ZMP
noxa1
Ensembl ID:
ZFIN ID:
Description:
NADPH oxidase activator 1 [Source:RefSeq peptide;Acc:NP_001025271]
Human Orthologue:
NOXA1
Human Description:
NADPH oxidase activator 1 [Source:HGNC Symbol;Acc:10668]
Mouse Orthologue:
Noxa1
Mouse Description:
NADPH oxidase activator 1 Gene [Source:MGI Symbol;Acc:MGI:2449980]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40448 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31445 | Nonsense | Available for shipment | Available now |
sa20441 | Essential Splice Site | Available for shipment | Available now |
sa12640 | Nonsense | Available for shipment | Available now |
sa2232 | Nonsense | F2 line generated | Not yet available |
sa20440 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40448
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 |
---|---|---|---|---|---|
ENSDART00000078469 | Nonsense | 22 | 269 | 2 | 6 |
The following transcripts of ENSDARG00000056047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 30790548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28551905 |
GRCz11 | 5 | 29152058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGATCCGCCTGTGGGATGAGGCCGTAAAGGCAATAGACATTCGGGACTG[G/A]CAGGGAGCTCTCAGTAAACTCAACCAGATCACGGATCATAACTGTCGCAC
Long Flanking Sequence:
TCTCTCTCTCTTCAGGGAATGCTGGACTTCCTGATGGCACTGAAACTGGGCGGCACCACAGATGTGTGTCACACTACAAATATTACTTCCCTAAGAGCCCACGCTTAAATACACCTGTTCAGGAGCTGCTCTGATATTCACGAGCAATCACTTCTAGAAAGCAAATTGAGTTCTTGACTTATTTCTGTTTGTTTTGTGTGCAGTGGTAAGTGTCAGTCATTGTATTAGTGTACAGGGCTTTCCTTTCATGGTTTTATTGACTAACAAGAACCTGCATAGCTGGTCTCACTTGTAACAGCTGTTATTCTTACATTCATTAGTGACTGAAGTATAATGTTTTATCAGTACAGCTTGATGATGATTTATTAACCTCTTTTTAAATTTGTGTAGCGTTCTAAAAATAATGTTTGATTATTTGTGTTTTGCTCTAGAGCCATGCTGTATATCGAGTTGATCCGCCTGTGGGATGAGGCCGTAAAGGCAATAGACATTCGGGACTG[G/A]CAGGGAGCTCTCAGTAAACTCAACCAGATCACGGATCATAACTGTCGCACTATGTTTGTGGTTGCGTCCACTCACATCGCCCTGGGTCAAGTGGATTTGGCCATTAAGGTACAAGCTACACGAACTGTCATAGAATTGTTTGATATCAATGACACTAAACAGTTATCTGTTTGTTTGTTGGTAAACTGCATTTGTGTTATTCAGGGGGTTTTAGACTTTAAGATGCAAGACCACCATCTTAAAATTTAAAAGGCAGTTTACATGTATAAAGACCTAGTTTTTAGTGTAAAATGTATCACTTAAGTTGATAAATGGGTGTAAATTTTAAGTTGGATTTTTATTTATTTTGTTTGTTTATTTTTTGTTTTGTTTTAATGTTATTCTATAACGTTTTACTACATTTCTGTTACATTGAATTATTTATTTCATCAGTTGTTGTATTTTTTTTTCATTTTTTTGTATTATTTATTTCACTTGTTTATTTAATTAAAGGGGTAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31445
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 |
---|---|---|---|---|---|
ENSDART00000078469 | Nonsense | 109 | 269 | 4 | 6 |
The following transcripts of ENSDARG00000056047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 30787818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28549175 |
GRCz11 | 5 | 29149328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGTATTTGGGCTCAGAAATACATGAGGGAAAACCCTGTCATTGACTA[C/A]AAGCAGCTGGGTCTTCGCTATAAACTCTACAGCTGGCAGGTCAGAGCATA
Long Flanking Sequence:
AATGATATATCATTGTTATACAAATTACAATTTAATAGGACTATGACAATTGTAAAAACTAGAAAAACTGTAGAAAAATAAAATGTGTCAAACAAAAAGTGGAATTTTATGTGCCTGACAATGTCAAATTATGTTTTTCAGGCTCTCGACCGAGTAATCGCCAAGGACTCATGCCTTGCTGTGGGATTTTTTCAGCGGTCTGCCGTTCATATGATGGCAAACAGGTGAGATTTCTCTGTTTTTCCACTGTAGCTTTCTATGTGTGAGTCGGCTATCGTGCTTGATACAACACAAACATTGACCTCTTTTGTATAAAGCTGATGTTCTGGACAGCTGATTCACTTTCATCTGACACTGCCTCTTTGTTCTCTTGCTCTCTCACTGTCTCGGTCTCTTTCTCTTTCTGTCTCTGTCATTTTTTCTAATGCCAGGCTTGAGGAGGCATTGTCTGATTGTATTTGGGCTCAGAAATACATGAGGGAAAACCCTGTCATTGACTA[C/A]AAGCAGCTGGGTCTTCGCTATAAACTCTACAGCTGGCAGGTCAGAGCATAAGTGTACTTCTGTCAAGAGTATATGAGATAAAACATGATGTTTTTTTTTTTTTTACTCTTTATTTAAATTTTTCATTGAAAAAAAAAAAAAAAACCTTCACACATATAGTACCACCTAAATACTTCCAAGAGAACTTTGATATATGCTCCGTTTCTTGTAAGTACTCACAGTGAATGTAGCTTACTACAAAAAGGAACTCAAAACCCTACCTTGCACCCCACCTATCTAACATCGATCAAAATATTTATGGAAGGTTCATAAAAATTAAATAATAGGCATTGATGAATTACATTTTCAATCATAATATGGAATTTTTTAAATTAGATTTTTTTATACATTTAAAATTGGAGCAAGGTGTACATGGACAATGAAACCAAGATTATTGTAAAATAAATAATGAAATTAATTAATTAATTAATTACCACAATAGTCTTGTAAAAAAATCTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20441
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078469 | Essential Splice Site | 168 | 269 | 6 | 6 |
The following transcripts of ENSDARG00000056047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 30781731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28543088 |
GRCz11 | 5 | 29143241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTATCACTGAACATTGTACTCACTTAATGATTCTGTCAATGGCATTTC[A/G]GAGGAAGGATGTTTTGGAGCCTCTTCTGCTTCCTGAGGGTGAAGTGTTTC
Long Flanking Sequence:
AGTGTTAACTTTTTTTTTCTTCAGAATTTGTAGATAAAGTTCAACAGATCAACTATTAAATTATTTTAAAGATAAATAGTTTGTAATGTTATACAGCAAATTACACTTTTGATCTGTTAAATGTGTCCTTGCTGAAGAAAAGCTTACTTTTTTAATAAGAAAAAAAACTTACTGACCCTAAATTCATTAATATTATCTAAATCTTTATTGTTATGGCATGTAATGTGTTCAACTTTTGTTTACAGTGTATGTGTGTGTGCTTGTGTGTGTTTATTAGGTGCTTTATAATGCAGCAGCCGTTCACTCTAGACTGCAACAATGGGACAAAGCTAGGGACATTTTGCTGGCGGCCTCACAGGAGAGAGGAGCAGGCCGGAGCAACCTGATAGACACGGCCCTAGAGGCTATTTCTGTACGTTTTAGAAACCTTTTGATTGCATTTTGCTGATAAAGTATCACTGAACATTGTACTCACTTAATGATTCTGTCAATGGCATTTC[A/G]GAGGAAGGATGTTTTGGAGCCTCTTCTGCTTCCTGAGGGTGAAGTGTTTCGTCCTAGGAAACTTGAGGTGGACCAGCTAAAACCGAGGGACTTCTTGGGTGAAGCAAAGGTGATTCAAATCTTCACGCTGTATTGCAGTTTTAATGCCTGTTCAAGTGCGGAATTTGAATACTGGATAAATATAAATGTTCAAAACCAATTATTACAGACAATATACGATAAGAAAGGGAATGCACCAAGTAAAGGGGTCTCAATGTTTTGCCCTTCAGCTCTCTGCACTTTTGTCTTTTCCAATTACCTAAAGATATAAGTTATTATATATTATCTTCCTCTTTATTTTGTTTTCTTTTTCGTCAAATAAGTTTTTTATTTGGTCGTTGAATAAACTTACAATATTCACAGATTCCAGGATTAGTTTTCTGAAATACCGTACATTTACAAAAACAAACAAAAACAAAAACAAACACTCCAAGCCCAGCCTGTAAGTATACAAAACTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12640
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 |
---|---|---|---|---|---|
ENSDART00000078469 | Nonsense | 199 | 269 | 6 | 6 |
The following transcripts of ENSDARG00000056047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 30781635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28542992 |
GRCz11 | 5 | 29143145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTCGTCCTAGGAAACTTGAGGTGGACCAGCTAAAACCGAGGGACTTCT[T/A]GGGTGAAGCRAAGGTGATTCAWATCTTCACRCTGTATTRCAGTTTTAATG
Long Flanking Sequence:
CAAATTACACTTTTGATCTGTTAAATGTGTCCTTGCTGAAGAAAAGCTTACTTTTTTAATAAGAAAAAAAACTTACTGACCCTAAATTCATTAATATTATCTAAATCTTTATTGTTATGGCATGTAATGTGTTCAACTTTTGTTTACAGTGTATGTGTGTGTGCTTGTGTGTGTTTATTAGGTGCTTTATAATGCAGCAGCCGTTCACTCTAGACTGCAACAATGGGACAAAGCTAGGGACATTTTGCTGGCGGCCTCACAGGAGAGAGGAGCAGGCCGGAGCAACCTGATAGACACGGCCCTAGAGGCTATTTCTGTACGTTTTAGAAACCTTTTGATTGCATTTTGCTGATAAAGTATCACTGAACATTGTACTCACTTAATGATTCTGTCAATGGCATTTCAGAGGAAGGATGTTTTGGAGCCTCTTCTGCTTCCTGAGGGTGAAGTGTTTCGTCCTAGGAAACTTGAGGTGGACCAGCTAAAACCGAGGGACTTCT[T/A]GGGTGAAGCAAAGGTGATTCAAATCTTCACGCTGTATTGCAGTTTTAATGCCTGTTCAAGTGCGGAATTTGAATACTGGATAAATATAAATGTTCAAAACCAATTATTACAGACAATATACGATAAGAAAGGGAATGCACCAAGTAAAGGGGTCTCAATGTTTTGCCCTTCAGCTCTCTGCACTTTTGTCTTTTCCAATTACCTAAAGATATAAGTTATTATATATTATCTTCCTCTTTATTTTGTTTTCTTTTTCGTCAAATAAGTTTTTTATTTGGTCGTTGAATAAACTTACAATATTCACAGATTCCAGGATTAGTTTTCTGAAATACCGTACATTTACAAAAACAAACAAAAACAAAAACAAACACTCCAAGCCCAGCCTGTAAGTATACAAAACTGCAATAATCAAAACAACTCCTCAAAGCAATGTATTGTAACTAAAAAAGTTACAATACATTGCTTTGGGGAGAAGAATTCCCCATGAAGGGACAAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2232
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078469 | Nonsense | 224 | 269 | 6 | 6 |
The following transcripts of ENSDARG00000056047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 30781559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28542916 |
GRCz11 | 5 | 29143069 |
KASP Assay ID:
554-2939.1 (used for ordering genotyping assays)
KASP Sequence:
TTCACGCTGTATTGCAGTTTTAATGCCTGTTCAAGTGCGGAATTTGAATA[C/A]TGGATAAATATAAATGTTCAAAACCAATTATTACAGACAATATACGATAA
Long Flanking Sequence:
TGACCCTAAATTCATTAATATTATCTAAATCTTTATTGTTATGGCATGTAATGTGTTCAACTTTTGTTTACAGTGTATGTGTGTGTGCTTGTGTGTGTTTATTAGGTGCTTTATAATGCAGCAGCCGTTCACTCTAGACTGCAACAATGGGACAAAGCTAGGGACATTTTGCTGGCGGCCTCACAGGAGAGAGGAGCAGGCCGGAGCAACCTGATAGACACGGCCCTAGAGGCTATTTCTGTACGTTTTAGAAACCTTTTGATTGCATTTTGCTGATAAAGTATCACTGAACATTGTACTCACTTAATGATTCTGTCAATGGCATTTCAGAGGAAGGATGTTTTGGAGCCTCTTCTGCTTCCTGAGGGTGAAGTGTTTCGTCCTAGGAAACTTGAGGTGGACCAGCTAAAACCGAGGGACTTCTTGGGTGAAGCAAAGGTGATTCAAATCTTCACGCTGTATTGCAGTTTTAATGCCTGTTCAAGTGCGGAATTTGAATA[C/A]TGGATAAATATAAATGTTCAAAACCAATTATTACAGACAATATACGATAAGAAAGGGAATGCACCAAGTAAAGGGGTCTCAATGTTTTGCCCTTCAGCTCTCTGCACTTTTGTCTTTTCCAATTACCTAAAGATATAAGTTATTATATATTATCTTCCTCTTTATTTTGTTTTCTTTTTCGTCAAATAAGTTTTTTATTTGGTCGTTGAATAAACTTACAATATTCACAGATTCCAGGATTAGTTTTCTGAAATACCGTACATTTACAAAAACAAACAAAAACAAAAACAAACACTCCAAGCCCAGCCTGTAAGTATACAAAACTGCAATAATCAAAACAACTCCTCAAAGCAATGTATTGTAACTAAAAAAGTTACAATACATTGCTTTGGGGAGAAGAATTCCCCATGAAGGGACAAAAGAAAGGGCCCCCATCTTCTGAAATTTTCCAATGTTGCCTTTTTAATATATATCTTGTTCGTTCCAAGTGCAGAGTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20440
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 |
---|---|---|---|---|---|
ENSDART00000078469 | Nonsense | 234 | 269 | 6 | 6 |
The following transcripts of ENSDARG00000056047 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 30781530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28542887 |
GRCz11 | 5 | 29143040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAGTGCGGAATTTGAATACTGGATAAATATAAATGTTCAAAACCAAT[T/A]ATTACAGACAATATACGATAAGAAAGGGAATGCACCAAGTAAAGGGGTCT
Long Flanking Sequence:
TCTTTATTGTTATGGCATGTAATGTGTTCAACTTTTGTTTACAGTGTATGTGTGTGTGCTTGTGTGTGTTTATTAGGTGCTTTATAATGCAGCAGCCGTTCACTCTAGACTGCAACAATGGGACAAAGCTAGGGACATTTTGCTGGCGGCCTCACAGGAGAGAGGAGCAGGCCGGAGCAACCTGATAGACACGGCCCTAGAGGCTATTTCTGTACGTTTTAGAAACCTTTTGATTGCATTTTGCTGATAAAGTATCACTGAACATTGTACTCACTTAATGATTCTGTCAATGGCATTTCAGAGGAAGGATGTTTTGGAGCCTCTTCTGCTTCCTGAGGGTGAAGTGTTTCGTCCTAGGAAACTTGAGGTGGACCAGCTAAAACCGAGGGACTTCTTGGGTGAAGCAAAGGTGATTCAAATCTTCACGCTGTATTGCAGTTTTAATGCCTGTTCAAGTGCGGAATTTGAATACTGGATAAATATAAATGTTCAAAACCAAT[T/A]ATTACAGACAATATACGATAAGAAAGGGAATGCACCAAGTAAAGGGGTCTCAATGTTTTGCCCTTCAGCTCTCTGCACTTTTGTCTTTTCCAATTACCTAAAGATATAAGTTATTATATATTATCTTCCTCTTTATTTTGTTTTCTTTTTCGTCAAATAAGTTTTTTATTTGGTCGTTGAATAAACTTACAATATTCACAGATTCCAGGATTAGTTTTCTGAAATACCGTACATTTACAAAAACAAACAAAAACAAAAACAAACACTCCAAGCCCAGCCTGTAAGTATACAAAACTGCAATAATCAAAACAACTCCTCAAAGCAATGTATTGTAACTAAAAAAGTTACAATACATTGCTTTGGGGAGAAGAATTCCCCATGAAGGGACAAAAGAAAGGGCCCCCATCTTCTGAAATTTTCCAATGTTGCCTTTTTAATATATATCTTGTTCGTTCCAAGTGCAGAGTAGATACTAATTCTTCAAGCCATAGTTTGGCAGC
Associated Phenotype:
Not determined