Tmco1 Gene Summary [Mouse]
Predicted to enable calcium channel activity and ribosome binding activity. Involved in calcium ion transmembrane transport; endoplasmic reticulum calcium ion homeostasis; and ossification. Predicted to be located in endoplasmic reticulum membrane. Predicted to be part of multi-pass translocon complex. Predicted to be active in endoplasmic reticulum. Is expressed in clavicle; mandible; maxilla; and rib. Used to study craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome. Human ortholog(s) of this gene implicated in craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1. Orthologous to human TMCO1 (transmembrane and coiled-coil domains 1). [provided by Alliance of Genome Resources, Jul 2025]
Details
| Type | Protein Coding |
| Official Symbol | Tmco1 |
| Official Name | transmembrane and coiled-coil domains 1 [Source:MGI Symbol;Acc:MGI:1921173] |
| Ensembl ID | ENSMUSG00000052428 |
| Bio databases IDs | |
| Aliases | transmembrane and coiled-coil domains 1 |
| Synonyms | 1190006A08RIK, 4930403O06Rik, CFSMR1, ESTM39, HP10122, LOC54499, PCIA3, PNAS-136, TMCC4, transmembrane and coiled-coil domains 1 |
| Species | Mouse, Mus musculus |
| 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 mouse Tmco1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- calcium channel
- ribosome binding
- Integral membrane protein EMC3/TMCO1-like
- protein binding
- ion channel
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- breast cancer
- neoplasia
- open-angle glaucoma
- normal tension glaucoma
- craniofacial dysmorphism skeletal anomalies and impaired intellectual development syndrome type 1
- glaucoma
- hereditary disorder
- cerebrofaciothoracic dysplasia
- agenesis of corpus callosum
- premature ovarian failure
role in cell
- apoptosis
- expression in
- quantity
- migration
- calcium homeostasis
- degeneration
- ossification by
- colony formation by
- calcium spike in
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Cytoplasm
- cellular membrane
- Endoplasmic Reticulum
- Mitochondria
- endoplasmic reticulum membrane
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the mouse Tmco1 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- ossification
- calcium ion transmembrane transport
- endoplasmic reticulum calcium ion homeostasis
- ER overload response
Cellular Component
Where in the cell the gene product is active
- endoplasmic reticulum membrane
- cytoplasm
- endoplasmic reticulum
- Golgi membrane
Molecular Function
What the gene product does at the molecular level
- protein binding
- ribosome binding
- calcium channel activity