PDCD5 programmed cell death 5

Information
Symbol
PDCD5
Type
protein-coding
Description
programmed cell death 5
Entrez Gene ID
9141
Genome
hg19
Position
chr19:33,072,096-33,078,359
Genome
hg38
Position
chr19:32,581,190-32,587,453
MIM
604583 OMIM
HGNC
HGNC:8764 HGNC
Ensembl
ENSG00000105185 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
16
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 TFAR19
MIM 604583 OMIM
HGNC HGNC:8764 HGNC
Ensembl ENSG00000105185 Ensembl
AllianceGenome HGNC:8764
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000590247.7 hg38 chr19 32,581,190 32,587,453 6,264
ENST00000379316.3 hg38 chr19 32,581,257 32,587,297 6,041
ENST00000419343.7 hg38 chr19 32,581,201 32,587,387 6,187
ENST00000586035.1 hg38 chr19 32,581,526 32,587,414 5,889
ENST00000592786.5 hg38 chr19 32,581,232 32,587,452 6,221
ENST00000590247.7 hg19 chr19 33,072,096 33,078,359 6,264
ENST00000419343.7 hg19 chr19 33,072,107 33,078,293 6,187
ENST00000592786.5 hg19 chr19 33,072,138 33,078,358 6,221
ENST00000379316.3 hg19 chr19 33,072,163 33,078,203 6,041
ENST00000586035.1 hg19 chr19 33,072,432 33,078,320 5,889
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