PRDM8 PR/SET domain 8

Information
Symbol
PRDM8
Type
protein-coding
Description
PR/SET domain 8
Entrez Gene ID
56978
Genome
hg19
Position
chr4:81,105,439-81,125,483
Genome
hg38
Position
chr4:80,184,285-80,204,329
MIM
616639 OMIM
HGNC
HGNC:13993 HGNC
Ensembl
ENSG00000152784 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 34
Likely benign 0 320
Uncertain significance 0 482
Ranking
ClinVar
0
0
70
762
2
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 EPM10
SYNONYM KMT8D
SYNONYM PFM5
MIM 616639 OMIM
HGNC HGNC:13993 HGNC
Ensembl ENSG00000152784 Ensembl
AllianceGenome HGNC:13993
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000504452.5 hg38 chr4 80,184,285 80,204,329 20,045
ENST00000339711.8 hg38 chr4 80,185,270 80,204,326 19,057
ENST00000415738.3 hg38 chr4 80,197,503 80,204,329 6,827
ENST00000504452.5 hg19 chr4 81,105,439 81,125,483 20,045
ENST00000339711.8 hg19 chr4 81,106,424 81,125,480 19,057
ENST00000415738.3 hg19 chr4 81,118,657 81,125,483 6,827
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