| Human Disease |
Chylomicron Retention Disease; CMRD OMIM ID: 246700 |
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| Synonyms | Anderson Disease; ANDD; Hypobetalipoproteinemia with Accumulation of Apolipoprotein B-Like Protein in Intestinal Cells; Lipid Transport Defect of Intestine | ||||||||||||||||||||||||||||
| 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 |
| Pitpnatm1Vab/Pitpnatm1Vab |
involves: 129S7/SvEvBrd | J:85204 | View |
| PitpnaGt(OST1152)Lex/PitpnaGt(OST1152)Lex |
involves: 129S5/SvEvBrd | J:85204 | 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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