Varaico: Literature-Extracted Genetic Variants

Gene:DNM2
Variant:p.D614N
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DNM2

NM_001005361.3:p.D614N

Associated Papers

A novel DNM2 variant associated with centronuclear myopathy: a case report.

Rimoldi M et al.

Frontiers in Genetics, 2025

40259930 (PubMed )
Supplement: DataSheet1.pdf

Effect of Pathogenic Mutations on the Formation of High-Order Dynamin 2 Assemblies in Living Cells.

Hedde PN et al.

Biochemistry, 2024

[The dynamin-2-gene related centronuclear myopathy].

Bitoun M

Medecine Sciences : M/s, 2023

Dynamins in human diseases: differential requirement of dynamin activity in distinct tissues.

Laiman J et al.

Current Opinion in Cell Biology, 2023

Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands.

Reumers SFI et al.

Clinical Genetics, 2021

Progression or Not - A Small Natural History Study of Genetical Confirmed Congenital Myopathies.

Werlauff U et al.

Journal of Neuromuscular Diseases, 2021

Dynamin 2 (DNM2) as Cause of, and Modifier for, Human Neuromuscular Disease.

Zhao M et al.

Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics, 2018

Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2.

Hohendahl A et al.

Journal of Structural Biology, 2016

Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2.

Sambuughin N et al.

Bmc Neurology, 2015

Myosin VI localization and expression in striated muscle pathology.

Karolczak J et al.

Anatomical Record (hoboken, N.j. : 2007), 2014

A mutation associated with centronuclear myopathy enhances the size and stability of dynamin 2 complexes in cells.

James NG et al.

Biochimica Et Biophysica Acta, 2014

Dynamin-2 in nervous system disorders.

González-Jamett AM et al.

Journal of Neurochemistry, 2014

Dynamin-2 function and dysfunction along the secretory pathway.

González-Jamett AM et al.

Frontiers in Endocrinology, 2013

A novel mutation in the DNM2 gene impairs dynamin 2 localization in skeletal muscle of a patient with late onset centronuclear myopathy.

Kierdaszuk B et al.

Neuromuscular Disorders : Nmd, 2013

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."