SLC20A2: Sodium-phosphate symporter which seems to play a fundamental housekeeping role in phosphate transport by absorbing phosphate from interstitial fluid for normal cellular functions such as cellular metabolism, signal transduction, and nucleic acid and lipid synthesis. In vitro, sodium-dependent phosphate uptake is not siginificantly affected by acidic and alkaline conditions, however sodium-independent phosphate uptake occurs at acidic conditions. May play a role in extracellular matrix, cartilage and vascular calcification. Functions as a retroviral receptor and confers human cells susceptibility to infection to amphotropic murine leukemia virus (A-MuLV), 10A1 murine leukemia virus (10A1 MLV) and some feline leukemia virus subgroup B (FeLV-B) variants. Defects in SLC20A2 are the cause of basal ganglia calcification, idiopathic, type 3 (IBGC3). An autosomal dominant condition characterized by symmetric calcification in the basal ganglia and other brain regions. Affected individuals can either be asymptomatic or show a wide spectrum of neuropsychiatric symptoms, including parkinsonism, dystonia, tremor, ataxia, dementia, psychosis, seizures, and chronic headache. Serum levels of calcium, phosphate, alkaline phosphatase and parathyroid hormone are normal. Belongs to the inorganic phosphate transporter (PiT) (TC 2.A.20) family.
Protein type: Transporter, SLC family; Membrane protein, integral; Transporter; Receptor, misc.; Membrane protein, multi-pass
Chromosomal Location of Human Ortholog: 8p11.21
Cellular Component: integral to plasma membrane; membrane; plasma membrane
Molecular Function: inorganic phosphate transmembrane transporter activity; receptor activity; sodium:inorganic phosphate symporter activity; sodium:phosphate symporter activity; viral receptor activity
Biological Process: entry of virus into host cell; ion transport; transmembrane transport; transport
Disease: Basal Ganglia Calcification, Idiopathic, 1
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