CHD7 Back

chromodomain helicase DNA binding protein 7

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NCBI Description of CHD7
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

Community Annotation of CHD7 Add / Edit CHD7: Annotations

No community annotations yet for CHD7.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

CHD7 is highly significantly mutated in
(none)
CHD7 is significantly mutated in
(none)
CHD7 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for CHD7