Gene

b4gat1

ID
ZDB-GENE-121001-5
Name
beta-1,4-glucuronyltransferase 1
Symbol
b4gat1 Nomenclature History
Previous Names
  • b3gnt1
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to have glucuronosyltransferase activity. Involved in muscle fiber development and protein glycosylation. Predicted to localize to Golgi apparatus. Used to study Walker-Warburg syndrome. Human ortholog(s) of this gene implicated in congenital muscular dystrophy-dystroglycanopathy type A13. Orthologous to human B4GAT1 (beta-1,4-glucuronyltransferase 1).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Buysse et al., 2013
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With b4gat1 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
congenital muscular dystrophy-dystroglycanopathy type A13 Alliance Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 615287
Associated With b4gat1 Via Experimental Models
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR043189 Beta-1,4-glucuronyltransferase 1
Domain Details Per Protein
Protein Length Beta-1,4-glucuronyltransferase 1
UniProtKB:L7YAI7 431
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