Variant ID | 7454 |
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Entrez Gene ID | 389207 |
Gene | GRXCR1 (GeneCards) |
Location | hg19 4:43025744-43025744
hg38 4:43023727-43023727 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000004.11:g.43025744 C>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 |
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EIGEN score | -0.1729 |
CADD Raw score (version 1.3) | 0.147886 (Deleterious) |
FATHMM raw prediction score | 0.10985 (Tolerated) |
Deleterious probability by DeFine | 0.3065 (Neutral) |
Entrez Gene ID | 389207 (NCBI Gene) |
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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 | 29217584.24 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
OMIM ID | 278700 |
Pubmed ID | 29217584 |
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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; |