About: HBG1 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
  • HBG1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 142200
GenBank_Accession_Number
  • NM_000559
Semantic_Type
  • Gene or Genome
Preferred_Name
  • HBG1 wt Allele
UMLS_CUI
  • C2827563
EntrezGene_ID
  • 3047
HGNC_ID
  • HGNC:4831
FULL_SYN
  • HBG1 wt AllelePTNCI
  • HBGASYNCI
  • HBGRSYNCI
  • Hemoglobin Gamma A wt AlleleSYNCI
  • HSGGL1SYNCI
  • PRO2979SYNCI
DEFINITION
  • Human HBG1 wt allele is located in the vicinity of 11p15.5 and is approximately 2 kb in length. This allele, which encodes hemoglobin subunit gamma-1 protein, plays a role in the transport of oxygen to tissues of the fetal and neonatal body. Mutations in this gene may be associated with beta-thalassemia.NCI
code
  • C84956
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