Entity Details

Primary name TRDN_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ13061
EntryNameTRDN_HUMAN
FullNameTriadin
TaxID9606
Evidenceevidence at protein level
Length729
SequenceStatuscomplete
DateCreated2000-05-30
DateModified2021-06-02

Ontological Relatives

GenesTRDN

GO terms

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GOName
GO:0005102 signaling receptor binding
GO:0005783 endoplasmic reticulum
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0006874 cellular calcium ion homeostasis
GO:0006936 muscle contraction
GO:0009617 response to bacterium
GO:0010649 regulation of cell communication by electrical coupling
GO:0010880 regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
GO:0014701 junctional sarcoplasmic reticulum membrane
GO:0014808 release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
GO:0016021 integral component of membrane
GO:0016529 sarcoplasmic reticulum
GO:0030314 junctional membrane complex
GO:0030674 protein-macromolecule adaptor activity
GO:0031122 cytoplasmic microtubule organization
GO:0033017 sarcoplasmic reticulum membrane
GO:0033018 sarcoplasmic reticulum lumen
GO:0034220 ion transmembrane transport
GO:0044325 transmembrane transporter binding
GO:0051279 regulation of release of sequestered calcium ion into cytosol
GO:0060047 heart contraction
GO:0060315 negative regulation of ryanodine-sensitive calcium-release channel activity
GO:0060316 positive regulation of ryanodine-sensitive calcium-release channel activity
GO:0086036 regulation of cardiac muscle cell membrane potential
GO:0090158 endoplasmic reticulum membrane organization
GO:1901846 positive regulation of cell communication by electrical coupling involved in cardiac conduction
GO:1903779 regulation of cardiac conduction

Subcellular Location

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Subcellular Location
Cell membrane
Sarcoplasmic reticulum membrane

Domains

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DomainNameCategoryType
IPR007943 Aspartyl beta-hydroxylase/Triadin domainDomainDomain
IPR010798 TriadinFamilyFamily

Diseases

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Disease IDSourceNameDescription
615441 OMIMVentricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness (CPVT5)An arrhythmogenic disorder characterized by stress-induced, bidirectional ventricular tachycardia that may degenerate into cardiac arrest and cause sudden death. Patients present with recurrent syncope, or sudden death after physical activity or emotional stress. Some patients have muscle weakness. CPVT5 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.