Genomic Feature
c262Tg
- ID
- ZDB-ALT-110805-3
- Name
- c262Tg
- Synonyms
-
- Tg(5xERE:EGFP)c262
- Affected Genomic Region
- This feature is representative of one or more unknown insertion sites.
- Construct
- Type
- Transgenic insertion (1)
- Protocol
- embryos treated with DNA
- Lab of Origin
- Halpern Lab
- Current Source
- Other Pages
Notes
| Comment | Citation |
|---|---|
| Insertion is located in an intron of cstf1 (formerly zgc:77560). | ZFIN Staff |
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Unmapped
- Nucleotide change
- Variant Notes
-
Insertion is located in an intron of cstf1 (formerly zgc:77560).
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