About: EGLN1 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
  • EGLN1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 606425
GenBank_Accession_Number
  • AJ310543
Semantic_Type
  • Gene or Genome
Preferred_Name
  • EGLN1 wt Allele
NCI_META_CUI
  • CL435962
EntrezGene_ID
  • 54583
HGNC_ID
  • HGNC:1232
FULL_SYN
  • DKFZp761F179SYNCI
  • EGLN1 wt AllelePTNCI
  • SM20SYNCI
  • PHD2SYNCI
  • HPH2SYNCI
  • SM-20SYNCI
  • HPH-2SYNCI
  • ECYT3SYNCI
  • HIFPH2SYNCI
  • HIF Prolyl Hydroxylase 2 GeneSYNCI
  • HIF-PH2SYNCI
  • C1orf12SYNCI
  • PNAS-118SYNCI
  • PNAS-137SYNCI
  • Egl Nine Homolog 1 (C. elegans) wt AlleleSYNCI
DEFINITION
  • Human EGLN1 wild-type allele is located in the vicinity of 1q42.1 and is approximately 61 kb in length. This allele, which encodes egl nine homolog 1 protein, is involved in the response to hypoxia. Mutation of the gene is associated with familial erythrocytosis type 3.NCI
code
  • C101544
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