Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

KCNQ3

potassium voltage-gated channel, KQT-like subfamily, member 3EBN2, Kv7.3


Gene KCNQ3 gene interaction
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MeSH term
FrequencyCondition_Probility

Adult

70.0

Amino Acid Sequence

130.0

Animals

350.0

Blotting, Western

20.0

Humans

540.0

Male

140.0

Molecular Sequence Data

140.0

Potassium Channels, Voltage-Gated

3258.0

Precipitin Tests

30.0

Rats

160.0

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

410.0

Sequence Homology, Amino Acid

40.0

Transfection

100.0

Ion Channels/*genetics/metabolism

225.0

Amino Acid Substitution

20.0

Cells, Cultured

90.0

Gene Expression

30.0

Genes, Dominant/genetics

32.0

Microinjections

31.0

Mutagenesis, Site-Directed

20.0

Mutation

80.0

Patch-Clamp Techniques

112.0

Pedigree

100.0

Potassium/metabolism

54.0

Potassium Channels/*genetics/metabolism

517.0

Protein Structure, Tertiary/physiology

21.0

Protein Subunits

20.0

Structure-Activity Relationship

30.0

Xenopus

71.0

Epilepsy, Benign Neonatal/genetics

266.0

Immunohistochemistry

40.0

Mice

80.0

Mice, Inbred C57BL

20.0

Organ Specificity

20.0

Potassium Channels/genetics/*metabolism

415.0

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

120.0

Gene Expression Regulation/genetics

21.0

Mutation/*genetics

40.0

Point Mutation

20.0

Electric Conductivity

42.0

Electrophysiology

61.0

Female

110.0

In Situ Hybridization

20.0

*Mutation

60.0

Potassium Channels/*genetics/physiology

228.0

Xenopus laevis

40.0

Anticonvulsants/*pharmacology

210.0

CHO Cells

70.0

Carbamates/*pharmacology

228.0

Hamsters

70.0

Indoles/pharmacology

73.0

Muscarinic Agonists/pharmacology

25.0

Phenylenediamines/*pharmacology

2100.0

*Potassium Channels, Voltage-Gated

134.0

Pyridines/pharmacology

62.0

Rats, Sprague-Dawley

20.0

Receptor, Muscarinic M1

28.0

Ion Channel Gating

22.0

Brain/cytology/metabolism

25.0

COS Cells

30.0

Cell Line

50.0

Cloning, Molecular

50.0

Neurons/cytology/drug effects/*metabolism

25.0

Tetraethylammonium/pharmacology

419.0

Tissue Distribution

30.0

Chromosome Mapping

50.0

Phenotype

40.0

Chromosomes, Human, Pair 6/genetics

21.0

DNA Mutational Analysis

30.0

Infant

20.0

Infant, Newborn

90.0

Potassium Channels/*genetics

86.0

Ion Transport

22.0

*Point Mutation

20.0

Base Sequence

40.0

Japan

20.0

Polymerase Chain Reaction

40.0

Seizures/congenital/*genetics

266.0

Sequence Alignment

30.0

Potassium Channels/*physiology

310.0

Neurons/*physiology

21.0

Variation (Genetics)

20.0

Epilepsy/*genetics

26.0

Anthracenes/pharmacology

210.0

English Abstract

30.0

Potassium Channels/genetics

48.0

*Chromosome Mapping

20.0

Electroencephalography

31.0

Epilepsy, Generalized/*genetics

310.0

Linkage (Genetics)

30.0

Myoclonic Epilepsy, Juvenile/*genetics

218.0

Benzimidazoles/pharmacology

24.0

Kinetics

30.0

Membrane Potentials/drug effects/physiology

22.0

Sulfanilamides/pharmacology

2100.0

Adolescent

30.0

Genetic Predisposition to Disease

20.0

Genotype

20.0

Middle Aged

30.0

DNA Primers

20.0

Dose-Response Relationship, Drug

30.0

Potassium Channel Blockers/pharmacology

413.0

Brain/metabolism

30.0

Oocytes

32.0

Ion Channel Gating/physiology

313.0

Aged

20.0

Child

20.0

Epilepsy, Benign Neonatal/*genetics

350.0

Comparative Study

30.0

Neurons/drug effects/*physiology

26.0

Potassium/pharmacology

23.0

Potassium Channels/chemistry/*physiology

2100.0

Hela Cells

20.0

Rats, Wistar

20.0

Oocytes/metabolism

31.0

RNA, Messenger/biosynthesis

20.0