Variant ID | 12241 |
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Entrez Gene ID | 9228 |
Gene | DLGAP2 (GeneCards) |
Location | hg19 8:1601255-1601255
hg38 8:1653089-1653089 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000008.10:g.1601255 G>A (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 | 146364022 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.4042 |
CADD Raw score (version 1.3) | -0.499581 (Deleterious) |
FATHMM raw prediction score | 0.05954 (Tolerated) |
Deleterious probability by DeFine | 0.4785 (Neutral) |
Entrez Gene ID | 9228 (NCBI Gene) |
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Official Gene Symbol | DLGAP2 (GeneCards) |
Number of variants in DLGAP2 in this database | 3 (view all the variants) |
Full name | DLG associated protein 2 |
Band | 8p23.3 |
Other IDs | Vega: OTTHUMG00000163599 OMIM: 605438 HGNC: HGNC:2906 Ensembl: ENSG00000198010 |
Other names | DAP2, SAPAP2, C8orf68, ERICH1-AS1 |
Summary | The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014] |
Individual ID | 29217584.12 (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; |