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- databases for immunodeficiency-causing variations

   FOXN1base
   Variation registry for  T-cell immunodeficiency, congenital alopecia, and nail dystrophy



Other resources

OMIM resources



FOXN1 Reference Sequences
Sequence type Accession number Description
Genomic sequence IDRefSeq: D0034
Homo sapiens chromosome 17, clone hRPK.192_H_23, complete sequence.
mRNA IDRefSeq: C0034
H.sapiens mRNA for whn transcription factor
Amino Acid Sequence O15353 Forkhead box protein N1 (Transcription factor winged-helix nude).