ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif 10
Information
- Symbol
- ADAMTS10
- Type
- protein-coding
- Description
- ADAM metallopeptidase with thrombospondin type 1 motif 10
- Entrez Gene ID
- 81794
- Genome
- hg19
- Position
- chr19:8,645,124-8,675,600
- Genome
- hg38
- Position
- chr19:8,580,240-8,610,715
- MIM
- 608990 OMIM
- HGNC
- HGNC:13201 HGNC
- Ensembl
- ENSG00000142303 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 34 |
Likely pathogenic | 0 | 18 |
Benign | 0 | 141 |
Likely benign | 0 | 780 |
Conflicting classifications of pathogenicity | 0 | 72 |
Uncertain significance | 0 | 644 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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180 |
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1,393 |
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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
[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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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 | |||
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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 |
---|---|
SYNONYM | ADAM-TS10 |
SYNONYM | ADAMTS-10 |
SYNONYM | WMS |
SYNONYM | WMS1 |
MIM | 608990 OMIM |
HGNC | HGNC:13201 HGNC |
Ensembl | ENSG00000142303 Ensembl |
AllianceGenome | HGNC:13201 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000595838.5 | hg38 | chr19 | 8,580,242 | 8,592,196 | 11,955 |
ENST00000597188.6 | hg38 | chr19 | 8,580,240 | 8,610,715 | 30,476 |
ENST00000270328.8 | hg38 | chr19 | 8,580,242 | 8,608,265 | 28,024 |
ENST00000597188.6 | hg19 | chr19 | 8,645,124 | 8,675,600 | 30,477 |
ENST00000595838.5 | hg19 | chr19 | 8,645,126 | 8,657,080 | 11,955 |
ENST00000270328.8 | hg19 | chr19 | 8,645,126 | 8,673,147 | 28,022 |
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