| Name |
|---|
CHR Genechromate resistance; sulfate transport |
LOC105369239 Genemultidrug resistance-associated protein 6 |
XRRA1 GeneX-ray radiation resistance associated 1 Involved in response to X-ray. Located in cytoplasm and nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
LOC104968398 Geneadriamycin resistance-associated |
BCAR1P2 Genebreast cancer anti-estrogen resistance 1 pseudogene 2 |
BCAR1P1 Genebreast cancer anti-estrogen resistance 1 pseudogene 1 |
LOC645405 Geneoxidation resistance 1 pseudogene |
SM1 GeneSchistosoma mansoni, susceptibility/resistance to |
UVRAG GeneUV radiation resistance associated This gene complements the ultraviolet sensitivity of xeroderma pigmentosum group C cells and encodes a protein with a C2 domain. The protein activates the Beclin1-PI(3)KC3 complex, promoting autophagy and suppressing the proliferation and tumorigenicity of human colon cancer cells. Chromosomal aberrations involving this gene are associated with left-right axis malformation and mutations in this gene have been associated with colon cancer. [provided by RefSeq, Jul 2008] |
BCAR4 Genebreast cancer anti-estrogen resistance 4 (non-protein coding) This gene produces a spliced long non-coding RNA (lncRNA) that has been implicated in breast cancer metastasis. It was originally identified in a screen for genes responsible for the development of resistance to anti-estrogens in breast cancer cells. It is thought that release of CCL21 enables this lncRNA to bind to the SNIP1 and PNUTS transcription factors, thereby activating a non-canonical GLI-dependent hedgehog signaling pathway that promotes cancer cell migration and invasion. A similar gene in cow expresses a protein in mature oocytes and preimplantation embryos. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Apr 2015] |
BCAR1 Genebreast cancer anti-estrogen resistance 1 The protein encoded by this gene is a member of the Crk-associated substrate (CAS) family of scaffold proteins, characterized by the presence of multiple protein-protein interaction domains and many serine and tyrosine phosphorylation sites. The encoded protein contains a Src-homology 3 (SH3) domain, a proline-rich domain, a substrate domain which contains 15 repeat of the YxxP consensus phosphorylation motif for Src family kinases, a serine-rich domain, and a bipartite Src-binding domain, which can bind both SH2 and SH3 domains. This adaptor protein functions in multiple cellular pathways, including in cell motility, apoptosis and cell cycle control. Dysregulation of this gene can have a wide range of effects, affecting different pathways, including cardiac development, vascular smooth muscle cells, liver and kidney function, endothelial migration, and cancer. [provided by RefSeq, Sep 2017] |
BCAR3 Genebreast cancer anti-estrogen resistance 3 Breast tumors are initially dependent on estrogens for growth and progression and can be inhibited by anti-estrogens such as tamoxifen. However, breast cancers progress to become anti-estrogen resistant. Breast cancer anti-estrogen resistance gene 3 was identified in the search for genes involved in the development of estrogen resistance. The gene encodes a component of intracellular signal transduction that causes estrogen-independent proliferation in human breast cancer cells. The protein contains a putative src homology 2 (SH2) domain, a hall mark of cellular tyrosine kinase signaling molecules, and is partly homologous to the cell division cycle protein CDC48. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012] |
OXR1 Geneoxidation resistance 1 Predicted to enable oxidoreductase activity. Predicted to be involved in response to oxidative stress. Predicted to act upstream of or within several processes, including adult walking behavior; negative regulation of cellular response to oxidative stress; and negative regulation of peptidyl-cysteine S-nitrosylation. Located in mitochondrion. Implicated in cerebellar hyplasia/atrophy, epilepsy, and global developmental delay. [provided by Alliance of Genome Resources, Mar 2025] |
SSD GeneSpeech-sound disorder |
OHDS GeneOrthostatic hypotensive disorder of Streeten |
MAFD9 GeneMajor affective disorder-9, susceptibility to |
MAFD8 GeneMajor affective disorder-8, susceptibility to |
MAFD5 GeneMajor affective disorder 5 |
MAFD1 Genemajor affective disorder 1 |
MAFD3 GeneMajor affective disorder 3, early onset |
MDD2 GeneMajor depressive disorder 2 |
MDD1 GeneMajor depressive disorder |
MAFD2 Genemajor affective disorder 2 |
MAFD4 GeneMajor affective disorder 4 |
MAFD6 GeneMajor affective disorder 6 |
ADHD2 GeneAttention deficit-hyperactivity disorder, susceptibility to, 2 |
HDL3 GeneHuntington-like neurodegenerative disorder 2 |
PAND1 GenePanic disorder 1 |
PAND2 Genepanic disorder 2 |
PAND3 Genepanic disorder 3 |
BDET GeneBleeding disorder, east Texas type |
ADHD4 GeneAttention deficit-hyperactivity disorder, susceptibility to, 4 |
ADHD5 GeneAttention deficit-hyperactivity disorder, susceptibility to, 5 |
ADHD6 GeneAttention deficit-hyperactivity disorder, susceptibility to, 6 |
ADHD1 GeneAttention deficit-hyperactivity disorder, susceptibility to, 1 |
ADHD3 GeneAttention deficit-hyperactivity disorder, susceptibility to, 2 |
SCZD8 Geneschizophrenia disorder 8 |
SCZD7 Geneschizophrenia disorder 7 |
SCZD6 Geneschizophrenia disorder 6 |
SCZD1 Geneschizophrenia disorder 1 |
SCZD3 Geneschizophrenia disorder 3 |
SCZD10 Geneschizophrenia disorder 10 (periodic catatonia) |
NDNC9 GeneNail disorder, nonsyndromic congenital, 9 |
CLA3 Genecerebellar ataxia 3 (cerebellar parenchyma disorder 1) |
SCZD2 Geneschizophrenia disorder 2 |
PDR Genepigment disorder, reticulate |