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Repository for lectin-assisted multimodality data
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MIRAGE
myelin protein zero
Summary
- Gene Symbol
-
- MPZ
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Charcot-Marie-Tooth disease
- Deafness
- Dejerine-Sottas syndrome
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Immunoglobulin domain
- Neurodegeneration
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A5F9ZI26 |
|
| P25189 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| chemical synaptic transmission |
|
|
| myelination |
|
|
| myelination |
|
|
| cell-cell adhesion |
|
|
| cell-cell adhesion |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| structural molecule activity |
|
|
| protein binding |
|
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- myelin protein P0
- Functional Category
-
- M: Cell wall/membrane/envelope biogenesis
- O: Posttranslational modification, protein turnover, chaperones
- P: Inorganic ion transport and metabolism
| Gene Ontology |
|---|
| myelination |
| InterPro |
|---|
| Immunoglobulin V-set domain |
| Immunoglobulin-like domain superfamily |
| Immunoglobulin-like domain |
| Immunoglobulin-like fold |
| Myelin P0 protein-related |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050540 | Charcot-Marie-Tooth disease type 3 | |
| DOID:0110152 | Charcot-Marie-Tooth disease type 1B | |
| DOID:0110157 | Charcot-Marie-Tooth disease type 2J | |
| DOID:0110158 | Charcot-Marie-Tooth disease type 2I | |
| DOID:0110200 | Charcot-Marie-Tooth disease dominant intermediate D | |
| DOID:10595 | Charcot-Marie-Tooth disease |
