Descriptor English: | Fanconi Anemia Complementation Group A Protein | ||||
Descriptor Spanish: |
Proteína del Grupo de Complementación A de la Anemia de Fanconi
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Descriptor Portuguese: | Proteína do Grupo de Complementação A da Anemia de Fanconi | ||||
Descriptor French: | Protéine du groupe de complémentation A de l'anémie de Fanconi | ||||
Entry term(s): |
FANCA Protein Fanconi Anemia Group A Complementing Protein Fanconi Anemia Group A Protein |
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Tree number(s): |
D12.776.313.500 D12.776.660.264 D12.776.744.476 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D052217 | ||||
Scope note: | 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. |
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Allowable Qualifiers: |
AD administration & dosage AE adverse effects AG agonists AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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Public MeSH Note: | 2006 |
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History Note: | 2006 |
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DeCS ID: | 51068 | ||||
Unique ID: | D052217 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 2006/01/01 | ||||
Date of Entry: | 2005/06/30 | ||||
Revision Date: | 2005/07/21 |
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CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins -
CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins -
CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins
|
Fanconi Anemia Complementation Group A Protein
- Preferred
Concept UI |
M0483788 |
Scope note | 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. |
Preferred term | Fanconi Anemia Complementation Group A Protein |
Entry term(s) |
FANCA Protein Fanconi Anemia Group A Complementing Protein Fanconi Anemia Group A Protein |
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