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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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Guidelines
MIRAGE
lectin, mannose binding 2 like
Summary
- Gene Symbol
-
- LMAN2L
- Aliases
-
- DKFZp564L2423
- VIP36-like
- VIPL
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Golgi apparatus
- Intellectual disability
- Lectin
- Metal-binding
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein folding | ||
| endoplasmic reticulum to Golgi vesicle-mediated transport | ||
| endoplasmic reticulum to Golgi vesicle-mediated transport | ||
| protein transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi membrane | ||
| endoplasmic reticulum membrane | ||
| endoplasmic reticulum membrane | ||
| endoplasmic reticulum-Golgi intermediate compartment | ||
| Golgi apparatus |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| mannose binding | ||
| mannose binding | ||
| metal ion binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Lectin
- Functional Category
-
- M: Cell wall/membrane/envelope biogenesis
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| mannose binding |
| InterPro |
|---|
| Concanavalin A-like lectin/glucanase domain superfamily |
| Legume-like lectin |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060307 | autosomal dominant intellectual developmental disorder | |
| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000718 | Aggressive behavior |
| HP:0000750 | Delayed speech and language development |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001263 | Global developmental delay |
| HP:0001344 | Absent speech |
| HP:0002069 | Bilateral tonic-clonic seizure |
| HP:0002080 | Intention tremor |
| Disease ID | Disease Name |
|---|---|
| OMIM:617863 |
|
| OMIM:616887 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 1139 | Xenbase:XB-GENE-999355 | ||
| 10960 | SGD:S000001752 | ||
| 11441 | Xenbase:XB-GENE-999355 | ||
| 25302 | Xenbase:XB-GENE-999355 | ||
| 34304 | Xenbase:XB-GENE-999355 | ||
| 66890 | SGD:S000001752 | ||
| 81562 | Xenbase:XB-GENE-999355 | ||
| 89832 | Xenbase:XB-GENE-999355 | ||
| 174262 | Xenbase:XB-GENE-999355 | ||
| 175072 | Xenbase:XB-GENE-999355 |
