FOXF2 forkhead box F2

Information
Symbol
FOXF2
Type
protein-coding
Description
forkhead box F2
Entrez Gene ID
2295
Genome
hg19
Position
chr6:1,389,811-1,395,838
Genome
hg38
Position
chr6:1,389,576-1,395,603
MIM
603250 OMIM
HGNC
HGNC:3810 HGNC
Ensembl
ENSG00000137273 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 16
not provided 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
72
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 :
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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 FKHL6
SYNONYM FREAC-2
SYNONYM FREAC2
MIM 603250 OMIM
HGNC HGNC:3810 HGNC
Ensembl ENSG00000137273 Ensembl
AllianceGenome HGNC:3810
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000645481.2 hg38 chr6 1,389,576 1,395,603 6,028
ENST00000645481.2 hg19 chr6 1,389,811 1,395,838 6,028
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