Wnt11 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt11
wingless-type MMTV integration site family, member 11
MGI:101948

5 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Fzd2^tm1.1Nat/Fzd2⁺ Fzd7^tm1.1Nat/Fzd7^tm1.1Nat Wnt11^tm1Amc/Wnt11⁺ involves: 129 * C57BL/6	abnormal heart morphology	J:189062
	cleft palate	J:189062
	ventricular septal defect	J:189062
Ret^tm1Cos/Ret⁺ Wnt11^tm1Amc/Wnt11⁺ involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * MF1	small kidney	J:83430
Ret^tm1Cos/Ret⁺ Wnt11^tm1Amc/Wnt11^tm1Amc involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * MF1	impaired branching involved in ureteric bud morphogenesis	J:83430
	small kidney	J:83430

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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