Genomic Feature
la017672Tg
- ID
- ZDB-ALT-120806-11681
- Name
- la017672Tg
- Synonyms
-
- la017672
- Affected Genomic Region
- Construct
- Type
- Allele caused by Transgenic insertion (2)
- Protocol
- embryos treated with DNA
- Lab of Origin
- Burgess & Lin Lab
- Current Source
- Other Pages
Notes
No data available
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Chr 11: 13296236 - 13296246 (Zv9) Details
- Nucleotide change
- Variant Notes
- None
Effect on DNA/cDNA, transcript, protein (from publications)
- DNA/cDNA Change
- None
- Transcript Consequence
- None
- Protein Consequence
- None
- Flanking Sequence
- None
- Additional Sequence
- GenBank:JS885916 (2)
Fish
Supplemental Information
- Genotyping protocol
- None