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TPM3

Tropomyosin 3

TPM3 is a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants.

Gene Name: Tropomyosin 3
Synonyms: TPM3, CFTD, Cytoskeletal tropomyosin TM30, Gamma-tropomyosin, NEM1, Hscp30, TM30nm, Tropomyosin alpha-3 chain, TM-5, TM5, TPMsk3, Tropomyosin 3, Tropomyosin-5, TM3, TM30, TRK, Tropomyosin-3, HTM5, OK/SW-cl.5, Tropomyosin gamma
Target Sequences: NM_152263 NP_689476.2 P06753

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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).