LCA5L Gene Summary [Human]
Predicted to be involved in intraciliary transport. Predicted to be active in axoneme. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Protein Coding |
| Official Symbol | LCA5L |
| Official Name | lebercilin LCA5 like [Source:HGNC Symbol;Acc:HGNC:1255] |
| Ensembl ID | ENSG00000157578 |
| Bio databases IDs | |
| Aliases | lebercilin LCA5 like |
| Synonyms | 4921526F01Rik, C21orf13, Lcca5l, lebercilin LCA5 like, Leber congenital amaurosis 5-like, MGC33295 |
| 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 LCA5L often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Ciliary protein causing Leber congenital amaurosis disease
- Growth-arrest specific micro-tubule binding
- protein binding
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Extracellular Space
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human LCA5L gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- intraflagellar transport
Cellular Component
Where in the cell the gene product is active
- axoneme
Molecular Function
What the gene product does at the molecular level
- protein binding