| Human Disease |
Telangiectasia, Hereditary Hemorrhagic, Type 2; HHT2 OMIM ID: 600376 |
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| View all models | View ALL (4) 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 |
| Acvrl1tm2Spo/Acvrl1tm2Spo Tg(Acvrl1-cre)L1Spo/0 |
involves: 129 * 129S4/SvJae * C57BL/6 * FVB | J:130020 | View |
| Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ |
involves: 129 * 129S1/Sv * 129X1/SvJ | J:154620 | View |
| Acvrl1tm1Enl/Acvrl1+ |
involves: C57BL/6 | J:82115 | View |
| Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Tg(Acvrl1-cre)L1Spo/0 |
involves: 129 * FVB | J:154620 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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