Structured Summary
Abstract
ATP-dependent DNA helicase that contains two N-terminal ZINC FINGERS and C-terminal ATP-binding and helicase domains. It functions in the regulation of gene transcription and CHROMATIN REMODELING. ATRX undergoes cell-cycle dependent phosphorylation, which causes it to translocate from the NUCLEAR MATRIX to CHROMATIN; thus, it may change its role from gene regulation during INTERPHASE to ensuring proper chromosome segregation at MITOSIS. Mutations in the ATRX gene are associated with cases of X-LINKED MENTAL RETARDATION co-morbid with ALPHA-THALASSEMIA (ATRX syndrome).
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Synonyms
5 entry terms
- ATRX Protein
- RAD54 Homolog Protein
- Homolog Protein, RAD54
- Nuclear Protein, X-linked
- X linked Nuclear Protein
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Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, 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.
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History Note
2018
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Previous Indexing
- DNA Helicases (1995-2017)
- Nuclear Proteins (1995-2017)
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References
- National Library of Medicine. X-linked Nuclear Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000075924. http://id.nlm.nih.gov/mesh/2026/D000075924
- X-linked Nuclear Protein. In: Wikidata. https://www.wikidata.org/wiki/Q21105313