FOXC2 forkhead box C2

Information
Symbol
FOXC2
Type
protein-coding
Description
forkhead box C2
Entrez Gene ID
2303
Genome
hg19
Position
chr16:86,600,435-86,603,334
Genome
hg38
Position
chr16:86,566,829-86,569,728
MIM
602402 OMIM
HGNC
HGNC:3801 HGNC
Ensembl
ENSG00000176692 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 64
Likely pathogenic 0 24
Benign 6 28
Likely benign 0 76
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 178
Ranking
ClinVar
0
0
40
290
30
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 FKHL14
SYNONYM LD
SYNONYM MFH-1
SYNONYM MFH1
MIM 602402 OMIM
HGNC HGNC:3801 HGNC
Ensembl ENSG00000176692 Ensembl
AllianceGenome HGNC:3801
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000649859.1 hg38 chr16 86,566,829 86,569,728 2,900
ENST00000649859.1 hg19 chr16 86,600,435 86,603,334 2,900
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