About Help FAQ

Symbol
Name
ID

Dll4
delta like canonical Notch ligand 4
MGI:1859388

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Oligohydramnios	Decreased fetal movement
Disease(s) Associated with DLL4	Oligohydramnios	Decreased fetal movement
Adams-Oliver syndrome

Mouse Phenotypes		abnormal umbilical artery morphology	abnormal placenta vasculature	abnormal vitelline vasculature morphology	absent vitelline blood vessels	embryo tissue necrosis	abnormal embryo development	embryonic growth retardation	abnormal visceral yolk sac morphology	abnormal vitelline vascular remodeling
Availability	Mouse Genotype	abnormal umbilical artery morphology	abnormal placenta vasculature	abnormal vitelline vasculature morphology	absent vitelline blood vessels	embryo tissue necrosis	abnormal embryo development	embryonic growth retardation	abnormal visceral yolk sac morphology	abnormal vitelline vascular remodeling
	Dll4^tm1Jrt/Dll4^tm1Jrt
	Dll4^tm1Grid/Dll4⁺
	Dll4^tm1Jrt/Dll4⁺
	Dll4^tm1Nwg/Dll4⁺
	Dll4^tm2.1Vlcg/Dll4⁺ Tg(Nanog-cre)#Vlcg/0 (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 05/28/2024 MGI 6.13