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Symbol Name ID |
Apoa1
apolipoprotein A-I MGI:88049 |
| Darker colors indicate more annotations |
| Human Phenotypes | Gastrointestinal hemorrhage |
Purpura |
Petechiae |
Pericarditis |
Coronary artery atherosclerosis |
Premature coronary artery atherosclerosis |
Hypertension |
Raynaud phenomenon |
Congestive heart failure |
Abnormal lymph node morphology |
Lymphadenopathy |
Splenomegaly |
Hepatosplenomegaly |
| Disease(s) Associated with APOA1 | |||||||||||||
| familial hypercholesterolemia | |||||||||||||
| familial visceral amyloidosis | |||||||||||||
| primary hypoalphalipoproteinemia 2 | |||||||||||||
| systemic lupus erythematosus |
| Mouse Phenotypes | abnormal vascular wound healing |
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| Availability | Mouse Genotype | |
| Apoa1tm1Unc/Apoa1tm1Unc | ||
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 05/28/2024 MGI 6.13 |
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