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Symbol
Name
ID

Slc20a2
solute carrier family 20, member 2
MGI:97851

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Horizontal nystagmus
Disease(s) Associated with SLC20A2	Horizontal nystagmus
basal ganglia calcification

Mouse Phenotypes		abnormal iris morphology	irregularly shaped pupil	abnormal lens morphology	cataract	narrow eye opening	eyelids fail to open
Availability	Mouse Genotype	abnormal iris morphology	irregularly shaped pupil	abnormal lens morphology	cataract	narrow eye opening	eyelids fail to open
	Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2^{tm1a(EUCOMM)Wtsi}
	Slc20a2^{tm1b(EUCOMM)Wtsi}/Slc20a2^{tm1b(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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