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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Ctdnep1tm1Ryn/Ctdnep1+
Wnt3tm1Brd/Wnt3+
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6
decreased primordial germ cell number J:199855
normal embryo phenotype J:199855
Eomestm1.1Rob/Eomes+
Wnt3tm1Brd/Wnt3+
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA
no abnormal phenotype detected J:131055
Lrp6Gw/Lrp6+
Wnt3tm1Brd/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
dilated hair follicle J:53379
short hair J:53379
Wnt3tm2Brd/Wnt3tm2Brd
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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory