Gene: PRCD ×
Source: BEFREE ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 768206
Gene Symbol: PRCD
PRCD 		0.130 GeneticVariation phenotype BEFREE Until now, the function of PRCD has remained enigmatic despite multiple demonstrations that its mutations cause blindness in humans and dogs. 31189593 2019
Entrez Id: 768206
Gene Symbol: PRCD
PRCD 		0.130 GeneticVariation phenotype BEFREE Remarkably, one of them is PRCD, a protein whose mutations have been shown to cause blindness, yet cellular localization remained completely unknown. 23672200 2013
Entrez Id: 768206
Gene Symbol: PRCD
PRCD 		0.130 Biomarker phenotype BEFREE Progressive rod-cone degeneration (prcd) is the most widespread hereditary retinal disease leading to blindness in dogs and phenotypically is the canine counterpart of retinitis pigmentosa (RP) in humans. 9501213 1998