RecName: Full=Chromodomain-helicase-DNA-binding protein 7; Short=CHD-7 - Protein

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CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction. [Genes (Basel). 2024]
CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction.
Driesen J, Van Hoecke H, Maes L, Janssens S, Acke F, De Leenheer E. Genes (Basel). 2024 May 19; 15(5). Epub 2024 May 19.
Maternal CHD7 gonosomal mosaicism in a fetus with CHARGE syndrome. [Am J Med Genet A. 2024]
Maternal CHD7 gonosomal mosaicism in a fetus with CHARGE syndrome.
Bai T, Shen Y, Yang Y, Dai S, Liu H. Am J Med Genet A. 2024 Apr; 194(4):e63491. Epub 2023 Dec 6.
A novel CHD7 variant in a chinese family with CHARGE syndrome. [Genes Genomics. 2024]
A novel CHD7 variant in a chinese family with CHARGE syndrome.
Shan Y, Yao L, Li L, Gao X, Jiang J. Genes Genomics. 2024 Mar; 46(3):379-387. Epub 2023 Jun 5.

RefSeq genomic sequence
See the genomic reference sequence for the CHD7 gene (NG_007009.1).
RefSeq protein isoforms
See 20 reference sequence protein isoforms for the CHD7 gene.

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Q9P2D1 [Domain Mapping of Disease Mut...]
Q9P2D1
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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reagent reviews [ExactAntigen/Labome]
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RecName: Full=Chromodomain-helicase-DNA-binding protein 7; Short=CHD-7; AltName:...
RecName: Full=Chromodomain-helicase-DNA-binding protein 7; Short=CHD-7; AltName: Full=ATP-dependent helicase CHD7
gi|148877246|sp|Q9P2D1.3|CHD7_HUMAN

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