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RPGRIP1

Official Full Name
RPGR interacting protein 1
Organism
Homo sapiens
GeneID
57096
Background
This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008]
Synonyms
LCA6; RGI1; RGRIP; CORD13; RPGRIP; RPGRIP1d;

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