Open Access Articles- Top Results for DNM2


External IDsOMIM602378 MGI109547 HomoloGene90883 ChEMBL: 5812 GeneCards: DNM2 Gene
EC number3.6.5.5
RefSeq (mRNA)NM_001005360NM_001039520
RefSeq (protein)NP_001005360NP_001034609
Location (UCSC)Chr 19:
10.72 – 10.83 Mb
Chr 9:
21.42 – 21.51 Mb
PubMed search[1][2]

Dynamin-2 is a protein that in humans is encoded by the DNM2 gene.[1][2]


Dynamins represent one of the subfamilies of GTP-binding proteins. These proteins share considerable sequence similarity over the N-terminal portion of the molecule, which contains the GTPase domain. Dynamins are associated with microtubules. They have been implicated in cell processes such as endocytosis and cell motility, and in alterations of the membrane that accompany certain activities such as bone resorption by osteoclasts. Dynamins bind many proteins that bind actin and other cytoskeletal proteins. Dynamins can also self-assemble, a process that stimulates GTPase activity. Four alternatively spliced transcripts encoding different proteins have been described. Additional alternatively spliced transcripts may exist, but their full-length nature has not been determined.[3]


DNM2 has been shown to interact with:

Clinical relevance

Mutations in this gene have been associated to cases of acute lymphoblastic leukaemia,[6] or congenital myopathy (centronuclear type).[7]


  1. ^ Diatloff-Zito C, Gordon AJ, Duchaud E, Merlin G (Nov 1995). "Isolation of an ubiquitously expressed cDNA encoding human dynamin II, a member of the large GTP-binding protein family". Gene 163 (2): 301–6. PMID 7590285. doi:10.1016/0378-1119(95)00275-B. 
  2. ^ Klocke R, Augustin A, Ronsiek M, Stief A, van der Putten H, Jockusch H (Jul 1997). "Dynamin genes Dnm1 and Dnm2 are located on proximal mouse chromosomes 2 and 9, respectively". Genomics 41 (2): 290–2. PMID 9143510. doi:10.1006/geno.1997.4634. 
  3. ^ "Entrez Gene: DNM2 dynamin 2". 
  4. ^ a b Okamoto PM, Gamby C, Wells D, Fallon J, Vallee RB (Dec 2001). "Dynamin isoform-specific interaction with the shank/ProSAP scaffolding proteins of the postsynaptic density and actin cytoskeleton". J. Biol. Chem. 276 (51): 48458–65. PMC 2715172. PMID 11583995. doi:10.1074/jbc.M104927200. 
  5. ^ Lundmark R, Carlsson SR (Nov 2003). "Sorting nexin 9 participates in clathrin-mediated endocytosis through interactions with the core components". J. Biol. Chem. 278 (47): 46772–81. PMID 12952949. doi:10.1074/jbc.M307334200. 
  6. ^ Zhang J, Ding L, Holmfeldt L, Wu G, Heatley SL, Payne-Turner D, Easton J, Chen X, Wang J, Rusch M, Lu C, Chen SC, Wei L, Collins-Underwood JR, Ma J, Roberts KG, Pounds SB, Ulyanov A, Becksfort J, Gupta P, Huether R, Kriwacki RW, Parker M, McGoldrick DJ, Zhao D, Alford D, Espy S, Bobba KC, Song G, Pei D, Cheng C, Roberts S, Barbato MI, Campana D, Coustan-Smith E, Shurtleff SA, Raimondi SC, Kleppe M, Cools J, Shimano KA, Hermiston ML, Doulatov S, Eppert K, Laurenti E, Notta F, Dick JE, Basso G, Hunger SP, Loh ML, Devidas M, Wood B, Winter S, Dunsmore KP, Fulton RS, Fulton LL, Hong X, Harris CC, Dooling DJ, Ochoa K, Johnson KJ, Obenauer JC, Evans WE, Pui CH, Naeve CW, Ley TJ, Mardis ER, Wilson RK, Downing JR, Mullighan CG (2012). "The genetic basis of early T-cell precursor acute lymphoblastic leukaemia". Nature 481 (7380): 157–63. PMC 3267575. PMID 22237106. doi:10.1038/nature10725. 
  7. ^ Jungbluth,, H. "Pathogenic mechanisms in centronuclear myopathies.". Front Aging Neurosci. PMID 25566070. doi:10.3389/fnagi.2014.00339. 

Further reading


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