Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD Identification of a novel nonsense mutation on the Pax3 gene in ENU-derived white belly spotting mice and its genetic interaction with c-Kit. 20095975

2010
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD A genetic risk factor for mouse neural tube defects: defining the embryonic basis. 10699180

2000
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD Neural crest is involved in development of abnormal myocardial function. 9344762

1997
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD Pax-3 is necessary for migration but not differentiation of limb muscle precursors in the mouse. 8631247

1996
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD NEW SPLOTCH ALLELES IN THE MOUSE. 14170406

1996
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD Regulation of Pax-3 expression in the dermomyotome and its role in muscle development. 7600971

1994
Entrez Id: 5077
Gene Symbol: PAX3
PAX3
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		1.000 Biomarker MGD Spinal ganglia reduction in the splotch-delayed mouse neural tube defect mutant. 2763211

1989