FOXN4 forkhead box N4

Information
Symbol
FOXN4
Type
protein-coding
Description
forkhead box N4
Entrez Gene ID
121643
Genome
hg19
Position
chr12:109,715,783-109,747,089
Genome
hg38
Position
chr12:109,277,978-109,309,284
MIM
609429 OMIM
HGNC
HGNC:21399 HGNC
Ensembl
ENSG00000139445 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 78
Ranking
ClinVar
0
0
0
78
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
MIM 609429 OMIM
HGNC HGNC:21399 HGNC
Ensembl ENSG00000139445 Ensembl
AllianceGenome HGNC:21399
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000299162.10 hg38 chr12 109,277,978 109,309,284 31,307
ENST00000355216.5 hg38 chr12 109,277,979 109,309,220 31,242
ENST00000299162.10 hg19 chr12 109,715,783 109,747,089 31,307
ENST00000355216.5 hg19 chr12 109,715,784 109,747,025 31,242
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