Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GenomicAlterations disease CGI
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CTD_human
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease HPO
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 CausalMutation disease CGI
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. 8681379 1996
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GeneticVariation disease LHGDN Mutations in SUFU predispose to medulloblastoma. 12068298 2002
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN Mutations in SUFU predispose to medulloblastoma. 12068298 2002
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease LHGDN Our results suggest that loss of function of SUFU results in overactivity of both the Sonic Hedgehog, and the WNT signaling pathways, leading to excessive proliferation and failure to differentiate resulting in MB. 15077159 2004
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease BEFREE Our results suggest that loss of function of SUFU results in overactivity of both the Sonic Hedgehog, and the WNT signaling pathways, leading to excessive proliferation and failure to differentiate resulting in MB. 15077159 2004
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GeneticVariation disease BEFREE Our results indicate that genetic alterations of the SUFU gene, do not contribute significantly to the molecular pathogenesis of MBs. 15488029 2004
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN Genetic elimination of Suppressor of fused reveals an essential repressor function in the mammalian Hedgehog signaling pathway. 16459298 2006
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN Loss of suppressor-of-fused function promotes tumorigenesis. 17452975 2007
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN A missense mutation in PTCH2 underlies dominantly inherited NBCCS in a Chinese family. 18285427 2008
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN We have identified the known c.1022 + 1G>A SUFU germ line splicing mutation in a family that was PTCH1-negative and who had signs and symptoms of GS, including medulloblastoma. 19533801 2009
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease GENOMICS_ENGLAND We have identified the known c.1022 + 1G>A SUFU germ line splicing mutation in a family that was PTCH1-negative and who had signs and symptoms of GS, including medulloblastoma. 19533801 2009
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease BEFREE Another component in this pathway, SUFU, is known to be involved in susceptibility to medulloblastoma but has never been reported in GS patients to date. 19533801 2009
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations. 19833601 2010
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GeneticVariation disease BEFREE Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations. 19833601 2010
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 GeneticVariation disease BEFREE We identified no PTCH1 mutations and two SUFU mutations that cause premature protein truncating in the series of sporadic non-familial medulloblastomas. 21188540 2011
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
Entrez Id: 51684
Gene Symbol: SUFU
SUFU
0.800 Biomarker disease CLINGEN Loss of Trp53 promotes medulloblastoma development but not skin tumorigenesis in Sufu heterozygous mutant mice. 21882258 2012
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 BEFREE A complete mutational analysis of the SUFU gene was performed on genomic DNA in all 131 consecutive patients treated for medulloblastoma in the pediatrics department of the Institut Gustave Roussy between 1972 and 2009 and for whom a blood sample was available. 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 GeneticVariation disease BEFREE Together with the previous report describing three cases of non-NBCCS medulloblastoma carrying a germline mutation in this gene, individuals with a SUFU germline mutation are expected to have a markedly high risk of developing medulloblastoma and probably meningioma. 22829011 2012