CPXCR1

GENE INFORMATION

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Gene name

CPXCR1 (HGNC Symbol)

Synonyms

CT77

Description

CPX chromosome region, candidate 1 (HGNC Symbol)

Entrez gene 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]

Chromosome

X (Chromosome progress)

Cytoband

q21.31

Chromosome location (bp)

88002226 - 88009786

Ensembl

ENSG00000147183 (version 73.37)

Entrez gene

53336

UniProt

Q8N123 (UniProt - Evidence at transcript level)

neXtProt

NX_Q8N123

Antibodypedia

CPXCR1 antibodies
 

PROTEIN VIEW

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CPXCR1-001
 
CPXCR1-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CPXCR1-001 ENSP00000276127
ENST00000276127
Q8N123
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Show » 301 34.7 No 0
CPXCR1-002 ENSP00000362203
ENST00000373111
Q8N123
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Show » 301 34.7 No 0