ZMP
tnikb
Ensembl ID:
ZFIN ID:
Description:
TRAF2 and NCK interacting kinase b [Source:UniProtKB/TrEMBL;Acc:Q32PQ9]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6774 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37905 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44157 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6774
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008374 | Nonsense | 41 | 537 | 2 | 14 |
ENSDART00000017384 | Nonsense | 41 | 522 | 2 | 14 |
ENSDART00000097792 | Nonsense | 41 | 1410 | 2 | 32 |
The following transcripts of ENSDARG00000009031 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 27402055)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 26460412 |
GRCz11 | 24 | 26605453 |
KASP Assay ID:
554-5019.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTGAGCTGGTGGAGCTTGTGGGAAATGGRACCTATGGACAAGTATAT[A/T]AGGTAAATATTGACTTTTCTGTTTGATMTGGTTCRTGTGATTGGCTGGAT
Long Flanking Sequence:
GTTTAAACCCCTTATAAAAATGACTTTTCATAATAGGTCTCCTTTAAAGTCTAAAATTTTGCACCTTGATGTAGTTCTTCTTTAACCTAAATTAGATAAGAACAATATCACCTGATTATTTTAGTATAATGATTATTACATAAATGAATTGTAAATAGAGCTAATAAAAATATGATTTTGCAAGGGAAATATTAAATCACAAGAAATATTGTTATCACTGTACTCAACAACATCTCATATTTTCCCAGTATTGCAGCCCTTGTAATACACTGTTATGTTCAAACAGATATTAAACTTTAATTCACACTCTTTGTTACATCTAATGACTGCAGAATCAGCATTTATGATGGCTCTAGTGTACATTCTATCTGTGATTGATTCATAATGTTCAATGACAGGATAATGCAATCTAATCTTCTGTTATTTTCTCCCCTAAGGATCCTGCGGGCATTTTTGAGCTGGTGGAGCTTGTGGGAAATGGGACCTATGGACAAGTATAT[A/T]AGGTAAATATTGACTTTTCTGTTTGATCTGGTTCATGTGATTGGCTGGATGTAGCTAGTTTAGTTCCAAAACATGTTTGGTGTTCCCCTCAGCTGTTTCTGCTCTTCCTCGAGTCTGAGATCTGCTCTTACCTGTTAGTGGCTCAGCAGCTTGCGTTATACATGTGGTATGTCCTGACATGTCAAGACTCATGTGTTATTTTGTACTACTAGATTCTTCGCCCTCTTCCATTGCCTGTTCAGAAAGTAGTGAGTCAGATTGTTCAATTGAAAGACTTGTTTGCATTTTTGGACGGGGTGATGTGTTAGCAAGGCTTAGGTTTTTTAAATGATATTGATGAAAATGTCAGGTTTAAGTTGCTGATGGAGTCTCTGTGGGGATTTGTAGAGTTTGTTACTGTCTGAACTAGAGGTGTAATGATACTTAAAAAAAACATTGTTCAGTATTTTGAAGTCATGTTTTTGGAACAGAAGTATGGGAAACTAAACATAAAATGGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37905
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 |
---|---|---|---|---|---|
ENSDART00000008374 | None | None | 537 | None | 14 |
ENSDART00000017384 | Nonsense | 421 | 522 | 13 | 14 |
ENSDART00000097792 | Nonsense | 421 | 1410 | 13 | 32 |
The following transcripts of ENSDARG00000009031 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 27345988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 26404345 |
GRCz11 | 24 | 26549386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCAACAGCGACGGGAGAGAGAGCTTCGCAAACAACAGGAGAGAGAG[C/T]AGAGGAGGCGCTATGAGGAGATGGAGCAGCTGCGGAGAGAGGAGGAGCGG
Long Flanking Sequence:
AAGTCACCACACATGTAAAGCGACTTTCACACCAGATGTGGAAAGCACTGCGATTTGAAACCCATTCATTTCAAAGGCTTGTGCAGCACAAGAATGGTTTGTTGCTATACTGACCAAAGCGCAAGAGCAGTGGTTTACACCTAGCTTGTGCACCCAACCCCTTATGACAACGCTGGTAAAATGACTGGTCTCGACTCTTTCATCCCAGAATTTTAATTTCGGTGCATCCCCACTTAACAGTTTTAGTTAAACTCGGCAAAAAACTTCATACGAGTCATTGTCCTCACTAGTTGACCATACCATGTATGTTCAGAAGCACTGCCACCTACTGGCCAAAAGTAGTAAATCATAAAACAATATTCCTGTAAAAATGACTCAATATTACACTAAAGTCTTGAATAACCAGTAATTGCTGCTTGCAGCTGTATTGAAGACTTGTGTTTGTACTCTTCCAGCAACAGCGACGGGAGAGAGAGCTTCGCAAACAACAGGAGAGAGAG[C/T]AGAGGAGGCGCTATGAGGAGATGGAGCAGCTGCGGAGAGAGGAGGAGCGGAGGCACGCCGAGAGGGAGCAGGTATATGCATGCCCTCAACCAGTATTTTTGCCCACTTTTATATCAATAGTAAAGTAGAAATAGGGCAAGAACTGACGGGCAGACTCCAAATATACATCATTATTCAGACTGTTATATGTTGGTCTATTATTACATACTGACCCATAATCTGCTCTGCAAAAAGAGATGGGGAAGCTCAGCCATGCTAGAAATGTCAGCTGAGCTCATGTGAACAGGAAGGGAAGAATAAGTGATGTGGCAGCTTCACACACTCACACTCTCCACACGCTAACAAACTCCCACTCATTCACCACTACAGAGATGGAGACGAGATGTACTTTGTTAATAAACTGCACATGTACAGAGATGAATAACTTTTTTTTTAAAGAGATACCAGTTGTTTCAGTGTTCAAGCCTTCAGAACTGATTTATTATTTTTTTTATGAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44157
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 |
---|---|---|---|---|---|
ENSDART00000008374 | Essential Splice Site | 510 | 537 | 13 | 14 |
ENSDART00000017384 | None | None | 522 | None | 14 |
ENSDART00000097792 | Essential Splice Site | 1383 | 1410 | 31 | 32 |
The following transcripts of ENSDARG00000009031 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 27293749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 26352106 |
GRCz11 | 24 | 26497147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACAAGCGAGCACAGCGACTGAAGTTCCTGTCTGAGAGAAATGATAAA[G/A]TATGTCAGCAGGATTGTTGTTTTGTTTGCCCCTATTTTATTAATCCTTTA
Long Flanking Sequence:
GACCATATCTAAATGTTTTGAAGTTCCAGTGGCTACAGTGCAAAGTCTTATTAAAAAATACAAGACATTCTGCACTGTGAAAAATCTCAGCGGGCGTGTTCAATATTTCACATTATGACTACTTCTTCCATGCATCTGAAGCACATGCATGTGTACAACATTCACTTAATCTAATTAAGAATGTAATGGAATAGGGGGATAGTGAATGAGAATCAAATCGAATCACACACCTGAATGGAAACCCAGCCCTATTGTTGACACTGAATGTGCAGGAATGAGGTTTTAATGTATTTTGGAGCTCTCCTGTCACTTCTTTCTCTTGTGTTTTTGTGTGTGTGTTCACTACTGTGTGTCCTGCAGCCTATATCCACTCCAACCAGATCATGGGCTGGGGAGAGAAAGCCATTGAGATCCGCTCCGTGGAAACGGGACACCTCGACGGAGTTTTCATGCACAAGCGAGCACAGCGACTGAAGTTCCTGTCTGAGAGAAATGATAAA[G/A]TATGTCAGCAGGATTGTTGTTTTGTTTGCCCCTATTTTATTAATCCTTTAAAAATGCATCATAATGTAATTTCTATTTTATTATTTTAATTTTTTTGTGTGTGTGTTTTTATTTTTAAGTGTTTGATGCAACAGTCCTTATATGACATTATGGAAAAATGTCTCATTTCATTGTTTGTTATATAAAGTTAATAATTGTTATACAAATGTTTATTTTTCAGTATAATGAAAACTACAAGTTTTTTATATTTGTATATAAAGTTTTAATACAAAATATATATTTTTTATATTTTAATCTTTTTATTTAAGTTTTTATTTGAATTTTTATCAAATTTTAGTTTTATCATTTTTATATAACATTTGTGTCGATTTAAATGTTCATTTATTTAATGTAGTTTAAGTTTAATTAGCTCACCATTTACTCATACTCTGATGTTTTAAAGGTGCTGTATGTACATTTTTGACTCAATAATACAATAATATGTTTGCAGATATTTAAAA
Associated Phenotype:
Not determined