Genomic Feature

hi1779Tg

ID
ZDB-ALT-040805-4
Name
hi1779Tg
Synonyms
  • hi1779 (1)
Affected Genomic Region
Construct
Type
Allele caused by Transgenic insertion (1)
Protocol
embryos treated with DNA
Lab of Origin
Hopkins Lab
Current Source
Zebrafish International Resource Center (ZIRC)    (order this)
Other Pages
Note
None
Genome Browser
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Variants
Variant Type
Transgenic Insertion
Variant Location
Chr 19: 40026771 - 40026772 (GRCz11) (1) Details
Nucleotide change
Variant Notes
The construct was inserted on the plus strand of the genome. The gene in which  ...
A 6-kb retroviral insertion at base 553 in the coding sequence leads to a  ...
Effect on DNA/cDNA, transcript, protein (from publications)
DNA/cDNA Change
Insertion in Exon 1 (1)
Transcript Consequence
None
Protein Consequence
Polypeptide Truncation: at position 197 (1)
Sequences
Flanking Sequence
None
Additional Sequence
None
Fish
Supplemental Information
Genotyping protocol
None
Citations