Gene: JAG1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 182
Gene Symbol: JAG1
JAG1 		0.300 Biomarker group CTD_human Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1. 12022040 2002
Entrez Id: 182
Gene Symbol: JAG1
JAG1 		0.300 Biomarker group CTD_human Mutations in the human Jagged1 gene are responsible for Alagille syndrome. 9207787 1997
Entrez Id: 182
Gene Symbol: JAG1
JAG1 		0.300 Biomarker group CTD_human Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. 9207788 1997