Variant ID | 23001 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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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; |