The OPN1SW gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol OPN1SW
Gene name opsin 1 (cone pigments), short-wave-sensitive
Chromosome 7
Chromosomal band q31.3-q32
Imprinted Unknown
Genomic reference NG_009094.1
Transcript reference NM_001708.2
Exon/intron information NM_001708.2 exon/intron table
Associated with diseases colorblindness, tritan
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 37
Unique public DNA variants reported 26
Individuals with public variants 11
Hidden variants -
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 performed by Johan den Dunnen, supported by Global Variome.
Date created July 06, 2012
Date last updated July 07, 2023
Version OPN1SW:230707

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_001708.2.
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/OPN1SW
HGNC 1012
Entrez Gene 611
PubMed articles OPN1SW
OMIM - Gene 613522
OMIM - Diseases colorblindness, tritan
HGMD OPN1SW
GeneCards OPN1SW
GeneTests OPN1SW
Orphanet OPN1SW


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00015058 7 opsin 1 (cone pigments), short-wave-sensitive NM_001708.2 NP_001699.1 37


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