Gene
ogt.2
- ID
- ZDB-GENE-051128-1
- Name
- O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 2
- Symbol
- ogt.2 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 14 Mapping Details/Browsers
- Description
- Exhibits protein N-acetylglucosaminyltransferase activity. Predicted to be involved in protein O-linked glycosylation. Human ortholog(s) of this gene implicated in X-linked mental retardation 106. Orthologous to human OGT (O-linked N-acetylglucosamine (GlcNAc) transferase).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Webster et al., 2009
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| non-syndromic X-linked intellectual disability 106 | Alliance | Intellectual developmental disorder, X-linked 106 | 300997 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | O-GlcNAc transferase, C-terminal | Tetratricopeptide-like helical domain superfamily | Tetratricopeptide repeat |
|---|---|---|---|---|
|
UniProtKB:A0A8M9QPC9
|
870 | |||
|
UniProtKB:A0A8M2B3B2
|
1092 | |||
|
UniProtKB:A0A0R4IVJ0
|
1102 |
Interactions and Pathways
No data available
Plasmids
No data available