DCTN3 dynactin subunit 3

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

Symbol: DCTN3
Type: protein-coding
Description: dynactin subunit 3
Entrez Gene ID: 11258
Genome: hg19
Position: chr9:34,613,543-34,620,492
Genome: hg38
Position: chr9:34,613,546-34,620,495
MIM: 607387 OMIM
HGNC: HGNC:2713 HGNC
Ensembl: ENSG00000137100 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	0	24

Ranking

	ClinVar
	0
	0
	0
	24
	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
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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

Search Word

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
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
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	DCTN-22
SYNONYM	DCTN22
MIM	607387 OMIM
HGNC	HGNC:2713 HGNC
Ensembl	ENSG00000137100 Ensembl
AllianceGenome	HGNC:2713

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000378916.8	hg38	chr9	34,613,545	34,620,523	6,979
ENST00000378913.6	hg38	chr9	34,614,187	34,620,481	6,295
ENST00000477738.6	hg38	chr9	34,613,604	34,620,468	6,865
ENST00000259632.12	hg38	chr9	34,613,546	34,620,495	6,950
ENST00000341694.6	hg38	chr9	34,613,551	34,620,474	6,924
ENST00000378916.8	hg19	chr9	34,613,542	34,620,520	6,979
ENST00000259632.12	hg19	chr9	34,613,543	34,620,492	6,950
ENST00000341694.6	hg19	chr9	34,613,548	34,620,471	6,924
ENST00000477738.6	hg19	chr9	34,613,601	34,620,465	6,865
ENST00000378913.6	hg19	chr9	34,614,184	34,620,478	6,295

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