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Symbol
Name
ID
Slc12a1
solute carrier family 12, member 1
MGI:103150
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Hyperchloriduria
Increased urinary potassium
Renal potassium wasting
Hypercalciuria
Renal salt wasting
Hyperprostaglandinuria
Hyposthenuria
Renal juxtaglomerular cell hypertrophy/hyperplasia
Nephrocalcinosis
Polyuria
Disease(s) Associated with SLC12A1
Bartter disease type 1

Mouse Phenotypes
decreased urine creatinine level
increased urine creatinine level
abnormal renal water reabsorbtion
increased urine potassium level
decreased urine sodium level
increased urine sodium level
abnormal urine homeostasis
increased urine calcium level
increased urine magnesium level
decreased urine osmolality
increased urine osmolality
increased urine prostaglandin level
abnormal urine urea nitrogen level
decreased urine uric acid level
pyelitis
pyelonephritis
abnormal kidney morphology
kidney papillary atrophy
hydronephrosis
abnormal renal tubule morphology
nephrocalcinosis
abnormal kidney physiology
increased creatinine clearance
abnormal renal reabsorbtion
abnormal tubuloglomerular feedback response
decreased tubuloglomerular feedback response
kidney failure
polyuria
Availability Mouse Genotype
Slc12a1tm1Haca/Slc12a1tm1Haca
Slc12a1tm1Tkh/Slc12a1tm1Tkh
Slc12a1tm2Haca/Slc12a1tm2Haca
Slc12a1urehr3/Slc12a1urehr3

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