CLCN5 Chromosome X

Cl-/H+ antiporter 5
116 variants 116 Health Risk

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What This Gene Does
This gene encodes a member of the ClC family of chloride ion channels and ion transporters. The encoded protein is primarily localized to endosomal membranes and may function to facilitate albumin uptake by the renal proximal tubule. Mutations in this gene have been found in Dent disease and renal tubular disorders complicated by nephrolithiasis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]
Gene Info
Gene Group
"CLC chloride channel and transporter family|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
Xp11.23
Ensembl
ENSG00000171365
Associated Conditions (19)
Dent disease type 1
X-linked recessive nephrolithiasis with renal failure
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
Hypophosphatemic rickets
X-linked recessive
Inborn genetic diseases
CLCN5-related disorder
Nonpapillary renal cell carcinoma
Hyperkalemia
Multiple small medullary renal cysts
Low-molecular-weight proteinuria
Thyroid cancer
nonmedullary
1
Nephrotic syndrome
Dent disease
Familial X-linked hypophosphatemic vitamin D refractory rickets
Key Variants
RS140312372
Conflicting classifications of pathogenicity
Dent disease type 1, Dent disease type 1
Health Risk
RS147798092
Conflicting classifications of pathogenicity
X-linked recessive nephrolithiasis with renal failure, Dent disease type 1, Proteinuria
Health Risk
RS148124447
Conflicting classifications of pathogenicity
Dent disease type 1, X-linked recessive nephrolithiasis with renal failure, Hypophosphatemic rickets
Health Risk
RS151340624
Conflicting classifications of pathogenicity
X-linked recessive nephrolithiasis with renal failure, CLCN5-related disorder, Proteinuria
Health Risk
RS151340626
Conflicting classifications of pathogenicity
Hypophosphatemic rickets, X-linked recessive, Dent disease type 1
Health Risk
RS2147605140
Conflicting classifications of pathogenicity
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
Health Risk
RS368039993
Conflicting classifications of pathogenicity
Dent disease type 1, Dent disease type 1
Health Risk
RS55676763
Conflicting classifications of pathogenicity
Dent disease type 1, Inborn genetic diseases, CLCN5-related disorder
Health Risk
RS781912440
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS781948493
Conflicting classifications of pathogenicity
Dent disease type 1, Dent disease type 1
Health Risk
RS782031818
Conflicting classifications of pathogenicity
Nonpapillary renal cell carcinoma, Nonpapillary renal cell carcinoma
Health Risk
RS782056386
Conflicting classifications of pathogenicity
Dent disease type 1, Hypophosphatemic rickets, X-linked recessive
Health Risk
All Variants (116)
RSID Category Clinical Significance Conditions
RS140312372 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Dent disease type 1
RS147798092 Health Risk Conflicting classifications of pathogenicity X-linked recessive nephrolithiasis with renal failure, Dent disease type 1, Proteinuria
RS148124447 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, X-linked recessive nephrolithiasis with renal failure, Hypophosphatemic rickets
RS151340624 Health Risk Conflicting classifications of pathogenicity X-linked recessive nephrolithiasis with renal failure, CLCN5-related disorder, Proteinuria
RS151340626 Health Risk Conflicting classifications of pathogenicity Hypophosphatemic rickets, X-linked recessive, Dent disease type 1
RS2147605140 Health Risk Conflicting classifications of pathogenicity Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
RS368039993 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Dent disease type 1
RS55676763 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Inborn genetic diseases, CLCN5-related disorder
RS781912440 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS781948493 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Dent disease type 1
RS782031818 Health Risk Conflicting classifications of pathogenicity Nonpapillary renal cell carcinoma, Nonpapillary renal cell carcinoma
RS782056386 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Hypophosphatemic rickets, X-linked recessive
RS782060809 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Inborn genetic diseases, Dent disease type 1
RS782071629 Health Risk Conflicting classifications of pathogenicity
RS782157715 Health Risk Conflicting classifications of pathogenicity X-linked recessive nephrolithiasis with renal failure, Dent disease type 1, Hypophosphatemic rickets
RS782177733 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Dent disease type 1
RS782191345 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782540790 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, X-linked recessive nephrolithiasis with renal failure, Hypophosphatemic rickets
RS782696367 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Inborn genetic diseases, Dent disease type 1
RS782744969 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Hypophosphatemic rickets, X-linked recessive
RS782746421 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782817681 Health Risk Conflicting classifications of pathogenicity Dent disease type 1, Dent disease type 1
RS1131691487 Health Risk Likely pathogenic
RS1131691678 Health Risk Likely pathogenic
RS1557194090 Health Risk Likely pathogenic Hyperkalemia, Multiple small medullary renal cysts, Low-molecular-weight proteinuria
RS1557194353 Health Risk Likely pathogenic Dent disease type 1, Hypophosphatemic rickets, X-linked recessive
RS1557194719 Health Risk Likely pathogenic
RS1933254834 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS1933257247 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS1933378481 Health Risk Likely pathogenic Thyroid cancer, nonmedullary, 1
RS1933713383 Health Risk Likely pathogenic Nephrotic syndrome, X-linked recessive nephrolithiasis with renal failure, Hypophosphatemic rickets
RS1933979876 Health Risk Likely pathogenic Dent disease type 1, X-linked recessive nephrolithiasis with renal failure, Proteinuria
RS1933984291 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS1934055157 Health Risk Likely pathogenic
RS2147605760 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2147606263 Health Risk Likely pathogenic Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
RS2519397087 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519397094 Health Risk Likely pathogenic
RS2519406899 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519419185 Health Risk Likely pathogenic
RS2519421939 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519422022 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519433029 Health Risk Likely pathogenic
RS2519434099 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519434988 Health Risk Likely pathogenic Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
RS2519435406 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519440356 Health Risk Likely pathogenic Dent disease type 1, Dent disease type 1
RS2519440480 Health Risk Likely pathogenic Dent disease type 1, Hypophosphatemic rickets, X-linked recessive
RS2519440912 Health Risk Likely pathogenic
RS2519444688 Health Risk Likely pathogenic CLCN5-related disorder, CLCN5-related disorder
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