Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
RPGR retinitis pigmentosa GTPase regulator CRD , RP3 , COD1 , PCDX , RP15 , XLRP3 , orf15 , CORDX1 Homo sapiens 25 protein-coding SERGEF , HERC3 , HERC5 , HERC6 , HERC4 312610

Summary

This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008]

GeneOntology

Gene Loss events - RPGR (1 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_TLP8Z2 Tupaia chinensis Scandentia LOF (frameshift, premature stop, ss) Full No 10.1093/icb/icy004