About: BTG1 wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • BTG1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 109580
GenBank_Accession_Number
  • NM_001731
Semantic_Type
  • Gene or Genome
Preferred_Name
  • BTG1 wt Allele
PubMedID_Primary_Reference
  • 19039135
UMLS_CUI
  • C2698303
EntrezGene_ID
  • 694
Legacy_Concept_Name
  • BTG1_wt_Allele
HGNC_ID
  • HGNC:1130
FULL_SYN
  • B-Cell Translocation Protein 1 GeneSYNCI
  • BTG1 wt AllelePTNCI
  • B-Cell Translocation Gene 1, Anti-Proliferative wt AlleleSYNCI
DEFINITION
  • Human BTG1 wild-type allele is located in the vicinity of 12q22 and is approximately 3 kb in length. This allele, which encodes protein BTG1, which plays a role in the modulation of cellular proliferation. Genetic variation may be associated with the relapse of acute lymphoblastic leukemia. The BTG1 gene and the MYC gene are involved in a chromosomal aberration, translocation t(8;12)(q24;q22), which may be associated with B-cell chronic lymphocytic leukemia.NCI
code
  • C80103
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