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 | Prominent sternum |
Disease(s) Associated with ALDH1A2 | |
congenital diaphragmatic hernia |
Mouse Phenotypes | skeleton phenotype |
abnormal laryngeal cartilage morphology |
abnormal cricoid cartilage morphology |
abnormal thyroid cartilage morphology |
abnormal tracheal cartilage morphology |
decreased tracheal cartilage ring number |
|
Availability | Mouse Genotype | ||||||
Aldh1a2tm1Dll/Aldh1a2tm1Dll | |||||||
Aldh1a2tm1Dll/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 09/03/2024 MGI 6.24 |
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