OPN1LW homepage - Eye diseases - LOVD - Leiden Open Variation Database

General information
Gene name	opsin 1 (cone pigments), long-wave-sensitive
Gene symbol	OPN1LW
Chromosome Location	Xq28
Database location	grenada.lumc.nl
Curator	LOVD-team, but with Curator vacancy
PubMed references	View all (unique) PubMed references in the OPN1LW database
Date of creation	July 04, 2012
Last update	July 04, 2012
Version	OPN1LW120704
Add sequence variant	Submit a sequence variant
First time submitters	Register here
Reference sequence file	Genomic reference sequence for describing sequence variants
Genomic refseq ID	NG_009105.1
Transcript refseq ID	NM_020061.4
Exon/intron information	Exon/intron information table
Total number of unique DNA variants reported	0
Total number of individuals with variant(s)	0
Total number of variants reported	0
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Graphical displays and utilities
Summary tables	Summary of all sequence variants in the OPN1LW 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

Eye diseases - LOVD