Gene
mpdu1b
- ID
- ZDB-GENE-040625-135
- Name
- mannose-P-dolichol utilization defect 1b
- Symbol
- mpdu1b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 7 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. Orthologous to human MPDU1 (mannose-P-dolichol utilization defect 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:6899615 (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 |
|---|---|---|---|
| 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:Q6IQH2
|
255 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
mpdu1b-201
(1)
|
Havana | 2019 nt | |
| ncRNA |
mpdu1b-002
(1)
|
Havana | 818 nt |
Interactions and Pathways
No data available
Plasmids
No data available