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All mouse models of plasma protein metabolism disease with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
polyclonal hypergammaglobulinemia | Copg1em1Geha/Copg1em1Geha | involves: C57BL/6 | J:345528 | View | ||||
alpha 1-antitrypsin deficiency | Serpina1em#Chmu/Serpina1em#Chmu | involves: C57BL/6J | J:259615 | View | ||||
Transgenes and Other Mutations | alpha 1-antitrypsin deficiency | Tg(SERPINA1*E342K)#Slcw/Tg(SERPINA1*E342K)#Slcw | involves: C57BL/6 * ICR | J:208016 | View |