Entity Details

Primary name CDHR1
Entity type gene
Source Source Link

Details

PrimaryID92211
RefseqGeneNG_028034
SymbolCDHR1
Namecadherin related family member 1
Chromosome10
Location10q23.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-07-12
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCDHR1_HUMAN

GO terms

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GOName
GO:0005509 calcium ion binding
GO:0005887 integral component of plasma membrane
GO:0007155 cell adhesion
GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
GO:0008594 photoreceptor cell morphogenesis
GO:0035845 photoreceptor cell outer segment organization
GO:0042622 photoreceptor outer segment membrane
GO:0045494 photoreceptor cell maintenance

Diseases

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Disease IDSourceNameDescription
613660 OMIMCone-rod dystrophy 15 (CORD15)An inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa, due to cone photoreceptors degenerating at a higher rate than rod photoreceptors. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CDHR1PROM1BioGRID18654668 details
CDHR1TMEM30BBioGRID, IntAct28514442 details
CDHR1ATP5POBioGRID, IntAct30021884 details
CDHR1RYKBioGRID21875946 details