About: PHGDH wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • PHGDH wt Allele
rdfs:subClassOf
OMIM_Number
  • 606879
GenBank_Accession_Number
  • BC011262
Semantic_Type
  • Gene or Genome
Preferred_Name
  • PHGDH wt Allele
PubMedID_Primary_Reference
  • 21760589
NCI_META_CUI
  • CL433322
EntrezGene_ID
  • 26227
HGNC_ID
  • HGNC:8923
FULL_SYN
  • RHOBSYNCI
  • 3-PGDHSYNCI
  • PGDHSYNCI
  • PDGSYNCI
  • PGDSYNCI
  • PHGDH wt AllelePTNCI
  • PGADSYNCI
  • 3PGDHSYNCI
  • PGDH3SYNCI
  • Phosphoglycerate Dehydrogenase wt AlleleSYNCI
DEFINITION
  • Human PHGDH wild-type allele is located in the vicinity of 1p12 and is approximately 84 kb in length. This allele, which encodes D-3-phosphoglycerate dehydrogenase protein, is involved in both amino acid biosynthesis and oxidoreductase activity. Mutation of the gene is associated with phosphoglycerate dehydrogenase deficiency.NCI
DesignNote
  • Recent studies have implicated aberrant expression of this gene and its role in serine synthesis in breast cancer tumorigenesis. (Nature. 2011; 476: 346-350.)
code
  • C99475
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