ZMP
ogdh
Ensembl ID:
ZFIN ID:
Description:
oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) [Source:RefSeq peptide;Acc:NP_957073]
Human Orthologue:
OGDH
Human Description:
oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) [Source:HGNC Symbol;Acc:8124]
Mouse Orthologue:
Ogdh
Mouse Description:
oxoglutarate dehydrogenase (lipoamide) Gene [Source:MGI Symbol;Acc:MGI:1098267]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34482 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31676 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34482
Status:
Mutation detected in F1 DNA
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022242 | Essential Splice Site | 312 | 1024 | 6 | 22 |
| ENSDART00000046064 | None | None | 175 | None | 3 |
| ENSDART00000132965 | None | None | 230 | None | 5 |
| ENSDART00000148206 | Essential Splice Site | 312 | 1022 | 7 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 47943162)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 45781420 |
| GRCz11 | 8 | 45789299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCAGTGAGAACGGCGTAGACACTGTCATCATGGGCATGCCTCACAGG[T/C]ACAGGACAAGATGCAGCGATAGAGATAGAAAGGATAGATAGAAGGAGAGA
Long Flanking Sequence:
GCATGTTGGAAAGGAAAAACACATTCTGTGGGAACCACCCCTAAGACTGAAAGACATCAAAGTGAAAGGAGTGTGCTGAAGCAGTTGCTAATGAAAGATGCTAAAACAGCTGAGCTTTCATTTTATAACGTTGTTTCATTATTAGTAGTAGTAGTAGTAGTAATAGTAGTAGTTATAATACTATGTGCTGTCTAATAAAACACACGCCAATCAAATTGAAATGTTTATTTTGACTGGATTGCATATAAACAACAAATACATGGATGTATGTATTTTTTGTCTTTAGTCGTTGAACCCCTATTTACATTTAAATCACAGCTTTGTTCTTGAGCATGTGTGTTGCTTTCTGAAGGTTTGAGGAGTTCCTGCAGAGGAAATGGTCATCTGAGAAACGCTTCGGACTGGAAGGCTGTGAAAGTCTGATCCCTGCACTCAAAACCATCATTGATAAATCCAGTGAGAACGGCGTAGACACTGTCATCATGGGCATGCCTCACAGG[T/C]ACAGGACAAGATGCAGCGATAGAGATAGAAAGGATAGATAGAAGGAGAGAAAATTGATACTACAGTGTCATACAGCGATTCATAATTGACCTTTTGTTATTTTTCTGCATTTTTTTGTAGAGGACGTTTGAACGTGCTTGCCAATGTGATCCGTAAGGAATTGGAGCAAATTTTCTGTCAGTTTGACTCTAAATTGGAAGCTGCTGATGAGGTCGGTGGCGTTTTGTTACTATTTGTTATTCTCATTTATTCATTTGATCAAACCTAAGATTTATTTGTTTGTTTGTTTGTGTCTCTGTACCTGCAATAGGGGTCAGGAGATGTCAAGTACCACTTGGGCATGTACCACAGGAGAATAAATCGTGTGACTAACAGGAATATTACCTTGTCATTGGTGGCCAACCCTTCCCATCTAGAAGCGGTGAACCCGGTGGTGCAGGGCAAGACTAAGGCTGAGCAGTTTTACAGCGGAGATACTGATGGAAAAAGGGTGAGATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31676
Status:
Available for shipment
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:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022242 | Essential Splice Site | 556 | 1024 | 11 | 22 |
| ENSDART00000046064 | None | None | 175 | None | 3 |
| ENSDART00000132965 | None | None | 230 | None | 5 |
| ENSDART00000148206 | Essential Splice Site | 556 | 1022 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 47940138)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 45778396 |
| GRCz11 | 8 | 45786275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCTGAGAAGCTCATTGCTGAAGGTGCCGTTACGCGACAGGAGTATGAG[G/A]TCCGTCAGCCAGAGATAATTTAGCTGCCTTTTATCCTCAGCTGGACCTTA
Long Flanking Sequence:
CAAATTAAATTGGCCGACCAGCTAAATTTGGCTTCAAGATATAGACCCTAGATTTCCTCATAATGTCTGCATCTCTCTTTCAGATCGGTTTCACTACAGATCCCCGTATGGCACGCTCATCTCCATATCCAACCGATGTTGCCCGTGTGGTCAATGCCCCTATCTTCCACGTCAATGCAGATGATCCTGAAGCTGTGATGTACGTGTGTAATGTGGCCGCAGAATGGAGGGCCACCTTCCACAAAGATGTGGTGGTGGATCTGGTGAGTTCTAGTGTATTTCTGACTTTTACCATCACAATTACTTTTATTTTCATGTTTTAGCTCTTATGACTTGTTTACATTTAGGTGTGCTATCGACGTAATGGCCACAACGAGATGGATGAGCCAATGTTCACTCAGCCACTGATGTACAAACAGATCAAGAAGCAGAAAGGAGTTCTGCAGAAATACGCTGAGAAGCTCATTGCTGAAGGTGCCGTTACGCGACAGGAGTATGAG[G/A]TCCGTCAGCCAGAGATAATTTAGCTGCCTTTTATCCTCAGCTGGACCTTAAAAGTGTTCTTCCATCTCTTTCCACAGGAAGAGATTGCGAAGTATGATAAAATCTGTGAGGAAGCTCATTCTCGCTCTAAGGATGAGAAGATCCTTCACATCAAGCACTGGCTGGACTCCCCCTGGCCAGGTGTGTACACAGTGTCTGAAAGCCGGTCCCCAGATGGCACAGTGCCCAGCACAAATTAGTATTTCTTAGAAAAAACTACTTCTTAGATCTTGCTTCAGAATTAAAGAGCTCCTATTATACATTATAAAAGGTCATATTTTGGTTTTGGGGGTCTCCAACAACAGGCTGATATGCATGCAAGCTCAAAAAACACTTTTATTGTCTCATAATATGCATTTATTTTTACCTAATTATCCCAGCTACTCCCATATTATTTGTTCAACTATTCATTTGTTCCCAAACCTATTCTTATAGCGATGCTAATCTGCGCTGATTGGTCT
Associated Phenotype:
Not determined