Genomic Feature
hi1779Tg
- ID
- ZDB-ALT-040805-4
- Name
- hi1779Tg
- Synonyms
-
- hi1779 (1)
- Affected Genomic Region
- Construct
- Type
- Allele caused by Transgenic insertion (1)
- Protocol
- embryos treated with DNA
- Lab of Origin
- Hopkins Lab
- Current Source
- Zebrafish International Resource Center (ZIRC) ( order this )
- Other Pages
Notes
| Comment | Citation |
|---|---|
| The construct was inserted on the plus strand of the genome. The gene in which ... | ZFIN Curated Data |
| A 6-kb retroviral insertion at base 553 in the coding sequence leads to a ... | Lowery et al., 2007 |
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Chr 19: 40026771 - 40026772 (GRCz11) (1) Details
- Nucleotide change
- Variant Notes
Effect on DNA/cDNA, transcript, protein (from publications)
- DNA/cDNA Change
- Insertion in Exon 1 (1)
- Transcript Consequence
- None
- Protein Consequence
- Polypeptide Truncation: at position 197 (1)
- Flanking Sequence
- None
- Additional Sequence
- None
Fish
Supplemental Information
- Genotyping protocol
- None