JAG1, jagged canonical Notch ligand 1, 182

N. diseases: 420; N. variants: 63
Disease: Alagille Syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 CausalMutation disease CLINVAR Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population. 11058898 2000
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 GeneticVariation disease UNIPROT Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population. 11058898 2000
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 GeneticVariation disease CLINVAR Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population. 11058898 2000
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 GeneticVariation disease UNIPROT Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome. 10220506 1999
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 CausalMutation disease CLINVAR Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome. 10220506 1999
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 GeneticVariation disease UNIPROT Jagged-1 mutation analysis in Italian Alagille syndrome patients. 10533065 1999
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 CausalMutation disease CLINVAR Jagged-1 mutation analysis in Italian Alagille syndrome patients. 10533065 1999
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 CausalMutation disease CLINVAR Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families. 9585603 1998
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 GeneticVariation disease UNIPROT Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families. 9585603 1998
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 Biomarker disease CTD_human Mutations in the human Jagged1 gene are responsible for Alagille syndrome. 9207787 1997
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 GeneticVariation disease UNIPROT Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. 9207788 1997
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 Biomarker disease CTD_human Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. 9207788 1997
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 CausalMutation disease CLINVAR Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. 9207788 1997
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		0.710 Biomarker disease GENOMICS_ENGLAND