|
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 |
Thalamic calcification |
Dysdiadochokinesis |
Limb dysmetria |
Bradykinesia |
Parkinsonism |
Athetosis |
Chorea |
Tremor |
Postural tremor |
Hand tremor |
Abnormal pyramidal sign |
Dysarthria |
Depression |
Anxiety |
Psychosis |
Bipolar affective disorder |
Apathy |
Impaired executive functioning |
Motor tics |
Attention deficit hyperactivity disorder |
Cognitive impairment |
Memory impairment |
Mental deterioration |
Dementia |
Micrographia |
Hyperreflexia |
Dyskinesia |
Dystonia |
Gait disturbance |
Postural instability |
Migraine |
Global developmental delay |
Seizure |
| Disease(s) Associated with SLC20A2 | ||||||||||||||||||||||||||||||||||||||
| basal ganglia calcification |
| Mouse Phenotypes | multiple persisting craniopharyngeal ducts |
microgliosis |
small superior cervical ganglion |
abnormal forebrain morphology |
abnormal basal ganglion morphology |
abnormal thalamus morphology |
abnormal cerebral cortex morphology |
calcified brain |
abnormal hypoglossal nerve topology |
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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 04/23/2024 MGI 6.23 |
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