Symbol Name ID |
Aldh1a2
aldehyde dehydrogenase family 1, subfamily A2 MGI:107928 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Congenital diaphragmatic hernia |
Aplasia/Hypoplasia of the diaphragm |
Agenesis of the diaphragm |
Disease(s) Associated with ALDH1A2 | |||
congenital diaphragmatic hernia |
Mouse Phenotypes | muscle phenotype |
abnormal myocardium layer morphology |
absent myocardial trabeculae |
thick myocardium |
|
Availability | Mouse Genotype | ||||
Aldh1a2tm1Ipc/Aldh1a2tm1Ipc | |||||
Aldh1a2tm1Dll/Aldh1a2tm1Ipc Tg(Rarb-cre)1Mrc/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 05/28/2024 MGI 6.13 |
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