The following gene names and symbols are associated with antigen Retinitis Pigmentosa GTPase Regulator across different species:

retinitis pigmentosa GTPase regulator (RPGR), retinitis pigmentosa GTPase regulator (Rpgr), retinitis pigmentosa GTPase regulator (rpgr), retinitis pigmentosa GTPase regulator (Bm1_19935), retinitis pigmentosa GTPase regulator (NAEGRDRAFT_80250)

Other aliases include:

CRD, RP3, COD1, PCDX, RP15, XLRP3, orf15, CORDX1, Rp3h, MGC187915, xrpgr

On the protein level the following designations are being used for antigen Retinitis Pigmentosa GTPase Regulator:

retinitis pigmentosa GTPase regulator – retinitis pigmentosa 15 – cone dystrophy 1 (X-linked) – retinitis pigmentosa 3 GTPase regulator – X-linked retinitis pigmentosa GTPase regulator – mRpgr – OTTMUSP00000018364 – OTTMUSP00000018365 – OTTMUSP00000018366 – OTTMUSP00000018367 – OTTMUSP00000018368 – retinitis pigmentosa GTP-ase regulator RPGR – RPGR 1-19 isoform – X-linked retinitis pigmentosa GTPase regulator-like

Retinitis Pigmentosa GTPase Regulator fulfills a number of functions:

guanyl-nucleotide exchange factor activity – protein binding – molecular_function

Retinitis Pigmentosa GTPase Regulator is relevant to the following processes:

intracellular protein transport – response to stimulus – visual perception – eye photoreceptor cell development – regulation of catalytic activity – biological_process

Locations for Retinitis Pigmentosa GTPase Regulator:

Golgi apparatus – cilium – cytoplasm – photoreceptor outer segment – cellular_component

Source: NCBI Entrez Gene, Gene Ontology