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Symbol
Name
ID
Slc12a5
solute carrier family 12, member 5
MGI:1862037
Phenotype annotations related to skeleton
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
Availability Mouse Genotype
Slc12a5em1(IMPC)Mbp/Slc12a5+

Contributing Projects:
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
The Jackson Laboratory