FOXL1 forkhead box L1

Information
Symbol
FOXL1
Type
protein-coding
Description
forkhead box L1
Entrez Gene ID
2300
Genome
hg19
Position
chr16:86,612,155-86,617,084
Genome
hg38
Position
chr16:86,578,549-86,583,478
MIM
603252 OMIM
HGNC
HGNC:3817 HGNC
Ensembl
ENSG00000176678 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 3 0
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
62
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
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 FKH6
SYNONYM FKHL11
SYNONYM FREAC7
SYNONYM OTSC11
MIM 603252 OMIM
HGNC HGNC:3817 HGNC
Ensembl ENSG00000176678 Ensembl
AllianceGenome HGNC:3817
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000320241.5 hg38 chr16 86,578,549 86,583,478 4,930
ENST00000320241.5 hg19 chr16 86,612,155 86,617,084 4,930
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