Genomic Feature
mn0067Gt
- ID
- ZDB-ALT-111118-5
- Name
- mn0067Gt
- Synonyms
-
- GBT0067 (1)
- Gt(GBT-RP2)mn0067
- Affected Genomic Region
- Construct
-
- Gt(GBT-rp2) (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
| Comment | Citation |
|---|---|
| integration site is located within intron 24 of myom3 (J. Xu et al., 2012) | Xu et al., 2012 |
Variants
- Variant Type
- Transgenic Insertion
- Variant Location
- Unmapped
- Nucleotide change
- Variant Notes
-
integration site is located within intron 24 of myom3 (J. Xu et al., 2012)
Effect on DNA/cDNA, transcript, protein (from publications)
- DNA/cDNA Change
- Insertion in Intron 24 (1)
- Transcript Consequence
- None
- Protein Consequence
- None
- Flanking Sequence
- None
- Additional Sequence
- None
Fish
Supplemental Information
- Genotyping protocol
- None