CPLX4 Gene Summary [Human]
This gene likely encodes a member of the complexin family. The encoded protein may be involved in synaptic vesicle exocytosis. [provided by RefSeq, Jan 2009]
Details
| Type | Protein Coding |
| Official Symbol | CPLX4 |
| Official Name | complexin 4 [Source:HGNC Symbol;Acc:HGNC:24330] |
| Ensembl ID | ENSG00000166569 |
| Bio databases IDs | |
| Aliases | complexin 4 |
| Synonyms | A930004D23Rik, complexin 4, CPX-IV, Gm957 |
| 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 CPLX4 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- SNARE binding
- Synaphin protein
- Complexin_NTD
- protein binding
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.
- Plasma Membrane
- synapse
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human CPLX4 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- regulation of neurotransmitter secretion
- synaptic vesicle exocytosis
- visual perception
Cellular Component
Where in the cell the gene product is active
- terminal button
- SNARE complex
- plasma membrane
Molecular Function
What the gene product does at the molecular level
- protein binding
- syntaxin binding
- SNARE binding