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Gene : BPNT2 Homo sapiens

Name  ? 3'(2'), 5'-bisphosphate nucleotidase 2 Cytological Location  8q12.1
Brief Description  3'(2'), 5'-bisphosphate nucleotidase 2
Description  This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]
  • synonyms:
  • IMPA3,
  • FLJ20421,
  • inositol monophosphatase domain containing 1,
  • IMP 3,
  • gPAPP,
  • HGNC:26019,
  • NM_017813,
  • BPNT2,
  • IMP-3,
  • IMPAD1,
  • GPAPP,
  • OTTHUMG00000164415,
  • IMPAD1,
  • Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase,
  • golgi-resident nucleotide phosphatase,
  • IMPA3,
  • uc003xte.5
  • identifiers:
  • 54928,
  • ENSG00000104331,
  • BPNT2

Genome feature

Region: gene ? Length: 35944  
Location: 8:56957931-56993874 reverse strand Cyto location: 8q12.1


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Disease

1 Diseases

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524 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results