Variant ID | 21597 |
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Entrez Gene ID | 1826 |
Gene | DSCAM (GeneCards) |
Location | hg19 21:41978496-41978496
hg38 21:40606569-40606569 |
Disease | Asymptomatic |
Method | HiSeq 2000 |
Mutation(HGVS format) | NC_000021.8:g.41978496 A>C (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 | 48129895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1309 |
CADD Raw score (version 1.3) | -0.28539 (Deleterious) |
FATHMM raw prediction score | 0.18347 (Tolerated) |
Deleterious probability by DeFine | 0.6416 (Deleterious) |
Entrez Gene ID | 1826 (NCBI Gene) |
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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 ID | 29217584.04 (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; |