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Repository for lectin-assisted multimodality data
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MIRAGE
WASH complex subunit 5
Summary
- Gene Symbol
-
- WASHC5
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cytoplasm
- Disease variant
- Endoplasmic reticulum
- Endosome
- Hereditary spastic paraplegia
- Intellectual disability
- Phosphoprotein
- Protein transport
- Proteomics identification
- Reference proteome
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| oocyte maturation | ||
| endosome organization | ||
| lysosome organization | ||
| positive regulation of neuron projection development | ||
| protein transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm |
|
|
| endosome | ||
| endosome | ||
| early endosome | ||
| endoplasmic reticulum |
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- wash complex subunit
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| actin filament polymerization |
| endosome fission |
| endosome organization |
| regulation of actin nucleation |
| InterPro |
|---|
| WASH complex, subunit strumpellin |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060571 | Ritscher-Schinzel syndrome 1 | |
| DOID:0110823 | hereditary spastic paraplegia 8 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 9897 | Xenbase:XB-GENE-5781989 | ||
| 223593 | MOUSE15208 | ||
| 362919 | RATNO39258 | ||
| 464385 | PANTR43246 | ||
| 475095 | CANLF03209 | ||
| 508040 | BOVIN05740 | ||
| 706857 | MACMU43525 | ||
| 100026267 | MONDO18155 | ||
| 100057703 | HORSE42649 | ||
| 100080157 | ORNAN20857 |
