RP2 Products

Description

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

Bioinformatics

Entrez	6102 Human
Uniprot	AAH43348 Human AAH43348.1 Human NM_006915 Human NP_008846 Human O75695 Human
Product By Gene ID	6102
Alternate Names	DELXp11.3 KIAA0215 NME10 protein XRP2 retinitis pigmentosa 2 (X-linked recessive) TBCCD2 XRP2

Research Areas for RP2

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Vision