ZMP
si:zfos-2326c3.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
NRK
Human Description:
Nik related kinase [Source:HGNC Symbol;Acc:25391]
Mouse Orthologue:
Nrk
Mouse Description:
Nik related kinase Gene [Source:MGI Symbol;Acc:MGI:1351326]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16332 | Nonsense | Available for shipment | Available now |
sa38982 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13811 | Nonsense | Available for shipment | Available now |
sa13810 | Essential Splice Site | Available for shipment | Available now |
sa42350 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16332
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 |
---|---|---|---|---|---|
ENSDART00000044203 | Nonsense | 296 | 1165 | 10 | 32 |
ENSDART00000138586 | Nonsense | 292 | 1063 | 10 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 9866284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 9361641 |
GRCz11 | 14 | 9667655 |
KASP Assay ID:
2260-7300.1 (used for ordering genotyping assays)
KASP Sequence:
CCACAGAGACGCTYTTACGSCATTCCTTTATTAAAGRCCTTCCCAATGAA[C/T]GACAAGTACGAATCACACTTAAAGATCAWCTGGACAGAACCAGGAAGAGG
Long Flanking Sequence:
CTTTAGTAATCTGTTTAACACATTTTTATCAGTTTTTTTTTAATAATTTTTATTATTTGTTTTCATTTTTCTTATACTTGTCTCTTTTATTCCTGTTTATAGAAAGCACTTTGAATTGCCACTGTGCATGAAATGTGCAACATAAATAAACTTGCCTTGCCTAAATCTTAAAATTGCACTTTAAGTTGAATACTAGTATCTTGCAAAATAATATAAAAATAGTATGTACTGCAAAGGTAAAATAAATTAATTAGAAATAAGACTATAATGTTTAAAGATGTGTTGGAAAAAAATATCTCCTTGAAGCAAAGAATTAAAATTTCACATGTGGGCTAATCATTTGGACTTCATATATCATAAACCCTTTTTATTTGAATTGCTCCTCAAGGTCTAAAAAGTTTCAGACTTTTGTGGACAGTTGTCTGGTGAAGAACTACCTCCACAGGCCATCCACAGAGACGCTTTTACGGCATTCCTTTATTAAAGACCTTCCCAATGAA[C/T]GACAAGTACGAATCACACTTAAAGATCATCTGGACAGAACCAGGAAGAGGAGACAAGAGAAAGGTATACCTGATAGACTGATTTTTTATTTTATGTTATTTAGTTTTGCGATTTTTAGATCAATGTGATTACAGGTTACGTTTCTTGTGCGTTTAAAAGTTCGGTGATTTTTACTGAAGCCTAAAATTTGAAGTGTCATTAAAAGCAACCGCAGTGGAATATTCCATTGATTCTAACAGTACTGTTGTTTTAAATTGTTTTCATCTCTGTTTCAAAATCAGATGGGAAGGAATATGAATATAGTGGAAGTGAAGATGAAGACGATGGTATAAATGAAGAAGAAGGTGAACCCAGGTATGTGTTAATCGTTTTTCCTGATCTCCTTGCAGAGTCAGCATCTTTACTTCTGCAAATAATGCTTCCCATAAGTCTAAATTGGATCTTTTCTGTATGGAGGCGGGTATTTGTTATAGAGGCAGAGCAACTGATTGCTTTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38982
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044203 | Essential Splice Site | 661 | 1165 | 20 | 32 |
ENSDART00000138586 | Essential Splice Site | 559 | 1063 | 17 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 9844591)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 9339948 |
GRCz11 | 14 | 9645962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATCCAAACAGAAACTCTCAAAGTCCAGGAGCATCACCACACAACCAG[G/A]TGTGAATCTGCATCACATGTATATCAGATGATTTTGCAGTTAGTTTAAGT
Long Flanking Sequence:
ATGACGCGATGCACTGAAGTAAACATTCTTCAGCGCTTTGATCGTAGGCTTAATAGAACAGCCAATGCTGATCACATCTGTGTTATCATACGCATCAAATGGTTAAAATTGTATTAATTTTTTCGTTCATTACTCGGTGATTCCTCCGTGCACCACTAGAAGTAAGCCCACACAATTTGCGAACCACTGTATTAAAGCAATATGAAAAGAAGAATGAATGGGAGTGAAGGGGATCATAAGTCTTGACACATTTAAGTTACATTGGCCACATGTGAGAAATAAGGTGGATAGATCATGGAAATTCATTTTTTTAGTTAGTAAGGTCATGGAAAAGTCAGGGAATTTGACATTTGTCTTAAAGTGGAAACAATGGCTTTTAAGTATATGTCAGTGAATGCTGTCATGTAGATGTTTTTGTTCTTGCAGGGTACTGTGTTCTGGATAATCCAGCTCATCCAAACAGAAACTCTCAAAGTCCAGGAGCATCACCACACAACCAG[G/A]TGTGAATCTGCATCACATGTATATCAGATGATTTTGCAGTTAGTTTAAGTAGACTGCTGACCCTATTTTATACATTACATTGTATAGGCAAATGTATAATGAATTTCTGATCATTTTCTGAATTTATAGTGTGAATCATAGAGATTATCACAATAAAATGGATTACTCATAATAACTTTCATAGCAATGTCAGATGTCTCTCTTTATCTTGCATTATTTACTGACAAATGCATCAAAATACAGTTGAAGTCAGAATTATTAGCCCCCTTTTGTTTTTTTTTTGTTTTTTTAAATATTTCCTAAATAATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTTCTTCTGGAGAAAGTCTTGTTTGTTTTATTTCGGCAAGAATAAAAGCAGCTTTAAATTTTTTAAAAACCATTTTCTGGACAAAATTATTAGCCCCTTTAAGCTATTTTTTTCGATAGTCTACAGAACAAACCATTAAAATACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13811
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 |
---|---|---|---|---|---|
ENSDART00000044203 | Nonsense | 718 | 1165 | 22 | 32 |
ENSDART00000138586 | Nonsense | 616 | 1063 | 19 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 9839024)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 9334381 |
GRCz11 | 14 | 9640395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGAGGGCAGACTAATGAAATCATTCTTCAGCCTCATCTCAATGTAAAA[C/T]AGCRGCAGGTAAARTCACCTTCACTATGTTGTTTTAGGGACMGTACGATA
Long Flanking Sequence:
TTATCTTAGCTGTCTACTATGGAGGATGAGGGAGCTCTCAAATTTCATCTAAAAAATTGTGTTCTAAAGATAAATGAATGTCTCGGGATTAGAATGAAATACAGCCAAGTAAATAATAGCAGAATTTTCATTTTTGGCTTAACTAATGCTTTGTTTTTACATTTGTGTCTATATTTTATTTGTGAAGTCTTAAGGGAAAATAGTAGTATGCTCCTCATGCAAAATCTAAAGCCCACGTGATCATCCCCTGTTGTCATTAGATGTGGGAATGAAGTGAACCTGTTGTTGTTGTTGTTGGTAAAAATGTGTTCTGTCGTACTGTATTCTTACCAGTGTTTGTAGTTTGCTGCATTGTTCATGGCCTGAAGGAACAAACGTTTTCTTTGACATCATTAAAATTGATCTGGTTGTTTTCCAGGTCTCCATCGAGCAATGGAAGGCCTGTGTTTTCCAGAGGGCAGACTAATGAAATCATTCTTCAGCCTCATCTCAATGTAAAA[C/T]AGCAGCAGGTAAAGTCACCTTCACTATGTTGTTTTAGGGACAGTACGATATACTGAGAAAAATAAGTCATTTTGTTTTGACATACTCTTGATTTTATCAGCCATTTAAAGCAAGGGTGTCAGACTCAGTTTCTTGAGGGCGGCAGCTCTGCACAGTTTAGTTCCATAAATGTAGTATAAAATAGAGTTTATTTATTTTTATCTTGCAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTCTGAACATATAAATTATAATTATAAATATTTTATATTATAATATAATTTTAATAAATCCTGTTTTGTTCAAATGCACCAAAATATATTGCCTATATTCACTGAAAAATGGATAAAAATATTTCTGGTTTTAAATTGGGATGTACTCATTTATGCTTAATTTACAGTGTTTCATAGATATTGTCAGTGCTTAAAACATGTCCTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13810
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044203 | Essential Splice Site | 809 | 1165 | 24 | 32 |
ENSDART00000138586 | Essential Splice Site | 707 | 1063 | 21 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 9835216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 9330573 |
GRCz11 | 14 | 9636587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGTTTGCTTCAGATTTCTCCACCTCTGAGTCCGCAGGGACACKGCCAGC[G/T]TGAGTCCACATGACTGACAGCCACTGACATACATGCATGTCACATTTACA
Long Flanking Sequence:
GTTTCTGAAATATTCAGACCAGCCCGTCTGGCACCAACAACCATGCCAGGTTCAAAGTCACTTAAATCACCTTTGTTCCTCATTCTGATGCTCAGTTTGAACTGCAGCAGATCGTCTTGACCTTATCTACATGCCTAATTGCACTTTGTTGCTGACGTGATTGGCTGATTAGAAATTTGCCTTAACAAGCAGTTGGATAGATATACCTAATAAAATGGCCAGTAAGTGTTATTGATGCTCATTGATGGTAAAAAAAAAAATGGTTTTCTATGAAAATGTAGTAAATTGTTTTTGTGATTTTTCATTTTGCAATATTGTATAAAGACGCAATTATTAGCGATCTCTATGTGATGTTTGCCCTGTTGTTCTGCATTTACAGAAACTACTCAATAACCAGCCAGGAAAAAGCGTGTCTTCTTCATCTTCCTCATTCTCAGCTTTCATTGACCCTCGTTTGCTTCAGATTTCTCCACCTCTGAGTCCGCAGGGACACGGCCAGC[G/T]TGAGTCCACATGACTGACAGCCACTGACATACATGCATGTCACATTTACAAACTCTCTGTCTGTCTCTCTGTGTGTGTTTCAGTGAATGGCAGGTGTGAGCCATGCGTTAGACAGCCTCACAGGAAGGGCTCAGTGGTGAACGTCAACCCCACCAACATTCGACCACAGAGTGACGCCCCAGAGATTCGCAAATATAAAAAGAAGTTCAACGCTGAGATCCTCTGTGCTAGTCTGTGGGGTGAGACACATTTGTATGCACACAACACAGCTGTGGAATGCAATGATGGCAAGTAACAACTGCCAGGAATCCCAGGGAAACTAGGAATTTCTGGAATATCATGGAATTTTAAAAGGTCTATTGCAGACATTTAAAGTCAGGGGATTAGTTTTTTTGGCCAAGGCATATTAAGGATTTTTGTTTGTTACTTTAAATTTTAGTTTCCCTTTAGTGCTATTTTCTATAGTTGTCCCTTGTTATTCGCGGGAGTTACGTTCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42350
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044203 | Nonsense | 952 | 1165 | 27 | 32 |
ENSDART00000138586 | Nonsense | 850 | 1063 | 24 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 9822422)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 9317779 |
GRCz11 | 14 | 9623793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAACAGGGCTGGACCTCTGTGGGGGACCTGGAGGGATGTGTCAGCTA[C/A]AAAGTAGGTGAGTCTAGAACTGATCTCTATACTCGTTACATTTCTGGTTC
Long Flanking Sequence:
TTACATGAAACATTAGGTCATGAATATTTATATAAAAAATTCTGGAAAAGTCATAGAATTTTAGTAGTAAAAAAGTGTATAAACCCTGAATATTCGCAGACTGTATGTCTTTGAATATATTGATAGTAGCAAGTCTCTGTATTTGCCCTCCCGTAATAATTAAAGCAGCAGCAGCTGCGTAGCAGATCTACTCCACCAAGACCAAACACATCCACACAGCCATATGCAAATTTATTACCATACTAAATCTCTCCAAGAGTTGTCTTGACAGAAATGAGCCTATTTCTGGAAAAAGTGGATTGTTTAATCTCTCCAAACTCAGTATGTGTATGCATAGCTTGAATCTCCTTTATTCGTTTTTTATTGTGGAAAGGTAAGAAAAACAAGCTGAGGCTGTACTACCTGTCATGGCTGAGGAATAAGATCCTGCATAATGATCCAGAGGTGGAAAAGAAACAGGGCTGGACCTCTGTGGGGGACCTGGAGGGATGTGTCAGCTA[C/A]AAAGTAGGTGAGTCTAGAACTGATCTCTATACTCGTTACATTTCTGGTTCTAATAAACTCTACCAACAACCATCAGTGTGCGAGAAATCAAGAGATTTTATTGGGCTAAACTGTTTTTAGCACATTGAAGGTAAGCTAAATTACATACAGTTGAAGTCAGAATTATTTCAGTCCTCAATTTTTATTATGTTTTTCAACAAATTTCTAAACATAATAGTTTTAATAACTCATTTCTGATAACTGATTTCTTTTATCTTTGCTATAATGACAGGAAATAATATTTTACTAGTCGTTGTTCAACTTACCAGCATTGTTTATAGTGACATTTAATGGCTTAACTAGGTTGATTAGGCAAGTTAGAGTAATTAGGCAAACCGTTGTGTAATGTGCTAATAATATTGACCTTAAAATGGTTTTAAACAAATTAAAAACTGATTATTCTAGCCGAAATAAAACAAATAAGACTTTCTTCAGAAGAAAAAAATATTATAGGACATGCT
Associated Phenotype:
Not determined