ZMP
si:dkey-39n1.2
Ensembl ID:
ZFIN ID:
Description:
sulfhydryl oxidase 1 [Source:RefSeq peptide;Acc:NP_001121836]
Human Orthologue:
QSOX1
Human Description:
quiescin Q6 sulfhydryl oxidase 1 [Source:HGNC Symbol;Acc:9756]
Mouse Orthologue:
Qsox1
Mouse Description:
quiescin Q6 sulfhydryl oxidase 1 Gene [Source:MGI Symbol;Acc:MGI:1330818]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34349 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41148 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16020 | Nonsense | Available for shipment | Available now |
| sa21226 | Nonsense | Available for shipment | Available now |
| sa7124 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41147 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34349
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 |
|---|---|---|---|---|---|
| ENSDART00000057645 | Nonsense | 170 | 778 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 15062214)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 14507558 |
| GRCz11 | 8 | 14545263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTTCGCCAATACATTATTGAGAATTTGGAGCTACATACCGAGGCTTG[G/A]CCGCCGGCTTGTCCACCTTTAGAGACGGCTAGGTTAGAATGCCATGTCTT
Long Flanking Sequence:
TCACACAGTAGAAATGTACAGCGATGGGAATTTAGAAGTGTGTTGATATTAGAGATGCACTGAATTTTTAGCCACCAAAAATTTATCAGCTGAAAATATGGTACGTTATTAATGAATCCTCTAATTTTTGTGGCTTCAGTCATTTTTAGGTACTCTTTTAAATATGCAAGCATTAACAAACTTATATTAAAATATATATCATTATCGTTAAATATGGACAATAATTATCGAGATAGCATTTTTGCCATATCACACAGCCCTGTTATGAATTCATCTTTTTGTATGAGAAGCATCCCTTCTGTCATAACTGTAGCTTTTGGATGAACTCTGCCTTTAAATACCCACTCTTACTTTAGTCTTCTAATCAAGATCTTATATGTATCGACTTTGCCTTTTTCTATGAATGAGCTTGTTTTCAACATTCACACAGGATTTTCAAGGGATGTGAGAGGACTTCGCCAATACATTATTGAGAATTTGGAGCTACATACCGAGGCTTG[G/A]CCGCCGGCTTGTCCACCTTTAGAGACGGCTAGGTTAGAATGCCATGTCTTTCTTTCCTTTTATATTTGCACTGAGAAATGTAAGGAGCTAGACCCATGTCATCTTTCTGTTGATTTAACAGTGCTGTAGTGTAAATAGCATTGCTTGTTGCAGTCAGTAAGCGTGTCAGTTTTGTGTGCTTTTAGTCAACATTGCTGTGTTCAAAAGGTCGCTCAAACAAGGAAGGAAAAGGACACGCCAAAACTTTGATGTGTATCACTCTTATTTCTGCATTCAAAGGCGTCTGACAAAACATGGCAGGAAATAAAAGAGGCGATTAAAAAGCACAGAAATGTCTAAAGTACGTTGGACTGTAGTTTAAGTATTTGATTGGTTTCAAATTTTAGAATCATTAGACTAATAACTATTTTGTTACAGTTAAACTTAAACGGTTAAAGTTAAGTAGACATATTTTTAGTTCAAGACTCGCTCAGATGTATTTAGGATATGAATAAAGAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41148
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 |
|---|---|---|---|---|---|
| ENSDART00000057645 | Nonsense | 204 | 778 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 15061558)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 14506902 |
| GRCz11 | 8 | 14544607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCTTTCCGGCCAACAATGTGAAGTATCTTGCTCTCGTGTTTGAGAAT[A/T]AAAAGTCTTACGTGGGAAGAGAGGTGAGATCAATTTGCATAATGCTGATT
Long Flanking Sequence:
AGTAAGCGTGTCAGTTTTGTGTGCTTTTAGTCAACATTGCTGTGTTCAAAAGGTCGCTCAAACAAGGAAGGAAAAGGACACGCCAAAACTTTGATGTGTATCACTCTTATTTCTGCATTCAAAGGCGTCTGACAAAACATGGCAGGAAATAAAAGAGGCGATTAAAAAGCACAGAAATGTCTAAAGTACGTTGGACTGTAGTTTAAGTATTTGATTGGTTTCAAATTTTAGAATCATTAGACTAATAACTATTTTGTTACAGTTAAACTTAAACGGTTAAAGTTAAGTAGACATATTTTTAGTTCAAGACTCGCTCAGATGTATTTAGGATATGAATAAAGAAGCTTAATTATTGTTATTATACACTGGTTTAATTGATTTTGTTAACTTATTTTATTAACTTATTTGAATCTAATTAATTTTCTCTCCCCAGTGAGGCAGAGGTACACCACTTCTTTCCGGCCAACAATGTGAAGTATCTTGCTCTCGTGTTTGAGAAT[A/T]AAAAGTCTTACGTGGGAAGAGAGGTGAGATCAATTTGCATAATGCTGATTTAGAGAAATAATTCACACAAAAAAAAAATGTAAATTTCCTAATTTATGCACCAAGCTTGAATTATTTTGCATGGAACGCATTTCTTCCAATCATCTTTTCAAAATTTGAAATTTATGTTGTTGTTTTTTTATTTATATATTATGTTAATTATGTTATTTTGTTAAATTTAATTTTTTTTGTTGATTATGATTTTTCTGTACAAAATATGTATTTAATTTGTTTTTTGTTTTTTTAGGTAACATTGGACTTGTTGCAGTATGAAAATATAGCTGTGCGCAGGGTTTTGGACACAGAGACGAATTTGGTGTCCAGGTTTGGTGTGACTGAATTTCCTTCCTGTTATCTCTACGACTCCTCTGGAAACATCACTAGGCTAAAAGTGTAAGTTTTTCCATTCATACAGTCCTACAGCAGATATAAAACTTCAAACTGATGTCATTGACATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16020
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000057645 | Nonsense | 207 | 778 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 15061547)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 14506891 |
| GRCz11 | 8 | 14544596 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAACAATGYSAAGTATCTTGCTCTCGTGTTTGAGAATAAAAAGTCTTA[C/A]GTGGGAAGAGAGGTGAGATCARTTTGCATAATGCTGATTTAGAGAAATAA
Long Flanking Sequence:
CAGTTTTGTGTGCTTTTAGTCAACATTGCTGTGTTCAAAAGGTCGCTCAAACAAGGAAGGAAAAGGACACGCCAAAACTTTGATGTGTATCACTCTTATTTCTGCATTCAAAGGCGTCTGACAAAACATGGCAGGAAATAAAAGAGGCGATTAAAAAGCACAGAAATGTCTAAAGTACGTTGGACTGTAGTTTAAGTATTTGATTGGTTTCAAATTTTAGAATCATTAGACTAATAACTATTTTGTTACAGTTAAACTTAAACGGTTAAAGTTAAGTAGACATATTTTTAGTTCAAGACTCGCTCAGATGTATTTAGGATATGAATAAAGAAGCTTAATTATTGTTATTATACACTGGTTTAATTGATTTTGTTAACTTATTTTATTAACTTATTTGAATCTAATTAATTTTCTCTCCCCAGTGAGGCAGAGGTACACCACTTCTTTCCGGCCAACAATGTGAAGTATCTTGCTCTCGTGTTTGAGAATAAAAAGTCTTA[C/A]GTGGGAAGAGAGGTGAGATCAATTTGCATAATGCTGATTTAGAGAAATAATTCACACAAAAAAAAAATGTAAATTTCCTAATTTATGCACCAAGCTTGAATTATTTTGCATGGAACGCATTTCTTCCAATCATCTTTTCAAAATTTGAAATTTATGTTGTTGTTTTTTTATTTATATATTATGTTAATTATGTTATTTTGTTAAATTTAATTTTTTTTGTTGATTATGATTTTTCTGTACAAAATATGTATTTAATTTGTTTTTTGTTTTTTTAGGTAACATTGGACTTGTTGCAGTATGAAAATATAGCTGTGCGCAGGGTTTTGGACACAGAGACGAATTTGGTGTCCAGGTTTGGTGTGACTGAATTTCCTTCCTGTTATCTCTACGACTCCTCTGGAAACATCACTAGGCTAAAAGTGTAAGTTTTTCCATTCATACAGTCCTACAGCAGATATAAAACTTCAAACTGATGTCATTGACATTTTTAGTACAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21226
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 |
|---|---|---|---|---|---|
| ENSDART00000057645 | Nonsense | 367 | 778 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 15039745)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 14485089 |
| GRCz11 | 8 | 14522794 |
KASP Assay ID:
2260-0290.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGGCCGTCCATCTGTAAAGAGTGCATTACAGGCTGTGGACAGTTGGT[T/A]ACAATCACAGAAGGGGACCGAGATCAAATATAGTGATTTCAGAGACGTCC
Long Flanking Sequence:
TCACTGCTTAAACTGACTTTGTAATGTTTTGCGTTTTTTCCTGGAAGGATTAATTAATATGCATCGGACTCTTTGTGCAAGGTTTGTTTTACTTGACAAGTTTTTTGCATATGAATATGAAGAAAACTCATACGAAAATTTTGCACTTCAGTGTGCAAAGACATTTATTCTTGTTTAAAGGGCCGCATTTTCATTGCTTGCTTCAAAGCACTGCAGTGTGTAGTTTTGCTGTCACTTAGCGTCTTAAAGTAGCACATTAGCGAATCTGGTGATCTCGCCATTTGACAGCATCTATTGGTATTGCAGAAATAGTCATCACATTTATTAGCTTTAAAAGGACTTATGGGAATTGATGAAATGTTTTATTCTAGCTTTGTCCCAAACACAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATTATATGTTTGTTATGTTTTTGCAGTATTTCCCAGGCCGTCCATCTGTAAAGAGTGCATTACAGGCTGTGGACAGTTGGT[T/A]ACAATCACAGAAGGGGACCGAGATCAAATATAGTGATTTCAGAGACGTCCTGGACAATGTCGTACAGGTTGGTCGACCCTACTTTAGTTTGTTTTCATATTTTATTTCTATTTGCGACTATAAACACTATTAGACATGATAAATAATAGTTTTGACAAGCAGAGGTTTGACTTATCAAAGGACTGCATTTACTTGAAAAGGTACCTGGACTTGTCAATACTTTGACGCAAGCATTTCTCCACTTAGACTTGGGTCATGAGGTCAGCGTATTGGGATGCTGTCACTCATTTAAATTTATTAAAACATCTATTTGAACTGTTTAAGCCAGTGCAAGCACAATTTCAAGCCTTGTCGTTCCACATCACATGCAGCCTGCATAAAAACTGTTTCATATGGCAAATGAATATGAGTTATGAGTTAGATGTTTAAATGTGGTTAAAAGTGCTGTGTTTACTTAAAAGGATAAGTATTCTGTCATCAGTTTCTCACCCACGTCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7124
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000057645 | Nonsense | 411 | 778 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 15036718)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 14482062 |
| GRCz11 | 8 | 14519767 |
KASP Assay ID:
554-4766.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCCTGAGGGCGTGCAGTGGGTGGGCTGTCAGGGATCTCAGGCCCGATA[T/A]CGTGGATACCCCTGTGCCGTTTGGACCCTCTTCCATGTGCTTACAGTGCA
Long Flanking Sequence:
CTTACATACCTTCACACACAAACATACACTGAAGCAGAGTTAGTGACATCATTAGCTTTTAGCAGCTCAATCAATGAATCAATAGATCAATGCGGAAGTAAGAAGGCCTCCGTAAGGAAATGAGCTGTTGTCATCAAGATCACCACCTCTTATAGGCAAACCTACCAATCAACTGATGAGTAAATCTGCACAGGAAACTGACCAAAAGGAGCTTTAAATGTGTTCCAAATCACAGTTTGATTCTGTTTATTATAGTCTTTTTCTATTTATGTATGTGTTTGAAAATTATCAGTGGGTTTTATTTCCTACAACAGCCGTACCTCATTTCATTGCTTCACTTCATTTGAGGAGTGACTGAAAGGAAAATTGATTGGCTTCAATTGATTCACAAGTGAAACGCACAAGTCAATTGAGAGTGTTTGTGTGTGCTTTTAGACGAGCGACGCAGTGCTGCCTGAGGGCGTGCAGTGGGTGGGCTGTCAGGGATCTCAGGCCCGATA[T/A]CGTGGATACCCCTGTGCCGTTTGGACCCTCTTCCATGTGCTTACAGTGCAGGCTAAAGAAATGGGAAGCACAGGTACTAATAATATGCACAGCACCTTGACAAAGTTCCCTTTAAGGCAAGTCATTTCAAGCCAAGCTATTAAATTTAATATTAGGAAACAACAATAACCAATGTCTCATTACTTTCATTTCTAAACATTCGAATCACACAAATTTGCAGAAACTCAGTCTGCTCCGAGCCCCTTCCCCGAAGAATCGTCAGTCTAAAGTAATCGATGATTGGCTCTTGTGCTAAAAGGCGGGGCTTCATTTGCACTTTTCCCCATTTAAAACTATACGAGTGACACATCTTGTGTATTCTATAGTCTTTGACCTTGACTACATCACACTGATAGTTATTAAGTGAAGCATGCCCGGGCTCCAGAGTGTAATTGCTTAGCATCAGCAACTGTTTTGGTATACTGTGGAGATTAGCAGAAGTGTTATATTGAAGTTAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41147
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 |
|---|---|---|---|---|---|
| ENSDART00000057645 | Nonsense | 473 | 778 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 15031597)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 14476941 |
| GRCz11 | 8 | 14514646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGCCGTGCGCAACTCACTTTGAGGCTATGGCCGCGGAGAGCATGGAT[C/T]AGGTCAACTCGCTGTCTGGCGCTGTCATTTGGTTGTGGTCACGCCACAAC
Long Flanking Sequence:
CGTGAGGGCTTATAATTTTGACTTTAACTATACATGCATCATATCTTGCAAATTTAAAGAAGAAACTGATATTTTTTTACTTCAACAATAAGTATAGGTTAATACTTTTTAATTCAAAATGTATTGTTTGTTGCAAAGTGAGTGACATACTTGATAATGGTTATAAAATAATAATGGAATAAAAAACAAAAACAGTTCCAAGATTATCATAGACTATAAATACTGCACACCCCTACAATGACATTCCTTTACTGAAATATATGAAGTCATTGAATGTTTTATGTTTTTTATGCATCCAAAAACATTGCTTCTTTAATAGCATTTTCATTTATCTTCCTCTTTTTTTCTCTCTCTCTCTTTTTTGTCCATTTCCTCTTTTCTGTGTGTTAGTCTCAGAGCCTCAGGAAGTGCTGCTGGCTATGAGAGGTTACGTCAGCAGTTTTTTCGGTTGCAGGCCGTGCGCAACTCACTTTGAGGCTATGGCCGCGGAGAGCATGGAT[C/T]AGGTCAACTCGCTGTCTGGCGCTGTCATTTGGTTGTGGTCACGCCACAACCGAGTCAACAACCGCCTGGCAGGTCAGTATTTTCAGTGCAAACAAATTTGAAGTGTTAAACACACATGACTAACACACCAGCAGCCCAAAGCAGTATTTGCACAGTATTTTTTAAATGTCACTTAAAGAGATATGTTCACCCTAAAATTTAAATTGTCAACATAATGTCCTCCTCTTGATTTAAGCTTATTTTGTTTCTTTCTTATGTTCAATTAAAAAAAAGATAATTTGAAGAATGATGGAAAACAGCAGCAATTAACTTCCTTTGTATTTTTTATCATATTATGAATGTCAATGGTCCTGCTGGCTTCTAACATTCTTCTTTATATCTACAGCGTTCAAGAGAAGAAAGAAATTCATAAAAGTTTATAACTACAGGGGTATAGAGTGTAAATAGTGAGGACATTTTCACATTGGGGTGAACTATCCTTTTAAAATTCAAAGCAATTA
Associated Phenotype:
Not determined