CLRN1-AS1
Appearance
(Redirected from CLRN1-AS1 (gene))
CLRN1-AS1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | CLRN1-AS1, CLRN1OS, UCRP, CLRN1 antisense RNA 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | GeneCards: CLRN1-AS1; OMA:CLRN1-AS1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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In molecular biology, CLRN1 antisense RNA 1 (CLRN1-AS1) (previously known as clarin 1 opposite strand, CLRN1OS or USH critical region pseudogene, UCRP) is a human gene encoding a long non-coding RNA. It was originally identified in a screen to identify the genes responsible for Usher syndrome type 3 and presumed to be an unprocessed pseudogene.[2]
See also
[edit]References
[edit]- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Joensuu, T.; Hämäläinen, R.; Yuan, B.; Johnson, C.; Tegelberg, S.; Gasparini, P.; Zelante, L.; Pirvola, U.; Pakarinen, L.; Lehesjoki, A. E.; De La Chapelle, A.; Sankila, E. M. (2001). "Mutations in a Novel Gene with Transmembrane Domains Underlie Usher Syndrome Type 3". The American Journal of Human Genetics. 69 (4): 673–684. doi:10.1086/323610. PMC 1226054. PMID 11524702.
Further reading
[edit]- Joensuu T, Hämäläinen R, Yuan B, et al. (2001). "Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3". Am. J. Hum. Genet. 69 (4): 673–684. doi:10.1086/323610. PMC 1226054. PMID 11524702.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–45. doi:10.1038/ng1285. PMID 14702039.
- Västinsalo H, Jalkanen R, Dinculescu A, et al. (2011). "Alternative splice variants of the USH3A gene Clarin 1 (CLRN1)". Eur. J. Hum. Genet. 19 (1): 30–35. doi:10.1038/ejhg.2010.140. PMC 3039507. PMID 20717163.
External links
[edit]- Human CLRN1-AS1 genome location and CLRN1-AS1 gene details page in the UCSC Genome Browser.