Entity Details

Primary name PRCD
Entity type gene
Source Source Link

Details

PrimaryID768206
RefseqGeneNG_016702
SymbolPRCD
Namephotoreceptor disc component
Chromosome17
Location17q25.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2006-10-14
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsPRCD_HUMAN

GO terms

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GOName
GO:0005576 extracellular region
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
GO:0005794 Golgi apparatus
GO:0007601 visual perception
GO:0042622 photoreceptor outer segment membrane
GO:0050896 response to stimulus

Diseases

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Disease IDSourceNameDescription
610599 OMIMRetinitis pigmentosa 36 (RP36)A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
PRCDCTBP2BioGRID30585266 details