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: 3773
MIM: 605722
HGNC: 6262
Ensembl: ENSG00000153822
Variants:
dbSNP: 3773
ClinVar: 3773
TCGA: ENSG00000153822
COSMIC: KCNJ16
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35809813 | 2022 | lncRNA XIST is associated with preeclampsia and mediates trophoblast cell invasion via miR-340-5p/KCNJ16 signaling pathway. | 8 |
| 35848616 | 2022 | Kir5.1 channels: potential role in epilepsy and seizure disorders. | 6 |
| 35809813 | 2022 | lncRNA XIST is associated with preeclampsia and mediates trophoblast cell invasion via miR-340-5p/KCNJ16 signaling pathway. | 8 |
| 35848616 | 2022 | Kir5.1 channels: potential role in epilepsy and seizure disorders. | 6 |
| 33811157 | 2021 | Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness. | 31 |
| 33811157 | 2021 | Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness. | 31 |
| 28577853 | 2017 | Loss of transcriptional activation of the potassium channel Kir5.1 by HNF1β drives autosomal dominant tubulointerstitial kidney disease. | 23 |
| 28577853 | 2017 | Loss of transcriptional activation of the potassium channel Kir5.1 by HNF1β drives autosomal dominant tubulointerstitial kidney disease. | 23 |
| 26663529 | 2016 | Variability in a three-generation family with Pierre Robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16. | 3 |
| 27599582 | 2016 | Elucidation of the molecular mechanisms of anaplastic thyroid carcinoma by integrated miRNA and mRNA analysis. | 9 |
| 26663529 | 2016 | Variability in a three-generation family with Pierre Robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16. | 3 |
| 27599582 | 2016 | Elucidation of the molecular mechanisms of anaplastic thyroid carcinoma by integrated miRNA and mRNA analysis. | 9 |
| 25339316 | 2014 | Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome. | 27 |
| 25339316 | 2014 | Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome. | 27 |
| 24193250 | 2013 | KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16. | 21 |
Citation
Dessen P
KCNJ16 (potassium inwardly rectifying channel subfamily J member 16)
Atlas Genet Cytogenet Oncol Haematol. 2017-04-01
Online version: http://atlasgeneticsoncology.org/gene/56740/kcnj16-(potassium-inwardly-rectifying-channel-subfamily-j-member-16)
