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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
sarcoglycan delta
Summary
- Gene Symbol
-
- SGCD
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cardiomyopathy
- Cell membrane
- Cytoskeleton
- Disease variant
- Disulfide bond
- Glycoprotein
- Limb-girdle muscular dystrophy
- Proteomics identification
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q92629 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| muscle organ development | ||
| calcium-mediated signaling | ||
| protein-containing complex localization | ||
| cardiac muscle tissue development | ||
| cardiac muscle cell development |
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoskeleton | ||
| plasma membrane | ||
| dystrophin-associated glycoprotein complex | ||
| sarcoglycan complex | ||
| sarcoplasmic reticulum |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- sarcoglycan
- Functional Category
-
- E: Amino acid transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| cardiac muscle tissue development |
| heart contraction |
| InterPro |
|---|
| Sarcoglycan complex subunit protein |
| Sarcoglycan gamma/delta/zeta |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
| DOID:0110436 | dilated cardiomyopathy 1L | |
| DOID:9884 | muscular dystrophy |
