PDCD2 programmed cell death 2

Information
Symbol
PDCD2
Type
protein-coding
Description
programmed cell death 2
Entrez Gene ID
5134
Genome
hg19
Position
chr6:170,884,383-170,893,725
Genome
hg38
Position
chr6:170,575,295-170,584,637
MIM
600866 OMIM
HGNC
HGNC:8762 HGNC
Ensembl
ENSG00000071994 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 46
Ranking
ClinVar
0
0
2
48
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 :
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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 RP8
SYNONYM ZMYND7
MIM 600866 OMIM
HGNC HGNC:8762 HGNC
Ensembl ENSG00000071994 Ensembl
AllianceGenome HGNC:8762
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537445.5 hg38 chr6 170,581,745 170,584,615 2,871
ENST00000443345.2 hg38 chr6 170,581,792 170,584,654 2,863
ENST00000542896.5 hg38 chr6 170,578,482 170,584,612 6,131
ENST00000392090.6 hg38 chr6 170,577,559 170,584,581 7,023
ENST00000541970.6 hg38 chr6 170,575,295 170,584,637 9,343
ENST00000453163.6 hg38 chr6 170,581,089 170,584,612 3,524
ENST00000614056.4 hg38 chr6 170,581,748 170,584,692 2,945
ENST00000541970.6 hg19 chr6 170,884,383 170,893,725 9,343
ENST00000392090.6 hg19 chr6 170,886,647 170,893,669 7,023
ENST00000542896.5 hg19 chr6 170,887,570 170,893,700 6,131
ENST00000453163.6 hg19 chr6 170,890,177 170,893,700 3,524
ENST00000537445.5 hg19 chr6 170,890,833 170,893,703 2,871
ENST00000614056.4 hg19 chr6 170,890,836 170,893,780 2,945
ENST00000443345.2 hg19 chr6 170,890,880 170,893,742 2,863
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