DCN decorin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Benign | 6 | 30 |
Likely benign | 0 | 12 |
Conflicting classifications of pathogenicity | 0 | 6 |
not provided | 0 | 2 |
Uncertain significance | 0 | 70 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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18 |
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92 |
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8 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CSCD |
SYNONYM | DSPG2 |
SYNONYM | PG40 |
SYNONYM | PGII |
SYNONYM | PGS2 |
SYNONYM | SLRR1B |
MIM | 125255 OMIM |
HGNC | HGNC:2705 HGNC |
Ensembl | ENSG00000011465 Ensembl |
AllianceGenome | HGNC:2705 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000546745.5 | hg38 | chr12 | 91,172,142 | 91,182,709 | 10,568 |
ENST00000552962.5 | hg38 | chr12 | 91,145,736 | 91,182,824 | 37,089 |
ENST00000420120.6 | hg38 | chr12 | 91,146,058 | 91,178,552 | 32,495 |
ENST00000546370.5 | hg38 | chr12 | 91,169,634 | 91,179,439 | 9,806 |
ENST00000441303.6 | hg38 | chr12 | 91,146,058 | 91,178,552 | 32,495 |
ENST00000550099.5 | hg38 | chr12 | 91,172,528 | 91,179,495 | 6,968 |
ENST00000551354.1 | hg38 | chr12 | 91,175,118 | 91,179,533 | 4,416 |
ENST00000456569.2 | hg38 | chr12 | 91,146,236 | 91,178,552 | 32,317 |
ENST00000547568.6 | hg38 | chr12 | 91,146,058 | 91,182,805 | 36,748 |
ENST00000052754.10 | hg38 | chr12 | 91,140,484 | 91,182,817 | 42,334 |
ENST00000425043.5 | hg38 | chr12 | 91,145,259 | 91,178,552 | 33,294 |
ENST00000052754.10 | hg19 | chr12 | 91,534,261 | 91,576,594 | 42,334 |
ENST00000425043.5 | hg19 | chr12 | 91,539,036 | 91,572,329 | 33,294 |
ENST00000420120.6 | hg19 | chr12 | 91,539,835 | 91,572,329 | 32,495 |
ENST00000441303.6 | hg19 | chr12 | 91,539,835 | 91,572,329 | 32,495 |
ENST00000547568.6 | hg19 | chr12 | 91,539,835 | 91,576,582 | 36,748 |
ENST00000456569.2 | hg19 | chr12 | 91,540,013 | 91,572,329 | 32,317 |
ENST00000546370.5 | hg19 | chr12 | 91,563,411 | 91,573,216 | 9,806 |
ENST00000546745.5 | hg19 | chr12 | 91,565,919 | 91,576,486 | 10,568 |
ENST00000550099.5 | hg19 | chr12 | 91,566,305 | 91,573,272 | 6,968 |
ENST00000551354.1 | hg19 | chr12 | 91,568,895 | 91,573,310 | 4,416 |
ENST00000552962.5 | hg19 | chr12 | 91,539,513 | 91,576,601 | 37,089 |
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