Identity
HGNC
LOCATION
6q22.31
LOCUSID
ALIAS
CPVT5,TDN,TRISK
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: 10345
MIM: 603283
HGNC: 12261
Ensembl: ENSG00000186439
Variants:
dbSNP: 10345
ClinVar: 10345
TCGA: ENSG00000186439
COSMIC: TRDN
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37163978 | 2023 | Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes. | 2 |
| 37163978 | 2023 | Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes. | 2 |
| 35862102 | 2022 | Cardiomyocyte-Specific Long Noncoding RNA Regulates Alternative Splicing of the Triadin Gene in the Heart. | 9 |
| 35862102 | 2022 | Cardiomyocyte-Specific Long Noncoding RNA Regulates Alternative Splicing of the Triadin Gene in the Heart. | 9 |
| 34415104 | 2021 | Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome. | 5 |
| 34736417 | 2021 | Association of decreased triadin expression level with apoptosis of dopaminergic cells in Parkinson's disease mouse model. | 0 |
| 34415104 | 2021 | Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome. | 5 |
| 34736417 | 2021 | Association of decreased triadin expression level with apoptosis of dopaminergic cells in Parkinson's disease mouse model. | 0 |
| 31437535 | 2020 | A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia. | 6 |
| 31437535 | 2020 | A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia. | 6 |
| 29126880 | 2018 | A heart-enriched antisense long non-coding RNA regulates the balance between cardiac and skeletal muscle triadin. | 8 |
| 29126880 | 2018 | A heart-enriched antisense long non-coding RNA regulates the balance between cardiac and skeletal muscle triadin. | 8 |
| 26768964 | 2016 | Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two Siblings. | 9 |
| 27562070 | 2016 | Triadin and CLIMP-63 form a link between triads and microtubules in muscle cells. | 20 |
| 26768964 | 2016 | Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two Siblings. | 9 |
Citation
Dessen P
TRDN (triadin)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/75128/trdn-(triadin)
