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Symbol Name ID |
Slc20a2
solute carrier family 20, member 2 MGI:97851 |
| Darker colors indicate more annotations |
| Human Phenotypes | 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 | abnormal incisor color |
abnormal spine curvature |
kyphosis |
fusion of vertebral arches |
decreased bone mineral content |
decreased bone mineral density |
ectopic cartilage |
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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 05/26/2026 MGI 6.24 |
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