Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol TNNT1 contributors: mct - updated : 03-04-2018
HGNC name troponin T type 1 (skeletal, slow)
HGNC id 11948
EXPRESSION
Type widely
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Cardiovascularheart   highly
Digestivemouth   highly
Endocrinepancreas    
Nervousbrain    
Reproductivemale systemprostate   
Urinarykidney    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Epithelialsecretoryglandularexocrine 
Muscularstriatumskeletal highly Homo sapiensAdult
Muscularstriatumcardiac highly Homo sapiens
Muscularstriatumskeletal   Homo sapiensFetal
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
conjugated PhosphoP
HOMOLOGY
interspecies ortholog to murine Tnnt1
homolog to C.elegans C05D11.13
Homologene
FAMILY
  • troponin T family
  • CATEGORY motor/contractile , regulatory , structural protein
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,cytosolic
    basic FUNCTION
  • involved in the attachment of the complex to tropomyosin and troponin I
  • regulating muscle contraction
  • sarcomeric thin filament anchoring subunit of the troponin complex in striated muscles
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS development
    text muscle development
    PATHWAY
    metabolism
    signaling
    a component
  • constituent of the troponin complex forming the calcium-sensitive molecular switch that regulates striated muscle contraction in response to modifications in intracellular concentration
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
  • binding to TPM3 and ACTA1
  • cardiac expression of TNNT1 strictly depends on the physical interaction between GATA4-ZFPM2 in the myocardium of both atria and ventricles
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) NEM5
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
  • marker for cardiac remodeling in hypertrophic cardiomyopathy
  • Therapy target
    ANIMAL & CELL MODELS