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Symbol
Name
ID
Erbb4
erb-b2 receptor tyrosine kinase 4
MGI:104771
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Amyotrophic lateral sclerosis
Dementia
Loss of ambulation
Disease(s) Associated with ERBB4
amyotrophic lateral sclerosis type 19

Mouse Phenotypes
abnormal motor neuron innervation pattern
abnormal sensory neuron innervation pattern
abnormal vestibulocochlear ganglion morphology
abnormal cranial ganglia morphology
abnormal geniculate ganglion morphology
abnormal trigeminal ganglion morphology
abnormal cranial nerve morphology
abnormal facial nerve morphology
abnormal glossopharyngeal nerve morphology
abnormal trigeminal nerve morphology
abnormal vestibulocochlear nerve morphology
enhanced long-term potentiation
abnormal prepulse inhibition
decreased prepulse inhibition
Availability Mouse Genotype
Erbb4tm1Grl/Erbb4tm1Grl
Erbb4tm1Grl/Erbb4+
Erbb4tm1Fej/Erbb4tm1Fej
Pvalbtm1(cre)Arbr/Pvalb+  (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