ATP2A2

GENERAL INFORMATION

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Gene name

ATP2A2

Gene description

ATPase, Ca++ transporting, cardiac muscle, slow twitch 2

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins
Transporters

Predicted localization

Intracellular,Membrane

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Group enriched (heart muscle, skeletal muscle)

Protein evidence

Evidence at protein level

Protein localization

Neurons and myocytes showed strong cytoplasmic positivity. Decidua, cells in seminiferous ducts, epididymis, intestine and respiratory epithelium in bronchus displayed moderate immunoreactivity. Other normal tissues were weakly stained or negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA062605
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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
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Heart muscle

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:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (heart muscle, skeletal muscle)

Organ

Expression



GENE INFORMATION

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Gene name

ATP2A2 (HGNC Symbol)

Synonyms

ATP2B, DAR, SERCA2

Description

ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 (HGNC Symbol)

Entrez gene summary

This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol into the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2008]

Chromosome

12

Cytoband

q24.11

Chromosome location (bp)

110280756 - 110351093

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000174437 (version 78.38)

Entrez gene

488

UniProt

P16615 (UniProt - Evidence at protein level)

neXtProt

NX_P16615

Antibodypedia

ATP2A2 antibodies


PROTEIN BROWSER

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ENST00000308664
 
ENST00000539276
 
ENST00000548169
 
ENST00000552636
 
ENST00000553144
 
 
 
 


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)

ATP2A2-001 ENSP00000311186
ENST00000308664
P16615
Show all »
Show » Show » 997 109.7 No >9
ATP2A2-003 ENSP00000440045
ENST00000539276
P16615
Show all »
Show » Show » 1042 114.8 No >9
ATP2A2-004 ENSP00000447406
ENST00000552636
F8W1Z7
Show all »
Show » 44 5.3 No 0
ATP2A2-006 ENSP00000449454
ENST00000548169
Show » Show » 933 102.5 No 9
ATP2A2-012 ENSP00000450407
ENST00000553144
P16615
Show all »
Show » Show » 46 5.3 No 0