Gene
magt1
- ID
- ZDB-GENE-030131-3667
- Name
- magnesium transporter 1
- Symbol
- magt1 Nomenclature History
- Previous Names
-
- fc49b02
- wu:fc49b02
- zgc:56218 (1)
- Type
- protein_coding_gene
- Location
- Chr: 14 Mapping Details/Browsers
- Description
- Predicted to have magnesium ion transmembrane transporter activity. Involved in magnesium ion transport. Predicted to localize to oligosaccharyltransferase complex. Human ortholog(s) of this gene implicated in X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia; congenital disorder of glycosylation; and non-syndromic X-linked intellectual disability. Orthologous to human MAGT1 (magnesium transporter 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:56218 (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 Icc | Alliance | Congenital disorder of glycosylation, type Icc | 301031 |
| X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | Alliance | Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia | 300853 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Oligosaccharyl transferase complex, subunit OST3/OST6 | Thioredoxin-like superfamily |
|---|---|---|---|
|
UniProtKB:Q7ZV50
|
328 |
Interactions and Pathways
No data available
Plasmids
No data available