| Human Disease |
Hyperlipidemia, Familial Combined; FCHL OMIM ID: 144250 |
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| Synonyms | Familial Combined Hyperlipidemia | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Apoetm1Unc/Apoetm1Unc Lpltm1Sem/Lpltm1Sem |
involves: 129P2/OlaHsd | J:151434 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ldlrtm1Her/Ldlrtm1Her Tg(APOC3)3707Bres/? |
involves: 129S7/SvEvBrd * C57BL/6J * CBA/J | J:37861 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tnfrsf1btm1Imx/Tnfrsf1btm1Imx |
involves: 129S7/SvEvBrd * C57BL/6 | J:45147 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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