Gene
nipa1
- ID
- ZDB-GENE-041010-164
- Name
- NIPA magnesium transporter 1
- Symbol
- nipa1 Nomenclature History
- Previous Names
-
- wu:fc12a05
- zgc:101743 (1)
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to have magnesium ion transmembrane transporter activity. Predicted to be involved in magnesium ion transport. Predicted to localize to membrane. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 6. Orthologous to human NIPA1 (NIPA magnesium transporter 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Messina et al., 2020
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 2 figures from Jardin et al., 2018
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| hereditary spastic paraplegia 6 | Alliance | Spastic paraplegia 6, autosomal dominant | 600363 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR008521 | Magnesium transporter NIPA |
Domain Details Per Protein
| Protein | Length | Magnesium transporter NIPA |
|---|---|---|
|
UniProtKB:Q5XJN7
|
306 |
Interactions and Pathways
No data available
Plasmids
No data available