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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 iris morphology |
irregularly shaped pupil |
abnormal lens morphology |
cataract |
narrow eye opening |
eyelids fail to open |
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| Availability | Mouse Genotype | ||||||
| Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2tm1a(EUCOMM)Wtsi | |||||||
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 04/16/2024 MGI 6.23 |
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