Gene
med27
- ID
- ZDB-GENE-040426-1601
- Name
- mediator complex subunit 27
- Symbol
- med27 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to enable transcription coactivator activity. Acts upstream of or within retinal cone cell development. Predicted to be located in nucleus. Predicted to be part of mediator complex. Orthologous to human MED27 (mediator complex subunit 27).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:66302 (1 image)
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 |
|---|---|---|---|
| Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia | 619286 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR021627 | Mediator complex, subunit Med27 |
Domain Details Per Protein
| Protein | Length | Mediator complex, subunit Med27 |
|---|---|---|
|
UniProtKB:Q6PFL0
|
311 | |
|
UniProtKB:A0A8M9QDN3
|
253 | |
|
UniProtKB:B2GNU2
|
311 |
Interactions and Pathways
No data available
Plasmids
No data available