SLC34A3

SLC34A3

Solute carrier family 34 (sodium phosphate), member 3, also known as SLC34A3, is a human gene.cite web | title = Entrez Gene: SLC34A3 solute carrier family 34 (sodium phosphate), member 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=142680| accessdate = ]

PBB_Summary
section_title =
summary_text = SLC34A3 contributes to the maintenance of inorganic phosphate concentration at the kidney (Segawa et al., 2002). [supplied by OMIM] cite web | title = Entrez Gene: SLC34A3 solute carrier family 34 (sodium phosphate), member 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=142680| accessdate = ]

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References

Further reading

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

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