Genomic Feature
fcc418p1Gt
- ID
- ZDB-ALT-160426-37
- Name
- fcc418p1Gt
- Synonyms
-
- Tg(GBT-B4)fcc418-P1 (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 2 dpf in the epiphysis, dorsal eye, hindbrain, spinal cord ... | Seiler et al., 2015 |
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Chr: 25 Details
- Nucleotide change
- Variant Notes
- None
Effect on DNA/cDNA, transcript, protein (from publications)
- DNA/cDNA Change
- None
- Transcript Consequence
- Splicing Variant (1)
- Protein Consequence
- Polypeptide Truncation (1)
- Flanking Sequence
- None
- Additional Sequence
- None
Fish
Supplemental Information
- Genotyping protocol
- None