KCNA5

GENERAL INFORMATION

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Gene name

KCNA5

Gene description

Potassium voltage-gated channel, shaker-related subfamily, member 5

Protein class

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

Predicted localization

Membrane

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (esophagus, heart muscle)
GTEx:Tissue enriched (heart muscle)

Protein evidence

Evidence at protein level

Protein localization

Membranous positivity in most glandular cells.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA021516 , CAB022562
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (esophagus, heart muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (heart muscle)

Organ

Expression



GENE INFORMATION

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Gene name

KCNA5 (HGNC Symbol)

Synonyms

HK2, HPCN1, Kv1.5

Description

Potassium voltage-gated channel, shaker-related subfamily, member 5 (HGNC Symbol)

Entrez gene summary

Potassium channels represent the most complex class of voltage-gated ino channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, the function of which could restore the resting membrane potential of beta cells after depolarization and thereby contribute to the regulation of insulin secretion. This gene is intronless, and the gene is clustered with genes KCNA1 and KCNA6 on chromosome 12. Defects in this gene are a cause of familial atrial fibrillation type 7 (ATFB7). [provided by RefSeq, May 2012]

Chromosome

12

Cytoband

p13.32

Chromosome location (bp)

5043989 - 5046788

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000130037 (version 78.38)

Entrez gene

3741

UniProt

P22460 (UniProt - Evidence at protein level)

neXtProt

NX_P22460

Antibodypedia

KCNA5 antibodies


PROTEIN BROWSER

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ENST00000252321
 
 
 
 


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)

KCNA5-001 ENSP00000252321
ENST00000252321
P22460
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