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All mouse models of pigmentation disease with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Bloch-Sulzberger syndrome | Ikbkgtm1Mka/Ikbkg+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:63054 | View | |||
| Bloch-Sulzberger syndrome | Ikbkgtm1Mpa/Ikbkg+ | involves: C57BL/6 | J:63055 | View | ||||
| | Bloch-Sulzberger syndrome | NsdhlStr-1H/Nsdhl+ | involves: 101/H * C3H/HeH | J:106524 | View | |||
| Transgenes and Other Mutations | neonatal jaundice | Ugt1tm1.1Afmu/Ugt1tm1.1Afmu | FVB.Cg-Ugt1tm1.1Afmu | J:216224 | View | |||