Symbol Name ID |
Wwox
WW domain-containing oxidoreductase MGI:1931237 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Sudden unexpected death in epilepsy |
Disease(s) Associated with WWOX | |
developmental and epileptic encephalopathy 28 |
Mouse Phenotypes | mortality/aging |
decreased survivor rate |
premature death |
postnatal lethality, complete penetrance |
|
Availability | Mouse Genotype | ||||
Wwoxem1Mald/Wwoxem1Mald | |||||
WwoxGt(XG218)Byg/WwoxGt(XG218)Byg | |||||
Wwoxtm1.1Mald/Wwoxtm1.1Mald | |||||
Wwoxtm1Mald/Wwoxtm1Mald | * | ||||
Wwoxtm1Ria/Wwoxtm1Ria | |||||
Wwoxtm2.1Ria/Wwoxtm2.1Ria |
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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