Genomic Feature
fcc382p2Gt
- ID
- ZDB-ALT-160426-35
- Name
- fcc382p2Gt
- Synonyms
-
- Tg(GBT-B4)fcc382-P2 (1)
- Affected Genomic Region
- Construct
- Type
- Allele caused by Transgenic insertion (1)
- Protocol
- embryos treated with DNA
- Lab of Origin
- Rhodes Lab
- Current Source
- Other Pages
Notes
| Comment | Citation |
|---|---|
| GFP expression at 6 dpf in nerves in the brain, vagus nerve and jaw. | Seiler et al., 2015 |
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Unmapped
- 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