ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
ift27
- ID
- ZDB-GENE-041212-9
- Name
- intraflagellar transport 27 homolog (Chlamydomonas)
- Symbol
- ift27 Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - rabl4
- zgc:101893
 
- Type
- protein_coding_gene
- Location
- Ambiguous Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable GTP binding activity and GTPase activity. Acts upstream of or within cilium assembly; kidney development; and regulation of melanosome transport. Predicted to be part of intraciliary transport particle B. Predicted to be active in Golgi membrane and cilium. Human ortholog(s) of this gene implicated in Bardet-Biedl syndrome 19. Orthologous to human IFT27 (intraflagellar transport 27).
- Genome Resources
- 
    
        
    
    
        
        - Alliance (1)
- Gene:494045 (1)
 
- Note
- None
- Comparative Information
- 
    
        
        
              
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- 
    
        
    
    
        
        - IMAGE:7148811 (1 image)
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Bardet-Biedl syndrome 19 | Alliance | Bardet-Biedl syndrome 19 | 615996 | 
| Human Disease | Fish | Conditions | Citations | 
|---|---|---|---|
| retinitis pigmentosa | ift27zf4178/zf4178 (AB) | standard conditions | Han et al., 2024 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Intraflagellar transport protein 27 homologue, eukaryotes | P-loop containing nucleoside triphosphate hydrolase | Ras-related protein Rab | Small GTPase | Small GTP-binding domain | 
|---|---|---|---|---|---|---|---|
| UniProtKB:Q5PR92 | InterPro | 186 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
- Comparative Orthology
- Alliance
