Retinitis pigmentosa GTPase regulator

RPGR
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4JHN, 4JHP, 4QAM
Identifiers
Aliases	RPGR, COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15, Retinitis pigmentosa GTPase regulator
External IDs	OMIM: 312610; MGI: 1344037; HomoloGene: 55455; GeneCards: RPGR; OMA:RPGR - orthologs
Gene location (Human) Chr. X chromosome (human) Band Xp11.4 Start 38,269,163 bp End 38,327,564 bp
Gene location (Mouse) Chr. X chromosome (mouse) Band X|X A1.1 Start 9,939,860 bp End 10,083,159 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in sperm bronchial epithelial cell right uterine tube right lung anterior pituitary tibial nerve subcutaneous adipose tissue upper lobe of left lung left uterine tube sural nerve Top expressed in saccule medial ganglionic eminence otic placode nucleus accumbens olfactory epithelium superior cervical ganglion substantia nigra spermatid pineal gland fossa More reference expression data BioGPS More reference expression data
Gene ontology Molecular function protein binding guanyl-nucleotide exchange factor activity RNA binding Cellular component cytoplasm ciliary basal body centrosome photoreceptor outer segment cell projection sperm flagellum cilium cytoskeleton microtubule organizing center Golgi apparatus motile cilium Biological process intracellular protein transport cell projection organization response to stimulus visual perception intraciliary transport cilium assembly regulation of molecular function Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 6103 19893 Ensembl ENSG00000156313 ENSMUSG00000031174 UniProt Q92834 Q9R0X5 RefSeq (mRNA) NM_000328 NM_001023582 NM_001034853 NM_001177950 NM_001177951 NM_001177952 NM_001177953 NM_001177954 NM_011285 RefSeq (protein) NP_000319 NP_001030025 NP_001354174 NP_001354175 NP_001354176 NP_001354177 NP_001354178 NP_001354179 NP_001354180 NP_001171421 NP_001171422 NP_001171423 NP_001171424 NP_001171425 NP_035415 Location (UCSC) Chr X: 38.27 – 38.33 Mb Chr X: 9.94 – 10.08 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

X-linked retinitis pigmentosa GTPase regulator is a GTPase-binding protein that in humans is encoded by the RPGR gene.

Function

This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. 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.

Interactions

Retinitis pigmentosa GTPase regulator has been shown to interact with PDE6D nephronophthisis (NPHP) proteins and RPGRIP1.

Further reading

• Jin ZB, Hayakawa M, Murakami A, Nao-i N (2007). "RCC1-like domain and ORF15: essentials in RPGR gene". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 29–33. doi:10.1007/0-387-32442-9_5. ISBN 978-0-387-28464-4. PMID 17249551.
• Ott J, Bhattacharya S, Chen JD, Denton MJ, Donald J, Dubay C, Farrar GJ, Fishman GA, Frey D, Gal A (Jan 1990). "Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests". Proceedings of the National Academy of Sciences of the United States of America. 87 (2): 701–4. doi:10.1073/pnas.87.2.701. PMC 53333. PMID 2300556.
• McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP (Jul 1995). "X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11". American Journal of Human Genetics. 57 (1): 87–94. PMC 1801245. PMID 7611300.
• Maruyama K, Sugano S (Jan 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
• Bonaldo MF, Lennon G, Soares MB (Sep 1996). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Research. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
• Fujita R, Buraczynska M, Gieser L, Wu W, Forsythe P, Abrahamson M, Jacobson SG, Sieving PA, Andréasson S, Swaroop A (Sep 1997). "Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families". American Journal of Human Genetics. 61 (3): 571–80. doi:10.1086/515523. PMC 1715956. PMID 9326322.
• Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (Oct 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
• Buraczynska M, Wu W, Fujita R, Buraczynska K, Phelps E, Andréasson S, Bennett J, Birch DG, Fishman GA, Hoffman DR, Inana G, Jacobson SG, Musarella MA, Sieving PA, Swaroop A (Dec 1997). "Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa". American Journal of Human Genetics. 61 (6): 1287–92. doi:10.1086/301646. PMC 1716085. PMID 9399904.
• Hardcastle AJ, David-Gray ZK, Jay M, Bird AC, Bhattacharya SS (Dec 1997). "Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp". Investigative Ophthalmology & Visual Science. 38 (13): 2750–5. PMID 9418727.
• Yan D, Swain PK, Breuer D, Tucker RM, Wu W, Fujita R, Rehemtulla A, Burke D, Swaroop A (Jul 1998). "Biochemical characterization and subcellular localization of the mouse retinitis pigmentosa GTPase regulator (mRpgr)". The Journal of Biological Chemistry. 273 (31): 19656–63. doi:10.1074/jbc.273.31.19656. PMID 9677393.
• Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A (Dec 1998). "X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60". Ophthalmology. 105 (12): 2286–96. doi:10.1016/S0161-6420(98)91231-3. PMID 9855162.
• Linari M, Ueffing M, Manson F, Wright A, Meitinger T, Becker J (Feb 1999). "The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase". Proceedings of the National Academy of Sciences of the United States of America. 96 (4): 1315–20. doi:10.1073/pnas.96.4.1315. PMC 15460. PMID 9990021.
• Dry KL, Manson FD, Lennon A, Bergen AA, Van Dorp DB, Wright AF (1999). "Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3)". Human Mutation. 13 (2): 141–5. doi:10.1002/(SICI)1098-1004(1999)13:2<141::AID-HUMU6>3.0.CO;2-Q. PMID 10094550.
• Kirschner R, Rosenberg T, Schultz-Heienbrok R, Lenzner S, Feil S, Roepman R, Cremers FP, Ropers HH, Berger W (Aug 1999). "RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa". Human Molecular Genetics. 8 (8): 1571–8. doi:10.1093/hmg/8.8.1571. PMID 10401007.
• Zito I, Thiselton DL, Gorin MB, Stout JT, Plant C, Bird AC, Bhattacharya SS, Hardcastle AJ (1999). "Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus". Human Genetics. 105 (1–2): 57–62. doi:10.1007/s004390051064. PMID 10480356.
• Miano MG, Testa F, Strazzullo M, Trujillo M, De Bernardo C, Grammatico B, Simonelli F, Mangino M, Torrente I, Ruberto G, Beneyto M, Antinolo G, Rinaldi E, Danesino C, Ventruto V, D'Urso M, Ayuso C, Baiget M, Ciccodicola A (Sep 1999). "Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa". European Journal of Human Genetics. 7 (6): 687–94. doi:10.1038/sj.ejhg.5200352. PMID 10482958.
• Hong DH, Pawlyk BS, Shang J, Sandberg MA, Berson EL, Li T (Mar 2000). "A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)". Proceedings of the National Academy of Sciences of the United States of America. 97 (7): 3649–54. doi:10.1073/pnas.060037497. PMC 16294. PMID 10725384.
• Zito I, Gorin MB, Plant C, Bird AC, Bhattacharya SS, Hardcastle AJ (Apr 2000). "Novel mutations of the RPGR gene in RP3 families". Human Mutation. 15 (4): 386. doi:10.1002/(SICI)1098-1004(200004)15:4<386::AID-HUMU23>3.0.CO;2-4. PMID 10737996.
• Rao KN, Li L, Anand M, Khanna H (2015). "Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition". Scientific Reports. 5: 11137. doi:10.1038/srep11137. PMC 4463945. PMID 26068394.