ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
meox1
- ID
 - ZDB-GENE-040718-149
 - Name
 - mesenchyme homeobox 1
 - Symbol
 - meox1 Nomenclature History
 - Previous Names
 - Type
 - protein_coding_gene
 - Location
 - Chr: 12 Mapping Details/Browsers
 - Genome Assembly
 - GRCz12tu
 - Annotation Status
 - Current
 - Description
 - Enables DNA-binding transcription factor activity; chromatin binding activity; and sequence-specific DNA binding activity. Involved in hematopoietic stem cell differentiation and somite development. Acts upstream of or within several processes, including developmental pigmentation; muscle cell development; and skeletal system development. Located in nucleus. Is expressed in several structures, including fast muscle myoblast; medial rectus; paraxial mesoderm; pectoral fin; and tail bud. Used to study Klippel-Feil syndrome. Human ortholog(s) of this gene implicated in Klippel-Feil syndrome 2. Orthologous to human MEOX1 (mesenchyme homeobox 1).
 - Genome Resources
 - Note
 - None
 - Comparative Information
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- All Expression Data
 - 12 figures from 6 publications
 - Cross-Species Comparison
 - High Throughput Data
 - Thisse Expression Data
 - No data available
 
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
 - 23 figures from 8 publications
 - Cross-Species Comparison
 - Alliance
 
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Klippel-Feil syndrome 2 | Alliance | Klippel-Feil syndrome 2 | 214300 | 
| Human Disease | Fish | Conditions | Citations | 
|---|---|---|---|
| Klippel-Feil syndrome | meox1tm26/tm26 (TU) | standard conditions | Dauer et al., 2018 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Homedomain-like superfamily | Homeobox, conserved site | Homeobox protein MOX-1/MOX-2 | Homeodomain | Homeodomain, metazoa | 
|---|---|---|---|---|---|---|---|
| UniProtKB:F1Q4R9 | InterPro | 253 | |||||
| UniProtKB:A0A8M9PW63 | InterPro | 181 | 
- Genome Browsers
 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers