ZMP
nostrin
Ensembl ID:
ZFIN ID:
Description:
nostrin [Source:RefSeq peptide;Acc:NP_001107076]
Human Orthologue:
NOSTRIN
Human Description:
nitric oxide synthase trafficker [Source:HGNC Symbol;Acc:20203]
Mouse Orthologue:
Nostrin
Mouse Description:
nitric oxide synthase trafficker Gene [Source:MGI Symbol;Acc:MGI:3606242]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15123 | Essential Splice Site | Available for shipment | Available now |
sa15830 | Essential Splice Site | Available for shipment | Available now |
sa9638 | Essential Splice Site | Available for shipment | Available now |
sa25441 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15123
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 |
---|---|---|---|---|---|
ENSDART00000113855 | Essential Splice Site | 87 | 537 | 4 | 16 |
ENSDART00000142338 | None | None | 65 | None | 2 |
ENSDART00000143102 | Essential Splice Site | 87 | 404 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 49905351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49160547 |
GRCz11 | 9 | 48858032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CYTGGTCCTTCATATCAGATGAGATGTTCRCCTCGGCAGATGCCCACCGG[T/C]ACCACACTACACTGCATCATTCTCCTCRCTTCATTATTCATGTGGCTGCT
Long Flanking Sequence:
AAAAGGAGGTCCCACCCAGTACTAGTAAGGTGTACCTAATAAAGTGGCCGGTGAGTGTTTATATTAAAAACAATAATTAATATAAAAAAGTACAGTAAAAAGTATTTTAAAAGTACATTTTCCCAAAAATTTTAAATGTTATTTTTATTCATAAAAATATCTTAAAATTCTTTGTGCAATTTACTTTCGAAATCAACAATATATTAAAATCTTAAACCTAAAAGTTCAAACCTTTAAAAATGACGCTTTGATTGAAGTATAAACAAGCGAAAACAACAAGTATTGCATGTCAGGTCCTTTTTACCCATAGAATTGGACAAAGAGTGAGACGAGTATTGTTCTTCAGTGTCGAGTTGTTTTCACCACATCAGCAGTGCAGGTTAATATTTGATGCAGTTGCTCTGCAAACTCATTGACAGTTTTTCCCTCTTCAAAGCTCCACGTATCATGCCTGGTCCTTCATATCAGATGAGATGTTCGCCTCGGCAGATGCCCACCGG[T/C]ACCACACTACACTGCATCATTCTCCTCGCTTCATTATTCATGTGGCTGCTGTGCATTTATATCTGCATTATTCTTACAGCATTCTGGGAAACGCTCTCAATCAGGATGTCATTCAGGAAATCCGGCAAATCCTGGATGAACACGGCAAACGAAAAAGGCCGGTATGTCACATCCAGTCACTAGTACTGCAGAGTACATTTTTTAATTCATCAAATTTTACATTTTGACCAATTATATACAGTAGTCAACATTTGAAGTGAATCAAAACCTTTCATCAAAGTTGTTCTGAATCTATTGAACAACATCCGTTCAAGTCCTAGGACAAACTTGAAAACCTTTTTTGATCCACTTCAATCGTTGACTACTGTTGCATGACAATATAACTACATGTATACATTTACAAAATGATGTTCAGCGGCATTTACATTAAGTCTTCATGTACACAGCTTGACAATGCAGTGGAGAAGTCTGGAAAGCTTGTTCTCACAAACTGGAGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15830
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113855 | Essential Splice Site | 87 | 537 | 5 | 16 |
ENSDART00000142338 | None | None | 65 | None | 2 |
ENSDART00000143102 | Essential Splice Site | 87 | 404 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 49905273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49160469 |
GRCz11 | 9 | 48857954 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RCTTCATTATTCATGTGGCTGCTGTGCATTTWTATCTGCATTATTCTTAC[A/C]GCATTCTGGGAAACGCTCTCAATCAGGAYGTCATTCAGGAAATCCGGCAA
Long Flanking Sequence:
AATATAAAAAAGTACAGTAAAAAGTATTTTAAAAGTACATTTTCCCAAAAATTTTAAATGTTATTTTTATTCATAAAAATATCTTAAAATTCTTTGTGCAATTTACTTTCGAAATCAACAATATATTAAAATCTTAAACCTAAAAGTTCAAACCTTTAAAAATGACGCTTTGATTGAAGTATAAACAAGCGAAAACAACAAGTATTGCATGTCAGGTCCTTTTTACCCATAGAATTGGACAAAGAGTGAGACGAGTATTGTTCTTCAGTGTCGAGTTGTTTTCACCACATCAGCAGTGCAGGTTAATATTTGATGCAGTTGCTCTGCAAACTCATTGACAGTTTTTCCCTCTTCAAAGCTCCACGTATCATGCCTGGTCCTTCATATCAGATGAGATGTTCGCCTCGGCAGATGCCCACCGGTACCACACTACACTGCATCATTCTCCTCGCTTCATTATTCATGTGGCTGCTGTGCATTTATATCTGCATTATTCTTAC[A/C]GCATTCTGGGAAACGCTCTCAATCAGGATGTCATTCAGGAAATCCGGCAAATCCTGGATGAACACGGCAAACGAAAAAGGCCGGTATGTCACATCCAGTCACTAGTACTGCAGAGTACATTTTTTAATTCATCAAATTTTACATTTTGACCAATTATATACAGTAGTCAACATTTGAAGTGAATCAAAACCTTTCATCAAAGTTGTTCTGAATCTATTGAACAACATCCGTTCAAGTCCTAGGACAAACTTGAAAACCTTTTTTGATCCACTTCAATCGTTGACTACTGTTGCATGACAATATAACTACATGTATACATTTACAAAATGATGTTCAGCGGCATTTACATTAAGTCTTCATGTACACAGCTTGACAATGCAGTGGAGAAGTCTGGAAAGCTTGTTCTCACAAACTGGAGTGAACAGATTAAGGTAAGAACATACAGCTGGAAGCTCTATAAGTCTTAGGGATTTGATCAAGGAATGTAAAATTAAATTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9638
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113855 | Essential Splice Site | 210 | 537 | 8 | 16 |
ENSDART00000142338 | None | None | 65 | None | 2 |
ENSDART00000143102 | Essential Splice Site | 210 | 404 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 49897168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49152364 |
GRCz11 | 9 | 48849849 |
KASP Assay ID:
554-6636.1 (used for ordering genotyping assays)
KASP Sequence:
GTCACCACATCCGCCTGAAGCTGGAGAACACGSTCAAAACATGCTACCAG[G/A]TTCAGATTGTTANNNTTTGAYACTTTYAGGAAGWTATTGAGTTTTGAYTKATT
Long Flanking Sequence:
CTCATCGTTACTGGCCGGTCACAATCCTGTCTACTGTCCGGAGCGTATTTCACGCTGGCCCCGGGCCACCGGGCAGTCCTTATTGTTGAGCCCTGGCTAATAATTTTGACCTCAACTGTGTATTTATTAATTTGTGTAAACAATTTATTATTATTTTTTTAATTAAAAGAAGTAGTAATGAGCAGAAATGTGTTTTTCTACAGCTAAAAAAGAAGCTGATCGGGTTGACAAGAGAACATGAAGCTCTCTTCAGCTTTGTAGAGAAAAACAAGCAAATCTGTACAGAGAAAGAAAAGCAGAAGGTATTTGTGACTAAGCTAAAGTGGGTTACCATTATGTTTTTGGACATCAGATGACTTTCTTTTTTATTCTAGATGTTCAACAGATTGAGTAAATCAGCAGAGCTTCAGGTCAGAGTGGATGAAGAATATTTCAACACTAACATGGAGGGTCACCACATCCGCCTGAAGCTGGAGAACACGCTCAAAACATGCTACCAG[G/A]TTCAGATTGTTATTTGATACTTTCAGGAAGTTATTGAGTTTTGACTTATTCTGGCCTGTATTTCAGATCGTTCAGGAGCTTGAGAAGCAAAGAATAGAGACTCTGGCCAACACCCTGAACAAGTACAGTCTCTTCATGACTGTTTATTCACAGACCGTCATTCATGTAAGCAAATCTATATGAAAATTATCAAAATGTCAACAAATAAAGCATAATGAATTGTCCCTTCGCTAAGCCCCACCCTCCTTGGTTACTGTTGCTACGCCTGCTTTCGTGCCTGGCACGCCTATAACAATATGTATGCGCCAGTGTCAGACATTGTCAGGGATATTATAGTCTTTTTTTTTTTAAATATTTATTTTTGGCCTTTTTTAGACAGGACAGAATTGAAACAGGAAGCGAAGTGGGAGAGAGAGAGAGAGGAGGTAGGTTAGGGAAATGTCCTCGAGCCGGGATTCGTACTCGCGATGTTCTGACGTGCTTTTGCACCATATGTCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25441
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 |
---|---|---|---|---|---|
ENSDART00000113855 | Nonsense | 323 | 537 | 12 | 16 |
ENSDART00000142338 | None | None | 65 | None | 2 |
ENSDART00000143102 | Nonsense | 323 | 404 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 49890425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49145621 |
GRCz11 | 9 | 48843106 |
KASP Assay ID:
554-7727.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGTACGCCTTTAGCTCAGCACTGACACATAAATCTGGTTTTCAGGTT[T/A]AGAGAAGATGGTGAAAGTCTATACAGAGCAACCAAACTTCTCAAACCAGA
Long Flanking Sequence:
ACCATTTTGTTGTTTGTCAACCGCCATTAAATTGAAGAAGACGAAGAAGAAGAAGCAGATTTACGTTATGCTTTAACAGGGGGCAAACACTTTCACACATTGTTTTACATATATTTTTAGATTTAGTTTTCTCTTAATGATAAAAACCTTCATTTCAGAACTGCATGATGTGTTTACTTGTGTTATCTATGACTAAAATTTCAATTTCTTAAATGATTTGAAACATTAATGTGTGACAAACATGCAAGCAATTAAGAAATCATTTTTAAGTACAACTGTATATGTATATATAATTTAAACATAACTTGTCTCTTGTCTGTCTGGTCAGGCGCAACGAGAGAAGTGGGAAACTGCTGGTGATTTTATGGAAAGCTAAATTTTGTGTGAAATGCCCCCTTTAAAAGAACATTTTATTCCTCAGAGATCTTATTAGGTGTTCCTGTGCTGTTATAATGTACGCCTTTAGCTCAGCACTGACACATAAATCTGGTTTTCAGGTT[T/A]AGAGAAGATGGTGAAAGTCTATACAGAGCAACCAAACTTCTCAAACCAGAAAAACCTGGAGGAAACCGAGCAGTTACTGGAGGAGGTGAGACACTCTTACATGTAATAACAAACATGTAACATCTAAATTACATTTTCATTGAGACTTTTTGACTATTTAAAGGTGCAGTATGTACGTTTTTGACTCTTTTAATGCATAATAATAGCATGCTACGTTTGCAGATATTTACCAAACAAGTGAACGTACTTGATTATCTGTTAAACATTGCTTAAAGTCAGTTATTCTCCTTGGAAAACGTGTATCACGGGTCAGTATGTCTGTCTCAGTTTTGGAATCTATAACCAGCCCACTGCCAGTTTACCCAATTATATTTCAGCACCTTGGGTTGCCTTGATAGTAAACAAACCGTTTTTTTCTTCAGTTATGAAGGCTGCATCGATGTATGCGGGTATGGCCAAAAATGCAGATACAGTGCTATAAAAATCCACATAAGCTGTTT
Associated Phenotype:
Not determined