FOXF1 forkhead box F1

Information
Symbol
FOXF1
Type
protein-coding
Description
forkhead box F1
Entrez Gene ID
2294
Genome
hg19
Position
chr16:86,544,133-86,549,028
Genome
hg38
Position
chr16:86,510,527-86,515,422
MIM
601089 OMIM
HGNC
HGNC:3809 HGNC
Ensembl
ENSG00000103241 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 78
Likely pathogenic 0 28
Benign 0 38
Likely benign 0 46
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 94
Ranking
ClinVar
0
0
34
196
52
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 ACDMPV
SYNONYM FKHL5
SYNONYM FREAC1
MIM 601089 OMIM
HGNC HGNC:3809 HGNC
Ensembl ENSG00000103241 Ensembl
AllianceGenome HGNC:3809
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000262426.6 hg38 chr16 86,510,527 86,515,422 4,896
ENST00000262426.6 hg19 chr16 86,544,133 86,549,028 4,896
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