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Symbol
Name
ID
Slc3a1
solute carrier family 3, member 1
MGI:1195264
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Hyperuricemia
Abnormality of amino acid metabolism
Hematuria
Hyperlysinuria
Argininuria
Cystinuria
Ornithinuria
Disease(s) Associated with SLC3A1
cystinuria

Mouse Phenotypes
argininuria
increased circulating creatinine level
lysinuria
ornithinuria
abnormal urine amino acid level
aminoaciduria
cystinuria
increased blood urea nitrogen level
increased circulating HDL cholesterol level
increased circulating LDL cholesterol level
increased circulating cholesterol level
increased circulating alkaline phosphatase level
uremia
crystalluria
Availability Mouse Genotype
Slc3a1m1Crl/Slc3a1m1Crl
Slc3a1pbl/Slc3a1pbl
Slc3a1tm1.1(KOMP)Vlcg/Slc3a1tm1.1(KOMP)Vlcg
Slc3a1tm1Jat/Slc3a1tm1Jat

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
04/30/2024
MGI 6.23
The Jackson Laboratory