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
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc24a1 Human Ortholog
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
Associated With slc24a1 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR004837 Sodium/calcium exchanger membrane region
Family IPR004481 Sodium/potassium/calcium exchanger
Homologous_superfamily IPR016024 Armadillo-type fold
Domain Details Per Protein
Protein Length Armadillo-type fold Sodium/calcium exchanger membrane region Sodium/potassium/calcium exchanger
UniProtKB:A0A2R8RLA2 696
UniProtKB:F1R8N3 724
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations