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: 2232
MIM: 103270
HGNC: 3642
Ensembl: ENSG00000161513
Variants:
dbSNP: 2232
ClinVar: 2232
TCGA: ENSG00000161513
COSMIC: FDXR
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36480042 | 2023 | Four Genes Predictive for the Severity of Hematological Damage Reveal a Similar Response after X Irradiation and Chemotherapy. | 0 |
| 37046037 | 2023 | FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy. | 0 |
| 37107710 | 2023 | FDXR-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. | 0 |
| 37481223 | 2023 | FDXR-associated disease in a Chinese cohort: Unraveling expanded ocular phenotypes and genetic spectrum. | 0 |
| 36480042 | 2023 | Four Genes Predictive for the Severity of Hematological Damage Reveal a Similar Response after X Irradiation and Chemotherapy. | 0 |
| 37046037 | 2023 | FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy. | 0 |
| 37107710 | 2023 | FDXR-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. | 0 |
| 37481223 | 2023 | FDXR-associated disease in a Chinese cohort: Unraveling expanded ocular phenotypes and genetic spectrum. | 0 |
| 34979083 | 2022 | Characterization of a Cleavable Fusion of Human CYP24A1 with Adrenodoxin Reveals the Variable Role of Hydrophobics in Redox Partner Binding. | 2 |
| 34979083 | 2022 | Characterization of a Cleavable Fusion of Human CYP24A1 with Adrenodoxin Reveals the Variable Role of Hydrophobics in Redox Partner Binding. | 2 |
| 33271253 | 2021 | Substrate-induced modulation of protein-protein interactions within human mitochondrial cytochrome P450-dependent system. | 7 |
| 33348459 | 2021 | Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significance. | 7 |
| 33938912 | 2021 | Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature. | 5 |
| 33271253 | 2021 | Substrate-induced modulation of protein-protein interactions within human mitochondrial cytochrome P450-dependent system. | 7 |
| 33348459 | 2021 | Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significance. | 7 |
Citation
Dessen P
FDXR (ferredoxin reductase)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/46873/fdxr
