Symbol
| TRDN
| contributors: mct/npt - updated : 09-05-2017
|
HGNC name
| triadin
|
HGNC id
| 12261
|
corresponding disease(s)
|
CPVT5
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
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constitutional
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displayed extensive T-wave inversions in precordial leads V1 through V4, with either persistent or transient QT prolongation and severe disease expression of exercise-induced cardiac arrest in early childhood | |
Variant & Polymorphism
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Candidate gene
Marker
Therapy target
| | | |
| triadin KO mouse presents objective muscle dysfunctions and is, therefore, undoubtedly suffering from myopathy as identical energy consumption produced a reduced strength (Oddoux 2009) |