Symbol Name ID |
Slc20a2
solute carrier family 20, member 2 MGI:97851 |
Darker colors indicate more annotations |
Human Phenotypes | Urinary incontinence |
Depression |
Bipolar affective disorder |
Apathy |
Impaired executive functioning |
Motor tics |
Attention deficit hyperactivity disorder |
Disease(s) Associated with SLC20A2 | |||||||
basal ganglia calcification |
Mouse Phenotypes | absent pinna reflex |
abnormal motor coordination/balance |
increased grip strength |
abnormal vocalization |
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Availability | Mouse Genotype | ||||
Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2tm1a(EUCOMM)Wtsi | |||||
Slc20a2tm1a(EUCOMM)Wtsi/Slc20a2+ | |||||
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 04/16/2024 MGI 6.23 |
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