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Symbol Name ID |
Aldh1a3
aldehyde dehydrogenase family 1, subfamily A3 MGI:1861722 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short palpebral fissure |
Entropion |
| Disease(s) Associated with ALDH1A3 | ||
| isolated microphthalmia 8 |
| Mouse Phenotypes | ethmoturbinate hypoplasia |
persistent nasal fins |
choanal atresia |
abnormal nasal cavity morphology |
absent maxillary sinus |
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| Availability | Mouse Genotype | |||||
| Aldh1a3tm1.1Pcn/Aldh1a3tm1.1Pcn | ||||||
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 04/16/2024 MGI 6.23 |
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