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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Wnt10btm1e.1(KOMP)Wtsi/Wnt10btm1e.1(KOMP)Wtsi
C57BL/6N-Wnt10btm1e.1(KOMP)Wtsi/Ucd
abnormal brain morphology J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased startle reflex J:211773
hydrocephaly J:211773
Wnt10btm1Ptr/Wnt10btm1Ptr
involves: FVB
abnormal muscle development J:99298
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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last database update
09/17/2019
MGI 6.14
The Jackson Laboratory