Busch Lab

ZMP

tnikb

Ensembl ID:
ENSDARG00000009031
ZFIN ID:
ZDB-GENE-051113-320
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.
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.
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.
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