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Symbol
Name
ID
Slc13a5
solute carrier family 13 (sodium-dependent citrate transporter), member 5
MGI:3037150
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Limb hypertonia
Spasticity
Axial hypotonia
Disease(s) Associated with SLC13A5
developmental and epileptic encephalopathy 25

Mouse Phenotypes
increased muscle cell glucose uptake
abnormal muscle physiology
Availability Mouse Genotype
Slc13a5tm1.2Helf/Slc13a5tm1.2Helf

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
04/16/2024
MGI 6.23
The Jackson Laboratory