Target intelligence / Profile preview

Sodium-dependent phosphate transport protein 2A (NaPi-2a)

Target
NaPi-2a
Molecular classification
Transporter, Sodium-phosphate cotransporter (Type II family), Solute carrier
01

Overview

Sodium-dependent phosphate transport protein 2A (NaPi-2a) is a membrane transporter primarily localized to the renal proximal tubule brush border membrane, where it facilitates the active reabsorption of phosphate from the filtrate via sodium-coupled cotransport, accounting for approximately 70–80% of phosphate reabsorption in the kidney[3][6][1]. This protein, encoded by the SLC34A1 gene, is regulated by parathyroid hormone and plays a crucial role in maintaining systemic phosphate homeostasis. Mutations in SLC34A1 can lead to disorders such as hypophosphatemia with kidney stones and/or osteoporosis[3][6]. The cotransporter typically operates with a stoichiometry of 3 sodium ions per one divalent phosphate ion, making the process electrogenic[3].

Other names
Na(+)-dependent phosphate cotransporter 2ANa(+)/Pi cotransporter 2ANaPi-2aNaPi-3NPT2SLC34A1Sodium-phosphate transport protein 2ASodium/phosphate cotransporter 2ASolute carrier family 34 member 1
02

Mechanism of action

Substrate (transporter for phosphate and sodium ions); Electrogenic sodium-phosphate cotransport

03

Biological functions

Renal phosphate reabsorptionPhosphate ion transmembrane transportIntracellular phosphate ion homeostasisCellular response to phosphate starvation
04

Disease associations

Hypophosphatemia nephrolithiasis/osteoporosis 1Other phosphate balance disorders
05

Safety considerations

Loss-of-function mutations cause phosphate wasting, nephrolithiasis, and/or bone diseaseDisruption may disturb phosphate homeostasis and calcium balance
06

Interacting drugs

Calcium phosphate

3 more in the full profile.

07

Biomarkers

Mutations in SLC34A1 for hypophosphatemia nephrolithiasis/osteoporosis 1

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