PRDM11 PR/SET domain 11

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Information
Clinical Significance
Ranking
Frequency
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Information

Symbol: PRDM11
Type: protein-coding
Description: PR/SET domain 11
Entrez Gene ID: 56981
Genome: hg19
Position: chr11:45,168,894-45,256,661
Genome: hg38
Position: chr11:45,147,343-45,235,110
MIM: 616347 OMIM
HGNC: HGNC:13996 HGNC
Ensembl: ENSG00000019485 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar

Ranking

	ClinVar
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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

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Target data	:	MGeND data only
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Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	PFM8
MIM	616347 OMIM
HGNC	HGNC:13996 HGNC
Ensembl	ENSG00000019485 Ensembl
AllianceGenome	HGNC:13996

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000683152.1	hg38	chr11	45,146,639	45,235,109	88,471
ENST00000534751.3	hg38	chr11	45,146,639	45,214,713	68,075
ENST00000622142.5	hg38	chr11	45,147,343	45,235,110	87,768
ENST00000424263.6	hg38	chr11	45,147,343	45,225,087	77,745
ENST00000530656.5	hg38	chr11	45,095,806	45,224,908	129,103
ENST00000530656.5	hg19	chr11	45,117,357	45,246,459	129,103
ENST00000534751.3	hg19	chr11	45,168,190	45,236,264	68,075
ENST00000683152.1	hg19	chr11	45,168,190	45,256,660	88,471
ENST00000424263.6	hg19	chr11	45,168,894	45,246,638	77,745
ENST00000622142.5	hg19	chr11	45,168,894	45,256,661	87,768

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