About Help FAQ

Symbol
Name
ID

Efnb1
ephrin B1
MGI:102708

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Low posterior hairline	Thickened nuchal skin fold	Short neck	Webbed neck	Hemihypotrophy of lower limb	Umbilical hernia	Congenital diaphragmatic hernia	Short stature
Disease(s) Associated with EFNB1
craniofrontonasal syndrome

Mouse Phenotypes		failure of palatal shelf elevation	absent palatal shelf	cleft secondary palate	cleft palate	omphalocele
Availability	Mouse Genotype	failure of palatal shelf elevation	absent palatal shelf	cleft secondary palate	cleft palate	omphalocele
	Efnb1^tm1.1Rha/Efnb1^tm1.1Rha
	Efnb1^tm1.1Sor/Efnb1^tm1.1Sor
	Efnb1^tm1Rha/Efnb1^tm1Rha
	Efnb1^tm1.1Sor/Y
	Efnb1^tm1Rha/Y
	Efnb1^tm1Rha/Efnb1⁺ Tg(Pgk1-cre)1Lni/? (conditional)
	Efnb1^tm1Sor/Efnb1⁺ H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ (conditional)
	Efnb1^tm1Rha/Y Tg(Pgk1-cre)1Lni/? (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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/09/2024 MGI 6.23