Wnt11 Phenotype Annotations

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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

18 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wnt11^{tm1.1(KOMP)Vlcg}/Wnt11^{tm1.1(KOMP)Vlcg} C57BL/6N-Wnt11^{tm1.1(KOMP)Vlcg}/Ucd	abnormal heart morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal testis morphology	J:211773
	abnormal uterus morphology	J:211773
	enlarged heart	J:211773
	hydrometra	J:211773
	increased blood urea nitrogen level	J:211773
	small testis	J:211773
Wnt11^tm1.1Khay/Wnt11^tm1.2Khay Pgr^tm2(cre)Lyd/Pgr⁺ involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	abnormal uterus physiology	J:170159
	increased endometrial gland number	J:170159
Wnt11^tm1Amc/Wnt11^tm1Amc 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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