| Human Disease |
Spherocytosis, Type 3; SPH3 OMIM ID: 270970 |
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| Synonyms | Spherocytosis, Hereditary, 3; HS3 | |||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Spta1ihj/Spta1ihj |
involves: HRS/J * LAH | J:157766 | View |
| Spta1sph-2Bc/Spta1sph-2Bc |
involves: SELH | J:7048, J:7501 | View |
| Spta1sph/Spta1sph |
either: (B6.C3-Spta1sph x WB.C3-Spta1sph)F1 or (WB.C3-Spta1sph x B6.C3-Spta1sph)F1 | J:6695 | View |
| Spta1sph-ha/Spta1sph-ha |
involves: DBA/1J | J:14946, J:30699 | View |
| Spta1sph/Spta1sph |
involves: C3H | J:12276 | 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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