Biology:LMOD3
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Short description: Protein-coding gene in humans
 Generic protein structure example |
Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene.[1][2]
Clinical significance
Dysfunction is associated with thin filament disorganisation and nemaline myopathy.[3]
References
- ↑ "Entrez Gene: LMOD3 leiomodin 3 (fetal)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=56203.
- ↑ "The evolution of compositionally and functionally distinct actin filaments". Journal of Cell Science 128 (11): 2009–19. June 2015. doi:10.1242/jcs.165563. PMID 25788699.
- ↑ "Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy". The Journal of Clinical Investigation 124 (11): 4693–708. November 2014. doi:10.1172/JCI75199. PMID 25250574.
Further reading
- "Risperidone-related weight gain: genetic and nongenetic predictors". Journal of Clinical Psychopharmacology 26 (2): 128–34. April 2006. doi:10.1097/01.jcp.0000203196.65710.2b. PMID 16633140.
- "The LIFEdb database in 2006". Nucleic Acids Research 34 (Database issue): D415-8. January 2006. doi:10.1093/nar/gkj139. PMID 16381901.
- "From ORFeome to biology: a functional genomics pipeline". Genome Research 14 (10B): 2136–44. October 2004. doi:10.1101/gr.2576704. PMID 15489336.
- "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Reports 1 (3): 287–92. September 2000. doi:10.1093/embo-reports/kvd058. PMID 11256614.
- "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Research 11 (3): 422–35. March 2001. doi:10.1101/gr.GR1547R. PMID 11230166.
- "DNA cloning using in vitro site-specific recombination". Genome Research 10 (11): 1788–95. November 2000. doi:10.1101/gr.143000. PMID 11076863.
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