Contents

DNM3

Protein-coding gene in the species Homo sapiens

DNM3
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3L43, 5A3F
Identifiers
Aliases	DNM3, Dyna III, dynamin 3
External IDs	OMIM: 611445; MGI: 1341299; HomoloGene: 22906; GeneCards: DNM3; OMA:DNM3 - orthologs
Gene location (Human) Chr. Chromosome 1 (human)[1] Band 1q24.3 Start 171,817,887 bp[1] End 172,418,466 bp[1]
Gene location (Mouse) Chr. Chromosome 1 (mouse)[2] Band 1|1 H2.1 Start 161,810,022 bp[2] End 162,305,603 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in lateral nuclear group of thalamus pons Brodmann area 46 corpus callosum Pars compacta postcentral gyrus superior vestibular nucleus dorsal motor nucleus of vagus nerve pars reticulata orbitofrontal cortex Top expressed in facial motor nucleus anterior horn of spinal cord superior colliculus central gray substance of midbrain inferior colliculus pontine nuclei medial vestibular nucleus substantia nigra dorsal tegmental nucleus nucleus of stria terminalis More reference expression data BioGPS More reference expression data
Gene ontology Molecular function nucleotide binding nitric-oxide synthase binding type 1 metabotropic glutamate receptor binding GTP binding type 5 metabotropic glutamate receptor binding protein binding hydrolase activity GTPase activity microtubule binding identical protein binding structural constituent of postsynapse Cellular component cytoplasm Golgi apparatus postsynaptic density photoreceptor inner segment dendritic spine synapse axon dendritic spine head mitochondrion perinuclear region of cytoplasm synaptic cleft microtubule extracellular exosome cytoskeleton mitochondrial membranes postsynaptic endocytic zone membrane plasma membrane membrane cytoplasmic vesicle postsynaptic membrane apical tubulobulbar complex basal tubulobulbar complex presynapse glutamatergic synapse Biological process endocytosis positive regulation of filopodium assembly regulation of dendritic spine morphogenesis negative regulation of dendritic spine morphogenesis mitochondrial fission dynamin family protein polymerization involved in mitochondrial fission synapse assembly filopodium assembly membrane fusion synaptic vesicle budding from presynaptic endocytic zone membrane postsynaptic neurotransmitter receptor internalization receptor internalization synaptic vesicle endocytosis regulation of synapse structure or activity postsynapse organization positive regulation of synaptic vesicle recycling Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 26052 103967 Ensembl ENSG00000197959 ENSMUSG00000040265 UniProt Q9UQ16 Q8BZ98 RefSeq (mRNA) NM_001136127 NM_001278252 NM_015569 NM_001350204 NM_001350205 NM_001350206 NM_001038619 NM_172646 RefSeq (protein) NP_001129599 NP_001265181 NP_056384 NP_001337133 NP_001337134 NP_001337135 NP_001033708 NP_766234 Location (UCSC) Chr 1: 171.82 – 172.42 Mb Chr 1: 161.81 – 162.31 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Dynamin-3 is a protein that in humans is encoded by the DNM3 gene.^[5][6] The protein encoded by this gene is a member of the dynamin family which possess mechanochemical properties involved in actin-membrane processes, predominantly in membrane budding.^[7] DNM3 is upregulated in Sézary's syndrome.^[8]

References[edit]

Further reading[edit]

External links[edit]

• Overview of all the structural information available in the PDB for UniProt: Q9UQ16 (Dynamin-3) at the PDBe-KB.

This article on a gene on human chromosome 1 is a stub. You can help Wikipedia by expanding it.