| Variant ID | 29699 |
|---|---|
| Entrez Gene ID | 26494 |
| Gene | OR8G1 (GeneCards) |
| Location | hg19 11:124120446-124120446
hg38 11:124249699-124249699 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| Method | MiSeq |
| Mutation(HGVS format) | NC_000011.9:g.124120446 A>C (Genome Assembly: hg19) |
| 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 | 135006516 |
| MAF in gnomAD genome (version 2.0.1) | 0 |
|---|---|
| CADD Raw score (version 1.3) | -1.382947 (Deleterious) |
| FATHMM raw prediction score | 0.16516 (Tolerated) |
| Deleterious probability by DeFine | 0.6561 (Deleterious) |
| Entrez Gene ID | 26494 (NCBI Gene) |
|---|---|
| Official Gene Symbol | OR8G1 (GeneCards) |
| Number of variants in OR8G1 in this database | 1 (view all the variants) |
| Full name | olfactory receptor family 8 subfamily G member 1 (gene/pseudogene) |
| Band | 11q24.2 |
| Other IDs | Vega: OTTHUMG00000189223 HGNC: HGNC:8484 Ensembl: ENSG00000197849 |
| Other names | OR8G1P, TPCR25, HSTPCR25 |
| Summary | Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. This family member represents a polymorphic pseudogene, whereby some individuals have a functional allele that encodes a full-length protein, while others have a non-functional allele due to the presence of an early stop codon and a 3' end deletion. [provided by RefSeq, Feb 2014] |
| Individual ID | 28714951.375 (view all the variants in this individual) |
|---|---|
| Pubmed ID | 28714951 |
| Whose mosaic mutation | Patient |
| Phenotype | 3 |
| Disease | Autism Spectrum Disorders (view all the variants in this disease) |
| OMIM ID | 209850 |
| Pubmed ID | 28714951 |
|---|---|
| Title | Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder |
| Journal | Nat Neurosci |
| Publication date | 2017.07 |
| Disease | Autism Spectrum Disorders |
| Incidence | 0.01 |
| Number of cases | cases of unknown sex: 376; |