Details
| Type | Protein Coding |
| Official Symbol | FAM167A |
| Official Name | family with sequence similarity 167 member A [Source:HGNC Symbol;Acc:HGNC:15549] |
| Ensembl ID | ENSG00000154319 |
| Bio databases IDs | |
| Aliases | family with sequence similarity 167 member A, disordered autoimmunity 1 |
| Synonyms | A030013D21, C8orf13, D8S265, DIORA-1, family with sequence similarity 167 member A, family with sequence similarity 167, member A, RGD1561302 |
| 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 FAM167A often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- FAM167
- protein binding
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- multiple sclerosis
- small cell lung cancer
- coronary artery disease
- neuroticism
- otosclerosis
- ototoxicity
- endometriosis
- small cell lung carcinoma
- thyroid carcinoma
- epithelial thyroid cancer
role in cell
- nilotinib resistance
- imatinib resistance
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Cytoplasm
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human FAM167A gene, providing context for its role in the cell.
Molecular Function
What the gene product does at the molecular level
- protein binding