Tropomyosin 3

Identifiers Symbols TPM3; CFTD; NEM1; OK/SW-cl.5; TM-5; TM3; TM30; TM30nm; TM5; TPMsk3; TRK; hTM5; hscp30 External IDs OMIM: 191030 HomoloGene: 81889 GeneCards: TPM3 Gene

Gene Ontology
Molecular function molecular_function
actin binding
Cellular component stress fiber
cytoplasm
cytosol
cytoskeleton
muscle thin filament tropomyosin
actin cytoskeleton
Biological process cellular component movement
muscle contraction
regulation of muscle contraction
muscle filament sliding
Sources: Amigo / QuickGO
Orthologs Species Human Mouse Entrez 7170 59069 Ensembl ENSG00000143549 ENSMUSG00000027940 UniProt P06753 P21107 RefSeq (mRNA) NM_001043351 NM_001253738 RefSeq (protein) NP_001036816 NP_001240667 Location (UCSC) Chr 1:
154.13 – 154.17 Mb Chr 3:
90.07 – 90.1 Mb PubMed search

Tropomyosin alpha-3 chain is a protein that in humans is encoded by the TPM3 gene.

This gene encodes a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosins are dimers of coiled-coil proteins that polymerize end-to-end along the major groove in most actin filaments. They provide stability to the filaments and regulate access of other actin-binding proteins. In muscle cells, they regulate muscle contraction by controlling the binding of myosin heads to the actin filament. Mutations in this gene result in autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this locus are associated with cancer. Multiple transcript variants encoding different isoforms have been found for this gene.