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Gene : CDHR1 Homo sapiens

Name  ? cadherin related family member 1 Cytological Location  10q23.1
Brief Description  cadherin related family member 1
Description  This gene belongs to the cadherin superfamily of calcium-dependent cell adhesion molecules. The encoded protein is a photoreceptor-specific cadherin that plays a role in outer segment disc morphogenesis. Mutations in this gene are associated with inherited retinal dystrophies. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2013]
  • synonyms:
  • OTTHUMG00000018634,
  • cadherin-related family member 1,
  • NM_033100,
  • uc001kcv.4,
  • PRCAD,
  • CORD15,
  • RP65,
  • HGNC:14550,
  • RP65,
  • CDHR1,
  • CORD15,
  • protocadherin 21,
  • AB053448,
  • KIAA1775,
  • PCDH21,
  • PCDH21
  • identifiers:
  • 92211,
  • ENSG00000148600,
  • CDHR1

Genome feature

Region: gene ? Length: 25085  
Location: 10:84194537-84219621 Cyto location: 10q23.1

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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


1 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

3740 SNPs

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results