disease:Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy [MIM:601705].,function:Transcriptional regulator involved in development.,online information:FOXN1 mutation db,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:Expressed in thymus.,
Nucleus.
Expressed in thymus.
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