FOXN2 forkhead box N2

Information
Symbol
FOXN2
Type
protein-coding
Description
forkhead box N2
Entrez Gene ID
3344
Genome
hg19
Position
chr2:48,541,821-48,606,434
Genome
hg38
Position
chr2:48,314,682-48,379,295
MIM
143089 OMIM
HGNC
HGNC:5281 HGNC
Ensembl
ENSG00000170802 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
58
0
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 HTLF
MIM 143089 OMIM
HGNC HGNC:5281 HGNC
Ensembl ENSG00000170802 Ensembl
AllianceGenome HGNC:5281
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000340553.8 hg38 chr2 48,314,682 48,379,295 64,614
ENST00000340553.8 hg19 chr2 48,541,821 48,606,434 64,614
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