Wnt10b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt10b
wingless-type MMTV integration site family, member 10B
MGI:108061

7 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wnt10b^{tm1e.1(KOMP)Wtsi}/Wnt10b^{tm1e.1(KOMP)Wtsi} C57BL/6N-Wnt10b^{tm1e.1(KOMP)Wtsi}/Ucd	abnormal brain morphology	J:211773
	abnormal cecum morphology	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	hydrocephaly	J:211773
Wnt10b^tm1Ptr/Wnt10b^tm1Ptr involves: FVB	abnormal muscle development	J:99298
Wnt10b^tm1Ptr/Wnt10b^tm1Ptr involves: FVB	abnormal muscle regeneration	J:99298

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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