Property Summary

NCBI Gene PubMed Count 6
PubMed Score 60.27
PubTator Score 2.50

Knowledge Summary


No data available


  Differential Expression (8)

Disease log2 FC p
astrocytic glioma -1.200 2.1e-02
ependymoma -1.500 2.4e-02
osteosarcoma 1.116 1.3e-05
atypical teratoid/rhabdoid tumor -1.300 3.1e-05
subependymal giant cell astrocytoma -1.614 6.2e-03
Pick disease -1.100 1.8e-03
progressive supranuclear palsy -1.100 2.2e-02
pituitary cancer 2.700 7.7e-08

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.