The PRKCG gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol PRKCG
Gene name protein kinase C, gamma
Chromosome 19
Chromosomal band q13.4
Imprinted Unknown
Genomic reference NG_009114.1
Transcript reference NM_002739.3
Exon/intron information NM_002739.3 exon/intron table
Associated with diseases SCA14
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 63
Unique public DNA variants reported 50
Individuals with public variants 8
Hidden variants 2
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 04, 2012
Date last updated May 16, 2022
Version PRKCG:220516

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_002739.3.
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/PRKCG
HGNC 9402
Entrez Gene 5582
PubMed articles PRKCG
OMIM - Gene 176980
OMIM - Diseases SCA14 (ataxia, spinocerebellar, type 14 (SCA-14))
HGMD PRKCG
GeneCards PRKCG
GeneTests PRKCG
Orphanet PRKCG


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00016839 19 protein kinase C, gamma NM_002739.3 NP_002730.1 63


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