Tmem169 Gene Summary [Mouse]
Predicted to be located in membrane. Orthologous to human TMEM169 (transmembrane protein 169). [provided by Alliance of Genome Resources, Jul 2025]
Details
| Type | Protein Coding |
| Official Symbol | Tmem169 |
| Official Name | transmembrane protein 169 [Source:MGI Symbol;Acc:MGI:2442781] |
| Ensembl ID | ENSMUSG00000026188 |
| Bio databases IDs | |
| Aliases | transmembrane protein 169 |
| Synonyms | A830020B06Rik, LOC679215, transmembrane protein 169 |
| Species | Mouse, Mus musculus |
| 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 mouse Tmem169 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- TMEM169 protein family
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- Hodgkin lymphoma
- Hodgkin disease
- Crohn disease
- nonalcoholic fatty liver disease
regulated by
role in cell
- morphology
- accumulation in
- elongation
- elongation in
- length
- thickness
- density
- accumulation
- complexity
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Unknown
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the mouse Tmem169 gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- membrane