FOXM1 forkhead box M1

Information
Symbol
FOXM1
Type
protein-coding
Description
forkhead box M1
Entrez Gene ID
2305
Genome
hg19
Position
chr12:2,966,849-2,986,152
Genome
hg38
Position
chr12:2,857,683-2,876,986
MIM
602341 OMIM
HGNC
HGNC:3818 HGNC
Ensembl
ENSG00000111206 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 20
Likely benign 0 12
Uncertain significance 0 100
Ranking
ClinVar
0
0
4
126
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 :
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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 FKHL16
SYNONYM FOXM1A
SYNONYM FOXM1B
SYNONYM FOXM1C
SYNONYM HFH-11
SYNONYM HFH11
SYNONYM HNF-3
SYNONYM INS-1
SYNONYM MPHOSPH2
SYNONYM MPP-2
SYNONYM MPP2
SYNONYM PIG29
SYNONYM TRIDENT
MIM 602341 OMIM
HGNC HGNC:3818 HGNC
Ensembl ENSG00000111206 Ensembl
AllianceGenome HGNC:3818
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000627656.2 hg38 chr12 2,857,681 2,877,155 19,475
ENST00000359843.8 hg38 chr12 2,857,680 2,877,174 19,495
ENST00000342628.6 hg38 chr12 2,857,683 2,876,986 19,304
ENST00000361953.7 hg38 chr12 2,857,683 2,877,040 19,358
ENST00000359843.8 hg19 chr12 2,966,846 2,986,340 19,495
ENST00000627656.2 hg19 chr12 2,966,847 2,986,321 19,475
ENST00000342628.6 hg19 chr12 2,966,849 2,986,152 19,304
ENST00000361953.7 hg19 chr12 2,966,849 2,986,206 19,358
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