Gene
mesd
- ID
- ZDB-GENE-070112-2142
- Name
- mesoderm development LRP chaperone
- Symbol
- mesd Nomenclature History
- Previous Names
-
- mesdc2
- zgc:158636 (1)
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Predicted to be involved in positive regulation of skeletal muscle acetylcholine-gated channel clustering. Predicted to act upstream of or within Wnt signaling pathway and protein folding. Predicted to be located in endoplasmic reticulum. Human ortholog(s) of this gene implicated in osteogenesis imperfecta type 20. Orthologous to human MESD (mesoderm development LRP chaperone).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| osteogenesis imperfecta type 20 | Alliance | Osteogenesis imperfecta, type XX | 618644 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019330 | LRP chaperone MESD |
Domain Details Per Protein
| Protein | Length | LRP chaperone MESD |
|---|---|---|
|
UniProtKB:A1L243
|
206 | |
|
UniProtKB:A0A8M9PP56
|
162 |
Interactions and Pathways
No data available
Plasmids
No data available