Terminology Service for NFDI4Health
TCF3/HLF Fusion Gene
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http://purl.obolibrary.org/obo/NCIT_C99289
A fusion gene (~4.4 kb) that results from a chromosomal translocation t(17;19)(q22;p13) which fuses intron 13 of the TCF3 gene with intron 3 of the HLF gene. This rearrangement is associated with childhood pre-B cell acute lymphoblastic leukemia. [ ]
Term info
Label
TCF3/HLF Fusion Gene
Synonyms
- E2A-HLF Fusion Gene
- E2A/HLF Fusion Gene
- HLF/E2A Fusion Gene
- TCF3-HLF Fusion Gene
- TCF3/HLF Fusion Gene
Subsets
NCIT_C116977, NCIT_C142800, NCIT_C142799
Contributing Source
CTRP
Display Name
TCF3/HLF Fusion Gene
GenBank Accession Number
M95586
Preferred Name
TCF3/HLF Fusion Gene
Related To Genetic Biomarker
http://purl.obolibrary.org/obo/NCIT_C97556, http://purl.obolibrary.org/obo/NCIT_C24846
Semantic Type
Gene or Genome
UMLS CUI
C1840636
code
C99289
Term relations
Subclass of:
- Fusion Gene
- Gene_Plays_Role_In_Process some Transcriptional Activation
- Gene_Has_Abnormality some t(17;19)(q22;p13)
Related from: