Overview

Variant ID 18887
Entrez Gene ID 161725
Gene OTUD7A (GeneCards)
Location hg19 15:31894914-31894914
hg38 15:31602711-31602711
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000015.9:g.31894914 T>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 102531392

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1166
CADD Raw score (version 1.3) 0.900794 (Deleterious)
FATHMM raw prediction score 0.25704 (Tolerated)
Deleterious probability by DeFine 0.0433 (Neutral)
Entrez Gene ID 161725 (NCBI Gene)
Official Gene Symbol OTUD7A (GeneCards)
Number of variants in OTUD7A in this database 4 (view all the variants)
Full name OTU deubiquitinase 7A
Band 15q13.3
Other IDs Vega: OTTHUMG00000129275
OMIM: 612024
HGNC: HGNC:20718
Ensembl: ENSG00000169918
Other names OTUD7, C15orf16, C16ORF15, CEZANNE2
Summary The protein encoded by this gene is a deubiquitinizing enzyme and possible tumor suppressor. The encoded protein acts on TNF receptor associated factor 6 (TRAF6) to control nuclear factor kappa B expression. However, this gene is downregulated by SNAIL1 in hepatocellular carcinoma cells, contributing to their progression and malignancy. [provided by RefSeq, Aug 2016]

Individual #1

Individual ID 29217584.08 (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;