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Protein-coding gene in humans
Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene .[ 5] [ 6] [ 7]
Clinical significance [ edit ] Dysfunction is associated with thin filament disorganisation and nemaline myopathy .[ 8]
^ a b c GRCh38: Ensembl release 89: ENSG00000163380 – Ensembl , May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000044086 – Ensembl , May 2017^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Entrez Gene: LMOD3 leiomodin 3 (fetal)" .^ Gunning PW, Ghoshdastider U, Whitaker S, Popp D, Robinson RC (June 2015). "The evolution of compositionally and functionally distinct actin filaments" . Journal of Cell Science . 128 (11): 2009–19. doi :10.1242/jcs.165563 PMID 25788699 . ^ ^ Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, et al. (November 2014). "Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy" . The Journal of Clinical Investigation . 124 (11): 4693–708. doi :10.1172/JCI75199 . PMC 4347224 PMID 25250574 .
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