About: FOXC2 wt Allele     Goto   Sponge   Distinct   Permalink

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

AttributesValues
rdf:type
rdfs:label
  • FOXC2 wt Allele
rdfs:subClassOf
OMIM_Number
  • 602402
GenBank_Accession_Number
  • NM_005251
Semantic_Type
  • Gene or Genome
Preferred_Name
  • FOXC2 wt Allele
UMLS_CUI
  • C1705360
EntrezGene_ID
  • 2303
Legacy_Concept_Name
  • Forkhead_Box_C2_wt_Allele
HGNC_ID
  • HGNC:3801
FULL_SYN
  • Mesenchyme Forkhead GeneSYNCI
  • Forkhead Box C2 wt AlleleSYNCI
  • LDSYNCI
  • FOXC2 wt AllelePTNCI
  • MFH1SYNCI
  • MFH-1SYNCI
  • FKHL14SYNCI
DEFINITION
  • Human FOXC2 wild-type allele is located within 16q22-16q24 and is approximately 2 kb in length. This allele, which encodes forkhead box protein C2, is involved in the modulation of transcription by RNA polymerase II.NCI
code
  • C52877
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