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: 100134444
MIM: 613236
HGNC: 39080
Ensembl: ENSG00000260458
Variants:
dbSNP: 100134444
ClinVar: 100134444
TCGA: ENSG00000260458
COSMIC: KCNJ18
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000260458 | ENST00000567955 | B7U540 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 31361309 | 2019 | Contribution of Asian Haplotype of KCNJ18 to Susceptibility to and Ethnic Differences in Thyrotoxic Periodic Paralysis. | 5 |
| 31361309 | 2019 | Contribution of Asian Haplotype of KCNJ18 to Susceptibility to and Ethnic Differences in Thyrotoxic Periodic Paralysis. | 5 |
| 28131627 | 2017 | Down-regulation of Kir2.6 channel by c-termini mutation D252N and its association with the susceptibility to Thyrotoxic Periodic Paralysis. | 5 |
| 28131627 | 2017 | Down-regulation of Kir2.6 channel by c-termini mutation D252N and its association with the susceptibility to Thyrotoxic Periodic Paralysis. | 5 |
| 25882930 | 2016 | Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients. | 6 |
| 27178871 | 2016 | A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. | 3 |
| 25882930 | 2016 | Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients. | 6 |
| 27178871 | 2016 | A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. | 3 |
| 25885757 | 2015 | The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. | 5 |
| 25885757 | 2015 | The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. | 5 |
| 22910584 | 2012 | Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis. | 6 |
| 22910584 | 2012 | Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis. | 6 |
| 21209095 | 2011 | Kir2.6 regulates the surface expression of Kir2.x inward rectifier potassium channels. | 13 |
| 21665951 | 2011 | Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. | 25 |
| 21209095 | 2011 | Kir2.6 regulates the surface expression of Kir2.x inward rectifier potassium channels. | 13 |
Citation
Dessen P
KCNJ18 (potassium inwardly rectifying channel subfamily J member 18)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64790/kcnj18-(potassium-inwardly-rectifying-channel-subfamily-j-member-18)
