Gene
dym
- ID
- ZDB-GENE-091204-348
- Name
- dymeclin
- Symbol
- dym Nomenclature History
- Previous Names
-
- si:ch211-167h3.1
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Predicted to be involved in Golgi organization. Predicted to localize to Golgi apparatus. Human ortholog(s) of this gene implicated in Dyggve-Melchior-Clausen disease; Smith-McCort dysplasia; and osteochondrodysplasia. Is expressed in ceratobranchial cartilage; ceratohyal cartilage; head; neuromast; and ventral mandibular arch. Orthologous to human DYM (dymeclin).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Denais et al., 2011
- 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 |
|---|---|---|---|
| Dyggve-Melchior-Clausen disease | Alliance | Dyggve-Melchior-Clausen disease | 223800 |
| Smith-McCort dysplasia 1 | Alliance | Smith-McCort dysplasia | 607326 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019142 | Dymeclin |
Domain Details Per Protein
| Protein | Length | Dymeclin |
|---|---|---|
|
UniProtKB:A0A8M6Z399
|
671 |
Interactions and Pathways
No data available
Plasmids
No data available