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  • Molecular assay reagents intended to identify mutations in the Fanconi anemia, complementation group G (FANCG) gene, located at chromosome 9p13, which encodes for a DNA repair protein that may operate in a postreplication repair or cell cycle checkpoint function and may also be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. The gene may be also a candidate for a tumor suppressor gene. Mutations at this locus have been identified in patients with Fanconi anemia (FA).
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