ZMP
TTBK1 (2 of 2)
Ensembl ID:
Description:
tau tubulin kinase 1 [Source:HGNC Symbol;Acc:19140]
Human Orthologue:
TTBK1
Human Description:
tau tubulin kinase 1 [Source:HGNC Symbol;Acc:19140]
Mouse Orthologue:
Ttbk1
Mouse Description:
tau tubulin kinase 1 Gene [Source:MGI Symbol;Acc:MGI:2147036]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45602 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9312 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36394 | Nonsense | Available for shipment | Available now |
sa6470 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45601 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23059 | Nonsense | Available for shipment | Available now |
sa36393 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45602
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 |
---|---|---|---|---|---|
ENSDART00000114470 | Nonsense | 82 | 1219 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21892292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22042441 |
GRCz11 | 17 | 22062277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCTGCCCAACAACCCAAACAAGTGCTAAAGATGGAGGTTGCTGTGCTA[A/T]AGAAACTACAAGGTGAGGAGACGGAGAGGATATATGTGCTGTTTTGTGTT
Long Flanking Sequence:
AATTATCATATGTTTATTTATTACCAGTCGTTGTGGTTTATACCAGGCAATTACCAATAAAGACCAAAATGAACTTTACAGTTTTCATTAAAACCAATGAAGTCATATGCCCTCAGATTGGAGCAGCTTAGGTAAATCAGCCAATCAAAGTTTGTCATACATTTATTGCATGTAAAGTAAATTCCATCCACACATTCATTTCTGCCAGATTAGGTGAGGAAATTGTTCGTTCTAATAGCAGAACTTCCACAGCATAATGTTTATGATATTATGCAAGACCAGCTCTGACTCTGAGTGAAACAGATTACAGACAGGTTAAATCGCTGCTCTGCCATGACTTACCTTGCTGTTGTTTGTGTATTCAGCTAAAGAAGATTGGGGGTGGAGGGTTTGGGGAGATATATGAGGCCTACGACTTGTTGACGCGGGAGAATGTGGCTCTTAAGGTGGAATCTGCCCAACAACCCAAACAAGTGCTAAAGATGGAGGTTGCTGTGCTA[A/T]AGAAACTACAAGGTGAGGAGACGGAGAGGATATATGTGCTGTTTTGTGTTTTTAATAACTAGCTTGAGTAATTAGTTTCTTGAAAAACAGATCATTGTGTTATTGCAGCATCACAATGTCGCTAAGAGCAGTCAGCATCCATCTCTTGTTAAAATCACACATCAGATAAAAAAAAAAAACAGGAGATTTGGGAATTTTATATCTCATGTTTTTGTTTTAATGGTTTAGTGGAAGAAATATTTATCATTACAAACTAGCCAAAATAAAGAAACTGTTCATAGTTATTTATAAAAATTATACTTTTATTTTATTTTTTATTTAAATTTCATCATATTGCATGTTTGTAAAACAATCATTAAAAATCATTGTTTTAATAGATGTGTTAAGCAGCAAAGCTTTTTTTTTTTCAAAATTGATGACAATAAGAATTGTTTACAAGAAGAAAATCAGTACTCTAAAAGATCATATGGCTCTGAAGAGTGGAAAACTAGCATGTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9312
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 |
---|---|---|---|---|---|
ENSDART00000114470 | Nonsense | 222 | 1219 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21884537)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22034686 |
GRCz11 | 17 | 22054522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCATACTCTGTTCTTTGTTTTTAACRGGAAATGGGTCGTCATGATGATT[T/A]GYGGTCGTTGTTTTATATGCTGGTAGAGTTTACCGTTGGACAATTACCAT
Long Flanking Sequence:
ATAACTGTGGACCTGAATATATGAAAGAGACAATTAATTGTGATTTAATCAGGCCAGGAATCCCAAAACTGGTCAAAAGGCATTAAAAAGCAGCTGAAACATACAGAATTCCTGTCGCTATACCCTTTCTTATATTTCCTTCCCATGGTTGCCTTGTTTTGATTATGTGCTCTTTTTCCAGCCTAAGTATAAAAAGTATCAAATGAAAGTGATGTGAATCCTTATTATGAGACTCTTTCAAATATTCTGCTTTAGCCCAGGTCAGTGGCTGGGTTCAGAGGAACGGTGCGATACGCTTCCATTAATGCTCATAAAAACAAGGTAAGTGCAGTCTAAAGTCTAGCATGCACAAAAAGTGACCAGGGTTGACTCTTTTTGCCAATCAGAATCAACTTTAATAAATCCAAATAAGGTTTTCAAGAATGAACAACAATATAGACAACTACATTTTTCATACTCTGTTCTTTGTTTTTAACAGGAAATGGGTCGTCATGATGATT[T/A]GTGGTCGTTGTTTTATATGCTGGTAGAGTTTACCGTTGGACAATTACCATGGCGTAAGATAAAAGATAAGGTAAGGCAAATGTATCACGCTCTCATCAACCAGTGACTATGAGCATAATGGGACTGAATTGAAGCAATTAACCCTTGCTGTGCTCAGTCTTAAGAGCTTTGTGTAAAATATTTAGGGCCTTCAGAGTGTTCTTGTTGTTAATAGTGTGTGTGTAATGTGCCTGATGAACAGGAGCAGGTGGGACAGATTAAAGAACGCTACGAGCACAGGATGCTGTTGAAACACATGCCTGCAGAGTTTCATATCTTTTATGATCATGTGCTGGATTTGGATTATTTCACCAAACCTGATTATCAGGTAAAGCAATACATACATCTCTTATCTTCTTCTGATTTCACTACCTCATTTCTAATATAAATGAGTTTTTCTTTGCGTTTGGCGTTATTATGTTCCAAGAACAGCAGTTGGATGATGTAAACAGTGTAAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36394
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114470 | Nonsense | 231 | 1219 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21884511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22034660 |
GRCz11 | 17 | 22054496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAATGGGTCGTCATGATGATTTGTGGTCGTTGTTTTATATGCTGGTA[G/T]AGTTTACCGTTGGACAATTACCATGGCGTAAGATAAAAGATAAGGTAAGG
Long Flanking Sequence:
GAGACAATTAATTGTGATTTAATCAGGCCAGGAATCCCAAAACTGGTCAAAAGGCATTAAAAAGCAGCTGAAACATACAGAATTCCTGTCGCTATACCCTTTCTTATATTTCCTTCCCATGGTTGCCTTGTTTTGATTATGTGCTCTTTTTCCAGCCTAAGTATAAAAAGTATCAAATGAAAGTGATGTGAATCCTTATTATGAGACTCTTTCAAATATTCTGCTTTAGCCCAGGTCAGTGGCTGGGTTCAGAGGAACGGTGCGATACGCTTCCATTAATGCTCATAAAAACAAGGTAAGTGCAGTCTAAAGTCTAGCATGCACAAAAAGTGACCAGGGTTGACTCTTTTTGCCAATCAGAATCAACTTTAATAAATCCAAATAAGGTTTTCAAGAATGAACAACAATATAGACAACTACATTTTTCATACTCTGTTCTTTGTTTTTAACAGGAAATGGGTCGTCATGATGATTTGTGGTCGTTGTTTTATATGCTGGTA[G/T]AGTTTACCGTTGGACAATTACCATGGCGTAAGATAAAAGATAAGGTAAGGCAAATGTATCACGCTCTCATCAACCAGTGACTATGAGCATAATGGGACTGAATTGAAGCAATTAACCCTTGCTGTGCTCAGTCTTAAGAGCTTTGTGTAAAATATTTAGGGCCTTCAGAGTGTTCTTGTTGTTAATAGTGTGTGTGTAATGTGCCTGATGAACAGGAGCAGGTGGGACAGATTAAAGAACGCTACGAGCACAGGATGCTGTTGAAACACATGCCTGCAGAGTTTCATATCTTTTATGATCATGTGCTGGATTTGGATTATTTCACCAAACCTGATTATCAGGTAAAGCAATACATACATCTCTTATCTTCTTCTGATTTCACTACCTCATTTCTAATATAAATGAGTTTTTCTTTGCGTTTGGCGTTATTATGTTCCAAGAACAGCAGTTGGATGATGTAAACAGTGTAAAGTGCATATTGTGTTTTTTTGGTAATCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6470
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 |
---|---|---|---|---|---|
ENSDART00000114470 | Essential Splice Site | 245 | 1219 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21884466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22034615 |
GRCz11 | 17 | 22054451 |
KASP Assay ID:
554-4659.1 (used for ordering genotyping assays)
KASP Sequence:
TGGTAGAGTTTACCGTTGGACAATTACCATGGCGTAAGATAAAAGATAAG[G/A]TAAGGCAAATGTATCACGCTCKCATCAACCAGTGACTATGAGCATAATGG
Long Flanking Sequence:
GTCAAAAGGCATTAAAAAGCAGCTGAAACATACAGAATTCCTGTCGCTATACCCTTTCTTATATTTCCTTCCCATGGTTGCCTTGTTTTGATTATGTGCTCTTTTTCCAGCCTAAGTATAAAAAGTATCAAATGAAAGTGATGTGAATCCTTATTATGAGACTCTTTCAAATATTCTGCTTTAGCCCAGGTCAGTGGCTGGGTTCAGAGGAACGGTGCGATACGCTTCCATTAATGCTCATAAAAACAAGGTAAGTGCAGTCTAAAGTCTAGCATGCACAAAAAGTGACCAGGGTTGACTCTTTTTGCCAATCAGAATCAACTTTAATAAATCCAAATAAGGTTTTCAAGAATGAACAACAATATAGACAACTACATTTTTCATACTCTGTTCTTTGTTTTTAACAGGAAATGGGTCGTCATGATGATTTGTGGTCGTTGTTTTATATGCTGGTAGAGTTTACCGTTGGACAATTACCATGGCGTAAGATAAAAGATAAG[G/A]TAAGGCAAATGTATCACGCTCTCATCAACCAGTGACTATGAGCATAATGGGACTGAATTGAAGCAATTAACCCTTGCTGTGCTCAGTCTTAAGAGCTTTGTGTAAAATATTTAGGGCCTTCAGAGTGTTCTTGTTGTTAATAGTGTGTGTGTAATGTGCCTGATGAACAGGAGCAGGTGGGACAGATTAAAGAACGCTACGAGCACAGGATGCTGTTGAAACACATGCCTGCAGAGTTTCATATCTTTTATGATCATGTGCTGGATTTGGATTATTTCACCAAACCTGATTATCAGGTAAAGCAATACATACATCTCTTATCTTCTTCTGATTTCACTACCTCATTTCTAATATAAATGAGTTTTTCTTTGCGTTTGGCGTTATTATGTTCCAAGAACAGCAGTTGGATGATGTAAACAGTGTAAAGTGCATATTGTGTTTTTTTGGTAATCAGAGGTAAAATTGCAGTAATTTTAGTTAAAATAAATGCTGTTTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45601
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 |
---|---|---|---|---|---|
ENSDART00000114470 | Essential Splice Site | 287 | 1219 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21884169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22034318 |
GRCz11 | 17 | 22054154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATGATCATGTGCTGGATTTGGATTATTTCACCAAACCTGATTATCAG[G/A]TAAAGCAATACATACATCTCTTATCTTCTTCTGATTTCACTACCTCATTT
Long Flanking Sequence:
ACTCTTTTTGCCAATCAGAATCAACTTTAATAAATCCAAATAAGGTTTTCAAGAATGAACAACAATATAGACAACTACATTTTTCATACTCTGTTCTTTGTTTTTAACAGGAAATGGGTCGTCATGATGATTTGTGGTCGTTGTTTTATATGCTGGTAGAGTTTACCGTTGGACAATTACCATGGCGTAAGATAAAAGATAAGGTAAGGCAAATGTATCACGCTCTCATCAACCAGTGACTATGAGCATAATGGGACTGAATTGAAGCAATTAACCCTTGCTGTGCTCAGTCTTAAGAGCTTTGTGTAAAATATTTAGGGCCTTCAGAGTGTTCTTGTTGTTAATAGTGTGTGTGTAATGTGCCTGATGAACAGGAGCAGGTGGGACAGATTAAAGAACGCTACGAGCACAGGATGCTGTTGAAACACATGCCTGCAGAGTTTCATATCTTTTATGATCATGTGCTGGATTTGGATTATTTCACCAAACCTGATTATCAG[G/A]TAAAGCAATACATACATCTCTTATCTTCTTCTGATTTCACTACCTCATTTCTAATATAAATGAGTTTTTCTTTGCGTTTGGCGTTATTATGTTCCAAGAACAGCAGTTGGATGATGTAAACAGTGTAAAGTGCATATTGTGTTTTTTTGGTAATCAGAGGTAAAATTGCAGTAATTTTAGTTAAAATAAATGCTGTTTTTTTAATCAAGTAATCCTGCAAAATGCTTTATGCATCAACAACAAATGAATGAATAAATGAACGAATGAACATTTTAAGTTGAAATATTGACTCACCATTATATTTTAAATTGTTTTCAGCTATTTTTAAAATGTGATTATTTGCTATTGAATAATTGCTGTCTTGATGAACATAGGCGACTTAAAAAAAAGTCAACATTTTGAATTGCTATATACATACAGTTGAAGTCAGAATTATTAGCCCCCTTTGAATTTTTTTTTTTTTTTTATATATATGCCAAATGATGTTTAACAGAGCAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23059
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 |
---|---|---|---|---|---|
ENSDART00000114470 | Nonsense | 902 | 1219 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21866250)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22016399 |
GRCz11 | 17 | 22036235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATAGCTATTAAAGAAAATATTTCAATAGAAACCAAATTAGATGACGAA[C/T]AAGATGGTGTCACAACAGAGAAAGAACAGGAGCAAGAAGAGAGTCCATCT
Long Flanking Sequence:
TGACACCGCAGGGAGAGCGACCTGTGCCAGAAGAATCTGAACCTGGCACTCTTTCCTCTGTCATTAAATCAGAGCCCAGGCCTATCGTCATGACAACTGCGGCTGTGATCACCAGTGGTTCTTCCTCGCCACCTTTTACTAAAGTGGAGCGCACTTTCATCCACATCGCTGAGACGTCACATCTTAATGTCATGACAGCCAGACACCGTCCGTCTGGATTCGATGAGCCGATATCTGTTGAGCGTGAGGAAATGGGGGAAGAGAAAGAGGATCGGGCAGGGCAACTAGTGGAGATAGAGAGGAATAGTGAAGGGATTAAGGTGGAAAGGGAAGGGGATGAGAAGAAAAAGGAAGAAAGTGAAGCTGAGAAGGAAAAGCAGGAAGTAGAAAATGTAATTATTAGTAGCAGAGAGGAAGCAGAGACTGTGTTTTTAGCTGAGCAGCCAGTGTCTATAGCTATTAAAGAAAATATTTCAATAGAAACCAAATTAGATGACGAA[C/T]AAGATGGTGTCACAACAGAGAAAGAACAGGAGCAAGAAGAGAGTCCATCTGTGTCCCCTGAACAAAACAGAGATGCTGAAGTAGAGGATGAGAAGGATGTGTCTCCACCAGAGGTGGAGTCACCTGATAGAAAGCCACTCCCACAAAGGCGGAGCCGTATTCCTGTGCTCATGTCAGAGGATGAAACGGGCTCAGACAAGTCATCGCAGACGAGTCAAGAGCAGTTGCAACGAACTCGCAAAAGCAGACACCAACAGTTGGCCCGTCTGGTTCTGGAGCGTAAACAAACGCATATGATGCGCTCTCGTTCTGCCTCCTCACACTCCCCAACACTCTCCACCACTGCATCTGAGGATGAAGCCCACCAATCTGATGACTCCGCTAAAGGAGCGGATGGGAAAATTAAGAGCAGGATCCCTCGGCCAGTCACGCCTATCAGGGGGTCTTACGACCTGTTAAAGTGCACGACTCTACCGCAAACCCAGAGATCTGTGTCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36393
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 |
---|---|---|---|---|---|
ENSDART00000114470 | Nonsense | 923 | 1219 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 21866187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22016336 |
GRCz11 | 17 | 22036172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGAGAAAGAACAGGAGCAAGAAGAGAGTCCATCTGTGTCCCCTGAA[C/T]AAAACAGAGATGCTGAAGTAGAGGATGAGAAGGATGTGTCTCCACCAGAG
Long Flanking Sequence:
TTAAATCAGAGCCCAGGCCTATCGTCATGACAACTGCGGCTGTGATCACCAGTGGTTCTTCCTCGCCACCTTTTACTAAAGTGGAGCGCACTTTCATCCACATCGCTGAGACGTCACATCTTAATGTCATGACAGCCAGACACCGTCCGTCTGGATTCGATGAGCCGATATCTGTTGAGCGTGAGGAAATGGGGGAAGAGAAAGAGGATCGGGCAGGGCAACTAGTGGAGATAGAGAGGAATAGTGAAGGGATTAAGGTGGAAAGGGAAGGGGATGAGAAGAAAAAGGAAGAAAGTGAAGCTGAGAAGGAAAAGCAGGAAGTAGAAAATGTAATTATTAGTAGCAGAGAGGAAGCAGAGACTGTGTTTTTAGCTGAGCAGCCAGTGTCTATAGCTATTAAAGAAAATATTTCAATAGAAACCAAATTAGATGACGAACAAGATGGTGTCACAACAGAGAAAGAACAGGAGCAAGAAGAGAGTCCATCTGTGTCCCCTGAA[C/T]AAAACAGAGATGCTGAAGTAGAGGATGAGAAGGATGTGTCTCCACCAGAGGTGGAGTCACCTGATAGAAAGCCACTCCCACAAAGGCGGAGCCGTATTCCTGTGCTCATGTCAGAGGATGAAACGGGCTCAGACAAGTCATCGCAGACGAGTCAAGAGCAGTTGCAACGAACTCGCAAAAGCAGACACCAACAGTTGGCCCGTCTGGTTCTGGAGCGTAAACAAACGCATATGATGCGCTCTCGTTCTGCCTCCTCACACTCCCCAACACTCTCCACCACTGCATCTGAGGATGAAGCCCACCAATCTGATGACTCCGCTAAAGGAGCGGATGGGAAAATTAAGAGCAGGATCCCTCGGCCAGTCACGCCTATCAGGGGGTCTTACGACCTGTTAAAGTGCACGACTCTACCGCAAACCCAGAGATCTGTGTCTTTTATTCAATACAGGTGGGTGGAGCAGAAAATTATTTGGTACTCATCAAAATTTTGAACATTTGTT
Associated Phenotype:
Not determined