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Symbol Name ID |
Wwox
WW domain-containing oxidoreductase MGI:1931237 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
| Disease(s) Associated with WWOX | |
| developmental and epileptic encephalopathy 28 |
| Mouse Phenotypes | abnormal fear/anxiety-related behavior |
increased thigmotaxis |
abnormal response to social novelty |
abnormal motor capabilities/coordination/movement |
limb grasping |
impaired coordination |
decreased locomotor activity |
decreased social investigation |
convulsive seizures |
tonic-clonic seizures |
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| Availability | Mouse Genotype | ||||||||||
| Wwoxem1Mald/Wwoxem1Mald | |||||||||||
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 05/14/2024 MGI 6.23 |
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