About: HBA2 wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • HBA2 wt Allele
rdfs:subClassOf
OMIM_Number
  • 141850
GenBank_Accession_Number
  • BC008572
Semantic_Type
  • Gene or Genome
Preferred_Name
  • HBA2 wt Allele
UMLS_CUI
  • C2697530
EntrezGene_ID
  • 3040
Legacy_Concept_Name
  • HBA2_wt_Allele
HGNC_ID
  • HGNC:4824
FULL_SYN
  • HBA2 wt AllelePTNCI
  • Hemoglobin, Alpha 2 wt AlleleSYNCI
DEFINITION
  • Human HBA2 wild-type allele is located in the vicinity of 16p13.3 and is approximately 1 kb in length. This allele, which encodes hemoglobin subunit alpha protein, is involved in the mediation of oxygen transport in the vasculature. Mutation or deletion of the gene is associated with alpha-thalassemia.NCI
DesignNote
  • The sequence of the coding region of the human HBA1 gene is identical to that of the human HBA2 gene. (Entrez Gene)
code
  • C75433
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