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FANCB

Official Full Name
FA complementation group B
Organism
Homo sapiens
GeneID
2187
Background
This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
Synonyms
FA2; FAB; FACB; FAAP90; FAAP95;

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