From Wikipedia, the free encyclopedia
Coiled-coil domain containing 151 is a protein that in humans is encoded by the CCDC151 gene.[5]
Clinical significance[]
Mutations in CCDC151 are associated to Primary ciliary dyskinesia.[6]
References[]
- ^ a b c GRCh38: Ensembl release 89: ENSG00000198003 - Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000039632 - 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: Coiled-coil domain containing 151".
- ^ Alsaadi MM, Erzurumluoglu AM, Rodriguez S, Guthrie PA, Gaunt TR, Omar HZ, Mubarak M, Alharbi KK, Al-Rikabi AC, Day IN (December 2014). "Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia". Human Mutation. 35 (12): 1446–8. doi:10.1002/humu.22698. PMC 4489323. PMID 25224326.
Further reading[]
External links[]
Categories:
- Genes on human chromosome 19
- Human chromosome 19 gene stubs