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SLC34A1, solute carrier family 34 member 1

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SLC34A1, solute carrier family 34 member 1

  • This gene encodes a member of the type II sodium-phosphate cotransporter family. Mutations in this gene are associated with hypophosphatemia nephrolithiasis/osteoporosis 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]

  • Gene Synonyms (sodium-dependent phosphate transport protein 2A, Na(+)-dependent phosphate cotransporter 2A, Na(+)/Pi cotransporter 2A, Na+-phosphate cotransporter type II, naPi-2a, renal sodium-dependent phosphate transporter, sodium-phosphate transport protein 2A, sodium/phosphate co-transporter, sodium/phosphate cotransporter 2A, solute carrier family 17 (sodium phosphate), member 2, solute carrier family 34 (sodium phosphate), member 1, solute carrier family 34 (type II sodium/phosphate cotransporter), member 1, FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2,)
  • NCBI Gene ID: 6569
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q06495
    UNIPROT ID#>>Q7Z725
    UNIPROT ID#>>Q86VN6
    UNIPROT ID#>>A0A024R7R9
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 34 member 1 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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