MIPOL1 Gene Summary [Human]
This gene encodes a coiled-coil domain-containing protein. The encoded protein may function as a tumor suppressor. A translocation that results in truncation of the protein encoded by this locus has been associated with mirror-image polydactyly, also known as Laurin-Sandrow Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Sep 2010]
Details
| Type | Protein Coding |
| Official Symbol | MIPOL1 |
| Official Name | mirror-image polydactyly 1 [Source:HGNC Symbol;Acc:HGNC:21460] |
| Ensembl ID | ENSG00000151338 |
| Bio databases IDs | |
| Aliases | mirror-image polydactyly 1 |
| Synonyms | 1700081O04Rik, 6030439O22Rik, CCDC193, D12Ertd19e, mirror-image polydactyly 1, TMIP |
| 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 MIPOL1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Tropomyosin
- protein binding
- identical 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.
- Nucleus
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human MIPOL1 gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- nucleus
Molecular Function
What the gene product does at the molecular level
- identical protein binding
- protein binding