Overview

Variant ID 8359
Entrez Gene ID 93166
Gene PRDM6 (GeneCards)
Location hg19 5:122443795-122443795
hg38 5:123108100-123108100
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000005.9:g.122443795 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 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003233
EIGEN score 1.1888
CADD Raw score (version 1.3) 2.258375 (Deleterious)
FATHMM raw prediction score 0.89341 (Tolerated)
Deleterious probability by DeFine 0.8382 (Deleterious)
Entrez Gene ID 93166 (NCBI Gene)
Official Gene Symbol PRDM6 (GeneCards)
Number of variants in PRDM6 in this database 6 (view all the variants)
Full name PR/SET domain 6
Band 5q23.2
Other IDs Vega: OTTHUMG00000150469
OMIM: 616982
HGNC: HGNC:9350
Ensembl: ENSG00000061455
Other names PDA3, KMT8C, PRISM
Summary The protein encoded by this gene is a transcriptional repressor and a member of the PRDM family. Family members contain a PR domain and multiple zinc-finger domains. The encoded protein is involved in regulation of vascular smooth muscle cells (VSMC) contractile proteins. Mutations in this gene result in patent ductus arteriosus 3 (PDA3). [provided by RefSeq, Apr 2017]

Individual #1

Individual ID 29217584.13 (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;