Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C0001916
Disease: Albinism
Albinism 		0.330 Biomarker MGD Novel ENU-induced eye mutations in the mouse: models for human eye disease. 11929848

2002
Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C0001916
Disease: Albinism
Albinism 		0.330 Biomarker MGD Saturation mutagenesis for dominant eye morphological defects in the mouse Mus musculus. 10886015

2000
Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C0001916
Disease: Albinism
Albinism 		0.330 Biomarker MGD Mitfmi-enu122 is a missense mutation in the HLH dimerization domain. 9501313

1998
Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C0001916
Disease: Albinism
Albinism 		0.330 Biomarker MGD Mast cells in spotted mutant mice (W Ph mi). 6127714

1982
Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C0001916
Disease: Albinism
Albinism 		0.330 Biomarker MGD The relationship between abnormalities of pigmentation and of the inner ear. 4392283

1970
Entrez Id: 4286
Gene Symbol: MITF
MITF
CUI: C0001916
Disease: Albinism
Albinism 		0.330 Biomarker MGD The eye and skeletal effects of two mutant alleles at the microphthalmia locus of Mus musculus. 4963367

1967