FOXB1 forkhead box B1

Information
Symbol
FOXB1
Type
protein-coding
Description
forkhead box B1
Entrez Gene ID
27023
Genome
hg19
Position
chr15:60,296,510-60,299,643
Genome
hg38
Position
chr15:60,004,311-60,007,444
MIM
619961 OMIM
HGNC
HGNC:3799 HGNC
Ensembl
ENSG00000171956 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
30
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 :
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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 FKH5
SYNONYM HFKH-5
MIM 619961 OMIM
HGNC HGNC:3799 HGNC
Ensembl ENSG00000171956 Ensembl
AllianceGenome HGNC:3799
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000396057.6 hg38 chr15 60,004,311 60,007,444 3,134
ENST00000396057.6 hg19 chr15 60,296,510 60,299,643 3,134
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