Symbol Name ID |
Apob
apolipoprotein B MGI:88052 |
Darker colors indicate more annotations |
Human Phenotypes | Stroke |
Ischemic stroke |
Abnormality of the nervous system |
Ataxia |
Reduced tendon reflexes |
Disease(s) Associated with APOB | |||||
familial hypobetalipoproteinemia 1 | |||||
sickle cell anemia |
Mouse Phenotypes | hydrocephaly |
exencephaly |
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Availability | Mouse Genotype | ||
Apobtm1Mae/Apobtm1Mae | |||
Apobtm1Unc/Apobtm1Unc | |||
Apobtm3Sgy/Apobtm3Sgy | |||
Apobtm4Sgy/Apobtm4Sgy | |||
Apobtm1Mae/Apob+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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