RPGRIP1
id:
rpgrip1-246-2110219
title:
RPGRIP1
text:
X-linked retinitis pigmentosa GTPase regulator-interacting protein 1 is a protein in the ciliary transition zone that in humans is encoded by the RPGRIP1 gene. RPGRIP1 is a multi-domain protein containing a coiled-coil domain at the N-terminus, two C2 domains and a C-terminal RPGR-interacting domain (RID). Defects in the gene result in the Leber congenital amaurosis (LCA) syndrome and in the eye disease glaucoma.
brand slug:
wiki
category slug:
encyclopedia
description:
Protein-coding gene in the species Homo sapiens
original url:
https://en.wikipedia.org/wiki/RPGRIP1
date created:
date modified:
2024-01-29T05:25:14Z
main entity:
{"identifier":"Q18042883","url":"https://www.wikidata.org/entity/Q18042883"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/f/fc/Human_RPGRIP1_C2_domain.png","width":711,"height":1217}
fields total:
13
integrity:
15