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Gene : ATP2B1 Homo sapiens

Name  ? ATPase plasma membrane Ca2+ transporting 1 Cytological Location  12q21.33
Brief Description  ATPase plasma membrane Ca2 transporting 1
Description  The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and play a critical role in intracellular calcium homeostasis. The mammalian plasma membrane calcium ATPase isoforms are encoded by at least four separate genes and the diversity of these enzymes is further increased by alternative splicing of transcripts. The expression of different isoforms and splice variants is regulated in a developmental, tissue- and cell type-specific manner, suggesting that these pumps are functionally adapted to the physiological needs of particular cells and tissues. This gene encodes the plasma membrane calcium ATPase isoform 1. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
  • synonyms:
  • PMCA1kb,
  • PMCA1,
  • J04027,
  • OTTHUMG00000169946,
  • ATP2B1,
  • PMCA1,
  • uc058rpj.1,
  • plasma membrane calcium-transporting ATPase 1,
  • NM_001682,
  • ATPase, Ca++ transporting, plasma membrane 1,
  • HGNC:814
  • identifiers:
  • 490,
  • ENSG00000070961,
  • ATP2B1

Genome feature

Region: gene ? Length: 121318  
Location: 12:89588049-89709366 reverse strand Cyto location: 12q21.33


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487 SN Ps

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18 Data Sets

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97 Rna Seq Results