ATP2B2 ATPase plasma membrane Ca2+ transporting 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 491)
Source: NCBI Gene (ID 491)
Symbol: ATP2B2
Full name: ATPase plasma membrane Ca2+ transporting 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: DFNA82; PMCA2; PMCA2a; PMCA2i
Summary: 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 2. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Expression: Biased expression in brain (RPKM 26.8), salivary gland (RPKM 5.2) and 1 other tissue
Orthologs: mouse
Gene size: 383985bp
Exon count: 34