SLC12A1 Chromosome 15

Solute carrier family 12 member 1
147 variants 147 Health Risk

Upload your DNA to see your personal genotypes for variants in SLC12A1.

What This Gene Does
This gene encodes a kidney-specific sodium-potassium-chloride cotransporter that is expressed on the luminal membrane of renal epithelial cells of the thick ascending limb of Henle's loop and the macula densa. It plays a key role in concentrating urine and accounts for most of the NaCl resorption. It is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their biological validity in humans has not been experimentally proven.[provided by RefSeq, May 2010]
Gene Info
Gene Group
Solute carrier family 12
Locus Type
gene with protein product
Location
15q21.1
Ensembl
ENSG00000074803
Associated Conditions (8)
Bartter disease type 1
Inborn genetic diseases
SLC12A1-related disorder
Clear cell carcinoma of kidney
Bartter syndrome
Nephrocalcinosis
Nephrolithiasis
See cases
Key Variants
RS116848967
Conflicting classifications of pathogenicity
Bartter disease type 1, Inborn genetic diseases, SLC12A1-related disorder
Health Risk
RS137893258
Conflicting classifications of pathogenicity
Bartter disease type 1, SLC12A1-related disorder, Bartter disease type 1
Health Risk
RS1380626543
Conflicting classifications of pathogenicity
SLC12A1-related disorder, Inborn genetic diseases, SLC12A1-related disorder
Health Risk
RS138382420
Conflicting classifications of pathogenicity
Bartter disease type 1, Inborn genetic diseases, Bartter disease type 1
Health Risk
RS139471047
Conflicting classifications of pathogenicity
Inborn genetic diseases, Bartter disease type 1, Inborn genetic diseases
Health Risk
RS139832082
Conflicting classifications of pathogenicity
Bartter disease type 1, SLC12A1-related disorder, Bartter disease type 1
Health Risk
RS140636270
Conflicting classifications of pathogenicity
Bartter disease type 1, Bartter disease type 1
Health Risk
RS140747686
Conflicting classifications of pathogenicity
Bartter disease type 1, Bartter disease type 1
Health Risk
RS141683652
Conflicting classifications of pathogenicity
Inborn genetic diseases, Bartter disease type 1, Inborn genetic diseases
Health Risk
RS142360465
Conflicting classifications of pathogenicity
Bartter disease type 1, Clear cell carcinoma of kidney, Bartter disease type 1
Health Risk
RS142646329
Conflicting classifications of pathogenicity
Health Risk
RS145003411
Conflicting classifications of pathogenicity
Bartter disease type 1, Bartter disease type 1
Health Risk
All Variants (147)
RSID Category Clinical Significance Conditions
RS2505099559 Health Risk Pathogenic
RS2505120564 Health Risk Pathogenic
RS2505137296 Health Risk Pathogenic
RS2505137368 Health Risk Pathogenic
RS2505182645 Health Risk Pathogenic
RS2505190434 Health Risk Pathogenic
RS2505218930 Health Risk Pathogenic
RS2505218935 Health Risk Pathogenic
RS2505219470 Health Risk Pathogenic
RS2505225464 Health Risk Pathogenic
RS35294392 Health Risk Pathogenic
RS375445813 Health Risk Pathogenic
RS539865839 Health Risk Pathogenic
RS6493311 Health Risk Pathogenic
RS745334373 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS746659421 Health Risk Pathogenic
RS750424494 Health Risk Pathogenic
RS756057922 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS761193706 Health Risk Pathogenic
RS761459796 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS766364222 Health Risk Pathogenic
RS773855120 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS773964647 Health Risk Pathogenic
RS774515747 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS779588655 Health Risk Pathogenic Bartter disease type 1, Nephrolithiasis, Nephrocalcinosis
RS781230604 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS901038678 Health Risk Pathogenic
RS1273695811 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS1318795841 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS1400209959 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS1413414501 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS1566861493 Health Risk Pathogenic/Likely pathogenic
RS1567311211 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS1567314296 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Inborn genetic diseases, Bartter disease type 1
RS1597456179 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS2042079691 Health Risk Pathogenic/Likely pathogenic Bartter syndrome, Bartter syndrome
RS2505053163 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS758166864 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS758291275 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS758961147 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS764247288 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS765347751 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS776346805 Health Risk Pathogenic/Likely pathogenic SLC12A1-related disorder, SLC12A1-related disorder
RS776749406 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS780619649 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS865973286 Health Risk Pathogenic/Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS896545456 Health Risk Pathogenic/Likely pathogenic Nephrolithiasis, Nephrocalcinosis, Bartter disease type 1
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