| Human Disease |
Term: Albinism, Ocular, Type I; OA1
OMIM ID: 300500
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| Synonyms |
Nettleship-Falls Type Ocular Albinism |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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  ...both mouse and human orthologous genes. |
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Mouse Models
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| Gpr143tm1Inc/Y |
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either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
J:66139
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1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes.
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Analysis Tools