About Help FAQ

Symbol
Name
ID

Erbb3
erb-b2 receptor tyrosine kinase 3
MGI:95411

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Polyhydramnios	Decreased fetal movement
Disease(s) Associated with ERBB3	Polyhydramnios	Decreased fetal movement
lethal congenital contracture syndrome 2

Mouse Phenotypes		abnormal neural crest cell migration	abnormal embryonic neuroepithelial layer differentiation
Availability	Mouse Genotype	abnormal neural crest cell migration	abnormal embryonic neuroepithelial layer differentiation
	Erbb3^tm1Gne/Erbb3^tm1Gne
	Erbb3^tm2Cbm/Erbb3^tm2Cbm

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 04/16/2024 MGI 6.23