SLC34A3

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Solute carrier family 34 (sodium phosphate), member 3
Identifiers
Symbols SLC34A3 ; FLJ38680; HHRH; NPTIIc
External IDs Template:OMIM5 Template:MGI HomoloGene15444
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

Solute carrier family 34 (sodium phosphate), member 3, also known as SLC34A3, is a human gene.[1]

SLC34A3 contributes to the maintenance of inorganic phosphate concentration at the kidney (Segawa et al., 2002).[supplied by OMIM][1] Both NPT2a and SLC34A3 (NPT2c) are regulated in a similar fashion by parathyroid hormone (PTH), FGF23, and dietary phosphate.[2] Phosphate deprivation increases NPT2a and NPT2c expression.[2] The relative expression of NPT2a is an order of magnitude higher than that of NPT2c in kidneys of organisms maintained on a normal phosphate diet.[2] Normal animals exhibit a more robust increase in NPT2c than in NPT2a in response to phosphate deprivation.[2] NPT2c is regulated by FGF23 and probably downregulated by PTH. As such SLC34A3 is involved in phosphate homeostasis.

See also

References

  1. 1.0 1.1 "Entrez Gene: SLC34A3 solute carrier family 34 (sodium phosphate), member 3".
  2. 2.0 2.1 2.2 2.3 Bergwitz C, Roslin NM, Tieder M, Loredo-Osti JC, Bastepe M, Abu-Zahra H, Frappier D, Burkett K, Carpenter TO, Anderson D, Garabedian M, Sermet I, Fujiwara TM, Morgan K, Tenenhouse HS, Juppner H (2006). "SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis". Am J Hum Genet. 78 (2): 179–92. PMID 16358214. Unknown parameter |month= ignored (help)

Further reading

  • Forster IC, Hernando N, Biber J, Murer H (2006). "Proximal tubular handling of phosphate: A molecular perspective". Kidney Int. 70 (9): 1548–59. doi:10.1038/sj.ki.5001813. PMID 16955105.
  • Yamamoto T, Michigami T, Aranami F; et al. (2007). "Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function". J. Bone Miner. Metab. 25 (6): 407–13. doi:10.1007/s00774-007-0776-6. PMID 17968493.
  • Lorenz-Depiereux B, Benet-Pages A, Eckstein G; et al. (2007). "Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3". Am. J. Hum. Genet. 78 (2): 193–201. doi:10.1086/499410. PMID 16358215.
  • Bergwitz C, Roslin NM, Tieder M; et al. (2007). "SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis". Am. J. Hum. Genet. 78 (2): 179–92. doi:10.1086/499409. PMID 16358214.
  • Ehnes C, Forster IC, Bacconi A; et al. (2005). "Structure-function relations of the first and fourth extracellular linkers of the type IIa Na+/Pi cotransporter: II. Substrate interaction and voltage dependency of two functionally important sites". J. Gen. Physiol. 124 (5): 489–503. doi:10.1085/jgp.200409061. PMID 15504899.
  • Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Gisler SM, Pribanic S, Bacic D; et al. (2004). "PDZK1: I. a major scaffolder in brush borders of proximal tubular cells". Kidney Int. 64 (5): 1733–45. doi:10.1046/j.1523-1755.2003.00266.x. PMID 14531806.
  • Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.
  • Segawa H, Kaneko I, Takahashi A; et al. (2002). "Growth-related renal type II Na/Pi cotransporter". J. Biol. Chem. 277 (22): 19665–72. doi:10.1074/jbc.M200943200. PMID 11880379.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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