About   Help   FAQ
Symbol
Name
ID
Erbb3
erb-b2 receptor tyrosine kinase 3
MGI:95411
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Episodic abdominal pain
Disease(s) Associated with ERBB3
lethal congenital contracture syndrome 2
neuronal intestinal dysplasia type A

Mouse Phenotypes
unresponsive to tactile stimuli
no spontaneous movement
Availability Mouse Genotype
Erbb3tm1Cbm/Erbb3tm1Cbm
Erbb3tm2Cbm/Erbb3tm2Cbm

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/19/2024
MGI 6.23
The Jackson Laboratory