| Variant ID | 21593 |
|---|---|
| Entrez Gene ID | 23181 |
| Gene | DIP2A (GeneCards) |
| Location | hg19 21:47940235-47940235
hg38 21:46520322-46520322 |
| Disease | Asymptomatic |
| Method | HiSeq 2000 |
| Mutation(HGVS format) | NC_000021.8:g.47940235 A>G (Genome Assembly: GRCh37) |
| 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 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | -0.0679 |
| CADD Raw score (version 1.3) | 0.70808 (Deleterious) |
| FATHMM raw prediction score | 0.22641 (Tolerated) |
| Deleterious probability by DeFine | 0.0845 (Neutral) |
| Entrez Gene ID | 23181 (NCBI Gene) |
|---|---|
| Official Gene Symbol | DIP2A (GeneCards) |
| Number of variants in DIP2A in this database | 4 (view all the variants) |
| Full name | disco interacting protein 2 homolog A |
| Band | 21q22.3 |
| Other IDs | Vega: OTTHUMG00000090717 OMIM: 607711 HGNC: HGNC:17217 Ensembl: ENSG00000160305 |
| Other names | DIP2, C21orf106 |
| Summary | The protein encoded by this gene may be involved in axon patterning in the central nervous system. This gene is not highly expressed. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009] |
| Individual ID | 29217584.04 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 29217584 |
| Whose mosaic mutation | Normal |
| Phenotype | 1 |
| Disease | Asymptomatic |
| OMIM ID |
| 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; |