Variant ID | 7202 |
---|---|
Entrez Gene ID | 389207 |
Gene | GRXCR1 (GeneCards) |
Location | hg19 4:43183609-43183609
hg38 4:43181592-43181592 |
Disease | Cockayne syndrome (view all the variants in this disease) |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000004.11:g.43183609 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 | 191154276 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | -0.2091 |
CADD Raw score (version 1.3) | -0.034622 (Deleterious) |
FATHMM raw prediction score | 0.09987 (Tolerated) |
Deleterious probability by DeFine | 0.3385 (Neutral) |
Entrez Gene ID | 389207 (NCBI Gene) |
---|---|
Official Gene Symbol | GRXCR1 (GeneCards) |
Number of variants in GRXCR1 in this database | 15 (view all the variants) |
Full name | glutaredoxin and cysteine rich domain containing 1 |
Band | 4p13 |
Other IDs | Vega: OTTHUMG00000160434 OMIM: 613283 HGNC: HGNC:31673 Ensembl: ENSG00000215203 |
Other names | DFNB25, PPP1R88 |
Summary | This gene is one of 60 loci associated with autosomal-recessive nonsyndromic hearing impairment. This gene encodes a protein which contains GRX-like domains; these domains play a role in the S-glutathionylation of proteins and may be involved in actin organization in hair cells. [provided by RefSeq, Sep 2010] |
Individual ID | 29217584.19 (view all the variants in this individual) |
---|---|
Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Cockayne syndrome (view all the variants in this disease) |
OMIM ID | 216400 |
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; |