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Gene : CPXCR1 Homo sapiens

Name  ? CPX chromosome region candidate 1 Cytological Location  Xq21.31
Brief Description  CPX chromosome region candidate 1
Description  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]
  • synonyms:
  • AL031116,
  • CPXCR1,
  • CT77,
  • uc004efd.5,
  • cancer/testis antigen 77,
  • HGNC:2332,
  • OTTHUMG00000021950,
  • NM_033048,
  • CT77
  • identifiers:
  • 53336,
  • ENSG00000147183,
  • CPXCR1

Genome feature

Region: gene ? Length: 7557  
Location: X:88747225-88754781 Cyto location: Xq21.31

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

29 SNPs

3 Cross References

13 Data Sets

1 Homologues

0 Located Features

97 Rna Seq Results