ZMP
LOC559207
Ensembl ID:
Human Orthologues:
OGDH, OGDHL
Human Descriptions:
oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) [Source:HGNC Symbol;Acc:8124]
oxoglutarate dehydrogenase-like [Source:HGNC Symbol;Acc:25590]
oxoglutarate dehydrogenase-like [Source:HGNC Symbol;Acc:25590]
Mouse Orthologues:
Ogdh, Ogdhl
Mouse Descriptions:
oxoglutarate dehydrogenase (lipoamide) Gene [Source:MGI Symbol;Acc:MGI:1098267]
oxoglutarate dehydrogenase-like Gene [Source:MGI Symbol;Acc:MGI:3616088]
oxoglutarate dehydrogenase-like Gene [Source:MGI Symbol;Acc:MGI:3616088]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10136 | Nonsense | Available for shipment | Available now |
sa30973 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18242 | Essential Splice Site | Available for shipment | Available now |
sa12904 | Nonsense | Available for shipment | Available now |
sa2685 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa10136
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113009 | Nonsense | 378 | 1008 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 29596588)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29242536 |
GRCz11 | 13 | 29372986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCACCTTGAGGCTGTAGATCCTGTCRTTCAGGGCAAGACCAAAGCAGAG[C/T]AGTTTTACAGAGGAGAYACTGAAGGAAGRAGGGTGAAACANNNATTTTCAGAT
Long Flanking Sequence:
CATCCCTGCGCTGAAGATGATCATCGACAAGTCCAGTGAAGCTGGTATAGAAAGTGTAATTATGGGAATGCCTCACAGGTACGTCTGAAACCTGCACCATTCAATCTCACCCTGCTCTTATGAATTCACCCCAGCAATAATAACACAACCTCCGCTTCACTCAGGGGAAGACTGAACGTTCTGGCCAACGTAGTTCGCAAGGATTTGGATCAAATATTCTGTCAGTTTGATCCCAAACTGGAGGCTGCAGATGAGGTGATTTAGTTTGAAGAGCGAGGATTTTGTCATCTCAAATACTTCATTCTCTTATGGTGCTTTTTCTAATGTAAGCTTTACACTTTAATCTACTCCAGGGCTCAGGAGATGTGAAATATCACTTGGGGATGTACCATGAACGGATAAACAGGGAAACGGATAAGAATATCACATTGTCACTAATGGCTAACCCATCTCACCTTGAGGCTGTAGATCCTGTCGTTCAGGGCAAGACCAAAGCAGAG[C/T]AGTTTTACAGAGGAGACACTGAAGGAAGGAGGGTGAAACAATTTTCAGATTATCATTACATATGAAAAACATAACCACATTTTCTGCCTTTTCTGTTATATAATGGCTCAACATTTTGGCATGTTAGAAGAATACAAATTAGATACACAAGATATTGGATAAAACTATTAGGAAAAAAGATGGCTTGAGTAGCTTAATTTGGAAAGAAACTGTAATTTTGTATTGCTCTGGGTAATTTTAGGGTAATGCATCTTCATAAAATATAAAAATTTCCAAGCATTGATAAATGCAATGAAGCTAAGATACAAACAATGCTTTGTGGCTTATATTCTGTTACTGAAATGTAATAATCAAATGTAAAATATCACTATATAGTCCTCATCTCATAAATAAATACCAACGATTTTTTTGTTAAAGCTACTATATTATTTCTTATGCCAGAATGCTTTAAACTAAGTTTAAATGCTTTTAAAAAGCTGCTTCTCCTATTTTCAAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30973
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113009 | Nonsense | 474 | 1008 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 29598087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29244035 |
GRCz11 | 13 | 29374485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCTTCCACGTCAACGCTGATGACCCAGAGGCTGTGATGTATGTGTGC[A/T]AGATTGCAGCAGAGTGGAGAACCACTTTCAACAAGGATGTGGTGATTGAC
Long Flanking Sequence:
TGTGGAGACTGGTAAAATCCGGACTTGAAATTTTACATTGATGCGTACATTGCGAGGTTGATCCTGAAATGATATATTGTGCAGCCCTGATATAAATAAATAGTTCAAATCATGAGTGAATTTGATTGTTCTCCAGGTGATGTCAATTCTCATGCATGGTGATGCTGCGTTTGCCGGTCAGGGAGTCGTCTATGAAACCTTCCATCTCAGTGAACTGCCTTCATATACTACTTATGGCACCATCCATGTGGTTGTCAATAATCAGGTTAGCATCAAACATCAGATTTTCCTATTAGAGTCCTGAGGTGAAGCAGGATCGTAACCCCTGACCTTTAGCATGTTGTAGATTGATGAGTGTTATCTGATGTTGCCAGATTGGATTCACAACTGATCCGCGAATGGCACGGTCATCGCCCTATCCAACAGATGTGGCTCGCGTGGTCAACGCACCCATCTTCCACGTCAACGCTGATGACCCAGAGGCTGTGATGTATGTGTGC[A/T]AGATTGCAGCAGAGTGGAGAACCACTTTCAACAAGGATGTGGTGATTGACCTGGTAAATTCTGTGAAGACACAGCCTACATATCACAAAAAAATTTAATTGAACGTGAAGATAAATCTCTTGAAAACTGCTCCAGTGCTTGACTAGAGATCCATTATCATGGTACAAGAATCATGTTTTCTCTTACAAAAAATCATGTTTTCTCTTAAAACTTAATTACTTCAATCTGAAAATAAAGCAATCTATCTAACAGACACAAATGTCAAAACTATGAGTGTAATTGACCCTTAATGATCATACTGACAGCATTTAACCATTTAACGCATAATCACCAAACACTGAAACACACTTAGTAAAATTTTTGCTCTCACATTATATTGTACAATGTACAATCAGGTACAATCAATTTTACACTGTAACTCTTTTTACTTATCTGTATGTAATTACATATGTTATTTATTTCTGCAATTACATTTATCCCAATACCTTGCTCATTACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18242
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113009 | Essential Splice Site | 491 | 1008 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 29598142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29244090 |
GRCz11 | 13 | 29374540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGCAGAGTGGAGAACCAYTTTCAACAAGGATGTGGTGATTGACCTGG[T/C]AAATKCTGTGAAGACACAGCCTACATATCACAAAAAAATTTAATTGAACG
Long Flanking Sequence:
GGTTGATCCTGAAATGATATATTGTGCAGCCCTGATATAAATAAATAGTTCAAATCATGAGTGAATTTGATTGTTCTCCAGGTGATGTCAATTCTCATGCATGGTGATGCTGCGTTTGCCGGTCAGGGAGTCGTCTATGAAACCTTCCATCTCAGTGAACTGCCTTCATATACTACTTATGGCACCATCCATGTGGTTGTCAATAATCAGGTTAGCATCAAACATCAGATTTTCCTATTAGAGTCCTGAGGTGAAGCAGGATCGTAACCCCTGACCTTTAGCATGTTGTAGATTGATGAGTGTTATCTGATGTTGCCAGATTGGATTCACAACTGATCCGCGAATGGCACGGTCATCGCCCTATCCAACAGATGTGGCTCGCGTGGTCAACGCACCCATCTTCCACGTCAACGCTGATGACCCAGAGGCTGTGATGTATGTGTGCAAGATTGCAGCAGAGTGGAGAACCACTTTCAACAAGGATGTGGTGATTGACCTGG[T/C]AAATTCTGTGAAGACACAGCCTACATATCACAAAAAAATTTAATTGAACGTGAAGATAAATCTCTTGAAAACTGCTCCAGTGCTTGACTAGAGATCCATTATCATGGTACAAGAATCATGTTTTCTCTTACAAAAAATCATGTTTTCTCTTAAAACTTAATTACTTCAATCTGAAAATAAAGCAATCTATCTAACAGACACAAATGTCAAAACTATGAGTGTAATTGACCCTTAATGATCATACTGACAGCATTTAACCATTTAACGCATAATCACCAAACACTGAAACACACTTAGTAAAATTTTTGCTCTCACATTATATTGTACAATGTACAATCAGGTACAATCAATTTTACACTGTAACTCTTTTTACTTATCTGTATGTAATTACATATGTTATTTATTTCTGCAATTACATTTATCCCAATACCTTGCTCATTACTCATACTAAACCTAAATCTGTCCCTGTTCCACCTCAAAAGCATCAAAGAATATGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12904
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113009 | Nonsense | 795 | 1008 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 29621406)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29267354 |
GRCz11 | 13 | 29397804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACGGCCTGAACGCTTCCTGCAGATGAGCAAAGATGACCCCGATCGCTA[T/A]CCGGTGAGTGGTCCTTCCTGCAATGCCTCATGCTGATGGCCACAGGTAGT
Long Flanking Sequence:
ACCATGAAATTCTACATGAAAATCATTTCTCCAGAATTTTCCCCCACTGTTTGTAAACATACAAGAATCTGTTCCATTTACATACGTAATTTAAAGCACCCAGGACATCAGCATAAATATCATGTAATATTTAACAGCTTATTTTCTCTGATTTGCCCAGTGAAACCCAGTGTTATTTTTAGAATCTGTTATGTACTGTAGATAACAACAGCCCATACAGATCACTGAATCTAATGATGTAAAAGACTGGCTAAACTCCTTTTGTTTCTTTTTACTCAAAGGCAGAATAGCAGTACTAAGATCAATAATGATGACTCAAGTTTGGTGTAAGCCGATAAATGAGGCTATAATTCTTCAGCTCAGTGTGCCGTTTGATAGAGCTCCTCTCATTAGCGCTGGTGTGTGTGTGTGTGTGTTTGCACTAATGAACAGGGCCCGGAGCACTCGTCAGCACGGCCTGAACGCTTCCTGCAGATGAGCAAAGATGACCCCGATCGCTA[T/A]CCGGTGAGTGGTCCTTCCTGCAATGCCTCATGCTGATGGCCACAGGTAGTTGGAAACGGACACACTTCACTGATTGCCAATTTGTTTGATGCTTAATATAGTTCTTGTTGATACTGCTTTCCTGTTTAGTCCAGCAGTGTCAGTCGCAGTGGCAGGGCATCATGAATAAACACATTCAGGGGTACAGGGATAGTAGTTACAGCTCTGATCAGTATTTAGAAGATGTAATCATTAAACAGGGAAAAGGCCAAACCAGACAGGAATTAGTTAATGGCAGGGTTATTATTTTTAACTAAAAGTAAATACTAATACTATGTATGCAGTGGTGTAAGTGTTTGTACCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCGTTTATTCGTTCATTAATTAATTTATTCATTTATTCATTCATGGAATAAAAGTAACACCAAATTTCAGAAAAAGACATCAGACCAGTAGTAAAATGTGGTGATGGTCTGGGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2685
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 |
---|---|---|---|---|---|
ENSDART00000113009 | Nonsense | 903 | 1008 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 29626004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29271952 |
GRCz11 | 13 | 29402402 |
KASP Assay ID:
554-2608.1 (used for ordering genotyping assays)
KASP Sequence:
TCATCTTCWGCACTGGAAAGGTGTACTATGAGCTAGCCAAAGAAAGAAAA[C/T]AGCTGAAGTTGGAAGAGAATGTTGCAATAGTCCGACTGGAGCAGGTCGCC
Long Flanking Sequence:
TGTTTTTGAGGTTTAACACTTTATTTAATAAAAAAAAGCATATTGCTACTCTGTTGTTAATTATTTTTTATGTATAATAATTTATCCAATTTCCATGTTTTTCCCAAGACTAGAAATAAATTTCAGTTTTCAAAATTGTTAAACTTCTTATATATTTCAGCTATATGGAAACCAAAGTTCTTGGATGTAAAATTATTGGATATTAAAAGGATAACTTAAAATAAGAAACATAAAAAAACAAGTTTTAAAAACTTCTTAAGCTTGTTTTCAACCACACTGTGTATGATTTTAGATCATATTGCCATGACCCCCTGATTGAAAACAATGGCTTTAAACTGTTCCCAACTTTGGTGGATAAAATTTCTAACTTTCTCTTTGCAGGGACAAAATTTATCAGGGTAATTCCAGATGATGGCCCTGCATCCAAAAACCCTGAAAAGGTCAAAAGGGTCATCTTCTGCACTGGAAAGGTGTACTATGAGCTAGCCAAAGAAAGAAAA[C/T]AGCTGAAGTTGGAAGAGAATGTTGCAATAGTCCGACTGGAGCAGGTCGCCATAATAGTTTCTTTATTTTAAGTACAATTGCACAGAAAAAAAAATTACTTTCTTTGTCAGAAACATCAAATACATTTTTTTTTTATCTTAGATATCGCCATTCCCTTTTGACCTCATCAAGGCTGAGGTTGAGAAGTACAGCAATGCTGAACTCATATGGTGTCAGGAGGAGCACAAGAACATGGGCTACTATGATTACATAAGGCCACGTTTCCTCACAGTCCAACCAAAGAATCCAATATGGTAAGTGTCTTTTGGAGATAAATGTTTGAGCCACTTAAACAAAAGTACAGTGGAGATCAAACTCAGGTCAGTGTTATGTCTTGTTTGAGATTATCCTAACATGATTAAAAGAGCATATATTTTAAAGGACAGTTTAATTTGTTTGGGTCTGATGGGAAACATTGTGCTCTATTTTAATTTAAGTGCATACAGTAGCACACATAATCT
Associated Phenotype:
Not determined