Identity
HGNC
LOCATION
17p13.3
LOCUSID
ALIAS
NRX,RRS2,TRG-4
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: 64359
MIM: 612895
HGNC: 18008
Ensembl: ENSG00000167693
Variants:
dbSNP: 64359
ClinVar: 64359
TCGA: ENSG00000167693
COSMIC: NXN
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000167693 | ENST00000336868 | Q6DKJ4 |
| ENSG00000167693 | ENST00000537628 | A0A0C4DGI2 |
| ENSG00000167693 | ENST00000571684 | I3L4V6 |
| ENSG00000167693 | ENST00000575801 | Q6DKJ4 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35406633 | 2022 | NXN Gene Epigenetic Changes in an Adult Neurogenesis Model of Alzheimer's Disease. | 3 |
| 35927236 | 2022 | NXN suppresses metastasis of hepatocellular carcinoma by promoting degradation of Snail through binding to DUB3. | 2 |
| 35406633 | 2022 | NXN Gene Epigenetic Changes in an Adult Neurogenesis Model of Alzheimer's Disease. | 3 |
| 35927236 | 2022 | NXN suppresses metastasis of hepatocellular carcinoma by promoting degradation of Snail through binding to DUB3. | 2 |
| 33048444 | 2021 | Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. | 13 |
| 33048444 | 2021 | Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. | 13 |
| 21251912 | 2011 | An interaction between human Sec63 and nucleoredoxin may provide the missing link between the SEC63 gene and polycystic liver disease. | 11 |
| 21251912 | 2011 | An interaction between human Sec63 and nucleoredoxin may provide the missing link between the SEC63 gene and polycystic liver disease. | 11 |
| 19308021 | 2009 | Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort. | 34 |
| 19308021 | 2009 | Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort. | 34 |
| 17567240 | 2007 | Nucleoredoxin, a novel thioredoxin family member involved in cell growth and differentiation. | 43 |
| 17567240 | 2007 | Nucleoredoxin, a novel thioredoxin family member involved in cell growth and differentiation. | 43 |
Citation
Dessen P
NXN (nucleoredoxin)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/71064/nxn-(nucleoredoxin)
