DCTN2 dynactin subunit 2

Information
Symbol
DCTN2
Type
protein-coding
Description
dynactin subunit 2
Entrez Gene ID
10540
Genome
hg19
Position
chr12:57,924,094-57,940,924
Genome
hg38
Position
chr12:57,530,311-57,547,141
MIM
607376 OMIM
HGNC
HGNC:2712 HGNC
Ensembl
ENSG00000175203 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
22
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 :
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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 DCTN50
SYNONYM DYNAMITIN
SYNONYM HEL-S-77
SYNONYM RBP50
MIM 607376 OMIM
HGNC HGNC:2712 HGNC
Ensembl ENSG00000175203 Ensembl
AllianceGenome HGNC:2712
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000678653.1 hg38 chr12 57,530,310 57,546,691 16,382
ENST00000678505.1 hg38 chr12 57,530,074 57,547,177 17,104
ENST00000543672.6 hg38 chr12 57,530,310 57,547,177 16,868
ENST00000434715.7 hg38 chr12 57,530,311 57,547,141 16,831
ENST00000548249.6 hg38 chr12 57,530,051 57,547,192 17,142
ENST00000548249.6 hg19 chr12 57,923,834 57,940,975 17,142
ENST00000434715.7 hg19 chr12 57,924,094 57,940,924 16,831
ENST00000543672.6 hg19 chr12 57,924,093 57,940,960 16,868
ENST00000678505.1 hg19 chr12 57,923,857 57,940,960 17,104
ENST00000678653.1 hg19 chr12 57,924,093 57,940,474 16,382
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