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Solute carrier family 34 (sodium phosphate), member 3
Identifiers
Symbols SLC34A3; FLJ38680; HHRH; NPTIIc
External IDs OMIM609826 MGI2159410 HomoloGene15444 GeneCards: SLC34A3 Gene
Orthologs
Species Human Mouse
Entrez 142680 142681
Ensembl ENSG00000198569 ENSMUSG00000006469
UniProt Q8N130 Q05AC3
RefSeq (mRNA) NP_543153 NM_080854
RefSeq (protein) NM_080877 NP_543130
Location (UCSC) Chr 9:
140.13 - 140.13 Mb
Chr 2:
25.05 - 25.06 Mb
PubMed search [1] [2]

Sodium-dependent phosphate transport protein 2C is a protein that in humans is encoded by the SLC34A3 gene.[1][2][3][4]

Contents

Function

SLC34A3 contributes to the maintenance of inorganic phosphate concentration at the kidney.[4]

Interactions

SLC34A3 has been shown to interact with PDZK1.[5]

Clinical Correlation

A mutation in the SLC34A3 gene has been known to cause the autosomal recessive condition hereditary hypophophatemic rickets with hypercalciuria. This gene is correlated closely with SLC34A1, an analogue sodium phosphate cotransporter protein. Symptoms include renal phosphate wasting in addition to increase levels of 1,25-dihydroxyvitamin D (yields the hypercalcuria).[2]

See also

References

  1. ^ Segawa H, Kaneko I, Takahashi A, Kuwahata M, Ito M, Ohkido I, Tatsumi S, Miyamoto K (May 2002). "Growth-related renal type II Na/Pi cotransporter". J Biol Chem 277 (22): 19665–72. doi:10.1074/jbc.M200943200. PMID 11880379.  
  2. ^ a b Lorenz-Depiereux B, Benet-Pages A, Eckstein G, Tenenbaum-Rakover Y, Wagenstaller J, Tiosano D, Gershoni-Baruch R, Albers N, Lichtner P, Schnabel D, Hochberg Z, Strom TM (Jan 2006). "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.  
  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 (Jan 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. doi:10.1086/499409. PMID 16358214.  
  4. ^ a b "Entrez Gene: SLC34A3 solute carrier family 34 (sodium phosphate), member 3". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=142680.  
  5. ^ Gisler SM, Pribanic S, Bacic D, Forrer P, Gantenbein A, Sabourin LA, Tsuji A, Zhao ZS, Manser E, Biber J, Murer H (November 2003). "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.  

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.  
  • 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.  

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

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