Gene

mpdu1b

ID
ZDB-GENE-040625-135
Name
mannose-P-dolichol utilization defect 1b
Symbol
mpdu1b Nomenclature History
Previous Names
  • fb18d03
  • wu:fb18d03 (1)
  • zgc:86765 (1)
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Involved in oligosaccharide biosynthetic process. Predicted to be located in membrane. Predicted to be 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
Expression
All Expression Data
1 figure from Thisse et al., 2004
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With mpdu1b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
congenital disorder of glycosylation If Alliance Congenital disorder of glycosylation, type If 609180
Associated With mpdu1b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR016817 Mannose-P-dolichol utilization defect 1 protein
Repeat IPR006603 PQ-loop repeat
Domain Details Per Protein
Protein Length Mannose-P-dolichol utilization defect 1 protein PQ-loop repeat
UniProtKB:Q6IQH2 255
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations