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RP2

Official Full Name
RP2 activator of ARL3 GTPase
Organism
Homo sapiens
GeneID
6102
Background
The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death [provided by RefSeq, Jul 2008]
Synonyms
XRP2; NME10; TBCCD2; NM23-H10; DELXp11.3;

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