Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22924
Gene Symbol: MAPRE3
MAPRE3
0.020 GeneticVariation disease BEFREE The YAC contains the CYBB locus in Xp21.1 and is thought to contain at least part of the RP3 gene responsible for X-linked retinitis pigmentosa. 7760861 1995
Entrez Id: 6990
Gene Symbol: DYNLT3
DYNLT3
0.020 GeneticVariation disease BEFREE The YAC contains the CYBB locus in Xp21.1 and is thought to contain at least part of the RP3 gene responsible for X-linked retinitis pigmentosa. 7760861 1995
Entrez Id: 1104
Gene Symbol: RCC1
RCC1
0.030 GeneticVariation disease BEFREE The cilia-expressed gene RPGR (retinitis pigmentosa GTPase regulator) is mutated in patients with X-linked retinitis pigmentosa (XLRP) and encodes multiple protein isoforms with a common N-terminal domain homologous to regulator of chromosome condensation 1 (RCC1), a guanine nucleotide exchange factor (GEF) for Ran GTPase. 20631154 2010
Entrez Id: 6654
Gene Symbol: SOS1
SOS1
0.030 GeneticVariation disease BEFREE The cilia-expressed gene RPGR (retinitis pigmentosa GTPase regulator) is mutated in patients with X-linked retinitis pigmentosa (XLRP) and encodes multiple protein isoforms with a common N-terminal domain homologous to regulator of chromosome condensation 1 (RCC1), a guanine nucleotide exchange factor (GEF) for Ran GTPase. 20631154 2010
Entrez Id: 5923
Gene Symbol: RASGRF1
RASGRF1
0.030 GeneticVariation disease BEFREE The cilia-expressed gene RPGR (retinitis pigmentosa GTPase regulator) is mutated in patients with X-linked retinitis pigmentosa (XLRP) and encodes multiple protein isoforms with a common N-terminal domain homologous to regulator of chromosome condensation 1 (RCC1), a guanine nucleotide exchange factor (GEF) for Ran GTPase. 20631154 2010
Entrez Id: 5923
Gene Symbol: RASGRF1
RASGRF1
0.030 GeneticVariation disease BEFREE Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1. 8817343 1996
Entrez Id: 5923
Gene Symbol: RASGRF1
RASGRF1
0.030 GeneticVariation disease BEFREE A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). 8673101 1996
Entrez Id: 6654
Gene Symbol: SOS1
SOS1
0.030 GeneticVariation disease BEFREE Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1. 8817343 1996
Entrez Id: 1104
Gene Symbol: RCC1
RCC1
0.030 GeneticVariation disease BEFREE Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1. 8817343 1996
Entrez Id: 1104
Gene Symbol: RCC1
RCC1
0.030 GeneticVariation disease BEFREE A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). 8673101 1996
Entrez Id: 6654
Gene Symbol: SOS1
SOS1
0.030 GeneticVariation disease BEFREE A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). 8673101 1996
Entrez Id: 5009
Gene Symbol: OTC
OTC
0.050 GeneticVariation disease BEFREE The gene for the most frequent from of X-linked retinitis pigmentosa (XLRP), RP3, has been assigned by genetic and physical mapping to a segment of less than 1000 kbp, which is flanked by the marker DXS1110 and the ornithine transcarbamylase (OTC) gene. 8776599 1996
Entrez Id: 5009
Gene Symbol: OTC
OTC
0.050 GeneticVariation disease BEFREE In one family, recombination events indicate a locus for XLRP outside the interval (DXS84-OTC-DXS255-DXS14), most likely on the centromeric side of DXS14. 1685699 1991
Entrez Id: 5009
Gene Symbol: OTC
OTC
0.050 GeneticVariation disease BEFREE In these kindreds the XLRP locus shows close linkage with Xp21 marker loci OTC and DXS206. 2568332 1989
Entrez Id: 5009
Gene Symbol: OTC
OTC
0.050 Biomarker disease BEFREE This putative location of the XLRP gene between L1.28 and 754 taken together with the tight linkage to OTC, a locus already located between L1.28 and 754, leads us to propose a gene order of centromere-L1.28-OTC/XLRP-754-telomere. 3422211 1988
Entrez Id: 5009
Gene Symbol: OTC
OTC
0.050 GeneticVariation disease BEFREE The XLRP locus was found to be excluded from the chromosome distal to ornithine transcarbamylase (OTC) (P = 6.5 X 10(-5]. 3477957 1987
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 GeneticVariation disease BEFREE A novel RP2 missense mutation Q158P identified in an X-linked retinitis pigmentosa family impaired RP2 protein stability. 31071385 2019
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 GeneticVariation disease BEFREE To identify novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene and retinitis pigmentosa 2 (RP2) gene underlying X-linked retinitis pigmentosa (XLRP) and assess genotype-phenotype correlations. 27768226 2017
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 GeneticVariation disease BEFREE An approximately 17Kb large deletion including the exon 4 and exon 5 of RP2 gene was found in an XLRP family. 28294154 2017
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 GeneticVariation disease BEFREE Screening for mutations in RPGR and RP2 genes in Jordanian families with X-linked retinitis pigmentosa. 27323122 2016
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 PosttranslationalModification disease BEFREE Using computational analysis, we revealed an extragenic tandem GAAA repeat 230-bp from the landmark CpG island of the human X-linked retinitis pigmentosa 2 RP2 promoter whose 5meCpG status correlates with XCI. 25078280 2014
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 AlteredExpression disease BEFREE RPGR and RP2 genes expressed in the photoreceptor sensory cilia are predominantly implicated in XLRP; however, the interpretation of genetic mutations and their correlation with clinical phenotypes remain unknown, and the role of these genes in photoreceptor cilia function is not completely elucidated. 23443027 2013
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 GeneticVariation disease BEFREE To identify mutations in the RPGR and RP2 genes from Chinese families with X-linked retinitis pigmentosa (XLRP). 20021257 2010
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 Biomarker disease BEFREE RPGR and RP2: targets for the treatment of X-linked retinitis pigmentosa? 19702441 2009
Entrez Id: 6102
Gene Symbol: RP2
RP2
0.100 GeneticVariation disease BEFREE Mutations in the RP2 gene are linked to the second most frequent form of X-linked retinitis pigmentosa. 16457815 2006