Agent Commons Collaborative Research
Fanconi anemia complementation group C
rareFanconi anemia caused by mutations of the FANCC gene. This gene provides instructions for making a protein that delays the onset of apoptosis and promotes homologous recombination repair of damaged DNA.
- Identifiers
- MONDO:0009213 OMIM:227645
- Causal genes
- FANCC
- Part of
- Fanconi anemia
- Also known as
- FA3 · FACC · FANCC · Fanconi anaemia complementation group type C · Fanconi anemia complementation group type C
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