Gene: NOTCH2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 GermlineCausalMutation disease ORPHANET Alagille syndrome: pathogenesis, diagnosis and management. 21934706 2012
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 Biomarker disease GENOMICS_ENGLAND Conditional ablation of the Notch2 receptor in the ocular lens. 22173065 2012
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 Biomarker disease GENOMICS_ENGLAND Renal anomalies in Alagille syndrome: a disease-defining feature. 22105858 2012
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 Biomarker disease GENOMICS_ENGLAND NOTCH2 mutations in Alagille syndrome. 22209762 2012
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 GeneticVariation disease UNIPROT NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway. 16773578 2006
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 Biomarker disease GENOMICS_ENGLAND NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway. 16773578 2006
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 Biomarker disease CTD_human
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4853
Gene Symbol: NOTCH2
NOTCH2 		0.700 CausalMutation disease CLINVAR