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Symbol
Name
ID
Erbb3
erb-b2 receptor tyrosine kinase 3
MGI:95411
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Arthrogryposis multiplex congenita
Skeletal muscle atrophy
Disease(s) Associated with ERBB3
lethal congenital contracture syndrome 2
neuronal intestinal dysplasia type A

Mouse Phenotypes
abnormal myocardium layer morphology
abnormal myocardial trabeculae morphology
Availability Mouse Genotype
Erbb3tm1Gne/Erbb3tm1Gne

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
04/09/2024
MGI 6.23
The Jackson Laboratory