Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4613
Gene Symbol: MYCN
MYCN
0.300 GeneticVariation disease ORPHANET Role of MYCN in retinoblastoma. 23498720 2013
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GermlineCausalMutation disease ORPHANET Gender-dependent histone deacetylases injury may contribute to differences in liver recovery rates of male and female mice. 23498780 2013
Entrez Id: 84260
Gene Symbol: TCHP
TCHP
0.010 GeneticVariation disease BEFREE The N-terminal domain of the retinoblastoma (Rb) tumor suppressor protein (RbN) harbors in-frame exon deletions in partially penetrant hereditary retinoblastomas and is known to impair cell growth and tumorigenesis. 26711265 2015
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma". 26753011 2016
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Familial retinoblastoma due to intronic LINE-1 insertion causes aberrant and noncanonical mRNA splicing of the RB1 gene. 26763876 2016
Entrez Id: 407041
Gene Symbol: MIR34B
MIR34B
0.010 Biomarker disease BEFREE A polymorphism in mir-34b/c as a potential biomarker for early onset of hereditary retinoblastoma. 28106538 2017
Entrez Id: 5925
Gene Symbol: RB1
RB1
0.600 GeneticVariation disease BEFREE Erratum to: "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma". 28331555 2019