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Mutated in human diseases

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F12
F5
FH
F13A
FAM20C
FAM83H
FANCD2
FBN1
FBN2
FCGR1A
FGB
FGD4
FGF10
FGF3
FGFR1
FGFR3
FIGLA
FLCN
FLNA
FLNB
FLNC
FMR1
FOXC1
FOXC2
FOXE1
FOXE3
FOXE3
FOXF1
FOXL2
FOXP2
FOXP3
FRAS1
FREM2