FIBCD1 Gene Summary [Human]
FIBCD1 is a conserved type II transmembrane endocytic receptor that binds chitin and is located primarily in the intestinal brush border (Schlosser et al., 2009 [PubMed 19710473]).[supplied by OMIM, Apr 2010]
Details
| Type | Protein Coding |
| Official Symbol | FIBCD1 |
| Official Name | fibrinogen C domain containing 1 [Source:HGNC Symbol;Acc:HGNC:25922] |
| Ensembl ID | ENSG00000130720 |
| Bio databases IDs | |
| Aliases | fibrinogen C domain containing 1 |
| Synonyms | AI448887, Fibcd1l1, fibrinogen C domain containing 1, LOC100909722, RGD1309097 |
| 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 FIBCD1 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
- chitin binding
- FReD
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.
- cellular membrane
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human FIBCD1 gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- extracellular space
- membrane
Molecular Function
What the gene product does at the molecular level
- chitin binding
- protein binding
- metal ion binding