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Symbol
Name
ID

Slc20a2
solute carrier family 20, member 2
MGI:97851

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Abnormal circulating calcium concentration	Calcification of the small brain vessels	Cerebellar calcifications	Cerebellar dentate nucleus calcification	Cerebral calcification	Basal ganglia calcification
Disease(s) Associated with SLC20A2
basal ganglia calcification

Mouse Phenotypes		increased circulating magnesium level	decreased circulating phosphate level	increased circulating alkaline phosphatase level	subcutaneous edema	impaired glucose tolerance	abnormal mineral level
Availability	Mouse Genotype	increased circulating magnesium level	decreased circulating phosphate level	increased circulating alkaline phosphatase level	subcutaneous edema	impaired glucose tolerance	abnormal mineral level
	Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2^{tm1a(EUCOMM)Wtsi}
	Slc20a2^{tm1b(EUCOMM)Wtsi}/Slc20a2⁺

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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