Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
laminin subunit alpha 2
Summary
- Gene Symbol
-
- LAMA2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Basement membrane
- Cell adhesion
- Coiled coil
- Congenital muscular dystrophy
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Laminin EGF-like domain
- Limb-girdle muscular dystrophy
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| P24043 |
|
| Q59H37 |
|
| A0A087WYF1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell adhesion | ||
| axon guidance | ||
| muscle organ development | ||
| Schwann cell differentiation | ||
| regulation of cell migration |
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
regulation of signaling [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region | ||
| basement membrane | ||
| basement membrane | ||
| neuromuscular junction | ||
| sarcolemma |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| signaling receptor binding | ||
| structural molecule activity | ||
| extracellular matrix structural constituent |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- laminin A
- Functional Category
-
- G: Carbohydrate transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- P: Inorganic ion transport and metabolism
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
| DOID:0110636 | congenital merosin-deficient muscular dystrophy 1A | |
| DOID:11830 | myopia | |
| DOID:9884 | muscular dystrophy |
