ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
tshba
- ID
- ZDB-GENE-030513-3
- Name
- thyroid stimulating hormone subunit beta a
- Symbol
- tshba Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - tshb (1)
 
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable hormone activity. Acts upstream of or within development of secondary sexual characteristics and regulation of thyroid hormone generation. Predicted to be located in extracellular region. Predicted to be active in cytoplasm and extracellular space. Is expressed in adenohypophyseal placode; head; hypophysis; and thyroid follicle. Human ortholog(s) of this gene implicated in congenital nongoitrous hypothyroidism 4 and hypothyroidism. Orthologous to human TSHB (thyroid stimulating hormone subunit beta).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 52 figures from 36 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 7 figures from Song et al., 2021
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| congenital nongoitrous hypothyroidism 4 | Alliance | Hypothyroidism, congenital, nongoitrous 4 | 275100 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cystine-knot cytokine | Glycoprotein hormone subunit beta | Gonadotropin, beta subunit | Gonadotropin, beta subunit, conserved site | 
|---|---|---|---|---|---|---|
| UniProtKB:A0A8M9PZI4 | InterPro | 129 | ||||
| UniProtKB:Q801K4 | InterPro | 148 | ||||
| UniProtKB:A0A8M9PLW7 | InterPro | 182 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
