| Human Disease |
Norrie Disease; ND OMIM ID: 310600 |
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| Synonyms | Atrophia Bulborum Hereditaria; Episkopi Blindness | ||||||||||||||||||||||||||||
| View all models | View ALL (3) mouse models for this human disease. | ||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ndptm1Wbrg/Y |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1 | J:77024 | View |
| Ndptm1Wbrg/Y |
involves: 129P2/OlaHsd * C57BL/6 | J:30902 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Fzd4tm1Nat/Fzd4tm1Nat |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:107732 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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