PRCD (photoreceptor disc component)

2014-11-01  

Identity

HGNC
LOCATION
17q25.1
LOCUSID
ALIAS
RP36
FUSION GENES

Other Information

Locus ID:

NCBI: 768206
MIM: 610598
HGNC: 32528
Ensembl: ENSG00000214140

Variants:

dbSNP: 768206
ClinVar: 768206
TCGA: ENSG00000214140
COSMIC: PRCD

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000214140ENST00000586148Q00LT1
ENSG00000214140ENST00000592014Q00LT1

Expression (GTEx)

0
5
10
15
20
25

References

Pubmed IDYearTitleCitations
205079252010Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.0
238050422013Identification of a novel mutation in the PRCD gene causing autosomal recessive retinitis pigmentosa in a Turkish family.0
276138642016Palmitoylation of Progressive Rod-Cone Degeneration (PRCD) Regulates Protein Stability and Localization.0

Citation

Dessen P

PRCD (photoreceptor disc component)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/72192/prcd