Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51684
Gene Symbol: SUFU
SUFU 		0.400 SusceptibilityMutation disease ORPHANET 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 		0.400 SusceptibilityMutation disease ORPHANET Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma. 21188540 2011
Entrez Id: 51684
Gene Symbol: SUFU
SUFU 		0.400 SusceptibilityMutation disease ORPHANET Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations. 19833601 2010
Entrez Id: 51684
Gene Symbol: SUFU
SUFU 		0.400 SusceptibilityMutation disease ORPHANET Mutations in SUFU predispose to medulloblastoma. 12068298 2002
Entrez Id: 51684
Gene Symbol: SUFU
SUFU 		0.400 CausalMutation disease CLINVAR
Entrez Id: 9623
Gene Symbol: TCL1B
TCL1B 		0.010 Biomarker disease BEFREE Thus, the clinically unfavorable "TCL1 MBEN" subset revealed transcriptome signatures composed of cancer-associated signaling pathways and disclosed a high frequency of clinically relevant germline PTCH1/SUFU alterations. 31781912 2020
Entrez Id: 8115
Gene Symbol: TCL1A
TCL1A 		0.010 Biomarker disease BEFREE Thus, the clinically unfavorable "TCL1 MBEN" subset revealed transcriptome signatures composed of cancer-associated signaling pathways and disclosed a high frequency of clinically relevant germline PTCH1/SUFU alterations. 31781912 2020
Entrez Id: 7447
Gene Symbol: VSNL1
VSNL1 		0.010 AlteredExpression disease BEFREE "TCL2 MBEN" also revealed strong and ubiquitous expression of VSNL1 (visinin-like protein 1) both at the mRNA and protein level, which was correlated with a favorable clinical course. 31781912 2020