Symbol Name ID |
Wls
wntless WNT ligand secretion mediator MGI:1915401 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Spastic gait |
Dilated fourth ventricle |
Hypoplasia of the corpus callosum |
Cerebellar vermis hypoplasia |
Intraventricular arachnoid cyst |
Delayed speech and language development |
Delayed early-childhood social milestone development |
Intellectual disability |
Hyperreflexia |
Unsteady gait |
Developmental regression |
Delayed fine motor development |
Delayed gross motor development |
Seizure |
Disease(s) Associated with WLS | |||||||||||||||
Zaki syndrome |
Mouse Phenotypes | abnormal neuron differentiation |
abnormal neural tube morphology |
abnormal neural tube closure |
abnormal brain morphology |
abnormal hindbrain development |
abnormal midbrain development |
abnormal midbrain-hindbrain boundary development |
absent midbrain-hindbrain boundary |
decreased forebrain size |
decreased brain size |
absent choroid plexus |
absent tectum |
absent tegmentum |
absent midbrain |
abnormal dentate gyrus morphology |
abnormal metencephalon morphology |
absent cerebellum |
abnormal nervous system development |
decreased neuron number |
abnormal cranial nerve morphology |
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Availability | Mouse Genotype | ||||||||||||||||||||
Wlsem1Jgg/Wlsem1Jgg | |||||||||||||||||||||
Wlsem2Jgg/Wlsem2Jgg | |||||||||||||||||||||
Wlstm1.1Lan/Wlstm1.1Lan H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Wlstm1.1Whsu/Wlstm1.1Whsu H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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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