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Symbol Name ID |
Aldh7a1
aldehyde dehydrogenase family 7, member A1 MGI:108186 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Prenatal movement abnormality |
Feeding difficulties |
Restlessness |
| Disease(s) Associated with ALDH7A1 | |||
| pyridoxine-dependent epilepsy |
| Mouse Phenotypes | behavior/neurological phenotype |
seizures |
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| Availability | Mouse Genotype | ||
| Aldh7a1tm1d(EUCOMM)Hmgu/Aldh7a1tm1d(EUCOMM)Hmgu | * | ||
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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