ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
nmnat1
- ID
 - ZDB-GENE-050417-101
 - Name
 - nicotinamide nucleotide adenylyltransferase 1
 - Symbol
 - nmnat1 Nomenclature History
 - Previous Names
 - 
    
        
    
    
        
        
- id:ibd5068
 - im:7144541
 - zgc:110243
 
 - Type
 - protein_coding_gene
 - Location
 - Chr: 23 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Predicted to enable nicotinamide-nucleotide adenylyltransferase activity and nicotinate-nucleotide adenylyltransferase activity. Predicted to be involved in NAD biosynthetic process. Predicted to act upstream of or within pyridine nucleotide biosynthetic process. Predicted to be active in nucleus. Is expressed in several structures, including Kupffer's vesicle; forerunner cell group; heart; liver; and yolk syncytial layer. Human ortholog(s) of this gene implicated in Leber congenital amaurosis 9 and spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis. Orthologous to human NMNAT1 (nicotinamide nucleotide adenylyltransferase 1).
 - Genome Resources
 - Note
 - None
 - Comparative Information
 - 
    
        
        
            
        
    
    
    
 
- All Expression Data
 - 8 figures from 2 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - 
    
        
    
    
        
        
- MGC:110243 (4 images)
 - IMAGE:7144541 (1 image)
 
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - No data available
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Leber congenital amaurosis 9 | Alliance | Leber congenital amaurosis 9 | 608553 | 
| spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis | Alliance | Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis | 619260 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Type | InterPro ID | Name | 
|---|---|---|
| Domain | IPR004821 | Cytidyltransferase-like domain | 
| Family | IPR005248 | Nicotinate/nicotinamide nucleotide adenylyltransferase | 
| Family | IPR045094 | Nicotinamide/nicotinate mononucleotide adenylyltransferase, eukaryotic | 
| Family | IPR051182 | Eukaryotic NMN adenylyltransferase | 
| Homologous_superfamily | IPR014729 | Rossmann-like alpha/beta/alpha sandwich fold | 
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Cytidyltransferase-like domain | Eukaryotic NMN adenylyltransferase | Nicotinamide/nicotinate mononucleotide adenylyltransferase, eukaryotic | Nicotinate/nicotinamide nucleotide adenylyltransferase | Rossmann-like alpha/beta/alpha sandwich fold | 
|---|---|---|---|---|---|---|---|
| UniProtKB:E9QH56 | InterPro | 271 | 
- Genome Browsers
 
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis | 
|---|---|---|---|---|---|
| mRNA | 
                    
                        
                        
                            nmnat1-201
                             (1)
                            
                                
 | 
                
                Ensembl | 1,107 nt | ||
| mRNA | 
                    
                        
                        
                            nmnat1-202
                             (1)
                            
                                
 | 
                
                Ensembl | 1,042 nt | 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers