U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

t(5;8)(p15;q13)

MedGen UID:
1789069
Concept ID:
C5447694
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation involving the genes AHRR on chromosome 5 and NCOA2 on chromosome 8 resulting in AHRR-NCOA2 fusion. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(5;8)(p15;q13)

Supplemental Content

Table of contents

    Practice guidelines

    • Bookshelf
      See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...