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Symbol
Name
ID
Wls
wntless WNT ligand secretion mediator
MGI:1915401
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Wlsem1Jgg/Wlsem1Jgg
Wlsem2Jgg/Wlsem2Jgg
Wlstm1.1Lan/Wlstm1.1Lan
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)
Wlstm1.1Whsu/Wlstm1.1Whsu
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)

Contributing Projects:
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
The Jackson Laboratory