Variant ID | 16624 |
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Entrez Gene ID | 80070 |
Gene | ADAMTS20 (GeneCards) |
Location | hg19 12:43952230-43952230
hg38 12:43558427-43558427 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000012.11:g.43952230 T>C (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 133851895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3316 |
CADD Raw score (version 1.3) | -0.119409 (Deleterious) |
FATHMM raw prediction score | 0.0817 (Tolerated) |
Deleterious probability by DeFine | 0.0561 (Neutral) |
Entrez Gene ID | 80070 (NCBI Gene) |
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Official Gene Symbol | ADAMTS20 (GeneCards) |
Number of variants in ADAMTS20 in this database | 5 (view all the variants) |
Full name | ADAM metallopeptidase with thrombospondin type 1 motif 20 |
Band | 12q12 |
Other IDs | Vega: OTTHUMG00000169353 OMIM: 611681 HGNC: HGNC:17178 Ensembl: ENSG00000173157 |
Other names | GON-1, ADAM-TS20, ADAMTS-20 |
Summary | The protein encoded by this gene is a member of the ADAMTS family of zinc-dependent proteases. The encoded protein has a signal peptide that is cleaved to release the mature peptide, which is secreted and found in the extracellular matrix. This protein may be involved in tissue remodeling. [provided by RefSeq, Sep 2011] |
Individual ID | 29217584.12 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
Journal | Science |
Publication date | 2018.02 |
Disease | Cockayne syndrome Xeroderma Pigmentosum |
Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |