About   Help   FAQ
Symbol
Name
ID
Slc3a1
solute carrier family 3, member 1
MGI:1195264
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Hematuria
Hyperlysinuria
Argininuria
Cystinuria
Ornithinuria
Nephrolithiasis
Renal insufficiency
Recurrent urinary tract infections
Disease(s) Associated with SLC3A1
cystinuria

Mouse Phenotypes
polycystic kidney
enlarged kidney
increased kidney weight
enlarged urinary bladder
argininuria
lysinuria
ornithinuria
abnormal urine amino acid level
aminoaciduria
cystinuria
crystalluria
kidney inflammation
tubulointerstitial nephritis
abnormal urinary bladder detrusor smooth muscle morphology
impaired contractility of urinary bladder detrusor smooth muscle
abnormal kidney morphology
abnormal kidney cortex morphology
abnormal renal glomerulus morphology
kidney cortex atrophy
kidney medulla atrophy
hydronephrosis
decreased kidney weight
small kidney
dilated renal tubule
nephrolithiasis
ureter obstruction
abnormal urinary bladder morphology
increased urinary bladder weight
cystolithiasis
urinary bladder obstruction
urolithiasis
abnormal urinary bladder physiology
abnormal bladder urine volume
abnormal urination
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory