Overview

Variant ID 8031
Entrez Gene ID 23037
Gene PDZD2 (GeneCards)
Location hg19 5:32035489-32035489
hg38 5:32035383-32035383
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000005.9:g.32035489 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 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.0004
EIGEN score -0.28
CADD Raw score (version 1.3) 0.021132 (Deleterious)
FATHMM raw prediction score 0.07098 (Tolerated)
Deleterious probability by DeFine 0.173 (Neutral)
Entrez Gene ID 23037 (NCBI Gene)
Official Gene Symbol PDZD2 (GeneCards)
Number of variants in PDZD2 in this database 3 (view all the variants)
Full name PDZ domain containing 2
Band 5p13.3
Other IDs Vega: OTTHUMG00000161981
OMIM: 610697
HGNC: HGNC:18486
Ensembl: ENSG00000133401
Other names AIPC, PIN1, PAPIN, PDZK3
Summary The protein encoded by this gene contains six PDZ domains and shares sequence similarity with pro-interleukin-16 (pro-IL-16). Like pro-IL-16, the encoded protein localizes to the endoplasmic reticulum and is thought to be cleaved by a caspase to produce a secreted peptide containing two PDZ domains. In addition, this gene is upregulated in primary prostate tumors and may be involved in the early stages of prostate tumorigenesis. [provided by RefSeq, Dec 2015]

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;