CPXCR1

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]

Description

CPX chromosome region, candidate 1

Protein family

-

Chromosome

X:q21.31 (88002226 - 88009786)

Ensembl ID

ENSG00000147183  (ver. 69.37)

Orthologs

Mouse Cpxcr1: ENSMUSG00000072995

Human splice variants
Mouse splice variants