PUBLICATION
            Retrieval and display of variant and flanking sequences
- Authors
- ZFIN Staff
- ID
- ZDB-PUB-191030-9
- Date
- 2019
- Source
- Semi-automated Curation : (Curation)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- none
            Citation
        
        
            ZFIN Staff (2019) Retrieval and display of variant and flanking sequences. Semi-automated Curation. .
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                ZFIN retrieves and displays flanking sequences for variants which have been mapped to an Ensembl genome build.
Genomic coordinates of variants are curated from publications by ZFIN curators, or submitted directly to ZFIN by collaborators. For variants that have been mapped to the latest genomic build, ZFIN retrieves 500 bp of upstream and downstream sequences flanking the variants, based on the curated/submitted coordinates.
The wild-type reference sequence, the variant sequence, and flanking sequences are displayed on feature pages in the following format:
Reference/Variant (in red)
500 bp downstream sequence
        
        
    
    
    The wild-type reference sequence, the variant sequence, and flanking sequences are displayed on feature pages in the following format:
500 bp upstream sequence
Reference/Variant (in red)
500 bp downstream sequence
All displayed sequences are on the forward (plus) genomic strand of the Ensembl genomic build specified in the "Location" section of the feature page. To obtain more detailed information about these processes or to send comments, please contact ZFIN.
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    