Symbol Name ID |
Slc20a2
solute carrier family 20, member 2 MGI:97851 |
Darker colors indicate more annotations |
Human Phenotypes | Horizontal nystagmus |
Disease(s) Associated with SLC20A2 | |
basal ganglia calcification |
Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal iris morphology |
irregularly shaped pupil |
abnormal lens morphology |
cataract |
narrow eye opening |
eyelids fail to open |
abnormal retina morphology |
decreased total retina thickness |
abnormal vitreous body morphology |
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Availability | Mouse Genotype | ||||||||||
Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2tm1a(EUCOMM)Wtsi | |||||||||||
Slc20a2tm1b(EUCOMM)Wtsi/Slc20a2tm1b(EUCOMM)Wtsi | |||||||||||
Slc20a2tm1b(EUCOMM)Wtsi/Slc20a2+ |
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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last database update 08/02/2024 MGI 6.24 |
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