DDIAS DNA damage induced apoptosis suppressor

Information
Symbol
DDIAS
Type
protein-coding
Description
DNA damage induced apoptosis suppressor
Entrez Gene ID
220042
Genome
hg19
Position
chr11:82,612,778-82,645,701
Genome
hg38
Position
chr11:82,901,736-82,934,659
MIM
618045 OMIM
HGNC
HGNC:26351 HGNC
Ensembl
ENSG00000165490 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 14
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
82
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 C11orf82
SYNONYM noxin
MIM 618045 OMIM
HGNC HGNC:26351 HGNC
Ensembl ENSG00000165490 Ensembl
AllianceGenome HGNC:26351
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000525388.5 hg38 chr11 82,901,742 82,932,216 30,475
ENST00000524921.5 hg38 chr11 82,901,698 82,931,822 30,125
ENST00000528759.5 hg38 chr11 82,901,698 82,934,655 32,958
ENST00000533655.6 hg38 chr11 82,901,736 82,934,659 32,924
ENST00000329143.4 hg38 chr11 82,914,689 82,934,655 19,967
ENST00000525361.5 hg38 chr11 82,901,698 82,958,277 56,580
ENST00000524921.5 hg19 chr11 82,612,740 82,642,864 30,125
ENST00000528759.5 hg19 chr11 82,612,740 82,645,697 32,958
ENST00000525361.5 hg19 chr11 82,612,740 82,669,319 56,580
ENST00000533655.6 hg19 chr11 82,612,778 82,645,701 32,924
ENST00000525388.5 hg19 chr11 82,612,784 82,643,258 30,475
ENST00000329143.4 hg19 chr11 82,625,731 82,645,697 19,967
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