Structured Summary
Abstract
A Fanconi anemia complementation group protein that undergoes mono-ubiquitination by FANCL PROTEIN in response to DNA DAMAGE. Also, in response to IONIZING RADIATION it can undergo PHOSPHORYLATION by ataxia telangiectasia mutated protein. Modified FANCD2 interacts with BRCA2 PROTEIN in a stable complex with CHROMATIN, and it is involved in DNA REPAIR by homologous RECOMBINATION.
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Classification
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Synonyms
3 entry terms
- FANCD2 Protein
- Fanconi Anemia Group D2 Complementing Protein
- Fanconi Anemia Group D2 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
2006(2001)
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AMA Style
References
- National Library of Medicine. Fanconi Anemia Complementation Group D2 Protein. Medical Subject Headings (MeSH). 2026. Unique ID D052236. http://id.nlm.nih.gov/mesh/2026/D052236
- Fanconi Anemia Complementation Group D2 Protein. In: Wikidata. https://www.wikidata.org/wiki/Q21100488