Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
A class of dynamin-like GTPases involved in the generation of the tubular ER network.
|
19665976 |
2009 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis.
|
12509422 |
2003 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome.
|
23092955 |
2013 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I.
|
21926968 |
2011 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Multiple forms of dynamin are encoded by shibire, a Drosophila gene involved in endocytosis.
|
1828536 |
1991 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Predominant and developmentally regulated expression of dynamin in neurons.
|
1832879 |
1991 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
A selective activity-dependent requirement for dynamin 1 in synaptic vesicle endocytosis.
|
17463283 |
2007 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Recruitment of endophilin to clathrin-coated pit necks is required for efficient vesicle uncoating after fission.
|
22099461 |
2011 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding.
|
7877694 |
1995 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Dynamin-like protein encoded by the Drosophila shibire gene associated with vesicular traffic.
|
1674590 |
1991 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
DNM1 encephalopathy: A new disease of vesicle fission.
|
28667181 |
2017 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Dynamin GTPase domain mutants block endocytic vesicle formation at morphologically distinct stages.
|
11553700 |
2001 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Cell- and stimulus-dependent heterogeneity of synaptic vesicle endocytic recycling mechanisms revealed by studies of dynamin 1-null neurons.
|
18250322 |
2008 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.
|
21441247 |
2011 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis.
|
12509422 |
2003 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
The crystal structure of dynamin.
|
21927001 |
2011 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice.
|
20700442 |
2010 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin.
|
19633650 |
2009 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
A selective activity-dependent requirement for dynamin 1 in synaptic vesicle endocytosis.
|
17463283 |
2007 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
A lethal defect of mitochondrial and peroxisomal fission.
|
17460227 |
2007 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Multiple forms of dynamin are encoded by shibire, a Drosophila gene involved in endocytosis.
|
1828536 |
1991 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice.
|
11879655 |
2002 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
|
15731758 |
2005 |
Entrez Id: |
1759 |
Gene Symbol: |
DNM1 |
DNM1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Dynamin GTPase domain mutants block endocytic vesicle formation at morphologically distinct stages.
|
11553700 |
2001 |