| Name |
|---|
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] |
IGAD1 Geneimmunoglobulin A (IgA) deficiency susceptibility 1 |
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 |
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. |
granulocytopenia Gene SetFrom HPO Gene-Disease Associations genes associated with the granulocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Granulocytopenia Severe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Granulocytopenia Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Granulocytopenia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Granulocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Clozapine-induced agranulocytosis/granulocytopenia in treatment-resistant schizophrenia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Clozapine-induced agranulocytosis/granulocytopenia in treatment-resistant schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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, 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 (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. |
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. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb 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 the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung 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 the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology 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. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humerus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of complement system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chorioretinal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sulfur amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sulfur amino acid metabolism 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 prothrombin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of coagulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cervical spine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carboxylic acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skeletal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lens Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body weight Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of temperature regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the systemic arterial tree Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the rib cage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retinal vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of ion homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of macrophages Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body height Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of polysaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intrinsic pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eosinophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the macula Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of epidermal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of higher mental function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ribs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nucleobase metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the forearm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of purine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of serum cytokine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology 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 the nephron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nephron 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. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the falx cerebri Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of gastrointestinal vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choanae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the immune system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reticulocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebellar peduncle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gingiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lung Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vena cava Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sharpey fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpophalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intrahepatic bile duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fluid regulation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pineal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the crus of the helix Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acetabulum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sense of smell Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of permanent molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the achilles tendon Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the myocardium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of complement system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood glucose concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal tubule Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the shoulder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome condensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prostaglandin metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neurodevelopmental abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of connective tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alanine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atlantoaxial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thrombocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vestibulocochlear nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of binocular vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thyroid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forebrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cerebral artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choroid plexus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choroid plexus 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. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the seventh cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acoustic reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubulointerstitial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dental pulp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cysteine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ganglioside metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of humoral immunity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sixth cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of calvarial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of calvarial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine bicarbonate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the genitourinary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fascia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the liver Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dental color Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alkaline phosphatase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the larynx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal abnormality 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. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the salivary glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of copper homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sacroiliac joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lacrimal duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal tibial epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic valve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corticospinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the endocrine system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the endocrine system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the soft palate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the adrenal glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the adrenal glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the periorbital region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the periorbital region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the respiratory system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fontanelles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the septum pellucidum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of renal excretion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of renal excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the premaxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
eeg abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the eeg abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of renin-angiotensin system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
c1-c2 vertebral abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pectoral muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pectoral muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of descemet's membrane Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of descemet's membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sclera Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sclera phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
phenotypic abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the phenotypic abnormality 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. |
abnormality of the radial head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radial head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of saccadic eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasolabial region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasolabial region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the uvea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of female external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of female external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of tyrosine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of tyrosine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of extrapyramidal motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the rectum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the rectum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the supraorbital ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the supraorbital ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the coagulation cascade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycosaminoglycan metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycosaminoglycan metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extrinsic pathway Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extrinsic pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skeletal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skeletal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the vestibule of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skin adnexa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skin adnexa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the mitral valve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the mitral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of orotic acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of orotic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of neutrophil physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of neutrophil physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of globe location Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of globe location phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scapula Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scapula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of t cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dicarboxylic acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dicarboxylic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the granulocytic lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the granulocytic lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femur Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pancreatic islet cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pancreatic islet cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of long bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of long bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lymphatic system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lymphatic system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mesangial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the mesangial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the patella Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
blood group antigen abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the optic disc Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the optic disc phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dermal melanosomes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dermal melanosomes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of leucine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of leucine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell number Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal cortex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ventricular septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ventricular septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the pelvis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fetal cardiovascular system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fetal cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the mandible Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pubic hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of proteoglycan metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the macula Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the styloid process of ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the styloid process of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skull ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia majora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the genital system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the genital system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humerus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lens shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lens shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the uvula Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lateral ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lateral ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome segregation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome segregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of higher mental function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of higher mental function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vitamin k metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vitamin k metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the conjunctiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the conjunctiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the chin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac atrium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac atrium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pain sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pain sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the menstrual cycle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior fontanelle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the plantar skin of foot Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the plantar skin of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pyruvate family amino acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pyruvate family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sacrococcygeal pilonidal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the sacrococcygeal pilonidal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of adrenal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of adrenal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of carpal bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of carpal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of male internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of male internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebral vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine hormone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of mast cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of mast cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of globe size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of globe size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vascular skin abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the vascular skin abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the foramen magnum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hand joint mobility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hand joint mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the urinary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the urinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dorsal column of the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dorsal column of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the costochondral junction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the costochondral junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiglottis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hair growth rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hair growth rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fatty-acid anion metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fatty-acid anion metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of magnesium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ureter Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ureter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of color vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of color vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vitamin e metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the foot Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of purine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of purine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nares Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nares phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the capitate bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the capitate bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of serum amino acid levels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of serum amino acid levels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the integument Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the integument phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retina Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sacrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of midbrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of midbrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebral subcortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of neuronal migration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of neuronal migration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ocular abduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ocular abduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hearing abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the hearing abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vagina Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of xanthine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of xanthine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the iris Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of renal resorption Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of renal resorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cranial sutures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cranial sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ankles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ankles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of phytanic acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of phytanic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of earlobe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radioulnar joints Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radioulnar joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thoracic cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thoracic cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the uterus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of facial soft tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of facial soft tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ischium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ischium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of parotid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of parotid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the spinal meninges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the spinal meninges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hindbrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hindbrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glutamine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glutamine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of small intestinal villus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of small intestinal villus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the calvaria Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the calvaria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of placental membranes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of placental membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of female internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of female internal genitalia 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. |
abnormality of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the striatum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the striatum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the right ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the right ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower-limb metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower-limb metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hair texture Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hair texture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fontanelles or cranial sutures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fontanelles or cranial sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the eyelid Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine calcium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine calcium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of coordination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lens Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip-girdle musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip-girdle musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the temporal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the temporal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hamate bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hamate bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of epidermal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of epidermal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the atrioventricular valves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the atrioventricular valves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of histidine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of histidine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpal epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpal epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dental eruption Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dental eruption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the metacarpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal pelvis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the talus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the talus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood and blood-forming tissues phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of bone mineral density Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the semicircular canal Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |