Bos taurus Gene: ATP2A2
Summary
InnateDB Gene IDBG-633099.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ATP2A2
Gene Name sarcoplasmic/endoplasmic reticulum calcium ATPase 2
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000001398
Encoded Proteins
ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000174437:
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:56458750-56512895
Strand Forward strand
Band
Transcripts
ENSBTAT00000001838 ENSBTAP00000001838
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 29 interaction(s) predicted by orthology.
Predicted by orthology
Total 29 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0005388 calcium-transporting ATPase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0008022 protein C-terminus binding
GO:0016787 hydrolase activity
GO:0019829 cation-transporting ATPase activity
GO:0019899 enzyme binding
GO:0044548 S100 protein binding
GO:0046872 metal ion binding
Biological Process
GO:0002026 regulation of the force of heart contraction
GO:0006812 cation transport
GO:0006816 calcium ion transport
GO:0006874 cellular calcium ion homeostasis
GO:0006984 ER-nucleus signaling pathway
GO:0008152 metabolic process
GO:0045822 negative regulation of heart contraction
GO:0070588 calcium ion transmembrane transport
Cellular Component
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016529 sarcoplasmic reticulum
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Reduction of cytosolic Ca++ levels pathway
Platelet homeostasis pathway
Ion transport by P-type ATPases pathway
Pre-NOTCH Processing in Golgi pathway
Transmembrane transport of small molecules pathway
Pre-NOTCH Expression and Processing pathway
Platelet calcium homeostasis pathway
Signal Transduction pathway
Ion channel transport pathway
Signaling by NOTCH pathway
Hemostasis pathway
Platelet homeostasis pathway
Hemostasis pathway
Platelet calcium homeostasis pathway
Reduction of cytosolic Ca++ levels pathway
Ion channel transport pathway
Transmembrane transport of small molecules pathway
Ion transport by P-type ATPases pathway
KEGG
Alzheimer's disease pathway
Calcium signaling pathway pathway
Arrhythmogenic right ventricular cardiomyopathy (ARVC) pathway
Hypertrophic cardiomyopathy (HCM) pathway
Cardiac muscle contraction pathway
Dilated cardiomyopathy pathway
Pancreatic secretion pathway
Calcium signaling pathway pathway
Alzheimer's disease pathway
Cardiac muscle contraction pathway
Arrhythmogenic right ventricular cardiomyopathy (ARVC) pathway
Hypertrophic cardiomyopathy (HCM) pathway
Dilated cardiomyopathy pathway
Pancreatic secretion pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL F1MPR3 Q5MA64
UniProt Splice Variant
Entrez Gene 540568
UniGene Bt.24649 Bt.68660
RefSeq NM_001191430
HUGO HGNC:812
OMIM
CCDS
HPRD
IMGT
EMBL AY860426 DAAA02045278
GenPept AAW29825
RNA Seq Atlas 540568