MED25 mediator complex subunit 25

Go to:

Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
Genome browser

Information

Symbol: MED25
Type: protein-coding
Description: mediator complex subunit 25
Entrez Gene ID: 81857
Genome: hg19
Position: chr19:50,321,546-50,343,640
Genome: hg38
Position: chr19:49,818,289-49,840,383
MIM: 610197 OMIM
HGNC: HGNC:28845 HGNC
Ensembl: ENSG00000104973 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	6
Likely pathogenic	0	12
Benign	0	82
Likely benign	0	696
Conflicting classifications of pathogenicity	0	28
Uncertain significance	0	642

Ranking

	ClinVar
	0
	0
	250
	1,154
	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
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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
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
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
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	ACID1
SYNONYM	ARC92
SYNONYM	BVSYS
SYNONYM	CMT2B2
SYNONYM	P78
SYNONYM	PTOV2
SYNONYM	TCBAP0758
MIM	610197 OMIM
HGNC	HGNC:28845 HGNC
Ensembl	ENSG00000104973 Ensembl
AllianceGenome	HGNC:28845

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000538643.5	hg38	chr19	49,818,342	49,836,962	18,621
ENST00000593767.3	hg38	chr19	49,818,289	49,840,383	22,095
ENST00000312865.10	hg38	chr19	49,818,289	49,836,979	18,691
ENST00000312865.10	hg19	chr19	50,321,546	50,340,236	18,691
ENST00000593767.3	hg19	chr19	50,321,546	50,343,640	22,095
ENST00000538643.5	hg19	chr19	50,321,599	50,340,219	18,621

Genome browser