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General information
Gene name G protein-coupled receptor 179
Gene symbol GPR179
Chromosome Location 17q21.1
Database location grenada.lumc.nl
Curator LOVD-team, but with Curator vacancy
PubMed references View all (unique) PubMed references in the GPR179 database
Date of creation July 13, 2012
Last update August 15, 2012
Version GPR179 120815
Add sequence variant Submit a sequence variant
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Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_032655.1
Transcript refseq ID NM_001004334.2
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 4
Total number of individuals with variant(s) 4
Total number of variants reported 4
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the GPR179 database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer
Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the GPR179 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the GPR179 database
Variants with no known pathogenicity Listing of all GPR179 variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)
Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms
Search through hidden entries Find the number of variant entries in the database (including hidden entries) matching your search terms.
Links to other resources
HGNC 31371
Entrez Gene 440435
OMIM - Gene 614515
OMIM - Disease Night blindness, congenital stationary, type 1E (CSNB1E)
UniProtKB (SwissProt/TrEMBL) Q6PRD1
HGMD GPR179
GeneCards GPR179
GeneTests GPR179

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