KCNQ3

GENERAL INFORMATION

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Gene name

KCNQ3

Gene description

Potassium voltage-gated channel, KQT-like subfamily, member 3

Protein class

Disease related genes
FDA approved drug targets
Predicted membrane proteins
Transporters
Voltage-gated ion channels

Predicted localization

Membrane

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (cerebral cortex)
GTEx:Tissue enhanced (cerebral cortex, hippocampus)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (cerebral cortex)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cerebral cortex, hippocampus)

Organ

Expression



GENE INFORMATION

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Gene name

KCNQ3 (HGNC Symbol)

Synonyms

EBN2, Kv7.3

Description

Potassium voltage-gated channel, KQT-like subfamily, member 3 (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]

Chromosome

8

Cytoband

q24.22

Chromosome location (bp)

132120859 - 132480953

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000184156 (version 78.38)

Entrez gene

3786

UniProt

O43525 (UniProt - Evidence at protein level)

neXtProt

NX_O43525

Antibodypedia

KCNQ3 antibodies


PROTEIN BROWSER

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ENST00000388996
 
ENST00000519445
 
ENST00000521134
 
ENST00000621976
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

KCNQ3-001 ENSP00000373648
ENST00000388996
O43525
Show all »
Show » Show » 872 96.7 No 5
KCNQ3-002 ENSP00000428790
ENST00000519445
E7ET42
Show all »
Show » Show » 860 95.4 No 5
KCNQ3-004 ENSP00000429799
ENST00000521134
O43525
Show all »
Show » Show » 752 84.8 Yes 4
KCNQ3-201 ENSP00000482510
ENST00000621976
Show » Show » 751 84.7 Yes 4