ENSG00000106976


Homo sapiens

Features
Gene ID: ENSG00000106976
  
Biological name :DNM1
  
Synonyms : DNM1 / dynamin 1 / Q05193
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 9
Strand: 1
Band: q34.11
Gene start: 128191655
Gene end: 128255248
  
Corresponding Affymetrix probe sets: 215116_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000486437
Ensembl peptide - ENSP00000420808
Ensembl peptide - ENSP00000486525
Ensembl peptide - ENSP00000490555
Ensembl peptide - ENSP00000490285
Ensembl peptide - ENSP00000489985
Ensembl peptide - ENSP00000489096
Ensembl peptide - ENSP00000487310
Ensembl peptide - ENSP00000486770
Ensembl peptide - ENSP00000345680
Ensembl peptide - ENSP00000362014
Ensembl peptide - ENSP00000377219
Ensembl peptide - ENSP00000419225
Ensembl peptide - ENSP00000420045
NCBI entrez gene - 1759     See in Manteia.
OMIM - 602377
RefSeq - XM_017014373
RefSeq - NM_001288737
RefSeq - NM_001288738
RefSeq - NM_001288739
RefSeq - NM_004408
RefSeq - XM_005251763
RefSeq - XM_005251768
RefSeq - XM_005251769
RefSeq - XM_006716992
RefSeq - XM_011518335
RefSeq - XM_011518336
RefSeq - XM_017014369
RefSeq - XM_017014370
RefSeq - XM_017014371
RefSeq - XM_017014372
RefSeq - NM_001005336
RefSeq Peptide - NP_001275666
RefSeq Peptide - NP_001275667
RefSeq Peptide - NP_001275668
RefSeq Peptide - NP_004399
RefSeq Peptide - NP_001005336
swissprot - A0A0D9SFE4
swissprot - H7C5U0
swissprot - Q05193
swissprot - A0A0D9SFB1
swissprot - A0A1B0GVK6
swissprot - A0A1B0GUX5
swissprot - A0A1B0GU67
swissprot - A0A0U1RQP1
swissprot - A0A0D9SFP1
Ensembl - ENSG00000106976
  
Related genetic diseases (OMIM): 616346 - Epileptic encephalopathy, early infantile, 31, 616346
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 dnm1aENSDARG00000010042Danio rerio
 dnm1bENSDARG00000009281Danio rerio
 DNM1ENSGALG00000004852Gallus gallus
 Dnm1ENSMUSG00000026825Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
DNM3 / Q9UQ16 / dynamin 3ENSG0000019795980
DNM2 / P50570 / dynamin 2ENSG0000007980579
DNM1L / O00429 / dynamin 1 likeENSG0000008747035
MX1 / P20591 / MX dynamin like GTPase 1ENSG0000015760122
MX2 / P20592 / MX dynamin like GTPase 2ENSG0000018348621


Protein motifs (from Interpro)
Interpro ID Name
 IPR000375  Dynamin central domain
 IPR001401  Dynamin, GTPase domain
 IPR001849  Pleckstrin homology domain
 IPR003130  Dynamin GTPase effector
 IPR011993  PH-like domain superfamily
 IPR019762  Dynamin, GTPase region, conserved site
 IPR020850  GTPase effector domain
 IPR022812  Dynamin superfamily
 IPR027417  P-loop containing nucleoside triphosphate hydrolase
 IPR027741  Dynamin-1
 IPR030381  Dynamin-type guanine nucleotide-binding (G) domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000266 mitochondrial fission IBA
 biological_processGO:0002031 G-protein coupled receptor internalization IEA
 biological_processGO:0003374 dynamin family protein polymerization involved in mitochondrial fission IBA
 biological_processGO:0006897 endocytosis TAS
 biological_processGO:0006898 receptor-mediated endocytosis IMP
 biological_processGO:0007032 endosome organization IMP
 biological_processGO:0007605 sensory perception of sound IEA
 biological_processGO:0008344 adult locomotory behavior IEA
 biological_processGO:0016185 synaptic vesicle budding from presynaptic endocytic zone membrane IEA
 biological_processGO:0031623 receptor internalization IEA
 biological_processGO:0048013 ephrin receptor signaling pathway TAS
 biological_processGO:0051262 protein tetramerization IEA
 biological_processGO:0051932 synaptic transmission, GABAergic IEA
 biological_processGO:0061025 membrane fusion IBA
 biological_processGO:0072583 clathrin-dependent endocytosis IEA
 biological_processGO:1901998 toxin transport IEA
 biological_processGO:1903423 positive regulation of synaptic vesicle recycling IEA
 cellular_componentGO:0001917 photoreceptor inner segment IEA
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005874 microtubule IEA
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0008021 synaptic vesicle IEA
 cellular_componentGO:0030117 membrane coat IEA
 cellular_componentGO:0031966 mitochondrial membrane IBA
 cellular_componentGO:0043196 varicosity IEA
 cellular_componentGO:0043209 myelin sheath IEA
 cellular_componentGO:0045202 synapse IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003723 RNA binding HDA
 molecular_functionGO:0003924 GTPase activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005525 GTP binding IEA
 molecular_functionGO:0008017 microtubule binding IBA
 molecular_functionGO:0008022 protein C-terminus binding IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0019901 protein kinase binding ISS
 molecular_functionGO:0031749 D2 dopamine receptor binding IEA
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0046983 protein dimerization activity IEA
 molecular_functionGO:0050998 nitric-oxide synthase binding IEA


Pathways (from Reactome)
Pathway description
Toll Like Receptor 4 (TLR4) Cascade
Retrograde neurotrophin signalling
Gap junction degradation
Formation of annular gap junctions
MHC class II antigen presentation
EPH-ephrin mediated repulsion of cells
Recycling pathway of L1
Clathrin-mediated endocytosis


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000718 Aggressive behavior "Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself." [HPO:curators]
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 HP:0000729 Pervasive developmental disorder 
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 HP:0000752 Hyperactivity 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001268 Mental deterioration 
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001298 Encephalopathy 
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 HP:0001336 Myoclonus "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators]
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 HP:0001344 Absent speech development 
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 HP:0002059 Cerebral atrophy 
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 HP:0002069 Generalized tonic-clonic seizures "Generalized tonic-clonic seizures are `generalized seizures` (HP:0002197) in which the patient suddenly loses conciousness, the eyes roll back, and the entire body musculature undergoes tonic contractions. In the clonic phase of the seizure, there are rhythmic contractions of the musculature alternating with relaxation of all muscle groups. Loss of sphincter control during the seizure is common. This form of seizure was formerly commonly called grand mal seizure." [HPO:curators]
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 HP:0002123 Myoclonic seizures "Myoclonic seizures are sudden, brief losses of consciousness and postural tone not associated with tonic muscular contractions. Myoclonic seizures may involve one body part or the entire body. In the latter case, the myoclonic seizure is accompanied by a violent fall but not by loss of consciousness." [HPO:curators]
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 HP:0002355 Difficulty walking 
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 HP:0002363 Abnormality of the brainstem 
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 HP:0002376 Developmental regression 
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 HP:0002527 Falls 
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 HP:0002540 Inability to walk 
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 HP:0007270 Atypical absence seizures 
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 HP:0007359 Partial seizures "Recurrent partial `seizures` (HP:0001250). In a partial seizure, the electrical disturbance is limited to one part or side of the brain. That is, partial epilepsies are epileptic disorders in which clinical or laboratory findings disclose a localized origin of seizures." [HPO:curators]
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 HP:0010818 Tonic seizures "A type of `seizure` (HP:0001250) characterized by a sudden increase in muscle tone whereby the body, arms, or legs make sudden stiffening movements and consciousness is usually preserved. Tonic seizures can occur during sleep. Tonic seizures usually affect both sides of the body, and cause a fall if the affected person was standing when the seizure started." [HPO:probinson]
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 HP:0010819 Atonic seizures "A type of `seizure` (HP:0001250) characterized by a suddenloss of musle tone. Usually, consciousness is retained. In an atonic seizure, the eyelids may droop, the head may nod, and the person may drop things and fall to the ground." [HPO:probinson]
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 HP:0011195 EEG with focal sharp slow waves "EEG with focal sharp transient waves of a duration between 80 and 200 msec followed by a slow wave." [HPO:jalbers]
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 HP:0012075 Personality disorder "An abnormality of mental functioning affecting the personality and behavioural tendencies of an individual and characterized by a rigid and unhealthy pattern of thinking and behavior. The definition of a personal disorder implies that the abnormality is not the result of damage or insult to the brain or from another psychiatric disorder." [HPO:probinson]
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 HP:0100716 Autoagression "Aggression towards oneself." [HPO:sdoelken]
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 HP:0200134 Epileptic encephalopathy 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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