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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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GALAXY
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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
- Reference proteome
- Repeat
- Signal
- Proteins
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
- Functional Category
-
- G: Carbohydrate transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- P: Inorganic ion transport and metabolism
| Gene Ontology |
|---|
| animal organ morphogenesis |
| regulation of cell adhesion |
| regulation of cell migration |
| regulation of embryonic development |
| signaling receptor binding |
| tissue development |
| InterPro |
|---|
| Concanavalin A-like lectin/glucanase domain superfamily |
| Laminin G domain |
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 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 3908 | Xenbase:XB-GENE-953878 | ||
| 16772 | FB:FBgn0261563 | ||
| 16773 | Xenbase:XB-GENE-953878 | MOUSE00027 | |
| 172952 | ZFIN:ZDB-GENE-060119-1 | ||
| 284217 | FB:FBgn0261563 | ||
| 309368 | RATNO19212 | ||
| 472122 | PANTR39036 | ||
| 715394 | MACMU34121 | ||
| 100030895 | MONDO12218 | ||
| 100073067 | HORSE02653 |
