E2F8 E2F transcription factor 8

Information
Symbol
E2F8
Type
protein-coding
Description
E2F transcription factor 8
Entrez Gene ID
79733
Genome
hg19
Position
chr11:19,245,610-19,262,492
Genome
hg38
Position
chr11:19,224,063-19,240,945
MIM
612047 OMIM
HGNC
HGNC:24727 HGNC
Ensembl
ENSG00000129173 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 10
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
116
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 E2F-8
MIM 612047 OMIM
HGNC HGNC:24727 HGNC
Ensembl ENSG00000129173 Ensembl
AllianceGenome HGNC:24727
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000527884.5 hg38 chr11 19,224,063 19,241,620 17,558
ENST00000250024.9 hg38 chr11 19,224,063 19,240,945 16,883
ENST00000620009.4 hg38 chr11 19,224,066 19,241,620 17,555
ENST00000250024.9 hg19 chr11 19,245,610 19,262,492 16,883
ENST00000527884.5 hg19 chr11 19,245,610 19,263,167 17,558
ENST00000620009.4 hg19 chr11 19,245,613 19,263,167 17,555
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