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Symbol
Name
ID

Gpr68
G protein-coupled receptor 68
MGI:2441763

Phenotype annotations related to skeleton

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

Human Phenotypes	Amelogenesis imperfecta	Enamel hypomineralization
Disease(s) Associated with GPR68	Amelogenesis imperfecta	Enamel hypomineralization
amelogenesis imperfecta type 2A6

Mouse Phenotypes		skeleton phenotype	abnormal osteoclast differentiation	abnormal osteoclast physiology
Availability	Mouse Genotype	skeleton phenotype	abnormal osteoclast differentiation	abnormal osteoclast physiology
	Gpr68^tm1.1Yaxu/Gpr68^tm1.1Yaxu	*
	Gpr68^tm1Yaxu/Gpr68^tm1Yaxu

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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