FOXN1 forkhead box N1

Information
Symbol
FOXN1
Type
protein-coding
Description
forkhead box N1
Entrez Gene ID
8456
Genome
hg19
Position
chr17:26,833,261-26,865,914
Genome
hg38
Position
chr17:28,506,243-28,538,896
MIM
600838 OMIM
HGNC
HGNC:12765 HGNC
Ensembl
ENSG00000109101 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 88
Likely pathogenic 0 26
Benign 0 68
Likely benign 0 642
Conflicting classifications of pathogenicity 0 50
Uncertain significance 0 606
Ranking
ClinVar
0
0
150
1,248
8
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM FKHL20
SYNONYM RONU
SYNONYM TIDAND
SYNONYM TLIND
SYNONYM WHN
MIM 600838 OMIM
HGNC HGNC:12765 HGNC
Ensembl ENSG00000109101 Ensembl
AllianceGenome HGNC:12765
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579795.6 hg38 chr17 28,506,348 28,538,900 32,553
ENST00000226247.2 hg38 chr17 28,523,941 28,538,896 14,956
ENST00000577936.2 hg38 chr17 28,506,243 28,538,896 32,654
ENST00000577936.2 hg19 chr17 26,833,261 26,865,914 32,654
ENST00000579795.6 hg19 chr17 26,833,366 26,865,918 32,553
ENST00000226247.2 hg19 chr17 26,850,959 26,865,914 14,956
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