Wnt7b Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt7b
wingless-type MMTV integration site family, member 7B
MGI:98962

6 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Edil3^{Tg(Sox2-cre)1Amc}/Edil3⁺ Wnt7a^tm1Amc/Wnt7a^tm1Amc Wnt7b^tm1Parr/Wnt7b^tm2Amc involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal blood-brain barrier function	J:142352
	abnormal vasculogenesis	J:142352
	embryonic lethality during organogenesis, complete penetrance	J:142352
	intracranial hemorrhage	J:142352
	spinal hemorrhage	J:142352
Gt(ROSA)26Sor^tm1Sor/? Wnt7b^tm2Amc/Wnt7b^tm2.1Amc Tg(Hoxb7-cre)13Amc/0 involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6	dilated kidney collecting duct	J:142685
Tg(Nes-cre)1Kln/0 Wnt7a^tm1Amc/Wnt7a^tm1Amc Wnt7b^tm1Parr/Wnt7b^tm2Amc involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	abnormal blood-brain barrier function	J:142352
	abnormal vasculogenesis	J:142352
	embryonic lethality during organogenesis, complete penetrance	J:142352
	intracranial hemorrhage	J:142352
	spinal hemorrhage	J:142352

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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