Genomic Feature

hi1841bTg

ID
ZDB-ALT-020426-34
Name
hi1841bTg
Synonyms
  • hi1841b (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
Notes
Comment Citation
The construct was inserted on the plus strand of the genome. The gene in which  ... ZFIN Curated Data
Genome Browser
Genome Build: GRCz11Chromosome: 17
Variants
Variant Type
Transgenic Insertion
Variant Location
Chr 17: 51744104 - 51744105 (GRCz11) (1) Details
Nucleotide change
Variant Notes
The construct was inserted on the plus strand of the genome. The gene in which  ...
Effect on DNA/cDNA, transcript, protein (from publications)
DNA/cDNA Change
Insertion in Intron 1 (1)
Transcript Consequence
None
Protein Consequence
None
Sequences
Flanking Sequence
None
Additional Sequence
None
Fish
Fish Genomic Feature Zygosity Parental Zygosity Affected Genomic Regions Phenotype Gene Expression
odc1hi1841bTg/hi1841bTgHomozygousUnknowntext only from Amsterdam et al., 2004
odc1hi1841bTg/+ (AB)HeterozygousUnknown
odc1hi1841bTg/+ (AB/TU)HeterozygousUnknown
odc1hi1841bTgUnknownUnknownFig. for (hi1841b) with image from Phenotype Annotation (1994-2006)
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Supplemental Information
Genotyping protocol
hi1841btg.pdf
Citations