Overview

Variant ID 5539
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)

Other information

Exon or Intron NA
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

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
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)
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 #1

Individual ID 29217584.14 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
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;