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Symbol
Name
ID

Slc20a2
solute carrier family 20, member 2
MGI:97851

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Urinary incontinence	Attention deficit hyperactivity disorder	Bipolar affective disorder	Impaired executive functioning	Motor tics
Disease(s) Associated with SLC20A2
basal ganglia calcification

Mouse Phenotypes		absent pinna reflex	abnormal motor coordination/balance	increased grip strength	abnormal vocalization
Availability	Mouse Genotype	absent pinna reflex	abnormal motor coordination/balance	increased grip strength	abnormal vocalization
	Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2^{tm1a(EUCOMM)Wtsi}
	Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2⁺
	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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