Mus musculus Gene: Atp2a2 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Gene | IDBG-198239.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | Atp2a2 | ||||||||||||||||||||||
Gene Name | ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 | ||||||||||||||||||||||
Synonyms | 9530097L16Rik; D5Wsu150e; mKIAA4195; SERCA2; SERCA2B | ||||||||||||||||||||||
Species | Mus musculus | ||||||||||||||||||||||
Ensembl Gene | ENSMUSG00000029467 | ||||||||||||||||||||||
Encoded Proteins |
ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
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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] |
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Gene Information | |||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||
Genomic Location | Chromosome 5:122442702-122502225 | ||||||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||||||
Band | F | ||||||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 19 experimentally validated interaction(s) in this database.
They are also associated with 30 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||
Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||
REACTOME |
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
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KEGG |
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
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INOH | |||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||
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
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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
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INOH | |||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | O55143 | ||||||||||||||||||||||
TrEMBL | Q5DTI2 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 11938 | ||||||||||||||||||||||
UniGene | Mm.227583 Mm.412722 | ||||||||||||||||||||||
RefSeq | NM_001110140 NM_009722 | ||||||||||||||||||||||
OMIM | |||||||||||||||||||||||
CCDS | CCDS57378 CCDS57379 | ||||||||||||||||||||||
HPRD | |||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
MGI ID | MGI:88110 | ||||||||||||||||||||||
MGI Symbol | Atp2a2 | ||||||||||||||||||||||
EMBL | AF029982 AJ131821 AJ131870 AJ223584 AK220538 BC054531 BC054748 CH466529 | ||||||||||||||||||||||
GenPept | AAD01889 AAH54531 AAH54748 BAD90532 CAA11450 CAB41017 CAB41018 CAB72436 EDL19677 | ||||||||||||||||||||||
RNA Seq Atlas | 11938 | ||||||||||||||||||||||