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Symbol
Name
ID
Slc12a1
solute carrier family 12, member 1
MGI:103150
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Chondrocalcinosis
Osteopenia
Disease(s) Associated with SLC12A1
Bartter disease type 1

Mouse Phenotypes
abnormal bone structure
decreased bone mineral density
Availability Mouse Genotype
Slc12a1urehr3/Slc12a1urehr3

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO)
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Funding Information
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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory