Fanconi anemia, complementation group C

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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 damaged DNA. Mutations in this gene result in Fanconi anemia, a human rare disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages.[6][7]

AliasesFANCC, Fancc, Facc, FA3, FAC, mir-3074-1, FACC, Fanconi anemia complementation group C, FA complementation group C
End95,426,796 bp[1]
Quick facts FANCC, Identifiers ...
FANCC
Identifiers
AliasesFANCC, Fancc, Facc, FA3, FAC, mir-3074-1, FACC, Fanconi anemia complementation group C, FA complementation group C
External IDsOMIM: 613899; MGI: 95480; HomoloGene: 109; GeneCards: FANCC; OMA:FANCC - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000136
NM_001243743
NM_001243744

NM_001042673
NM_001282942
NM_007985
NM_001347514
NM_001347515

RefSeq (protein)

NP_000127
NP_001230672
NP_001230673

NP_001036138
NP_001269871
NP_001334443
NP_001334444
NP_032011

Location (UCSC)Chr 9: 95.1 – 95.43 MbChr 13: 63.43 – 63.65 Mb
PubMed search[3][4]
Wikidata
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Structure

Quick facts Identifiers, Symbol ...
Fanconi anaemia group C protein
Identifiers
SymbolFanconi_C
PfamPF02106
InterProIPR000686
Available protein structures:
PDB  IPR000686 PF02106 (ECOD; PDBsum)  
AlphaFold
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Function

A nuclear complex containing FANCC protein (as well as FANCA, FANCF and FANCG) is essential for the activation of the FANCD2 protein to the mono-ubiquitinated isoform.[8] In normal, non-mutant, cells FANCD2 is mono-ubiquinated in response to DNA damage. FANCC together with FANCE acts as the substrate adaptor for this reaction [9] Activated FANCD2 protein co-localizes with BRCA1 (breast cancer susceptibility protein) at ionizing radiation-induced foci and in synaptonemal complexes of meiotic chromosomes. Activated FANCD2 protein may function prior to the initiation of meiotic recombination, perhaps to prepare chromosomes for synapsis, or to regulate subsequent recombination events.[8]

FANCC(-/-) mutant male and female mice have compromised gametogenesis, leading to markedly impaired fertility, a characteristic of Fanconi anemia patients.[10] Both male and female FANCC mutant mice have reduced numbers of germ cells.[11]

Interactions

Fanconi anemia, complementation group C has been shown to interact with:

References

Further reading

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