| Name | solute carrier family 34 (sodium phosphate), member 1 |
| Symbol | SLC34A1 |
| Aliases | NPT2; SLC11; NAPI-3; NPTIIa; SLC17A2; sodium/phosphate co-transporter; solute carrier family 17 (sodium phosphate), member 2 |
| Gene Product | - solute carrier family 34 (sodium phosphate), member 1
|
| Category | |
| UniGene |
Hs.936
|
| Reference Sequence |
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| OMIM and SNP |
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| Locus |
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| Gene Ontology | |
| Expression | | EST (22 ESTs, 8 libraries) |
| Tissue | Breadth ? |
CPM ? |
| kidney |  | | | nervous |  | | | skin | | | | uncharacterized tissue | | |
|
| SAGE (155907 tags, 3 libraries) |
| Tissue | Breadth ? |
CPM ? |
| cerebellum | | | | mammary gland | | | | uncharacterized tissue | | |
|
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| Evidence | Mutation in Nephrolithiasis
- Prie D, Huart V, Bakouh N, Planelles G, Dellis O, Gerard B, Hulin P, Benque-Blanchet F, Silve C, Grandchamp B, Friedlander G Nephrolithiasis and osteoporosis associated with hypophosphatemia causedby mutations in the type 2a sodium-phosphate cotransporter. N Engl J Med 2002 Sep 26;347(13):983-91.
Other key publications related to this gene
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