The FANCC gene provides instructions for making a protein that is involved in a process known as the Fanconi anemia (FA) pathway. The FA pathway turns on (activates) when the process …

Fanconi anemia group C protein is a protein that in humans is encoded by the FANCC gene. [5][6] This protein delays the onset of apoptosis and promotes homologous recombination repair of …

Mar 30, 2025 · Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal …

Fanconi anemia, complementation group C (FANCC) is a gene that encodes a protein that is a member of the Fanconi anemia complementation group. The protein complex functions in the …

FANCC was the first gene causal for FA to be identified, and consequently has been the most intensively studied. Loss of function studies have demonstrated an important role for FANCC …

Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and …

Fanconi anemia (FA) is a rare genetic disorder that results from DNA repair defects arising from pathogenic variants (PVs) in at least 22 genes (FANCA, FANCB, FANCC, FANCD1/BRCA2, …

Nov 8, 2011 · HGNC Approved Gene Symbol: FANCC. The FANCC gene is one of a group of classical Fanconi anemia genes whose protein products physically interact in a multiprotein …

The FANCC gene provides instructions for making a protein that is involved in a process known as the Fanconi anemia (FA) pathway. The FA pathway turns on ( activates) when the process …

Clinical resource with information about FANCC, Fanconi anemia complementation group C, and available tests. There are links to practice guidelines and authoritative resources like …