Chemicals and Drugs

Fanconi Anemia Complementation Group A Protein

A Fanconi anemia complementation group protein that is the most commonly mutated protein in FANCONI ANEMIA. It undergoes PHOSPHORYLATION by PROTEIN KINASE B and forms a complex with FANCC PROTEIN in the CELL NUCLEUS.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

A Fanconi anemia complementation group protein that is the most commonly mutated protein in FANCONI ANEMIA. It undergoes PHOSPHORYLATION by PROTEIN KINASE B and forms a complex with FANCC PROTEIN in the CELL NUCLEUS.

MeSH Record

Classification

Broader headings

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MeSH Record

Synonyms

3 entry terms
  • FANCA Protein
  • Fanconi Anemia Group A Complementing Protein
  • Fanconi Anemia Group A 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

MeSH Hierarchy

Tree Numbers

  1. D12.776w.313.500
  2. D12.776w.660w.264
  3. D12.776w.744w.476

AMA Style

References

  1. National Library of Medicine. Fanconi Anemia Complementation Group A Protein. Medical Subject Headings (MeSH). 2026. Unique ID D052217. http://id.nlm.nih.gov/mesh/2026/D052217
  2. Fanconi Anemia Complementation Group A Protein. In: Wikidata. https://www.wikidata.org/wiki/Q21101242