Gene
slc24a1
- ID
- ZDB-GENE-060503-191
- Name
- solute carrier family 24 member 1
- Symbol
- slc24a1 Nomenclature History
- Previous Names
-
- si:ch211-117i10.3
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to have calcium channel activity and calcium, potassium:sodium antiporter activity. Predicted to be involved in calcium ion transmembrane transport; cellular calcium ion homeostasis; and regulation of synaptic plasticity. Predicted to localize to integral component of plasma membrane. Human ortholog(s) of this gene implicated in congenital stationary night blindness 1D. Orthologous to human SLC24A1 (solute carrier family 24 member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Clifford et al., 2022
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
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 stationary night blindness 1D | Alliance | Night blindness, congenital stationary (complete), 1D, autosomal recessive | 613830 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Armadillo-type fold | NCX, central ion-binding domain superfamily | Sodium/calcium exchanger membrane region | Sodium/potassium/calcium exchanger |
|---|---|---|---|---|---|
|
UniProtKB:A0A8M9Q2S5
|
724 | ||||
|
UniProtKB:A0A2R8RLA2
|
696 | ||||
|
UniProtKB:A0A8M3B2X1
|
696 | ||||
|
UniProtKB:A0A8M3AJK7
|
741 | ||||
|
UniProtKB:A0A8M9P1C0
|
741 | ||||
|
UniProtKB:F1R8N3
|
724 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
slc24a1-202
(1)
|
Havana | 3753 nt |
Interactions and Pathways
No data available
Plasmids
No data available