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CPXCR1

CPX chromosome region, candidate 1

Synonyms:
CT77
Species:
Human CPXCR1 (53336), Mouse Cpxcr1 (382239)
UniProtKB ID:
Q8N123, B2R9F9, D3DTE7, Q96RS3
Gene ID:
  • Human(53336) Summary: This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
  • Mouse(382239) CPX chromosome region, candidate 1

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