DMWD Gene Summary [Human]
Predicted to be located in dendrite; nucleus; and perikaryon. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Protein Coding |
| Official Symbol | DMWD |
| Official Name | DM1 locus, WD repeat containing [Source:HGNC Symbol;Acc:HGNC:2936] |
| Ensembl ID | ENSG00000185800 |
| Bio databases IDs | |
| Aliases | DM1 locus, WD repeat containing |
| Synonyms | D19S593E, DM1 locus, WD repeat containing, DM9, DMR-N9, Dystrophia myotonica containing wd repeat, dystrophia myotonica-containing WD repeat motif, gene59 |
| Species | Human, Homo sapiens |
| Orthologies |
Protein Domains
A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human DMWD often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- WD40 repeats
- protein binding
- protease activator
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Nucleus
- Cytoplasm
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human DMWD gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- dendrite
- nucleus
- cytoplasm
- perikaryon
Molecular Function
What the gene product does at the molecular level
- protein binding
- ubiquitin-specific protease activator activity