Genomic Feature

hi3821Tg

ID
ZDB-ALT-040721-8
Name
hi3821Tg
Synonyms
  • hi3821 (1)
Affected Genomic Region
Construct
Type
Allele caused by Transgenic insertion (1)
Protocol
embryos treated with DNA
Lab of Origin
Hopkins Lab
Current Source
Other Pages
Note
None
Genome Browser
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Variants
Variant Type
Transgenic Insertion
Variant Location
Chr 23: 12880216 - 12880217 (GRCz11) (1) Details
Nucleotide change
Variant Notes
The construct was inserted on the minus strand of the genome. The gene in which  ...
Effect on DNA/cDNA, transcript, protein (from publications)
DNA/cDNA Change
Insertion in Exon 16 (1)
Transcript Consequence
None
Protein Consequence
None
Sequences
Flanking Sequence
None
Additional Sequence
None
Fish
Supplemental Information
Genotyping protocol
None
Citations