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Protein Coding Gene : Trdn triadin
Primary Identifier  MGI:1924007 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  76757
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable signaling receptor binding activity. Involved in heart contraction. Acts upstream of or within establishment of localization in cell; release of sequestered calcium ion into cytosol by sarcoplasmic reticulum; and response to bacterium. Predicted to be located in cytosol; nucleoplasm; and sarcoplasmic reticulum. Predicted to be part of calcium channel complex and junctional membrane complex. Predicted to be active in junctional sarcoplasmic reticulum membrane and plasma membrane. Is expressed in embryo and heart. Human ortholog(s) of this gene implicated in catecholaminergic polymorphic ventricular tachycardia and catecholaminergic polymorphic ventricular tachycardia 5. Orthologous to human TRDN (triadin).
PHENOTYPE: Mice homozygous for a null allele exhibit a loss of transverse orientation of triads within skeletal muscle cells. [provided by MGI curators]
  • synonyms:
  • triadin-2,
  • triadin 2,
  • 2310045H21Rik,
  • RIKEN cDNA 2310045H21 gene,
  • EG432451,
  • triadin 1,
  • triadin-3,
  • MGI:3646337,
  • triadin,
  • Trdn,
  • triadin 3,
  • triadin-1,
  • predicted gene, EG432451
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2 Involved In Mutations

Trail: ProteinCodingGene

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6 Pathways

Trail: ProteinCodingGene

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