| Human Disease |
Priapism, Familial Idiopathic OMIM ID: 176620 |
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| 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 |
| Arntltm1Bra/Arntltm1Bra |
B6.129-Arntltm1Bra | J:191844 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Hbatm1Paz/Hbatm1Paz Hbbtm1Tow/Hbbtm1Tow Tg(HBA-HBBs)41Paz/0 |
involves: 129 * Black Swiss * C57BL/6 * DBA/2 * FVB/N | J:135978 | 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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