Overview

Variant ID 21589
Entrez Gene ID 1826
Gene DSCAM (GeneCards)
Location hg19 21:41597602-41597602
hg38 21:40225675-40225675
Disease Asymptomatic
Method HiSeq 2000
Mutation(HGVS format) NC_000021.8:g.41597602 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 48129895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.0851
CADD Raw score (version 1.3) 0.302346 (Deleterious)
FATHMM raw prediction score 0.13342 (Tolerated)
Deleterious probability by DeFine 0.4758 (Neutral)
Entrez Gene ID 1826 (NCBI Gene)
Official Gene Symbol DSCAM (GeneCards)
Number of variants in DSCAM in this database 12 (view all the variants)
Full name DS cell adhesion molecule
Band 21q22.2
Other IDs Vega: OTTHUMG00000086732
OMIM: 602523
HGNC: HGNC:3039
Ensembl: ENSG00000171587
Other names CHD2, CHD2-42, CHD2-52
Summary This gene is a member of the immunoglobulin superfamily of cell adhesion molecules (Ig-CAMs), and is involved in human central and peripheral nervous system development. This gene is a candidate for Down syndrome and congenital heart disease (DSCHD). A gene encoding a similar Ig-CAM protein is located on chromosome 11. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]

Individual #1

Individual ID 29217584.04 (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;