|
Symbol Name ID |
Aldh7a1
aldehyde dehydrogenase family 7, member A1 MGI:108186 |
| Darker colors indicate more annotations |
| Human Phenotypes | Delayed CNS myelination |
Ventriculomegaly |
Hypoplasia of the corpus callosum |
Brain atrophy |
Widened subarachnoid space |
EEG with generalized slow activity |
Multifocal epileptiform discharges |
EEG with generalized epileptiform discharges |
EEG with burst suppression |
EEG with generalized sharp slow waves |
Hypsarrhythmia |
Irritability |
Restlessness |
Intellectual disability |
Neurodevelopmental delay |
Seizure |
Early onset absence seizures |
Focal-onset seizure |
Focal aware motor seizure |
Focal myoclonic seizure |
Atonic seizure |
Epileptic spasm |
Status epilepticus |
| Disease(s) Associated with ALDH7A1 | |||||||||||||||||||||||
| pyridoxine-dependent epilepsy |
| Mouse Phenotypes | 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 04/30/2024 MGI 6.23 |
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