FOXN1 gene homepage

General information
Gene symbol FOXN1
Gene name forkhead box N1
Chromosome 17
Chromosomal band q11-q12
Imprinted Unknown
Genomic reference LRG_61
Transcript reference NM_003593.2
Exon/intron information NM_003593.2 exon/intron table
Associated with diseases T-cell immunodeficiency, congenital alopecia and nail dystrophy
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 8
Unique public DNA variants reported 7
Individuals with public variants 11
Hidden variants 0
Download all this gene's data Download all data
Notes Alias WHN.
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated January 13, 2018
Version FOXN1:180113

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_003593.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/FOXN1
HGNC 12765
Entrez Gene 8456
PubMed articles FOXN1
OMIM - Gene 600838
OMIM - Diseases T-cell immunodeficiency, congenital alopecia and nail dystrophy
HGMD FOXN1
GeneCards FOXN1
GeneTests FOXN1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008099 17 forkhead box N1 NM_003593.2 NP_003584.2 8


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