Variant ID | 8031 |
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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) |
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) | 0.0004 |
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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) |
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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 ID | 29217584.10 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |