Commd1 Gene Summary [Mouse]
Predicted to enable several functions, including low-density lipoprotein particle receptor binding activity; phosphatidylinositol-3,4-bisphosphate binding activity; and phospholipid binding activity. Acts upstream of or within several processes, including cholesterol homeostasis; low-density lipoprotein particle clearance; and positive regulation of protein localization. Located in endosome. Is expressed in several structures, including central nervous system; extraembryonic component; future brain; limb bud; and otocyst. Orthologous to human COMMD1 (copper metabolism domain containing 1). [provided by Alliance of Genome Resources, Jul 2025]
Details
| Type | Protein Coding |
| Official Symbol | Commd1 |
| Official Name | COMM domain containing 1 [Source:MGI Symbol;Acc:MGI:109474] |
| Ensembl ID | ENSMUSG00000051355 |
| Bio databases IDs | |
| Aliases | COMM domain containing 1 |
| Synonyms | C2orf5, COMM domain containing 1, copper metabolism domain containing 1, MURR1, U2/Mu |
| 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 Commd1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- COMMD1 N-terminal domain
- phospholipid binding
- low-density lipoprotein receptor binding
- protein binding
- Commd
- identical protein binding
- phosphatidylinositol binding
- sodium channel inhibitor
- copper ion binding
- binding protein
- phosphatidylinositol-3,4,5-triphosphate binding
- phosphatidylinositol-4,5-bisphosphate binding
- protein homodimerization
- COMM domain
- transporter
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- proliferative diabetic retinopathy
- nonalcoholic fatty liver disease
- Parkinson disease
- growth failure
- age-related nuclear cataract disorder
role in cell
- activation in
- binding in
- homeostasis in
- replication in
- degradation in
- association
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
- nuclear fraction
- Cytoplasm
- endosomes
- cytoplasmic aggregates
- cytosol
- nucleoplasm
- recycling endosomes
- early endosomes
- cytosolic fraction
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the mouse Commd1 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- negative regulation of protein localization at cell surface
- negative regulation of NF-kappaB transcription factor activity
- protein transport
- positive regulation of protein ubiquitination
- Golgi to plasma membrane transport
- nucleotide-excision repair
- plasma membrane to endosome transport
- regulation of proteasomal ubiquitin-dependent protein catabolic process
- copper ion homeostasis
Cellular Component
Where in the cell the gene product is active
- nucleus
- early endosome
- endosome
- cytoplasm
- cytosol
- endosome membrane
- recycling endosome
- Cul2-RING ubiquitin ligase complex
- nucleoplasm
Molecular Function
What the gene product does at the molecular level
- phosphatidylinositol-3,4,5-trisphosphate binding
- phosphatidylinositol-4,5-bisphosphate binding
- identical protein binding
- protein homodimerization activity
- protein binding
- copper ion binding
- phosphatidylinositol-3,5-bisphosphate binding
- sodium channel inhibitor activity
- phosphatidic acid binding
- phosphatidylinositol-3,4-bisphosphate binding