Wnt3 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt3
wingless-type MMTV integration site family, member 3
MGI:98955

10 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ctdnep1^tm1Ryn/Ctdnep1⁺ Wnt3^tm1Brd/Wnt3⁺ involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	decreased primordial germ cell number	J:199855
	normal embryo phenotype	J:199855
Eomes^tm1.1Rob/Eomes⁺ Wnt3^tm1Brd/Wnt3⁺ involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA	no abnormal phenotype detected	J:131055
Lrp6^Gw/Lrp6⁺ Wnt3^tm1Brd/Wnt3⁺ involves: 101/H * 129S7/SvEvBrd * BALB/c * C3H	kinked tail	J:170646
Tg(Wnt3)7Gsb/0 either: FVB/N or (involves: C57BL/6 * FVB/N)	alopecia	J:53379
Tg(Wnt3)7Gsb/Tg(Wnt3)7Gsb either: FVB/N or (involves: C57BL/6 * FVB/N)	abnormal hair shaft morphology	J:53379
	alopecia	J:53379
	dermal cyst	J:53379
	distended hair follicles	J:53379
	short hair	J:53379
Wnt3^tm2Brd/Wnt3^tm2Brd involves: 129S7/SvEvBrd * C57BL/6Brd	prenatal lethality, complete penetrance	J:56548

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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