rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
21305656
2011
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
21305656
2011
rs151340626
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Hypophosphatemic Rickets, X-Linked Recessive
0.800
GeneticVariation
UNIPROT
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
21305656
2011
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
21305656
2011
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing.
19657328
2009
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.
19019917
2009
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing.
19657328
2009
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.
19019917
2009
rs151340628
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis
0.800
GeneticVariation
UNIPROT
Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.
19019917
2009
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing.
19657328
2009
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.
19019917
2009
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.
18025833
2007
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
A missense mutation in the chloride/proton ClC-5 antiporter gene results in increased expression of an alternative mRNA form that lacks exons 10 and 11. Identification of seven new CLCN5 mutations in patients with Dent's disease.
17262170
2007
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
A missense mutation in the chloride/proton ClC-5 antiporter gene results in increased expression of an alternative mRNA form that lacks exons 10 and 11. Identification of seven new CLCN5 mutations in patients with Dent's disease.
17262170
2007
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.
18025833
2007
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.
18025833
2007
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
A missense mutation in the chloride/proton ClC-5 antiporter gene results in increased expression of an alternative mRNA form that lacks exons 10 and 11. Identification of seven new CLCN5 mutations in patients with Dent's disease.
17262170
2007
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study.
16822791
2006
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Dent's disease and prevalence of renal stones in dialysis patients in Northeastern Italy.
16247550
2006
rs151340622
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Family history may be misleading in the diagnosis of Dent's disease.
16416111
2006
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study.
16822791
2006
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Family history may be misleading in the diagnosis of Dent's disease.
16416111
2006
rs151340623
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Dent's disease and prevalence of renal stones in dialysis patients in Northeastern Italy.
16247550
2006
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study.
16822791
2006
rs151340630
×
Entrez Id:
1184
Gene Symbol:
CLCN5
CLCN5
Dent disease 1
0.800
GeneticVariation
UNIPROT
Family history may be misleading in the diagnosis of Dent's disease.
16416111
2006