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RP2 gene

RP2 activator of ARL3 GTPase

Key facts

Official symbol
RP2
Full name
RP2
Chromosome
X
Map location
Xp11.3
Organism
Homo sapiens
NCBI Gene ID
6102
Also known as
DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2

Function summary

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].

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Data source: NCBI Gene · alsesAI Gene Library