Overview

Variant ID 22486
Entrez Gene ID 7799
Gene PRDM2 (GeneCards)
Location hg19 1:14227380-14227380
hg38 1:13900885-13900885
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000001.10:g.14227380 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 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.0119
CADD Raw score (version 1.3) -0.113824 (Deleterious)
FATHMM raw prediction score 0.06367 (Tolerated)
Deleterious probability by DeFine 0.5432 (Deleterious)
Entrez Gene ID 7799 (NCBI Gene)
Official Gene Symbol PRDM2 (GeneCards)
Number of variants in PRDM2 in this database 8 (view all the variants)
Full name PR/SET domain 2
Band 1p36.21
Other IDs Vega: OTTHUMG00000007917
OMIM: 601196
HGNC: HGNC:9347
Ensembl: ENSG00000116731
Other names RIZ, KMT8, RIZ1, RIZ2, KMT8A, MTB-ZF, HUMHOXY1
Summary This tumor suppressor gene is a member of a nuclear histone/protein methyltransferase superfamily. It encodes a zinc finger protein that can bind to retinoblastoma protein, estrogen receptor, and the TPA-responsive element (MTE) of the heme-oxygenase-1 gene. Although the functions of this protein have not been fully characterized, it may (1) play a role in transcriptional regulation during neuronal differentiation and pathogenesis of retinoblastoma, (2) act as a transcriptional activator of the heme-oxygenase-1 gene, and (3) be a specific effector of estrogen action. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]

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;