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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|
| endoplasmic reticulum to Golgi vesicle-mediated transport | ||
| protein folding |
|
|
| protein transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| COPII-coated ER to Golgi transport vesicle | ||
| endoplasmic reticulum-Golgi intermediate compartment | ||
| endoplasmic reticulum membrane | ||
| membrane |
|
|
| Golgi apparatus |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| mannose binding | ||
| metal ion binding | ||
| protein binding |
GO Hierarchy
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:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0060307 | autosomal dominant intellectual developmental disorder | |
| DOID:0060810 | syndromic X-linked intellectual disability type 10 | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | |
| DOID:10907 | microcephaly | |
| DOID:10930 | borderline personality disorder | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:11832 | visual epilepsy | |
| DOID:12139 | dysthymic disorder |
- 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 |
|---|---|---|---|
| 180423 | WB:WBGene00002071 | ||
| 42872 | FB:FBgn0039160 | ||
| 403038 | ZFIN:ZDB-GENE-040715-4 | ||
| 767766 | ZFIN:ZDB-GENE-060929-256 | ||
| 108260377 | ICTPU23252 | ||
| 113588081 | ELEEL40727 | ||
| 106563290 | SALSA56874 | ||
| 115204064 | SALTR78093 | ||
| 115541612 | GADMO44979 | ||
| 100701135 | ORENI65164 |
