Terminology Service for NFDI4Health

P2RY8/CRLF2 Fusion Gene

Go to external page http://purl.obolibrary.org/obo/NCIT_C99389


A fusion gene that results from an intrachromosomal deletion of the pseudoautosomal region 1of Xp22.3 and Yp11.3 which fuses the noncoding exon 1 of the P2RY8 gene to the entire coding region of the CRLF2 gene. This rearrangement is associated with Down syndrome-associated acute lymphoblastic leukemia. [ ]

Term info

Label

P2RY8/CRLF2 Fusion Gene

Synonyms
  • CRLF2/P2RY8 Fusion Gene
  • P2RY8-CRLF2 Fusion Gene
  • P2RY8/CRLF2 Fusion Gene
Subsets

NCIT_C116977, NCIT_C142800, NCIT_C142799

DesignNote

The P2RY8/CRLF2 gene fusion causes aberrant expression of the CRLF2 gene.

Display Name

P2RY8/CRLF2 Fusion Gene

Preferred Name

P2RY8/CRLF2 Fusion Gene

Related To Genetic Biomarker

http://purl.obolibrary.org/obo/NCIT_C97430, http://purl.obolibrary.org/obo/NCIT_C97683

Semantic Type

Gene or Genome

UMLS CUI

C3275246

code

C99389

Term relations