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Symbol
Name
ID
Zeb2
zinc finger E-box binding homeobox 2
MGI:1344407
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Drooling
Abnormal enteric ganglion morphology
Aganglionic megacolon
Dysphagia
Spasticity
Morphological central nervous system abnormality
Ventriculomegaly
Polymicrogyria
Focal cortical dysplasia
Large basal ganglia
Abnormal cerebral white matter morphology
Abnormal corpus callosum morphology
Agenesis of corpus callosum
Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the cerebral white matter
Focal white matter lesions
Abnormal hippocampus morphology
Agenesis of cerebellar vermis
Cerebellar vermis hypoplasia
Enlarged cerebellum
Periventricular heterotopia
Ataxia
EEG with generalized slow activity
EEG with spike-wave complexes
Absent speech
Expressive aphasia
Delayed speech and language development
Anxiety
Happy demeanor
Reduced social reciprocity
Motor stereotypy
Bruxism
Intellectual disability
Intellectual disability, moderate
Intellectual disability, severe
Sleep abnormality
Broad-based gait
Inability to walk
Developmental regression
Neurodevelopmental delay
Motor delay
Delayed fine motor development
Delayed ability to walk
Seizure
Atypical absence seizure
Focal-onset seizure
Status epilepticus
Impaired pain sensation
Disease(s) Associated with ZEB2
Hirschsprung's disease
Mowat-Wilson syndrome

Mouse Phenotypes
nervous system phenotype
abnormal neural plate morphology
abnormal melanoblast morphology
absent vagal neural crest cells
open neural tube
Availability Mouse Genotype
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
Zeb2tm1.2Yhi/Zeb2+ *
Zeb2tm1.1Yhi/Zeb2tm1.1Yhi
Tg(Dct-lacZ)A12Jkn/0
Tg(Tyr-cre)1Lru/Y  (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
04/16/2024
MGI 6.23
The Jackson Laboratory