ZMP
atp5o
Ensembl ID:
ZFIN ID:
Description:
ATP synthase subunit O, mitochondrial [Source:RefSeq peptide;Acc:NP_001003843]
Human Orthologues:
AP000304.12, ATP5O
Human Description:
ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit [Source:HGNC Symbol;Acc:850]
Mouse Orthologues:
Atp5o, Gm5436
Mouse Descriptions:
ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit Gene [Source:MGI Symbol;Acc:MGI:1
predicted pseudogene 5436 Pseudogene [Source:MGI Symbol;Acc:MGI:3643291]
predicted pseudogene 5436 Pseudogene [Source:MGI Symbol;Acc:MGI:3643291]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17805 | Essential Splice Site | Available for shipment | Available now |
| sa21522 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17805
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 |
|---|---|---|---|---|---|
| ENSDART00000005879 | Essential Splice Site | 9 | 209 | None | 7 |
The following transcripts of ENSDARG00000001788 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 34178923)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 33334869 |
| GRCz11 | 9 | 33145615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTACACAGTCGCAGGAGAAAATGGCAGCGCTTGGAGTGGGGCTGCAGG[T/C]ATGACTTTCTGAAAACCTTGTACTCGCTTTATAGAAAATCAACAAATGTG
Long Flanking Sequence:
TAAAAAGTATGTGTTTGTTAGACACATTTTTATTTATTGTAATGAACATTTATATTATTTATTTGAATATTTTATTTACTGTTTTATAAAAGAATAATATTTATTTGACTCCAAATCAAGTCAAATCAAATCAAATGAACGCCCTTCATCAATAACATGTTGTCAAGCTTTCTGTATCAGTAAGCTATTTGAATTTTTACAAAATCTAAAAATAATTTGATTTGTGTTGCCAATAAAATAAATGTTAGGCTAATCAGTGGTATATAGTGGTAAATAAGGTATTGTCCCAAATAAAAAGGGGAAGTTATATACTTTAGGCCTTTACCCAAACTAATCCAGTCATTGGTCAGAGTAATTTTCCACTGATCTGTCTAACTACATTACCCATAATGCACGAGCGCAGCTCTTGCGTATTTCATCCCAGACCAGTACGCATGCGCAGTTCTTTTGACCTACACAGTCGCAGGAGAAAATGGCAGCGCTTGGAGTGGGGCTGCAGG[T/C]ATGACTTTCTGAAAACCTTGTACTCGCTTTATAGAAAATCAACAAATGTGTGCCTTTTTATTCATAACACTATGTAAACAGTAAGAATTGTAAATATTTGAGTGGTTGGAACGAACGTGATATGTCTGGAAACTGAGCGAGGCCTTGACAGGCAGTGTCGAATCCGCAACAGACAGTCATTCAAACCGTGCGCTCTTGTAGTTCGTTACATAGTAAATAATGTTAATTTGCGTATCACCCTTTCAATTGAAAGCCTTTATTTACTTGTTTGTAAAGTACAATGATCACCAAATGAGTTTTTGCTTCTCAATGCTCAATCTGGAGTATGCAGCGCTCAAAATGTGACTGAACATGCGTTTTAAACTCTCTAACGTTATATCATGCAGTGTAGTGGCTTTTGTGACGCAGTGAGTCATGGACCATATATCTATATTCATGATTTTACAGTTTGCAATACTTGATAAATCTGCAAATAATTGTTTTCCTCTTCCTGCAGGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21522
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005879 | Nonsense | 133 | 209 | 5 | 7 |
The following transcripts of ENSDARG00000001788 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 34180609)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 33336555 |
| GRCz11 | 9 | 33147301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTGACCCCTGATGTCATCGCTGCTTTTAGCAAAATGATGAGCGCCCAC[A/T]GAGGAGAGGTCACATGCTCAGTCACCACCGCTCAGGTAAGCGTTATATAA
Long Flanking Sequence:
TGTTCTCTGCTGCCAGCAAGCAGAAGAGCCTCGACAAGGTGGAACAGGAACTTGGACGTGTGTCTGTGAGTTTCCCTGTCAATATTTATTTTAAATCTTTTTCCAGTTCTCATACTCAATACTCCTCAATACTCATTTCTTCACTTTCTAGAGCCTAATTAAGGACCCTAAGCTGTCAGGTATTGTGATGAACCCCCATGTCAAGCGCTCTGTCAAGCAAAAGACTTTTGTGGACGCCTTGACCAAGGCTAAAGTCTCCCCCATAACCATCAACCTCATCAGTGAGTTTTCTGTGTTACCCAGGTTGAGCTATTGTGCAAATTTTCAAGTACTTTTGAAAAATAAATATAGATTTTTGCTTTTAGAAAAAGGAGGGAGCATGTTATTGATTATATTATGTGTTTTAATTATTTATATCCACAGATGTCCTATCAGAAAATGGCCGCTTGACCTTGACCCCTGATGTCATCGCTGCTTTTAGCAAAATGATGAGCGCCCAC[A/T]GAGGAGAGGTCACATGCTCAGTCACCACCGCTCAGGTAAGCGTTATATAAATTAGATTGGTTGCTTGTTTATAATCTTATTATCAGTCTTAAATGGTTTGTGGTCTGTCTAATAGTTAAATTGATGCGTTTTGATGATCATTGGTATTGAATTAAACCCCTTTTGTCTAACTAATATGTCCATATTTTTACAGCCTCTGGATGAAGCTAGTCTTGCAGAGCTGAAAGTGGCACTGAATGGTTTCCTTGCAAAGGGAGAGACCATCAAGCTTGAGACCAAGGTATGTTTATTTTTTCCACAGGGTGGTCTTTTTGTCTTCTTTCTCTAATCATTTTAAACATGTTCAGTTTTTAAAAAGCAGAAATGTTCATTTATAATGTAACATACCTGTTATAGCATATTGACTATTCACTTAGAATACAGAAATTATTGTGATAAGTGATGTTATTGTTATTTTAACAACATGTTATGCCACTGAATAGATGCAACACAATAATAAT
Associated Phenotype:
Not determined