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Gene : FTCD Homo sapiens

Name  ? formimidoyltransferase cyclodeaminase Cytological Location  21q22.3
Brief Description  formimidoyltransferase cyclodeaminase
description  The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009]
  • synonyms:
  • U91541,
  • HGNC:3974,
  • FTCD,
  • LCHC1,
  • OTTHUMG00000090488,
  • NM_006657,
  • uc010gqg.2,
  • formiminotransferase cyclodeaminase
  • identifiers:
  • 10841,
  • ENSG00000160282,
  • FTCD

Genome feature

Region: gene ? Length: 20502  
Location: 21:46135981-46156482 reverse strand Cyto location: 21q22.3


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Disease

1 Diseases

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Expression

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2011 SN Ps

5 Cross References

19 Data Sets

4 Homologues

0 Located Features

90 Rna Seq Results