Gene
slc41a1
- ID
- ZDB-GENE-030131-4700
- Name
- solute carrier family 41 member 1
- Symbol
- slc41a1 Nomenclature History
- Previous Names
-
- fd54c09
- wu:fd54c09
- Type
- protein_coding_gene
- Location
- Chr: 11 Mapping Details/Browsers
- Description
- Predicted to have cation transmembrane transporter activity. Involved in chordate embryonic development; magnesium ion homeostasis; and pronephros development. Predicted to localize to plasma membrane. Is expressed in brain; corpuscles of Stannius; gill; liver; and pleuroperitoneal region. Orthologous to human SLC41A1 (solute carrier family 41 member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| ?Nephronophthisis-like nephropathy 2 | 619468 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | SLC41A divalent cation transporter | SLC41A/MgtE divalent cation transporters, integral membrane domain superfamily | SLC41A/MgtE, integral membrane domain |
|---|---|---|---|---|
|
UniProtKB:A0A8M9Q0L4
|
544 | |||
|
UniProtKB:E7EXX2
|
544 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
slc41a1-201
(1)
|
Havana | 3144 nt | |
| mRNA |
slc41a1-202
(1)
|
Ensembl | 1635 nt |
Interactions and Pathways
No data available
Plasmids
No data available