COPE COPI coat complex subunit epsilon

Information
Symbol
COPE
Type
protein-coding
Description
COPI coat complex subunit epsilon
Entrez Gene ID
11316
Genome
hg19
Position
chr19:19,010,372-19,030,189
Genome
hg38
Position
chr19:18,899,563-18,919,380
MIM
606942 OMIM
HGNC
HGNC:2234 HGNC
Ensembl
ENSG00000105669 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
36
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
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 :
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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
Entry Origin Type Annotation
TypeID
SYNONYM epsilon-COP
MIM 606942 OMIM
HGNC HGNC:2234 HGNC
Ensembl ENSG00000105669 Ensembl
AllianceGenome HGNC:2234
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000349893.8 hg38 chr19 18,899,517 18,919,363 19,847
ENST00000262812.9 hg38 chr19 18,899,514 18,919,387 19,874
ENST00000351079.8 hg38 chr19 18,899,573 18,919,375 19,803
ENST00000600932.5 hg38 chr19 18,899,563 18,919,380 19,818
ENST00000262812.9 hg19 chr19 19,010,323 19,030,196 19,874
ENST00000349893.8 hg19 chr19 19,010,326 19,030,172 19,847
ENST00000600932.5 hg19 chr19 19,010,372 19,030,189 19,818
ENST00000351079.8 hg19 chr19 19,010,382 19,030,184 19,803
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