Gene
mpdu1a
- ID
- ZDB-GENE-040912-9
- Name
- mannose-P-dolichol utilization defect 1a
- Symbol
- mpdu1a Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to be involved in oligosaccharide biosynthetic process. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation If. Is expressed in brain and ventricular zone. Orthologous to human MPDU1 (mannose-P-dolichol utilization defect 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 6 figures from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:7160534 (2 images)
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 |
|---|---|---|---|
| congenital disorder of glycosylation If | Alliance | Congenital disorder of glycosylation, type If | 609180 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mannose-P-dolichol utilization defect 1 protein | PQ-loop repeat |
|---|---|---|---|
|
UniProtKB:Q66I07
|
258 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
mpdu1a-201
(1)
|
Havana | 2689 nt |
Interactions and Pathways
No data available
Plasmids
No data available