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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Fzd2tm1.1Nat/Fzd2+
Fzd7tm1.1Nat/Fzd7tm1.1Nat
Wnt11tm1Amc/Wnt11+
involves: 129 * C57BL/6
abnormal heart morphology J:189062
cleft palate J:189062
ventricular septal defect J:189062
Rettm1Cos/Ret+
Wnt11tm1Amc/Wnt11+
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * MF1
small kidney J:83430
Rettm1Cos/Ret+
Wnt11tm1Amc/Wnt11tm1Amc
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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory