E2F6 E2F transcription factor 6

Information
Symbol
E2F6
Type
protein-coding
Description
E2F transcription factor 6
Entrez Gene ID
1876
Genome
hg19
Position
chr2:11,584,501-11,606,287
Genome
hg38
Position
chr2:11,444,375-11,466,161
MIM
602944 OMIM
HGNC
HGNC:3120 HGNC
Ensembl
ENSG00000169016 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 0
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
22
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 :
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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 E2F-6
MIM 602944 OMIM
HGNC HGNC:3120 HGNC
Ensembl ENSG00000169016 Ensembl
AllianceGenome HGNC:3120
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000546212.2 hg38 chr2 11,444,375 11,466,177 21,803
ENST00000381525.8 hg38 chr2 11,444,375 11,466,161 21,787
ENST00000542100.5 hg38 chr2 11,444,375 11,466,177 21,803
ENST00000307236.8 hg38 chr2 11,444,375 11,466,177 21,803
ENST00000381525.8 hg19 chr2 11,584,501 11,606,287 21,787
ENST00000307236.8 hg19 chr2 11,584,501 11,606,303 21,803
ENST00000542100.5 hg19 chr2 11,584,501 11,606,303 21,803
ENST00000546212.2 hg19 chr2 11,584,501 11,606,303 21,803
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