ZMP
si:ch211-229p19.3
Ensembl ID:
ZFIN ID:
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11227 | Nonsense | Available for shipment | Available now |
sa34993 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11227
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 |
---|---|---|---|---|---|
ENSDART00000013485 | Nonsense | 534 | 1023 | 11 | 22 |
ENSDART00000139214 | Nonsense | 534 | 1023 | 12 | 23 |
The following transcripts of ENSDARG00000073805 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 46172846)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45338230 |
GRCz11 | 10 | 45184842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAYGAGCCCATGTTTACTCAACCGCTGATGTACAAACAGATCAAGAAG[C/T]AGAAACCTGTTCWGCAGAAATATGYGGAGAAGCTGATCGCAGAAGGAGCT
Long Flanking Sequence:
GGCAGGTTTATTTATATAGCACATTTCATACACAATGGTAATTCAAAGTGCTTTACAAGGAATAAAATTGATTAAAAACAGATTAAAATTTTTTAAAGGAATGAAAAGGAAAAGAGAGACATAATCGTGTGATCTGAGCTCATTCAGTAAAGGCACAGCTAAACAGATGTGTGTTCAGTGTTGATGTGCATGTGCCTAATGTTGGTGCACACGTATAGTAAAGTTGATGTGTATAGGGTGGACAGCCTTTATAGACTATACACTACATAAGCTGTCCACCCTATACACATCAACTTAACTGTCTGATTTTGATTGTAATGTATTAACATGCACCTTTTGTAAAGCTTACATAATAACCTATAATAATTGTGAAAAGCACCATGCAAATGAGACTGAACTGAATACGTTGTTGTGTACAGGTGTCCTACAGACGGAACGGCCACAACGAGATGGACGAGCCCATGTTTACTCAACCGCTGATGTACAAACAGATCAAGAAG[C/T]AGAAACCTGTTCTGCAGAAATATGCGGAGAAGCTGATCGCAGAAGGAGCTGTGACCAGACAGGAATACGAGGTCAGGACAAACCTGTTTTTACTATTTAACCCCTAAATGGTGCTTTGAAATGTGCATTTTTTAATTCGATGTTTGACGCAATCTCAGCTGAAACATGAAGAGAGGGTGGGACATAGTGTAGCTCCTCCTCCTTAAAAAAATAGCCAATAACGTGTTGTTTTTCTTACAGCTCTGCCAGTGAGAGTGGTTAAGCTCAAGCTCATTAAGTGAAAAGCCAATGAAAAGAAGGGGGCGGGGCATGTCAGACACTAGAGAGCATTTGATTGGTCGAAATATTTGATGATGAACTGAAGTATAAGGAGACGGCAAAAATCCTTGATCCATTAAGGCTGAAAAGACATACAGCAAACTGTGTTTTTATCTTCTAAATGTAAAATGTGATTGAGCCACAAAGAAAATGAATAAATGGTTTATATTCTACATAGGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34993
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013485 | Nonsense | 648 | 1023 | 14 | 22 |
ENSDART00000139214 | Nonsense | 648 | 1023 | 15 | 23 |
The following transcripts of ENSDARG00000073805 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 46170249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 45340827 |
GRCz11 | 10 | 45187439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGTTTGCAGGTCTGAGCCGTATCTTGAAGAGCCGGTCGCTGATGGTG[C/T]AGAACCGCTCTGTGGACTGGGCTCTGGGCGAATATATGGCGTTCGGTTCG
Long Flanking Sequence:
CCATGAGCTGTCCGTCCACTGGCCTCAGTGAGGAAACTCTGGCGCACATCGGGCAGACGGCTTCATCCGTTCCTGTGGAGGATTTCACTATACATGGAGGTGTGTGTGTGTTACACGGCTGTCAGGAATACTGTATTCTGATTGGTCAGTTGTGGCATTTCCAGGTCTGTTATTGCCAGATAACACCCGCTGAATAACACAGACTCATATGGATGAACATCTTTACTTACGGTGATTCTCAGCTCCTGGATGAGTGTGTGTTATTTAGCGGGTGTTATCTGGCATTAGCAGAGCTTGGATTGTCACGACTGACCAATCCGAATCCAGTATTCCACACAGCCGTGTAATAATCTGCAATAACGACCTCCTGGATGTACTTTATCCCTTACTTAAGATGCTTGTAGCTCAGAAAAAGGCTCACGCCCCATCATCATTATTACCCAGAGTTCCCTCTGTTTGCAGGTCTGAGCCGTATCTTGAAGAGCCGGTCGCTGATGGTG[C/T]AGAACCGCTCTGTGGACTGGGCTCTGGGCGAATATATGGCGTTCGGTTCGCTGCTGAAGGAGGGCATTCATGTGCGGCTCAGCGGGCAGGACGTGGAAAGAGGAACATTCAGGTGACACCCATACACATATTACCACTGTATTGACCTTATTTCCTGGTGGGTAGCGCTGTCGCCTTACAGCAAGAAGGTCACTGGTTTGAGTCTCGGCTGAGTCAGTTGTCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTCGGCGTGGGTTTCCTCCGGGTGCTCCGGTTTTCCCCACAGTCCAAACACATGCGCTATAGGGGAACTGATCAACTAAACTAGCCATAGTGTATGAGTGTGTGTGTGTGTGTGAATGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTGCATCTGGGAGAGCATCCGCTGTGTAAAACATATGCTGGAATAGTTGGCGGTTCATTCCCTGACAGATAAAGGGACTAAGCCGAAGGAAAATTTATG
Associated Phenotype:
Not determined