Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding. 7877694

1995

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy. 14985377

2004

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Predominant and developmentally regulated expression of dynamin in neurons. 1832879

1991

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Multiple forms of dynamin are encoded by shibire, a Drosophila gene involved in endocytosis. 1828536

1991

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Cell- and stimulus-dependent heterogeneity of synaptic vesicle endocytic recycling mechanisms revealed by studies of dynamin 1-null neurons. 18250322

2008

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Mitochondrial fusion and fission in cell life and death. 21102612

2010

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR A novel member of the dynamin family of GTP-binding proteins is expressed specifically in the testis. 8360266

1993

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Recruitment of endophilin to clathrin-coated pit necks is required for efficient vesicle uncoating after fission. 22099461

2011

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Dominant-negative inhibition of receptor-mediated endocytosis by a dynamin-1 mutant with a defective pleckstrin homology domain. 10074457

1999

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Dynamin GTPase domain mutants block endocytic vesicle formation at morphologically distinct stages. 11553700

2001

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR De novo DNM1 mutations in two cases of epileptic encephalopathy. 26611353

2016

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice. 11879655

2002

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR A lethal defect of mitochondrial and peroxisomal fission. 17460227

2007

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR A selective activity-dependent requirement for dynamin 1 in synaptic vesicle endocytosis. 17463283

2007

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion. 26648591

2016

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Possible temperature-dependent blockage of synaptic vesicle recycling induced by a single gene mutation in Drosophila. 6304244

1983

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function. 21441247

2011

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice. 20700442

2010

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin. 19633650

2009

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR DNM1 encephalopathy: A new disease of vesicle fission. 28667181

2017

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Large-scale discovery of novel genetic causes of developmental disorders. 25533962

2015

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Induction of mutant dynamin specifically blocks endocytic coated vesicle formation. 7962076

1994

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C. elegans. 9294229

1997

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy. 19502294

2009

dbSNP: rs1554767317
rs1554767317
A 0.700 GeneticVariation CLINVAR Building a fission machine--structural insights into dynamin assembly and activation. 23781021

2013