Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 CausalMutation disease CLINVAR Each SUFU-positive family included a single case of medulloblastoma, whereas only two (1.7%) of 115 individuals with Gorlin syndrome and a PTCH1 mutation developed medulloblastoma. 25403219 2014
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GeneticVariation disease CLINVAR Each SUFU-positive family included a single case of medulloblastoma, whereas only two (1.7%) of 115 individuals with Gorlin syndrome and a PTCH1 mutation developed medulloblastoma. 25403219 2014
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 CausalMutation disease CLINVAR High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age. 22508808 2012
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GeneticVariation disease CLINVAR High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age. 22508808 2012
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 CausalMutation disease CLINVAR Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma. 21188540 2011