Sgca Gene Summary [Mouse]
This gene encodes a member of the sarcoglycan alpha/epsilon family of transmembrane proteins. The encoded protein is part of the dystrophin-glycoprotein complex which links the extracellular matrix to the cytoskeleton in muscle fibers. Disruption of this gene results in progressive muscular dystrophy and is associated with the development of embryonal rhabdomysarcoma. [provided by RefSeq, Dec 2012]
Details
| Type | Protein Coding |
| Official Symbol | Sgca |
| Official Name | sarcoglycan, alpha (dystrophin-associated glycoprotein) [Source:MGI Symbol;Acc:MGI:894698] |
| Ensembl ID | ENSMUSG00000001508 |
| Bio databases IDs | |
| Aliases | sarcoglycan, alpha (dystrophin-associated glycoprotein) |
| Synonyms | 50-DAG, adhalin, ADL, alpha SARCOGLYCAN, Asg, DAG2, DMDA2, LGMD2D, LGMDR3, SARCOGLYCAN alpha, sarcoglycan, alpha, sarcoglycan, alpha (dystrophin-associated glycoprotein), Sarcoglycan α, sarcoglycan, α, sarcoglycan, α (dystrophin-associated glycoprotein), SCARMD1, α SARCOGLYCAN |
| 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 Sgca often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Sarcoglycan alpha/epsilon
- X25 domain of Bacillus acidopullulyticus pullulanase and similar proteins
- intracellular domain
- Cadherin repeat-like domain
- protein binding
- Dystroglycan-type cadherin-like domains
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- limb-girdle muscular dystrophy type 2D
- dystrophy
- limb-girdle muscular dystrophy type 2
- sarcoglycanopathies
- muscular dystrophy
- fibrosis
- cardiac fibrosis
- cardiomyopathy
- limb-girdle muscular dystrophy type 2B
- centronuclear myopathy
role in cell
- damage
- organization
- centralization
- abnormal morphology
- replication in
- permeability
- centralization 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.
- Plasma Membrane
- microsomal fraction
- intercellular junctions
- endoplasmic reticulum membrane
- microsome
- Golgi membrane
- sarcolemma
- membrane rafts
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the mouse Sgca gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- muscle organ development
- response to denervation involved in regulation of muscle adaptation
- muscle contraction
- skeletal muscle tissue regeneration
Cellular Component
Where in the cell the gene product is active
- cytoskeleton
- cell-cell junction
- cytoplasm
- sarcolemma
- membrane raft
- dystrophin-associated glycoprotein complex
- sarcoglycan complex
Molecular Function
What the gene product does at the molecular level
- protein binding
- calcium ion binding