ZMP
zgc:66484
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC327557 [Source:RefSeq peptide;Acc:NP_956121]
Human Orthologues:
PAOX, SMOX
Human Descriptions:
polyamine oxidase (exo-N4-amino) [Source:HGNC Symbol;Acc:20837]
spermine oxidase [Source:HGNC Symbol;Acc:15862]
spermine oxidase [Source:HGNC Symbol;Acc:15862]
Mouse Orthologues:
Paox, Smox
Mouse Descriptions:
polyamine oxidase (exo-N4-amino) Gene [Source:MGI Symbol;Acc:MGI:1916983]
spermine oxidase Gene [Source:MGI Symbol;Acc:MGI:2445356]
spermine oxidase Gene [Source:MGI Symbol;Acc:MGI:2445356]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34757 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17098 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34757
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044880 | Nonsense | 314 | 406 | 3 | 4 |
ENSDART00000131252 | None | None | 237 | None | 2 |
ENSDART00000138316 | Nonsense | 403 | 495 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 45969010)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 45100675 |
GRCz11 | 9 | 44901627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATATCTCTATATGTATTTTTAAAGGTTGCTCAGGTCTTCAACAGGCT[G/A]GCCAGTACCAGAAGTGTCAAAGACGCTGATCTCCAGATGGGGCTCTGATC
Long Flanking Sequence:
GCGTAATCTGGAACAGGTGCGTGTGAGAGGTGCATGACTGGATCTTGCAGTCCATATACCAACGGATTTGTAGTTTTTTAGCGAACTGCATGTTTACCAGTGATCTGCCGGGATTAAATCGCTAGTGATTGTGATAGGTAATTAGGCAAGTTATTGTATGATGATTGTTTGTTCTGTTGACATTCAAAAAATATTGCTTTAGGGGGCTAATAATATTGACCCCTAAAATGTTTTTTTTTTTTTAAACTGCTTTTATTCTAGTGAAATAAGACTTTCTCCAGAGGAAAAAAATATTATAGGAAATACTGTGAAAAATTCCTTGCTCTGTTAAACATTTTGGGAAATATTTGAAAAAGGAAAAAAAAGGCTAATAATTTTGACCTCAACTGTATGTCACAATTTAAGCTCTTAATTGTTTTTTTGTTGTTGTATTTGTTGTCACTAATAAACTGAATATCTCTATATGTATTTTTAAAGGTTGCTCAGGTCTTCAACAGGCT[G/A]GCCAGTACCAGAAGTGTCAAAGACGCTGATCTCCAGATGGGGCTCTGATCCTCAAGTCCGCGGCTCCTATACATTTGTACCTGATGGTGTTGATGGAGTGGAAGCACACAAGGCTTTAGCGTCCCCTCTTCCCCCTAAACACAGGTCCAGGGGGAGGAAGGTAACCATTTGATATTGTATATATTAAATGTTTGAAAGATTAATATTACACAGATGTTTATTTTTTATTGTAAAGTGTAAAATGTATGAAATCTGATTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTTTTACAAAGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACAAACACACACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17098
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 |
---|---|---|---|---|---|
ENSDART00000044880 | Nonsense | 395 | 406 | 4 | 4 |
ENSDART00000131252 | None | None | 237 | None | 2 |
ENSDART00000138316 | Nonsense | 484 | 495 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 45967253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 45098918 |
GRCz11 | 9 | 44899870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCATGTGAACTTCTACACCACCACCCATGGAGCCTATTTATCCGGACAG[C/T]GAGAAGCAGAAAGACTCAWCAGCTATTACTCTGACTGAACATACAGTCGC
Long Flanking Sequence:
ATGGCAGATACTAGAGAGCATTTGATTGGTCTGAAGATTTGATGAGAAGTGATGTCATTTATTTATTTTTTTTTTTTTTATGCGTTTAGAGTGAAGTTACACACTGCAAGCTTTGGATGTTTATGACTTCTTAATGTACATTTGGTCACACTACACTGTATACAAGTTGACTCAACTTAAAATCGTATAGAAACTTGCGGCACAGCTTTTTTTGAGTTCACTTAACTTTTAACCCAAGCACTGCACTAAAAAAGCTCTGCAGCGAACCGCCCTTTTTAGATTTAAACTTGTTTTTTTGTTTATTTACAGTGTAGCTTATATATATATCCTTATAACTAACATATTCATACTAATTTCTAAAATGCTTGATTCTGATTTCACAGGGACTTTAATAACAGTTTTTTTCTCTGTTTCTGAAGAACCTTCAGGTTTTGTTTGCTGGTGAAGCGACGCATGTGAACTTCTACACCACCACCCATGGAGCCTATTTATCCGGACAG[C/T]GAGAAGCAGAAAGACTCATCAGCTATTACTCTGACTGAACATACAGTCGCAAAGACAGGGGAACATACACTTTGGTCTTATGAAGAAACATTTTATAAGCGTAAAGCACTTTATAGACTTGCTCTTACATCATATAGTTTGCGTTTTGTCTCTGCCTGACCCAGAAGCAGTTTATAGCTTAACTGTGAGTGCTTGCAAATGACATCCACCTGCTCGTGTTATCATGCATATCTCCGTCCTGTTAATTGTTAAACATCAACGACGTGTTGTACATGTAGTACTGATAAAGAAATAGTCTTTTGCACTTGCCAAGCATTTATACTGTTATGGAGAAAAAAATGAAAAGACCTCTTGAAAATTCCCAGTCTCTCTGGATTTAATATGTGTGTTTATGATTAATATTATTTGTTTTATTCTATAAATTTTTAATATATAAAATAATTCTTTCATATTTTTTTGGTTTAGTCCCTTTATTAATCAGGGGTCACCACTGCGGAATG
Associated Phenotype:
Not determined