FAM177A1 Gene Summary [Human]
This gene encodes a member of a conserved protein family. Alternative splicing results in multiple transcript variants. This gene is thought to be associated with susceptibility to juvenile idiopathic arthritis. [provided by RefSeq, Apr 2017]
Details
| Type | Protein Coding |
| Official Symbol | FAM177A1 |
| Official Name | family with sequence similarity 177 member A1 [Source:HGNC Symbol;Acc:HGNC:19829] |
| Ensembl ID | ENSG00000151327 |
| Bio databases IDs | |
| Aliases | family with sequence similarity 177 member A1 |
| Synonyms | 1700047I17Rik2, C14orf24, Fam177a2, family with sequence similarity 177 member A1, family with sequence similarity 177, member A1, family with sequence similarity 177 member A2 |
| 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 FAM177A1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- protein binding
- FAM177 family
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.
- Unknown