Symbol Name ID |
Abcc9
ATP-binding cassette, sub-family C member 9 MGI:1352630 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Lymphedema |
Exercise intolerance |
Disease(s) Associated with ABCC9 | ||
familial atrial fibrillation | ||
hypertrichotic osteochondrodysplasia Cantu type |
Mouse Phenotypes | homeostasis/metabolism phenotype |
abnormal response to cardiac infarction |
decreased myocardial infarct size |
decreased fatty acid oxidation |
decreased oxygen consumption |
hypoxia |
abnormal physiological response to xenobiotic |
|
Availability | Mouse Genotype | |||||||
Abcc9em3Nich/Abcc9em3Nich | ||||||||
Tg(CMV-Abcc9)1Ajo/? | ||||||||
Abcc9tm1.1Mcn/Abcc9tm1.1Mcn Tg(Tagln-cre)1Her/0 (conditional) |
* |
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 04/23/2024 MGI 6.23 |
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