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CABP4

Official Full Name
calcium binding protein 4
Organism
Homo sapiens
GeneID
57010
Background
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. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Synonyms
CRSD; CSNB2B;

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