Busch Lab

ZMP

si:dkey-267j14.4

Ensembl ID:
ENSDARG00000086933
ZFIN ID:
ZDB-GENE-081104-399
Human Orthologue:
TNNI3K
Human Description:
TNNI3 interacting kinase [Source:HGNC Symbol;Acc:19661]
Mouse Orthologue:
Tnni3k
Mouse Description:
TNNI3 interacting kinase Gene [Source:MGI Symbol;Acc:MGI:2443276]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41170 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34364 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41170
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129148 Essential Splice Site 556 835 16 25
Genomic Location (Zv9):
Chromosome 8 (position 18487600)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 17932488
GRCz11 8 17968200
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACGTTTCTGGAGGATCCCTGTTCTCGCTACTGCACGAACAAAAGAGG[T/A]CATTTCAAGAGTATTATTACAATGAATGTATTAAAACACATTAATACTAT
Long Flanking Sequence:
ACTGTGACAATAACTTATTTTCTTTACATTAGACTAAAAATATATCATGGAAATCACAACAATCGACAGACTTTTTAAAAATAGTTTTTGGTCTGTAGTGTCTTGCCTTAAATATCAAATAACAACACACATTAAACCTTAATCCACTAAAACAACTGCATTCATACAGGCTCCTTCGGAAAGGTCTACAAAGGAAAATGTCGCAATAAGATAGTAGCAATTAAGCGGTAAGAGTTTCTTTTAACTTGTTTTGTCCACATCATGTATATAAAGTGAACTGCATTACCTTCATACCTTTCCACAGGTACCGACCAAACACATATTGCTCAAAGTCTGACACGGATATGTTCTGTCGAGAAGTGTCTATCCTGTGTCGCCTCAACCATCCCTGCGTTATCCAGTTTGTGGGAGCGTGTCTGGACGACCCCAGTCAGTTTGCCATCGTAACCCAATACGTTTCTGGAGGATCCCTGTTCTCGCTACTGCACGAACAAAAGAGG[T/A]CATTTCAAGAGTATTATTACAATGAATGTATTAAAACACATTAATACTATTATTTGTTACAAAAAACTTTTATTTGACTTCATATTGATCAAACTATCATGATAAACAGATTATTTACCACTAAATTGTTAAGCAGCTGCTTTCAACATTGCTAATAATAAGAAATGCTTCACTAGTACAAATCAGAATCACATCAGAAGCATCTTGACACTAAAAGTAATGTAATGTAATGTAAAAGTAATGGCTATGATTTATAGTTAATAATTTTAATTTAAAAACTGATCACATTCTTAACTCAAAGGAAAAATTATTTTAATCATTTCTTTGCATAAAATAAAAAAGTGTCATGTTTCAGATGTGTATATGCAGTTTTAGACAATGTGATGCAAATGTTTTAATTTCAAATGTTGAATAACACTTATTTTCATTTAGAACAATTGAAAAAAATTCTGAAAAAAAAAGCCTGTTAATGATTTTATTATGCTATACTCTAAAACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34364
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129148 Nonsense 702 835 21 25
Genomic Location (Zv9):
Chromosome 8 (position 18482110)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 17926998
GRCz11 8 17962710
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGGATACTCAATCCCCAAACCCATCTCAGCACTGCTCATGAGGGGCT[G/A]GAACGTTTGTCCAGAGGTCAGTGGGCCACATCTACCTGAAAATATAACAC
Long Flanking Sequence:
GTTTCATCCACAGAGGTTCAGAGCTGACAACTTAAAGTTCAAAAGCAGAAGACTTACCCACTGAAGTGATATCTATCTTCTTTAAATTTTATACATCTGTGCAACGAATCACATTTATCTCCAGAGCTGAAACGAAAACCAAAACACATTCTTCCACAAGATGCAAGCAGTTATATTTATTAACCACTATAAGGCCAAAAGTTACATACCTACCTTTAAATTGAGGTTTCAATTGTAGTTTTATGTGTAACAACCAAGAGGACTTCAAGAACAGATGAACTAAATGTCTGATTAAATGTTGAACTATATACTTCAAATTTTAGCATTTAAAACAATCCTAGTGTTATGTTAATGTAATTCTAATGAAGTTTTAATAAAAATGTCTCACGTGTGTGAAATGCTTACAGCTGCAGCCGCTGCAGATATGGCCTATCATCATGTTCGTCCACCGATTGGATACTCAATCCCCAAACCCATCTCAGCACTGCTCATGAGGGGCT[G/A]GAACGTTTGTCCAGAGGTCAGTGGGCCACATCTACCTGAAAATATAACACATATACAACACTGTAAAAAATCCAGGCTTTCACTCAATTCATTCATGTTGTCCAAACACTGATTAAGTTAACCGCAACAATTGTGATTCTTCGGCTCATTTTAAATAAGTAATTTGAACAAGCAGGTGATTTATTAAGAGATATGAAACTATTTTATATTTATTTTACTTTAAATCCATTTAAAAAAGTAAGAAATAAACTATGAATTTACTATTATGAAAAACTATAAACATAATATTAGTTGCTTTTGCAGAGGTTTGTTGAAATGATCAAATTCACAGCATCTTGTTTAAAATTAAGGAAAACGTATGGAAAGGATAACATTTTATTAATTTAACTATTGTATGCTTCTTAAATTCATTCTTGAACAACCTATCTGTTGTGCCGAGTTCATCTATAATCCTTCAGATTACCCAGAATCCCTCATCTCTGGAGCTCAGGGCGAGTTTG
Associated Phenotype:
Not determined