Variant: rs121918369 

    present in Gene: PRCD;CYGB
    present in Chromosome: 17
    Position on Chromosome: 76540146
    Alleles of this Variant: G/A

rs121918369 in PRCD;CYGB gene and RETINITIS PIGMENTOSA 36 PMID 16938425 2006 Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans.

PMID 24992209 2014 The progressive rod-cone degeneration (PRCD) protein is secreted through the conventional ER/Golgi-dependent pathway.

PMID 27613864 2016 Palmitoylation of Progressive Rod-Cone Degeneration (PRCD) Regulates Protein Stability and Localization.