|
Symbol Name ID |
Wdr4
WD repeat domain 4 MGI:1889002 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Aqueductal stenosis |
Pachygyria |
Partial agenesis of the corpus callosum |
Abnormality of neuronal migration |
Hemiplegia/hemiparesis |
EEG abnormality |
Absent speech |
Cognitive impairment |
Brisk reflexes |
Global developmental delay |
Profound global developmental delay |
Seizure |
Status epilepticus |
| Disease(s) Associated with WDR4 | |||||||||||||||
| Galloway-Mowat syndrome | |||||||||||||||
| microcephaly, growth deficiency, seizures, and brain malformations |
| Mouse Phenotypes | abnormal brain development |
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| Availability | Mouse Genotype | |
| Wdr4tm1.1Hsi/Wdr4tm1.1Hsi | ||
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 04/23/2024 MGI 6.23 |
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