About Help FAQ

Symbol
Name
ID

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

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Aplasia of the maxilla	Enamel hypoplasia	Finger aplasia	Foot oligodactyly	Toe syndactyly	Finger syndactyly	Split foot	Split hand
Disease(s) Associated with WNT10B	Aplasia of the maxilla	Enamel hypoplasia	Finger aplasia	Foot oligodactyly	Toe syndactyly	Finger syndactyly	Split foot	Split hand
split hand-foot malformation 6
tooth agenesis

Mouse Phenotypes		decreased bone mineral content	decreased bone mineral density
Availability	Mouse Genotype
	Wnt10b^{tm1e.1(KOMP)Wtsi}/Wnt10b^{tm1e.1(KOMP)Wtsi}

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/09/2024 MGI 6.23