About: APOE wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • APOE wt Allele
rdfs:subClassOf
OMIM_Number
  • 107741
GenBank_Accession_Number
  • K00396
Semantic_Type
  • Gene or Genome
Preferred_Name
  • APOE wt Allele
UMLS_CUI
  • C2827465
EntrezGene_ID
  • 348
HGNC_ID
  • HGNC:613
FULL_SYN
  • APOE wt AllelePTNCI
  • AD2SYNCI
  • LPGSYNCI
  • Apolipoprotein E wt AlleleSYNCI
  • Alzheimer Disease 2 (APOE*E4-Associated, Late Onset) GeneSYNCI
  • LDLCQ5SYNCI
  • MGC1571SYNCI
DEFINITION
  • Human APOE wild-type allele is located in the vicinity of 19q13.2 and is approximately 4 kb in length. This allele, which encodes apolipoprotein E protein, plays a role in the mediation of lipid transport and metabolism. Genetic variation is involved in both cardiovascular disease and Alzheimer's disease. Mutation of the gene is associated with type III hyperlipoproteinemia.NCI
code
  • C84469
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