Structured Summary
Abstract
A transcriptional co-repressor that contains a MYND-type zinc finger (MYND DOMAIN) at its C-terminal and functions as a homo-oligomer. It associates with DNA-binding transcription factors, other repressor proteins, and HISTONE ACETYLTRANSFERASES to repress expression of genes involved in cell growth and differentiation such as MATRIX METALLOPROTEINASE 7 and TCF12. A CHROMOSOMAL TRANSLOCATION involving the RUNX1T1 and CORE BINDING FACTOR ALPHA 2 SUBUNIT (RUNX1) genes frequently occurs in cells of leukemia patients; the resulting fusion protein (AML1-ETO or RUNX1-RUNX1T1) plays a critical role in leukemogenesis.
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Classification
Broader headings
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Synonyms
2 entry terms
- Eight Twenty One Protein
- RUNX1T1 Protein
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2018
MeSH Record
Previous Indexing
- DNA-Binding Proteins (1993-2017)
- Proto-Oncogene Proteins (1993-2017)
- Transcription Factors (2008-2017)
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AMA Style
References
- National Library of Medicine. RUNX1 Translocation Partner 1 Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000075142. http://id.nlm.nih.gov/mesh/2026/D000075142
- RUNX1 Translocation Partner 1 Protein. In: Wikidata. https://www.wikidata.org/wiki/Q24779617