FOXK2 forkhead box K2

Information
Symbol
FOXK2
Type
protein-coding
Description
forkhead box K2
Entrez Gene ID
3607
Genome
hg19
Position
chr17:80,477,608-80,562,478
Genome
hg38
Position
chr17:82,519,732-82,604,602
MIM
147685 OMIM
HGNC
HGNC:6036 HGNC
Ensembl
ENSG00000141568 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 32
Likely benign 0 32
Uncertain significance 0 102
Ranking
ClinVar
0
0
4
160
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 :
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 ILF
SYNONYM ILF-1
SYNONYM ILF1
SYNONYM nGTBP
MIM 147685 OMIM
HGNC HGNC:6036 HGNC
Ensembl ENSG00000141568 Ensembl
AllianceGenome HGNC:6036
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335255.10 hg38 chr17 82,519,732 82,604,602 84,871
ENST00000335255.10 hg19 chr17 80,477,608 80,562,478 84,871
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