FOXE1 forkhead box E1

Information
Symbol
FOXE1
Type
protein-coding
Description
forkhead box E1
Entrez Gene ID
2304
Genome
hg19
Position
chr9:100,615,508-100,618,999
Genome
hg38
Position
chr9:97,853,226-97,856,717
MIM
602617 OMIM
HGNC
HGNC:3806 HGNC
Ensembl
ENSG00000178919 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Benign 0 40
Likely benign 0 14
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 42
Ranking
ClinVar
0
0
12
82
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 :
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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 BAMLAZ
SYNONYM FKHL15
SYNONYM FOXE2
SYNONYM HFKH4
SYNONYM HFKL5
SYNONYM NMTC4
SYNONYM TITF2
SYNONYM TTF-2
SYNONYM TTF2
MIM 602617 OMIM
HGNC HGNC:3806 HGNC
Ensembl ENSG00000178919 Ensembl
AllianceGenome HGNC:3806
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000375123.5 hg38 chr9 97,853,226 97,856,717 3,492
ENST00000375123.5 hg19 chr9 100,615,508 100,618,999 3,492
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