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Merck
CN

CPXCR1

CPX chromosome region, candidate 1

Synonyms:
CT77
Species:
UniProtKB ID:
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

Custom & Knockdown Gene Products

Antibodies

Product Number
Description
Species Reactivity
Application
Anti-CPXCR1 antibody produced in rabbit, IgG fraction of antiserum,
Species Reactivity
human
Application
western blot

esiRNA

Product Number
Description
Species
MISSION® esiRNA, targeting mouse Cpxcr1,
Species
mouse