Overview

Variant ID 23001
Entrez Gene ID 93166
Gene PRDM6 (GeneCards)
Location hg19 5:122449410-122449410
hg38 5:123113715-123113715
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000005.9:g.122449410 C>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
EIGEN score 0.0539
CADD Raw score (version 1.3) 0.021682 (Deleterious)
FATHMM raw prediction score 0.24083 (Tolerated)
Deleterious probability by DeFine 0.4906 (Neutral)
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 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;