Wnt2 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt2
wingless-type MMTV integration site family, member 2
MGI:98954

15 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
\Wnt2^{tm1.1(rtTA)Eem}/\Wnt2^{tm1.1(rtTA)Eem} involves: 129X1/SvJ * C57BL/6	abnormal lung vasculature morphology	J:153098
	abnormal lung-associated mesenchyme development	J:153098
	abnormal respiratory system physiology	J:153098
	cyanosis	J:153098
	decreased mesenchymal cell proliferation involved in lung development	J:153098
	neonatal lethality, incomplete penetrance	J:153098
	pulmonary hypoplasia	J:153098
\Wnt2^tm1Bjw/\Wnt2^tm1Bjw involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal fetal growth/weight/body size	J:36835
	abnormal placenta development	J:36835
	abnormal placenta labyrinth morphology	J:36835
	abnormal placenta morphology	J:36835
	abnormal placenta vasculature	J:36835
	decreased body size	J:36835
	decreased body weight	J:36835
	perinatal lethality, incomplete penetrance	J:36835

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 03/25/2025 MGI 6.24