Variant ID | 5539 |
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Entrez Gene ID | 57337 |
Gene | SENP7 (GeneCards) |
Location | hg19 3:101073493-101073493
hg38 3:101354649-101354649 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000003.11:g.101073493 G>A (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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.4255 |
CADD Raw score (version 1.3) | -0.285353 (Deleterious) |
FATHMM raw prediction score | 0.06184 (Tolerated) |
Deleterious probability by DeFine | 0.2161 (Neutral) |
Entrez Gene ID | 57337 (NCBI Gene) |
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Official Gene Symbol | SENP7 (GeneCards) |
Number of variants in SENP7 in this database | 3 (view all the variants) |
Full name | SUMO specific peptidase 7 |
Band | 3q12.3 |
Other IDs | Vega: OTTHUMG00000149927 OMIM: 612846 HGNC: HGNC:30402 Ensembl: ENSG00000138468 |
Other names | None |
Summary | The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1; MIM 601912) is required for many cellular processes. SUMO-specific proteases, such as SENP7, process SUMO precursors to generate a C-terminal diglycine motif required for the conjugation reaction. They also display isopeptidase activity for deconjugation of SUMO-conjugated substrates (Lima and Reverter, 2008 [PubMed 18799455]).[supplied by OMIM, Jun 2009] |
Individual ID | 29217584.14 (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; |