Genomic Feature
mn0001Gt
- ID
- ZDB-ALT-111117-3
- Name
- mn0001Gt
- Synonyms
-
- GBT0001 (1)
- Gt(GBT-R15)mn0001
- Affected Genomic Region
- Construct
-
- Gt(GBT-R15) (1)
- Type
- Allele caused by Transgenic insertion (1)
- Protocol
- embryos treated with DNA
- Lab of Origin
- Stephen C. Ekker Laboratory
- Current Source
- Other Pages
Notes
No data available
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Chr: 23 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
- None
Fish
Supplemental Information
- Genotyping protocol
- None