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Gene : SLC20A2 Homo sapiens

Name  ? solute carrier family 20 member 2 Cytological Location  8p11.21
Brief Description  solute carrier family 20 member 2
Description  This gene encodes a member of the inorganic phosphate transporter family. The encoded protein is a type 3 sodium-dependent phosphate symporter that plays an important role in phosphate homeostasis by mediating cellular phosphate uptake. The encoded protein also confers susceptibility to viral infection as a gamma-retroviral receptor. Mutations in this gene may play a role in familial idiopathic basal ganglia calcification. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]
  • synonyms:
  • uc003xpe.5,
  • solute carrier family 20 (phosphate transporter), member 2,
  • NM_001257180,
  • Ram-1,
  • PIT-2,
  • HGNC:10947,
  • murine leukemia virus, amphotropic; receptor,
  • PIT2,
  • IBGC1,
  • GLVR2,
  • GLVR2,
  • PiT-2,
  • OTTHUMG00000164169,
  • Glvr-2,
  • SLC20A2,
  • GLVR-2,
  • RAM1,
  • MLVAR,
  • IBGC3,
  • MLVAR,
  • Ram-1
  • identifiers:
  • 6575,
  • ENSG00000168575,
  • SLC20A2

Genome feature

Region: gene ? Length: 125682  
Location: 8:42416462-42542143 reverse strand Cyto location: 8p11.21

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Gene -> HPO annotation (Human Phenotype Ontology)

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1 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

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3756 SN Ps

5 Cross References

19 Data Sets

12 Homologues

0 Located Features

97 Rna Seq Results