TRPV5
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Transient receptor potential cation channel, subfamily V, member 5 | |||||||||||||
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Identifiers | |||||||||||||
Symbols | TRPV5 ; CAT2; ECAC1; OTRPC3 | ||||||||||||
External IDs | OMIM: 606679 MGI: 2429764 HomoloGene: 10520 IUPHAR: 511 ChEMBL: 1628474 GeneCards: TRPV5 Gene | ||||||||||||
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RNA expression pattern | |||||||||||||
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More reference expression data | |||||||||||||
Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 56302 | 194352 | |||||||||||
Ensembl | ENSG00000127412 | ENSMUSG00000036899 | |||||||||||
UniProt | Q9NQA5 | P69744 | |||||||||||
RefSeq (mRNA) | NM_019841 | NM_001007572 | |||||||||||
RefSeq (protein) | NP_062815 | NP_001007573 | |||||||||||
Location (UCSC) | Chr 7: 142.91 – 142.93 Mb |
Chr 6: 41.65 – 41.68 Mb |
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PubMed search | [1] | [2] | |||||||||||
Transient receptor potential cation channel subfamily V member 5 is a protein that in humans is encoded by the TRPV5 gene.[1][2][3]
TRPV5 is mainly expressed in kidney epithelial cells, where it plays an important role in the reabsorption of Ca2+.[4] Genetic deletion of TRPV5 in mice leads to Ca2+ loss in the urine, and consequentual hyperparathyroidism, and bone loss.[5]
Function
This gene is a member of the transient receptor family and the TRPV subfamily. The calcium-selective channel , TRPV5, encoded by this gene has 6 transmembrane-spanning domains, multiple potential phosphorylation sites, an N-linked glycosylation site, and 5 ANK repeats. This protein forms homotetramers or heterotetramers and is activated by a low internal calcium level.[6]
Interactions
TRPV5 has been shown to interact with S100A10.[7]
See also
References
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Further reading
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External links
- TRPV5 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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