ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
runx2b
- ID
- ZDB-GENE-040629-4
- Name
- RUNX family transcription factor 2b
- Symbol
- runx2b Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Enables DNA-binding transcription factor activity and nuclear vitamin D receptor binding activity. Acts upstream of or within chondrocyte differentiation; dorsal/ventral pattern formation; and positive regulation of DNA-templated transcription. Predicted to be located in nucleus. Is expressed in several structures, including EVL; fin; osteoblast; pharyngeal arch; and skeletal system. Human ortholog(s) of this gene implicated in cleidocranial dysplasia; lung non-small cell carcinoma; and metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome. Orthologous to human RUNX2 (RUNX family transcription factor 2).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 95 figures from 72 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 | 
|---|---|---|---|
| cleidocranial dysplasia | Alliance | Cleidocranial dysplasia | 119600 | 
| cleidocranial dysplasia | Alliance | Cleidocranial dysplasia, forme fruste, dental anomalies only | 119600 | 
| cleidocranial dysplasia | Alliance | Cleidocranial dysplasia, forme fruste, with brachydactyly | 119600 | 
| metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome | Alliance | Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly | 156510 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Type | InterPro ID | Name | 
|---|---|---|
| Domain | IPR013524 | Runt domain | 
| Domain | IPR013711 | Runx, C-terminal domain | 
| Family | IPR000040 | Acute myeloid leukemia 1 protein (AML1)/Runt | 
| Family | IPR016554 | Runt-related transcription factor RUNX | 
| Homologous_superfamily | IPR008967 | p53-like transcription factor, DNA-binding domain superfamily | 
| Homologous_superfamily | IPR012346 | p53/RUNT-type transcription factor, DNA-binding domain superfamily | 
| Homologous_superfamily | IPR027384 | Runx, central domain superfamily | 
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | Acute myeloid leukemia 1 protein (AML1)/Runt | p53-like transcription factor, DNA-binding domain superfamily | p53/RUNT-type transcription factor, DNA-binding domain superfamily | Runt domain | Runt-related transcription factor RUNX | Runx, central domain superfamily | Runx, C-terminal domain | 
|---|---|---|---|---|---|---|---|---|---|
| UniProtKB:A0A8M1PMM2 | InterPro | 464 | |||||||
| UniProtKB:A0A8M9PSK4 | InterPro | 323 | |||||||
| UniProtKB:A0AB32T894 | InterPro | 646 | |||||||
| UniProtKB:A0AB32T8Z6 | InterPro | 619 | |||||||
| UniProtKB:A0AB32TA58 | InterPro | 501 | |||||||
| UniProtKB:A0AB32TDW2 | InterPro | 502 | 
- Genome Browsers
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis | 
|---|---|---|---|---|---|
| mRNA | runx2b-201
                             (1) | Ensembl | 1,707 nt | ||
| mRNA | runx2b-202
                             (1) | Ensembl | 1,533 nt | ||
| mRNA | runx2b-203
                             (1) | Ensembl | 1,128 nt | ||
| mRNA | runx2b-204
                             (1) | Ensembl | 675 nt | ||
| mRNA | runx2b-205
                             (1) | Ensembl | 2,491 nt | 
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
