Symbol Name ID |
Slc12a5
solute carrier family 12, member 5 MGI:1862037 |
Darker colors indicate more annotations |
Human Phenotypes | Secondary microcephaly |
Disease(s) Associated with SLC12A5 | |
developmental and epileptic encephalopathy 34 |
Mouse Phenotypes | decreased bone mineral content |
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Availability | Mouse Genotype | |
Slc12a5em1(IMPC)Mbp/Slc12a5+ |
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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