Genomic Feature

nkhg21cEt

ID
ZDB-ALT-100113-6
Name
nkhg21cEt
Synonyms
  • Et(T2KHG)nkhg21c (1)
  • nkhg21c (1)
Affected Genomic Region
Construct
Type
Allele caused by Transgenic insertion
Protocol
embryos treated with DNA
Lab of Origin
K. Kawakami Lab
Current Source
Other Pages
Notes
Comment Citation
AB353984; Fin folds ZFIN Staff
Genome Browser
Variants
Variant Type
Transgenic Insertion
Variant Location
Chr: 21 Details
Nucleotide change
Variant Notes
AB353984; Fin folds
Effect on DNA/cDNA, transcript, protein (from publications)
DNA/cDNA Change
None
Transcript Consequence
None
Protein Consequence
None
Sequences
Flanking Sequence
None
Additional Sequence
GenBank:AB353984 (1)
Fish
Supplemental Information
Genotyping protocol
None
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.