CABP4 Back

calcium binding protein 4

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NCBI Description of CABP4
This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. 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 CABP4 Add / Edit CABP4: Annotations

No community annotations yet for CABP4.
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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

CABP4 is highly significantly mutated in
(none)
CABP4 is significantly mutated in
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CABP4 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 CABP4