The PRCD gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol PRCD
Gene name progressive rod-cone degeneration
Chromosome 17
Chromosomal band q25.1
Imprinted Unknown
Genomic reference NG_016702.1
Transcript reference NM_001077620.2
Exon/intron information NM_001077620.2 exon/intron table
Associated with diseases RP36
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 25
Unique public DNA variants reported 11
Individuals with public variants 38
Hidden variants 0
Download all this gene's data Download all data
Notes This database is one of the "Eye disease" gene variant databases.
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created July 16, 2012
Date last updated June 03, 2021
Version PRCD:210603

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001077620.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/PRCD
HGNC 32528
Entrez Gene 768206
PubMed articles PRCD
OMIM - Gene 610598
OMIM - Diseases RP36 (retinitis pigmentosa, type 36 (RP36))
HGMD PRCD
GeneCards PRCD
GeneTests PRCD
Orphanet PRCD


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00016771 17 transcript variant 1 NM_001077620.2 NP_001071088.1 25


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