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 clustering of voltage-gated sodium channels. Predicted to localize to integral component of membrane. 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