ZMP
hibadhb
Ensembl ID:
ZFIN ID:
Description:
3-hydroxyisobutyrate dehydrogenase b [Source:RefSeq peptide;Acc:NP_957454]
Human Orthologue:
HIBADH
Human Description:
3-hydroxyisobutyrate dehydrogenase [Source:HGNC Symbol;Acc:4907]
Mouse Orthologue:
Hibadh
Mouse Description:
3-hydroxyisobutyrate dehydrogenase Gene [Source:MGI Symbol;Acc:MGI:1889802]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2861 | Nonsense | F2 line generated | Not yet available |
| sa5622 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa2861
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006429 | Nonsense | 72 | 329 | 2 | 8 |
| ENSDART00000006429 | Nonsense | 72 | 329 | 2 | 8 |
The following transcripts of ENSDARG00000007959 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 22958695)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 21068446 |
| GRCz11 | 16 | 20874265 |
KASP Assay ID:
554-3070.1 (used for ordering genotyping assays)
KASP Sequence:
GATATCCAGTGATCGCCACAGATGTATTTCCAGAATCTTGCAAAGAGCTG[C/T]AGGAACTCGGAGCTCAGGTCAGGATAACAGACATAAAACTTTATAACATC
Long Flanking Sequence:
AGTTATTCCTTGCATAATTTCATTTAATCAGCCATATGTGTTTAGGGGTTAGTTTATCTAAAAATTTTAGTTTACTTACCCTCAAGTGGTTCTGAACTGGTTTAAAGTTTCTTTCATCTGTTGAACACAAAATAAGTTATTTTGTAAAATGTTAGATGCCTTTAACCATTGATGACATTGACACATTTTTCTAAATATCTTCTTTTGTGTTCAACGAAAGAAAGAAACTCCAACAGGTTTGTGACACATGAATGAGTAAATTTTCAGTTTTGTGTGAACTATCCTTTTAAATGCAAATATATTCAAAGTGAACTTCTAAAATTGACACTAAATATATAATGCATGTCTCTTCTTAAGTCTCCATCAGGTCAATGGCTTCTAAAACCCAGGTGGGCTTCATTGGCCTGGGGAACATGGGCAACCCAATGGCAAAGAACCTCATAAAACATGGATATCCAGTGATCGCCACAGATGTATTTCCAGAATCTTGCAAAGAGCTG[C/T]AGGAACTCGGAGCTCAGGTCAGGATAACAGACATAAAACTTTATAACATCTGATTTGTGTTAAATACCTTGATGTACAGGCTTTGTATGATTGATTTGGTAGTTGTTTTAGTCTGACAGTGTAGAGACCTATTTTATTTCTGACTGTTCTCAGATCCTGGATAGCCCTGCAGATGTAGCAGACAAGGCAGATCGCATCATCACAATGCTTCCCTCCAACCCCAATGTTGTAGATGTGTATACCGGACCAAATGGTATTTTAAAGTAAGGAGATCTTTTCTGTATGGACTAAATATTTTTATCTTAAGCACAACCTTTTAATTAAAAGTAACTCTTGAGTTTTAAAGAAAACAAATACAAATTCAACTTGGATTCAGTTTACTCTTTGGCCACACTTTATGTGTGTGTTTTGAAAAGGGGGTAAATCAGGGGCCTGTTTCAGTAAGGAGGTTCAAACAACTCAGAGTTTAAACTTGAACTCTGAGTTGATCTACCGAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5622
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006429 | Nonsense | 72 | 329 | 2 | 8 |
| ENSDART00000006429 | Nonsense | 72 | 329 | 2 | 8 |
The following transcripts of ENSDARG00000007959 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 22958695)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 21068446 |
| GRCz11 | 16 | 20874265 |
KASP Assay ID:
554-3070.1 (used for ordering genotyping assays)
KASP Sequence:
GATATCCAGTGATCGCCACAGATGTATTTCCAGAATCTTGCAAAGAGCTG[C/T]AGGAACTCGGAGCTCAGGTCAGGATAACAGACATAAAACTTTATAACATC
Long Flanking Sequence:
AGTTATTCCTTGCATAATTTCATTTAATCAGCCATATGTGTTTAGGGGTTAGTTTATCTAAAAATTTTAGTTTACTTACCCTCAAGTGGTTCTGAACTGGTTTAAAGTTTCTTTCATCTGTTGAACACAAAATAAGTTATTTTGTAAAATGTTAGATGCCTTTAACCATTGATGACATTGACACATTTTTCTAAATATCTTCTTTTGTGTTCAACGAAAGAAAGAAACTCCAACAGGTTTGTGACACATGAATGAGTAAATTTTCAGTTTTGTGTGAACTATCCTTTTAAATGCAAATATATTCAAAGTGAACTTCTAAAATTGACACTAAATATATAATGCATGTCTCTTCTTAAGTCTCCATCAGGTCAATGGCTTCTAAAACCCAGGTGGGCTTCATTGGCCTGGGGAACATGGGCAACCCAATGGCAAAGAACCTCATAAAACATGGATATCCAGTGATCGCCACAGATGTATTTCCAGAATCTTGCAAAGAGCTG[C/T]AGGAACTCGGAGCTCAGGTCAGGATAACAGACATAAAACTTTATAACATCTGATTTGTGTTAAATACCTTGATGTACAGGCTTTGTATGATTGATTTGGTAGTTGTTTTAGTCTGACAGTGTAGAGACCTATTTTATTTCTGACTGTTCTCAGATCCTGGATAGCCCTGCAGATGTAGCAGACAAGGCAGATCGCATCATCACAATGCTTCCCTCCAACCCCAATGTTGTAGATGTGTATACCGGACCAAATGGTATTTTAAAGTAAGGAGATCTTTTCTGTATGGACTAAATATTTTTATCTTAAGCACAACCTTTTAATTAAAAGTAACTCTTGAGTTTTAAAGAAAACAAATACAAATTCAACTTGGATTCAGTTTACTCTTTGGCCACACTTTATGTGTGTGTTTTGAAAAGGGGGTAAATCAGGGGCCTGTTTCAGTAAGGAGGTTCAAACAACTCAGAGTTTAAACTTGAACTCTGAGTTGATCTACCGAGAGA
Associated Phenotype:
Not determined