Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

KCNH2

potassium voltage-gated channel, subfamily H (eag-related), member 2HERG, Kv11.1


Gene KCNH2 gene interaction
View Neighborhood Gene

Result number fewer <<<< << < ALL > >> >>> more

MeSH term
FrequencyCondition_Probility

Animals

100.0

Benzopyrans/pharmacology

28.0

Cell Line

40.0

Humans

300.0

Immunoblotting

20.0

In Vitro

20.0

Patch-Clamp Techniques

61.0

Piperidines/pharmacology

23.0

Potassium/metabolism

32.0

*Potassium Channels, Voltage-Gated

228.0

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

240.0

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

120.0

Adult

130.0

Aged

70.0

Aged, 80 and over

40.0

DNA Mutational Analysis

70.0

Electrocardiography

92.0

Family Health

40.0

Follow-Up Studies

20.0

Genetic Predisposition to Disease/genetics

30.0

Genotype

50.0

Long QT Syndrome/*genetics

1128.0

Male

180.0

Middle Aged

80.0

Mutation/*genetics

30.0

Pedigree

80.0

Phenotype

100.0

Potassium Channels/genetics

510.0

Female

160.0

*Mutation

80.0

Mutation, Missense

40.0

Polymorphism, Single-Stranded Conformational

60.0

Potassium Channels/*genetics

96.0

Sodium Channels/*genetics

33.0

*Cation Transport Proteins

156.0

*DNA-Binding Proteins

130.0

Mice

20.0

Potassium Channels/*genetics/*metabolism

218.0

*Trans-Activators

132.0

Reproducibility of Results

20.0

Gene Expression

30.0

Mutation

50.0

Polymerase Chain Reaction

40.0

Adolescent

70.0

Adrenergic beta-Antagonists/*therapeutic use

25.0

Child

40.0

Long QT Syndrome/*drug therapy/*genetics

2100.0

Treatment Outcome

20.0

COS Cells

30.0

Cloning, Molecular

20.0

Genes, Dominant

20.0

Alleles

20.0

Asian Continental Ancestry Group

20.0

Base Sequence

50.0

China

30.0

Electrophysiology

30.0

European Continental Ancestry Group

20.0

*Genetic Screening

21.0

Molecular Sequence Data

50.0

Mutagenesis, Site-Directed

40.0

*Polymorphism, Genetic

30.0

Potassium Channels, Voltage-Gated/*genetics

337.0

Transfection

20.0

Amino Acid Sequence

30.0

Electric Conductivity

21.0

Potassium Channels/*genetics/metabolism

310.0

Syndrome

20.0

Comparative Study

30.0

Infant

40.0

Long QT Syndrome/genetics/physiopathology

360.0

Chromatography, High Pressure Liquid/*methods

21.0

Heterozygote

20.0

Nucleic Acid Denaturation

22.0

Child, Preschool

30.0

Sequence Alignment

20.0

Long QT Syndrome/*genetics/physiopathology

225.0