ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 motif 20
Information
- Symbol
- ADAMTS20
- Type
- protein-coding
- Description
- ADAM metallopeptidase with thrombospondin type 1 motif 20
- Entrez Gene ID
- 80070
- Genome
- hg19
- Position
- chr12:43,747,669-43,946,006
- Genome
- hg38
- Position
- chr12:43,353,866-43,552,203
- MIM
- 611681 OMIM
- HGNC
- HGNC:17178 HGNC
- Ensembl
- ENSG00000173157 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 28 |
| Uncertain significance | 0 | 186 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
218 |
 |
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
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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | ADAM-TS20 |
| SYNONYM | ADAMTS-20 |
| SYNONYM | GON-1 |
| MIM | 611681 OMIM |
| HGNC | HGNC:17178 HGNC |
| Ensembl | ENSG00000173157 Ensembl |
| AllianceGenome | HGNC:17178 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000553158.5 | hg38 | chr12 | 43,423,576 | 43,551,921 | 128,346 |
| ENST00000389420.8 | hg38 | chr12 | 43,353,866 | 43,552,203 | 198,338 |
| ENST00000389420.8 | hg19 | chr12 | 43,747,669 | 43,946,006 | 198,338 |
| ENST00000553158.5 | hg19 | chr12 | 43,817,379 | 43,945,724 | 128,346 |
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