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other RP genes

Other RP and photoreceptor degeneration disorder-associated genes  fall into process/pathway categories such as ciliary transport, extracellular matrix and channel activity, retinal development, metabolism and splicing. For more information, check PMIDs 20212494 and 23701314. Several representative genes implicated in RP are listed with aliases in parentheses, full names and links to gene report pages:

Crx (CORD2, CRD, LCA7) – cone-rod homeobox
EYS – eyes shut homolog (Drosophila) (human gene)
NR2E3 (ESCS) – nuclear receptor subfamily 2 group E member 3 (human gene)
Prpf8 (U5) – pre-mRNA processing factor 8
Prpf31 (hPrp31) – pre-mRNA processing factor 31
Rp1 (ORP1) – RP1, axonemal microtubule associated
Rpgr (COD1, CORDX1) – retinitis pigmentosa GTPase regulator
Tulp1 (LCA15) – tubby like protein 1

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.