======= TPM3 ======= == Gene Information == * **Official Symbol**: TPM3 * **Official Name**: tropomyosin 3 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=7170|7170]] * **UniProt**: [[https://www.uniprot.org/uniprot/P06753|P06753]] * **Interactions**: [[https://thebiogrid.org/search.php?search=TPM3&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20TPM3|Open PubMed]] * **OMIM**: [[https://omim.org/entry/191030|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes 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. [provided by RefSeq, May 2013]. * **UniProt Summary**: N/A |Tropomyosin| |Tropomyosin 1| |Laminin II| |muscle thin filament tropomyosin| |muscle filament sliding| |actin-myosin filament sliding| |stress fiber| |actin filament| |actin-mediated cell contraction| |actin filament-based movement| |actin filament binding| |actin cytoskeleton| |actin filament organization| |muscle contraction| |muscle system process| |cytoskeleton| |supramolecular fiber organization| |actin cytoskeleton organization| |actin filament-based process| |molecular function| |cytoskeleton organization| |movement of cell or subcellular component| |system process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp375|Lenalidomide 20μM R07 exp375]]|-2.06| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 11318 * **Expression level (log2 read counts)**: 8.08 {{:chemogenomics:nalm6 dist.png?nolink |}}