Identity
HGNC
LOCATION
4p13
LOCUSID
ALIAS
DFNB25,PPP1R88
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 389207
MIM: 613283
HGNC: 31673
Ensembl: ENSG00000215203
Variants:
dbSNP: 389207
ClinVar: 389207
TCGA: ENSG00000215203
COSMIC: GRXCR1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000215203 | ENST00000399770 | A8MXD5 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 25802247 | 2015 | Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. | 6 |
| 25802247 | 2015 | Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. | 6 |
| 20137778 | 2010 | Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. | 33 |
| 20137778 | 2010 | Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. | 33 |
Citation
Dessen P
GRXCR1 (glutaredoxin and cysteine rich domain containing 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64063/chromosome-explorer/new-content/
