About: BCL11A wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • BCL11A wt Allele
rdfs:subClassOf
OMIM_Number
  • 606557
GenBank_Accession_Number
  • AJ404611
Semantic_Type
  • Gene or Genome
Preferred_Name
  • BCL11A wt Allele
NCI_META_CUI
  • CL429886
EntrezGene_ID
  • 53335
HGNC_ID
  • HGNC:13221
FULL_SYN
  • B-Cell CLL/Lymphoma 11A (Zinc Finger Protein) wt AlleleSYNCI
  • BCL11A wt AllelePTNCI
  • EVI9SYNCI
  • CTIP1SYNCI
  • ZNF856SYNCI
  • Ecotropic Viral Integration Site 9 GeneSYNCI
  • HBFQTL5SYNCI
  • FLJ10173SYNCI
  • KIAA1809SYNCI
  • BCL11A-LSYNCI
  • FLJ34997SYNCI
  • BCL11A-SSYNCI
  • BCL11A-XLSYNCI
DEFINITION
  • Human BCL11A wild-type allele is located in the vicinity of 2p16.1 and is approximately 102 kb in length. This allele, which encodes B-cell lymphoma/leukemia 11A protein, plays a role in both lymphopoiesis and cell shape. Overexpression of the gene is associated with a translocation t(2;14)(p13;q32.3) as well as chronic lymphocytic leukemia and other B-cell malignancies.NCI
DesignNote
  • Multiple transcript variants encoding several different isoforms have been found for the BCL11A gene. (EntrezGene)
  • Variation of the BCL11A gene underlies the fetal hemoglobin quantitative trait locus 5 which is associated with variation in the production of erythrocytes containing measurable amounts of fetal hemoglobin (HbF). (UniProt)
code
  • C97395
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