| Name |
|---|
IGAT GeneImmune response to synthetic polypeptide--IRGAT |
TCIRG1 GeneT-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3 This gene encodes a subunit of a large protein complex known as a vacuolar H+-ATPase (V-ATPase). The protein complex acts as a pump to move protons across the membrane. This movement of protons helps regulate the pH of cells and their surrounding environment. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, and receptor-mediated endocytosis. V-ATPase is comprised of a cytosolic V1 domain and a transmembrane V0 domain. Alternative splicing results in multiple transcript variants. Mutations in this gene are associated with infantile malignant osteopetrosis. [provided by RefSeq, May 2017] |
ISCW GeneImmune suppression to streptococcal antigen |
IGLP1 Geneimmune response to synthetic polypeptides 1 |
IGLP2 Geneimmune response to synthetic polypeptides 2 |
TCIM Genetranscriptional and immune response regulator This gene encodes a small, monomeric, predominantly unstructured protein that functions as a positive regulator of the Wnt/beta-catenin signaling pathway. This protein interacts with a repressor of beta-catenin mediated transcription at nuclear speckles. It is thought to competitively block interactions of the repressor with beta-catenin, resulting in up-regulation of beta-catenin target genes. The encoded protein may also play a role in the NF-kappaB and ERK1/2 signaling pathways. Expression of this gene may play a role in the proliferation of several types of cancer including thyroid cancer, breast cancer and hematological malignancies. [provided by RefSeq, Nov 2011] |
CYCSP38 Genecytochrome c, somatic pseudogene 38 |
CYCSP39 Genecytochrome c, somatic pseudogene 39 |
CYCSP34 Genecytochrome c, somatic pseudogene 34 |
CYCSP35 Genecytochrome c, somatic pseudogene 35 |
CYCSP30 Genecytochrome c, somatic pseudogene 30 |
CYCSP32 Genecytochrome c, somatic pseudogene 32 |
CYCSP49 Genecytochrome c, somatic pseudogene 49 |
CYCSP48 Genecytochrome c, somatic pseudogene 48 |
CYCSP46 Genecytochrome c, somatic pseudogene 46 |
CYCSP41 Genecytochrome c, somatic pseudogene 41 |
CYCSP40 Genecytochrome c, somatic pseudogene 40 |
CYCSP43 Genecytochrome c, somatic pseudogene 43 |
CYCSP42 Genecytochrome c, somatic pseudogene 42 |
CYCSP45 Genecytochrome c, somatic pseudogene 45 |
CYCSP44 Genecytochrome c, somatic pseudogene 44 |
CYCSP16 Genecytochrome c, somatic pseudogene 16 |
CYCSP17 Genecytochrome c, somatic pseudogene 17 |
CYCSP14 Genecytochrome c, somatic pseudogene 14 |
CYCSP12 Genecytochrome c, somatic pseudogene 12 |
CYCSP10 Genecytochrome c, somatic pseudogene 10 |
CYCSP11 Genecytochrome c, somatic pseudogene 11 |
CYCSP18 Genecytochrome c, somatic pseudogene 18 |
CYCSP19 Genecytochrome c, somatic pseudogene 19 |
CYCSP33 Genecytochrome c, somatic pseudogene 33 |
CYCSP29 Genecytochrome c, somatic pseudogene 29 |
CYCSP28 Genecytochrome c, somatic pseudogene 28 |
CYCSP27 Genecytochrome c, somatic pseudogene 27 |
CYCSP26 Genecytochrome c, somatic pseudogene 26 |
CYCSP24 Genecytochrome c, somatic pseudogene 24 |
CYCSP23 Genecytochrome c, somatic pseudogene 23 |
CYCSP22 Genecytochrome c, somatic pseudogene 22 |
CYCSP20 Genecytochrome c, somatic pseudogene 20 |
CYCSP25 Genecytochrome c, somatic pseudogene 25 |
CYCSP8 Genecytochrome c, somatic pseudogene 8 |
CYCSP4 Genecytochrome c, somatic pseudogene 4 |
CYCSP5 Genecytochrome c, somatic pseudogene 5 |
CYCSP6 Genecytochrome c, somatic pseudogene 6 |
CYCSP7 Genecytochrome c, somatic pseudogene 7 |
CYCSP1 Genecytochrome c, somatic pseudogene 1 |
CYCSP2 Genecytochrome c, somatic pseudogene 2 |
CYCSP3 Genecytochrome c, somatic pseudogene 3 |
CYCSP52 Genecytochrome c, somatic pseudogene 52 |
CYCSP53 Genecytochrome c, somatic pseudogene 53 |
CYCSP51 Genecytochrome c, somatic pseudogene 51 |
CYCSP55 Genecytochrome c, somatic pseudogene 55 |
CYCS Genecytochrome c, somatic This gene encodes a small heme protein that functions as a central component of the electron transport chain in mitochondria. The encoded protein associates with the inner membrane of the mitochondrion where it accepts electrons from cytochrome b and transfers them to the cytochrome oxidase complex. This protein is also involved in initiation of apoptosis. Mutations in this gene are associated with autosomal dominant nonsyndromic thrombocytopenia. Numerous processed pseudogenes of this gene are found throughout the human genome.[provided by RefSeq, Jul 2010] |