Property Summary

NCBI Gene PubMed Count 6
PubMed Score 60.27
PubTator Score 2.50

Knowledge Summary


No data available


  Disease Sources (3)

Disease Target Count P-value
pituitary cancer 1972 7.6805316496622E-8
osteosarcoma 7933 1.34149578716104E-5
atypical teratoid/rhabdoid tumor 1095 3.0869423782246E-5
Pick disease 1893 0.00178203061627947
subependymal giant cell astrocytoma 2287 0.00621443571432701
astrocytic glioma 2241 0.0205162388862237
progressive supranuclear palsy 674 0.0218576583434037
ependymoma 2514 0.0239067399924666


  Differential Expression (8)

Disease log2 FC p
astrocytic glioma -1.200 0.021
ependymoma -1.500 0.024
osteosarcoma 1.116 0.000
atypical teratoid/rhabdoid tumor -1.300 0.000
subependymal giant cell astrocytoma -1.614 0.006
Pick disease -1.100 0.002
progressive supranuclear palsy -1.100 0.022
pituitary cancer 2.700 0.000


Accession Q00LT1 B9EJD4
Symbols RP36


  Ortholog (5)

Gene RIF (2)

23805042 The identification of a third mutation in PRCD confirms its role in the pathogenesis of retinitis pigmentosa.
20507925 The identification of a second pathogenic mutation of PRCD in multiple retinitis pigmentosa (RP) patients confirms the role of PRCD in the aetiology of RP in humans.

AA Sequence


Text Mined References (6)

PMID Year Title
23805042 2013 Identification of a novel mutation in the PRCD gene causing autosomal recessive retinitis pigmentosa in a Turkish family.
20507925 2010 Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.
16938425 2006 Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
14702039 2004 Complete sequencing and characterization of 21,243 full-length human cDNAs.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.