| Variant ID | 9140 |
|---|---|
| Entrez Gene ID | 577 |
| Gene | ADGRB3 (GeneCards) |
| Location | hg19 6:70159745-70159745
hg38 6:69449853-69449853 |
| Disease | Asymptomatic |
| Method | HiSeq X Ten |
| Mutation(HGVS format) | NC_000006.11:g.70159745 G>A (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 | 171115067 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| EIGEN score | 0.0147 |
| CADD Raw score (version 1.3) | 1.358646 (Deleterious) |
| FATHMM raw prediction score | 0.43199 (Tolerated) |
| Deleterious probability by DeFine | 0.0792 (Neutral) |
| Entrez Gene ID | 577 (NCBI Gene) |
|---|---|
| Official Gene Symbol | ADGRB3 (GeneCards) |
| Number of variants in ADGRB3 in this database | 111 (view all the variants) |
| Full name | adhesion G protein-coupled receptor B3 |
| Band | 6q12-q13 |
| Other IDs | Vega: OTTHUMG00000014982 OMIM: 602684 HGNC: HGNC:945 Ensembl: ENSG00000135298 |
| Other names | BAI3 |
| Summary | This p53-target gene encodes a brain-specific angiogenesis inhibitor, a seven-span transmembrane protein, and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities, and may also play a role in angiogenesis. [provided by RefSeq, Jul 2008] |
| Individual ID | 29217584.06 (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; |