Gene

stt3a

ID
ZDB-GENE-021015-3
Name
STT3 oligosaccharyltransferase complex catalytic subunit A
Symbol
stt3a Nomenclature History
Previous Names
  • cb437 (1)
  • itm1
  • wu:fb38c11
Type
protein_coding_gene
Location
Chr: 10 Mapping Details/Browsers
Description
Predicted to have dolichyl-diphosphooligosaccharide-protein glycotransferase activity. Predicted to be involved in post-translational protein modification and protein N-linked glycosylation via asparagine. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation Iw. Is expressed in axial mesoderm; hatching gland; musculature system; notochord; and otic placode. Orthologous to human STT3A (STT3 oligosaccharyltransferase complex catalytic subunit A).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
7 figures from 2 publications
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 stt3a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
congenital disorder of glycosylation Iw Alliance Congenital disorder of glycosylation, type Iw, autosomal recessive 615596
Congenital disorder of glycosylation, type Iw, autosomal dominant 619714
Associated With stt3a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR003674 Oligosaccharyl transferase, STT3 subunit
Domain Details Per Protein
Protein Length Oligosaccharyl transferase, STT3 subunit
UniProtKB:Q7ZUY9 705
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