ZMP
si:dkey-57m14.4
Ensembl ID:
ZFIN IDs:
Description:
nitric oxide synthase 2a, inducible [Source:RefSeq peptide;Acc:NP_001098407]
Human Orthologues:
AC015688.1, NOS2
Human Description:
nitric oxide synthase 2, inducible [Source:HGNC Symbol;Acc:7873]
Mouse Orthologue:
Nos2
Mouse Description:
nitric oxide synthase 2, inducible Gene [Source:MGI Symbol;Acc:MGI:97361]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14427 | Nonsense | Available for shipment | Available now |
| sa14328 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14427
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 |
|---|---|---|---|---|---|
| ENSDART00000019431 | Nonsense | 188 | 1079 | 5 | 25 |
| ENSDART00000130355 | Nonsense | 188 | 1079 | 7 | 27 |
| ENSDART00000019431 | Nonsense | 188 | 1079 | 5 | 25 |
| ENSDART00000130355 | Nonsense | 188 | 1079 | 7 | 27 |
The following transcripts of ENSDARG00000026925 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 45404154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 43185419 |
| GRCz11 | 5 | 43785572 |
KASP Assay ID:
2259-6389.1 (used for ordering genotyping assays)
KASP Sequence:
KTTTMATGCCTTGTGCACTCATCTWAAGTATGCCACCAACGGAGGAAACT[T/A]GAGGTGAGGGGANTTTTTTATTTAACCCCNGTAAAACCTAAAATATCAAAAA
Long Flanking Sequence:
ACAAGTGAGGATTCAGCAACTCGAACGAGAAAAACAGCTTTACTTTTATCAATGACAAGAAAATGAAATAAAACATTACTGTTCTGTCGACTTGATAAACACGATGGGAGTGTGAAAGTCGATTTACCTTGCTAAATTAAAAGGTCATTCTTACCTTTTTACGCAGCCCGGGCTCGACGGAGCAGCAAGCGCGGATTGACAGGATCGCGCTGGAGATCACTCTGACCGGGACCTACTCTCTCACCACCGAGGAACTCGCTTTTGGGGCCAAACAGGCGTGGAGAAATGCGCCAAGATGCATTGGCAGGATCCAGTGGTCCAATTTACAGGTTAGAGATTTTTTTTAATGTCGCTTTTTGCAAGCATAGCTCTCGCGAGTTTTTAAACACGTAACAAGTCTTATCTTTTGCAGCTTTTCGATGCCCGTGATTGTAAAACCGCTGAGGACATGTTTCATGCCTTGTGCACTCATCTTAAGTATGCCACCAACGGAGGAAACT[T/A]GAGGTGAGGGGATTTTTTATTTAACCCCGTAAAACCTAAAATATCAAAAATAGGCAGAAACTAGACCTGAGATGTTTATTAAACCATTTAGCGAAATAAATATAAAAAAAAAATCATAAACATTTTTTCATGATATTTATTTTGTATTACATTTGATACATCAGGCGTTTGTGCAACTTTTTGTTCATAACAATGTAAATTTTAATTACAAAAAAATAAAAATAAATTGCCCTTAACTTTTGGTCAACAGAGAACATTTCAGGCAGTTTTTATCTTTGTTTTTTTTTTACATTAAATACTTTAAAGACTTGTATTATTTCACTTTGTGGTAGGCGTAATTGCAGTTTCAGTCCTTGTACAGGCAAAGATTCACTTTACACTTACAGAGTACACAGAGGTTTGAAGTGATTGCTGGAGCAGTGCTTTTATCTTCTGTCTGTTTCTCCAGTTTCATGCTTTCTAACATCAAAAGGCACACTGCAACTTGACCTTTTATAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14328
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 |
|---|---|---|---|---|---|
| ENSDART00000019431 | Nonsense | 188 | 1079 | 5 | 25 |
| ENSDART00000130355 | Nonsense | 188 | 1079 | 7 | 27 |
| ENSDART00000019431 | Nonsense | 188 | 1079 | 5 | 25 |
| ENSDART00000130355 | Nonsense | 188 | 1079 | 7 | 27 |
The following transcripts of ENSDARG00000026925 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 45404154)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 43185419 |
| GRCz11 | 5 | 43785572 |
KASP Assay ID:
2259-6389.1 (used for ordering genotyping assays)
KASP Sequence:
KTTTMATGCCTTGTGCACTCATCTWAAGTATGCCACCAACGGAGGAAACT[T/A]GAGGTGAGGGGANTTTTTTATTTAACCCCNGTAAAACCTAAAATATCAAAAA
Long Flanking Sequence:
ACAAGTGAGGATTCAGCAACTCGAACGAGAAAAACAGCTTTACTTTTATCAATGACAAGAAAATGAAATAAAACATTACTGTTCTGTCGACTTGATAAACACGATGGGAGTGTGAAAGTCGATTTACCTTGCTAAATTAAAAGGTCATTCTTACCTTTTTACGCAGCCCGGGCTCGACGGAGCAGCAAGCGCGGATTGACAGGATCGCGCTGGAGATCACTCTGACCGGGACCTACTCTCTCACCACCGAGGAACTCGCTTTTGGGGCCAAACAGGCGTGGAGAAATGCGCCAAGATGCATTGGCAGGATCCAGTGGTCCAATTTACAGGTTAGAGATTTTTTTTAATGTCGCTTTTTGCAAGCATAGCTCTCGCGAGTTTTTAAACACGTAACAAGTCTTATCTTTTGCAGCTTTTCGATGCCCGTGATTGTAAAACCGCTGAGGACATGTTTCATGCCTTGTGCACTCATCTTAAGTATGCCACCAACGGAGGAAACT[T/A]GAGGTGAGGGGATTTTTTATTTAACCCCGTAAAACCTAAAATATCAAAAATAGGCAGAAACTAGACCTGAGATGTTTATTAAACCATTTAGCGAAATAAATATAAAAAAAAAATCATAAACATTTTTTCATGATATTTATTTTGTATTACATTTGATACATCAGGCGTTTGTGCAACTTTTTGTTCATAACAATGTAAATTTTAATTACAAAAAAATAAAAATAAATTGCCCTTAACTTTTGGTCAACAGAGAACATTTCAGGCAGTTTTTATCTTTGTTTTTTTTTTACATTAAATACTTTAAAGACTTGTATTATTTCACTTTGTGGTAGGCGTAATTGCAGTTTCAGTCCTTGTACAGGCAAAGATTCACTTTACACTTACAGAGTACACAGAGGTTTGAAGTGATTGCTGGAGCAGTGCTTTTATCTTCTGTCTGTTTCTCCAGTTTCATGCTTTCTAACATCAAAAGGCACACTGCAACTTGACCTTTTATAATG
Associated Phenotype:
Not determined