ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
grnb
- ID
- ZDB-GENE-030131-7393
- Name
- granulin b
- Symbol
- grnb Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - fj14b08
- wu:fj14b08
- zfPGRN-B (1)
- zgc:111858
 
- Type
- protein_coding_gene
- Location
- Chr: 24 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Acts upstream of or within axon extension. Predicted to be active in extracellular region. Is expressed in several structures, including central nervous system; gut; immature eye; mesoderm; and pleuroperitoneal region. Human ortholog(s) of this gene implicated in dementia (multiple); neurodegenerative disease (multiple); neuronal ceroid lipofuscinosis 11; and primary progressive multiple sclerosis. Orthologous to human GRN (granulin precursor).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 9 figures from 6 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
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        - MGC:111858 (1 image)
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- 1 Figure from Laird et al., 2010
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | Alliance | Aphasia, primary progressive | 607485 | 
| GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | Alliance | Frontotemporal dementia 2 | 607485 | 
| neuronal ceroid lipofuscinosis 11 | Alliance | Ceroid lipofuscinosis, neuronal, 11 | 614706 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Granulin | Granulin family | Granulin superfamily | 
|---|---|---|---|---|---|
| UniProtKB:F1R6I2 | InterPro | 729 | |||
| UniProtKB:Q7T3M4 | InterPro | 729 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
