About: F2 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
  • F2 wt Allele
rdfs:subClassOf
OMIM_Number
  • 176930
GenBank_Accession_Number
  • M33031
Semantic_Type
  • Gene or Genome
Preferred_Name
  • F2 wt Allele
UMLS_CUI
  • C2826539
EntrezGene_ID
  • 2147
Legacy_Concept_Name
  • F2_wt_Allele
HGNC_ID
  • HGNC:3535
FULL_SYN
  • F2 wt AllelePTNCI
  • PTSYNCI
  • Coagulation Factor II (Thrombin) wt AlleleSYNCI
DEFINITION
  • Human F2 wild-type allele is located in the vicinity of 11p11 and is approximately 20 kb in length. This allele, which encodes prothrombin protein, is involved in the regulation of coagulation. Mutation of the gene is associated with dysprothrombinemia and genetic variation may affect susceptibility to ischemic stroke.NCIUniProt
code
  • C82853
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