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: 643226
MIM: 615762
HGNC: 33862
Ensembl: ENSG00000204928
Variants:
dbSNP: 643226
ClinVar: 643226
TCGA: ENSG00000204928
COSMIC: GRXCR2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000204928 | ENST00000377976 | A6NFK2 |
| ENSG00000204928 | ENST00000639411 | A0A1W2PQQ7 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33528103 | 2021 | Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon. | 6 |
| 33528103 | 2021 | Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon. | 6 |
| 30157177 | 2018 | Grxcr2 is required for stereocilia morphogenesis in the cochlea. | 10 |
| 30157177 | 2018 | Grxcr2 is required for stereocilia morphogenesis in the cochlea. | 10 |
| 24619944 | 2014 | A frameshift mutation in GRXCR2 causes recessively inherited hearing loss. | 25 |
| 24619944 | 2014 | A frameshift mutation in GRXCR2 causes recessively inherited hearing loss. | 25 |
Citation
Dessen P
GRXCR2 (glutaredoxin and cysteine rich domain containing 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64064/grxcr2-(glutaredoxin-and-cysteine-rich-domain-containing-2)
