Symbol
Name
ID

Wnt10a
wingless-type MMTV integration site family, member 10A
MGI:108071

Phenotype annotations related to skeleton

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Aplasia of the maxilla	Enamel hypoplasia
Disease(s) Associated with WNT10A	Aplasia of the maxilla	Enamel hypoplasia
tooth agenesis

Mouse Phenotypes

skeleton phenotype

abnormal alveolar process morphology

dental pulp stones

taurodontia

abnormal incisor morphology

abnormal molar morphology

abnormal molar crown morphology

abnormal molar cusp morphology

abnormal molar root morphology

absent molars

small molars

supernumerary molars

abnormal dentin mineralization

abnormal dentin morphology

abnormal tooth root resorption

short tibia

increased bone mineral content

Availability

Mouse Genotype

Wnt10a^{tm1.1(KOMP)Vlcg}/Wnt10a^{tm1.1(KOMP)Vlcg}

Wnt10a^tm1.1Smr/Wnt10a^tm1.1Smr

Wnt10a^tm1Smr/Wnt10a^tm1Smr
Tg(KRT14-cre)#Smr/0 (conditional)

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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