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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
15 phenotypes from 4 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Wnt11tm1.1(KOMP)Vlcg/Wnt11tm1.1(KOMP)Vlcg
C57BL/6N-Wnt11tm1.1(KOMP)Vlcg/Ucd
abnormal kidney morphology J:211773
abnormal testis morphology J:211773
decreased body length J:211773
increased blood urea nitrogen level J:211773
small testis J:211773
Wnt11tm1.1Khay/Wnt11tm1.2Khay
Pgrtm2(cre)Lyd/Pgr+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
abnormal uterus physiology J:170159
increased endometrial gland number J:170159
Wnt11tm1Amc/Wnt11tm1Amc
involves: 129S1/Sv * 129X1/SvJ
abnormal ureteric bud tip morphology J:83430
decreased renal glomerulus number J:83430
delayed kidney development J:83430
embryonic lethality during organogenesis, incomplete penetrance J:83430
impaired branching involved in ureteric bud morphogenesis J:83430
neonatal lethality, complete penetrance J:83430
renal hypoplasia 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
11/12/2024
MGI 6.24
The Jackson Laboratory