Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-18255
Nat Genet May 1, 1996; 13 (1): 35-42.

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3).

Meindl A , Dry K , Herrmann K , Manson F , Ciccodicola A , Edgar A , Carvalho MR , Achatz H , Hellebrand H , Lennon A , Migliaccio C , Porter K , Zrenner E , Bird A , Jay M , Lorenz B , Wittwer B , D'Urso M , Meitinger T , Wright A .


Abstract
X-linked retinitis pigmentosa (xlRP) is a severe progressive retinal degeneration which affects about 1 in 25,000 of the population. The most common form of xlRP, RP3, has been localised to the interval between CYBB and OTC in Xp21.1 by linkage analysis and deletion mapping. Identification of microdeletions within this region has now led to the positional cloning of a gene, RPGR, that spans 60 kg of genomic DNA and is ubiquitously expressed. The predicted 90 kD protein contains in its N-terminal half a tandem repeat structure highly similar to RCC1 (regulator of chromosome condensation), suggesting an interaction with a small GTPase. The C-terminal half contains a domain, rich in acidic residues, and ends in a potential isoprenylation anchorage site. The two intragenic deletions, two nonsense and three missense mutations within conserved domains provide evidence that RPGR (retinitis pigmentosa GTPase regulator) is the RP3 gene.

PubMed ID: 8673101
Article link: Nat Genet
Grant support: [+]

Species referenced: Xenopus
Genes referenced: cybb mapre3 otc rcc1 rpgr

Disease Ontology terms: retinitis pigmentosa
OMIMs: RETINITIS PIGMENTOSA 3; RP3