geneimmunoglobulin kappa variable 3-31 (pseudogene) |
IGKV3OR2-5 Geneimmunoglobulin kappa variable 3/OR2-5 (pseudogene) |
IGHV3-19 Geneimmunoglobulin heavy variable 3-19 (pseudogene) |
IGHV3-15 Geneimmunoglobulin heavy variable 3-15 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-16 Geneimmunoglobulin heavy variable 3-16 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-13 Geneimmunoglobulin heavy variable 3-13 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVI-20 Geneimmunoglobulin lambda variable (I)-20 (pseudogene) |
KIR2DS4 Genekiller cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 4 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DS3 Genekiller cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DS1 Genekiller cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
IGHVII-43-1 Geneimmunoglobulin heavy variable (II)-43-1 (pseudogene) |
IGDCC3 Geneimmunoglobulin superfamily, DCC subclass, member 3 Predicted to be involved in cell-cell adhesion. Predicted to act upstream of or within neuromuscular process controlling balance. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGDCC4 Geneimmunoglobulin superfamily, DCC subclass, member 4 Predicted to be involved in cell-cell adhesion. Predicted to be located in plasma membrane. [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] |
IGHV4-55 Geneimmunoglobulin heavy variable 4-55 (pseudogene) |
LOC391405 Geneimmunoglobulin kappa light chain variable region |
IGKV1-27 Geneimmunoglobulin kappa variable 1-27 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-22 Geneimmunoglobulin kappa variable 1-22 (pseudogene) |
IGHVIV-44-1 Geneimmunoglobulin heavy variable (IV)-44-1 (pseudogene) |
LOC105371448 Geneimmunoglobulin superfamily DCC subclass member 3-like |
IGHV4-34 Geneimmunoglobulin heavy variable 4-34 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2-23 Geneimmunoglobulin kappa variable 2-23 (pseudogene) |
IGKV2-26 Geneimmunoglobulin kappa variable 2-26 (pseudogene) |
IGKV2-28 Geneimmunoglobulin kappa variable 2-28 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2-29 Geneimmunoglobulin kappa variable 2-29 (gene/pseudogene) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKJ1 Geneimmunoglobulin kappa joining 1 Predicted to be involved in adaptive immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKJ3 Geneimmunoglobulin kappa joining 3 |
IGKJ5 Geneimmunoglobulin kappa joining 5 |
IGKJ@ Geneimmunoglobulin kappa joining cluster Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains (see MIM 147100) and 2 identical light chains, either kappa or lambda (see MIM 147220), joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. The kappa and lambda light chains have no apparent functional differences. Each Ig kappa light chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by a C region gene (IGKC; MIM 147200), that provides signaling functions. The kappa light chain V region is encoded by 2 types of genes: V genes (see MIM 146980) and joining (J) genes. Random selection of just 1 gene of each type to assemble a V region accounts for the great diversity of V regions among Ig molecules. The kappa light chain locus on chromosome 2 contains approximately 40 functional V genes, followed by approximately 5 functional J genes. Due to polymorphism, the numbers of functional V and J genes differ among individuals (Janeway et al., 2005).[supplied by OMIM, Apr 2008] |
IGHVIII-47-1 Geneimmunoglobulin heavy variable (III)-47-1 (pseudogene) |
IGHD4OR15-4B Geneimmunoglobulin heavy diversity 4/OR15-4B (non-functional) |
IGHD2-21 Geneimmunoglobulin heavy diversity 2-21 |
IGHVII-40-1 Geneimmunoglobulin heavy variable (II)-40-1 (pseudogene) |
IGHD Geneimmunoglobulin heavy constant delta Predicted to enable antigen binding activity. Involved in positive regulation of interleukin-1 production. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVVI-25-1 Geneimmunoglobulin lambda variable (VI)-25-1 (pseudogene) |
IGHD1-20 Geneimmunoglobulin heavy diversity 1-20 |
IGHD1-26 Geneimmunoglobulin heavy diversity 1-26 |
IGHV6-1 Geneimmunoglobulin heavy variable 6-1 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1OR-3 Geneimmunoglobulin kappa variable 1/OR-3 (pseudogene) |
IGKV1OR-2 Geneimmunoglobulin kappa variable 1/OR-2 (pseudogene) |
IGKV1OR-4 Geneimmunoglobulin kappa variable 1/OR-4 (pseudogene) |
IGLVVII-41-1 Geneimmunoglobulin lambda variable (VII)-41-1 (pseudogene) |
IGHVII-65-1 Geneimmunoglobulin heavy variable (II)-65-1 (pseudogene) |
IGHE Geneimmunoglobulin heavy constant epsilon Enables immunoglobulin receptor binding activity. Involved in several processes, including B cell mediated immunity; Fc receptor-mediated immune complex endocytosis; and leukocyte degranulation. Located in extracellular space and plasma membrane. Part of IgE B cell receptor complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD6-6 Geneimmunoglobulin heavy diversity 6-6 |
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] |
IGKV2OR22-3 Geneimmunoglobulin kappa variable 2/OR22-3 (pseudogene) |
IGKV2OR22-4 Geneimmunoglobulin kappa variable 2/OR22-4 (pseudogene) |
IGHVII-53-1 Geneimmunoglobulin heavy variable (II)-53-1 (pseudogene) |
IGFN1 Geneimmunoglobulin-like and fibronectin type III domain containing 1 Predicted to be located in Z disc and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV@ Geneimmunoglobulin lambda variable cluster Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains (see MIM 147100) and 2 identical light chains, either kappa (see MIM 147200) or lambda, joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. The kappa and lambda light chains have no apparent functional differences. Each Ig lambda light chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by a C region gene (IGLC1; MIM 147220), that provides signaling functions. The lambda light chain V region is encoded by 2 types of genes: V genes and joining (J) genes (see MIM 147230). Random selection of just 1 gene of each type to assemble a V region accounts for the great diversity of V regions among Ig molecules. The lambda light chain locus on chromosome 22 contains approximately 30 functional V genes, followed by approximately 4 functional J genes. Due to polymorphism, the numbers of functional V and J genes differ among individuals (Janeway et al., 2005).[supplied by OMIM, Apr 2008] |
IGHV4-61 Geneimmunoglobulin heavy variable 4-61 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVII-62-1 Geneimmunoglobulin heavy variable (II)-62-1 (pseudogene) |
IGHVII-20-1 Geneimmunoglobulin heavy variable (II)-20-1 (pseudogene) |
IGHA2 Geneimmunoglobulin heavy constant alpha 2 (A2m marker) Contributes to immunoglobulin receptor binding activity. Involved in glomerular filtration and positive regulation of respiratory burst. Located in extracellular space. Part of monomeric IgA immunoglobulin complex and secretory dimeric IgA immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHA1 Geneimmunoglobulin heavy constant alpha 1 Contributes to immunoglobulin receptor binding activity. Involved in glomerular filtration and positive regulation of respiratory burst. Located in extracellular space. Part of monomeric IgA immunoglobulin complex and secretory dimeric IgA immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC338667 GeneV-set and immunoglobulin domain-containing protein 10-like Predicted to enable cell adhesion molecule binding activity. Predicted to be involved in cell-cell adhesion. Predicted to be located in membrane. Predicted to be active in cell-cell junction and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVII-28-1 Geneimmunoglobulin heavy variable (II)-28-1 (pseudogene) |
IGLV5-37 Geneimmunoglobulin lambda variable 5-37 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV5-39 Geneimmunoglobulin lambda variable 5-39 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3OR16-12 Geneimmunoglobulin heavy variable 3/OR16-12 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3OR16-11 Geneimmunoglobulin heavy variable 3/OR16-11 (pseudogene) |
IGHV3OR16-10 Geneimmunoglobulin heavy variable 3/OR16-10 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3OR16-16 Geneimmunoglobulin heavy variable 3/OR16-16 (pseudogene) |
IGHV3OR16-15 Geneimmunoglobulin heavy variable 3/OR16-15 (pseudogene) |
TIE1 Genetyrosine kinase with immunoglobulin-like and EGF-like domains 1 This gene encodes a member of the tyrosine protein kinase family. The encoded protein plays a critical role in angiogenesis and blood vessel stability by inhibiting angiopoietin 1 signaling through the endothelial receptor tyrosine kinase Tie2. Ectodomain cleavage of the encoded protein relieves inhibition of Tie2 and is mediated by multiple factors including vascular endothelial growth factor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
IGKV2-24 Geneimmunoglobulin kappa variable 2-24 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
BIVM Genebasic, immunoglobulin-like variable motif containing Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV4-60 Geneimmunoglobulin lambda variable 4-60 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV4-69 Geneimmunoglobulin lambda variable 4-69 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKJ2 Geneimmunoglobulin kappa joining 2 |
IGKJ4 Geneimmunoglobulin kappa joining 4 |
IGHV3-25 Geneimmunoglobulin heavy variable 3-25 (pseudogene) |
IGHV3-20 Geneimmunoglobulin heavy variable 3-20 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-21 Geneimmunoglobulin heavy variable 3-21 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-22 Geneimmunoglobulin heavy variable 3-22 (pseudogene) |
IGHV3-23 Geneimmunoglobulin heavy variable 3-23 IGHV3-23 belongs to a cluster of approximately 40 functional variable (V) genes in the immunoglobulin (Ig) heavy chain locus on chromosome 14. For background information on the Ig heavy chain and the V gene cluster, see (MIM 147070).[supplied by OMIM, Apr 2008] |
IGLVI-70 Geneimmunoglobulin lambda variable (I)-70 (pseudogene) |
IGHV3-29 Geneimmunoglobulin heavy variable 3-29 (pseudogene) |
IGHV7-27 Geneimmunoglobulin heavy variable 7-27 (pseudogene) |
IGLC4 Geneimmunoglobulin lambda constant 4 (pseudogene) |
IGLC5 Geneimmunoglobulin lambda constant 5 (pseudogene) |
IGLC6 Geneimmunoglobulin lambda constant 6 (Kern+Oz- marker, gene/pseudogene) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
IGLC7 Geneimmunoglobulin lambda constant 7 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of IgG immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLC1 Geneimmunoglobulin lambda constant 1 (Mcg marker) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLC2 Geneimmunoglobulin lambda constant 2 (Kern-Oz- marker) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLC3 Geneimmunoglobulin lambda constant 3 (Kern-Oz+ marker) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in blood microparticle and extracellular exosome. Part of IgG immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3OR15-7 Geneimmunoglobulin heavy variable 3/OR15-7 (pseudogene) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC390714 Geneimmunoglobulin heavy chain variable region Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGES Geneimmunoglobulin E concentration, serum |
IGKV3D-20 Geneimmunoglobulin kappa variable 3D-20 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV3D-25 Geneimmunoglobulin kappa variable 3D-25 (pseudogene) |
IGHVII-15-1 Geneimmunoglobulin heavy variable (II)-15-1 (pseudogene) |
IGLVVI-22-1 Geneimmunoglobulin lambda variable (VI)-22-1 (pseudogene) |
KIR3DS1 Genekiller cell immunoglobulin-like receptor, three domains, short cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
IGHVIII-25-1 Geneimmunoglobulin heavy variable (III)-25-1 (pseudogene) |
IGLV2-34 Geneimmunoglobulin lambda variable 2-34 (pseudogene) |
IGLV2-33 Geneimmunoglobulin lambda variable 2-33 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421901 Geneimmunoglobulin (CD79A) binding protein 1 pseudogene |
IGHD4OR15-4A Geneimmunoglobulin heavy diversity 4/OR15-4A (non-functional) |
IGHVIII-67-4 Geneimmunoglobulin heavy variable (III)-67-4 (pseudogene) |
IGHVIII-67-2 Geneimmunoglobulin heavy variable (III)-67-2 (pseudogene) |
IGHVIII-67-3 Geneimmunoglobulin heavy variable (III)-67-3 (pseudogene) |
IGKV1OR2-3 Geneimmunoglobulin kappa variable 1/OR2-3 (pseudogene) |
IGKV1OR2-0 Geneimmunoglobulin kappa variable 1/OR2-0 (non-functional) |
IGKV1OR2-1 Geneimmunoglobulin kappa variable 1/OR2-1 (pseudogene) |
IGKV1OR2-6 Geneimmunoglobulin kappa variable 1/OR2-6 (pseudogene) |
IGLV6-57 Geneimmunoglobulin lambda variable 6-57 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC102725034 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
CYAT1 Geneimmunoglobulin lambda light chain-like |
IGHV3OR16-9 Geneimmunoglobulin heavy variable 3/OR16-9 (non-functional) Predicted to be involved in adaptive immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3OR16-8 Geneimmunoglobulin heavy variable 3/OR16-8 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHM Geneimmunoglobulin heavy constant mu Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains and 2 identical light chains (see MIM 147200) joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. Each Ig heavy chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by an individual C region gene, that determines the isotype of the antibody and provides effector or signaling functions. The heavy chain V region is encoded by 1 each of 3 types of genes: V genes (see MIM 147070), joining (J) genes (see MIM 147010), and diversity (D) genes (see MIM 146910). The C region genes are clustered downstream of the V region genes within the heavy chain locus on chromosome 14. The IGHM gene encodes the C region of the mu heavy chain, which defines the IgM isotype. Naive B cells express the transmembrane forms of IgM and IgD (see IGHD; MIM 1471770) on their surface. During an antibody response, activated B cells can switch to the expression of individual downstream heavy chain C region genes by a process of somatic recombination known as isotype switching. In addition, secreted Ig forms that act as antibodies can be produced by alternative RNA processing of the heavy chain C region sequences. Although the membrane forms of all Ig isotypes are monomeric, secreted IgM forms pentamers, and occasionally hexamers, in plasma (summary by Janeway et al., 2005).[supplied by OMIM, Aug 2010] |
IGHV1OR15-5 Geneimmunoglobulin heavy variable 1/OR15-5 (non-functional) |
IGHV2-5 Geneimmunoglobulin heavy variable 2-5 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLL3P Geneimmunoglobulin lambda-like polypeptide 3, pseudogene |
IGHV4-59 Geneimmunoglobulin heavy variable 4-59 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1OR22-1 Geneimmunoglobulin kappa variable 1/OR22-1 (pseudogene) |
IGKV1OR22-5 Geneimmunoglobulin kappa variable 1/OR22-5 (pseudogene) |
IGKV6D-21 Geneimmunoglobulin kappa variable 6D-21 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-33-2 Geneimmunoglobulin heavy variable 3-33-2 (pseudogene) |
LOC100887081 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 6 pseudogene |
LOC102725031 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
IGHVIII-22-2 Geneimmunoglobulin heavy variable (III)-22-2 (pseudogene) |
IGKV1D-39 Geneimmunoglobulin kappa variable 1D-39 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1D-33 Geneimmunoglobulin kappa variable 1D-33 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1D-32 Geneimmunoglobulin kappa variable 1D-32 (pseudogene) |
IGKV1D-35 Geneimmunoglobulin kappa variable 1D-35 (pseudogene) |
IGKV1D-37 Geneimmunoglobulin kappa variable 1D-37 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
KIR2DL5B Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL5A Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
IGHV3-79 Geneimmunoglobulin heavy variable 3-79 (pseudogene) |
IGHV3-73 Geneimmunoglobulin heavy variable 3-73 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-72 Geneimmunoglobulin heavy variable 3-72 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-71 Geneimmunoglobulin heavy variable 3-71 (pseudogene) |
IGHV3-76 Geneimmunoglobulin heavy variable 3-76 (pseudogene) |
IGHV3-75 Geneimmunoglobulin heavy variable 3-75 (pseudogene) |
IGHV3-74 Geneimmunoglobulin heavy variable 3-74 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVI-42 Geneimmunoglobulin lambda variable (I)-42 (pseudogene) |
IGLV8OR8-1 Geneimmunoglobulin lambda variable 8/OR8-1 (pseudogene) |
IGKV1OR2-108 Geneimmunoglobulin kappa variable 1/OR2-108 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3OR16-14 Geneimmunoglobulin heavy variable 3/OR16-14 (pseudogene) |
IGHV3OR16-6 Geneimmunoglobulin heavy variable 3/OR16-6 (pseudogene) |
IGHV3-7 Geneimmunoglobulin heavy variable 3-7 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-6 Geneimmunoglobulin heavy variable 3-6 (pseudogene) |
IGHV3-9 Geneimmunoglobulin heavy variable 3-9 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVIII-51-1 Geneimmunoglobulin heavy variable (III)-51-1 (pseudogene) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-46 Geneimmunoglobulin heavy variable 1-46 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-10 Geneimmunoglobulin lambda variable 3-10 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-13 Geneimmunoglobulin lambda variable 3-13 (pseudogene) |
IGLV3-12 Geneimmunoglobulin lambda variable 3-12 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-15 Geneimmunoglobulin lambda variable 3-15 (pseudogene) |
IGLV3-17 Geneimmunoglobulin lambda variable 3-17 (pseudogene) |
IGLV3-16 Geneimmunoglobulin lambda variable 3-16 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-19 Geneimmunoglobulin lambda variable 3-19 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1OR2-11 Geneimmunoglobulin kappa variable 1/OR2-11 (pseudogene) |
IGKV3D-11 Geneimmunoglobulin kappa variable 3D-11 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV3D-15 Geneimmunoglobulin kappa variable 3D-15 (gene/pseudogene) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHDOR15@ Geneimmunoglobulin heavy diversity orphans on chromosome 15 |
LILRB5 Geneleukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 5 This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). Several other LIR subfamily B receptors are expressed on immune cells where they bind to MHC class I molecules on antigen-presenting cells and inhibit stimulation of an immune response. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LILRB4 Geneleukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 4 This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. The receptor can also function in antigen capture and presentation. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LILRB3 Geneleukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 3 This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LILRB2 Geneleukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 2 This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LILRB1 Geneleukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 1 This gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains, a transmembrane domain, and two to four cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs). The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response. It is thought to control inflammatory responses and cytotoxicity to help focus the immune response and limit autoreactivity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
IGLV1-41 Geneimmunoglobulin lambda variable 1-41 (pseudogene) |
IGLV1-44 Geneimmunoglobulin lambda variable 1-44 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV1-47 Geneimmunoglobulin lambda variable 1-47 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379662 Genekiller cell immunoglobulin-like receptor 2DS1 |
IGKV2-40 Geneimmunoglobulin kappa variable 2-40 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV7-4-1 Geneimmunoglobulin heavy variable 7-4-1 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD1-7 Geneimmunoglobulin heavy diversity 1-7 |
IGHD1-1 Geneimmunoglobulin heavy diversity 1-1 Predicted to be involved in adaptive immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-5 Geneimmunoglobulin kappa variable 1-5 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2OR2-2 Geneimmunoglobulin kappa variable 2/OR2-2 (pseudogene) |
IGKV2OR2-1 Geneimmunoglobulin kappa variable 2/OR2-1 (pseudogene) |
IGKV2OR2-7 Geneimmunoglobulin kappa variable 2/OR2-7 (pseudogene) |
IGKV2OR2-4 Geneimmunoglobulin kappa variable 2/OR2-4 (pseudogene) |
IGHD3-16 Geneimmunoglobulin heavy diversity 3-16 |
IGHD3-10 Geneimmunoglobulin heavy diversity 3-10 |
IGHV1OR16-1 Geneimmunoglobulin heavy variable 1/OR16-1 (pseudogene) |
IGHV1OR16-3 Geneimmunoglobulin heavy variable 1/OR16-3 (pseudogene) |
IGHV1OR16-2 Geneimmunoglobulin heavy variable 1/OR16-2 (pseudogene) |
IGHV1OR16-4 Geneimmunoglobulin heavy variable 1/OR16-4 (pseudogene) |
IGKV6-21 Geneimmunoglobulin kappa variable 6-21 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-58 Geneimmunoglobulin heavy variable 1-58 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
MILR1 Genemast cell immunoglobulin-like receptor 1 Predicted to enable transmembrane signaling receptor activity. Predicted to be involved in cell surface receptor signaling pathway; mast cell degranulation; and negative regulation of mast cell activation. Predicted to be located in plasma membrane. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGHJ2P Geneimmunoglobulin heavy joining 2P (pseudogene) |
IGHVIII-76-1 Geneimmunoglobulin heavy variable (III)-76-1 (pseudogene) |
LOC102724123 Geneimmunoglobulin superfamily member 3-like |
IGHV2OR16-5 Geneimmunoglobulin heavy variable 2/OR16-5 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1OR9-1 Geneimmunoglobulin kappa variable 1/OR9-1 (pseudogene) |
RBPJ Generecombination signal binding protein for immunoglobulin kappa J region The protein encoded by this gene is a transcriptional regulator important in the Notch signaling pathway. The encoded protein acts as a repressor when not bound to Notch proteins and an activator when bound to Notch proteins. It is thought to function by recruiting chromatin remodeling complexes containing histone deacetylase or histone acetylase proteins to Notch signaling pathway genes. Several transcript variants encoding different isoforms have been found for this gene, and several pseudogenes of this gene exist on chromosome 9. [provided by RefSeq, Oct 2013] |
IGHD4-23 Geneimmunoglobulin heavy diversity 4-23 (non-functional) |
IGHV4-80 Geneimmunoglobulin heavy variable 4-80 (pseudogene) |
IGHV7-81 Geneimmunoglobulin heavy variable 7-81 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV1-24 Geneimmunoglobulin heavy variable 1-24 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD4-4 Geneimmunoglobulin heavy diversity 4-4 |
IGLV3-29 Geneimmunoglobulin lambda variable 3-29 (pseudogene) |
IGLV3-21 Geneimmunoglobulin lambda variable 3-21 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-22 Geneimmunoglobulin lambda variable 3-22 (gene/pseudogene) Predicted to be involved in immune response. Predicted to act upstream of or within apoptotic signaling pathway; negative regulation of stem cell proliferation; and regulation of G1/S transition of mitotic cell cycle. Predicted to be located in cytoplasm and extracellular space. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-24 Geneimmunoglobulin lambda variable 3-24 (pseudogene) |
IGLV3-25 Geneimmunoglobulin lambda variable 3-25 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-26 Geneimmunoglobulin lambda variable 3-26 (pseudogene) |
IGLV3-27 Geneimmunoglobulin lambda variable 3-27 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD5OR15-5B Geneimmunoglobulin heavy diversity 5/OR15-5B (non-functional) |
IGHD5OR15-5A Geneimmunoglobulin heavy diversity 5/OR15-5A (non-functional) |
IGLV5-52 Geneimmunoglobulin lambda variable 5-52 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LILRA6 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 6 Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LILRA4 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 4 This gene encodes an immunoglobulin-like cell surface protein that is expressed predominantly on plasmacytoid dendritic cells (PDCs) and modulates the function of these cells in the immune response. Expression of this gene is downregulated by interleukin 3 (IL3). This gene is one of a cluster of highly related genes located at chromosomal region 19q13.4. [provided by RefSeq, Jan 2015] |
LILRA5 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 5 The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008] |
LILRA2 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 2 This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014] |
LILRA3 Geneleukocyte immunoglobulin-like receptor, subfamily A (without TM domain), member 3 This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014] |
LILRA1 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 1 This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013] |
IGHD1OR15-1B Geneimmunoglobulin heavy diversity 1/OR15-1B (non-functional) |
IGHD1OR15-1A Geneimmunoglobulin heavy diversity 1/OR15-1A (non-functional) |
IGHVII-78-1 Geneimmunoglobulin heavy variable (II)-78-1 (pseudogene) |
IGHV1OR21-1 Geneimmunoglobulin heavy variable 1/OR21-1 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD5-18 Geneimmunoglobulin heavy diversity 5-18 |
IGHD5-12 Geneimmunoglobulin heavy diversity 5-12 |
PIGR Genepolymeric immunoglobulin receptor This gene is a member of the immunoglobulin superfamily. The encoded poly-Ig receptor binds polymeric immunoglobulin molecules at the basolateral surface of epithelial cells; the complex is then transported across the cell to be secreted at the apical surface. A significant association was found between immunoglobulin A nephropathy and several SNPs in this gene.[provided by RefSeq, Sep 2009] |
IGKV1-35 Geneimmunoglobulin kappa variable 1-35 (pseudogene) |
IGKV1-37 Geneimmunoglobulin kappa variable 1-37 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-32 Geneimmunoglobulin kappa variable 1-32 (pseudogene) |
IGKV1-33 Geneimmunoglobulin kappa variable 1-33 Enables identical protein binding activity. Predicted to be involved in immune response. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-39 Geneimmunoglobulin kappa variable 1-39 (gene/pseudogene) Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379433 Geneimmunoglobulin superfamily member 2-like |
IGHVIII-5-2 Geneimmunoglobulin heavy variable (III)-5-2 (pseudogene) |
IGHVIII-5-1 Geneimmunoglobulin heavy variable (III)-5-1 (pseudogene) |
IGHV5-51 Geneimmunoglobulin heavy variable 5-51 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD5-5 Geneimmunoglobulin heavy diversity 5-5 |
IGLV2-11 Geneimmunoglobulin lambda variable 2-11 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV2-14 Geneimmunoglobulin lambda variable 2-14 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV2-18 Geneimmunoglobulin lambda variable 2-18 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-6 Geneimmunoglobulin kappa variable 1-6 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-8 Geneimmunoglobulin kappa variable 1-8 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1-9 Geneimmunoglobulin kappa variable 1-9 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-64D Geneimmunoglobulin heavy variable 3-64D Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-38-3 Geneimmunoglobulin heavy variable 3-38-3 (non-functional) Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
PVRIG Genepoliovirus receptor related immunoglobulin domain containing Enables phosphatase binding activity and signaling receptor activity. Involved in negative regulation of T cell receptor signaling pathway. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV4-30-4 Geneimmunoglobulin heavy variable 4-30-4 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV4-30-2 Geneimmunoglobulin heavy variable 4-30-2 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV4-30-1 Geneimmunoglobulin heavy variable 4-30-1 |
IGKV2-19 Geneimmunoglobulin kappa variable 2-19 (pseudogene) |
IGKV2-18 Geneimmunoglobulin kappa variable 2-18 (pseudogene) |
IGKV2-14 Geneimmunoglobulin kappa variable 2-14 (pseudogene) |
IGKV2-10 Geneimmunoglobulin kappa variable 2-10 (pseudogene) |
IGHVIII-38-1 Geneimmunoglobulin heavy variable (III)-38-1 (pseudogene) |
IGHVIII-82 Geneimmunoglobulin heavy variable (III)-82 (pseudogene) |
IGLV11-55 Geneimmunoglobulin lambda variable 11-55 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVIV-65 Geneimmunoglobulin lambda variable (IV)-65 (pseudogene) |
IGLVIV-64 Geneimmunoglobulin lambda variable (IV)-64 (pseudogene) |
IGLV1-40 Geneimmunoglobulin lambda variable 1-40 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVII-33-1 Geneimmunoglobulin heavy variable (II)-33-1 (pseudogene) |
IGKV2D-38 Geneimmunoglobulin kappa variable 2D-38 (pseudogene) |
IGKV2D-36 Geneimmunoglobulin kappa variable 2D-36 (pseudogene) |
IGKV2D-30 Geneimmunoglobulin kappa variable 2D-30 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV5-10-1 Geneimmunoglobulin heavy variable 5-10-1 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV2OR2-7D Geneimmunoglobulin kappa variable 2/OR2-7D (pseudogene) |
LOC105369139 Genekiller cell immunoglobulin-like receptor 2DS3 |
IGLV9-49 Geneimmunoglobulin lambda variable 9-49 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV2-8 Geneimmunoglobulin lambda variable 2-8 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV2-5 Geneimmunoglobulin lambda variable 2-5 (pseudogene) |
CD79B GeneCD79b molecule, immunoglobulin-associated beta The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-beta protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008] |
CD79A GeneCD79a molecule, immunoglobulin-associated alpha The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-alpha protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008] |
IGLJ@ Geneimmunoglobulin lambda joining cluster Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains (see MIM 147100) and 2 identical light chains, either kappa (see MIM 147200) or lambda, joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. The kappa and lambda light chains have no apparent functional differences. Each Ig lambda light chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by a C region gene (IGLC1; MIM 147220), that provides signaling functions. The lambda light chain V region is encoded by 2 types of genes: V genes (see MIM 147240) and joining (J) genes. Random selection of just 1 gene of each type to assemble a V region accounts for the great diversity of V regions among Ig molecules. The lambda light chain locus on chromosome 22 contains approximately 30 functional V genes, followed by approximately 4 functional J genes. Due to polymorphism, the numbers of functional V and J genes differ among individuals (Janeway et al., 2005).[supplied by OMIM, Apr 2008] |
IGLJ3 Geneimmunoglobulin lambda joining 3 |
IGLJ2 Geneimmunoglobulin lambda joining 2 |
IGLJ1 Geneimmunoglobulin lambda joining 1 Predicted to be involved in adaptive immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLJ7 Geneimmunoglobulin lambda joining 7 |
IGLJ6 Geneimmunoglobulin lambda joining 6 |
IGLJ5 Geneimmunoglobulin lambda joining 5 (non-functional) |
IGLJ4 Geneimmunoglobulin lambda joining 4 (non-functional) |
IGKV3OR2-268 Geneimmunoglobulin kappa variable 3/OR2-268 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region. Predicted to be part of immunoglobulin complex. [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] |
IGHVIII-11-1 Geneimmunoglobulin heavy variable (III)-11-1 (pseudogene) |
IGHVIII-13-1 Geneimmunoglobulin heavy variable (III)-13-1 (pseudogene) |
IGHVII-46-1 Geneimmunoglobulin heavy variable (II)-46-1 (pseudogene) |
IGHVII-1-1 Geneimmunoglobulin heavy variable (II)-1-1 (pseudogene) |
IGKV1D-17 Geneimmunoglobulin kappa variable 1D-17 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1D-16 Geneimmunoglobulin kappa variable 1D-16 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1D-13 Geneimmunoglobulin kappa variable 1D-13 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1D-12 Geneimmunoglobulin kappa variable 1D-12 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD7-27 Geneimmunoglobulin heavy diversity 7-27 |
IGLVV-66 Geneimmunoglobulin lambda variable (V)-66 (pseudogene) |
IGHV3-50 Geneimmunoglobulin heavy variable 3-50 (pseudogene) |
IGHV3-53 Geneimmunoglobulin heavy variable 3-53 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-52 Geneimmunoglobulin heavy variable 3-52 (pseudogene) |
IGHV3-54 Geneimmunoglobulin heavy variable 3-54 (pseudogene) |
IGHV3-57 Geneimmunoglobulin heavy variable 3-57 (pseudogene) |
IGLVI-63 Geneimmunoglobulin lambda variable (I)-63 (pseudogene) |
IGLVI-68 Geneimmunoglobulin lambda variable (I)-68 (pseudogene) |
SEMA3A Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A This gene is a member of the semaphorin family and encodes a protein with an Ig-like C2-type (immunoglobulin-like) domain, a PSI domain and a Sema domain. This secreted protein can function as either a chemorepulsive agent, inhibiting axonal outgrowth, or as a chemoattractive agent, stimulating the growth of apical dendrites. In both cases, the protein is vital for normal neuronal pattern development. Increased expression of this protein is associated with schizophrenia and is seen in a variety of human tumor cell lines. Also, aberrant release of this protein is associated with the progression of Alzheimer's disease. [provided by RefSeq, Jul 2008] |
SEMA3C Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017] |
SEMA3B Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B The protein encoded by this gene belongs to the class-3 semaphorin/collapsin family, whose members function in growth cone guidance during neuronal development. This family member inhibits axonal extension and has been shown to act as a tumor suppressor by inducing apoptosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
SEMA3E Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. This gene encodes a class 4 semaphorin. This gene encodes a class 3 semaphorin. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010] |
SEMA3D Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin like domain and a C-terminal basic domain. The protein encoded by this gene binds neuropilin and plays an important role in cardiovascular development. [provided by RefSeq, Aug 2016] |
SEMA3G Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G The transcription of this gene is activated by PPAR-gamma, and the resulting protein product plays a role in endothelial cell migration. Expression of this gene also inhibits tumor cell migration and invasion. [provided by RefSeq, Jul 2016] |
SEMA3F Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin loop and a C-terminal basic domain. This gene is expressed by the endothelial cells where it was found to act in an autocrine fashion to induce apoptosis, inhibit cell proliferation and survival, and function as an anti-tumorigenic agent. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
IGHVII-67-1 Geneimmunoglobulin heavy variable (II)-67-1 (pseudogene) |
IGKV@ Geneimmunoglobulin kappa variable cluster Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains (see MIM 147100) and 2 identical light chains, either kappa or lambda (see MIM 147220), joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. The kappa and lambda light chains have no apparent functional differences. Each Ig kappa light chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by a C region gene (IGKC; MIM 147200), that provides signaling functions. The kappa light chain V region is encoded by 2 types of genes: V genes and joining (J) genes (see MIM 146970). Random selection of just 1 gene of each type to assemble a V region accounts for the great diversity of V regions among Ig molecules. The kappa light chain locus on chromosome 2 contains approximately 40 functional V genes, followed by approximately 5 functional J genes. Due to polymorphism, the numbers of functional V and J genes differ among individuals (Janeway et al., 2005).[supplied by OMIM, Apr 2008] |
IGHD5-24 Geneimmunoglobulin heavy diversity 5-24 (non-functional) |
IGLV3-4 Geneimmunoglobulin lambda variable 3-4 (pseudogene) |
IGLV3-7 Geneimmunoglobulin lambda variable 3-7 (pseudogene) |
IGLV3-6 Geneimmunoglobulin lambda variable 3-6 (pseudogene) |
IGLV3-1 Geneimmunoglobulin lambda variable 3-1 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV3-2 Geneimmunoglobulin lambda variable 3-2 (pseudogene) |
IGLV3-9 Geneimmunoglobulin lambda variable 3-9 (gene/pseudogene) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHVII-74-1 Geneimmunoglobulin heavy variable (II)-74-1 (pseudogene) |
IGKV3D-34 Geneimmunoglobulin kappa variable 3D-34 (pseudogene) |
IGKV3D-31 Geneimmunoglobulin kappa variable 3D-31 (pseudogene) |
KIR3DP1 Genekiller cell immunoglobulin-like receptor, three domains, pseudogene 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence of transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result of a recombinantion event, has two copies of this gene, one of which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011] |
VSIG10 GeneV-set and immunoglobulin domain containing 10 Predicted to enable cell adhesion molecule binding activity. Predicted to be involved in cell-cell adhesion. Predicted to be located in membrane. Predicted to be active in cell-cell junction and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC642131 Geneputative V-set and immunoglobulin domain-containing-like protein IGHV4OR15-8 |
IGKV3OR22-2 Geneimmunoglobulin kappa variable 3/OR22-2 (pseudogene) |
LOC100631370 Geneimmunoglobulin superfamily, DCC subclass, member 3 pseudogene |
IGLV1-62 Geneimmunoglobulin lambda variable 1-62 (pseudogene) |
TIMD4 GeneT-cell immunoglobulin and mucin domain containing 4 Predicted to enable phosphatidylserine binding activity. Predicted to be involved in apoptotic cell clearance and cytoskeletal rearrangement involved in phagocytosis, engulfment. Predicted to be located in extracellular region and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV7-56 Geneimmunoglobulin heavy variable 7-56 (pseudogene) |
IGKV5-2 Geneimmunoglobulin kappa variable 5-2 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV7-3 Geneimmunoglobulin kappa variable 7-3 (pseudogene) |
IGKV2D-40 Geneimmunoglobulin kappa variable 2D-40 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVIV-66-1 Geneimmunoglobulin lambda variable (IV)-66-1 (pseudogene) |
VSIG8 GeneV-set and immunoglobulin domain containing 8 Enables RNA binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
VSIG4 GeneV-set and immunoglobulin domain containing 4 This gene encodes a v-set and immunoglobulin-domain containing protein that is structurally related to the B7 family of immune regulatory proteins. The encoded protein may be a negative regulator of T-cell responses. This protein is also a receptor for the complement component 3 fragments C3b and iC3b. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
VSIG2 GeneV-set and immunoglobulin domain containing 2 Predicted to be involved in lipid metabolic process. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
VSIG1 GeneV-set and immunoglobulin domain containing 1 This gene encodes a member of the junctional adhesion molecule (JAM) family. The encoded protein contains multiple glycosylation sites at the N-terminal region, and multiple phosphorylation sites and glutamic acid/proline (EP) repeats at the C-terminal region. The gene is expressed in normal stomach and testis, as well as in gastric, esophageal and ovarian cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009] |
KIR2DP1 Genekiller cell immunoglobulin-like receptor, two domains, pseudogene 1 Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
IGLL2P Geneimmunoglobulin lambda-like polypeptide 2, pseudogene This locus represents a pseudogene of immunoglobulin lambda-like polypeptide 1. However, it appears to be co-transcribed with an adjacent glucuronidase, beta pseudogene. The transcript including sequence for both pseudogenes is represented by NR_024448, GeneID 91316. [provided by RefSeq, Jul 2011] |
IGHV4-28 Geneimmunoglobulin heavy variable 4-28 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHD2-15 Geneimmunoglobulin heavy diversity 2-15 |
IGHV1-17 Geneimmunoglobulin heavy variable 1-17 (pseudogene) |
IGHV1-18 Geneimmunoglobulin heavy variable 1-18 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLVV-58 Geneimmunoglobulin lambda variable (V)-58 (pseudogene) |
IGKV1OR1-1 Geneimmunoglobulin kappa variable 1/OR1-1 (pseudogene) |
IGKV4-1 Geneimmunoglobulin kappa variable 4-1 Predicted to enable antigen binding activity. Predicted to be involved in immune response. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
IGSF23 Geneimmunoglobulin superfamily, member 23 This gene encodes a protein that has one immunoglobulin (Ig) domain and is a member of the immunoglobulin superfamily. Proteins in this superfamily are usually found on or in cell membranes and act as receptors in immune response pathways. [provided by RefSeq, Nov 2011] |
IGSF22 Geneimmunoglobulin superfamily, member 22 |
IGHV1-69D Geneimmunoglobulin heavy variable 1-69D Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGLV4-3 Geneimmunoglobulin lambda variable 4-3 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV2-10 Geneimmunoglobulin heavy variable 2-10 (pseudogene) |
TMIGD1 Genetransmembrane and immunoglobulin domain containing 1 Predicted to enable cell-cell adhesion mediator activity and protein homodimerization activity. Involved in several processes, including negative regulation of apoptotic process; regulation of cell migration; and regulation of membrane permeability. Located in cytosol; mitochondrion; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4A Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010] |
SEMA4B Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B Predicted to enable chemorepellent activity; neuropilin binding activity; and semaphorin receptor binding activity. Predicted to be involved in several processes, including axon guidance; neural crest cell migration; and semaphorin-plexin signaling pathway. Predicted to be located in membrane and synapse. Predicted to be active in glutamatergic synapse and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4C Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C Predicted to enable chemorepellent activity; neuropilin binding activity; and semaphorin receptor binding activity. Involved in muscle cell differentiation and positive regulation of stress-activated MAPK cascade. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4D Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D Enables identical protein binding activity; semaphorin receptor binding activity; and transmembrane signaling receptor activity. Involved in several processes, including ossification involved in bone maturation; positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and regulation of neuron projection development. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4F Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F This gene encodes a transmembrane class IV semaphorin family protein, which plays a role in neural development. This gene may be involved in neurogenesis in prostate cancer, the development of neurofibromas, and breast cancer tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
SEMA4G Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011] |
IGHV3-60 Geneimmunoglobulin heavy variable 3-60 (pseudogene) |
IGHV3-62 Geneimmunoglobulin heavy variable 3-62 (pseudogene) |
IGHV3-63 Geneimmunoglobulin heavy variable 3-63 (pseudogene) |
IGHV3-64 Geneimmunoglobulin heavy variable 3-64 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGHV3-65 Geneimmunoglobulin heavy variable 3-65 (pseudogene) |
IGHV3-66 Geneimmunoglobulin heavy variable 3-66 Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
KIR2DL3 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL2 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL1 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008] |
KIR2DL4 Genekiller cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4 Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules; thus, KIR proteins are thought to play an important role in regulation of the immune response. This gene is one of the `framework` loci that is present on all haplotypes. Alternate alleles of this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some of which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016] |
IGKV1OR2-118 Geneimmunoglobulin kappa variable 1/OR2-118 (pseudogene) |
IGL Geneimmunoglobulin lambda locus Immunoglobulins recognize foreign antigens and initiate immune responses such as phagocytosis and the complement system. Each immunoglobulin molecule consists of two identical heavy chains and two identical light chains. There are two classes of light chains, kappa and lambda. This region represents the germline organization of the lambda light chain locus. The locus includes V (variable), J (joining), and C (constant) segments. During B cell development, a recombination event at the DNA level joins a single V segment with a J segment; the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase, and by somatic hypermutation, which occurs during B cell maturation in the spleen and lymph nodes. Several V segments and three C segments are known to be incapable of encoding a protein and are considered pseudogenes. The locus also includes several non-immunoglobulin genes, many of which are pseudogenes or are predicted by automated computational analysis or homology to other species. [provided by RefSeq, Jul 2008] |
IGK Geneimmunoglobulin kappa locus |
IGH Geneimmunoglobulin heavy locus Immunoglobulins recognize foreign antigens and initiate immune responses such as phagocytosis and the complement system. Each immunoglobulin molecule consists of two identical heavy chains and two identical light chains. This region represents the germline organization of the heavy chain locus. The locus includes V (variable), D (diversity), J (joining), and C (constant) segments. During B cell development, a recombination event at the DNA level joins a single D segment with a J segment; this partially rearranged D-J gene is then joined to a V segment. The rearranged V-D-J is then transcribed with the IGHM constant region; this transcript encodes a mu heavy chain. Later in development B cells generate V-D-J-Cmu-Cdelta pre-messenger RNA, which is alternatively spliced to encode either a mu or a delta heavy chain. Mature B cells in the lymph nodes undergo switch recombination, so that the V-D-J gene is brought in proximity to one of the IGHG, IGHA, or IGHE genes and each cell expresses either the gamma, alpha, or epsilon heavy chain. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random addition of nucleotides by terminal deoxynucleotidyltransferase, and by somatic hypermutation, which occurs during B cell maturation in the spleen and lymph nodes. Due to polymorphism, the numbers of functional V, J, and D genes differ among individuals and some V, D, J, and C segments may be pseudogenes. [provided by RefSeq, Dec 2017] |
PVRIG2P Genepoliovirus receptor related immunoglobulin domain containing 2, pseudogene |
IGHVII-51-2 Geneimmunoglobulin heavy variable (II)-51-2 (pseudogene) |
IGKV3-20 Geneimmunoglobulin kappa variable 3-20 Predicted to enable antigen binding activity. Involved in glomerular filtration. Located in extracellular space. Part of monomeric IgA immunoglobulin complex; pentameric IgM immunoglobulin complex; and secretory IgA immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV3-25 Geneimmunoglobulin kappa variable 3-25 (pseudogene) |
IGKV1D-42 Geneimmunoglobulin kappa variable 1D-42 (non-functional) Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
IGKV1D-43 Geneimmunoglobulin kappa variable 1D-43 Predicted to be involved in immune response. Predicted to be located in extracellular region and plasma membrane. Predicted to be part of immunoglobulin complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC107987462 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
LOC107987425 Geneleukocyte immunoglobulin-like receptor subfamily B member 3 |
LOC124905743 Genelow affinity immunoglobulin gamma Fc region receptor III-B |
LOC112268354 Genekiller cell immunoglobulin-like receptor 2DL4-like |
ITGA2B Geneintegrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) This gene encodes a member of the integrin alpha chain family of proteins. The encoded preproprotein is proteolytically processed to generate light and heavy chains that associate through disulfide linkages to form a subunit of the alpha-IIb/beta-3 integrin cell adhesion receptor. This receptor plays a crucial role in the blood coagulation system, by mediating platelet aggregation. Mutations in this gene are associated with platelet-type bleeding disorders, which are characterized by a failure of platelet aggregation, including Glanzmann thrombasthenia. [provided by RefSeq, Jan 2016] |
LOC100421559 Geneadaptor-related protein complex 5, mu 1 subunit pseudogene |
TRAPPC6A Genetrafficking protein particle complex 6A This gene encodes a component of the trafficking protein particle complex, which tethers transport vesicles to the cis-Golgi membrane. Loss of expression of the related gene in mouse affects coat and eye pigmentation, suggesting that the encoded protein may be involved in melanosome biogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012] |
TRAPPC6B Genetrafficking protein particle complex 6B TRAPPC6B is a component of TRAPP complexes, which are tethering complexes involved in vesicle transport (Kummel et al., 2005 [PubMed 16025134]).[supplied by OMIM, Mar 2008] |
HLA-DQB1 Genemajor histocompatibility complex, class II, DQ beta 1 HLA-DQB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and it contains six exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011] |
HLA-DQB3 Genemajor histocompatibility complex, class II, DQ beta 3 Predicted to be involved in adaptive immune response and antigen processing and presentation of peptide or polysaccharide antigen via MHC class II. Predicted to be located in endosome membrane and lysosomal membrane. Predicted to be part of MHC class II protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-DQB2 Genemajor histocompatibility complex, class II, DQ beta 2 HLA-DQB2 belongs to the family of HLA class II beta chain paralogs. Class II molecules are heterodimers consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. They play a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). Polymorphisms in the alpha and beta chains specify the peptide binding specificity, and typing for these polymorphisms is routinely done for bone marrow transplantation. However this gene, HLA-DQB2, is not routinely typed, as it is not thought to have an effect on transplantation. There is conflicting evidence in the literature and public sequence databases for the protein-coding capacity of HLA-DQB2. Because there is evidence of transcription and an intact ORF, HLA-DQB2 is represented in Entrez Gene and in RefSeq as a protein-coding locus. [provided by RefSeq, Oct 2010] |
LY6G6C Genelymphocyte antigen 6 complex, locus G6C LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008] |
LY6G6E Genelymphocyte antigen 6 complex, locus G6E (pseudogene) LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008] |
ATP5C1 GeneATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the gamma subunit of the catalytic core. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene also has a pseudogene on chromosome 14. [provided by RefSeq, Jul 2008] |
SYCE1 Genesynaptonemal complex central element protein 1 This gene encodes a member of the synaptonemal complex, which links homologous chromosomes during prophase I of meiosis. The tripartite structure of the complex is highly conserved amongst metazoans. It consists of two lateral elements and a central region formed by transverse elements and a central element. The protein encoded by this gene localizes to the central element and is required for initiation and elongation of the synapsis. Allelic variants of this gene have been associated with premature ovarian failure and spermatogenic failure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016] |
DRC7 Genedynein regulatory complex subunit 7 Predicted to be involved in sperm axoneme assembly. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
DRC1 Genedynein regulatory complex subunit 1 This gene encodes a central component of the nexin-dynein complex (N-DRC), which regulates the assembly of ciliary dynein. Mutations in this gene can cause ciliary dyskinesia. [provided by RefSeq, Aug 2015] |
TCP1P1 Genet-complex 1 pseudogene 1 |
TCP1P2 Genet-complex 1 pseudogene 2 |
TCP1P3 Genet-complex 1 pseudogene 3 |
OSTCP7 Geneoligosaccharyltransferase complex subunit pseudogene 7 |
OSTCP4 Geneoligosaccharyltransferase complex subunit pseudogene 4 |
OSTCP2 Geneoligosaccharyltransferase complex subunit pseudogene 2 |
SKA1 Genespindle and kinetochore associated complex subunit 1 Enables microtubule binding activity. Involved in attachment of mitotic spindle microtubules to kinetochore; negative regulation of mitotic spindle assembly checkpoint signaling; and positive regulation of microtubule polymerization. Located in intercellular bridge; kinetochore; and microtubule cytoskeleton. Part of SKA complex. [provided by Alliance of Genome Resources, Mar 2025] |
SKA3 Genespindle and kinetochore associated complex subunit 3 This gene encodes a component of the spindle and kinetochore-associated protein complex that regulates microtubule attachment to the kinetochores during mitosis. The encoded protein localizes to the outer kinetechore and may be required for normal chromosome segregation and cell division. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
SKA2 Genespindle and kinetochore associated complex subunit 2 Enables microtubule binding activity. Involved in attachment of mitotic spindle microtubules to kinetochore and regulation of microtubule polymerization or depolymerization. Located in spindle microtubule. Part of SKA complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-DMB Genemajor histocompatibility complex, class II, DM beta HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008] |
NCAPD2P1 Genenon-SMC condensin I complex, subunit D2 pseudogene 1 |
ELP6 Geneelongator acetyltransferase complex subunit 6 Predicted to be involved in positive regulation of cell migration. Predicted to act upstream of or within several processes, including autophagosome maturation; gene expression; and homeostasis of number of retina cells. Located in cytosol and nucleus. Part of elongator holoenzyme complex. [provided by Alliance of Genome Resources, Mar 2025] |
ELP5 Geneelongator acetyltransferase complex subunit 5 Predicted to contribute to tRNA binding activity. Predicted to be involved in positive regulation of cell migration and tRNA modification. Located in cytosol and nucleoplasm. Part of elongator holoenzyme complex. [provided by Alliance of Genome Resources, Mar 2025] |
ELP4 Geneelongator acetyltransferase complex subunit 4 This gene encodes a component of the six subunit elongator complex, a histone acetyltransferase complex that associates directly with RNA polymerase II during transcriptional elongation. The human gene can partially complement sensitivity phenotypes of yeast ELP4 deletion mutants. This gene has also been associated with Rolandic epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013] |
ELP3 Geneelongator acetyltransferase complex subunit 3 Enables acetyltransferase activity and phosphorylase kinase regulator activity. Involved in regulation of transcription by RNA polymerase II and tRNA wobble uridine modification. Located in cytosol and nucleolus. Part of elongator holoenzyme complex. [provided by Alliance of Genome Resources, Mar 2025] |
ELP2 Geneelongator acetyltransferase complex subunit 2 The protein encoded by this gene is a core subunit of the elongator complex, a histone acetyltransferase complex that associates with RNA polymerase II. In addition to histone acetylation, the encoded protein effects transcriptional elongation and may help remodel chromatin. [provided by RefSeq, May 2016] |
HLA-K Genemajor histocompatibility complex, class I, K (pseudogene) |
HLA-J Genemajor histocompatibility complex, class I, J (pseudogene) This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. [provided by RefSeq, May 2010] |
HLA-L Genemajor histocompatibility complex, class I, L (pseudogene) Predicted to be involved in antigen processing and presentation of peptide antigen via MHC class I. Predicted to be located in lumenal side of endoplasmic reticulum membrane and phagocytic vesicle membrane. Predicted to be part of MHC class I protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-B Genemajor histocompatibility complex, class I, B HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008] |
HLA-A Genemajor histocompatibility complex, class I, A HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. More than 6000 HLA-A alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020] |
HLA-G Genemajor histocompatibility complex, class I, G HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008] |
HLA-F Genemajor histocompatibility complex, class I, F This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008] |
MT-ND1 GeneNADH dehydrogenase, subunit 1 (complex I) Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Located in mitochondrial membrane. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in several diseases, including MELAS syndrome; neurodegenerative disease (multiple); optic nerve disease (multiple); toxic shock syndrome; and type 2 diabetes mellitus. Biomarker of Alzheimer's disease; Parkinson's disease; and multiple sclerosis. [provided by Alliance of Genome Resources, Mar 2025] |
MT-ND3 GeneNADH dehydrogenase, subunit 3 (complex I) Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in Leber hereditary optic neuropathy; Leigh disease; and Parkinson's disease. [provided by Alliance of Genome Resources, Mar 2025] |
MT-ND4 GeneNADH dehydrogenase, subunit 4 (complex I) Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in Leber hereditary optic neuropathy; Parkinson's disease; macular degeneration; and schizophrenia. Biomarker of Alzheimer's disease. [provided by Alliance of Genome Resources, Mar 2025] |
MT-ND5 GeneNADH dehydrogenase, subunit 5 (complex I) Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in Leber hereditary optic neuropathy; Leigh disease; and MELAS syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
MT-ND6 GeneNADH dehydrogenase, subunit 6 (complex I) Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Located in mitochondrion. Part of mitochondrial inner membrane. Implicated in Leber hereditary optic neuropathy; Leigh disease; and spinal muscular atrophy with lower extremity predominant 2B. [provided by Alliance of Genome Resources, Mar 2025] |
SCHLAP1 GeneSWI/SNF complex antagonist associated with prostate cancer 1 (non-protein coding) |
LY6G6D Genelymphocyte antigen 6 complex, locus G6D LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009] |
ANAPC1 Geneanaphase promoting complex subunit 1 This gene encodes a subunit of the anaphase-promoting complex. This complex is an E3 ubiquitin ligase that regulates progression through the metaphase to anaphase portion of the cell cycle by ubiquitinating proteins which targets them for degradation. [provided by RefSeq, Dec 2011] |
ANAPC2 Geneanaphase promoting complex subunit 2 A large protein complex, termed the anaphase-promoting complex (APC), or the cyclosome, promotes metaphase-anaphase transition by ubiquitinating its specific substrates such as mitotic cyclins and anaphase inhibitor, which are subsequently degraded by the 26S proteasome. Biochemical studies have shown that the vertebrate APC contains eight subunits. The composition of the APC is highly conserved in organisms from yeast to humans. The product of this gene is a component of the complex and shares sequence similarity with a recently identified family of proteins called cullins, which may also be involved in ubiquitin-mediated degradation. [provided by RefSeq, Jul 2008] |
ANAPC5 Geneanaphase promoting complex subunit 5 This gene encodes a tetratricopeptide repeat-containing component of the anaphase promoting complex/cyclosome (APC/C), a large E3 ubiquitin ligase that controls cell cycle progression by targeting a number of cell cycle regulators such as B-type cyclins for 26S proteasome-mediated degradation through ubiquitination. The encoded protein is required for the proper ubiquitination function of APC/C and for the interaction of APC/C with transcription coactivators. It also interacts with polyA binding protein and represses internal ribosome entry site-mediated translation. Multiple transcript variants encoding different isoforms have been found for this gene. These differences cause translation initiation at a downstream AUG and result in a shorter protein (isoform b), compared to isoform a. [provided by RefSeq, Nov 2008] |
ANAPC4 Geneanaphase promoting complex subunit 4 A large protein complex, termed the anaphase-promoting complex (APC), or the cyclosome, promotes metaphase-anaphase transition by ubiquitinating its specific substrates such as mitotic cyclins and anaphase inhibitor, which are subsequently degraded by the 26S proteasome. Biochemical studies have shown that the vertebrate APC contains eight subunits. The composition of the APC is highly conserved in organisms from yeast to humans. The exact function of this gene product is not known. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
ANAPC7 Geneanaphase promoting complex subunit 7 This gene encodes a tetratricopeptide repeat containing component of the anaphase promoting complex/cyclosome (APC/C), a large E3 ubiquitin ligase that controls cell cycle progression by targeting a number of cell cycle regulators such as B-type cyclins for 26S proteasome-mediated degradation through ubiquitination. The encoded protein is required for proper protein ubiquitination function of APC/C and for the interaction of APC/C with certain transcription coactivators. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008] |
BLOC1S6 Genebiogenesis of lysosomal organelles complex-1, subunit 6, pallidin The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome. [provided by RefSeq, Aug 2015] |
BLOC1S1 Genebiogenesis of lysosomal organelles complex-1, subunit 1 BLOC1S1 is a component of the ubiquitously expressed BLOC1 multisubunit protein complex. BLOC1 is required for normal biogenesis of specialized organelles of the endosomal-lysosomal system, such as melanosomes and platelet dense granules (Starcevic and Dell'Angelica, 2004 [PubMed 15102850]).[supplied by OMIM, Mar 2008] |
ANAPC1P1 Geneanaphase promoting complex subunit 1 pseudogene 1 |
AP1S1 Geneadaptor-related protein complex 1, sigma 1 subunit The protein encoded by this gene is part of the clathrin coat assembly complex which links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. This protein, as well as beta-prime-adaptin, gamma-adaptin, and the medium (mu) chain AP47, form the AP-1 assembly protein complex located at the Golgi vesicle. [provided by RefSeq, Jul 2008] |
ATP5L2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit G2 Predicted to enable proton transmembrane transporter activity. Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven ATP synthesis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
NACA Genenascent polypeptide-associated complex alpha subunit This gene encodes a protein that associates with basic transcription factor 3 (BTF3) to form the nascent polypeptide-associated complex (NAC). This complex binds to nascent proteins that lack a signal peptide motif as they emerge from the ribosome, blocking interaction with the signal recognition particle (SRP) and preventing mistranslocation to the endoplasmic reticulum. This protein is an IgE autoantigen in atopic dermatitis patients. Alternative splicing results in multiple transcript variants, but the full length nature of some of these variants, including those encoding very large proteins, has not been determined. There are multiple pseudogenes of this gene on different chromosomes. [provided by RefSeq, Feb 2016] |
HCG18 GeneHLA complex group 18 (non-protein coding) |
INTS12 Geneintegrator complex subunit 12 INTS12 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008] |
INTS10 Geneintegrator complex subunit 10 INTS10 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008] |
HCG4P11 GeneHLA complex group 4 pseudogene 11 |
LOC100127892 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene |
AP5B1 Geneadaptor-related protein complex 5, beta 1 subunit Involved in endosomal transport. Located in lysosomal membrane. Part of AP-type membrane coat adaptor complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-DOA Genemajor histocompatibility complex, class II, DO alpha HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008] |
HLA-DOB Genemajor histocompatibility complex, class II, DO beta HLA-DOB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DOA) and a beta chain (DOB), both anchored in the membrane. It is located in intracellular vesicles. DO suppresses peptide loading of MHC class II molecules by inhibiting HLA-DM. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008] |
HLA-DQA1 Genemajor histocompatibility complex, class II, DQ alpha 1 HLA-DQA1 belongs to the HLA class II alpha chain paralogues. The class II molecule is a heterodimer consisting of an alpha (DQA) and a beta chain (DQB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B Lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa. It is encoded by 5 exons; exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DQ molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to four different molecules. Typing for these polymorphisms is routinely done for bone marrow transplantation. [provided by RefSeq, Jul 2008] |
HLA-DQA2 Genemajor histocompatibility complex, class II, DQ alpha 2 This gene belongs to the HLA class II alpha chain family. The encoded protein forms a heterodimer with a class II beta chain. It is located in intracellular vesicles and plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (B lymphocytes, dendritic cells, macrophages) and are used to present antigenic peptides on the cell surface to be recognized by CD4 T-cells. [provided by RefSeq, Jun 2010] |
PDHX Genepyruvate dehydrogenase complex, component X The pyruvate dehydrogenase (PDH) complex is located in the mitochondrial matrix and catalyzes the conversion of pyruvate to acetyl coenzyme A. The PDH complex thereby links glycolysis to Krebs cycle. The PDH complex contains three catalytic subunits, E1, E2, and E3, two regulatory subunits, E1 kinase and E1 phosphatase, and a non-catalytic subunit, E3 binding protein (E3BP). This gene encodes the E3 binding protein subunit; also known as component X of the pyruvate dehydrogenase complex. This protein tethers E3 dimers to the E2 core of the PDH complex. Defects in this gene are a cause of pyruvate dehydrogenase deficiency which results in neurological dysfunction and lactic acidosis in infancy and early childhood. This protein is also a minor antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC eventually leads to cirrhosis and liver failure. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009] |
AP5Z1 Geneadaptor-related protein complex 5, zeta 1 subunit This gene was identified by genome-wide screen for genes involved in homologous recombination DNA double-strand break repair (HR-DSBR). The encoded protein was found in a complex with other proteins that have a role in HR-DSBR. Knockdown of this gene reduced homologous recombination, and mutations in this gene were found in patients with spastic paraplegia. It was concluded that this gene likely encodes a helicase (PMID:20613862). [provided by RefSeq, Jan 2011] |
TRAPPC9 Genetrafficking protein particle complex 9 This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive cognitive disability. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010] |
TRAPPC8 Genetrafficking protein particle complex 8 Involved in Golgi organization and collagen biosynthetic process. Part of TRAPP complex. [provided by Alliance of Genome Resources, Mar 2025] |
TRAPPC1 Genetrafficking protein particle complex 1 This gene product plays a role in vesicular transport of proteins to the Golgi apparatus from the endoplasmic reticulum. The encoded protein is a component of the multisubunit transport protein particle (TRAPP) complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009] |
TRAPPC3 Genetrafficking protein particle complex 3 This gene encodes a component of the trafficking protein particle complex, which tethers transport vesicles to the cis-Golgi membrane. The encoded protein participates in the regulation of transport from the endoplasmic reticulum to the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012] |
TRAPPC2 Genetrafficking protein particle complex 2 The protein encoded by this gene is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010] |
TRAPPC5 Genetrafficking protein particle complex 5 Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport. Part of TRAPP complex. [provided by Alliance of Genome Resources, Mar 2025] |
TRAPPC4 Genetrafficking protein particle complex 4 Involved in autophagy and endoplasmic reticulum to Golgi vesicle-mediated transport. Part of TRAPP complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421096 Genenon-SMC condensin I complex, subunit G pseudogene |
NCAPH2 Genenon-SMC condensin II complex, subunit H2 This gene encodes one of the non-SMC subunits of the condensin II complex. This complex plays an essential role in mitotic chromosome assembly. Alternate splicing of this gene results in multiple transcript variants.[provided by RefSeq, May 2010] |
RICTOR GeneRPTOR independent companion of MTOR, complex 2 RICTOR and MTOR (FRAP1; MIM 601231) are components of a protein complex that integrates nutrient- and growth factor-derived signals to regulate cell growth (Sarbassov et al., 2004 [PubMed 15268862]).[supplied by OMIM, Mar 2008] |
LOC646709 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 1 pseudogene |
BRK1P2 GeneBRICK1, SCAR/WAVE actin-nucleating complex subunit pseudogene 2 |
MED13P1 Genemediator complex subunit 13 pseudogene 1 |
INTS4P1 Geneintegrator complex subunit 4 pseudogene 1 |
INTS4P2 Geneintegrator complex subunit 4 pseudogene 2 |
TRAPPC2P5 Genetrafficking protein particle complex 2 pseudogene 5 |
TRAPPC2P4 Genetrafficking protein particle complex 2 pseudogene 4 |
TRAPPC2P7 Genetrafficking protein particle complex 2 pseudogene 7 |
TRAPPC2P6 Genetrafficking protein particle complex 2 pseudogene 6 |
TRAPPC2P3 Genetrafficking protein particle complex 2 pseudogene 3 |
TRAPPC2P2 Genetrafficking protein particle complex 2 pseudogene 2 |
TRAPPC2P9 Genetrafficking protein particle complex 2 pseudogene 9 |
TRAPPC2P8 Genetrafficking protein particle complex 2 pseudogene 8 |
SKA2P1 Genespindle and kinetochore associated complex subunit 2 pseudogene 1 |
AP2B1 Geneadaptor-related protein complex 2, beta 1 subunit The protein encoded by this gene is one of two large chain components of the assembly protein complex 2, which serves to link clathrin to receptors in coated vesicles. The encoded protein is found on the cytoplasmic face of coated vesicles in the plasma membrane. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
MED15P7 Genemediator complex subunit 15 pseudogene 7 |
MED15P6 Genemediator complex subunit 15 pseudogene 6 |
MED15P5 Genemediator complex subunit 15 pseudogene 5 |
MED15P4 Genemediator complex subunit 15 pseudogene 4 |
MED15P1 Genemediator complex subunit 15 pseudogene 1 |
MED15P9 Genemediator complex subunit 15 pseudogene 9 |
INO80 GeneINO80 complex subunit This gene encodes a subunit of the chromatin remodeling complex, which is classified into subfamilies depending on sequence features apart from the conserved ATPase domain. This protein is the catalytic ATPase subunit of the INO80 chromatin remodeling complex, which is characterized by a DNA-binding domain. This protein is proposed to bind DNA and be recruited by the YY1 transcription factor to activate certain genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
KANSL1L GeneKAT8 regulatory NSL complex subunit 1-like Predicted to enable histone acetyltransferase binding activity. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be part of NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
CTC1 GeneCTS telomere maintenance complex component 1 This gene encodes a component of the CST complex. This complex plays an essential role in protecting telomeres from degradation. This protein also forms a heterodimer with the CST complex subunit STN1 to form the enzyme alpha accessory factor. This enzyme regulates DNA replication. Mutations in this gene are the cause of cerebroretinal microangiopathy with calcifications and cysts. Alternate splicing results in both coding and non-coding variants. [provided by RefSeq, Mar 2012] |
TCP10L Genet-complex 10-like Enables DNA-binding transcription factor binding activity; identical protein binding activity; and transcription corepressor activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289091 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit G2 pseudogene |
HCG4 GeneHLA complex group 4 (non-protein coding) |
HCG9 GeneHLA complex group 9 (non-protein coding) This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009] |
ATP5BP1 GeneATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide pseudogene 1 |
SNAPC3 Genesmall nuclear RNA activating complex, polypeptide 3, 50kDa Predicted to enable RNA polymerase III type 3 promoter sequence-specific DNA binding activity and bent DNA binding activity. Predicted to contribute to RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and core promoter sequence-specific DNA binding activity. Predicted to be involved in snRNA transcription by RNA polymerase II and snRNA transcription by RNA polymerase III. Located in nuclear body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAPC2 Genesmall nuclear RNA activating complex, polypeptide 2, 45kDa This gene encodes a subunit of the snRNA-activating protein complex which is associated with the TATA box-binding protein. The encoded protein is necessary for RNA polymerase II and III dependent small-nuclear RNA gene transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009] |
SNAPC1 Genesmall nuclear RNA activating complex, polypeptide 1, 43kDa Predicted to enable sequence-specific DNA binding activity. Predicted to be involved in snRNA transcription by RNA polymerase II and snRNA transcription by RNA polymerase III. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SNAPC5 Genesmall nuclear RNA activating complex, polypeptide 5, 19kDa This gene encodes a subunit of the small nuclear RNA (snRNA)-activating protein complex that plays a role in the transcription of snRNA genes. This complex binds to the promoters of snRNA genes transcribed by either RNA polymerase II or III and recruits other regulatory factors to activate snRNA gene transcription. The encoded protein may play a role in stabilizing this complex. A pseudogene of this gene has been identified on chromosome 6. [provided by RefSeq, Jul 2016] |
SNAPC4 Genesmall nuclear RNA activating complex, polypeptide 4, 190kDa This gene encodes the largest subunit of the small nuclear RNA-activating protein (SNAP) complex. The encoded protein contains a Myb DNA-binding domain, and is essential for RNA polymerase II and III polymerase transcription from small nuclear RNA promoters. A mutation in this gene is associated with ankylosing spondylitis. [provided by RefSeq, Jul 2016] |
LOC100192388 Geneanaphase promoting complex subunit 13 pseudogene |
LOC100192389 Geneanaphase promoting complex subunit 13 pseudogene |
CHRAC1 Genechromatin accessibility complex 1 CHRAC1 is a histone-fold protein that interacts with other histone-fold proteins to bind DNA in a sequence-independent manner. These histone-fold protein dimers combine within larger enzymatic complexes for DNA transcription, replication, and packaging.[supplied by OMIM, Apr 2004] |
CNOT4 GeneCCR4-NOT transcription complex, subunit 4 The protein encoded by this gene is a subunit of the CCR4-NOT complex, a global transcriptional regulator. The encoded protein interacts with CNOT1 and has E3 ubiquitin ligase activity. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010] |
LOC100418484 GeneKAT8 regulatory NSL complex subunit 1 pseudogene |
LOC390846 Genegolgi SNAP receptor complex member 2 pseudogene |
TCP11X1 Genet-complex 11 family, X-linked 1 Predicted to be involved in protein kinase A signaling and regulation of sperm capacitation. Predicted to be active in acrosomal vesicle and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
TCP11X2 Genet-complex 11 family, X-linked 2 Predicted to be involved in protein kinase A signaling and regulation of sperm capacitation. Predicted to be active in acrosomal vesicle and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
ARPC5L Geneactin related protein 2/3 complex, subunit 5-like Predicted to enable actin filament binding activity. Predicted to be involved in Arp2/3 complex-mediated actin nucleation and cell migration. Located in extracellular exosome and focal adhesion. [provided by Alliance of Genome Resources, Mar 2025] |
HCG25 GeneHLA complex group 25 (non-protein coding) |
HCG27 GeneHLA complex group 27 (non-protein coding) |
MCM8 Geneminichromosome maintenance complex component 8 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the mini-chromosome maintenance proteins is a key component of the pre-replication complex and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein contains the central domain that is conserved among the mini-chromosome maintenance proteins. The encoded protein may interact with other mini-chromosome maintenance proteins and play a role in DNA replication. This gene may be associated with length of reproductive lifespan and menopause. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013] |
LOC646112 Geneorigin recognition complex, subunit 3-like (yeast) pseudogene |
TPGS2 Genetubulin polyglutamylase complex subunit 2 This gene encodes a protein that is a component of the neuronal polyglutamylase complex, which plays a role in post-translational addition of glutamate residues to C-terminal tubulin tails. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2012] |
TPGS1 Genetubulin polyglutamylase complex subunit 1 Predicted to enable microtubule binding activity and tubulin-glutamic acid ligase activity. Predicted to be involved in sperm axoneme assembly. Predicted to act upstream of or within several processes, including adult behavior; chemical synaptic transmission; and protein polyglutamylation. Located in centrosome. [provided by Alliance of Genome Resources, Mar 2025] |
LOC653653 Geneadaptor-related protein complex 1, sigma 2 subunit pseudogene |
CNOT7P2 GeneCCR4-NOT transcription complex, subunit 7 pseudogene 2 |
CNOT7P1 GeneCCR4-NOT transcription complex, subunit 7 pseudogene 1 |
ATP5J2LP GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2-like pseudogene |
DGCR8 GeneDGCR8 microprocessor complex subunit This gene encodes a subunit of the microprocessor complex which mediates the biogenesis of microRNAs from the primary microRNA transcript. The encoded protein is a double-stranded RNA binding protein that functions as the non-catalytic subunit of the microprocessor complex. This protein is required for binding the double-stranded RNA substrate and facilitates cleavage of the RNA by the ribonuclease III protein, Drosha. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010] |
IKBKAP Geneinhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein The protein encoded by this gene is a scaffold protein and a regulator for three different kinases involved in proinflammatory signaling. The encoded protein can bind NF-kappa-B-inducing kinase and I-kappa-B kinases through separate domains and assemble them into an active kinase complex. Mutations in this gene have been associated with familial dysautonomia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
CACTIN Genecactin, spliceosome C complex subunit Enables RNA binding activity. Involved in several processes, including cellular response to cytokine stimulus; negative regulation of cytokine production; and negative regulation of signal transduction. Located in cytosol and nuclear speck. Part of catalytic step 2 spliceosome. [provided by Alliance of Genome Resources, Mar 2025] |
GCOM2 GeneGRINL1B complex locus 2, pseudogene |
GCOM1 GeneGRINL1A complex locus 1 This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013] |
LOC100288416 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene |
LOC643454 Geneadaptor-related protein complex 3, sigma 1 subunit pseudogene |
AP3M1 Geneadaptor-related protein complex 3, mu 1 subunit The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane, and it may directly function in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
AP3M2 Geneadaptor-related protein complex 3, mu 2 subunit This gene encodes a subunit of the heterotetrameric adaptor-related protein comlex 3 (AP-3), which belongs to the adaptor complexes medium subunits family. The AP-3 complex plays a role in protein trafficking to lysosomes and specialized organelles. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Aug 2008] |
HCG21 GeneHLA complex group 21 (non-protein coding) |
HCG20 GeneHLA complex group 20 (non-protein coding) |
HCG23 GeneHLA complex group 23 (non-protein coding) |
HCG22 GeneHLA complex group 22 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289381 Geneadaptor-related protein complex 3, sigma 1 subunit pseudogene |
DSN1 GeneDSN1, MIS12 kinetochore complex component This gene encodes a kinetochore protein that functions as part of the minichromosome instability-12 centromere complex. The encoded protein is required for proper kinetochore assembly and progression through the cell cycle. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009] |
BRCC3P1 GeneBRCA1/BRCA2-containing complex, subunit 3 pseudogene 1 |
NPIPP1 Genenuclear pore complex interacting protein pseudogene 1 |
LOC102724200 Genetrafficking protein particle complex subunit 10-like |
ICE2P2 Geneinteractor of little elongation complex ELL subunit 2 pseudogene 2 |
ICE2P1 Geneinteractor of little elongation complex ELL subunit 2 pseudogene 1 |
NPIP Genenuclear pore complex interacting protein family, member A1 pseudogene |
TRAPPC11 Genetrafficking protein particle complex 11 The protein encoded by this gene is a subunit of the TRAPP (transport protein particle) tethering complex, which functions in intracellular vesicle trafficking. This subunit is involved in early stage endoplasmic reticulum-to-Golgi vesicle transport. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2013] |
TRAPPC10 Genetrafficking protein particle complex 10 The protein encoded by this gene is a transmembrane protein found in the cis-Golgi complex. The encoded protein is part of the multisubunit transport protein particle (TRAPP) complex and may be involved in vesicular transport from the endoplasmic reticulum to the Golgi. Mutations in this gene could be responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy, or for autoimmune polyglandular disease type 1. [provided by RefSeq, Jul 2008] |
TRAPPC13 Genetrafficking protein particle complex 13 Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport; vesicle coating; and vesicle tethering. Predicted to be located in cytosol. Predicted to be part of TRAPPIII protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
TRAPPC12 Genetrafficking protein particle complex 12 Involved in several processes, including endoplasmic reticulum to Golgi vesicle-mediated transport; positive regulation of protein localization to kinetochore; and regulation of kinetochore assembly. Located in several cellular components, including endoplasmic reticulum-Golgi intermediate compartment; kinetochore; and perinuclear region of cytoplasm. Part of TRAPP complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC260421 Geneactin related protein 2/3 complex subunit 1A pseudogene |
LOC260422 Geneactin related protein 2/3 complex subunit 1A pseudogene |
AP4B1 Geneadaptor-related protein complex 4, beta 1 subunit This gene encodes a subunit of a heterotetrameric adapter-like complex 4 that is involved in targeting proteins from the trans-Golgi network to the endosomal-lysosomal system. Mutations in this gene are associated with cerebral palsy spastic quadriplegic type 5 (CPSQ5) disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] |
STT3B GeneSTT3B, subunit of the oligosaccharyltransferase complex (catalytic) The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014] |
STT3A GeneSTT3A, subunit of the oligosaccharyltransferase complex (catalytic) The protein encoded by this gene is a catalytic subunit of the N-oligosaccharyltransferase (OST) complex, which functions in the endoplasmic reticulum to transfer glycan chains to asparagine residues of target proteins. A separate complex containing a similar catalytic subunit with an overlapping function also exists. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015] |
NSL1 GeneNSL1, MIS12 kinetochore complex component This gene encodes a protein with two coiled-coil domains that localizes to kinetochores, which are chromosome-associated structures that attach to microtubules and mediate chromosome movements during cell division. The encoded protein is part of a conserved protein complex that includes two chromodomain-containing proteins and a component of the outer plate of the kinetochore. This protein complex is proposed to bridge centromeric heterochromatin with the outer kinetochore structure. Multiple transcript variants encoding different isoforms have been found for this gene. There is a pseudogene of the 3' UTR region of this gene on chromosome X. [provided by RefSeq, Jul 2014] |
SWAP70 GeneSWAP switching B-cell complex 70kDa subunit Enables cadherin binding activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to act upstream of or within isotype switching. Located in actin cytoskeleton; cytoplasm; and plasma membrane. Is active in postsynapse. [provided by Alliance of Genome Resources, Mar 2025] |
LEO1 GeneLeo1, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) LEO1, parafibromin (CDC73; MIM 607393), CTR9 (MIM 609366), and PAF1 (MIM 610506) form the PAF protein complex that associates with the RNA polymerase II subunit POLR2A (MIM 180660) and with a histone methyltransferase complex (Rozenblatt-Rosen et al., 2005 [PubMed 15632063]).[supplied by OMIM, Mar 2008] |
MR1 Genemajor histocompatibility complex, class I-related MAIT (mucosal-associated invariant T-cells) lymphocytes represent a small population of T-cells primarily found in the gut. The protein encoded by this gene is an antigen-presenting molecule that presents metabolites of microbial vitamin B to MAITs. This presentation may activate the MAITs to regulate the amounts of specific types of bacteria in the gut. Several transcript variants encoding different isoforms have been found for this gene, and a pseudogene of it has been detected about 36 kbp upstream on the same chromosome. [provided by RefSeq, Jul 2015] |
MECOM GeneMDS1 and EVI1 complex locus The protein encoded by this gene is a transcriptional regulator and oncoprotein that may be involved in hematopoiesis, apoptosis, development, and cell differentiation and proliferation. The encoded protein can interact with CTBP1, SMAD3, CREBBP, KAT2B, MAPK8, and MAPK9. This gene can undergo translocation with the AML1 gene, resulting in overexpression of this gene and the onset of leukemia. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Mar 2011] |
AP2A1 Geneadaptor-related protein complex 2, alpha 1 subunit This gene encodes the alpha 1 adaptin subunit of the adaptor protein 2 (AP-2) complex found in clathrin coated vesicles. The AP-2 complex is a heterotetramer consisting of two large adaptins (alpha or beta), a medium adaptin (mu), and a small adaptin (sigma). The complex is part of the protein coat on the cytoplasmic face of coated vesicles which links clathrin to receptors in vesicles. Alternative splicing of this gene results in two transcript variants encoding two different isoforms. A third transcript variant has been described, but its full length nature has not been determined. [provided by RefSeq, Jul 2008] |
AP2A2 Geneadaptor-related protein complex 2, alpha 2 subunit The protein encoded by this gene is a subunit of the AP-2 adaptor protein complex, which is involved in linking lipid and protein membrane components with the clathrin lattice. This interaction supports the formation of clathrin-coated vesicles, and the encoded subunit aids in the process by binding polyphosphoinositide-containing lipids in the cell membrane. [provided by RefSeq, Nov 2016] |
ATP5JP1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6 pseudogene 1 |
ATP5A1 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, using an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the alpha subunit of the catalytic core. Alternatively spliced transcript variants encoding the different isoforms have been identified. Pseudogenes of this gene are located on chromosomes 9, 2, and 16. [provided by RefSeq, Mar 2012] |
SNAPC5P1 Genesmall nuclear RNA activating complex, polypeptide 5, 19kDa pseudogene 1 |
NACA2 Genenascent polypeptide-associated complex alpha subunit 2 Predicted to enable unfolded protein binding activity. Predicted to be involved in protein targeting to membrane. Predicted to be located in nucleus. Predicted to be part of nascent polypeptide-associated complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130035 Genebiogenesis of lysosome-related organelles complex 1 subunit 6-like |
LOC644310 Geneubiquinol-cytochrome c reductase, complex III subunit X pseudogene |
HCG9P5 GeneHLA complex group 9 pseudogene 5 |
HCG9P3 GeneHLA complex group 9 pseudogene 3 |
HCG9P2 GeneHLA complex group 9 pseudogene 2 |
LOC100131348 Geneadaptor-related protein complex 2, beta 1 subunit pseudogene |
NCAPG2 Genenon-SMC condensin II complex, subunit G2 This gene encodes a protein that belongs to the Condensin2nSMC family of proteins. The encoded protein is a regulatory subunit of the condensin II complex which, along with the condensin I complex, plays a role in chromosome assembly and segregation during mitosis. A similar protein in mouse is required for early development of the embryo. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
LOC100422044 Geneactin related protein 2/3 complex, subunit 1A, 41kDa pseudogene |
NPIPB15 Genenuclear pore complex interacting protein family, member B15 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
ATP5J2P6 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 6 |
ATP5J2P4 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 4 |
ATP5J2P5 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 5 |
ATP5J2P2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 2 |
ATP5J2P3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 3 |
LOC391247 GeneGINS complex subunit 2 (Psf2 homolog) pseudogene |
ATP5S GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit s (factor B) This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. This gene encodes the subunit s, also known as factor B, of the proton channel. This subunit is necessary for the energy transduction activity of the ATP synthase complexes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
ATP5J GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6 Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo complex has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the F6 subunit of the Fo complex. The F6 subunit is required for F1 and Fo interactions. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has 1 or more pseudogenes. [provided by RefSeq, Feb 2016] |
ATP5I GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit E Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the e subunit of the Fo complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010] |
ATP5H GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit d Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq, Jun 2010] |
ATP5O GeneATP synthase, H+ transporting, mitochondrial F1 complex, O subunit The protein encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane proton channel. The encoded protein appears to be part of the connector linking these two components and may be involved in transmission of conformational changes or proton conductance. [provided by RefSeq, Jul 2008] |
ATP5B GeneATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the beta subunit of the catalytic core. [provided by RefSeq, Jul 2008] |
ATP5E GeneATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the epsilon subunit of the catalytic core. Two pseudogenes of this gene are located on chromosomes 4 and 13. Read-through transcripts that include exons from this gene are expressed from the upstream gene SLMO2.[provided by RefSeq, Mar 2011] |
ATP5D GeneATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the delta subunit of the catalytic core. Alternatively spliced transcript variants encoding the same isoform have been identified. [provided by RefSeq, Jul 2008] |
LOC105379604 Geneset1/Ash2 histone methyltransferase complex subunit ASH2 pseudogene |
LOC100132849 GeneATP synthase, H+ transporting, mitochondrial F1 complex, O subunit pseudogene |
HAUS8P1 GeneHAUS augmin-like complex, subunit 8 pseudogene 1 |
BABAM1 GeneBRISC and BRCA1 A complex member 1 Enables identical protein binding activity. Involved in several processes, including DNA repair-dependent chromatin remodeling; mitotic G2 DNA damage checkpoint signaling; and positive regulation of DNA repair. Located in cytosol and nuclear body. Part of BRCA1-A complex and BRISC complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC727681 GeneNSL1, MIND kinetochore complex component, homolog (S. cerevisiae) pseudogene |
LOC100421148 Genenon-SMC condensin I complex, subunit G pseudogene |
3.8-1.4 GeneHLA complex group 26 (non-protein coding) pseudogene |
3.8-1.5 GeneHLA complex group 26 (non-protein coding) pseudogene |
3.8-1.2 GeneHLA complex group 26 (non-protein coding) pseudogene |
ATP5C1P1 GeneATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 pseudogene 1 |
LOC727919 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 2 pseudogene |
LOC285074 Geneanaphase promoting complex subunit 1 pseudogene |
ARPC4 Geneactin related protein 2/3 complex, subunit 4, 20kDa This gene encodes one of seven subunits of the human Arp2/3 protein complex. This complex controls actin polymerization in cells and has been conserved throughout eukaryotic evolution. This gene encodes the p20 subunit, which is necessary for actin nucleation and high-affinity binding to F-actin. Alternative splicing results in multiple transcript variants. Naturally occurring read-through transcription exists between this gene and the downstream tubulin tyrosine ligase-like family, member 3 (TTLL3), which results in the production of a fusion protein. [provided by RefSeq, Nov 2010] |
LOC100507083 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene |
LOC440353 Genenuclear pore complex interacting protein family, member A1 pseudogene Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
NOC2L Genenucleolar complex associated 2 homolog (S. cerevisiae) Histone modification by histone acetyltransferases (HAT) and histone deacetylases (HDAC) can control major aspects of transcriptional regulation. NOC2L represents a novel HDAC-independent inhibitor of histone acetyltransferase (INHAT) (Hublitz et al., 2005 [PubMed 16322561]).[supplied by OMIM, Mar 2008] |
EZH2P1 Geneenhancer of zeste 2 polycomb repressive complex 2 subunit pseudogene 1 |
ARPC3P4 Geneactin related protein 2/3 complex, subunit 3 pseudogene 4 |
HLA-H Genemajor histocompatibility complex, class I, H (pseudogene) This major histocompatibility complex gene represents a transcribed pseudogene, possibly derived from HLA-A. This gene displays extensive variation. [provided by RefSeq, May 2010] |
HLA-N Genemajor histocompatibility complex, class I, N (pseudogene) |
HLA-C Genemajor histocompatibility complex, class I, C HLA-C belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. About 6000 HLA-C alleles have been described. The HLA system plays an important role in the occurrence and outcome of infectious diseases, including those caused by the malaria parasite, the human immunodeficiency virus (HIV), and the severe acute respiratory syndrome coronavirus (SARS-CoV). The structural spike and the nucleocapsid proteins of the novel coronavirus SARS-CoV-2, which causes coronavirus disease 2019 (COVID-19), are reported to contain multiple Class I epitopes with predicted HLA restrictions. Individual HLA genetic variation may help explain different immune responses to a virus across a population.[provided by RefSeq, Aug 2020] |
HLA-E Genemajor histocompatibility complex, class I, E HLA-E belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-E binds a restricted subset of peptides derived from the leader peptides of other class I molecules. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. [provided by RefSeq, Jul 2008] |
HLA-Z Genemajor histocompatibility complex, class I, Z (pseudogene) |
HLA-Y Genemajor histocompatibility complex, class I, Y (pseudogene) |
HLA-X Genemajor histocompatibility complex, class I, X (pseudogene) |
HLA-S Genemajor histocompatibility complex, class I, S (pseudogene) |
HLA-P Genemajor histocompatibility complex, class I, P (pseudogene) |
HLA-W Genemajor histocompatibility complex, class I, W (pseudogene) |
HLA-V Genemajor histocompatibility complex, class I, V (pseudogene) |
HLA-U Genemajor histocompatibility complex, class I, U (pseudogene) |
HLA-T Genemajor histocompatibility complex, class I, T (pseudogene) |
XKRYP6 GeneXK, Kell blood group complex subunit-related, Y-linked pseudogene 6 |
XKRYP4 GeneXK, Kell blood group complex subunit-related, Y-linked pseudogene 4 |
XKRYP5 GeneXK, Kell blood group complex subunit-related, Y-linked pseudogene 5 |
XKRYP2 GeneXK, Kell blood group complex subunit-related, Y-linked pseudogene 2 |
XKRYP3 GeneXK, Kell blood group complex subunit-related, Y-linked pseudogene 3 |
XKRYP1 GeneXK, Kell blood group complex subunit-related, Y-linked pseudogene 1 |
LOC102723574 GeneHAUS augmin-like complex subunit 6 pseudogene |
LOC101060346 GeneT-complex protein 11 X-linked protein 2-like |
AP1S2 Geneadaptor-related protein complex 1, sigma 2 subunit Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as the small subunit of this complex and is a member of the adaptin protein family. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013] |
AP1S3 Geneadaptor-related protein complex 1, sigma 3 subunit This gene encodes a member of the adaptor-related protein complex 1, sigma subunit genes. The encoded protein is a component of adaptor protein complex 1 (AP-1), one of the AP complexes involved in claathrin-mediated vesicular transport from the Golgi or endosomes. Disruption of the pathway for display of HIV-1 antigens, which prevents recognition of the virus by cytotoxic T cells, has been shown to involve the AP-1 complex (PMID: 15569716). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ATP5J2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The catalytic portion of mitochondrial ATP synthase consists of five different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the f subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has multiple pseudogenes. Naturally occurring read-through transcription also exists between this gene and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene. [provided by RefSeq, Nov 2010] |
LOC100420889 Geneanaphase promoting complex subunit 1 pseudogene |
TRAPPC2L Genetrafficking protein particle complex 2-like This gene encodes a protein that interacts with the tethering factor trafficking protein particle (TRAPP complex). TRAPP complexes mediate the contact between vescicles and target membranes, and thus, are involved in vescicle-mediated transport of proteins and lipids. The encoded protein is related to the X-linked trafficking protein particle complex 2. A related pseudogene is located on the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
TRAPPC2B Genetrafficking protein particle complex 2B Enables transcription corepressor binding activity; transcription regulator inhibitor activity; and transmembrane transporter binding activity. Involved in positive regulation of gene expression and skeletal system development. Located in endoplasmic reticulum; nucleus; and perinuclear region of cytoplasm. Part of TRAPP complex. [provided by Alliance of Genome Resources, Mar 2025] |
AP4E1 Geneadaptor-related protein complex 4, epsilon 1 subunit This gene encodes a member of the adaptor complexes large subunit protein family. These proteins are components of the heterotetrameric adaptor protein complexes, which play important roles in the secretory and endocytic pathways by mediating vesicle formation and sorting of integral membrane proteins. The encoded protein is a large subunit of adaptor protein complex-4, which is associated with both clathrin- and nonclathrin-coated vesicles. Disruption of this gene may be associated with cerebral palsy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
NUF2 GeneNUF2, NDC80 kinetochore complex component This gene encodes a protein that is highly similar to yeast Nuf2, a component of a conserved protein complex associated with the centromere. Yeast Nuf2 disappears from the centromere during meiotic prophase when centromeres lose their connection to the spindle pole body, and plays a regulatory role in chromosome segregation. The encoded protein is found to be associated with centromeres of mitotic HeLa cells, which suggests that this protein is a functional homolog of yeast Nuf2. Alternatively spliced transcript variants that encode the same protein have been described. [provided by RefSeq, Jul 2008] |
MED30 Genemediator complex subunit 30 The multiprotein TRAP/Mediator complex facilitates gene expression through a wide variety of transcriptional activators. MED30 is a component of this complex that appears to be metazoan specific (Baek et al., 2002 [PubMed 11909976]).[supplied by OMIM, Nov 2010] |
MED31 Genemediator complex subunit 31 Predicted to enable transcription coregulator activity and ubiquitin protein ligase activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within limb development and negative regulation of fibroblast proliferation. Part of core mediator complex. [provided by Alliance of Genome Resources, Mar 2025] |
EXOC6B Geneexocyst complex component 6B This gene encodes a protein which is a part of the evolutionarily conserved exocyst, a multimeric protein complex necessary for exocytosis, which in turn, is crucial for cell growth, polarity and migration. Disruption of this gene may be associated with phenotypes exhibiting multiple symptoms including intellectual disability and developmental delay (DD). [provided by RefSeq, Jun 2016] |
MED23 Genemediator complex subunit 23 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein also acts as a metastasis suppressor. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2012] |
UQCR10 Geneubiquinol-cytochrome c reductase, complex III subunit X UCRC is a subunit of mitochondrial complex III (ubiquinol-cytochrome c reductase; EC 1.10.2.2), which forms the middle segment of the respiratory chain of the inner mitochondrial membrane (Schagger et al., 1995 [PubMed 8592474]).[supplied by OMIM, Mar 2008] |
UQCR11 Geneubiquinol-cytochrome c reductase, complex III subunit XI This gene encodes the smallest known component of the ubiquinol-cytochrome c reductase complex, which forms part of the mitochondrial respiratory chain. The encoded protein may function as a binding factor for the iron-sulfur protein in this complex. [provided by RefSeq, Oct 2009] |
MED14P1 Genemediator complex subunit 14 pseudogene 1 |
NCAPH Genenon-SMC condensin I complex, subunit H This gene encodes a member of the barr gene family and a regulatory subunit of the condensin complex. This complex is required for the conversion of interphase chromatin into condensed chromosomes. The protein encoded by this gene is associated with mitotic chromosomes, except during the early phase of chromosome condensation. During interphase, the protein has a distinct punctate nucleolar localization. Alternatively spliced transcript variants encoding different proteins have been described. [provided by RefSeq, Jul 2013] |
NCAPG Genenon-SMC condensin I complex, subunit G This gene encodes a subunit of the condensin complex, which is responsible for the condensation and stabilization of chromosomes during mitosis and meiosis. Phosphorylation of the encoded protein activates the condensin complex. There are pseudogenes for this gene on chromosomes 8 and 15. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012] |
NDUFAF5 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 5 The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes a mitochondrial protein that is associated with the matrix face of the mitochondrial inner membrane and is required for complex I assembly. A mutation in this gene results in mitochondrial complex I deficiency. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009] |
NDUFAF4 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 4 NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene are a cause of mitochondrial complex I deficiency. [provided by RefSeq, Oct 2009] |
NDUFAF7 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 7 This gene encodes an assembly factor protein which helps in the assembly and stabilization of Complex I, a large multi-subunit enzyme in the mitochondrial respiratory chain. Complex I is involved in several physiological activities in the cell, including metabolite transport and ATP synthesis. The encoded protein is a methyltransferase which methylates Arg85 of a subunit of Complex I in the early stages of its assembly. A pseudogene related to this gene is located on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
NDUFAF6 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 6 This gene encodes a protein that localizes to mitochondria and contains a predicted phytoene synthase domain. The encoded protein plays an important role in the assembly of complex I (NADH-ubiquinone oxidoreductase) of the mitochondrial respiratory chain through regulation of subunit ND1 biogenesis. Mutations in this gene are associated with complex I enzymatic deficiency. [provided by RefSeq, Nov 2011] |
NDUFAF1 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 1 This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Dec 2011] |
NDUFAF3 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 3 This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009] |
NDUFAF2 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 2 NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency. [provided by RefSeq, Jul 2008] |
HLA-DMA Genemajor histocompatibility complex, class II, DM alpha HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. [provided by RefSeq, Jul 2008] |
LY6G5C Genelymphocyte antigen 6 complex, locus G5C LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008] |
LY6G5B Genelymphocyte antigen 6 complex, locus G5B LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008] |
UQCRQ Geneubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa This gene encodes a ubiquinone-binding protein of low molecular mass. This protein is a small core-associated protein and a subunit of ubiquinol-cytochrome c reductase complex III, which is part of the mitochondrial respiratory chain. [provided by RefSeq, Jul 2008] |
LOC100288031 GeneBRICK1, SCAR/WAVE actin-nucleating complex subunit pseudogene |
AP4M1 Geneadaptor-related protein complex 4, mu 1 subunit This gene encodes a subunit of the heterotetrameric AP-4 complex. The encoded protein belongs to the adaptor complexes medium subunits family. This AP-4 complex is involved in the recognition and sorting of cargo proteins with tyrosine-based motifs from the trans-golgi network to the endosomal-lysosomal system. [provided by RefSeq, Jul 2008] |
SDHA Genesuccinate dehydrogenase complex, subunit A, flavoprotein (Fp) This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014] |
SDHC Genesuccinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa This gene encodes one of four nuclear-encoded subunits that comprise succinate dehydrogenase, also known as mitochondrial complex II, a key enzyme complex of the tricarboxylic acid cycle and aerobic respiratory chains of mitochondria. The encoded protein is one of two integral membrane proteins that anchor other subunits of the complex, which form the catalytic core, to the inner mitochondrial membrane. There are several related pseudogenes for this gene on different chromosomes. Mutations in this gene have been associated with paragangliomas. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2013] |
SDHB Genesuccinate dehydrogenase complex, subunit B, iron sulfur (Ip) This tumor suppressor gene encodes the iron-sulfur protein subunit of the succinate dehydrogenase (SDH) enzyme complex which plays a critical role in mitochondria. The SDH enzyme complex is composed of four nuclear-encoded subunits. This enzyme complex converts succinate to fumarate which releases electrons as part of the citric acid cycle, and the enzyme complex additionally provides an attachment site for released electrons to be transferred to the oxidative phosphorylation pathway. The SDH enzyme complex plays a role in oxygen-related gene regulation through its conversion of succinate, which is an oxygen sensor that stabilizes the hypoxia-inducible factor 1 (HIF1) transcription factor. Sporadic and familial mutations in this gene result in paragangliomas, pheochromocytoma, and gastrointestinal stromal tumors, supporting a link between mitochondrial dysfunction and tumorigenesis. Mutations in this gene are also implicated in nuclear type 4 mitochondrial complex II deficiency. [provided by RefSeq, Jun 2022] |
SDHD Genesuccinate dehydrogenase complex, subunit D, integral membrane protein This gene encodes a member of complex II of the respiratory chain, which is responsible for the oxidation of succinate. The encoded protein is one of two integral membrane proteins anchoring the complex to the matrix side of the mitochondrial inner membrane. Mutations in this gene are associated with the formation of tumors, including hereditary paraganglioma. Transmission of disease occurs almost exclusively through the paternal allele, suggesting that this locus may be maternally imprinted. There are pseudogenes for this gene on chromosomes 1, 2, 3, 7, and 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013] |
CNOT6LP1 GeneCCR4-NOT transcription complex, subunit 6-like pseudogene 1 |
MIS12 GeneMIS12 kinetochore complex component Involved in attachment of mitotic spindle microtubules to kinetochore and kinetochore assembly. Located in kinetochore and nucleus. Part of MIS12/MIND type complex. [provided by Alliance of Genome Resources, Mar 2025] |
MED12L Genemediator complex subunit 12-like The protein encoded by this gene is part of the Mediator complex, which is involved in transcriptional coactivation of nearly all RNA polymerase II-dependent genes. The Mediator complex links gene-specific transcriptional activators with the basal transcription machinery. [provided by RefSeq, May 2010] |
LIN54 Genelin-54 DREAM MuvB core complex component LIN54 is a component of the LIN, or DREAM, complex, an essential regulator of cell cycle genes (Schmit et al., 2009 [PubMed 19725879]).[supplied by OMIM, Dec 2010] |
LIN52 Genelin-52 DREAM MuvB core complex component Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleoplasm. Predicted to be part of DRM complex. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB5 Genenuclear pore complex interacting protein family, member B5 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC613037 Genenuclear pore complex interacting protein pseudogene Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ATP5EP1 GeneATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 1 |
ATP5EP2 GeneATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 2 Predicted to enable hydrolase activity. Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven mitochondrial ATP synthesis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
COPB1 Genecoatomer protein complex, subunit beta 1 This gene encodes a protein subunit of the coatomer complex associated with non-clathrin coated vesicles. The coatomer complex, also known as the coat protein complex 1, forms in the cytoplasm and is recruited to the Golgi by activated guanosine triphosphatases. Once at the Golgi membrane, the coatomer complex may assist in the movement of protein and lipid components back to the endoplasmic reticulum. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009] |
COPB2 Genecoatomer protein complex, subunit beta 2 (beta prime) The Golgi coatomer complex (see MIM 601924) constitutes the coat of nonclathrin-coated vesicles and is essential for Golgi budding and vesicular trafficking. It consists of 7 protein subunits, including COPB2.[supplied by OMIM, Jul 2002] |
LOC100288663 Geneactin related protein 2/3 complex, subunit 1A, 41kDa pseudogene |
NELFB Genenegative elongation factor complex member B NELFB is a subunit of negative elongation factor (NELF), which also includes NELFA (WHSC2; MIM 606026), either NELFC or NELFD (TH1L; MIM 605297), and NELFE (RDBP; MIM 154040). NELF acts with DRB sensitivity-inducing factor (DSIF), a heterodimer of SPT4 (SUPT4H1; MIM 603555) and SPT5 (SUPT5H; MIM 602102), to cause transcriptional pausing of RNA polymerase II (see MIM 180660) (Narita et al., 2003 [PubMed 12612062]).[supplied by OMIM, Mar 2008] |
NELFA Genenegative elongation factor complex member A This gene is expressed ubiquitously with higher levels in fetal than in adult tissues. It encodes a protein sharing 93% sequence identity with the mouse protein. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome. The encoded protein is found to be capable of reacting with HLA-A2-restricted and tumor-specific cytotoxic T lymphocytes, suggesting a target for use in specific immunotherapy for a large number of cancer patients. This protein has also been shown to be a member of the NELF (negative elongation factor) protein complex that participates in the regulation of RNA polymerase II transcription elongation. [provided by RefSeq, Jul 2008] |
NELFE Genenegative elongation factor complex member E The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008] |
ATP5G2P1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 1 |
ATP5G2P3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 3 |
ATP5G2P2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 2 |
ATP5G2P4 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 4 |
MED1 Genemediator complex subunit 1 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. It also regulates p53-dependent apoptosis and it is essential for adipogenesis. This protein is known to have the ability to self-oligomerize. [provided by RefSeq, Jul 2008] |
MED6 Genemediator complex subunit 6 Enables transcription coactivator activity and transcription coactivator binding activity. Acts upstream of or within positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of core mediator complex and mediator complex. [provided by Alliance of Genome Resources, Mar 2025] |
MED4 Genemediator complex subunit 4 This gene encodes a component of the Mediator complex. The Mediator complex interacts with DNA-binding gene-specific transcription factors to modulate transcription by RNA polymerase II. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
MED8 Genemediator complex subunit 8 This gene encodes a protein component of the mediator complex, which aids in transcriptional activation through interaction with RNA polymerase II and gene-specific transcription factors. The encoded protein may also function in ubiquitin ligation and protein degradation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013] |
MED9 Genemediator complex subunit 9 The multiprotein Mediator complex is a coactivator required for activation of RNA polymerase II transcription by DNA bound transcription factors. The protein encoded by this gene is thought to be a subunit of the Mediator complex. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
AP3S2 Geneadaptor-related protein complex 3, sigma 2 subunit Predicted to be involved in anterograde synaptic vesicle transport and vesicle-mediated transport. Located in intracellular membrane-bounded organelle. Part of AP-3 adaptor complex. [provided by Alliance of Genome Resources, Mar 2025] |
AP3S1 Geneadaptor-related protein complex 3, sigma 1 subunit This gene encodes a subunit of the AP3 adaptor complex. This complex functions in the formation of subcellular vesicles budded from the Golgi body. Several related pseudogenes of this gene have been found. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
LOC340569 Geneorigin recognition complex, subunit 1 pseudogene |
HCG4P1 GeneHLA complex group 4 pseudogene 1 |
HCG4P2 GeneHLA complex group 4 pseudogene 2 |
HCG4P3 GeneHLA complex group 4 pseudogene 3 |
HCG4P4 GeneHLA complex group 4 pseudogene 4 |
HCG4P5 GeneHLA complex group 4 pseudogene 5 |
HCG4P7 GeneHLA complex group 4 pseudogene 7 |
HCG4P8 GeneHLA complex group 4 pseudogene 8 |
HCG4P9 GeneHLA complex group 4 pseudogene 9 |
CD3D GeneCD3d molecule, delta (CD3-TCR complex) The protein encoded by this gene is part of the T-cell receptor/CD3 complex (TCR/CD3 complex) and is involved in T-cell development and signal transduction. The encoded membrane protein represents the delta subunit of the CD3 complex, and along with four other CD3 subunits, binds either TCR alpha/beta or TCR gamma/delta to form the TCR/CD3 complex on the surface of T-cells. Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK). Two transcript variants encoding different isoforms have been found for this gene. Other variants may also exist, but the full-length natures of their transcripts has yet to be defined. [provided by RefSeq, Feb 2009] |
CD3E GeneCD3e molecule, epsilon (CD3-TCR complex) The protein encoded by this gene is the CD3-epsilon polypeptide, which together with CD3-gamma, -delta and -zeta, and the T-cell receptor alpha/beta and gamma/delta heterodimers, forms the T-cell receptor-CD3 complex. This complex plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. The genes encoding the epsilon, gamma and delta polypeptides are located in the same cluster on chromosome 11. The epsilon polypeptide plays an essential role in T-cell development. Defects in this gene cause immunodeficiency. This gene has also been linked to a susceptibility to type I diabetes in women. [provided by RefSeq, Jul 2008] |
CD3G GeneCD3g molecule, gamma (CD3-TCR complex) The protein encoded by this gene is the CD3-gamma polypeptide, which together with CD3-epsilon, -delta and -zeta, and the T-cell receptor alpha/beta and gamma/delta heterodimers, forms the T-cell receptor-CD3 complex. This complex plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. The genes encoding the epsilon, gamma and delta polypeptides are located in the same cluster on chromosome 11. Defects in this gene are associated with T cell immunodeficiency. [provided by RefSeq, Jul 2008] |
HCG24 GeneHLA complex group 24 (non-protein coding) |
HCG26 GeneHLA complex group 26 (non-protein coding) |
VKORC1 Genevitamin K epoxide reductase complex, subunit 1 This gene encodes the catalytic subunit of the vitamin K epoxide reductase complex, which is responsible for the reduction of inactive vitamin K 2,3-epoxide to active vitamin K in the endoplasmic reticulum membrane. Vitamin K is a required co-factor for carboxylation of glutamic acid residues by vitamin K-dependent gamma-carboxylase in blood-clotting enzymes. Allelic variation in this gene is associated with vitamin k-dependent clotting factors combined deficiency of 2, and increased resistance or sensitivity to warfarin, an inhibitor of vitamin K epoxide reductase. Pseudogenes of this gene are located on chromosomes 1 and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
ATP5HP1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 1 |
ATP5HP3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 3 |
ATP5HP2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 2 |
ATP5HP4 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 4 |
VKORC1L1 Genevitamin K epoxide reductase complex, subunit 1-like 1 This gene encodes an enzyme important in the vitamin K cycle, which is involved in the carboxylation of glutamate residues present in vitamin K-dependent proteins. The encoded enzyme catalyzes the de-epoxidation of vitamin K 2,3-epoxide. Oxidative stress may upregulate expression of this gene and the encoded protein may protect cells and membrane proteins form oxidative damage. This gene and a related gene (Gene ID: 79001) may have arisen by gene duplication of an ancestral gene. [provided by RefSeq, Oct 2016] |
LOC646794 GeneSNF8, ESCRT-II complex subunit, homolog (S. cerevisiae) pseudogene |
BLOC1S5 Genebiogenesis of lysosomal organelles complex-1, subunit 5, muted This gene encodes a component of BLOC-1 (biogenesis of lysosome-related organelles complex 1). Components of this complex are involved in the biogenesis of organelles such as melanosomes and platelet-dense granules. A mouse model for Hermansky-Pudlak Syndrome is mutated in the murine version of this gene. Alternative splicing results in multiple transcript variants. Read-through transcription exists between this gene and the upstream EEF1E1 (eukaryotic translation elongation factor 1 epsilon 1) gene, as well as with the downstream TXNDC5 (thioredoxin domain containing 5) gene. [provided by RefSeq, Dec 2010] |
BLOC1S3 Genebiogenesis of lysosomal organelles complex-1, subunit 3 This gene encodes a protein that is a component of the BLOC1 multi-subunit protein complex. This complex is necessary for the biogenesis of specialized organelles of the endosomal-lysosomal system, including platelet dense granules and melanosomes. Mutations in this gene cause Hermansky-Pudlak syndrome 8, a disease characterized by lysosomal storage defects, bleeding due to platelet storage pool deficiency, and oculocutaneous albinism. [provided by RefSeq, Jul 2008] |
BLOC1S2 Genebiogenesis of lysosomal organelles complex-1, subunit 2 This gene encodes a protein with multiple functions. The encoded protein has been found in association with the centrosome, shown to co-localize with gamma-tubulin, and also found to be one of the proteins in the BLOC-1 complex which functions in the formation of lysosome-related organelles. A pseudogene of this gene is located on the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
EMC9 GeneER membrane protein complex subunit 9 Contributes to membrane insertase activity. Involved in protein insertion into ER membrane by stop-transfer membrane-anchor sequence and tail-anchored membrane protein insertion into ER membrane. Located in cytoplasm. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
EMC8 GeneER membrane protein complex subunit 8 Contributes to membrane insertase activity. Involved in protein insertion into ER membrane by stop-transfer membrane-anchor sequence and tail-anchored membrane protein insertion into ER membrane. Located in Golgi apparatus and endoplasmic reticulum. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
EMC3 GeneER membrane protein complex subunit 3 Contributes to membrane insertase activity. Involved in protein insertion into ER membrane by stop-transfer membrane-anchor sequence and tail-anchored membrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
EMC2 GeneER membrane protein complex subunit 2 Contributes to membrane insertase activity. Involved in protein insertion into ER membrane by stop-transfer membrane-anchor sequence and tail-anchored membrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane. Is extrinsic component of endoplasmic reticulum membrane. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
EMC1 GeneER membrane protein complex subunit 1 This gene encodes a single-pass type I transmembrane protein, which is a subunit of the endoplasmic reticulum membrane protein complex (EMC). Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2012] |
EMC7 GeneER membrane protein complex subunit 7 Contributes to membrane insertase activity. Involved in protein insertion into ER membrane by stop-transfer membrane-anchor sequence and tail-anchored membrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
EMC6 GeneER membrane protein complex subunit 6 Contributes to membrane insertase activity. Involved in autophagosome assembly; protein insertion into ER membrane by stop-transfer membrane-anchor sequence; and tail-anchored membrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane and omegasome membrane. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
EMC4 GeneER membrane protein complex subunit 4 Contributes to membrane insertase activity. Involved in protein insertion into ER membrane by stop-transfer membrane-anchor sequence and tail-anchored membrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
CNC2 GeneCarney complex type 2, multiple neoplasia and lentiginosis |
EXOC2 Geneexocyst complex component 2 The protein encoded by this gene is a component of the exocyst complex, a multi-protein complex essential for the polarized targeting of exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and the functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. This interaction has been shown to mediate filopodia formation in fibroblasts. This protein has been shown to interact with the Ral subfamily of GTPases and thereby mediate exocytosis by tethering vesicles to the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012] |
EXOC3 Geneexocyst complex component 3 The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. The complex is also essential for the biogenesis of epithelial cell surface polarity. [provided by RefSeq, Jul 2008] |
EXOC1 Geneexocyst complex component 1 The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008] |
EXOC6 Geneexocyst complex component 6 The protein encoded by this gene is highly similar to the Saccharomyces cerevisiae SEC15 gene product, which is essential for vesicular traffic from the Golgi apparatus to the cell surface in yeast. It is one of the components of a multiprotein complex required for exocytosis. The 5' portion of this gene and two neighboring cytochrome p450 genes are included in a deletion that results in an autosomal-dominant form of nonsyndromic optic nerve aplasia (ONA). Alternative splicing and the use of alternative promoters results in multiple transcript variants. A paralogous gene encoding a similar protein is present on chromosome 2. [provided by RefSeq, Jan 2016] |
EXOC7 Geneexocyst complex component 7 The protein encoded by this gene is a component of the exocyst complex. The exocyst complex plays a critical role in vesicular trafficking and the secretory pathway by targeting post-Golgi vesicles to the plasma membrane. The encoded protein is required for assembly of the exocyst complex and docking of the complex to the plasma membrane. The encoded protein may also play a role in pre-mRNA splicing through interactions with pre-mRNA-processing factor 19. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Nov 2011] |
EXOC4 Geneexocyst complex component 4 The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. The complex is also essential for the biogenesis of epithelial cell surface polarity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
EXOC5 Geneexocyst complex component 5 The protein encoded by this gene is a component of the exocyst complex, a multiple protein complex essential for targeting exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and functions of exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. The complex is also essential for the biogenesis of epithelial cell surface polarity. [provided by RefSeq, Jul 2008] |
EXOC8 Geneexocyst complex component 8 This gene encodes a component of the exocyst complex, an evolutionarily conserved multi-protein complex that plays a critical role in vesicular trafficking and the secretory pathway by targeting post-Golgi vesicles to the plasma membrane. This protein is a target of activated Ral subfamily of GTPases and thereby regulates exocytosis by tethering vesicles to the plasma membrane. Mutations in this gene may be related to Joubert syndrome. [provided by RefSeq, Sep 2016] |
EZH1 Geneenhancer of zeste 1 polycomb repressive complex 2 subunit EZH1 is a component of a noncanonical Polycomb repressive complex-2 (PRC2) that mediates methylation of histone H3 (see MIM 602812) lys27 (H3K27) and functions in the maintenance of embryonic stem cell pluripotency and plasticity (Shen et al., 2008 [PubMed 19026780]).[supplied by OMIM, Mar 2009] |
EZH2 Geneenhancer of zeste 2 polycomb repressive complex 2 subunit This gene encodes a member of the Polycomb-group (PcG) family. PcG family members form multimeric protein complexes, which are involved in maintaining the transcriptional repressive state of genes over successive cell generations. This protein associates with the embryonic ectoderm development protein, the VAV1 oncoprotein, and the X-linked nuclear protein. This protein may play a role in the hematopoietic and central nervous systems. Multiple alternatively splcied transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Feb 2011] |
TEN1 GeneTEN1 CST complex subunit C17ORF106, or TEN1, appears to function in a telomere-associated complex with STN1 (OBFC1; MIM 613128) and CTC1 (C17ORF68; MIM 613129) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009] |
KANSL3 GeneKAT8 regulatory NSL complex subunit 3 Involved in regulation of mitochondrial transcription. Located in mitochondrion and nucleoplasm. Part of NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
KANSL2 GeneKAT8 regulatory NSL complex subunit 2 Predicted to be involved in positive regulation of DNA-templated transcription. Located in several cellular components, including actin cytoskeleton; cytosol; and nucleoplasm. Part of NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
KANSL1 GeneKAT8 regulatory NSL complex subunit 1 This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The encoded protein has been implicated in a variety of cellular processes including enhancer regulation, cell proliferation, and mitosis. Mutations in this gene are associated with Koolen-de Vries Syndrome. [provided by RefSeq, May 2022] |
MCMBP Geneminichromosome maintenance complex binding protein This gene encodes a protein which is a component of the hexameric minichromosome maintenance (MCM) complex which regulates initiation and elongation of DNA. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012] |
LOC441241 Genevitamin K epoxide reductase complex, subunit 1-like 1 pseudogene |
SPCS2P1 Genesignal peptidase complex subunit 2 homolog (S. cerevisiae) pseudogene 1 |
SPCS2P2 Genesignal peptidase complex subunit 2 homolog (S. cerevisiae) pseudogene 2 |
INTS3 Geneintegrator complex subunit 3 The protein encoded by this gene can form a complex with human single-strand DNA binding proteins 1 or 2 (hSSB1 and hSSB2) and other proteins to mediate genome stability and the DNA damage response. The encoded protein is also part of a multiprotein complex that interacts with the C-terminal domain of RNA polymerase II large subunit to help regulate processing of U1 and U2 small nuclear RNAs. [provided by RefSeq, May 2016] |
INTS2 Geneintegrator complex subunit 2 INTS2 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008] |
INTS1 Geneintegrator complex subunit 1 INTS1 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008] |
INTS7 Geneintegrator complex subunit 7 This gene encodes a subunit of the integrator complex. The integrator complex associates with the C-terminal domain of RNA polymerase II and mediates 3'-end processing of the small nuclear RNAs U1 and U2. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010] |
INTS6 Geneintegrator complex subunit 6 DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. The protein encoded by this gene is a DEAD box protein that is part of a complex that interacts with the C-terminus of RNA polymerase II and is involved in 3' end processing of snRNAs. In addition, this gene is a candidate tumor suppressor and is located in the critical region of loss of heterozygosity (LOH). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2015] |
INTS5 Geneintegrator complex subunit 5 The Integrator complex is a complex that associates with the C-terminal domain of RNA polymerase II large subunit. This complex is brought to U1 and U2 small nuclear RNA genes, where it is involved in the transcription and processing of their transcripts. The protein encoded by this gene represents a subunit of the Integrator complex. [provided by RefSeq, Aug 2016] |
INTS4 Geneintegrator complex subunit 4 INTS4 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008] |
INTS9 Geneintegrator complex subunit 9 This gene encodes a subunit of the Integrator complex. This protein complex binds the C-terminal domain of RNA polymerase II and likely plays a role in small nuclear RNA processing. The encoded protein has similarities to the subunits of the cleavage and polyadenylation specificity factor complex. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010] |
INTS8 Geneintegrator complex subunit 8 This gene encodes a subunit of the Integrator complex which is involved in the cleavage of small nuclear RNAs U1 and U2 within the nucleus. The encoded protein associates with RNA polymerase II and is recruited to the U1 and U2 small nuclear RNA genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
LOC642502 Genesuccinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa pseudogene |
ATP5G3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C3 (subunit 9) This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding different proteins have been identified. [provided by RefSeq, Jun 2010] |
ATP5G2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). There are three separate genes which encode subunit c of the proton channel and they specify precursors with different import sequences but identical mature proteins. The protein encoded by this gene is one of three precursors of subunit c. This gene has multiple pseudogenes. [provided by RefSeq, Jan 2018] |
SNF8 GeneSNF8, ESCRT-II complex subunit The protein encoded by this gene is a component of the endosomal sorting complex required for transport II (ESCRT-II), which regulates the movement of ubiquitinylated transmembrane proteins to the lysosome for degradation. This complex also interacts with the RNA polymerase II elongation factor (ELL) to overcome the repressive effects of ELL on RNA polymerase II activity. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
DGS2 GeneDiGeorge syndrome/velocardiofacial syndrome complex 2 |
HLA-DPA1 Genemajor histocompatibility complex, class II, DP alpha 1 HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008] |
HLA-DPA3 Genemajor histocompatibility complex, class II, DP alpha 3 (pseudogene) |
HLA-DPA2 Genemajor histocompatibility complex, class II, DP alpha 2 (pseudogene) |
MED28P3 Genemediator complex subunit 28 pseudogene 3 |
MED28P1 Genemediator complex subunit 28 pseudogene 1 |
MED28P7 Genemediator complex subunit 28 pseudogene 7 |
MED28P4 Genemediator complex subunit 28 pseudogene 4 |
MED28P8 Genemediator complex subunit 28 pseudogene 8 |
CNOT4P1 GeneCCR4-NOT transcription complex, subunit 4 pseudogene 1 |
GID4 GeneGID complex subunit 4 The multiprotein Mediator complex is a coactivator required for activation of RNA polymerase II transcription by DNA bound transcription factors. The protein encoded by this gene is thought to be a subunit of the Mediator complex. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
GID8 GeneGID complex subunit 8 Predicted to enable protein homodimerization activity. Involved in positive regulation of canonical Wnt signaling pathway and positive regulation of cell population proliferation. Located in cell junction; cytosol; and nucleoplasm. Part of ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
ANAPC13 Geneanaphase promoting complex subunit 13 This gene encodes a component of the anaphase promoting complex, a large ubiquitin-protein ligase that controls cell cycle progression by regulating the degradation of cell cycle regulators such as B-type cyclins. The encoded protein is evolutionarily conserved and is required for the integrity and ubiquitin ligase activity of the anaphase promoting complex. Pseudogenes and splice variants have been found for this gene; however, the biological validity of some of the splice variants has not been determined. [provided by RefSeq, Nov 2008] |
LOC730268 Geneanaphase-promoting complex subunit 1-like |
LOC101060275 Genenuclear pore complex-interacting protein family member B4-like |
LOC102724642 Geneanaphase-promoting complex subunit 1-like |
LOC101060022 Genenascent polypeptide-associated complex subunit alpha, muscle-specific form-like |
HLA-DRB8 Genemajor histocompatibility complex, class II, DR beta 8 (pseudogene) |
HLA-DRB9 Genemajor histocompatibility complex, class II, DR beta 9 (pseudogene) Predicted to be involved in antigen processing and presentation and immune response. Predicted to be located in membrane. Predicted to be part of MHC class II protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-DRB2 Genemajor histocompatibility complex, class II, DR beta 2 (pseudogene) Predicted to be involved in adaptive immune response and antigen processing and presentation of peptide or polysaccharide antigen via MHC class II. Predicted to be located in endosome membrane and lysosomal membrane. Predicted to be part of MHC class II protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-DRB3 Genemajor histocompatibility complex, class II, DR beta 3 HLA-DRB3 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020] |
HLA-DRB1 Genemajor histocompatibility complex, class II, DR beta 1 HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 6 exons. Exon one encodes the leader peptide; exons 2 and 3 encode the two extracellular domains; exon 4 encodes the transmembrane domain; and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020] |
HLA-DRB6 Genemajor histocompatibility complex, class II, DR beta 6 (pseudogene) |
HLA-DRB7 Genemajor histocompatibility complex, class II, DR beta 7 (pseudogene) Predicted to be involved in antigen processing and presentation and immune response. Predicted to be located in membrane. Predicted to be part of MHC class II protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
HLA-DRB4 Genemajor histocompatibility complex, class II, DR beta 4 HLA-DRB4 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020] |
HLA-DRB5 Genemajor histocompatibility complex, class II, DR beta 5 HLA-DRB5 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. There are multiple pseudogenes of this gene. [provided by RefSeq, Feb 2020] |
LOC100420746 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 7 pseudogene |
CNOT6L GeneCCR4-NOT transcription complex, subunit 6-like Predicted to enable poly(A)-specific ribonuclease activity. Involved in positive regulation of cell population proliferation and positive regulation of cytoplasmic mRNA processing body assembly. Located in cytosol and nucleus. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Mar 2025] |
SPEG GeneSPEG complex locus This gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Along with the desmin gene, expression of this gene may be controlled by the desmin locus control region. Mutations in this gene are associated with centronuclear myopathy 5. [provided by RefSeq, Jun 2016] |
GNAS GeneGNAS complex locus This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012] |
INTS6P1 Geneintegrator complex subunit 6 pseudogene 1 |
NPIPA8 Genenuclear pore complex interacting protein family, member A8 |
NPIPA5 Genenuclear pore complex interacting protein family, member A5 |
NPIPA7 Genenuclear pore complex interacting protein family, member A7 |
NPIPA1 Genenuclear pore complex interacting protein family, member A1 Predicted to be involved in mRNA transport and protein transport. Predicted to be located in nuclear membrane. Predicted to be part of nuclear pore. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPA2 Genenuclear pore complex interacting protein family, member A2 Predicted to be involved in mRNA transport and protein transport. Predicted to be located in nuclear membrane. Predicted to be part of nuclear pore. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPA3 Genenuclear pore complex interacting protein family, member A3 |
LOC101928892 Genenascent polypeptide-associated complex subunit alpha, muscle-specific form-like |
COPZ1 Genecoatomer protein complex, subunit zeta 1 This gene encodes a subunit of the cytoplasmic coatamer protein complex, which is involved in autophagy and intracellular protein trafficking. The coatomer protein complex is comprised of seven subunits and functions as the coat protein of coat protein complex (COP)I-vesicles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
COPZ2 Genecoatomer protein complex, subunit zeta 2 This gene encodes a member of the adaptor complexes small subunit family. The encoded protein is a subunit of the coatomer protein complex, a seven-subunit complex that functions in the formation of COPI-type, non-clathrin-coated vesicles. COPI vesicles function in the retrograde Golgi-to-ER transport of dilysine-tagged proteins. [provided by RefSeq, Feb 2014] |
TCP11 Genet-complex 11, testis-specific Involved in germ cell development. Located in acrosomal vesicle and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
TCP10 Genet-complex 10 |
SYCE3 Genesynaptonemal complex central element protein 3 Predicted to be involved in reciprocal meiotic recombination; spermatogenesis; and synaptonemal complex assembly. Predicted to act upstream of or within positive regulation of apoptotic process; positive regulation of developmental process; and positive regulation of reproductive process. Predicted to be located in chromosome and nucleus. Predicted to be active in central element. [provided by Alliance of Genome Resources, Mar 2025] |
COPG2 Genecoatomer protein complex, subunit gamma 2 Predicted to enable structural molecule activity. Involved in intra-Golgi vesicle-mediated transport. Part of COPI vesicle coat. [provided by Alliance of Genome Resources, Mar 2025] |
COPG1 Genecoatomer protein complex, subunit gamma 1 Predicted to enable structural molecule activity. Predicted to be involved in several processes, including Golgi vesicle transport; establishment of Golgi localization; and organelle transport along microtubule. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
SDHCP1 Genesuccinate dehydrogenase complex, subunit C pseudogene 1 |
SDHCP2 Genesuccinate dehydrogenase complex, subunit C pseudogene 2 |
SDHCP3 Genesuccinate dehydrogenase complex, subunit C pseudogene 3 |
SDHCP4 Genesuccinate dehydrogenase complex, subunit C pseudogene 4 |
HCG15 GeneHLA complex group 15 (non-protein coding) |
HCG11 GeneHLA complex group 11 (non-protein coding) |
LOC100420127 Genemediator complex subunit 13 pseudogene |
NOC4L Genenucleolar complex associated 4 homolog (S. cerevisiae) Enables RNA binding activity. Predicted to be involved in rRNA processing. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
KHDC3L GeneKH domain containing 3-like, subcortical maternal complex member The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole. [provided by RefSeq, Dec 2011] |
CD74 GeneCD74 molecule, major histocompatibility complex, class II invariant chain The protein encoded by this gene associates with class II major histocompatibility complex (MHC) and is an important chaperone that regulates antigen presentation for immune response. It also serves as cell surface receptor for the cytokine macrophage migration inhibitory factor (MIF) which, when bound to the encoded protein, initiates survival pathways and cell proliferation. This protein also interacts with amyloid precursor protein (APP) and suppresses the production of amyloid beta (Abeta). Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011] |
EXOC7P1 Geneexocyst complex component 7 pseudogene 1 |
HCG19P GeneHLA complex group 19 pseudogene |
ASCC3 Geneactivating signal cointegrator 1 complex subunit 3 This gene encodes a protein that belongs to a family of helicases that are involved in the ATP-dependent unwinding of nucleic acid duplexes. The encoded protein is the largest subunit of the activating signal cointegrator 1 complex that is involved in DNA repair and resistance to alkylation damage. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
ASCC2 Geneactivating signal cointegrator 1 complex subunit 2 Enables K63-linked polyubiquitin modification-dependent protein binding activity. Involved in regulation of DNA-templated transcription; rescue of stalled ribosome; and ribosome-associated ubiquitin-dependent protein catabolic process. Located in nucleus. Part of DNA repair complex and activating signal cointegrator 1 complex. Is active in cytosolic ribosome. [provided by Alliance of Genome Resources, Mar 2025] |
ASCC1 Geneactivating signal cointegrator 1 complex subunit 1 This gene encodes a subunit of the activating signal cointegrator 1 (ASC-1) complex. The ASC-1 complex is a transcriptional coactivator that plays an important role in gene transactivation by multiple transcription factors including activating protein 1 (AP-1), nuclear factor kappa-B (NF-kB) and serum response factor (SRF). The encoded protein contains an N-terminal KH-type RNA-binding motif which is required for AP-1 transactivation by the ASC-1 complex. Mutations in this gene are associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011] |
LOC105379572 GeneKAT8 regulatory NSL complex subunit 1-like |
SPCS2P4 Genesignal peptidase complex subunit 2 homolog (S. cerevisiae) pseudogene 4 |
SPCS2P3 Genesignal peptidase complex subunit 2 homolog (S. cerevisiae) pseudogene 3 |
ATP5A1P4 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 4 |
ATP5A1P5 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 5 |
ATP5A1P7 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 7 |
ATP5A1P2 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 2 |
ATP5A1P3 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 3 |
ATP5A1P8 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 8 |
LY6G6F Genelymphocyte antigen 6 complex, locus G6F The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008] |
AP2S1 Geneadaptor-related protein complex 2, sigma 1 subunit One of two major clathrin-associated adaptor complexes, AP-2, is a heterotetramer which is associated with the plasma membrane. This complex is composed of two large chains, a medium chain, and a small chain. This gene encodes the small chain of this complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
NDUFA4 GeneNDUFA4, mitochondrial complex associated The protein encoded by this gene belongs to the complex I 9kDa subunit family. Mammalian complex I of mitochondrial respiratory chain is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. [provided by RefSeq, Jul 2008] |
SYCE2 Genesynaptonemal complex central element protein 2 The protein encoded by this gene is part of the synaptonemal complex formed between homologous chromosomes during meiotic prophase. The encoded protein associates with SYCP1 and SYCE1 and is found only where chromosome cores are synapsed. [provided by RefSeq, Dec 2012] |
HAUS8 GeneHAUS augmin-like complex, subunit 8 HAUS8 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010] |
HAUS6 GeneHAUS augmin-like complex, subunit 6 The protein encoded by this gene is a subunit of the augmin complex. The augmin complex plays a role in microtubule attachment to the kinetochore and central spindle formation. This protein may have a role in efficient chromosome congression and segregation by promoting microtubule-dependent microtubule amplification. Pseudogenes of this gene are located on chromosomes 7 and 20. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012] |
HAUS7 GeneHAUS augmin-like complex, subunit 7 This gene encodes a subunit of the augmin complex, which regulates centrosome and mitotic spindle integrity, and is necessary for the completion of cytokinesis. The encoded protein was identified by interaction with ubiquitin C-terminal hydrolase 37. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012] |
HAUS4 GeneHAUS augmin-like complex, subunit 4 This gene encodes a subunit of the centrosome complex termed the human augmin complex. The encoded protein localizes to the spindle microtubules and may play a role in mitotic spindle assembly and maintenance of centrosome integrity during cell division. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 1. [provided by RefSeq, Oct 2009] |
HAUS5 GeneHAUS augmin-like complex, subunit 5 HAUS5 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010] |
HAUS2 GeneHAUS augmin-like complex, subunit 2 The protein encoded by this gene is a subunit of the augmin complex. The augmin complex plays a role in microtubule attachment to the kinetochore and central spindle formation. [provided by RefSeq, Apr 2016] |
HAUS3 GeneHAUS augmin-like complex, subunit 3 This gene encodes a component of the HAUS augmin-like protein complex, which plays a key role in cytokinesis and mitosis. Disruption of the encoded protein causes mitotic defects resulting from fragmentation of centrosomes and microtubule destabilization. This gene shares its 5' exons with some transcripts from overlapping GeneID: 353497, which encodes a DNA polymerase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
HAUS1 GeneHAUS augmin-like complex, subunit 1 HAUS1 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010] |
ATP5A1P10 GeneATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 10 |
ARPIN Geneactin-related protein 2/3 complex inhibitor Involved in directional locomotion; negative regulation of cell migration; and negative regulation of cellular component organization. Predicted to be located in lamellipodium. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130783 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 2 pseudogene |
LOC401010 Genenucleolar complex associated 2 homolog (S. cerevisiae) pseudogene |
GOSR2 Genegolgi SNAP receptor complex member 2 This gene encodes a trafficking membrane protein which transports proteins among the medial- and trans-Golgi compartments. Due to its chromosomal location and trafficking function, this gene may be involved in familial essential hypertension. [provided by RefSeq, Mar 2016] |
LOC100132812 Genenascent polypeptide-associated complex alpha subunit 2 pseudogene |
CIITA Geneclass II, major histocompatibility complex, transactivator This gene encodes a protein with an acidic transcriptional activation domain, 4 LRRs (leucine-rich repeats) and a GTP binding domain. The protein is located in the nucleus and acts as a positive regulator of class II major histocompatibility complex gene transcription, and is referred to as the `master control factor` for the expression of these genes. The protein also binds GTP and uses GTP binding to facilitate its own transport into the nucleus. Once in the nucleus it does not bind DNA but rather uses an intrinsic acetyltransferase (AT) activity to act in a coactivator-like fashion. Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency), increased susceptibility to rheumatoid arthritis, multiple sclerosis, and possibly myocardial infarction. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
MED10 Genemediator complex subunit 10 MED10 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008] |
MED11 Genemediator complex subunit 11 MED11 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008] |
MED12 Genemediator complex subunit 12 The initiation of transcription is controlled in part by a large protein assembly known as the preinitiation complex. A component of this preinitiation complex is a 1.2 MDa protein aggregate called Mediator. This Mediator component binds with a CDK8 subcomplex which contains the protein encoded by this gene, mediator complex subunit 12 (MED12), along with MED13, CDK8 kinase, and cyclin C. The CDK8 subcomplex modulates Mediator-polymerase II interactions and thereby regulates transcription initiation and reinitation rates. The MED12 protein is essential for activating CDK8 kinase. Defects in this gene cause X-linked Opitz-Kaveggia syndrome, also known as FG syndrome, and Lujan-Fryns syndrome. [provided by RefSeq, Aug 2009] |
MED13 Genemediator complex subunit 13 This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, possibly by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. The product of this gene is proposed to form a sub-complex with MED12, cyclin C, and CDK8 that can negatively regulate transactivation by mediator. [provided by RefSeq, Jul 2008] |
MED14 Genemediator complex subunit 14 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein contains a bipartite nuclear localization signal. This gene is known to escape chromosome X-inactivation. [provided by RefSeq, Jul 2008] |
MED15 Genemediator complex subunit 15 The protein encoded by this gene is a subunit of the multiprotein complexes PC2 and ARC/DRIP and may function as a transcriptional coactivator in RNA polymerase II transcription. This gene contains stretches of trinucleotide repeats and is located in the chromosome 22 region which is deleted in DiGeorge syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014] |
MED16 Genemediator complex subunit 16 Enables nuclear thyroid hormone receptor binding activity and transcription coactivator activity. Involved in positive regulation of transcription initiation by RNA polymerase II. Located in membrane. Part of core mediator complex and mediator complex. [provided by Alliance of Genome Resources, Mar 2025] |
MED17 Genemediator complex subunit 17 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008] |
MED18 Genemediator complex subunit 18 MED18 is a component of the Mediator complex, which is a coactivator for DNA-binding factors that activate transcription via RNA polymerase II (Sato et al., 2003 [PubMed 12584197]).[supplied by OMIM, Oct 2008] |
MED19 Genemediator complex subunit 19 The protein encoded by this gene is a subunit of the Mediator complex, which binds to gene-specific regulatory factors and provides support for the basal RNA polymerase II transcription machinery. This gene has been implicated in the growth of several types of cancer, and inhibition of its expression inhibits the growth and spread of these cancers. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
HLA-DPB1 Genemajor histocompatibility complex, class II, DP beta 1 HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008] |
HLA-DPB2 Genemajor histocompatibility complex, class II, DP beta 2 (pseudogene) |
XKR9 GeneXK, Kell blood group complex subunit-related family, member 9 Predicted to enable phospholipid scramblase activity. Predicted to be involved in apoptotic process involved in development; engulfment of apoptotic cell; and phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
XKR8 GeneXK, Kell blood group complex subunit-related family, member 8 Enables phospholipid scramblase activity. Involved in engulfment of apoptotic cell; phosphatidylserine exposure on apoptotic cell surface; and positive regulation of myoblast differentiation. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ATP5F1P1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 1 |
ATP5F1P3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 3 |
ATP5F1P5 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 5 |
ATP5F1P4 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 4 |
ATP5F1P7 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 7 |
ATP5F1P6 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 6 |
CRSP8P Genemediator complex subunit 27 pseudogene |
LOC100420890 Geneanaphase promoting complex subunit 1 pseudogene |
UGT1A GeneUDP glucuronosyltransferase 1 family, polypeptide A complex locus This RefSeq represents a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. [provided by RefSeq, Jul 2008] |
LOC100130270 GeneNDUFA4, mitochondrial complex associated pseudogene |
LIN37 Genelin-37 DREAM MuvB core complex component This gene encodes a protein expressed in the eye. [provided by RefSeq, Jul 2008] |
AP3D1 Geneadaptor-related protein complex 3, delta 1 subunit The protein encoded by this gene is a subunit of the AP3 adaptor-like complex, which is not clathrin-associated, but is associated with the golgi region, as well as more peripheral structures. The AP-3 complex facilitates the budding of vesicles from the golgi membrane, and may be directly involved in trafficking to lysosomes. This subunit is implicated in intracellular biogenesis and trafficking of pigment granules, and possibly platelet dense granules and neurotransmitter vesicles. Defects in this gene are a cause of a new type of Hermansky-Pudlak syndrome. [provided by RefSeq, Feb 2017] |
BRK1 GeneBRICK1, SCAR/WAVE actin-nucleating complex subunit Enables identical protein binding activity. Contributes to small GTPase binding activity. Involved in Rac protein signal transduction and positive regulation of cellular component organization. Located in extracellular exosome. Part of SCAR complex. [provided by Alliance of Genome Resources, Mar 2025] |
TCP1 Genet-complex 1 The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternate transcriptional splice variants of this gene, encoding different isoforms, have been characterized. In addition, three pseudogenes that appear to be derived from this gene have been found. [provided by RefSeq, Jun 2010] |
SYCP3 Genesynaptonemal complex protein 3 This gene encodes an essential structural component of the synaptonemal complex. This complex is involved in synapsis, recombination and segregation of meiotic chromosomes. Mutations in this gene are associated with azoospermia in males and susceptibility to pregnancy loss in females. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2010] |
LOC105369271 Genenuclear pore complex-interacting protein family member B7-like |
LOC100289568 GeneUDP glucuronosyltransferase 2 family, polypeptide A1, complex locus pseudogene |
AP1M2 Geneadaptor-related protein complex 1, mu 2 subunit This gene encodes a subunit of the heterotetrameric adaptor-related protein comlex 1 (AP-1), which belongs to the adaptor complexes medium subunits family. This protein is capable of interacting with tyrosine-based sorting signals. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
AP1M1 Geneadaptor-related protein complex 1, mu 1 subunit The protein encoded by this gene is the medium chain of the trans-Golgi network clathrin-associated protein complex AP-1. The other components of this complex are beta-prime-adaptin, gamma-adaptin, and the small chain AP1S1. This complex is located at the Golgi vesicle and links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. Alternatively spliced transcript variants encoding distinct protein isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
ATPAF2 GeneATP synthase mitochondrial F1 complex assembly factor 2 This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008] |
ATPAF1 GeneATP synthase mitochondrial F1 complex assembly factor 1 This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 beta subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011] |
MCM7 Geneminichromosome maintenance complex component 7 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 4 and 6 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. Cyclin D1-dependent kinase, CDK4, is found to associate with this protein, and may regulate the binding of this protein with the tumorsuppressor protein RB1/RB. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
MCM6 Geneminichromosome maintenance complex component 6 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 4 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of the complex by CDC2 kinase reduces the helicase activity, suggesting a role in the regulation of DNA replication. Single nucleotide polymorphisms in the intron regions of this gene are associated with differential transcriptional activation of the promoter of the neighboring lactase gene and, thereby, influence lactose intolerance in early adulthood. [provided by RefSeq, May 2012] |
MCM5 Geneminichromosome maintenance complex component 5 The protein encoded by this gene is structurally very similar to the CDC46 protein from S. cerevisiae, a protein involved in the initiation of DNA replication. The encoded protein is a member of the MCM family of chromatin-binding proteins and can interact with at least two other members of this family. The encoded protein is upregulated in the transition from the G0 to G1/S phase of the cell cycle and may actively participate in cell cycle regulation. [provided by RefSeq, Jul 2008] |
MCM4 Geneminichromosome maintenance complex component 4 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 6 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of this protein by CDC2 kinase reduces the DNA helicase activity and chromatin binding of the MCM complex. This gene is mapped to a region on the chromosome 8 head-to-head next to the PRKDC/DNA-PK, a DNA-activated protein kinase involved in the repair of DNA double-strand breaks. Alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008] |
MCM2 Geneminichromosome maintenance complex component 2 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein forms a complex with MCM4, 6, and 7, and has been shown to regulate the helicase activity of the complex. This protein is phosphorylated, and thus regulated by, protein kinases CDC2 and CDC7. Multiple alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been defined. [provided by RefSeq, Oct 2012] |
DUSP11 Genedual specificity phosphatase 11 (RNA/RNP complex 1-interacting) The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product is localized to the nucleus and binds directly to RNA and splicing factors, and thus it is suggested to participate in nuclear mRNA metabolism. [provided by RefSeq, Sep 2008] |
MCM9 Geneminichromosome maintenance complex component 9 The protein encoded by this gene is a member of the mini-chromosome maintenance (MCM) protein family that are essential for the initiation of eukaryotic genome replication. Binding of this protein to chromatin has been shown to be a pre-requisite for recruiting the MCM2-7 helicase to DNA replication origins. This protein also binds, and is a positive regulator of, the chromatin licensing and DNA replication factor 1, CDT1. [provided by RefSeq, Nov 2010] |
ATP5LP5 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 5 |
ATP5LP4 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 4 |
ATP5LP7 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 7 |
ATP5LP6 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 6 |
ATP5LP1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 1 |
ATP5LP3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 3 |
ATP5LP2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 2 |
ATP5LP8 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 8 |
MED7 Genemediator complex subunit 7 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008] |
HAUS4P1 GeneHAUS augmin-like complex, subunit 4 pseudogene 1 |
HCG9P1 GeneHLA complex group 9 pseudogene 1 |
AIMP1P1 Geneaminoacyl tRNA synthetase complex-interacting multifunctional protein 1 pseudogene 1 |
AIMP1P2 Geneaminoacyl tRNA synthetase complex-interacting multifunctional protein 1 pseudogene 2 |
EMC10 GeneER membrane protein complex subunit 10 Contributes to membrane insertase activity. Involved in positive regulation of angiogenesis; positive regulation of endothelial cell proliferation; and protein insertion into ER membrane. Located in endoplasmic reticulum membrane and extracellular region. Part of EMC complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421462 Genetrafficking protein particle complex 2-like pseudogene |
OSTCP6 Geneoligosaccharyltransferase complex subunit pseudogene 6 |
OSTCP5 Geneoligosaccharyltransferase complex subunit pseudogene 5 |
OSTCP3 Geneoligosaccharyltransferase complex subunit pseudogene 3 |
OSTCP1 Geneoligosaccharyltransferase complex subunit pseudogene 1 |
OSTCP8 Geneoligosaccharyltransferase complex subunit pseudogene 8 |
RPTOR Generegulatory associated protein of MTOR, complex 1 This gene encodes a component of a signaling pathway that regulates cell growth in response to nutrient and insulin levels. The encoded protein forms a stoichiometric complex with the mTOR kinase, and also associates with eukaryotic initiation factor 4E-binding protein-1 and ribosomal protein S6 kinase. The protein positively regulates the downstream effector ribosomal protein S6 kinase, and negatively regulates the mTOR kinase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
LOC220729 Genesuccinate dehydrogenase complex, subunit A, flavoprotein (Fp) pseudogene |
LOC101060016 Genesignal peptidase complex subunit 3-like |
ATP5G1P3 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 3 |
ATP5G1P1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 1 |
SUZ12 GeneSUZ12 polycomb repressive complex 2 subunit This zinc finger gene has been identified at the breakpoints of a recurrent chromosomal translocation reported in endometrial stromal sarcoma. Recombination of these breakpoints results in the fusion of this gene and JAZF1. The protein encoded by this gene contains a zinc finger domain in the C terminus of the coding region. [provided by RefSeq, Jul 2009] |
AP4S1 Geneadaptor-related protein complex 4, sigma 1 subunit This gene encodes a member of the adaptor complexes small subunit protein family. These proteins are components of the heterotetrameric adaptor protein complexes, which play important roles in the secretory and endocytic pathways by mediating vesicle formation and sorting of integral membrane proteins. The encoded protein is the small subunit of adaptor protein complex-4, which is associated with both clathrin- and nonclathrin-coated vesicles. Mutations in this gene are associated with spastic quadriplegic cerebral palsy-6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 6. [provided by RefSeq, Dec 2011] |
LOC100652955 GeneCOP9 signalosome complex subunit 3 pseudogene |
LOC391707 Genechromatin accessibility complex 1 pseudogene |
BLOC1S4 Genebiogenesis of lysosomal organelles complex-1, subunit 4, cappuccino This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. A similar protein in mouse is a component of a protein complex termed biogenesis of lysosome-related organelles complex 1 (BLOC-1), and is a model for Hermansky-Pudlak syndrome. The encoded protein may play a role in intracellular vesicular trafficking. [provided by RefSeq, Jul 2008] |
NDUFAF4P4 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 4 pseudogene 4 |
NDUFAF4P3 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 4 pseudogene 3 |
NDUFAF4P2 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 4 pseudogene 2 |
NDUFAF4P1 GeneNADH dehydrogenase (ubiquinone) complex I, assembly factor 4 pseudogene 1 |
ARPC1B Geneactin related protein 2/3 complex, subunit 1B, 41kDa This gene encodes one of seven subunits of the human Arp2/3 protein complex. This subunit is a member of the SOP2 family of proteins and is most similar to the protein encoded by gene ARPC1A. The similarity between these two proteins suggests that they both may function as p41 subunit of the human Arp2/3 complex that has been implicated in the control of actin polymerization in cells. It is possible that the p41 subunit is involved in assembling and maintaining the structure of the Arp2/3 complex. Multiple versions of the p41 subunit may adapt the functions of the complex to different cell types or developmental stages. This protein also has a role in centrosomal homeostasis by being an activator and substrate of the Aurora A kinase. [provided by RefSeq, Mar 2011] |
ARPC1A Geneactin related protein 2/3 complex, subunit 1A, 41kDa This gene encodes one of seven subunits of the human Arp2/3 protein complex. This subunit is a member of the SOP2 family of proteins and is most similar to the protein encoded by gene ARPC1B. The similarity between these two proteins suggests that they both may function as p41 subunit of the human Arp2/3 complex that has been implicated in the control of actin polymerization in cells. It is possible that the p41 subunit is involved in assembling and maintaining the structure of the Arp2/3 complex. Multiple versions of the p41 subunit may adapt the functions of the complex to different cell types or developmental stages. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010] |
TRAPPC13P1 Genetrafficking protein particle complex 13 pseudogene 1 |
MOV10 GeneMov10 RISC complex RNA helicase Enables 5'-3' RNA helicase activity and RNA binding activity. Involved in defense response to virus and mRNA destabilization. Located in P-body and cytosol. Implicated in hypertension. [provided by Alliance of Genome Resources, Mar 2025] |
SYCP2L Genesynaptonemal complex protein 2-like Predicted to be involved in meiotic recombination checkpoint signaling and synaptonemal complex assembly. Predicted to act upstream of or within negative regulation of programmed cell death. Located in condensed chromosome, centromeric region and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC643276 Genenucleolar complex associated 2 homolog (S. cerevisiae) pseudogene |
LOC402096 Geneanaphase-promoting complex subunit 1-like |
LOC100420902 Geneexocyst complex component 3-like 4 pseudogene |
SDHDP7 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 7 |
SDHDP6 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 6 |
SDHDP5 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 5 |
SDHDP4 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 4 |
SDHDP3 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 3 |
SDHDP2 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 2 |
SDHDP1 Genesuccinate dehydrogenase complex, subunit D, integral membrane protein pseudogene 1 |
CTR9 GeneCTR9, Paf1/RNA polymerase II complex component The protein encoded by this gene is a component of the PAF1 complex, which associates with RNA polymerase II and functions in transcriptional regulation and elongation. This complex also plays a role in the modification of histones. [provided by RefSeq, Oct 2016] |
XKRY2 GeneXK, Kell blood group complex subunit-related, Y-linked 2 This probable pseudogene is located in the nonrecombining portion of the Y chromosome, and is expressed specifically in testis. It is similar to the XK (X-linked Kell blood group precursor) gene, which encodes a putative membrane transport protein. This gene is present as two identical copies within a palindromic region; this record represents the more telomeric copy. [provided by RefSeq, Nov 2020] |
AP5S1 Geneadaptor-related protein complex 5, sigma 1 subunit Involved in double-strand break repair via homologous recombination and endosomal transport. Located in several cellular components, including late endosome; lysosome; and nucleoplasm. Part of AP-type membrane coat adaptor complex. [provided by Alliance of Genome Resources, Mar 2025] |
ATP5F1P2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 2 |
MED29 Genemediator complex subunit 29 MED29 is a subunit of the Mediator complex, a multiprotein coactivator of RNA transcription that interacts with DNA-bound transcriptional activators, RNA polymerase II (see MIM 180660), and general initiation factors (Sato et al., 2003 [PubMed 14576168]).[supplied by OMIM, Aug 2009] |
MED28 Genemediator complex subunit 28 Predicted to enable actin binding activity. Predicted to be involved in RNA polymerase II preinitiation complex assembly; positive regulation of transcription elongation by RNA polymerase II; and positive regulation of transcription initiation by RNA polymerase II. Predicted to act upstream of or within negative regulation of smooth muscle cell differentiation and somatic stem cell population maintenance. Located in nucleoplasm. Part of core mediator complex. [provided by Alliance of Genome Resources, Mar 2025] |
MED21 Genemediator complex subunit 21 This gene encodes a member of the mediator complex subunit 21 family. The encoded protein interacts with the human RNA polymerase II holoenzyme and is involved in transcriptional regulation of RNA polymerase II transcribed genes. A pseudogene of this gene is located on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
MED20 Genemediator complex subunit 20 This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. A mutation in this gene has been associated with a novel infantile-onset neurodegenerative movement disorder. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015] |
MED22 Genemediator complex subunit 22 This gene encodes a protein component of the mediator complex, which functions in the regulation of transcription by bridging interactions between gene-specific regulatory factors, RNA polymerase II, and general transcription factors. Alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2013] |
MED25 Genemediator complex subunit 25 This gene encodes a component of the transcriptional coactivator complex termed the Mediator complex. This complex is required for transcription of most RNA polymerase II-dependent genes. The encoded protein plays a role in chromatin modification and in preinitiation complex assembly. Mutations in this gene are associated with Charcot-Marie-Tooth disease type 2B2. [provided by RefSeq, Apr 2010] |
MED24 Genemediator complex subunit 24 This gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, possibly by interacting with RNA polymerase II and promoting the formation of a transcriptional pre-initiation complex. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
MED27 Genemediator complex subunit 27 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Dec 2011] |
TRAPPC2P10 Genetrafficking protein particle complex 2 pseudogene 10 |
SDHAF1 Genesuccinate dehydrogenase complex assembly factor 1 The succinate dehydrogenase (SDH) complex (or complex II) of the mitochondrial respiratory chain is composed of 4 individual subunits. The protein encoded by this gene resides in the mitochondria, and is essential for SDH assembly, but does not physically associate with the complex in vivo. Mutations in this gene are associated with SDH-defective infantile leukoencephalopathy (mitochondrial complex II deficiency).[provided by RefSeq, Mar 2010] |
SDHAF2 Genesuccinate dehydrogenase complex assembly factor 2 This gene encodes a mitochondrial assembly factor needed for the flavination of a succinate dehydrogenase complex subunit (SDHA), which is required for activity of the succinate dehydrogenase complex. Mutations in this gene are associated with paraganglioma. [provided by RefSeq, May 2022] |
SDHAF3 Genesuccinate dehydrogenase complex assembly factor 3 Predicted to be involved in mitochondrial respiratory chain complex II assembly; regulation of gluconeogenesis; and succinate metabolic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SDHAF4 Genesuccinate dehydrogenase complex assembly factor 4 Predicted to enable enzyme activator activity. Involved in cellular respiration and mitochondrial respiratory chain complex II assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105369248 Genenuclear pore complex-interacting protein family member B5-like |
LOC101928010 Genehistone deacetylase complex subunit SAP25 pseudogene |
AP1B1P1 Geneadaptor-related protein complex 1, beta 1 subunit pseudogene 1 |
AP1B1P2 Geneadaptor-related protein complex 1, beta 1 subunit pseudogene 2 |
NACAP1 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 1 Predicted to enable unfolded protein binding activity. Predicted to be involved in protein targeting to membrane. Predicted to be part of nascent polypeptide-associated complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
NACAP3 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 3 |
NACAP2 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 2 |
NACAP5 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 5 |
NACAP4 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 4 |
NACAP7 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 7 |
NACAP6 Genenascent-polypeptide-associated complex alpha polypeptide pseudogene 6 |
LOC100418617 Genemajor histocompatibility complex, class I, B pseudogene |
MCM10 Geneminichromosome maintenance complex component 10 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre-RC) and it may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein can interact with MCM2 and MCM6, as well as with the origin recognition protein ORC2. It is regulated by proteolysis and phosphorylation in a cell cycle-dependent manner. Studies of a similar protein in Xenopus suggest that the chromatin binding of this protein at the onset of DNA replication is after pre-RC assembly and before origin unwinding. Alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008] |
MR1P1 Genemajor histocompatibility complex, class I-related pseudogene |
HAUS1P1 GeneHAUS augmin-like complex, subunit 1 pseudogene 1 |
HAUS1P3 GeneHAUS augmin-like complex, subunit 1 pseudogene 3 |
HAUS1P2 GeneHAUS augmin-like complex, subunit 1 pseudogene 2 |
GOSR1 Genegolgi SNAP receptor complex member 1 This gene encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi and between Golgi compartments. This protein is considered an essential component of the Golgi SNAP receptor (SNARE) complex. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
ATP5L GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit G Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the g subunit of the Fo complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010] |
TCP11L1 Genet-complex 11, testis-specific-like 1 Predicted to be involved in signal transduction. Located in microtubule. [provided by Alliance of Genome Resources, Mar 2025] |
TCP11L2 Genet-complex 11, testis-specific-like 2 Predicted to be involved in muscle cell migration and signal transduction. Predicted to be located in cytoskeleton. Predicted to be part of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SYCP2 Genesynaptonemal complex protein 2 The synaptonemal complex is a proteinaceous structure that links homologous chromosomes during the prophase of meiosis. The protein encoded by this gene is a major component of the synaptonemal complex and may bind DNA at scaffold attachment regions. The encoded protein requires synaptonemal complex protein 3, but not 1, for inclusion in the synaptonemal complex. [provided by RefSeq, Jul 2008] |
SYCP1 Genesynaptonemal complex protein 1 Enables double-stranded DNA binding activity. Involved in protein homotetramerization. Predicted to be located in synaptonemal complex. Predicted to be active in central element; male germ cell nucleus; and transverse filament. [provided by Alliance of Genome Resources, Mar 2025] |
MED13L Genemediator complex subunit 13-like The protein encoded by this gene is a subunit of the Mediator complex, a large complex of proteins that functions as a transcriptional coactivator for most RNA polymerase II-transcribed genes. The encoded protein is involved in early development of the heart and brain. Defects in this gene are a cause of transposition of the great arteries, dextro-looped (DTGA).[provided by RefSeq, Jul 2010] |
ATP5G1P2 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 2 |
ATP5G1P6 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 6 |
ATP5G1P7 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 7 |
ATP5G1P4 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 4 |
ATP5G1P5 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 5 |
ATP5G1P8 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 8 |
HCG16 GeneHLA complex group 16 (non-protein coding) |
FRAS1 GeneFraser extracellular matrix complex subunit 1 This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
LOC105379735 Geneintegrator complex subunit 4-like protein 2 |
LOC101929322 Geneintegrator complex subunit 4-like protein 2 |
AP1B1 Geneadaptor-related protein complex 1, beta 1 subunit Adaptor protein complex 1 is found at the cytoplasmic face of coated vesicles located at the Golgi complex, where it mediates both the recruitment of clathrin to the membrane and the recognition of sorting signals within the cytosolic tails of transmembrane receptors. This complex is a heterotetramer composed of two large, one medium, and one small adaptin subunit. The protein encoded by this gene serves as one of the large subunits of this complex and is a member of the adaptin protein family. This gene is a candidate meningioma gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
PCDHA@ Geneprotocadherin alpha cluster, complex locus The protocadherin alpha gene cluster is one of three related clusters tandemly linked on chromosome five. The clusters have a genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 genes and 1 pseudogene, which are members of the cadherin superfamily and related to the mouse CNR genes. The sequence of the 13 upstream genes and the pseudogene are highly similar to one another, while a subfamily (C) contains two more distantly related coding sequences. The alpha cluster genes are organized in a tandem array of 15 large, variable region exons followed by a constant region, which contains 3 exons shared by all genes in the cluster. Each variable region exon encodes an extracellular domain comprised of 6 cadherin ectodomains and a transmembrane region. The constant region exons encode a common cytoplasmic tail. These neural adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the alpha cluster genes. [provided by RefSeq, Jul 2008] |
BRCC3 GeneBRCA1/BRCA2-containing complex, subunit 3 This gene encodes a subunit of the BRCA1-BRCA2-containing complex (BRCC), which is an E3 ubiquitin ligase. This complex plays a role in the DNA damage response, where it is responsible for the stable accumulation of BRCA1 at DNA break sites. The component encoded by this gene can specifically cleave Lys 63-linked polyubiquitin chains, and it regulates the abundance of these polyubiquitin chains in chromatin. The loss of this gene results in abnormal angiogenesis and is associated with syndromic moyamoya, a cerebrovascular angiopathy. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 5. [provided by RefSeq, Jun 2011] |
MT-ND4L GeneNADH dehydrogenase, subunit 4L (complex I) Enables NADH dehydrogenase (ubiquinone) activity. Predicted to be involved in mitochondrial electron transport, NADH to ubiquinone and proton motive force-driven mitochondrial ATP synthesis. Located in mitochondrion. Part of mitochondrial inner membrane and respiratory chain complex I. Implicated in Leber hereditary optic neuropathy and diabetes mellitus. [provided by Alliance of Genome Resources, Mar 2025] |
INO80D GeneINO80 complex subunit D Involved in several processes, including chromatin remodeling; regulation of chromosome organization; and regulation of nucleobase-containing compound metabolic process. Part of Ino80 complex. [provided by Alliance of Genome Resources, Mar 2025] |
INO80E GeneINO80 complex subunit E Involved in several processes, including chromatin remodeling; regulation of chromosome organization; and regulation of nucleobase-containing compound metabolic process. Located in nucleolus and nucleoplasm. Part of Ino80 complex. [provided by Alliance of Genome Resources, Mar 2025] |
INO80B GeneINO80 complex subunit B This gene encodes a subunit of an ATP-dependent chromatin remodeling complex, INO80, which plays a role in DNA and nucleosome-activated ATPase activity and ATP-dependent nucleosome sliding. Readthrough transcription of this gene into the neighboring downstream gene, which encodes WW domain-binding protein 1, generates a non-coding transcript. [provided by RefSeq, Feb 2011] |
INO80C GeneINO80 complex subunit C Involved in several processes, including chromatin remodeling; regulation of chromosome organization; and regulation of nucleobase-containing compound metabolic process. Part of Ino80 complex and MLL1 complex. [provided by Alliance of Genome Resources, Mar 2025] |
AP2M1 Geneadaptor-related protein complex 2, mu 1 subunit This gene encodes a subunit of the heterotetrameric coat assembly protein complex 2 (AP2), which belongs to the adaptor complexes medium subunits family. The encoded protein is required for the activity of a vacuolar ATPase, which is responsible for proton pumping occurring in the acidification of endosomes and lysosomes. The encoded protein may also play an important role in regulating the intracellular trafficking and function of CTLA-4 protein. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015] |
HCG14 GeneHLA complex group 14 (non-protein coding) |
HCG17 GeneHLA complex group 17 (non-protein coding) |
UQCC1 Geneubiquinol-cytochrome c reductase complex assembly factor 1 This gene encodes a transmembrane protein that is structurally similar to the mouse basic fibroblast growth factor repressed ZIC-binding protein. In mouse this protein may be involved in fibroblast growth factor regulated growth control. In humans, polymorphisms in this gene are associated with variation in human height and osteoarthritis. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
UQCC3 Geneubiquinol-cytochrome c reductase complex assembly factor 3 Complex III is a mitochondrial inner membrane protein complex that transfers electrons from ubiquinol to cytochrome c. This gene encodes a protein that functions in complex III assembly. Mutations in this gene result in Mitochondrial complex III deficiency, nuclear type 9. [provided by RefSeq, Dec 2014] |
UQCC2 Geneubiquinol-cytochrome c reductase complex assembly factor 2 This gene encodes a nucleoid protein localized to the mitochondria inner membrane. The encoded protein affects regulation of insulin secretion, mitochondrial ATP production, and myogenesis through modulation of mitochondrial respiratory chain activity. [provided by RefSeq, Oct 2012] |
HAUS6P2 GeneHAUS augmin-like complex, subunit 6 pseudogene 2 |
HAUS6P1 GeneHAUS augmin-like complex, subunit 6 pseudogene 1 |
NPIPB9 Genenuclear pore complex interacting protein family, member B9 |
LOC100422556 GeneLeo1, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) pseudogene |
HLA-DRA Genemajor histocompatibility complex, class II, DR alpha HLA-DRA is one of the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha and a beta chain, both anchored in the membrane. This molecule is expressed on the surface of various antigen presenting cells such as B lymphocytes, dendritic cells, and monocytes/macrophages, and plays a central role in the immune system and response by presenting peptides derived from extracellular proteins, in particular, pathogen-derived peptides to T cells. The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, and exon 4 encodes the transmembrane domain and the cytoplasmic tail. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5. [provided by RefSeq, Aug 2020] |
ICE2 Geneinteractor of little elongation complex ELL subunit 2 This gene encodes a protein component of the little elongation complex (LEC), which plays a role in small nuclear RNA (snRNA) transcription. The LEC regulates snRNA transcription by enhancing both RNA Polymerase II occupancy and transcriptional elongation. The encoded protein and other LEC components have been shown to localize to Cajal bodies, which are sites of ribonucleoprotein (RNP) complex assembly. Pseudogenes of this gene have been identified on chromosomes 3 and 4. [provided by RefSeq, May 2017] |
ICE1 Geneinteractor of little elongation complex ELL subunit 1 Enables protein-macromolecule adaptor activity. Involved in several processes, including positive regulation of intracellular protein transport; positive regulation of transcription by RNA polymerase III; and snRNA transcription. Located in Cajal body; euchromatin; and histone locus body. Part of transcription elongation factor complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379556 Genenascent polypeptide-associated complex subunit alpha, muscle-specific form-like |
LOC101060099 GeneCST complex subunit TEN1-like |
RTF1 GeneRtf1, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) This locus may represent a gene involved in regulation of transcription elongation and chromatin remodeling, based on studies of similar proteins in other organisms. The encoded protein may bind single-stranded DNA. [provided by RefSeq, Sep 2010] |
LOC101929932 GeneAP-3 complex subunit sigma-1 pseudogene |
COG8 Genecomponent of oligomeric golgi complex 8 This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008] |
COG3 Genecomponent of oligomeric golgi complex 3 This gene encodes a component of the conserved oligomeric Golgi (COG) complex which is composed of eight different subunits and is required for normal Golgi morphology and localization. Defects in the COG complex result in multiple deficiencies in protein glycosylation. The protein encoded by this gene is involved in ER-Golgi transport.[provided by RefSeq, Jun 2011] |
COG2 Genecomponent of oligomeric golgi complex 2 This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi complex. The encoded protein specifically interacts with the USO1 vesicle docking protein and may be necessary for normal Golgi ribbon formation and trafficking of Golgi enzymes. Mutations of this gene are associated with abnormal glycosylation within the Golgi apparatus. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009] |
COG1 Genecomponent of oligomeric golgi complex 1 The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. It is thought that this protein is required for steps in the normal medial and trans Golgi-associated processing of glycoconjugates and plays a role in the organization of the Golgi-localized complex. [provided by RefSeq, Jul 2008] |
COG7 Genecomponent of oligomeric golgi complex 7 The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010] |
COG6 Genecomponent of oligomeric golgi complex 6 This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi apparatus. The encoded protein is organized with conserved oligomeric Golgi complex components 5, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009] |
COG5 Genecomponent of oligomeric golgi complex 5 The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. The encoded protein is organized with conserved oligomeric Golgi complex components 6, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants. Mutations in this gene result in congenital disorder of glycosylation type 2I.[provided by RefSeq, Jan 2011] |
COG4 Genecomponent of oligomeric golgi complex 4 The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010] |
LOC100129130 GeneTHO complex 4 pseudogene |
LOC100422641 GeneSTT3A, subunit of the oligosaccharyltransferase complex (catalytic) pseudogene |
CNOT8 GeneCCR4-NOT transcription complex, subunit 8 Enables poly(A)-specific ribonuclease activity. Involved in miRNA-mediated gene silencing by mRNA destabilization and positive regulation of cell population proliferation. Located in nucleus. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Mar 2025] |
CNOT3 GeneCCR4-NOT transcription complex, subunit 3 Involved in regulation of stem cell population maintenance. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Mar 2025] |
CNOT2 GeneCCR4-NOT transcription complex, subunit 2 This gene encodes a subunit of the multi-component CCR4-NOT complex. The CCR4-NOT complex regulates mRNA synthesis and degradation and is also thought to be involved in mRNA splicing, transport and localization. The encoded protein interacts with histone deacetylases and functions as a repressor of polymerase II transcription. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010] |
CNOT1 GeneCCR4-NOT transcription complex, subunit 1 Enables armadillo repeat domain binding activity; molecular adaptor activity; and nuclear receptor binding activity. Contributes to poly(A)-specific ribonuclease activity. Involved in several processes, including negative regulation of intracellular signal transduction; positive regulation of cytoplasmic mRNA processing body assembly; and regulation of gene expression. Located in P-body and cytosol. Part of CCR4-NOT complex. Implicated in Vissers-Bodmer syndrome and holoprosencephaly 12. [provided by Alliance of Genome Resources, Mar 2025] |
CNOT7 GeneCCR4-NOT transcription complex, subunit 7 The protein encoded by this gene binds to an anti-proliferative protein, B-cell translocation protein 1, which negatively regulates cell proliferation. Binding of the two proteins, which is driven by phosphorylation of the anti-proliferative protein, causes signaling events in cell division that lead to changes in cell proliferation associated with cell-cell contact. The encoded protein downregulates the innate immune response and therefore provides a therapeutic target for enhancing its antimicrobial activity against foreign agents. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and X. [provided by RefSeq, Apr 2016] |
CNOT6 GeneCCR4-NOT transcription complex, subunit 6 This gene encodes the catalytic component of the CCR4-NOT core transcriptional regulation complex. The encoded protein has a 3'-5' RNase activity and prefers polyadenylated substrates. The CCR4-NOT complex plays a role in many cellular processes, including miRNA-mediated repression, mRNA degradation, and transcriptional regulation. [provided by RefSeq, Dec 2014] |
NELFCD Genenegative elongation factor complex member C/D The NELF complex of proteins interacts with the DSIF protein complex to repress transcriptional elongation by RNA polymerase II. The protein encoded by this gene is an essential part of the NELF complex. Alternative translation initiation site usage results in the formation of two isoforms with different N-termini. [provided by RefSeq, Jul 2008] |
ATP5F1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the b subunit of the proton channel. [provided by RefSeq, Jul 2008] |
EXOC3L4 Geneexocyst complex component 3-like 4 Predicted to enable SNARE binding activity. Predicted to be involved in exocyst localization and exocytosis. Predicted to be part of exocyst. [provided by Alliance of Genome Resources, Mar 2025] |
EXOC3L2 Geneexocyst complex component 3-like 2 The protein encoded by this gene is upregulated by vascular endothelial growth factor A and interacts with exocyst complex component 4. The encoded protein may be part of an exocyst complex that plays a role in cell membrane dynamics. Mutations in this gene may be associated with Alzheimer's disease. [provided by RefSeq, May 2017] |
EXOC3L1 Geneexocyst complex component 3-like 1 Predicted to enable SNARE binding activity. Predicted to be involved in exocyst localization; exocytosis; and peptide hormone secretion. Predicted to be located in secretory granule. Predicted to be part of exocyst. [provided by Alliance of Genome Resources, Mar 2025] |
HCG13P GeneHLA complex group 13 pseudogene |
ORC6 Geneorigin recognition complex, subunit 6 The origin recognition complex (ORC) is a highly conserved six subunit protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. Gene silencing studies with small interfering RNA demonstrated that this protein plays an essential role in coordinating chromosome replication and segregation with cytokinesis. [provided by RefSeq, Oct 2010] |
ORC4 Geneorigin recognition complex, subunit 4 The origin recognition complex (ORC) is a highly conserved six subunit protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. This gene encodes a subunit of the ORC complex. Several alternatively spliced transcript variants, some of which encode the same protein, have been reported for this gene. [provided by RefSeq, Oct 2010] |
ORC5 Geneorigin recognition complex, subunit 5 The origin recognition complex (ORC) is a highly conserved six subunit protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Oct 2010] |
ORC2 Geneorigin recognition complex, subunit 2 The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. This protein forms a core complex with ORC3, -4, and -5. It also interacts with CDC45 and MCM10, which are proteins known to be important for the initiation of DNA replication. This protein has been demonstrated to specifically associate with the origin of replication of Epstein-Barr virus in human cells, and is thought to be required for DNA replication from viral origin of replication. Alternatively spliced transcript variants have been found, one of which is a nonsense-mediated mRNA decay candidate. [provided by RefSeq, Oct 2010] |
ORC3 Geneorigin recognition complex, subunit 3 The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is a subunit of the ORC complex. Studies of a similar gene in Drosophila suggested a possible role of this protein in neuronal proliferation and olfactory memory. Alternatively spliced transcript variants encoding distinct isoforms have been reported for this gene. [provided by RefSeq, Jul 2008] |
ORC1 Geneorigin recognition complex, subunit 1 The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is the largest subunit of the ORC complex. While other ORC subunits are stable throughout the cell cycle, the levels of this protein vary during the cell cycle, which has been shown to be controlled by ubiquitin-mediated proteolysis after initiation of DNA replication. This protein is found to be selectively phosphorylated during mitosis. It is also reported to interact with MYST histone acetyltransferase 2 (MyST2/HBO1), a protein involved in control of transcription silencing. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010] |
EXOC5P1 Geneexocyst complex component 5 pseudogene 1 |
SYCE1L Genesynaptonemal complex central element protein 1-like Predicted to be involved in synaptonemal complex assembly. Located in intermediate filament cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
THOC3 GeneTHO complex 3 This gene encodes a component of the nuclear THO transcription elongation complex, which is part of the larger transcription export (TREX) complex that couples messenger RNA processing and export. In humans, the transcription export complex is recruited to the 5'-end of messenger RNAs in a splicing- and cap-dependent manner. Studies of a related complex in mouse suggest that the metazoan transcription export complex is involved in cell differentiation and development. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, May 2013] |
THOC2 GeneTHO complex 2 The TREX multiprotein complex binds specifically to spliced mRNAs to facilitate mRNA export. The protein encoded by this gene is a member of the THO complex, a subset of the TREX complex. The encoded protein interacts with the THOC1 protein.[provided by RefSeq, Jun 2010] |
THOC1 GeneTHO complex 1 Predicted to enable DNA binding activity and RNA binding activity. Involved in mRNA export from nucleus. Located in chromosome, telomeric region; cytoplasm; and nuclear speck. Part of THO complex part of transcription export complex. Implicated in autosomal dominant nonsyndromic deafness 86. [provided by Alliance of Genome Resources, Mar 2025] |
THOC7 GeneTHO complex 7 Predicted to enable RNA binding activity. Involved in mRNA export from nucleus. Located in chromosome, telomeric region; cytosol; and nuclear speck. Part of THO complex part of transcription export complex. [provided by Alliance of Genome Resources, Mar 2025] |
THOC6 GeneTHO complex 6 This gene encodes a subunit of the multi-protein THO complex, which is involved in coordination between transcription and mRNA processing. The THO complex is a component of the TREX (transcription/export) complex, which is involved in transcription and export of mRNAs. A missense mutation in this gene is associated with a neurodevelopmental disorder called Beaulieu-Boycott-Innes syndrome. [provided by RefSeq, Dec 2016] |
THOC5 GeneTHO complex 5 Predicted to enable mRNA binding activity. Involved in mRNA export from nucleus and monocyte differentiation. Located in chromosome, telomeric region and nucleoplasm. Part of THO complex part of transcription export complex. Implicated in breast carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB11 Genenuclear pore complex interacting protein family, member B11 Predicted to act upstream of or within prevention of polyspermy. Predicted to be located in external side of plasma membrane and sperm head plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB1P Genenuclear pore complex interacting protein family, member B1, pseudogene |
GINS2 GeneGINS complex subunit 2 (Psf2 homolog) The yeast heterotetrameric GINS complex is made up of Sld5 (GINS4; MIM 610611), Psf1 (GINS1; MIM 610608), Psf2, and Psf3 (GINS3; MIM 610610). The formation of this complex is essential for the initiation of DNA replication in yeast and Xenopus egg extracts (Ueno et al., 2005 [PubMed 16287864]). See GINS1 for additional information about the GINS complex.[supplied by OMIM, Mar 2008] |
GINS3 GeneGINS complex subunit 3 (Psf3 homolog) This gene encodes a protein subunit of the GINS heterotetrameric complex, which is essential for the initiation of DNA replication and replisome progression in eukaryotes. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008] |
GINS1 GeneGINS complex subunit 1 (Psf1 homolog) The yeast heterotetrameric GINS complex is made up of Sld5 (GINS4; MIM 610611), Psf1, Psf2 (GINS2; MIM 610609), and Psf3 (GINS3; MIM 610610). The formation of the GINS complex is essential for the initiation of DNA replication in yeast and Xenopus egg extracts (Ueno et al., 2005 [PubMed 16287864]).[supplied by OMIM, Mar 2008] |
GINS4 GeneGINS complex subunit 4 (Sld5 homolog) The yeast heterotetrameric GINS complex is made up of Sld5, Psf1 (GINS1; MIM 610608), Psf2 (GINS2; MIM 610609), and Psf3 (GINS3; MIM 610610). The formation of the GINS complex is essential for the initiation of DNA replication in yeast and Xenopus egg extracts (Ueno et al., 2005 [PubMed 16287864]). See GINS1 for additional information about the GINS complex.[supplied by OMIM, Mar 2008] |
AP3B1 Geneadaptor-related protein complex 3, beta 1 subunit This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012] |
AP3B2 Geneadaptor-related protein complex 3, beta 2 subunit Adaptor protein complex 3 (AP-3 complex) is a heterotrimeric protein complex involved in the formation of clathrin-coated synaptic vesicles. The protein encoded by this gene represents the beta subunit of the neuron-specific AP-3 complex and was first identified as the target antigen in human paraneoplastic neurologic disorders. The encoded subunit binds clathrin and is phosphorylated by a casein kinase-like protein, which mediates synaptic vesicle coat assembly. Defects in this gene are a cause of early-onset epileptic encephalopathy. [provided by RefSeq, Feb 2017] |
ARPC3 Geneactin related protein 2/3 complex, subunit 3, 21kDa This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been conserved through evolution and is implicated in the control of actin polymerization in cells. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013] |
ARPC2 Geneactin related protein 2/3 complex, subunit 2, 34kDa This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved through evolution. The exact role of the protein encoded by this gene, the p34 subunit, has yet to be determined. Two alternatively spliced variants have been characterized to date. Additional alternatively spliced variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008] |
ARPC5 Geneactin related protein 2/3 complex, subunit 5, 16kDa This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved through evolution. The exact role of the protein encoded by this gene, the p16 subunit, has yet to be determined. Alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
HCP5B GeneHLA complex P5B (non-protein coding) |
LOC102724998 Geneset1/Ash2 histone methyltransferase complex subunit ASH2-like |
TCTE3 Genet-complex-associated-testis-expressed 3 Predicted to enable dynein intermediate chain binding activity. Predicted to be involved in microtubule-based movement. Predicted to be located in cytosol and sperm flagellum. Predicted to be part of cytoplasmic dynein complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TCTE1 Genet-complex-associated-testis-expressed 1 Predicted to be involved in flagellated sperm motility. Predicted to be located in sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
COPA Genecoatomer protein complex, subunit alpha In eukaryotic cells, protein transport between the endoplasmic reticulum and Golgi compartments is mediated in part by non-clathrin-coated vesicular coat proteins (COPs). Seven coat proteins have been identified, and they represent subunits of a complex known as coatomer. The subunits are designated alpha-COP, beta-COP, beta-prime-COP, gamma-COP, delta-COP, epsilon-COP, and zeta-COP. The alpha-COP, encoded by COPA, shares high sequence similarity with RET1P, the alpha subunit of the coatomer complex in yeast. Also, the N-terminal 25 amino acids of alpha-COP encode the bioactive peptide, xenin, which stimulates exocrine pancreatic secretion and may act as a gastrointestinal hormone. Alternative splicing results in multiple splice forms encoding distinct isoforms. [provided by RefSeq, Jul 2008] |
COPE Genecoatomer protein complex, subunit epsilon The product of this gene is an epsilon subunit of coatomer protein complex. Coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles. It is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. Coatomer complex consists of at least the alpha, beta, beta', gamma, delta, epsilon and zeta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
VCPIP1 Genevalosin containing protein (p97)/p47 complex interacting protein 1 Enables cysteine-type deubiquitinase activity. Involved in protein deubiquitination; protein-DNA covalent cross-linking repair; and regulation of protein localization to chromatin. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB3 Genenuclear pore complex interacting protein family, member B3 Predicted to be located in nuclear envelope. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB4 Genenuclear pore complex interacting protein family, member B4 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB7 Genenuclear pore complex interacting protein family, member B7 Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB6 Genenuclear pore complex interacting protein family, member B6 |
NPIPB8 Genenuclear pore complex interacting protein family, member B8 |
LOC100533936 Genemajor histocompatibility complex, class I, B pseudogene |
MOV10L1 GeneMov10 RISC complex RNA helicase like 1 This gene is similar to a mouse gene that encodes a putative RNA helicase and shows testis-specific expression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009] |
AP5M1 Geneadaptor-related protein complex 5, mu 1 subunit Involved in endosomal transport. Located in several cellular components, including cytosol; late endosome; and lysosome. Part of AP-type membrane coat adaptor complex. [provided by Alliance of Genome Resources, Mar 2025] |
NCAPD2 Genenon-SMC condensin I complex, subunit D2 Enables histone binding activity. Involved in mitotic chromosome condensation and positive regulation of chromosome condensation. Located in condensed chromosome; cytosol; and nuclear lumen. Part of condensin complex. Implicated in primary autosomal recessive microcephaly. [provided by Alliance of Genome Resources, Mar 2025] |
NCAPD3 Genenon-SMC condensin II complex, subunit D3 Condensin complexes I and II play essential roles in mitotic chromosome assembly and segregation. Both condensins contain 2 invariant structural maintenance of chromosome (SMC) subunits, SMC2 (MIM 605576) and SMC4 (MIM 605575), but they contain different sets of non-SMC subunits. NCAPD3 is 1 of 3 non-SMC subunits that define condensin II (Ono et al., 2003 [PubMed 14532007]).[supplied by OMIM, Mar 2008] |
ARPC3P2 Geneactin related protein 2/3 complex, subunit 3 pseudogene 2 |
ARPC3P3 Geneactin related protein 2/3 complex, subunit 3 pseudogene 3 |
ARPC3P1 Geneactin related protein 2/3 complex, subunit 3 pseudogene 1 |
ARPC3P5 Geneactin related protein 2/3 complex, subunit 3 pseudogene 5 |
LOC101101841 Genemediator complex subunit 21 pseudogene |
UGT2A1 GeneUDP glucuronosyltransferase 2 family, polypeptide A1, complex locus The protein encoded by this gene belongs to the UDP-glycosyltransferase family. Members of this protein family play a role in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. The encoded enzyme is expressed in the olfactory neuroepithelium, which lines the posterior nasal cavity and is exposed to a wide range of odorants and airborne toxic compounds. Hence, this protein has been suggested to be involved in clearing lipophilic odorant molecules from the sensory epithelium. This gene shares exon structure with the UDP glucuronosyltransferase 2A2 family member, which encodes N-terminally distinct isoforms. Polymorphisms in this gene may be associated with the loss of taste and smell that is reported by some individuals during SARS-CoV-2 infection. [provided by RefSeq, Jan 2022] |
MCM3 Geneminichromosome maintenance complex component 3 The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are involved in the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein is a subunit of the protein complex that consists of MCM2-7. It has been shown to interact directly with MCM5/CDC46. This protein also interacts with and is acetylated by MCM3AP, a chromatin-associated acetyltransferase. The acetylation of this protein inhibits the initiation of DNA replication and cell cycle progression. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2018] |
AIMP2 Geneaminoacyl tRNA synthetase complex-interacting multifunctional protein 2 The protein encoded by this gene is part of the aminoacyl-tRNA synthetase complex, which contains nine different aminoacyl-tRNA synthetases and three non-enzymatic factors. The encoded protein is one of the non-enzymatic factors and is required for assembly and stability of the complex. [provided by RefSeq, May 2016] |
AIMP1 Geneaminoacyl tRNA synthetase complex-interacting multifunctional protein 1 The protein encoded by this gene is a cytokine that is specifically induced by apoptosis, and it is involved in the control of angiogenesis, inflammation, and wound healing. The release of this cytokine renders the tumor-associated vasculature sensitive to tumor necrosis factor. The precursor protein is identical to the p43 subunit, which is associated with the multi-tRNA synthetase complex, and it modulates aminoacylation activity of tRNA synthetase in normal cells. This protein is also involved in the stimulation of inflammatory responses after proteolytic cleavage in tumor cells. Multiple transcript variants encoding different isoforms have been found for this gene. A pseudogene has been identified on chromosome 20. [provided by RefSeq, Dec 2008] |
LOC102725157 Genenuclear pore complex-interacting protein family member B5-like |
ANAPC15 Geneanaphase promoting complex subunit 15 Involved in anaphase-promoting complex-dependent catabolic process; protein polyubiquitination; and regulation of mitotic cell cycle spindle assembly checkpoint. Part of anaphase-promoting complex. [provided by Alliance of Genome Resources, Mar 2025] |
ANAPC16 Geneanaphase promoting complex subunit 16 Involved in anaphase-promoting complex-dependent catabolic process and protein polyubiquitination. Located in cytosol and kinetochore. Part of anaphase-promoting complex. [provided by Alliance of Genome Resources, Mar 2025] |
ANAPC11 Geneanaphase promoting complex subunit 11 Enables cullin family protein binding activity and ubiquitin-ubiquitin ligase activity. Contributes to ubiquitin-protein transferase activity. Involved in anaphase-promoting complex-dependent catabolic process; positive regulation of mitotic metaphase/anaphase transition; and protein polyubiquitination. Located in nucleolus and nucleoplasm. Part of anaphase-promoting complex. [provided by Alliance of Genome Resources, Mar 2025] |
ANAPC10 Geneanaphase promoting complex subunit 10 ANAPC10 is a core subunit of the anaphase-promoting complex (APC), or cyclosome, a ubiquitin protein ligase that is essential for progression through the cell cycle. APC initiates sister chromatid separation by ubiquitinating the anaphase inhibitor securin (PTTG1; MIM 604147) and triggers exit from mitosis by ubiquitinating cyclin B (CCNB1; MIM 123836), the activating subunit of cyclin-dependent kinase-1 (CDK1; MIM 116940) (summary by Wendt et al., 2001 [PubMed 11524682]).[supplied by OMIM, Feb 2011] |
SPC25 GeneSPC25, NDC80 kinetochore complex component This gene encodes a protein that may be involved in kinetochore-microtubule interaction and spindle checkpoint activity. [provided by RefSeq, Jul 2008] |
SPC24 GeneSPC24, NDC80 kinetochore complex component Predicted to contribute to microtubule binding activity. Involved in attachment of spindle microtubules to kinetochore. Located in nucleolus and nucleoplasm. Part of Ndc80 complex. [provided by Alliance of Genome Resources, Mar 2025] |
OSTC Geneoligosaccharyltransferase complex subunit (non-catalytic) Predicted to contribute to dolichyl-diphosphooligosaccharide-protein glycotransferase activity. Predicted to be involved in protein N-linked glycosylation. Part of oligosaccharyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131124 Geneadaptor-related protein complex 4, sigma 1 subunit pseudogene |
CNOT11 GeneCCR4-NOT transcription complex, subunit 11 Predicted to be involved in nuclear-transcribed mRNA poly(A) tail shortening. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Mar 2025] |
CNOT10 GeneCCR4-NOT transcription complex, subunit 10 Predicted to be involved in mRNA catabolic process and negative regulation of translation. Located in membrane. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC204800 Geneactin related protein 2/3 complex, subunit 1A, 41kDa pseudogene |
SDHAP2 Genesuccinate dehydrogenase complex, subunit A, flavoprotein pseudogene 2 |
SDHAP3 Genesuccinate dehydrogenase complex, subunit A, flavoprotein pseudogene 3 |
SDHAP1 Genesuccinate dehydrogenase complex, subunit A, flavoprotein pseudogene 1 |
LY6E Genelymphocyte antigen 6 complex, locus E This gene belongs to the human Ly6 gene family and encodes a glycosylphosphatidyl-inositol (GPI)-anchored cell surface protein. The protein plays an important role in T cell physiology, oncogenesis and immunological regulation. The protein is also involved in modulation of viral infection by coronaviruses, SARS-CoV, MERS-CoV and SARS-CoV-2. [provided by RefSeq, Aug 2021] |
LY6D Genelymphocyte antigen 6 complex, locus D Predicted to be involved in lymphocyte differentiation. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in cell surface. [provided by Alliance of Genome Resources, Mar 2025] |
LY6K Genelymphocyte antigen 6 complex, locus K Predicted to be involved in binding activity of sperm to zona pellucida. Predicted to act upstream of or within flagellated sperm motility. Predicted to be located in cell surface and plasma membrane. Predicted to be active in acrosomal vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
LY6H Genelymphocyte antigen 6 complex, locus H Predicted to enable acetylcholine receptor binding activity and acetylcholine receptor inhibitor activity. Predicted to be involved in acetylcholine receptor signaling pathway. Predicted to be located in extracellular region. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TCP10L2 Genet-complex 10-like 2 |
AP1G1 Geneadaptor-related protein complex 1, gamma 1 subunit Adaptins are important components of clathrin-coated vesicles transporting ligand-receptor complexes from the plasma membrane or from the trans-Golgi network to lysosomes. The adaptin family of proteins is composed of four classes of molecules named alpha, beta-, beta prime- and gamma- adaptins. Adaptins, together with medium and small subunits, form a heterotetrameric complex called an adaptor, whose role is to promote the formation of clathrin-coated pits and vesicles. The protein encoded by this gene is a gamma-adaptin protein and it belongs to the adaptor complexes large subunits family. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
AP1G2 Geneadaptor-related protein complex 1, gamma 2 subunit Adaptins are important components of clathrin-coated vesicles transporting ligand-receptor complexes from the plasma membrane or from the trans-Golgi network to lysosomes. The adaptin family of proteins is composed of four classes of molecules named alpha, beta-, beta prime- and gamma- adaptins. Adaptins, together with medium and small subunits, form a heterotetrameric complex called an adaptor, whose role is to promote the formation of clathrin-coated pits and vesicles. The protein encoded by this gene is a gamma-adaptin protein and it belongs to the adaptor complexes large subunits family. This protein along with the complex is thought to function at some trafficking step in the complex pathways between the trans-Golgi network and the cell surface. [provided by RefSeq, Aug 2017] |
XKRY GeneXK, Kell blood group complex subunit-related, Y-linked This probable pseudogene is located in the nonrecombining portion of the Y chromosome, and is expressed specifically in testis. It is similar to the XK (X-linked Kell blood group precursor) gene, which encodes a putative membrane transport protein. This gene is present as two identical copies within a palindromic region; this record represents the more centromeric copy. [provided by RefSeq, Nov 2020] |
XKRX GeneXK, Kell blood group complex subunit-related, X-linked This gene encodes a protein that is related to a component of the XK/Kell complex of the Kell blood group system. The encoded protein includes several transmembrane domains, is known to be exposed to the cell surface, and may function as a membrane transporter. [provided by RefSeq, May 2010] |
LOC252862 GeneCDC26 subunit of anaphase promoting complex-related gene |
XKR5 GeneXK, Kell blood group complex subunit-related family, member 5 Predicted to be involved in apoptotic process involved in development; engulfment of apoptotic cell; and phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
XKR4 GeneXK, Kell blood group complex subunit-related family, member 4 Enables phospholipid scramblase activity. Involved in phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
XKR7 GeneXK, Kell blood group complex subunit-related family, member 7 Predicted to be involved in apoptotic process involved in development; engulfment of apoptotic cell; and phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
XKR6 GeneXK, Kell blood group complex subunit-related family, member 6 Predicted to be involved in apoptotic process involved in development; engulfment of apoptotic cell; and phosphatidylserine exposure on apoptotic cell surface. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
XKR3 GeneXK, Kell blood group complex subunit-related family, member 3 XKRX (MIM 300684) and XKR3 are homologs of the Kell blood group precursor XK (MIM 314850), which is a putative membrane transporter and a component of the XK/Kell complex of the Kell blood group system (Calenda et al., 2006 [PubMed 16431037]).[supplied by OMIM, Mar 2008] |
LOC401602 Geneadaptor-related protein complex 2, beta 1 subunit pseudogene |
LOC645388 Geneadaptor-related protein complex 1, mu 2 subunit pseudogene |
NDC80 GeneNDC80 kinetochore complex component This gene encodes a component of the NDC80 kinetochore complex. The encoded protein consists of an N-terminal microtubule binding domain and a C-terminal coiled-coiled domain that interacts with other components of the complex. This protein functions to organize and stabilize microtubule-kinetochore interactions and is required for proper chromosome segregation. [provided by RefSeq, Oct 2011] |
LOC101928722 Genenascent polypeptide-associated complex subunit alpha, muscle-specific form-like |
DLST Genedihydrolipoamide S-succinyltransferase (E2 component of 2-oxo-glutarate complex) This gene encodes a mitochondrial protein that belongs to the 2-oxoacid dehydrogenase family. This protein is one of the three components (the E2 component) of the 2-oxoglutarate dehydrogenase complex that catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2011] |
MED26 Genemediator complex subunit 26 The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008] |
HCP5 GeneHLA complex P5 (non-protein coding) |
MCM3AP Geneminichromosome maintenance complex component 3 associated protein The minichromosome maintenance protein 3 (MCM3) is one of the MCM proteins essential for the initiation of DNA replication. The protein encoded by this gene is a MCM3 binding protein. It was reported to have phosphorylation-dependent DNA-primase activity, which was up-regulated in antigen immunization induced germinal center. This protein was demonstrated to be an acetyltransferase that acetylates MCM3 and plays a role in DNA replication. The mutagenesis of a nuclear localization signal of MCM3 affects the binding of this protein with MCM3, suggesting that this protein may also facilitate MCM3 nuclear localization. This gene is expressed in the brain or in neuronal tissue. An allelic variant encoding amino acid Lys at 915, instead of conserved Glu, has been identified in patients with mild intellectual disability. [provided by RefSeq, Jan 2014] |
LOC644145 Geneexocyst complex component 1 pseudogene |
AP1AR Geneadaptor-related protein complex 1 associated regulatory protein Enables AP-1 adaptor complex binding activity and kinesin binding activity. Involved in negative regulation of receptor recycling and vesicle targeting, trans-Golgi to endosome. Acts upstream of or within negative regulation of substrate adhesion-dependent cell spreading. Located in Golgi apparatus and transport vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
BLOC1S2P1 Genebiogenesis of lysosomal organelles complex-1, subunit 2 pseudogene 1 |
LOC100421179 Genecomponent of oligomeric golgi complex 1 pseudogene |
3.8-1.3 GeneHLA complex group 26 (non-protein coding) pseudogene |
NOC3L Genenucleolar complex associated 3 homolog (S. cerevisiae) Enables RNA binding activity. Predicted to be involved in DNA replication initiation. Predicted to act upstream of or within fat cell differentiation. Located in mitochondrion; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RIC1 GeneRAB6A GEF complex partner 1 Enables guanyl-nucleotide exchange factor activity and small GTPase binding activity. Involved in several processes, including positive regulation of GTPase activity; regulation of extracellular matrix constituent secretion; and retrograde transport, endosome to Golgi. Located in cytosol and membrane. Part of Ric1-Rgp1 guanyl-nucleotide exchange factor complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100287498 GeneNDUFA4, mitochondrial complex associated pseudogene |
LOC100422671 Genecell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) pseudogene |
SPCS1 Genesignal peptidase complex subunit 1 homolog (S. cerevisiae) Predicted to enable ribosome binding activity. Involved in signal peptide processing; viral protein processing; and virion assembly. Located in endoplasmic reticulum membrane. Part of signal peptidase complex. [provided by Alliance of Genome Resources, Mar 2025] |
SPCS2 Genesignal peptidase complex subunit 2 homolog (S. cerevisiae) Predicted to enable peptidase activity. Involved in signal peptide processing. Part of signal peptidase complex. [provided by Alliance of Genome Resources, Mar 2025] |
SPCS3 Genesignal peptidase complex subunit 3 homolog (S. cerevisiae) Involved in signal peptide processing and viral protein processing. Located in endoplasmic reticulum. Part of signal peptidase complex. [provided by Alliance of Genome Resources, Mar 2025] |
LIN9 Genelin-9 DREAM MuvB core complex component This gene encodes a tumor suppressor protein that inhibits DNA synthesis and oncogenic transformation through association with the retinoblastoma 1 protein. The encoded protein also interacts with a complex of other cell cycle regulators to repress cell cycle-dependent gene expression in non-dividing cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
ATP5G1 GeneATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008] |
LOC729978 Genenuclear pore complex interacting protein pseudogene Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421655 Geneadaptor-related protein complex 3, mu 2 subunit pseudogene |
HCG4B GeneHLA complex group 4B (non-protein coding) |
LOC728554 GeneTHO complex 3 pseudogene |
TRAPPC3L Genetrafficking protein particle complex 3-like Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport and intra-Golgi vesicle-mediated transport. Part of TRAPP complex. [provided by Alliance of Genome Resources, Mar 2025] |
PACERR GenePTGS2 antisense NFKB1 complex-mediated expression regulator RNA This gene represents transcription of a long non-coding RNA produced in antisense to the prostaglandin-endoperoxide synthase 2 (PTGS2) gene. This transcript interacts with NF-kB transcriptional regulators to promote expression of PTGS2. [provided by RefSeq, Feb 2015] |
HCG8 GeneHLA complex group 8 |
TUBGCP2 Genetubulin, gamma complex associated protein 2 Predicted to enable gamma-tubulin binding activity. Predicted to contribute to microtubule minus-end binding activity. Involved in brain development and neuron migration. Located in centrosome and nucleoplasm. Implicated in pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures. [provided by Alliance of Genome Resources, Mar 2025] |
TUBGCP3 Genetubulin, gamma complex associated protein 3 Enables gamma-tubulin binding activity. Predicted to be involved in meiotic cell cycle; microtubule cytoskeleton organization; and mitotic cell cycle. Located in cytoplasm and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
TUBGCP4 Genetubulin, gamma complex associated protein 4 This gene encodes a component of the gamma-tubulin ring complex, which is required for microtubule nucleation. In mammalian cells, the protein localizes to centrosomes in association with gamma-tubulin. Crystal structure analysis revealed a structure composed of five helical bundles arranged around conserved hydrophobic cores. An exposed surface area located in the C-terminal domain is essential and sufficient for direct binding to gamma-tubulin. Mutations in this gene that alter microtubule organization are associated with microcephaly and chorioretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015] |
TUBGCP5 Genetubulin, gamma complex associated protein 5 Enables microtubule binding activity. Involved in microtubule nucleation. Located in centrosome and cytosol. Part of gamma-tubulin ring complex. [provided by Alliance of Genome Resources, Mar 2025] |
TUBGCP6 Genetubulin, gamma complex associated protein 6 The protein encoded by this gene is part of a large multisubunit complex required for microtubule nucleation at the centrosome. [provided by RefSeq, Jul 2008] |
ANAPC10P1 Geneanaphase promoting complex subunit 10 pseudogene 1 |
MED6P1 Genemediator complex subunit 6 pseudogene 1 |
LOC105371186 Genenuclear pore complex-interacting protein family member A5-like |
LOC105371189 Genenuclear pore complex-interacting protein family member B9-like |
BORCS6 GeneBLOC-1 related complex subunit 6 Enables identical protein binding activity. Involved in lysosome localization. Part of BORC complex. [provided by Alliance of Genome Resources, Mar 2025] |
PYM1 GenePYM homolog 1, exon junction complex associated factor Enables ribosome binding activity. Involved in exon-exon junction complex disassembly; nuclear-transcribed mRNA catabolic process, nonsense-mediated decay; and positive regulation of translation. Located in cell junction; cytosol; and nuclear lumen. Part of exon-exon junction complex. [provided by Alliance of Genome Resources, Mar 2025] |
BORCS7 GeneBLOC-1 related complex subunit 7 Predicted to be involved in organelle transport along microtubule; regulation of endosome size; and regulation of lysosome size. Predicted to act upstream of or within several processes, including lysosome localization; motor behavior; and response to cycloheximide. Part of BORC complex. [provided by Alliance of Genome Resources, Mar 2025] |
WASHC5 GeneWASH complex subunit 5 This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq, Aug 2009] |
INTS13 Geneintegrator complex subunit 13 Involved in regulation of mitotic cell cycle. Acts upstream of or within centrosome localization; mitotic spindle organization; and protein localization to nuclear envelope. Located in cytoplasm and nuclear body. Part of integrator complex. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SGF29 GeneSAGA complex associated factor 29 CCDC101 is a subunit of 2 histone acetyltransferase complexes: the ADA2A (TADA2A; MIM 602276)-containing (ATAC) complex and the SPT3 (SUPT3H; MIM 602947)-TAF9 (MIM 600822)-GCN5 (KAT2A; MIM 602301)/PCAF (KAT2B; MIM 602303) acetylase (STAGA) complex. Both of these complexes contain either GCN5 or PCAF, which are paralogous acetyltransferases (Wang et al., 2008 [PubMed 18838386]).[supplied by OMIM, Apr 2010] |
INTS11 Geneintegrator complex subunit 11 The Integrator complex contains at least 12 subunits and associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates the 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690). INTS11, or CPSF3L, is the catalytic subunit of the Integrator complex (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008] |
NSMCE3 GeneNSE3 homolog, SMC5-SMC6 complex component The protein encoded by this gene is part of the SMC5-6 chromatin reorganizing complex and is a member of the MAGE superfamily. This is an intronless gene. [provided by RefSeq, May 2011] |
INTS14 Geneintegrator complex subunit 14 Predicted to be involved in snRNA 3'-end processing. Located in cytoplasm. Part of integrator complex. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ABRAXAS2 Geneabraxas 2, BRISC complex subunit Enables microtubule binding activity and polyubiquitin modification-dependent protein binding activity. Involved in nuclear chromosome segregation; protein K63-linked deubiquitination; and response to ischemia. Located in cytoplasm; microtubule cytoskeleton; and midbody. Part of BRISC complex. [provided by Alliance of Genome Resources, Mar 2025] |
CNOT9 GeneCCR4-NOT transcription complex subunit 9 This gene encodes a member of the highly conserved RCD1 protein family. The encoded protein is a transcriptional cofactor and a core protein of the CCR4-NOT complex. It may be involved in signal transduction as well as retinoic acid-regulated cell differentiation and development. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2012] |
ELP1 Geneelongator acetyltransferase complex subunit 1 The protein encoded by this gene is a scaffold protein and a regulator for three different kinases involved in proinflammatory signaling. The encoded protein can bind NF-kappa-B-inducing kinase and I-kappa-B kinases through separate domains and assemble them into an active kinase complex. Mutations in this gene have been associated with familial dysautonomia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
WASHC3 GeneWASH complex subunit 3 Predicted to be involved in actin filament polymerization and exocytosis. Part of WASH complex. [provided by Alliance of Genome Resources, Mar 2025] |
SINHCAF GeneSIN3-HDAC complex associated factor Involved in negative regulation of cell migration. Part of Sin3-type complex. [provided by Alliance of Genome Resources, Mar 2025] |
BORCS5 GeneBLOC-1 related complex subunit 5 Involved in lysosome localization and organelle transport along microtubule. Located in cytoplasmic side of lysosomal membrane; plasma membrane; and plus-end kinesin complex. Part of BORC complex. Implicated in colorectal adenocarcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
FMC1 Geneformation of mitochondrial complex V assembly factor 1 homolog Involved in mitochondrial proton-transporting ATP synthase complex assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
WASHC2A GeneWASH complex subunit 2A Predicted to enable phosphatidylinositol phosphate binding activity and retromer complex binding activity. Involved in protein localization to endosome. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
BABAM2 GeneBRISC and BRCA1 A complex member 2 This gene encodes an anti-apoptotic, death receptor-associated protein that interacts with tumor necrosis factor-receptor-1. The encoded protein acts as an adapter in several protein complexes, including the BRCA1-A complex and the BRISC complex. The BRCA1-A complex possesses ubiquitinase activity and targets sites of double strand DNA breaks, while the BRISC complex exhibits deubiquitinase activity and is involved in mitotic spindle assembly. This gene is upregulated in several types of cancer. [provided by RefSeq, Jun 2016] |
WASHC4 GeneWASH complex subunit 4 This gene encodes a component of the WASH complex, which functions in the intracellular transport of endosomes. Mutations in this gene have been detected in individuals with autosomal recessive cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014] |
PATJ GenePATJ crumbs cell polarity complex component This gene encodes a protein with multiple PDZ domains. PDZ domains mediate protein-protein interactions, and proteins with multiple PDZ domains often organize multimeric complexes at the plasma membrane. This protein localizes to tight junctions and to the apical membrane of epithelial cells. A similar protein in Drosophila is a scaffolding protein which tethers several members of a multimeric signaling complex in photoreceptors. [provided by RefSeq, Jul 2008] |
BORCS8 GeneBLOC-1 related complex subunit 8 Involved in heart development. Part of BORC complex. [provided by Alliance of Genome Resources, Mar 2025] |
ODAD1 Geneouter dynein arm docking complex subunit 1 This gene encodes a coiled-coil domain-containing protein that is a component of the outer dynein arm docking complex in cilia cells. Mutations in this gene may cause primary ciliary dyskinesia 20. [provided by RefSeq, May 2013] |
GON7 GeneGON7 subunit of KEOPS complex Involved in tRNA threonylcarbamoyladenosine modification. Located in cytosol; nucleolus; and nucleoplasm. Part of EKC/KEOPS complex. Implicated in Galloway-Mowat syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
MRNIP GeneMRN complex interacting protein Enables chromatin binding activity. Involved in several processes, including mitotic G2 DNA damage checkpoint signaling; regulation of double-strand break repair; and response to ionizing radiation. Located in Mre11 complex and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CPLANE1 Geneciliogenesis and planar polarity effector complex subunit 1 The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012] |
BICRA GeneBRD4 interacting chromatin remodeling complex associated protein Enables transcription regulator activator activity. Involved in positive regulation of DNA-templated transcription. Located in nucleus. Part of SWI/SNF complex. Implicated in Coffin-Siris syndrome 12. [provided by Alliance of Genome Resources, Mar 2025] |
SLF2 GeneSMC5-SMC6 complex localization factor 2 Enables ubiquitin protein ligase binding activity. Involved in several processes, including positive regulation of cellular component organization; positive regulation of double-strand break repair; and protein localization to site of double-strand break. Located in PML body; chromatin; and site of double-strand break. Implicated in mosaic variegated aneuploidy syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
STN1 GeneSTN1 subunit of CST complex OBFC1 and C17ORF68 (MIM 613129) are subunits of an alpha accessory factor (AAF) that stimulates the activity of DNA polymerase-alpha-primase (see MIM 176636), the enzyme that initiates DNA replication (Casteel et al., 2009 [PubMed 19119139]). OBFC1 also appears to function in a telomere-associated complex with C17ORF68 and TEN1 (C17ORF106; MIM 613130) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009] |
SLF1 GeneSMC5-SMC6 complex localization factor 1 Enables ubiquitin protein ligase binding activity. Involved in several processes, including positive regulation of cellular component organization; positive regulation of double-strand break repair; and protein localization to site of double-strand break. Located in nucleoplasm and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
WASHC2C GeneWASH complex subunit 2C Enables phosphatidylinositol phosphate binding activity; phosphatidylinositol-3,4-bisphosphate binding activity; and retromer complex binding activity. Involved in several processes, including endosomal transport; negative regulation of barbed-end actin filament capping; and protein localization to endosome. Located in cytosol; early endosome; and nucleolus. Part of WASH complex. [provided by Alliance of Genome Resources, Mar 2025] |
TEPSIN GeneTEPSIN adaptor related protein complex 4 accessory protein Located in coated vesicle membrane and trans-Golgi network membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SHLD2 Geneshieldin complex subunit 2 Involved in negative regulation of double-strand break repair via homologous recombination; positive regulation of double-strand break repair via nonhomologous end joining; and positive regulation of isotype switching. Located in actin cytoskeleton; nucleoplasm; and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
EPOP Geneelongin BC and polycomb repressive complex 2 associated protein Predicted to enable chromatin binding activity. Predicted to be involved in neuron fate commitment; regulation of transcription by RNA polymerase II; and stem cell differentiation. Predicted to be located in chromosome and nucleus. Predicted to be part of ESC/E(Z) complex and elongin complex. [provided by Alliance of Genome Resources, Mar 2025] |
TEDC1 Genetubulin epsilon and delta complex 1 Predicted to be involved in positive regulation of smoothened signaling pathway. Predicted to be located in centriole and cilium. [provided by Alliance of Genome Resources, Mar 2025] |
FAAP24 GeneFA core complex associated protein 24 FAAP24 is a component of the Fanconi anemia (FA) core complex (see MIM 227650), which plays a crucial role in DNA damage response (Ciccia et al., 2007 [PubMed 17289582]).[supplied by OMIM, Mar 2008] |
BICRAL GeneBICRA like chromatin remodeling complex associated protein Predicted to be involved in positive regulation of DNA-templated transcription. Part of SWI/SNF complex. [provided by Alliance of Genome Resources, Mar 2025] |
TEDC2 Genetubulin epsilon and delta complex 2 Predicted to be involved in positive regulation of smoothened signaling pathway. Predicted to be located in centriole and cilium. [provided by Alliance of Genome Resources, Mar 2025] |
ABRAXAS1 Geneabraxas 1, BRCA1 A complex subunit This gene encodes a protein that binds to the C-terminal repeats of breast cancer 1 (BRCA1) through a phospho-SXXF motif. The encoded protein recruits ubiquitin interaction motif containing 1 protein to BRCA1 protein and is required for DNA damage resistance, DNA repair, and cell cycle checkpoint control. Pseudogenes of this gene are found on chromosomes 3 and 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
FAAP100 GeneFA core complex associated protein 100 FAAP100 is a component of the Fanconi anemia (FA; MIM 277650) core complex and is required for core complex stability and FANCD2 (see MIM 227646) monoubiquitination (Ling et al., 2007 [PubMed 17396147]).[supplied by OMIM, Mar 2008] |
SKIC2 GeneSKI2 subunit of superkiller complex DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is a human homologue of yeast SKI2 and may be involved in antiviral activity by blocking translation of poly(A) deficient mRNAs. This gene is located in the class III region of the major histocompatibility complex. [provided by RefSeq, Jul 2008] |
SKIC8 GeneSKI8 subunit of superkiller complex WDR61 is a subunit of the human PAF and SKI complexes, which function in transcriptional regulation and are involved in events downstream of RNA synthesis, such as RNA surveillance (Zhu et al., 2005 [PubMed 16024656]).[supplied by OMIM, Mar 2008] |
CSTPP1 Genecentriolar satellite-associated tubulin polyglutamylase complex regulator 1 Enables protein-macromolecule adaptor activity. Involved in regulation of protein complex stability. Is active in centriolar satellite. [provided by Alliance of Genome Resources, Mar 2025] |
SKIC3 GeneSKI3 subunit of superkiller complex This gene encodes a protein with twenty tetratricopeptide (TPR) repeats. Tetratricopeptide repeat containing motifs are found in a variety of proteins and may mediate protein-protein interactions and chaperone activity. Mutations in this gene are associated with trichohepatoenteric syndrome. [provided by RefSeq, Jul 2010] |
FHIP2B GeneFHF complex subunit HOOK interacting protein 2B |
INTS15 Geneintegrator complex subunit 15 Part of integrator complex. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TRAPPC14 Genetrafficking protein particle complex subunit 14 Enables alpha-tubulin binding activity. Involved in cilium assembly and regulation of cell population proliferation. Located in several cellular components, including microtubule cytoskeleton; midbody; and plasma membrane. Part of TRAPPII protein complex. Implicated in primary autosomal recessive microcephaly. [provided by Alliance of Genome Resources, Mar 2025] |
HYCC2 Genehyccin PI4KA lipid kinase complex subunit 2 Predicted to be involved in phosphatidylinositol phosphate biosynthetic process and protein localization to plasma membrane. Predicted to be located in cytosol and membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
VPS50 GeneVPS50 subunit of EARP/GARPII complex Enables SNARE binding activity. Acts upstream of or within endocytic recycling. Located in recycling endosome. Part of EARP complex. [provided by Alliance of Genome Resources, Mar 2025] |
UQCC4 Geneubiquinol-cytochrome c reductase complex assembly factor 4 Predicted to be involved in mitochondrial respiratory chain complex III assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
INTS6L Geneintegrator complex subunit 6 like Predicted to be involved in snRNA 3'-end processing. Predicted to be part of integrator complex. [provided by Alliance of Genome Resources, Mar 2025] |
ODAD4 Geneouter dynein arm docking complex subunit 4 This gene encodes a tetratricopeptide repeat domain-containing protein that localizes to ciliary axonmenes and plays a role in the docking of the outer dynein arm to cilia. Mutations in this gene cause severely reduced ciliary motility and the disorder CILD35 (ciliary dyskinesia,primary, 35). Primary ciliary dyskinesia is often associated with recurrent respiratory infections, immotile spermatozoa, and situs inversus; an inversion in left-right body symmetry. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017] |
WASHC1 GeneWASH complex subunit 1 Enables alpha-tubulin binding activity and ubiquitin protein ligase binding activity. Involved in several processes, including Arp2/3 complex-mediated actin nucleation; endosomal transport; and positive regulation of pseudopodium assembly. Located in several cellular components, including endosome; exocyst; and lamellipodium. Part of WASH complex. [provided by Alliance of Genome Resources, Mar 2025] |
RIMOC1 GeneRAB7A interacting MON1-CCZ1 complex subunit 1 Involved in mitophagy. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
FHIP1B GeneFHF complex subunit HOOK interacting protein 1B The protein encoded by this gene is part of the FTS/Hook/FHIP (FHF) complex, which can interact with members of the homotypic vesicular protein sorting (HOPS) complex. This interaction suggests that the encoded protein is involved in vesicle trafficking. [provided by RefSeq, Dec 2016] |
CPLANE2 Geneciliogenesis and planar polarity effector complex subunit 2 Predicted to enable GTP binding activity. Predicted to be involved in cilium assembly; protein localization; and regulation of vesicle-mediated transport. Predicted to act upstream of or within several processes, including axoneme assembly; endocardial cushion fusion; and regulation of smoothened signaling pathway. Located in centriole; ciliary basal body; and ciliary transition zone. [provided by Alliance of Genome Resources, Mar 2025] |
FHIP1A GeneFHF complex subunit HOOK interacting protein 1A Involved in protein localization to perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
UQCC6 Geneubiquinol-cytochrome c reductase complex assembly factor 6 Involved in mitochondrial cytochrome c oxidase assembly and mitochondrial respiratory chain complex III assembly. Located in mitochondrion. Is active in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025] |
FAAP20 GeneFA core complex associated protein 20 Enables K63-linked polyubiquitin modification-dependent protein binding activity and ubiquitin-modified protein reader activity. Involved in interstrand cross-link repair and translesion synthesis. Located in cell junction; chromosome; and nuclear body. Part of Fanconi anaemia nuclear complex and chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
SHLD1 Geneshieldin complex subunit 1 Involved in negative regulation of double-strand break repair via homologous recombination; positive regulation of double-strand break repair via nonhomologous end joining; and positive regulation of isotype switching. Located in site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
HYCC1 Genehyccin PI4KA lipid kinase complex subunit 1 The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008] |
FHIP2A GeneFHF complex subunit HOOK interacting protein 2A |
ODAD2 Geneouter dynein arm docking complex subunit 2 The protein encoded by this gene contains ten Armadillo repeat motifs (ARMs) and one HEAT repeat, and is thought to be involved in ciliary and flagellar movement. This protein has been shown to localize to the ciliary axonemes and at the ciliary base of respiratory cells. Studies indicate that mutations in this gene cause partial outer dynein arm (ODA) defects in respiratory cilia. The cilia of cells with mutations in this gene displayed either reduced ciliary beat frequency and amplitude, or, complete immotility. Some individuals with primary ciliary dyskensia (PCD) have been shown to have mutations in this gene. PCD is characterized by chronic airway disease and left/right body asymmetry defects. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
NDUFAF8 GeneNADH:ubiquinone oxidoreductase complex assembly factor 8 Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrial matrix. Implicated in nuclear type mitochondrial complex I deficiency 34. [provided by Alliance of Genome Resources, Mar 2025] |
ODAD3 Geneouter dynein arm docking complex subunit 3 This gene encodes a protein containing coiled-coil domains. The encoded protein functions in outer dynein arm assembly and is required for motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014] |
JHY Genejunctional cadherin complex regulator Predicted to be involved in axoneme assembly and brain development. Predicted to act upstream of or within several processes, including cerebrospinal fluid circulation; motile cilium assembly; and regulation of establishment of planar polarity. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
TCP10L3 Genet-complex 10 like 3, pseudogene |
NPIPB2 Genenuclear pore complex interacting protein family member B2 Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
UQCC5 Geneubiquinol-cytochrome c reductase complex assembly factor 5 Enables mitochondrial ribosome binding activity. Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrion. Is active in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SHLD3 Geneshieldin complex subunit 3 Involved in negative regulation of double-strand break repair via homologous recombination; positive regulation of double-strand break repair via nonhomologous end joining; and positive regulation of isotype switching. Located in nucleolus; nucleoplasm; and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB13 Genenuclear pore complex interacting protein family, member B13 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
NPIPB12 Genenuclear pore complex interacting protein family member B12 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SHLD2P3 Geneshieldin complex subunit 2 pseudogene 3 |
NPIPB14P Genenuclear pore complex interacting protein family member B14, pseudogene |
NPIPA6 Genenuclear pore complex interacting protein family, member A6 |
DRC3 Genedynein regulatory complex subunit 3 Located in axoneme. [provided by Alliance of Genome Resources, Mar 2025] |
FERRY3 GeneFERRY endosomal RAB5 effector complex subunit 3 This gene is highly conserved from nematodes to humans. In rat, the orthologous gene encodes a cytoplasmic protein that is involved in mast cell degranulation. The human gene has been implicated in autosomal recessive intellectual disability. [provided by RefSeq, Sep 2016] |
EXOC1L Geneexocyst complex component 1 like |
MSL3B GeneMSL complex subunit 3B Predicted to be involved in chromatin organization and regulation of DNA-templated transcription. Predicted to be located in nucleus. Predicted to be part of MSL complex and NuA4 histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
DRC5 Genedynein regulatory complex subunit 5 Predicted to be involved in flagellated sperm motility. Predicted to be located in sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
DRC2 Genedynein regulatory complex subunit 2 |
DRC9 Genedynein regulatory complex subunit 9 Enables Hsp70 protein binding activity and calmodulin binding activity. Predicted to be involved in sperm axoneme assembly. Located in actin cytoskeleton and cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
DRC4 Genedynein regulatory complex subunit 4 |
DRC10 Genedynein regulatory complex subunit 10 Located in ciliary basal body. [provided by Alliance of Genome Resources, Mar 2025] |
DRC8 Genedynein regulatory complex subunit 8 |
DRC11 Genedynein regulatory complex subunit 11 |
DRC11L Genedynein regulatory complex subunit 11 like Predicted to enable ATP hydrolysis activity and microtubule severing ATPase activity. Predicted to be involved in microtubule cytoskeleton organization. [provided by Alliance of Genome Resources, Mar 2025] |
TSLIG1 GenetRNA splicing ligase complex subunit 1 Predicted to enable metal ion binding activity. Involved in tRNA splicing, via endonucleolytic cleavage and ligation. Part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
TSLIG3B GenetRNA splicing ligase complex subunit 3B Enables identical protein binding activity and protein methyltransferase activity. Involved in positive regulation of cell population proliferation; positive regulation of gene expression; and protein methylation. Located in cytoplasm and nucleoplasm. Part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
TSLIG2 GenetRNA splicing ligase complex subunit 2 Predicted to be involved in tRNA splicing, via endonucleolytic cleavage and ligation. Located in nucleoplasm. Part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
CNOT12 GeneCCR4-NOT transcription complex subunit 12 Enables ankyrin repeat binding activity and enzyme binding activity. Involved in cellular response to ionizing radiation; double-strand break repair; and positive regulation of protein phosphorylation. Located in several cellular components, including adherens junction; heterochromatin; and nucleus. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Mar 2025] |
TSLIG3C GenetRNA splicing ligase complex subunit 3C Predicted to be part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
TSLIG3A GenetRNA splicing ligase complex subunit 3A Enables protein methyltransferase activity. Involved in positive regulation of cell population proliferation; positive regulation of gene expression; and protein methylation. Predicted to be part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
iga immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the iga immunoglobulin complex, circulating cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
iga immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the iga immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
iga immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the iga immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
IgA immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the IgA immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
IgA immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the IgA immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
IgA immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the IgA immunoglobulin complex, circulating cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
IgA immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgA immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
secretory iga immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the secretory iga immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
monomeric iga immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the monomeric iga immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
iga immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the iga immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
dimeric iga immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dimeric iga immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
secretory dimeric iga immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the secretory dimeric iga immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
polymeric iga immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the polymeric iga immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
secretory iga immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the secretory iga immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
iga immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the iga immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
polymeric iga immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the polymeric iga immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
secretory iga immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the secretory iga immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
monomeric iga immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the monomeric iga immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
iga immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the iga immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
dimeric iga immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the dimeric iga immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
secretory dimeric iga immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the secretory dimeric iga immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
polymeric iga immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the polymeric iga immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
monomeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the monomeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
dimeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the dimeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
secretory IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the secretory IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
secretory dimeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the secretory dimeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
polymeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the polymeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
monomeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the monomeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
dimeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the dimeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
secretory IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the secretory IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
secretory dimeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the secretory dimeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
polymeric IgA immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the polymeric IgA immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the IgA immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Secretory dimeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Secretory dimeric IgA immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Secretory IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Secretory IgA immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Polymeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Polymeric IgA immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Monomeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Monomeric IgA immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Dimeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Dimeric IgA immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgA immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Monomeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Monomeric IgA immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Secretory dimeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Secretory dimeric IgA immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Dimeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Dimeric IgA immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Secretory IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Secretory IgA immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Polymeric IgA immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Polymeric IgA immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
glomerulonephritis, iga; iga glomerulonephritides; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; henoch-schoenlein purpura; iga glomerulonephritides; nephritis; purpura, schoenlein-henoch Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; henoch-schoenlein purpura; iga glomerulonephritides; nephritis; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; iga glomerulonephritides; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; hypertension; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; hypertension; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; iga glomerulonephritides; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; iga glomerulonephritides; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; iga glomerulonephritides; nephrotic syndrome; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; nephrotic syndrome; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
focal segmental glomsclerosis; glomerulonephritis, iga; glomerulosclerosis, focal segmental; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulonephritis, iga; glomerulosclerosis, focal segmental; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; iga glomerulonephritides; lupus nephritis; nephritis sle Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; lupus nephritis; nephritis sle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Composite immunoglobulin trait (IgA x IgG) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Composite immunoglobulin trait (IgA x IgG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Composite immunoglobulin trait (IgA/IgG) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Composite immunoglobulin trait (IgA/IgG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Composite immunoglobulin trait (IgA x IgG x IgM) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Composite immunoglobulin trait (IgA x IgG x IgM) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Composite immunoglobulin trait (IgA/IgM) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Composite immunoglobulin trait (IgA/IgM) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Composite immunoglobulin trait (IgA x IgG/IgM) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Composite immunoglobulin trait (IgA x IgG/IgM) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the immunoglobulin complex, circulating cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
igm immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the igm immunoglobulin complex, circulating cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
ige immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ige immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
igm immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the igm immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
IgM immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the IgM immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
IgM immunoglobulin complex, circulating Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the IgM immunoglobulin complex, circulating cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Immunoglobulin complex, circulating cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
IgM immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the IgM immunoglobulin complex, circulating cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgG immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgG immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgM immunoglobulin complex, circulating Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgM immunoglobulin complex, circulating cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
igg immunoglobulin transcytosis in epithelial cells mediated by fcrn immunoglobulin receptor Gene SetFrom GO Biological Process Annotations 2015 genes participating in the igg immunoglobulin transcytosis in epithelial cells mediated by fcrn immunoglobulin receptor biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin production involved in immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin production involved in immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor Gene SetFrom GO Biological Process Annotations 2023 genes participating in the immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor biological process from the curated GO Biological Process Annotations 2023 dataset. |
IgG immunoglobulin transcytosis in epithelial cells mediated by FcRn immunoglobulin receptor Gene SetFrom GO Biological Process Annotations 2023 genes participating in the IgG immunoglobulin transcytosis in epithelial cells mediated by FcRn immunoglobulin receptor biological process from the curated GO Biological Process Annotations 2023 dataset. |
immunoglobulin production involved in immunoglobulin-mediated immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the immunoglobulin production involved in immunoglobulin-mediated immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor Gene SetFrom GO Biological Process Annotations 2025 genes participating in the immunoglobulin transcytosis in epithelial cells mediated by polymeric immunoglobulin receptor biological process from the curated GO Biological Process Annotations 2025 dataset. |
IgG immunoglobulin transcytosis in epithelial cells mediated by FcRn immunoglobulin receptor Gene SetFrom GO Biological Process Annotations 2025 genes participating in the IgG immunoglobulin transcytosis in epithelial cells mediated by FcRn immunoglobulin receptor biological process from the curated GO Biological Process Annotations 2025 dataset. |
immunoglobulin production involved in immunoglobulin-mediated immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the immunoglobulin production involved in immunoglobulin-mediated immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2015 dataset. |
humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2015 dataset. |
humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2023 dataset. |
humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of humoral immune response mediated by circulating immunoglobulin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of humoral immune response mediated by circulating immunoglobulin biological process from the curated GO Biological Process Annotations 2025 dataset. |
iga b cell receptor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the iga b cell receptor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
IgA B cell receptor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgA B cell receptor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
pentameric igm immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pentameric igm immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
igm immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the igm immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
hexameric igm immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the hexameric igm immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
igd immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the igd immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
igg immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the igg immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
igm immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the igm immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
ige immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ige immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
heavy chain immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the heavy chain immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
igy immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the igy immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
pentameric igm immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the pentameric igm immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
igm immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the igm immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
hexameric igm immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the hexameric igm immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Immunoglobulin/major histocompatibility complex, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin/major histocompatibility complex, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
hexameric IgM immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the hexameric IgM immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
pentameric IgM immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the pentameric IgM immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
hexameric IgM immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the hexameric IgM immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
pentameric IgM immunoglobulin complex Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the pentameric IgM immunoglobulin complex cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
IgM immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the IgM immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Pentameric IgM immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Pentameric IgM immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
IgG immunoglobulin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the IgG immunoglobulin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgM immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgM immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgE immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgE immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgG immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgG immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Heavy chain immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Heavy chain immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgD immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgD immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgW immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgW immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgZ immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgZ immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgY immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgY immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Hexameric IgM immunoglobulin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Hexameric IgM immunoglobulin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgD immunoglobulin complex, GPI-anchored Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the IgD immunoglobulin complex, GPI-anchored cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
IgA Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease IgA Deficiency from the curated CTD Gene-Disease Associations dataset. |
Glomerulonephritis, IGA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulonephritis, IGA from the curated CTD Gene-Disease Associations dataset. |
Glomerulonephritis, IGA Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Glomerulonephritis, IGA in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
iga glomerulonephritis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease iga glomerulonephritis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
iga glomerulonephritis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease iga glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
selective iga deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease selective iga deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
iga deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; iga deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; iga deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; kidney failure, chronic; polycystic kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; kidney failure, chronic; polycystic kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, iga Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, iga in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iga deficiency and common variable immunodeficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iga deficiency and common variable immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
systemic lupus erythematosus; nephropathy, iga Gene SetFrom GAD Gene-Disease Associations genes associated with the disease systemic lupus erythematosus; nephropathy, iga in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; common variable immunodeficiency; iga deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; common variable immunodeficiency; iga deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iga, igd, igg, igm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iga, igd, igg, igm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iga Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term iga in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
positive regulation of isotype switching to iga isotypes Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of isotype switching to iga isotypes biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of isotype switching to iga isotypes Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of isotype switching to iga isotypes biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of isotype switching to iga isotypes Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of isotype switching to iga isotypes biological process from the curated GO Biological Process Annotations 2015 dataset. |
iga binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iga binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Serum IgA levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Serum IgA levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
IgA nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the IgA nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
selective iga deficiency disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease selective iga deficiency disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
iga glomerulonephritis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease iga glomerulonephritis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
iga deficiency Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the iga deficiency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
iga deposition in the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the iga deposition in the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
iga deficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the iga deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased iga level Gene SetFrom HPO Gene-Disease Associations genes associated with the increased iga level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
IgA Deficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the IgA Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Glomerulonephritis, IGA Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Glomerulonephritis, IGA phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal iga level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal iga level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased iga level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased iga level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased iga level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased iga level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iga nephropathy, susceptibility to, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the iga nephropathy, susceptibility to, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{iga nephropathy, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {iga nephropathy, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Iga Glomerulonephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iga Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iga Myeloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iga Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Linear Iga Bullous Dermatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Linear Iga Bullous Dermatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iga Pemphigus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iga Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iga Nephropathy, Susceptibility To, 3 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iga Nephropathy, Susceptibility To, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Iga Deficiency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Iga Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Iga Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Iga Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iga Deposition In The Glomerulus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iga Deposition In The Glomerulus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
positive regulation of isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2023 dataset. |
isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2023 genes participating in the isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2023 dataset. |
IgA binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the IgA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
increased IgA level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased IgA level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased IgA level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased IgA level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Tonsil - L2 - Mature IgA+ PC Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - Mature IgA+ PC cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Tonsil - L2 - MBC derived IgA+ PC Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Tonsil - L2 - MBC derived IgA+ PC cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
IgA memory B cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the IgA memory B cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
IgA lamina propria lymphocyte_Small intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the IgA lamina propria lymphocyte_Small intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
IgA+ Regulatory B cell_Intestine_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the IgA+ Regulatory B cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
positive regulation of isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2025 dataset. |
isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2025 genes participating in the isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of isotype switching to IgA isotypes Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of isotype switching to IgA isotypes biological process from the curated GO Biological Process Annotations 2025 dataset. |
IgA binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the IgA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
IgA receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the IgA receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
IgA glomerulonephritis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease IgA glomerulonephritis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
IgA glomerulonephritis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease IgA glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Selective IgA deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Selective IgA deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
IgA pemphigus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease IgA pemphigus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
IgA nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the IgA nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Serum IgA levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum IgA levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
IgA levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the IgA levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Serum galactose-deficient IgA1 levels in IgA nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum galactose-deficient IgA1 levels in IgA nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Selective IgA deficiency Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Selective IgA deficiency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intestinal immune network for IgA production Gene SetFrom KEGG Pathways 2026 proteins participating in the Intestinal immune network for IgA production pathway from the KEGG Pathways 2026 dataset. |
Immunoglobulin a deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunoglobulin a deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
Immunoglobulin a deficiency 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunoglobulin a deficiency 1 from the curated CTD Gene-Disease Associations dataset. |
Immunoglobulin E Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Immunoglobulin E in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Immunoglobulin A Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Immunoglobulin A in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
immunoglobulin alpha deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease immunoglobulin alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
selective immunoglobulin deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease selective immunoglobulin deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Intravenous Immunoglobulin Gene Setinteracting proteins for the Intravenous Immunoglobulin drug from the curated DrugBank Drug Targets dataset. |
immunoglobulin e receptor-mediated histamine release from basophils Gene SetFrom GAD Gene-Disease Associations genes associated with the disease immunoglobulin e receptor-mediated histamine release from basophils in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
immunoglobulin e Gene SetFrom GAD Gene-Disease Associations genes associated with the disease immunoglobulin e in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
immunoglobulin a Gene SetFrom GAD Gene-Disease Associations genes associated with the disease immunoglobulin a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
immunoglobulin Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term immunoglobulin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of immunoglobulin biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of immunoglobulin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
somatic recombination of immunoglobulin gene segments Gene SetFrom GO Biological Process Annotations 2015 genes participating in the somatic recombination of immunoglobulin gene segments biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin production biological process from the curated GO Biological Process Annotations 2015 dataset. |
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2015 genes participating in the adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin transcytosis in epithelial cells Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin transcytosis in epithelial cells biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2015 dataset. |
somatic recombination of immunoglobulin genes involved in immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the somatic recombination of immunoglobulin genes involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of immunoglobulin secretion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of immunoglobulin secretion biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin secretion involved in immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin secretion involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of immunoglobulin secretion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of immunoglobulin secretion biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin secretion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin secretion biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin v(d)j recombination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin v(d)j recombination biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2015 dataset. |
somatic hypermutation of immunoglobulin genes Gene SetFrom GO Biological Process Annotations 2015 genes participating in the somatic hypermutation of immunoglobulin genes biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of immunoglobulin secretion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of immunoglobulin secretion biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of immunoglobulin biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of immunoglobulin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
immunoglobulin receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the immunoglobulin receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
polymeric immunoglobulin receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the polymeric immunoglobulin receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
immunoglobulin receptor binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the immunoglobulin receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
immunoglobulin binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the immunoglobulin binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Immunoglobulin A Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Immunoglobulin A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
immunoglobulin alpha deficiency Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease immunoglobulin alpha deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
selective immunoglobulin deficiency disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease selective immunoglobulin deficiency disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
immunoglobulin igg2 deficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the immunoglobulin igg2 deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
High affinity immunoglobulin epsilon receptor subunit beta Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High affinity immunoglobulin epsilon receptor subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin C1-set Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin C1-set protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin C2-set Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin C2-set protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin V-set domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin V-set domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin J chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin J chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin subtype Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin subtype protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
V-set and immunoglobulin domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the V-set and immunoglobulin domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycoside hydrolase, family 2/20, immunoglobulin-like beta-sandwich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, family 2/20, immunoglobulin-like beta-sandwich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin I-set Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin I-set protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin C2-set-like, ligand-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin C2-set-like, ligand-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin-like fold Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin-like fold protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CD80-like, immunoglobulin C2-set Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CD80-like, immunoglobulin C2-set protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CD47 immunoglobulin-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CD47 immunoglobulin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adhesion molecule, immunoglobulin-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adhesion molecule, immunoglobulin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Natural killer cell receptor 2B4 immunoglobulin domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Natural killer cell receptor 2B4 immunoglobulin domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin subtype 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin subtype 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alpha-1B-glycoprotein/leukocyte immunoglobulin-like receptor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha-1B-glycoprotein/leukocyte immunoglobulin-like receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Immunoglobulin E-set Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Immunoglobulin E-set protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycoside hydrolase, family 2, immunoglobulin-like beta-sandwich Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoside hydrolase, family 2, immunoglobulin-like beta-sandwich protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal immunoglobulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased immunoglobulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased immunoglobulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immunoglobulin v(d)j recombination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin v(d)j recombination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immunoglobulin transcytosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin transcytosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immunoglobulin heavy chain v(d)j recombination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin heavy chain v(d)j recombination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased immunoglobulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased immunoglobulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immunoglobulin light chain v-j recombination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin light chain v-j recombination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
immunoglobulin a deficiency 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunoglobulin a deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunoglobulin a deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunoglobulin a deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
Primary Immunoglobulin A Nephropathy (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Immunoglobulin A Nephropathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Selective Immunoglobulin A Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Selective Immunoglobulin A Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Granulocytopenia With Immunoglobulin Abnormality Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Granulocytopenia With Immunoglobulin Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Immunoglobulin A Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Immunoglobulin A Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Monoclonal Immunoglobulin M Proteinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Monoclonal Immunoglobulin M Proteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Immunoglobulin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Immunoglobulin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
stimulatory killer cell immunoglobulin-like receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stimulatory killer cell immunoglobulin-like receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
somatic hypermutation of immunoglobulin genes Gene SetFrom GO Biological Process Annotations 2023 genes participating in the somatic hypermutation of immunoglobulin genes biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2023 dataset. |
immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
immunoglobulin V(D)J recombination Gene SetFrom GO Biological Process Annotations 2023 genes participating in the immunoglobulin V(D)J recombination biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
somatic recombination of immunoglobulin gene segments Gene SetFrom GO Biological Process Annotations 2023 genes participating in the somatic recombination of immunoglobulin gene segments biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2023 dataset. |
somatic recombination of immunoglobulin genes involved in immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the somatic recombination of immunoglobulin genes involved in immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2023 genes participating in the adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2023 dataset. |
immunoglobulin receptor binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the immunoglobulin receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
polymeric immunoglobulin receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the polymeric immunoglobulin receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
immunoglobulin receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the immunoglobulin receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal immunoglobulin V(D)J recombination Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin V(D)J recombination phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased immunoglobulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased immunoglobulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immunoglobulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal glomerular immunoglobulin deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerular immunoglobulin deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased immunoglobulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased immunoglobulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immunoglobulin transcytosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin transcytosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immunoglobulin heavy chain V(D)J recombination Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin heavy chain V(D)J recombination phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immunoglobulin light chain V-J recombination Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin light chain V-J recombination phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
stimulatory killer cell immunoglobulin-like receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stimulatory killer cell immunoglobulin-like receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
somatic hypermutation of immunoglobulin genes Gene SetFrom GO Biological Process Annotations 2025 genes participating in the somatic hypermutation of immunoglobulin genes biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2025 dataset. |
immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
immunoglobulin V(D)J recombination Gene SetFrom GO Biological Process Annotations 2025 genes participating in the immunoglobulin V(D)J recombination biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
somatic recombination of immunoglobulin gene segments Gene SetFrom GO Biological Process Annotations 2025 genes participating in the somatic recombination of immunoglobulin gene segments biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2025 dataset. |
somatic recombination of immunoglobulin genes involved in immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the somatic recombination of immunoglobulin genes involved in immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2025 genes participating in the adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of immunoglobulin production Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of immunoglobulin production biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of immunoglobulin mediated immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of immunoglobulin mediated immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of immunoglobulin production in mucosal tissue Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of immunoglobulin production in mucosal tissue biological process from the curated GO Biological Process Annotations 2025 dataset. |
immunoglobulin receptor binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the immunoglobulin receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
polymeric immunoglobulin binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the polymeric immunoglobulin binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
polymeric immunoglobulin receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the polymeric immunoglobulin receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
immunoglobulin receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the immunoglobulin receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Immunoglobulin alpha deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin alpha deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin light chain amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin light chain amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Selective immunoglobulin deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Selective immunoglobulin deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin heavy-and-light chain Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin heavy-and-light chain in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin heavy chain amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin heavy chain amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunoglobulin A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Immunoglobulin-mediated membranoproliferative glomerulonephritis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunoglobulin-mediated membranoproliferative glomerulonephritis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
T-Cell Immunoglobulin and Mucin domain 1 levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the T-Cell Immunoglobulin and Mucin domain 1 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin G index levels in multiple sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin G index levels in multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Composite immunoglobulin trait (IgG/IgM) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Composite immunoglobulin trait (IgG/IgM) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin A Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin measurement (zinc sulfate turbidity test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin measurement (zinc sulfate turbidity test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin M against phosphorylcholine (IgM anti-PC) levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin M against phosphorylcholine (IgM anti-PC) levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to intravenous immunoglobulin treatment in Kawasaki disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to intravenous immunoglobulin treatment in Kawasaki disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin A vasculitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin A vasculitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (liver involvement) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (liver involvement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thymic Factor, Circulating Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Thymic Factor, Circulating from the curated CTD Gene-Chemical Interactions dataset. |
circulating protein c levels and thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease circulating protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased circulating c4 and predominant mesangial c4 deposition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased circulating c4 and predominant mesangial c4 deposition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased circulating high density lipoprotein cholesterol levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased circulating high density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased number of circulating vldl and idl particles Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased number of circulating vldl and idl particles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
circulating levels of plasminogen activator inhibitor-1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease circulating levels of plasminogen activator inhibitor-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
circulating fibrinogen levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease circulating fibrinogen levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
circulating Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term circulating in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of vasoconstriction by circulating norepinephrine Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of vasoconstriction by circulating norepinephrine biological process from the curated GO Biological Process Annotations 2015 dataset. |
Circulating myeloperoxidase levels (plasma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Circulating myeloperoxidase levels (plasma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Circulating vasoactive peptide levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Circulating vasoactive peptide levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Circulating myeloperoxidase levels (serum) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Circulating myeloperoxidase levels (serum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating leptin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
decreased circulating aldosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased circulating aldosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased circulating cortisol level Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased circulating cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating protein level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased circulating very-low-density lipoprotein cholesterol Gene SetFrom HPO Gene-Disease Associations genes associated with the increased circulating very-low-density lipoprotein cholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating hormone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating adrenocorticotropin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating adrenocorticotropin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating renin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased circulating acth level Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased circulating acth level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased circulating renin level Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased circulating renin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased circulating renin level Gene SetFrom HPO Gene-Disease Associations genes associated with the increased circulating renin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased circulating cortisol level Gene SetFrom HPO Gene-Disease Associations genes associated with the increased circulating cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating aldosterone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating creatinine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating leptin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating leptin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated circulating catecholamine level Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated circulating catecholamine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating fibrinogen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased circulating acth level Gene SetFrom HPO Gene-Disease Associations genes associated with the increased circulating acth level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating enzyme level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating enzyme level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated circulating parathyroid hormone (pth) level Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated circulating parathyroid hormone (pth) level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating glucocorticoid level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating catecholamine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating catecholamine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Neoplasm Circulating Cells Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasm Circulating Cells phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neoplastic Cells, Circulating Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplastic Cells, Circulating phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
decreased circulating thyroid-stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating thyroid-stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interferon-alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-12 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-2 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-2 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent circulating noradrenaline Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent circulating noradrenaline phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating prolactin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating prolactin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating ghrelin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating haptoglobin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating haptoglobin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating estradiol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating complement protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucagon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating serum albumin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating serum albumin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pyruvate kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pyruvate kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
suppressed circulating follicle stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the suppressed circulating follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating prothrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating prothrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating creatine kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating magnesium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating gastrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating gastrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating ketone body level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sodium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sodium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating magnesium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating factor ix level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating factor ix level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating chloride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-17 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-17 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating atrial natriuretic factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating atrial natriuretic factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating gonadotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating gonadotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating corticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating unsaturated transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating unsaturated transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating alanine transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating alanine transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating unsaturated transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating unsaturated transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pituitary hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-17 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-17 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating total protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating complement protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating bicarbonate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating noradrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating glycerol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-13 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-13 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating adrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating apolipoprotein e level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating apolipoprotein e level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-18 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-18 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating amylase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating amylase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating atrial natriuretic factor Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating atrial natriuretic factor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating pituitary hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-10 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-10 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-1 beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-1 beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating dihydrotestosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating dihydrotestosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-4 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-4 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-16 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-16 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating vldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating vldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating creatine kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-6 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-6 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating antithrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating antithrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating progesterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating renin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-6 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-6 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating gonadotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating gonadotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-12 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating c-reactive protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating c-reactive protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating corticotropin-releasing hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating corticotropin-releasing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating insulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating insulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating potassium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ketone body level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating alkaline phosphatase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating alkaline phosphatase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating glucagon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating creatine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating calcium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating glucocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating insulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating insulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating ghrelin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interferon-gamma level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-gamma level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-4 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-4 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating total protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating bilirubin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating ferritin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating erythropoietin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating erythropoietin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-5 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-5 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating prothrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating prothrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating ceruloplasmin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ceruloplasmin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating mineralocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating apolipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating apolipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-13 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-13 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-10 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-10 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating glutamate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating glutamate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating hdl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating testosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating testosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-16 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-16 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating prolactin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating prolactin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ghrelin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating potassium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating ammonia level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-1 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-1 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating adrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating parathyroid hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating parathyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating adrenocorticotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating estrogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating estrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating glucagon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent circulating adrenaline Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent circulating adrenaline phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating potassium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating adrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating amylase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating amylase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-2 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-2 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating hdl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating serum amyloid protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating serum amyloid protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating ldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating ldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating free fatty acids level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating dihydrotestosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating dihydrotestosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating erythropoietin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating erythropoietin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating bicarbonate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-12b level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-12b level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating phospholipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating phospholipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating phosphate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating gastrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating gastrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating estrogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating estrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating phospholipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating phospholipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-18 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-18 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating parathyroid hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating parathyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating glycerol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating corticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating testosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating testosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating mineral level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating mineral level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating pituitary hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating ferritin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-4 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-4 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating alkaline phosphatase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating alkaline phosphatase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating vldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating vldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating androgen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating androgen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating luteinizing hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ferritin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating noradrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating phospholipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating phospholipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating glucocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating estradiol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating fructosamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating fructosamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating fibrinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating fibrinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating renin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon-beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon-beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating levels of thyroid hormone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating levels of thyroid hormone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating calcium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-9 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-9 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating cytokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating cytokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating plant sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating plant sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating bilirubin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating carnitine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating carnitine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating alkaline phosphatase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating alkaline phosphatase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interferon-beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interferon-beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-3 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-3 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-3 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-3 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating growth hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating growth hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating parathyroid hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating parathyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating vldl triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating vldl triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-18 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-18 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating leptin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating leptin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-13 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-13 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating hdl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating free fatty acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating free fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ammonia level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating creatine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating non-hdl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating non-hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating factor ix level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating factor ix level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating bicarbonate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating dihydrotestosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating dihydrotestosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating lactate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating lactate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-12b level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-12b level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating creatine kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-6 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-6 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating free fatty acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating free fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-10 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-10 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating bilirubin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating phosphate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating leptin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating leptin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating mineralocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating gastrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating gastrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating insulin-like growth factor i level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating insulin-like growth factor i level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating calcium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating total protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating thyroid-stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating thyroid-stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating aspartate transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating aspartate transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating corticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating chloride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating serum albumin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating serum albumin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating creatine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interferon-gamma level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interferon-gamma level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating follicle stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-5 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-5 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating creatinine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating thyroxine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating thyroxine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating testosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating testosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating carnitine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating carnitine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating progesterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating follicle stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating magnesium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating vldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating vldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating lipase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating lipase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interferon-alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interferon-alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating homocysteine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating homocysteine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating levels of thyroid hormone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating levels of thyroid hormone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating carnitine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating carnitine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating mineralocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon-gamma level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon-gamma level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating fructosamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating fructosamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating estradiol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-1 beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-1 beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating fructosamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating fructosamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating renin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating amino acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating amino acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating antithrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating antithrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating insulin-like growth factor i level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating insulin-like growth factor i level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating aspartate transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating aspartate transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating serum albumin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating serum albumin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating ketone body level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating amylase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating amylase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating luteinizing hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glutamate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glutamate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating fibrinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating fibrinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-12 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating aspartate transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating aspartate transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon-alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon-alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating osteocalcin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating osteocalcin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interleukin-17 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-17 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating interferon-beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating unsaturated transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating unsaturated transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating ldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating estrogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating estrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating sodium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating sodium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating lactate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating lactate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating sodium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating sodium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating vldl triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating vldl triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating insulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating insulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-5 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-5 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating adrenocorticotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating thyroxine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating thyroxine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating alanine transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating alanine transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating enzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating enzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating interleukin-2 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating interleukin-2 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating gonadotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating gonadotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating growth hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating growth hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased fasted circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating factor viii level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating factor viii level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-12b level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-12b level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-9 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-9 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating atrial natriuretic factor Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating atrial natriuretic factor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fasted circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased fasted circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating phosphate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating creatinine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating noradrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating progesterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chloride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating factor viii level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating factor viii level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating plant sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating plant sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glycerol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating thyroxine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating thyroxine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating leptin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating leptin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating insulin-like growth factor i level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating insulin-like growth factor i level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating alanine transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating alanine transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[sex hormone-binding blobulin circulating level qtl 1] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [sex hormone-binding blobulin circulating level qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Abnormal Circulating Renin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Circulating Renin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Decreased Circulating Aldosterone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Aldosterone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Cortisol Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Cortisol Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Circulating Enzyme Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Circulating Enzyme Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Free Fatty Acid Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Free Fatty Acid Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Acth Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Acth Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Acth Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Acth Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Parathyroid Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Parathyroid Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Cortisol Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Cortisol Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Circulating Insulin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Circulating Insulin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Follicle Stimulating Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Follicle Stimulating Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Luteinizing Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Luteinizing Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Circulating Follicle Stimulating Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Circulating Follicle Stimulating Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Circulating Luteinizing Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Circulating Luteinizing Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Renin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Renin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Gonadotropin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Gonadotropin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Circulating Parathyroid Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Circulating Parathyroid Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Beta-2-Microglobulin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Beta-2-Microglobulin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Renin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Renin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Androgen Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Androgen Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Circulating Aldosterone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Circulating Aldosterone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Androgen Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Androgen Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Progesterone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Progesterone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Circulating Follicle-Stimulating Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Circulating Follicle-Stimulating Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Osteocalcin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Osteocalcin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Proportion Circulating T-Helper Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Proportion Circulating T-Helper Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Gonadotropin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Gonadotropin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Circulating Cortisol Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Circulating Cortisol Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Circulating Leptin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Circulating Leptin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Circulating Adrenocorticotropin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Circulating Adrenocorticotropin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Circulating Dehydroepiandrosterone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Circulating Dehydroepiandrosterone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Circulating Ribitol Concentration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Circulating Ribitol Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Circulating Catecholamine Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Circulating Catecholamine Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Circulating Thyroglobulin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Circulating Thyroglobulin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
decreased circulating growth hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating growth hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating HDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating HDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating HDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating HDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating insulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating insulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating insulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating insulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating phosphate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating phosphate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating follicle stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating follicle stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating luteinizing hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating luteinizing hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating alkaline phosphatase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating alkaline phosphatase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating alkaline phosphatase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating alkaline phosphatase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating insulin-like growth factor I level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating insulin-like growth factor I level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating amino acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating amino acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating ammonia level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating ammonia level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating citrulline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating citrulline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating ornithine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating ornithine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating ornithine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating ornithine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating arginine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating arginine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating phenylalanine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating phenylalanine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating LDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating LDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating VLDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating VLDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating creatinine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating creatinine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating free fatty acids level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating corticosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating corticosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating free fatty acids level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating leptin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating leptin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-6 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-6 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-12 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-12 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating glucagon level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating glucagon level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating insulin-like growth factor I level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating insulin-like growth factor I level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating free fatty acids level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating antidiuretic hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating antidiuretic hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating renin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating renin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating ketone body level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating ketone body level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating tumor necrosis factor level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating tumor necrosis factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating tumor necrosis factor level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating tumor necrosis factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating phospholipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating phospholipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating testosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating testosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating LDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating LDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating VLDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating VLDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating sodium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating sodium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating chloride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating chloride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating bicarbonate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating bicarbonate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating leptin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating leptin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating adiponectin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating adiponectin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent circulating adrenaline Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent circulating adrenaline phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent circulating noradrenaline Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent circulating noradrenaline phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating enzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating enzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating bilirubin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating bilirubin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating HDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating HDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating LDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating LDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating follicle stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating follicle stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating growth hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating growth hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating estradiol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating estradiol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating cysteine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating cysteine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating parathyroid hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating parathyroid hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating magnesium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating magnesium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating creatine kinase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating creatine kinase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating pyruvate kinase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating pyruvate kinase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating serum albumin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating serum albumin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating tyrosine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating tyrosine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating progesterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating progesterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating progesterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating progesterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interferon-gamma level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interferon-gamma level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-6 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-6 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating serum amyloid protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating serum amyloid protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating aldosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating aldosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating renin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating renin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating mineral level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating mineral level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating luteinizing hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating luteinizing hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating prolactin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating prolactin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating potassium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating potassium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating sodium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating sodium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating estradiol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating estradiol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating phospholipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating phospholipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating testosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating testosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating gastrin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating gastrin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating total protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating total protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating homocysteine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating homocysteine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating osteocalcin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating osteocalcin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating alanine transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating alanine transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating alanine transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating alanine transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating ferritin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating ferritin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating carnitine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating carnitine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating adrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating adrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating ketone body level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating ketone body level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-1 beta level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-1 beta level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating aspartate transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating aspartate transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating thyroid-stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating thyroid-stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating thyroxine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating thyroxine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating proline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating proline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating prolactin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating prolactin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating dihydrotestosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating dihydrotestosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating serum albumin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating serum albumin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating total protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating total protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
suppressed circulating follicle stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the suppressed circulating follicle stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating homocysteine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating homocysteine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating methionine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating methionine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-3 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-3 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating VLDL triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating VLDL triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating citrulline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating citrulline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating bilirubin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating bilirubin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating alanine transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating alanine transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating alkaline phosphatase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating alkaline phosphatase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating aspartate transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating aspartate transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-13 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-13 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating triiodothyronine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating triiodothyronine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interferon-gamma level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interferon-gamma level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased fasting circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fasting circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating triiodothyronine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating triiodothyronine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating levels of thyroid hormone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating levels of thyroid hormone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating corticosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating corticosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating adrenocorticotropin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating adrenocorticotropin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating arginine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating arginine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating potassium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating potassium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating adrenocorticotropin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating adrenocorticotropin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating estrogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating estrogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating thyroid-stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating thyroid-stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating thyroxine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating thyroxine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating sodium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating sodium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating potassium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating potassium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating aldosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating aldosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating progesterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating progesterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-1 alpha level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-1 alpha level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-1 beta level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-1 beta level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating estrogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating estrogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-4 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-4 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating renin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating renin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating corticotropin-releasing hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating corticotropin-releasing hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating complement protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating glycerol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glycerol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating osteocalcin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating osteocalcin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating serum albumin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating serum albumin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating creatinine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating creatinine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating histidine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating histidine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating proline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating proline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating CXCL10 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating CXCL10 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating carnitine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating carnitine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating VLDL triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating VLDL triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating lactate dehydrogenase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating lactate dehydrogenase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating haptoglobin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating haptoglobin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating tumor necrosis factor level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating tumor necrosis factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating phosphate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating phosphate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating ferritin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating ferritin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating pituitary hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating pituitary hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating glucagon level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glucagon level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-1 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-1 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating adiponectin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating adiponectin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating von Willebrand factor level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating von Willebrand factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating cytokine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating cytokine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-10 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-10 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating antidiuretic hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating antidiuretic hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating phytosterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating phytosterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating phytosterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating phytosterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-12 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-12 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating insulin-like growth factor I level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating insulin-like growth factor I level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating parathyroid hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating parathyroid hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating taurine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating taurine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating glycine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glycine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating insulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating insulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating gastrin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating gastrin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating lactate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating lactate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating alanine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating alanine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating magnesium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating magnesium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating ketone body level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating ketone body level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating corticosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating corticosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating estradiol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating angiotensin II level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating angiotensin II level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating ghrelin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating ghrelin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interferon-alpha level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interferon-alpha level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating type I collagen C-terminal telopeptide level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating type I collagen C-terminal telopeptide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating creatine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating creatine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating ceruloplasmin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating ceruloplasmin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating glycerol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating glycerol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-4 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-4 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-5 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-5 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating histamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating histamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating amylase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating amylase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating type I collagen C-terminal telopeptide level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating type I collagen C-terminal telopeptide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating adrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating adrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-12b level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-12b level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased fasting circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fasting circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating magnesium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating magnesium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating serine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating serine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating glutamic acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glutamic acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating gonadotropin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating gonadotropin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating creatinine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating creatinine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating dihydrotestosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating dihydrotestosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating cortisol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating cortisol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-12b level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-12b level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interferon level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interferon level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating phospholipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating phospholipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-16 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-16 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating chloride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating chloride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating serum amyloid protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating serum amyloid protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating tyrosine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating tyrosine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating phenylalanine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating phenylalanine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating angiotensinogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating angiotensinogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating aspartate transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating aspartate transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-6 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-6 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating serum amyloid protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating serum amyloid protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating noradrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating noradrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating glutamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating glutamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating cysteine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating cysteine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating angiotensinogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating angiotensinogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating haptoglobin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating haptoglobin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating phosphate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating phosphate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating antithrombin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating antithrombin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-2 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-2 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating atrial natriuretic factor Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating atrial natriuretic factor phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating amylase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating amylase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating hypoxanthine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating hypoxanthine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating xanthine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating xanthine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating noradrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating noradrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating glutamate dehydrogenase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating glutamate dehydrogenase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating leptin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating leptin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating chemokine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating adrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating adrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating noradrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating noradrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating homocysteine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating homocysteine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating creatine kinase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating creatine kinase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating lactate dehydrogenase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating lactate dehydrogenase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interleukin-18 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interleukin-18 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating lactate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating lactate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating glucocorticoid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating interferon-beta level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating interferon-beta level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating angiotensin II level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating angiotensin II level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating fibrinogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating fibrinogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating atrial natriuretic factor Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating atrial natriuretic factor phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating lipocalin 2 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating lipocalin 2 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating hyaluronic acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating hyaluronic acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating interleukin-18 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating interleukin-18 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating apolipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating apolipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating triiodothyronine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating triiodothyronine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interferon-gamma level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interferon-gamma level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |