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    TNNC1 troponin C1, slow skeletal and cardiac type [ Homo sapiens (human) ]

    Gene ID: 7134, updated on 2-Nov-2024

    Summary

    Official Symbol
    TNNC1provided by HGNC
    Official Full Name
    troponin C1, slow skeletal and cardiac typeprovided by HGNC
    Primary source
    HGNC:HGNC:11943
    See related
    Ensembl:ENSG00000114854 MIM:191040; AllianceGenome:HGNC:11943
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    TNC; TN-C; TNNC; CMD1Z; CMH13
    Summary
    Troponin is a central regulatory protein of striated muscle contraction, and together with tropomyosin, is located on the actin filament. Troponin consists of 3 subunits: TnI, which is the inhibitor of actomyosin ATPase; TnT, which contains the binding site for tropomyosin; and TnC, the protein encoded by this gene. The binding of calcium to TnC abolishes the inhibitory action of TnI, thus allowing the interaction of actin with myosin, the hydrolysis of ATP, and the generation of tension. Mutations in this gene are associated with cardiomyopathy dilated type 1Z. [provided by RefSeq, Oct 2008]
    Expression
    Restricted expression toward heart (RPKM 1964.8) See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See TNNC1 in Genome Data Viewer
    Location:
    3p21.1
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (52451100..52454041, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (52484001..52486942, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (52485116..52488057, complement)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:52443693-52444241 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14443 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19941 Neighboring gene PHD finger protein 7 Neighboring gene VISTA enhancer hs2179 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:52471583-52472088 Neighboring gene semaphorin 3G Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:52478216-52479092 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:52479093-52479969 Neighboring gene Sharpr-MPRA regulatory region 2927 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:52486099-52486919 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14444 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:52490599-52491274 Neighboring gene nischarin Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:52505250-52505750 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:52538009-52538514 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:52538515-52539020 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:52540387-52540986 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:52540987-52541588 Neighboring gene stabilin 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:52553072-52553680 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:52553681-52554287 Neighboring gene 5'-nucleotidase domain containing 2

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Dilated cardiomyopathy 1Z
    MedGen: C2678475 OMIM: 611879 GeneReviews: Not available
    Compare labs
    Hypertrophic cardiomyopathy 13
    MedGen: C2750472 OMIM: 613243 GeneReviews: Not available
    Compare labs

    EBI GWAS Catalog

    Description
    Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
    EBI GWAS Catalog
    Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.
    EBI GWAS Catalog

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    retropepsin gag-pol HIV-1 protease hydrolyzes troponin C at amino acid residues 101-102 PubMed

    Go to the HIV-1, Human Interaction Database

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables actin filament binding ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables calcium ion binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables calcium ion binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables calcium-dependent protein binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables calcium-dependent protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables protein homodimerization activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables troponin I binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables troponin I binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables troponin I binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables troponin T binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in cardiac muscle contraction IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cardiac muscle contraction IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in cardiac muscle contraction IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in diaphragm contraction IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in regulation of ATP-dependent activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in regulation of muscle contraction IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in regulation of muscle contraction TAS
    Traceable Author Statement
    more info
    PubMed 
    involved_in regulation of muscle filament sliding speed ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in response to metal ion IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in skeletal muscle contraction IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in transition between fast and slow fiber IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in ventricular cardiac muscle tissue morphogenesis IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    part_of cardiac Troponin complex IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of cardiac Troponin complex IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytosol TAS
    Traceable Author Statement
    more info
     
    part_of troponin complex IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    troponin C, slow skeletal and cardiac muscles
    Names
    cardiac troponin C
    slow twitch skeletal/cardiac muscle troponin C
    troponin C type 1 (slow)

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_008963.1 RefSeqGene

      Range
      5001..7951
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_378

    mRNA and Protein(s)

    1. NM_003280.3 → NP_003271.1  troponin C, slow skeletal and cardiac muscles

      See identical proteins and their annotated locations for NP_003271.1

      Status: REVIEWED

      Source sequence(s)
      AJ574625, X07897
      Consensus CDS
      CCDS2857.1
      UniProtKB/Swiss-Prot
      O14800, P02590, P04463, P63316
      UniProtKB/TrEMBL
      A0A024R2Z4, Q6FH91
      Related
      ENSP00000232975.3, ENST00000232975.8
      Conserved Domains (1) summary
      PTZ00184
      Location:9 → 157
      PTZ00184; calmodulin; Provisional

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

      Range
      52451100..52454041 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      52484001..52486942 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)