PRDM13 PR/SET domain 13

Information
Symbol
PRDM13
Type
protein-coding
Description
PR/SET domain 13
Entrez Gene ID
59336
Genome
hg19
Position
chr6:100,054,709-100,063,438
Genome
hg38
Position
chr6:99,606,833-99,615,562
MIM
616741 OMIM
HGNC
HGNC:13998 HGNC
Ensembl
ENSG00000112238 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Benign 0 34
Likely benign 0 348
Uncertain significance 0 562
Ranking
ClinVar
0
0
76
858
8
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 CDIDHH
SYNONYM MU-MB-20.220
SYNONYM PCH17
SYNONYM PFM10
MIM 616741 OMIM
HGNC HGNC:13998 HGNC
Ensembl ENSG00000112238 Ensembl
AllianceGenome HGNC:13998
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000369215.5 hg38 chr6 99,606,833 99,615,562 8,730
ENST00000369215.5 hg19 chr6 100,054,709 100,063,438 8,730
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