ZMP
LOC556172
Ensembl ID:
Human Orthologue:
TAOK2
Human Description:
TAO kinase 2 [Source:HGNC Symbol;Acc:16835]
Mouse Orthologue:
Taok2
Mouse Description:
TAO kinase 2 Gene [Source:MGI Symbol;Acc:MGI:1915919]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa998 | Essential Splice Site | Available for shipment | Available now |
| sa40050 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40049 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19988 | Essential Splice Site | Available for shipment | Available now |
| sa33147 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15028 | Essential Splice Site | Available for shipment | Available now |
| sa19987 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa998
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114631 | Essential Splice Site | 44 | 1141 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21379525)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21035916 |
| GRCz11 | 3 | 21166464 |
KASP Assay ID:
554-0902.1 (used for ordering genotyping assays)
KASP Sequence:
CACTGACCTCCGGGAGATTGGTCATGGCAGCTTTGGAGCRGTGTACTTTG[T/A]GAGCAAGCCACACCATTATTTATCAATGAATGTGTTTGAATGTAKGTTTA
Long Flanking Sequence:
GTTTTGCCACATGGCATTTTGGAAAAAACGTGAGATATCTCAGACAAACCTGTGTACGAAGATTTGAAATGAGATGGTTAAATAACAACAGATAATGTCTGCGAAGACGGTACTTGATTCAAATCATGCATGTCATTCACGTCATGTCAGGGCCACTATCTTTTTTTCAATCAGTGCATTTGTTTCTAATGAAGTCGTCAGCCACTGGGTGACCTTTTATTTGCTCAAAGCCATTTTATATTCTCTGTGATTTGGGATTATTTAAAAACAGAAGTCCACACTTGTAGATGTGTGGTGTTTTAAGGAGTTTCTTGAGGTTTTTCTAATGTCTCTTCTTTTTTTTTAAACTATGTTTCAGGAGCCAGTCATGCCTGCCAGTGTGCGTACTGGGACCCTGAAGGACTCTGAGGTGTCTGAGCTCTTCTATAGAGATGATCCAGAGAAGCTCTTCACTGACCTCCGGGAGATTGGTCATGGCAGCTTTGGAGCAGTGTACTTTG[T/A]GAGCAAGCCACACCATTATTTATCAATGAATGTGTTTGAATGTATGTTTAAAGGCTCTTGACCATATTTTCCTTTCAGGCTCACGATGTGCGGTCCAACGAAGTGGTGGCCATCAAGAAGATGTCGTTCAGTGGCAAACAGTCTAATGAGGTCAGAATCATAACCAGATGTATAATAGTAGGACTGGGGGTATGACAAAAGAAACTAAAGGTTTGACTAATTCATGAAAATGATAACTGTTGTTTTATATAAATTTCACCCAGAAATTATCATTTGTAGTTGGTTTACTCTGGTTATCCAAGATGTTGTAGATTTTGTCAACATCTCAATGTCAAAAATTGTTCAAGTTAACATTTTAAGAGTCAAGCAAAACATGAATAGACAACAAATAAATTGAAACCCACAAAATTTATTCTGTTATTATCCCTGTATGATTAGTAAAGTGTTATTTCAGTCAGTCACACATGGTTATTCATGGTTAAGATCAGGTTAAGTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40050
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114631 | Essential Splice Site | 68 | 1141 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21379373)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21035764 |
| GRCz11 | 3 | 21166312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGTGGCCATCAAGAAGATGTCGTTCAGTGGCAAACAGTCTAATGAGG[T/G]CAGAATCATAACCAGATGTATAATAGTAGGACTGGGGGTATGACAAAAGA
Long Flanking Sequence:
CCACTATCTTTTTTTCAATCAGTGCATTTGTTTCTAATGAAGTCGTCAGCCACTGGGTGACCTTTTATTTGCTCAAAGCCATTTTATATTCTCTGTGATTTGGGATTATTTAAAAACAGAAGTCCACACTTGTAGATGTGTGGTGTTTTAAGGAGTTTCTTGAGGTTTTTCTAATGTCTCTTCTTTTTTTTTAAACTATGTTTCAGGAGCCAGTCATGCCTGCCAGTGTGCGTACTGGGACCCTGAAGGACTCTGAGGTGTCTGAGCTCTTCTATAGAGATGATCCAGAGAAGCTCTTCACTGACCTCCGGGAGATTGGTCATGGCAGCTTTGGAGCAGTGTACTTTGTGAGCAAGCCACACCATTATTTATCAATGAATGTGTTTGAATGTATGTTTAAAGGCTCTTGACCATATTTTCCTTTCAGGCTCACGATGTGCGGTCCAACGAAGTGGTGGCCATCAAGAAGATGTCGTTCAGTGGCAAACAGTCTAATGAGG[T/G]CAGAATCATAACCAGATGTATAATAGTAGGACTGGGGGTATGACAAAAGAAACTAAAGGTTTGACTAATTCATGAAAATGATAACTGTTGTTTTATATAAATTTCACCCAGAAATTATCATTTGTAGTTGGTTTACTCTGGTTATCCAAGATGTTGTAGATTTTGTCAACATCTCAATGTCAAAAATTGTTCAAGTTAACATTTTAAGAGTCAAGCAAAACATGAATAGACAACAAATAAATTGAAACCCACAAAATTTATTCTGTTATTATCCCTGTATGATTAGTAAAGTGTTATTTCAGTCAGTCACACATGGTTATTCATGGTTAAGATCAGGTTAAGTTGTTTCATAACGCTTGATATAAACATTCTGTCTCACCTTAGGGTTATCCCAGAGTTTGCAATTAACTCTGGAACACATGAAAGTGTGACGTGTGCAACAAACAGCCACTTACACAACACATGAGAGAGTCAGTTTGATTCCAATGCAATTCAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40049
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 |
|---|---|---|---|---|---|
| ENSDART00000114631 | Essential Splice Site | 150 | 1141 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21377233)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21033624 |
| GRCz11 | 3 | 21164172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGCACTTCAGGGCCTTGCCTACCTTCACTCTCATAACATGATACACAG[G/A]TGAGATCACGGACCCTCAAGCTTTTCTGTTTATCTCTATTTTTATTTTCA
Long Flanking Sequence:
AATATAAAGGGTGCTACCTCAGAGAGCACACAGCATGGGTAAGTGTCTACACATTAGTCTGTGAGCGACGTGTTTGTCTGACGTGTGTTAATGTGTCTGTATCTCCTGTTAGCTGGTGATGGAATACTGTCTAGGATCAGCCTCTGATCTGTTAGAGGGTGAGTAGCTCAATTTTACCCTTCCTCTTGTTATTTCTTTTTTTTATTTTACAAAAAAGCTGTTATAATCCCTCTCATCTACCCTGTCTGACATTAGAGGTGTCCAATTGTATTTTCGGTGTTGTATTTGTGCTACCATGATCATTTGGAGGAAAATGCTGGTGTAAATATTGTAATCATCAGATTTCTGGATTGTGGTGTTTTCCCACGGTGAAATATTTTGTTGTTGTTTTTCCCCCCTGCAGTGCATAAAAAGCCTCTGCAGGAGATGGAAATAGCTGCTATTACCCACGGTGCACTTCAGGGCCTTGCCTACCTTCACTCTCATAACATGATACACAG[G/A]TGAGATCACGGACCCTCAAGCTTTTCTGTTTATCTCTATTTTTATTTTCATAGCTCACTTTAAGACTTTCTCCTGCTGACTTCTTGCCATTTGGTTTTCACCTTATGTTTTTGTGTCAGTGCTGTAACATACCTGTTTTTTTTTTTTATTATTATCCAGAGATGTGAAGGCTGGAAATATTCTGCTAACTGAGCCTGGTCAGGTGAAGCTTGGAGATTTTGGCTCTGCCTCAATCGTTTCTCCTGCCAACTCTTTTGTGGGTACACCTTACTGGTAAGTCGTGAATGCAAGGGGTTATTTGGTTTTGGCTGTAGTCTGAGAGTTTAATATTATTATTTTTTACCCATCTGACGACAACTTATAATTAGTGATGCACCAAATTGACAAATCAGGGCCCAAACCGAAAATTCTGTATGCACTTGACCTAAAACTGAAACCAAAAATTTTTGATTATTATTTTATTAAATAATATAAAGTAATTATGTGAGACTTTTTCGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19988
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114631 | Essential Splice Site | 715 | 1141 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21360424)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21016815 |
| GRCz11 | 3 | 21147363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGTCAGAAACATGCTGTGGAGGTCCGCCAGCAACCCAAAAGCTTAAAG[G/A]TGAAAGGATAGGGTTTTTTCTTTTTTCTTAATGTGGTGCATTCTACAATA
Long Flanking Sequence:
TCATACACTACGGACAATTTAGCTTACCTAATTATCCTGTACCGCAAGTCTTTGGACTTGTGGGGAAAACCGGAGCACTGTAGAAAACCCACGCAAACTCAGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCGAGGCTTGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCGACTGCATTGCCTACCTTTTATTTCTTATCTGTTAATCTTTTGTCTGTTTTTCCATGTAGGACCTAAATAAGCGTCAAACCCAGAAGGATTTGGAGTGTGCCATGTTGTTGAGGCATCACGAGTCCACTCAGGAGCTGGAGTTCAGGCAGCTGGCATTGGTCCAACGCACTCGAGCCGATCTGATCCGAACGCAGCACCAGAGTGAACTGGCCAATCAGATGGAGTACAATAAACGGCGTGAGCAGGAGCTTCGTCAGAAACATGCTGTGGAGGTCCGCCAGCAACCCAAAAGCTTAAAG[G/A]TGAAAGGATAGGGTTTTTTCTTTTTTCTTAATGTGGTGCATTCTACAATAAAACACACTGAGTGGAAATTTGCATTTTATATAATTTTGCAGATACATTTCAGAGTTAAAAAAATTAAATATTGCAATTTTAATTTGAAGTGAATTGGGAAATGAACGAGAACATAGTATTGCTTTATTAACTGCATTGTTAATACATGAGTAGCATTGGTGTATCAATTAGATTTCATTTGGATTTATTGTAAAATAGGTTACCAGTAGACCTAAATTAAACAAAAGTTGCTTTTCCACTATCTTGCTCAATGGTTGTTCCATTCCGTGCCAATCTGGGTCAGTCAGCATTGGGTACATTTAAAATTTTCCAAGGAGGTGCTGATAATGCAGCTTTCTGGAATGCAATAAAAAATGCGCCGTAGTAACCCAAGTATAATGTAAACAGTGAAATGGAAGATGATCAGATATTTCTGTTTTTGACACTACTTTTTGAGATTACCTAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33147
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 |
|---|---|---|---|---|---|
| ENSDART00000114631 | Essential Splice Site | 790 | 1141 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21358247)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21014638 |
| GRCz11 | 3 | 21145186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCATTGGCTGCTTCTCTACTGATGTCCCACCTCTTTGTTTTCGTAACA[G/A]TTGCGATTGGATGAGACACAGGAGGATGAGTATCGAGCACTGCGCATGCA
Long Flanking Sequence:
GGAATAATGTATGTATGTGTAAACATGCATGGGTCAATCACACAAAAATGGTCAAGAACATGGTCACTTTTCACTCCGTACAAATGATATTTATGTTGAGTTACTATTGTCTTTTTTATGAATAGCTTATTCTTATTAAAATACGCATTATTATATGCATAAAATTATATTAAATATTATTTAAATATATTTAAAGTTTTTATCGTATTTTTTGCTTTTATATTTTATTATATATATTTTTGTAAATAAAATAAAATATGCTGAATCTAATAATAATGCCTTAGTAATAATAATATTGCTTTAATAATTATAATAATAATAAATTGTAAGTATATAAATATGTCTTTTTATTATTATTTTAAAGTTGACCATTGTCGGATAATGTTTTTGACTGGTTTTTGAGATTCTCCTTCTTATAGTTAATTAATCAATTCTAAAGCCATCACGTGTCTTCATTGGCTGCTTCTCTACTGATGTCCCACCTCTTTGTTTTCGTAACA[G/A]TTGCGATTGGATGAGACACAGGAGGATGAGTATCGAGCACTGCGCATGCAGCTACAGCAGGAGTTGGAGCTGCTCAACGCCTATCAGAGCAAAATCAAGATGCACACAGACACGCAACACGAGAGAGAGGTCAAAGACCTGGAGCAGAGGGTGTCCATACGGAGAGCTCTTCTTGAACAAAGGGTAGGAGAGAGAGAAAAGGAATTGGACTGAATGTTGCTCGTTAAATAGGTTCAAGCAGCACGCAACATGGTTGTCATATAACCAAAATGGCCACAACAACAACAAAAAGTCATAGAAACTTTTCTAAATCATCAACATCACCGAACATACTGTGCATCCGGAAAGTATTCAAAGCGCTTCACTTTTTCCACATTTTTTTATGTTACAGCCTTATTCCAAAATGGATTAAAATTCACTTATTTCCTCAACTCTGCACACAATACCCCATAATGACAATGTGAAAAAAGATTTTTTGAAATTGTTGCAAATTTATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15028
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114631 | Essential Splice Site | 850 | 1141 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21358063)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21014454 |
| GRCz11 | 3 | 21145002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACCTGGAGCAGAGGGTGTCCATACGGAGAGCTCTTCTTGAACAAAGG[G/A]TAGGAGAGAGAGAAAAGGAATTGGACTGAATGTTGCTCGTTAAATAKGTT
Long Flanking Sequence:
ATATATTTAAAGTTTTTATCGTATTTTTTGCTTTTATATTTTATTATATATATTTTTGTAAATAAAATAAAATATGCTGAATCTAATAATAATGCCTTAGTAATAATAATATTGCTTTAATAATTATAATAATAATAAATTGTAAGTATATAAATATGTCTTTTTATTATTATTTTAAAGTTGACCATTGTCGGATAATGTTTTTGACTGGTTTTTGAGATTCTCCTTCTTATAGTTAATTAATCAATTCTAAAGCCATCACGTGTCTTCATTGGCTGCTTCTCTACTGATGTCCCACCTCTTTGTTTTCGTAACAGTTGCGATTGGATGAGACACAGGAGGATGAGTATCGAGCACTGCGCATGCAGCTACAGCAGGAGTTGGAGCTGCTCAACGCCTATCAGAGCAAAATCAAGATGCACACAGACACGCAACACGAGAGAGAGGTCAAAGACCTGGAGCAGAGGGTGTCCATACGGAGAGCTCTTCTTGAACAAAGG[G/A]TAGGAGAGAGAGAAAAGGAATTGGACTGAATGTTGCTCGTTAAATAGGTTCAAGCAGCACGCAACATGGTTGTCATATAACCAAAATGGCCACAACAACAACAAAAAGTCATAGAAACTTTTCTAAATCATCAACATCACCGAACATACTGTGCATCCGGAAAGTATTCAAAGCGCTTCACTTTTTCCACATTTTTTTATGTTACAGCCTTATTCCAAAATGGATTAAAATTCACTTATTTCCTCAACTCTGCACACAATACCCCATAATGACAATGTGAAAAAAGATTTTTTGAAATTGTTGCAAATTTATTAAAAATAAAAAAACCTGAAAAATCAGATATACATCAGTATTTGCAGTCTTTGCCATGAAGCTCTAAATTGAGCTCAGGTACATTCTGTTTCCACTGATCATTCTTGAGATGTTTCAGCAGCTAAATTCACCAAAGGAGTTCACCTGTGGTAAATTCAGTTCATTGGACATGATTTGAAAAGACATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19987
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 |
|---|---|---|---|---|---|
| ENSDART00000114631 | Nonsense | 1008 | 1141 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 3 (position 21355933)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 21012324 |
| GRCz11 | 3 | 21142872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTTCCTCGCATCATCACCTCCGCTACATCCCGCAGCAGTACCACCAT[C/T]AGAGCACCCCACACCTGTACCGCGACAGCCGAGAGAGAGAGTGGGGAAGT
Long Flanking Sequence:
TTGCTTTTCTCTTACACATTTGTCTTTAGATTGAGGAAGAGATGTTGTCTCTGCAGAACGAGCGCTCAGAGCGAATCCGAGCTTTGCTTGAACAACAGGCTCGGGAAATAGAGTCTTTTGACTCTGAGAGCATGCGCTTGGGCTTCAGTAACATGGCTTTGAGTGGCATCCCTGCTGAGGCTTACAATCAGGGCTACTCCAACCCTCCTTCATCCGGGCCTGGAGGCTGGCCGTCCCGTCCTGTCCCCCGCTCAGGCAGCCAGTGGAGCCATGGTGTCCAGAACTCAGCTGCGCCGCCCTCCTGGCGCAGTCAGAACAGCACAGCCGGATTCAGCCGAGCAGAGCAAATGTCCAGTCGGGAGAGAGATCGAGACCGGGAGCTGGAGAGCATGGCCGCCCGTGCCTATCCAGGCTCTCGCTCCTCCGCCTCATCGGCATCATCATCATCATCATCTTCCTCGCATCATCACCTCCGCTACATCCCGCAGCAGTACCACCAT[C/T]AGAGCACCCCACACCTGTACCGCGACAGCCGAGAGAGAGAGTGGGGAAGTGGAGGAGGAGGTCACCACTCTTCCTCATCCTCCTCTCATGGCCACTCGCATCACATTTCTGCCCAATCCCTCGCCCTCCTCCCTCCACCGCCGCCTCCTCCACCCATCTCTCTTTCCTCCTCTTCTCCTCCATCTTCCTCCTCATCTTCATCCTCTCAGAGTGGCTACGGAGGAAGGGGCGAAGGTTTGGTTGTCCGAGGCCCCAGTCTGATGGCTCTGAGAAACAGCCCCGGGCCCCTGCGAAGAACAGCCTCAGGTGGAGGTGCCGGCGGGTCAGGCGGAGACGGAGGTTTGAGCCGGAGTACTTCAGTGACGTCACACATCTCCAACGGATCTCACCTGTCGTATTCCTAGAGGGCGAAGTTCAGATGGTGCCATTTTTATTTCTTTATTTTTTTAGAGGGAAGGCCTTCACGCAGGAAGGCGGAGAGAGGACTTTTTAGATGGGCA
Associated Phenotype:
Not determined