KCNJ2

GENERAL INFORMATION

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Gene name

KCNJ2

Gene description

Potassium inwardly-rectifying channel, subfamily J, member 2

Protein class

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

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Most normal cells displayed moderate to strong cytoplasmic positivity with a few cases of membranous staining. Glial cells and lymphoid cells outside reaction centra were generally negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA029109
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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

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

KCNJ2 (HGNC Symbol)

Synonyms

IRK1, Kir2.1, LQT7

Description

Potassium inwardly-rectifying channel, subfamily J, member 2 (HGNC Symbol)

Entrez gene summary

Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq, Jul 2008]

Chromosome

17

Cytoband

q24.3

Chromosome location (bp)

70168673 - 70180048

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000123700 (version 78.38)

Entrez gene

3759

UniProt

P63252 (UniProt - Evidence at protein level)

neXtProt

NX_P63252

Antibodypedia

KCNJ2 antibodies


PROTEIN BROWSER

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ENST00000243457
 
ENST00000535240
 
 
 
 


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)

KCNJ2-001 ENSP00000441848
ENST00000535240
P63252
Show all »
Show » Show » 427 48.3 No 2
KCNJ2-002 ENSP00000243457
ENST00000243457
P63252
Show all »
Show » Show » 427 48.3 No 2