SLC34A3
From Wikipedia, the free encyclopedia
Solute carrier family 34 (sodium phosphate), member 3
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Identifiers | ||||||||||||||
Symbol(s) | SLC34A3; FLJ38680; HHRH; NPTIIc | |||||||||||||
External IDs | OMIM: 609826 MGI: 2159410 HomoloGene: 15444 | |||||||||||||
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Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 142680 | 142681 | ||||||||||||
Ensembl | n/a | ENSMUSG00000006469 | ||||||||||||
Uniprot | n/a | Q05AC3 | ||||||||||||
Refseq | XM_001133456 (mRNA) XP_001133456 (protein) |
NM_080854 (mRNA) NP_543130 (protein) |
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Location | n/a | Chr 2: 25.05 - 25.06 Mb | ||||||||||||
Pubmed search | [1] | [2] |
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]
[edit] See also
[edit] References
[edit] 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: . 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: . 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: . 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: . 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: . 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: . 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: . 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: . 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: . PMID 11880379.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.