KRT222 Gene Summary [Human]
Predicted to enable structural molecule activity. Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Nonsense Mediated Decay |
| Official Symbol | KRT222 |
| Official Name | keratin 222 [Source:HGNC Symbol;Acc:HGNC:28695] |
| Ensembl ID | ENSG00000213424 |
| Bio databases IDs | |
| Aliases | keratin 222 |
| Synonyms | 6330509G02Rik, KA21, Ka21p, keratin 222, KRT222P, KRT22P, RGD1560383 |
| 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 KRT222 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
Pathways
Biological processes and signaling networks where the KRT222 gene in human plays a role, providing insight into its function and relevance in health or disease.
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
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human KRT222 gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- intermediate filament
Molecular Function
What the gene product does at the molecular level
- protein binding
- structural molecule activity