Coiled-coil domain containing 151 [Homo sapiens]

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Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome. [Biosci Rep. 2020]
Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome.
Deng S, Wu S, Xia H, Xiong W, Deng X, Liao J, Deng H, Yuan L. Biosci Rep. 2020 Jun 26; 40(6).
Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus. [J Hum Genet. 2019]
Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus.
Zhang W, Li D, Wei S, Guo T, Wang J, Luo H, Yang Y, Tan Z. J Hum Genet. 2019 Mar; 64(3):249-252. Epub 2018 Nov 30.
Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia. [Hum Mutat. 2014]
Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia.
Alsaadi MM, Erzurumluoglu AM, Rodriguez S, Guthrie PA, Gaunt TR, Omar HZ, Mubarak M, Alharbi KK, Al-Rikabi AC, Day IN. Hum Mutat. 2014 Dec; 35(12):1446-8.

RefSeq genomic sequence
See the genomic reference sequence for the ODAD3 gene (NG_041777.1).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the ODAD3 gene.

Nucleotide
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Protein