AEN apoptosis enhancing nuclease

Information
Symbol
AEN
Type
protein-coding
Description
apoptosis enhancing nuclease
Entrez Gene ID
64782
Genome
hg19
Position
chr15:89,164,571-89,175,512
Genome
hg38
Position
chr15:88,621,340-88,632,281
MIM
610177 OMIM
HGNC
HGNC:25722 HGNC
Ensembl
ENSG00000181026 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
50
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 ISG20L1
SYNONYM pp12744
MIM 610177 OMIM
HGNC HGNC:25722 HGNC
Ensembl ENSG00000181026 Ensembl
AllianceGenome HGNC:25722
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000332810.4 hg38 chr15 88,621,340 88,632,281 10,942
ENST00000332810.4 hg19 chr15 89,164,571 89,175,512 10,942
Genome browser