INF2

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INF2

A gene on chromosome 14q32.33 that encodes a diaphanous formin, which in mice plays a role in polymerisation and depolymerisation of actin filaments.

Molecular pathology
INF2 mutations are associated with focal segmental glomerulosclerosis type 5, as well as some cases of Charcot-Tooth-Marie neuropathy.