Gene
gldn
- ID
- ZDB-GENE-050119-4
- Name
- gliomedin
- Symbol
- gldn Nomenclature History
- Previous Names
-
- collomin
- colm
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to be involved in signal transduction. Predicted to act upstream of or within clustering of voltage-gated sodium channels. Predicted to be located in membrane. Predicted to be active in cell surface and extracellular space. Human ortholog(s) of this gene implicated in lethal congenital contracture syndrome. Orthologous to human GLDN (gliomedin).
- 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 |
|---|---|---|---|
| Lethal congenital contracture syndrome 11 | 617194 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Collagen triple helix repeat | Olfactomedin-like domain | Olfactomedin-like domain-containing protein |
|---|---|---|---|---|
|
UniProtKB:F2Z4S9
|
542 | |||
|
UniProtKB:A0A8M9P157
|
564 |
Interactions and Pathways
No data available
Plasmids
No data available