ZMP
tnika
Ensembl ID:
ZFIN ID:
Description:
TRAF2 and NCK interacting kinase a [Source:RefSeq peptide;Acc:NP_955997]
Human Orthologue:
TNIK
Human Description:
TRAF2 and NCK interacting kinase [Source:HGNC Symbol;Acc:30765]
Mouse Orthologue:
Tnik
Mouse Description:
TRAF2 and NCK interacting kinase Gene [Source:MGI Symbol;Acc:MGI:1916264]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32926 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19764 | Nonsense | Available for shipment | Available now |
sa25812 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8613 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32926
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 |
---|---|---|---|---|---|
ENSDART00000051234 | Nonsense | 321 | 1303 | 11 | 31 |
Genomic Location (Zv9):
Chromosome 2 (position 25919983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26116179 |
GRCz11 | 2 | 25771813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGAAATGTGACTGCTGAATGTTTTCACACCTACAGATGAGACGGAGTA[T/A]GAGTACAGCGGGAGTGAAGAGGAGGAAGAGGCCATGCTTGAGATTGGAGA
Long Flanking Sequence:
CATAAAAGTTTCACATTATTACTAATATGTAGTTTTATCAAAAGTAATTTTGGTGTGCACAAAAATCTTACAGATCCCAAATGACATATATTTAGACTTTGAAGTTGTTGATCATCATCTTTGGAAAATGTTTTTCTCGTATTGTGTTTGTGCCATACTACTTGTGATAACTACCACTTGTCTGATATTCAGTTGAATATTGTTTGTCTCTGTAAAGCTAGGGTAGTACAGCTTGTGCAATTTTAAGTGTCATCGAGAGATGGCCATTAAATCTAAAAATCTGTTTGTGAATGCTGCTGCAAACCTTGAACATCCTACAGTAAAGTGCACTTCAGGGGGGAAAAAGCTACAAAATCATTGATTTTTGGCACTTTAAAAGCAGCCAGATGCTTTAAGGACACTGAATGTCAAGATACCTGTCAGGGATCCCATCAGGGAGGGCTTTGCATGTCTGAAATGTGACTGCTGAATGTTTTCACACCTACAGATGAGACGGAGTA[T/A]GAGTACAGCGGGAGTGAAGAGGAGGAAGAGGCCATGCTTGAGATTGGAGAACCCAGGTAGAGCATGCATCAGATTTTTGGGGTTGTATTTGAGTTGTATTTAAGTATTTAAAGGAAAAAGGCTTGAAACCTTCATTTGTTTCCATGTAGCTCCATTATCAACATACCCGGCGAGTCGACTCTACGGCGGGATTTCCTGCGCCTGCAGGTGGCCAATAAGGAGCGTTCAGACGCCCTGCGTAGACAACAGCTTGAGCAGCAGCAGAACGAGGGACACAAACATCAACTGCTGGCAGAGAGGCAGAAACGCATCGAGGAACAGAAAGAACAGAGGCGCCGATTAGAAGAGGTAAACATCTAGAGATGATTCTTCCTGATGTTATTCGATCACCTATGAGTGAGCACAACCCTAGTTATTCGAGACTTCTGGCCTCATTTACTTCCATTGATTAAAGAAAAACAGCTTATGCTTTTTTTAATCTATAGTCATAAACACAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19764
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 |
---|---|---|---|---|---|
ENSDART00000051234 | Nonsense | 373 | 1303 | 12 | 31 |
Genomic Location (Zv9):
Chromosome 2 (position 25920230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26116426 |
GRCz11 | 2 | 25772060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCCTGCAGGTGGCCAATAAGGAGCGTTCAGACGCCCTGCGTAGACAA[C/T]AGCTTGAGCAGCAGCAGAACGAGGGACACAAACATCAACTGCTGGCAGAG
Long Flanking Sequence:
TGTCATCGAGAGATGGCCATTAAATCTAAAAATCTGTTTGTGAATGCTGCTGCAAACCTTGAACATCCTACAGTAAAGTGCACTTCAGGGGGGAAAAAGCTACAAAATCATTGATTTTTGGCACTTTAAAAGCAGCCAGATGCTTTAAGGACACTGAATGTCAAGATACCTGTCAGGGATCCCATCAGGGAGGGCTTTGCATGTCTGAAATGTGACTGCTGAATGTTTTCACACCTACAGATGAGACGGAGTATGAGTACAGCGGGAGTGAAGAGGAGGAAGAGGCCATGCTTGAGATTGGAGAACCCAGGTAGAGCATGCATCAGATTTTTGGGGTTGTATTTGAGTTGTATTTAAGTATTTAAAGGAAAAAGGCTTGAAACCTTCATTTGTTTCCATGTAGCTCCATTATCAACATACCCGGCGAGTCGACTCTACGGCGGGATTTCCTGCGCCTGCAGGTGGCCAATAAGGAGCGTTCAGACGCCCTGCGTAGACAA[C/T]AGCTTGAGCAGCAGCAGAACGAGGGACACAAACATCAACTGCTGGCAGAGAGGCAGAAACGCATCGAGGAACAGAAAGAACAGAGGCGCCGATTAGAAGAGGTAAACATCTAGAGATGATTCTTCCTGATGTTATTCGATCACCTATGAGTGAGCACAACCCTAGTTATTCGAGACTTCTGGCCTCATTTACTTCCATTGATTAAAGAAAAACAGCTTATGCTTTTTTTAATCTATAGTCATAAACACAATTGTTTGTTGAGCAAGTAGTTCAATGGTGTTTGTTATTCCTAGTCATTTCCAAATAGGCCAATAAATCAGAAGTCAAAATTGCAGAAAAGAGCTTACTTTCACATTGAGGAAACCGAGACGGGCCGTTGACGTGCCCACCTGCTTTCAAAGATGATATAATGAATAAACCGCTAGCAAAAGATTTGGGGGTTTTGATTTGGGGTTCCAGTGTTTATGAAAATGGTTTGTGTCAATATGTTGATCCACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25812
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 |
---|---|---|---|---|---|
ENSDART00000051234 | Nonsense | 1064 | 1303 | 26 | 31 |
Genomic Location (Zv9):
Chromosome 2 (position 25946824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26143020 |
GRCz11 | 2 | 25798654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGAAAAAAAATAAGCTCCGTGTGTACTACTTGTCATGGCTAAGAAAC[C/T]GAATACTGCACAATGACCCGGAGGTGGAGAAGAAGCAGGGCTGGATCACT
Long Flanking Sequence:
TCACAATATCAGTTTTGGCCAATATTGTGCAGGGCTAGTAAGCGGAGATTATTGTTCCTAATTTATTTAAAGGTATAGTTAAAATTTTTTCCAAAACTGTTTTTTTCTTATGTTGATCGCAAATGAAGACATTTTAAAAAATTGTATCTGGTTACCACTTACTATGACTTTTTTTTTTCTTTAATAGGGATATCAGTTTCTAACATTATTCAAAATATCTTCTTTTGTGTTAAACAGAAATAAGAAACCTTTATAAATATTTGGAACCACTTTTTTTCCATTTTTGGTTAAATGTGCATTTAGGGTTACTGAGGAAATGTCCTCAAACCAATATGACATAAAAGAAACTTCCCTCCCCCTAAAATGTTATTGAATCTGGTGGCATCTTTTTGGGATACACATATTTTGTTTTAAGCTAATGACATTAACATGTCTCATCATTATTTATTGCAGGGAAAAAAAATAAGCTCCGTGTGTACTACTTGTCATGGCTAAGAAAC[C/T]GAATACTGCACAATGACCCGGAGGTGGAGAAGAAGCAGGGCTGGATCACTGTTGGTGAACTCGAAGGCTGCATCCACTATAAAGTTGGTATGTGAATTATATTTATAAAGGGTTGTGGCAGTGAGATTTTGTACCAATAAACACTTAAGCATTTAAGTTATTATTGAATCATATTTGAATAAATTAAGATACATCTTAATTAGGTTTTCAGTTAAATATTTTCAGAAAATATTAAGTGTGGTGTGATTTTTAACTTGTCAATATTGTTGCTTAAAAAAAAATGGACCCAACTTTTTAAAACATTTCAATATTAATTTTATTTCATAATTTTAGTAATGTTAGCAGTATATTTGACAATTGGATTAGCTGCAATTTATAGTAGTTGGTATTGTAAAGTAACAAAATACAAATACTCAAATTACTAACGAGTAGTTTTTCTGAGGAAGTGTACTTTACTAATTAGTTTAAAATGTGTCATGTTTAGTGCTGTATCGGCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39838
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051234 | Nonsense | 1148 | 1303 | 28 | 31 |
Genomic Location (Zv9):
Chromosome 2 (position 25948999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26145195 |
GRCz11 | 2 | 25800829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCACAGACCTCAGCTGGTGGACCTCACAGTAGAAGAGGGTCAGAGGT[T/G]AAAGGTCATCTACGGCTCTAGTGTGGGCTTTCACGTCATCGATGTGGATT
Long Flanking Sequence:
AAATCTTGTAGATTGTCATTCTGGTTGCCTCTCAGTGCACAGAGAGGCCCAGCGGGACATGGTCTGCTTCCTTGTTATAAATATGATAGACTGCAACTGTGAGCTGCAGGTAACTGAACGCACGGTTTACTTTGTTTTCAGTGAAATACGAGAGAATCAAATTCCTGGTGATTGCACTGAAGAACTCGGTAGAGATTTACGCATGGGCCCCCAAGCCGTACCATAAATTCATGGCTTTCAAGGTATGGTGCTCTAAGAACATTTTCTCATCTCTCAGTTTTTCTCTGCATTTCTTACATGCTTGCTTTTCTGCCTATTTAGCCAGTTTGTGACAGAATCATTTGTAAAGGGTAAAAATGCCTTTGAGGTTTGCGTGCATTAACTGCCTGTTTATCCAATTGTTAAGTCTTGACATGCATCTCTTTCTGCCTGGCAGTCGTTCACAGAGCTGCAGCACAGACCTCAGCTGGTGGACCTCACAGTAGAAGAGGGTCAGAGGT[T/G]AAAGGTCATCTACGGCTCTAGTGTGGGCTTTCACGTCATCGATGTGGATTCCGGAAGCCCCTACGACATCTACATACCGTCACATGTAAGTGATGTGATTGTAAATATTATCAACTGAACAAAAACAGTAGTTTCATACTGAATAGTGCTGCAATTTTATTGTGAAAATAAAATCACTTGATAAACTAAATAATTAAGACATATAGGAAGTATTTACATGTGTTGACACTTTTCTGAGGTAGGTGAGAGAACTCAAAAGGGCGGCAAGTTAAGGAAATCTGTTCATATAAAAAGCATCAACAAATAGAGAAATAATTATAATCAGCTTGAAAACACTTGCGCACACAAATTCTCACAACACATGCAAATACAGAAATATGCTGCAAATAGCACAGATCACAACAAAAATGTGCCGGGGCACCATAATAAGTAACAAACCCAGCTGCTTCCTGTTTTGAGTGGTGTTTCAGGGATCTAAGAGGTGAGTTTTCTTTTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8613
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051234 | Essential Splice Site | 1177 | 1303 | 29 | 31 |
Genomic Location (Zv9):
Chromosome 2 (position 25952592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 26148788 |
GRCz11 | 2 | 25804422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACTGGTCTCCTTTAGCACTGCAGCCTGTAACATCTTTTTTTCWTCCTT[A/T]GATTCAGAGCACTGTGACTCCTCATGCCATCGTGGTGCTTCCGAAGACTG
Long Flanking Sequence:
TTCATCAAATGAGAAATAATGTTCTATCTGTCTAATAATGTGTTTAAGCGGAAATATGCTTAAATATATGTGCCAAAATTAGTTGAGCAATTTATTGCATTTTTTCCTTGTGTACATTTTTAAAAAATAAAGCTTCTTTAGTGACATTGATAGTTCAATGATGAACATTTGATGTCTGTGGAACAAATATTATTTAAATTCAAAAAGGTTCTTTAAATTAGTAGTTTATCTTCAGATAATAAAAAAAATGCTTATGAATTTTTCATTAAAAATTTTATTCATTTTTAATGAATTTTTAATGAACCAAAGAAGTTCTTATATGACACCAATGCAAATACTTCTTTTAATGTTTCTTTTTTTGTTTTTTGTTTTGTTAATAGTGCACTTTTGCAGTACATTCCCTTAAATTCCCAGTAAACATTAATGAACAAGATTGGAAAATGTGGCCCTCTACTGGTCTCCTTTAGCACTGCAGCCTGTAACATCTTTTTTTCTTCCTT[A/T]GATTCAGAGCACTGTGACTCCTCATGCCATCGTGGTGCTTCCGAAGACTGATGGCATGGAGATGCTGCTGTGTTATGAAGATGAGGGCGTTTATGTCAATACCTACGGCAGAATCACCAAGGACGTTGTCTTGCAGTGGGGAGAGATGCCCACCTCTGTTGGTAAGTCTGCCACAATGACATATGTCATACTGTAGTTGGTGCTATATTTGTTTTAGGACTTACTTGCAGTCATTTAAAAAACTATGTTTTATAAAGCAGGATTTAAAGCTTGATTTAGGCGATGCAGTGGCACAGTAGGTGGTGCTATCGCCTCACAGCAAGAAGGTCGCTGATTCGAACCTCGGCTCAGTTGGCTTTCTGTGTGGAATTTGCATGTTCTCCCTGCGTTCGGGTAGTCCGGTTTCCCTCAAAGTCCAAAGACATGTGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGCAGTTTGAGTGCATGTGTGTGTGTGGCTGTTTCCCAGAAA
Associated Phenotype:
Not determined