The RPGRIP1 gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol RPGRIP1
Gene name retinitis pigmentosa GTPase regulator interacting protein 1
Chromosome 14
Chromosomal band q11.2
Imprinted Unknown
Genomic reference NG_008933.1
Transcript reference NM_020366.3
Exon/intron information NM_020366.3 exon/intron table
Associated with diseases CORD-13, LCA-6
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 236
Unique public DNA variants reported 141
Individuals with public variants 326
Hidden variants 3
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 European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created February 13, 2012
Date last updated March 07, 2021
Version RPGRIP1:210307

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_020366.3.
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
External URL Orphanet
HGNC 13436
Entrez Gene 57096
PubMed articles RPGRIP1
OMIM - Gene 605446
OMIM - Diseases CORD-13 (dystrophy, cone-rod, type 13 (CORD-13))
LCA-6 (Leber congenital amaurosis, type 6 (LCA-6))
GeneCards RPGRIP1
GeneTests RPGRIP1
Orphanet RPGRIP1

Active transcripts




NCBI ID     

NCBI Protein ID     

00018070 14 retinitis pigmentosa GTPase regulator interacting protein 1 NM_020366.3 NP_065099.3 236

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2012-2021. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.