Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 Biomarker disease CTD_human
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE By using three independent sets of amplification reactions, which cover 26% of the RB1 gene coding region, we identified RB1 gene deletions in the DNA of peripheral blood cells in 3 out of 24 (12.5%) unrelated patients with hereditary retinoblastoma. 1577465 1992
Entrez Id: 5973
Gene Symbol: RENBP
RENBP
0.010 Biomarker disease BEFREE We further analyzed this parental age factor by measuring the relative risk of age groups and comparing the incidence of sporadic hereditary retinoblastoma in the various parental age groups with the incidence of sporadic hereditary retinoblastoma in the total population. 2248323 1990
Entrez Id: 2098
Gene Symbol: ESD
ESD
0.040 Biomarker disease BEFREE Esterase D: evaluation of a potential derived gene marker for hereditary retinoblastoma. 3164261 1988
Entrez Id: 8102
Gene Symbol: XRS
XRS
0.010 Biomarker disease BEFREE X-ray sensitivity of fibroblasts from patients with hereditary retinoblastoma and their families. 3620303 1987
Entrez Id: 2098
Gene Symbol: ESD
ESD
0.040 GeneticVariation disease BEFREE We analyzed a three-generation family that demonstrates cosegregation of alleles at the EsD locus and the Rb locus. 3862370 1985
Entrez Id: 2098
Gene Symbol: ESD
ESD
0.040 Biomarker disease BEFREE Linkage of genes for human esterase D and hereditary retinoblastoma. 6731533 1984
Entrez Id: 2098
Gene Symbol: ESD
ESD
0.040 GeneticVariation disease BEFREE Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. 6823558 1983
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma. 7704558 1994
Entrez Id: 1081
Gene Symbol: CGA
CGA
0.010 GeneticVariation disease BEFREE Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma. 7704558 1994
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE We have performed a mutation survey of the RB1 gene in 232 patients with hereditary or non hereditary retinoblastoma. 7795591 1995
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma. 7927327 1994
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Germline mutations in the RB1 gene in patients with hereditary retinoblastoma. 8605116 1995
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE We have performed RB1 gene mutation analysis in 45 patients with hereditary retinoblastoma. 10671068 1998
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Our data indicate that lipoma predisposition in hereditary retinoblastoma is not associated with specific RB1 gene mutations but is influenced by modifying factors linked to this gene. 11571558 2001
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE This paper reports the first clinical experience of preimplantation genetic diagnosis (PGD) for hereditary retinoblastoma using two highly polymorphic microsatellite markers RB1.20 and D13S284, located within and close to the RB1 gene respectively. 12569181 2003
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.010 GeneticVariation disease BEFREE In contrast, the relative amounts of hMSH2 or RB1 mRNAs carrying premature termination codons were significantly reduced compared with those of wild-type mRNAs in lymphocytes from carriers of hereditary, nonpolyposis, colorectal cancer and hereditary retinoblastoma. 15480874 2004
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Complementary constitutional chromosome and fluorescent in situ hybridization (FISH) analyses of RB1 gene were applied in cases where hereditary retinoblastoma was suspected despite negative detection. 16343894 2006
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GermlineCausalMutation disease ORPHANET Hereditary retinoblastoma constitutes a cancer predisposition syndrome: a subject constitutionally carrying an RB1 gene mutation has a greater than 90% risk of developing retinoblastoma but is also at increased risk of developing other types of cancers.Diagnosis is made by fundoscopy. 16934146 2006
Entrez Id: 4193
Gene Symbol: MDM2
MDM2
0.020 GeneticVariation disease BEFREE p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma. 21814224 2011
Entrez Id: 4193
Gene Symbol: MDM2
MDM2
0.020 Biomarker disease BEFREE Influence of MDM2 and MDM4 on development and survival in hereditary retinoblastoma. 22180099 2012
Entrez Id: 4194
Gene Symbol: MDM4
MDM4
0.010 Biomarker disease BEFREE Influence of MDM2 and MDM4 on development and survival in hereditary retinoblastoma. 22180099 2012
Entrez Id: 6794
Gene Symbol: STK11
STK11
0.010 GeneticVariation disease BEFREE Germline loss of function mutations in tumor suppressor genes RB1 and LKB1/STK11 are associated with the autosomal dominant cancer predisposing syndromes familial retinoblastoma and Peutz-Jeghers syndrome (PJS), respectively. 23463749 2013
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GermlineCausalMutation disease ORPHANET Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies. 23498719 2013
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
0.300 GeneticVariation disease ORPHANET Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies. 23498719 2013