Wnt2 Phenotype Annotations

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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)
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