Variant ID | 7755 |
---|---|
Entrez Gene ID | 84059 |
Gene | ADGRV1 (GeneCards) |
Location | hg19 5:89907206-89907206
hg38 5:90611389-90611389 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000005.9:g.89907206 A>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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | 0.0143 |
CADD Raw score (version 1.3) | -0.168124 (Deleterious) |
FATHMM raw prediction score | 0.09626 (Tolerated) |
Deleterious probability by DeFine | 0.4117 (Neutral) |
Entrez Gene ID | 84059 (NCBI Gene) |
---|---|
Official Gene Symbol | ADGRV1 (GeneCards) |
Number of variants in ADGRV1 in this database | 6 (view all the variants) |
Full name | adhesion G protein-coupled receptor V1 |
Band | 5q14.3 |
Other IDs | Vega: OTTHUMG00000162668 OMIM: 602851 HGNC: HGNC:17416 Ensembl: ENSG00000164199 |
Other names | FEB4, GPR98, MASS1, USH2B, USH2C, VLGR1, VLGR1b |
Summary | This gene encodes a member of the G-protein coupled receptor superfamily. The encoded protein contains a 7-transmembrane receptor domain, binds calcium and is expressed in the central nervous system. Mutations in this gene are associated with Usher syndrome 2 and familial febrile seizures. Several alternatively spliced transcripts have been described. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.07 (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; |