TMEM169 Gene Summary [Human]
Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Protein Coding |
| Official Symbol | TMEM169 |
| Official Name | transmembrane protein 169 [Source:HGNC Symbol;Acc:HGNC:25130] |
| Ensembl ID | ENSG00000163449 |
| Bio databases IDs | |
| Aliases | transmembrane protein 169 |
| Synonyms | A830020B06Rik, LOC679215, transmembrane protein 169 |
| 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 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 human TMEM169 gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- membrane