ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
gfi1b
- ID
 - ZDB-GENE-091118-129
 - Name
 - growth factor independent 1B transcription repressor
 - Symbol
 - gfi1b Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- si:ch211-231o6.2
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 21 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to enable metal ion binding activity. Acts upstream of or within definitive hemopoiesis and erythrocyte differentiation. Predicted to be active in nucleus. Is expressed in ectoderm; erythroblast; hematopoietic system; otic vesicle; and posterior lateral mesoderm. Human ortholog(s) of this gene implicated in gray platelet syndrome and platelet-type bleeding disorder 17. Orthologous to human GFI1B (growth factor independent 1B transcriptional repressor).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 6 figures from 4 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 | 
|---|---|---|---|
| platelet-type bleeding disorder 17 | Alliance | Bleeding disorder, platelet-type, 17 | 187900 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Zinc finger C2H2 superfamily | Zinc finger C2H2-type | 
|---|---|---|---|---|
| UniProtKB:E7FBX7 | InterPro | 334 | ||
| UniProtKB:J9PE59 | InterPro | 334 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers