Overview

Variant ID 14272
Entrez Gene ID 26091
Gene HERC4 (GeneCards)
Location hg19 10:69729291-69729291
hg38 10:67969534-67969534
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000010.10:g.69729291 C>T (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 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1952
CADD Raw score (version 1.3) 0.161492 (Deleterious)
FATHMM raw prediction score 0.09749 (Tolerated)
Deleterious probability by DeFine 0.2052 (Neutral)
Entrez Gene ID 26091 (NCBI Gene)
Official Gene Symbol HERC4 (GeneCards)
Number of variants in HERC4 in this database 3 (view all the variants)
Full name HECT and RLD domain containing E3 ubiquitin protein ligase 4
Band 10q21.3
Other IDs Vega: OTTHUMG00000018343
OMIM: 609248
HGNC: HGNC:24521
Ensembl: ENSG00000148634
Other names None
Summary HERC4 belongs to the HERC family of ubiquitin ligases, all of which contain a HECT domain and at least 1 RCC1 (MIM 179710)-like domain (RLD). The 350-amino acid HECT domain is predicted to catalyze the formation of a thioester with ubiquitin before transferring it to a substrate, and the RLD is predicted to act as a guanine nucleotide exchange factor for small G proteins (Hochrainer et al., 2005 [PubMed 15676274]).[supplied by OMIM, Mar 2008]

Individual #1

Individual ID 29217584.10 (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;