Genomic Feature
hu1798
- ID
- ZDB-ALT-180814-2
- Name
- hu1798
- Synonyms
- None
- Affected Genomic Region
- Construct
- None
- Type
- Allele with one point mutation (1)
- Protocol
- adult males treated with ENU
- Lab of Origin
- Schulte-Merker
- Current Source
- Other Pages
Notes
No data available
Variants
- Variant Type
- Point Mutation
- Variant Location
- Chr: 19 Details
- Nucleotide change
- Variant Notes
-
Missense mutation H239Q caused by an A>T substitution in exon 5
Effect on DNA/cDNA, transcript, protein (from publications)
- DNA/cDNA Change
- A>T in Exon 5 (1)
- Transcript Consequence
- Missense (1)
- Protein Consequence
- Amino Acid Substitution: His>Gln at position 239 (1)
- Flanking Sequence
-
- Additional Sequence
- None
Fish
Supplemental Information
- Genotyping protocol
- None