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NUMA1/RARA Fusion Gene

Go to external page http://purl.obolibrary.org/obo/NCIT_C99359

A fusion gene that results from a chromosomal translocation t(11;17)(q13;q21) which fuses the 5' half of the NUMA gene to the most of the RARA gene. This rearrangement may be associated with acute promyelocytic leukemia. [ ]

Term info

Label

NUMA1/RARA Fusion Gene

Synonyms
  • NUMA-RARA Fusion Gene
  • NUMA1-RARA Fusion Gene
  • NUMA1/RARA Fusion Gene
  • NuMA/RARA Fusion Gene
  • RARA/NUMA1 Fusion Gene
Subsets

NCIT_C116977, NCIT_C142800, NCIT_C142799

Display Name

NUMA1/RARA Fusion Gene

Preferred Name

NUMA1/RARA Fusion Gene

Related To Genetic Biomarker

http://purl.obolibrary.org/obo/NCIT_C21571, http://purl.obolibrary.org/obo/NCIT_C24648

Semantic Type

Gene or Genome

UMLS CUI

C1834115

code

C99359