ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
iba57
- ID
- ZDB-GENE-060929-712
- Name
- iron-sulfur cluster assembly factor IBA57
- Symbol
- iba57 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - zgc:153540
 
- Type
- protein_coding_gene
- Location
- Chr: 2 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable transferase activity, transferring one-carbon groups. Acts upstream of or within heme biosynthetic process. Predicted to be located in mitochondrion. Predicted to be active in mitochondrial matrix. Is expressed in intermediate cell mass of mesoderm. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 74 and multiple mitochondrial dysfunctions syndrome 3. Orthologous to human IBA57 (iron-sulfur cluster assembly factor IBA57).
- Genome Resources
- Note
- None
- Comparative Information
- 
    
        
        
              
- All Expression Data
- 1 figure from Nilsson et al., 2009
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 1 Figure from Nilsson et al., 2009
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| hereditary spastic paraplegia 74 | Alliance | ?Spastic paraplegia 74, autosomal recessive | 616451 | 
| multiple mitochondrial dysfunctions syndrome 3 | Alliance | Multiple mitochondrial dysfunctions syndrome 3 | 615330 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | GTP-binding protein TrmE/Aminomethyltransferase GcvT, domain 1 | YgfZ/GcvT | YgfZ/GcvT conserved site | 
|---|---|---|---|---|---|
| UniProtKB:B8JMH0 | InterPro | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
