LMOD3

LMOD3
Identifiers
Aliases	LMOD3, NEM10, leiomodin 3
External IDs	OMIM: 616112 MGI: 2444169 HomoloGene: 28097 GeneCards: LMOD3
Gene location (Human)
Chr.	Chromosome 3 (human)[1]
End	69,123,032 bp[1]
Gene location (Mouse)
Chr.	Chromosome 6 (mouse)[2]
End	97,252,759 bp[2]
RNA expression pattern
	; ;
	More reference expression data
Gene ontology
Molecular function	• actin monomer binding; • tropomyosin binding;
Cellular component	• cytoskeleton; • A band; • cytoplasm; • striated muscle thin filament; • M band; • myofibril;
Biological process	• pointed-end actin filament capping; • skeletal muscle fiber development; • muscle contraction; • actin filament organization; • myofibril assembly; • striated muscle contraction; • skeletal muscle thin filament assembly; • actin nucleation; • positive regulation of skeletal muscle fiber development;
	Sources:Amigo / QuickGO
Orthologs
	56203
	320502
	ENSG00000163380
	ENSMUSG00000044086
	Q0VAK6
	E9QA62
	NM_198271; NM_001304418
	NM_001081157
	NP_001291347; NP_938012
	NP_001074626
	Wikidata
View/Edit Human	View/Edit Mouse

Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene.[5][6]

Clinical significance

Dysfunction is associated with thin filament disorganisation and nemaline myopathy.[7]

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References

GRCh38: Ensembl release 89: ENSG00000163380 - Ensembl, May 2017
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.

Lane HY, Liu YC, Huang CL, Chang YC, Wu PL, Lu CT, Chang WH (April 2006). "Risperidone-related weight gain: genetic and nongenetic predictors". Journal of Clinical Psychopharmacology. 26 (2): 128–34. doi:10.1097/01.jcp.0000203196.65710.2b. PMID 16633140.
Mehrle A, Rosenfelder H, Schupp I, del Val C, Arlt D, Hahne F, Bechtel S, Simpson J, Hofmann O, Hide W, Glatting KH, Huber W, Pepperkok R, Poustka A, Wiemann S (January 2006). "The LIFEdb database in 2006". Nucleic Acids Research. 34 (Database issue): D415-8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
Wiemann S, Arlt D, Huber W, Wellenreuther R, Schleeger S, Mehrle A, Bechtel S, Sauermann M, Korf U, Pepperkok R, Sültmann H, Poustka A (October 2004). "From ORFeome to biology: a functional genomics pipeline". Genome Research. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
Simpson JC, Wellenreuther R, Poustka A, Pepperkok R, Wiemann S (September 2000). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Reports. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Böcher M, Blöcker H, Bauersachs S, Blum H, Lauber J, Düsterhöft A, Beyer A, Köhrer K, Strack N, Mewes HW, Ottenwälder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (March 2001). "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. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
Hartley JL, Temple GF, Brasch MA (November 2000). "DNA cloning using in vitro site-specific recombination". Genome Research. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000163380 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000044086 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: LMOD3 leiomodin 3 (fetal)".

[pmid25788699-6] 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.

[pmid25250574-7] 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.

LMOD3

Clinical significance

References

Further reading