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
RS1479511052 Health Risk Likely pathogenic Bartter disease type 1, Inborn genetic diseases, Bartter disease type 1
RS1486622300 Health Risk Likely pathogenic
RS1555466999 Health Risk Likely pathogenic Nephrocalcinosis, Nephrolithiasis, Bartter disease type 1
RS1566857461 Health Risk Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS201696514 Health Risk Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS201930377 Health Risk Likely pathogenic
RS2041199779 Health Risk Likely pathogenic Bartter syndrome, Bartter syndrome
RS2041206341 Health Risk Likely pathogenic
RS2041650191 Health Risk Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS2141064916 Health Risk Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS2141115303 Health Risk Likely pathogenic
RS2505026310 Health Risk Likely pathogenic See cases, See cases
RS2505027099 Health Risk Likely pathogenic
RS2505034797 Health Risk Likely pathogenic
RS2505087341 Health Risk Likely pathogenic
RS2505087791 Health Risk Likely pathogenic Bartter syndrome, Bartter disease type 1, Bartter syndrome
RS2505087861 Health Risk Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS2505136920 Health Risk Likely pathogenic
RS2505141958 Health Risk Likely pathogenic
RS2505190299 Health Risk Likely pathogenic Bartter syndrome, Bartter syndrome
RS2505191463 Health Risk Likely pathogenic
RS2505192006 Health Risk Likely pathogenic See cases, See cases
RS2505225672 Health Risk Likely pathogenic SLC12A1-related disorder, SLC12A1-related disorder
RS770400317 Health Risk Likely pathogenic Bartter disease type 1, Bartter syndrome, Bartter disease type 1
RS886039870 Health Risk Likely pathogenic Bartter disease type 1, Bartter disease type 1
RS1048935147 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS1057519608 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS1057520300 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS1057520302 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS1057520303 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS1057520304 Health Risk Pathogenic Bartter disease type 1, Inborn genetic diseases, Bartter disease type 1
RS1193100543 Health Risk Pathogenic
RS1295566242 Health Risk Pathogenic
RS137853158 Health Risk Pathogenic Bartter disease type 1, Bartter disease type 1
RS137853159 Health Risk Pathogenic Bartter disease type 1, SLC12A1-related disorder, Bartter disease type 1
RS1419151341 Health Risk Pathogenic
RS180847164 Health Risk Pathogenic
RS199877869 Health Risk Pathogenic Bartter syndrome, Bartter disease type 1, Bartter syndrome
RS2041000812 Health Risk Pathogenic
RS2041559629 Health Risk Pathogenic
RS2140999192 Health Risk Pathogenic
RS2505026251 Health Risk Pathogenic
RS2505026270 Health Risk Pathogenic
RS2505034727 Health Risk Pathogenic
RS2505080056 Health Risk Pathogenic
RS2505085696 Health Risk Pathogenic
RS2505087651 Health Risk Pathogenic
RS2505093961 Health Risk Pathogenic
RS2505099370 Health Risk Pathogenic
RS2505099397 Health Risk Pathogenic
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