Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

CLCN5

chloride channel 5 (nephrolithiasis 2, X-linked, Dent disease)DENTS, XLRH, XRN, hClC-K2, hCIC-K2, CLC5


Gene CLCN5 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Chloride Channels/*genetics

1732.0

Gene Deletion

20.0

Humans

290.0

Proteinuria/genetics

323.0

Reverse Transcriptase Polymerase Chain Reaction

20.0

Adult

150.0

Calcium/urine

311.0

Child

150.0

Child, Preschool

130.0

DNA Mutational Analysis

50.0

Exons

60.0

Female

150.0

Japan

20.0

Kidney Calculi/*genetics

646.0

Linkage (Genetics)

80.0

Male

210.0

Middle Aged

70.0

Pedigree

120.0

Research Support, Non-U.S. Gov't

170.0

Transcription, Genetic

20.0

X Chromosome

61.0

Amino Acid Sequence/genetics

31.0

Animals

100.0

Chloride Channels/*genetics/metabolism

333.0

DNA/genetics

50.0

Frameshift Mutation

20.0

Gene Expression

20.0

Infant

40.0

Kidney/*metabolism

21.0

Kidney Diseases/*genetics

25.0

Mutation/*genetics

20.0

Xenopus/genetics

29.0

*Linkage (Genetics)

40.0

Molecular Sequence Data

120.0

Syndrome

40.0

X Chromosome/*genetics

20.0

Adolescent

90.0

Calcium/*urine

412.0

*Mutation

90.0

Rats

20.0

Research Support, U.S. Gov't, P.H.S.

60.0

Amino Acid Sequence

90.0

Fanconi Syndrome/*genetics

360.0

Polymerase Chain Reaction

40.0

Polymorphism, Single-Stranded Conformational

30.0

*X Chromosome

40.0

Base Sequence

60.0

Introns

30.0

Mice

20.0

Open Reading Frames

20.0

Promoter Regions (Genetics)

20.0

RNA, Messenger/genetics/metabolism

20.0

Sequence Analysis, DNA

50.0

Sequence Homology, Amino Acid

20.0

Mutation/*genetics/*physiology

240.0

Oocytes/metabolism

21.0

Proteinuria/*genetics

342.0

Xenopus

20.0

Aged

20.0

Japan/ethnology

22.0

Molecular Weight

20.0

Proteins/chemistry

24.0

Mutation

30.0

Chromosomes, Human, X/*genetics

26.0

Haplotypes

20.0

Phenotype

20.0

Chromosome Mapping

20.0

Gene Expression Regulation

20.0