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Gene : SLC34A1 Homo sapiens

Name  ? solute carrier family 34 member 1 Cytological Location  5q35.3
Brief Description  solute carrier family 34 member 1
Description  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]
  • synonyms:
  • NPTIIa,
  • FRTS2,
  • SLC11,
  • sodium/phosphate co-transporter,
  • solute carrier family 34 (sodium phosphate), member 1,
  • NAPI-3,
  • NPT2,
  • NAPI-3,
  • SLC17A2,
  • Na+-phosphate cotransporter type II,
  • NM_003052,
  • uc003mgk.5,
  • NPT2,
  • SLC11,
  • NPHLOP1,
  • HGNC:11019,
  • NPTIIa,
  • SLC17A2,
  • L13258,
  • solute carrier family 34 (type II sodium/phosphate cotransporter), member 1,
  • OTTHUMG00000130857,
  • HCINF2,
  • SLC34A1,
  • solute carrier family 17 (sodium phosphate), member 2
  • identifiers:
  • 6569,
  • ENSG00000131183,
  • SLC34A1

Genome feature

Region: gene ? Length: 27588  
Location: 5:177384434-177412021 Cyto location: 5q35.3


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Gene -> HPO annotation (Human Phenotype Ontology)

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Proteins

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SNPs

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Disease

3 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Gene -> HPO annotation (Human Phenotype Ontology)

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Expression

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Other

88 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results