ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
slc16a2
- ID
- ZDB-GENE-120117-1
- Name
- solute carrier family 16 member 2
- Symbol
- slc16a2 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - MCT8 (1)
 
- Type
- protein_coding_gene
- Location
- Ambiguous Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Enables thyroid hormone binding activity and thyroid hormone transmembrane transporter activity. Acts upstream of or within several processes, including nervous system development; optomotor response; and thyroid gland development. Predicted to be located in apical plasma membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including cardiovascular system; central nervous system; digestive system; eye; and hindbrain neural keel. Used to study Allan-Herndon-Dudley syndrome. Human ortholog(s) of this gene implicated in Allan-Herndon-Dudley syndrome and intellectual disability. Orthologous to human SLC16A2 (solute carrier family 16 member 2).
- Genome Resources
- Note
- None
- Comparative Information
- 
    
        
        
              
- All Expression Data
- 10 figures from 8 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 35 figures from 9 publications
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Allan-Herndon-Dudley syndrome | Alliance | Allan-Herndon-Dudley syndrome | 300523 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Major facilitator superfamily | Major facilitator superfamily domain | MFS transporter superfamily | Proton-linked Monocarboxylate Transporter | 
|---|---|---|---|---|---|---|
| UniProtKB:G8XYX6 | InterPro | 526 | 
- Genome Browsers
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis | 
|---|---|---|---|---|---|
| mRNA | slc16a2-201
                             (1) | Ensembl | 1,581 nt | ||
| mRNA | slc16a2-202
                             (1) | Ensembl | 1,587 nt | 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
- Comparative Orthology
- Alliance
