| Variant ID | 22155 |
|---|---|
| Entrez Gene ID | 27334 |
| Gene | P2RY10 (GeneCards) |
| Location | hg19 X:78300328-78300328
hg38 X:79044831-79044831 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000023.10:g.78300328 C>T (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 | 155270560 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| CADD Raw score (version 1.3) | 0.124181 (Deleterious) |
| FATHMM raw prediction score | 0.04152 (Tolerated) |
| Deleterious probability by DeFine | 0.0653 (Neutral) |
| Entrez Gene ID | 27334 (NCBI Gene) |
|---|---|
| Official Gene Symbol | P2RY10 (GeneCards) |
| Number of variants in P2RY10 in this database | 2 (view all the variants) |
| Full name | P2Y receptor family member 10 |
| Band | Xq21.1 |
| Other IDs | Vega: OTTHUMG00000021896 OMIM: 300529 HGNC: HGNC:19906 Ensembl: ENSG00000078589 |
| Other names | P2Y10, LYPSR2 |
| Summary | The protein encoded by this gene belongs to the family of G-protein coupled receptors that are preferentially activated by adenosine and uridine nucleotides. There is a pseudogene for this gene nearby on chromosome X. Multiple alternatively spliced transcripts have been observed. [provided by RefSeq, Apr 2016] |
| Individual ID | 29217584.11 (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; |