ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
nup88
- ID
 - ZDB-GENE-050522-297
 - Name
 - nucleoporin 88
 - Symbol
 - nup88 Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- ik:tdsubc_2f7
 - wu:fb16f10
 - wu:fb33e09
 - xx:tdsubc_2f7
 - zgc:112439
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 5 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to be a structural constituent of nuclear pore. Predicted to be involved in nucleocytoplasmic transport. Predicted to act upstream of or within mRNA transport; nucleocytoplasmic transport; and protein transport. Predicted to be located in nucleus. Predicted to be part of nuclear pore. Is expressed in several structures, including brain; eye; immature eye; otic vesicle; and yolk syncytial layer. Human ortholog(s) of this gene implicated in fetal akinesia deformation sequence syndrome 4. Orthologous to human NUP88 (nucleoporin 88).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 14 figures from 2 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 | 
|---|---|---|---|
| fetal akinesia deformation sequence syndrome 4 | Alliance | Fetal akinesia deformation sequence 4 | 618393 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Nucleoporin Nup88 | Nucleoporin NUP88/NUP82 | 
|---|---|---|---|---|
| UniProtKB:A0A8D3IZM5 | InterPro | |||
| UniProtKB:A2CEI4 | InterPro | 720 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers