Gene: LOC105377982

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

Gene: TRDN

Alternate names for this Gene: CPVT5|TDN|TRISK

Gene Summary: This gene encodes an integral membrane protein that contains a single transmembrane domain. As similar protein in rabbits plays a role in skeletal muscle excitation-contraction coupling as part of the calcium release complex in association with the ryanodine receptor. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and single nucleotide polymorphisms in this gene may be markers for IgA nephritis.

Gene is located in Chromosome: 6

Location in Chromosome : 6q22.31

Description of this Gene: triadin

Type of Gene: protein-coding

rs11154178 in LOC105377982;TRDN gene and Diabetes Mellitus, Insulin-Dependent PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs11154178 in LOC105377982;TRDN gene and Diabetes Mellitus, Non-Insulin-Dependent PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs11154178 in LOC105377982;TRDN gene and Diabetic Foot PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs11154178 in LOC105377982;TRDN gene and Hereditary and idiopathic neuropathy, unspecified PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs11154178 in LOC105377982;TRDN gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs11154178 in LOC105377982;TRDN gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 3 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs11154178 in LOC105377982;TRDN gene and Neuropathy PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs768049331 in LOC105377982;TRDN gene and VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) PMID 25922419 2015 Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.

PMID 22422768 2012 Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.

rs397515459 in LOC105377982;TRDN gene and VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS PMID 22422768 2012 Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.