KIAA1530
KIAA1530 is a protein that in humans that is encoded by the KIAA1530 gene, also known as UVSSA.[5] Mutations in this gene have been identified to cause the UV-sensitive syndrome and recently, its important role in Transcription-coupled repair has been identified.[6]
| UVSSA | |||||||||||||||||||||||||
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| Aliases | UVSSA, KIAA1530, UVSS3, UV stimulated scaffold protein A | ||||||||||||||||||||||||
| External IDs | OMIM: 614632 MGI: 1918351 HomoloGene: 13807 GeneCards: UVSSA | ||||||||||||||||||||||||
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| Species | Human | Mouse | |||||||||||||||||||||||
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| Location (UCSC) | Chr 4: 1.35 – 1.4 Mb | Chr 5: 33.54 – 33.58 Mb | |||||||||||||||||||||||
| PubMed search | [3] | [4] | |||||||||||||||||||||||
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Clinical relevance
Mutations in this gene cause UV-sensitive syndrome.[7]
References
- GRCh38: Ensembl release 89: ENSG00000163945 - Ensembl, May 2017
- GRCm38: Ensembl release 89: ENSMUSG00000037355 - Ensembl, May 2017
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: KIAA1530". Retrieved 2012-05-07.
- Schwertman P, Lagarou A, Dekkers DH, Raams A, van der Hoek AC, Laffeber C, Hoeijmakers JH, Demmers JA, Fousteri M, Vermeulen W, Marteijn JA (May 2012). "UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair". Nat. Genet. 44 (5): 598–602. doi:10.1038/ng.2230. PMID 22466611. S2CID 5486230.
- Zhang X, Horibata K, Saijo M, Ishigami C, Ukai A, Kanno S, Tahara H, Neilan EG, Honma M, Nohmi T, Yasui A, Tanaka K (May 2012). "Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair". Nat. Genet. 44 (5): 593–7. doi:10.1038/ng.2228. PMID 22466612. S2CID 5094505.
Further reading
- Yashin AI, Wu D, Arbeev KG, Ukraintseva SV (September 2010). "Joint influence of small-effect genetic variants on human longevity". Aging. 2 (9): 612–20. doi:10.18632/aging.100191. PMC 2984609. PMID 20834067.
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