Overview

Variant ID 7523
Entrez Gene ID 5144
Gene PDE4D (GeneCards)
Location hg19 5:58679734-58679734
hg38 5:59383908-59383908
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000005.9:g.58679734 G>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 -0.3548
CADD Raw score (version 1.3) -0.139903 (Deleterious)
FATHMM raw prediction score 0.05954 (Tolerated)
Deleterious probability by DeFine 0.3645 (Neutral)
Entrez Gene ID 5144 (NCBI Gene)
Official Gene Symbol PDE4D (GeneCards)
Number of variants in PDE4D in this database 26 (view all the variants)
Full name phosphodiesterase 4D
Band 5q11.2-q12.1
Other IDs Vega: OTTHUMG00000162218
OMIM: 600129
HGNC: HGNC:8783
Ensembl: ENSG00000113448
Other names DPDE3, PDE43, STRK1, ACRDYS2, HSPDE4D, PDE4DN2
Summary This gene encodes one of four mammalian counterparts to the fruit fly 'dunce' gene. The encoded protein has 3',5'-cyclic-AMP phosphodiesterase activity and degrades cAMP, which acts as a signal transduction molecule in multiple cell types. This gene uses different promoters to generate multiple alternatively spliced transcript variants that encode functional proteins.[provided by RefSeq, Sep 2009]

Individual #1

Individual ID 29217584.03 (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;