ZMP
AATK (2 of 2)
Ensembl ID:
Description:
apoptosis-associated tyrosine kinase [Source:HGNC Symbol;Acc:21]
Human Orthologue:
AATK
Human Description:
apoptosis-associated tyrosine kinase [Source:HGNC Symbol;Acc:21]
Mouse Orthologue:
Aatk
Mouse Description:
apoptosis-associated tyrosine kinase Gene [Source:MGI Symbol;Acc:MGI:1197518]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35358 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22160 | Nonsense | Available for shipment | Available now |
sa42084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45475 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11207 | Nonsense | Available for shipment | Available now |
sa19043 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35358
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111560 | Essential Splice Site | 146 | 1657 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 12 (position 38056826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 36021842 |
GRCz11 | 12 | 35716097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGAGTTTGCTCTACATTAAGGAGATTGGAAATGGCTGGTTTGGCAAGG[T/C]AAATCTAGTCAGTTTGTTGTTTCATTTGTTTTATATGTGCGCCTCGCAGA
Long Flanking Sequence:
TCACCCCTAAAAATAGTGAAATAACTGAACATAAATATAGGAGGCTACGAAAATAATAATTTCAGATGGCACTTAGAGGCTGCATTGAGCTCAATATATATAGGATTAAGAAATGGCAGAGTTTTAATTTGGATTGGAAGTCAATAATGACAGTTTTCAATTATTTTTATTTTTTTTTTTACATCCAGTAAAGTCTTGATGACAGCAGAATTGTCTCAAAGTTTGAGAATGAATCAAAGACCATCTTGTACTGTACCTAAAAATCGAATTAATTCCTTCATTTATAGTATGTTCTGTTCTTTATTTATGTTTTCTATCTAAATGTTCTAGACTCTGAGTGGCAGATCTTCTGTTTGGCCCATTAACTAATTACTGTCTTGTTCTGTCTCTGTCTTTTCTTGCTGATAATGGTCTTTCAGTCCAGCTCCTGAGATCCACCGATCTTGGCCGCCAGAGTTTGCTCTACATTAAGGAGATTGGAAATGGCTGGTTTGGCAAGG[T/C]AAATCTAGTCAGTTTGTTGTTTCATTTGTTTTATATGTGCGCCTCGCAGACATCAATGCTCTAAGCATGTACTGTACTGCAGCGGATCAAAGGTTTAGCTCTATAGTTTAGTCCCGAGGATGTGAAAATATCGTCCATGCTACATTACCAGCTCCTCGTCTGTGCTTTGATGTTGGGCCGGTGTCTTGACTGTTCCCTCAGAGAATTTGATGTTATTTCTATGTAGCAGTGAAGCAGTTTAAAATTTCACAGGAATAACTGAGCCTCTTTCATTCTCATTCTCTCTTTCTTTCTCTCTACTTCTTTGTCTTTTGTAACACACATACATAAACACACACACTTCCCCAATTACCCCAACTTCCCATTGAATGGGTATGTCCATCTGTATGTGTGTCTCTGTGGCTGCATGTTTACCAATGTCCCATCTGGTTTTGTGTTGTTTGGTCTGTCTGCGTTTCCATTTGAGCATGATTCCTGGACTTCTTTTGATCCTTATTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22160
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 |
---|---|---|---|---|---|
ENSDART00000111560 | Nonsense | 353 | 1657 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 12 (position 38064202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 36014466 |
GRCz11 | 12 | 35708721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGCTGTTTGAGTTAGGGAATCAGCCGTACCGCCATTATTCAGACCGA[C/T]AGGTTCTCAGTTATGCTGTGAAGGATCAGCAATTGAAGCTGTCCAAGCCT
Long Flanking Sequence:
TACAAGGCATGTACACTTTAATCTATACTTTTTTATTACTTTATCAATAACAAAGTCCATTATACGAATAATACTAACATGTAAGCATGACTTTCAGATTTTCATAGTTTCATAGATACTTTCATAGTTTGTATATTTTATTAACATTAACCATAGCCCCCTCTCTTCATGTTTTTTTTTTTTTTTTCCAGGATGACTACTTTGTGACATCAGACCAGACCTGGGTACCTTTACGCTGGATTGCCCCTGAACTGGTGGATGAGGTTCATGGCAATTTGCTGGTAGTGGACCAAACCAAGGAAAGCAACATCTGGTCAGTATATTTAGCGTATTTAGGCAGTTTAGGAAGAATAAATCATTTTTATTGTTGAATATAAATGCATTAATTGCTGTTATTTTCCAGAGTTCTATGTTCTTCTCTGTTTTTAAGGTCACTTGGTGTAACCATCTGGGAGCTGTTTGAGTTAGGGAATCAGCCGTACCGCCATTATTCAGACCGA[C/T]AGGTTCTCAGTTATGCTGTGAAGGATCAGCAATTGAAGCTGTCCAAGCCTATTCTTAAGTACCCACTTGCTGACCGCTGGTGGGTGTCTAATAAACTTTATATAGCTCTTCTTACACAATCCATTTACCATTACTTAGAGTTAGAGCCTTGACTTTTTGCTTCAGTAGAGCTTTTCAATCTTCACCCCTCTCTTTTGTAAAGTCCGTGCCCTTAAACACATTAAATATTGCACTTTTTCCATATTTGGATCTTATTCATTACATTTTGCTGTAAATTCAAATACTTCAAATTTCTTTTATATAATGGAGGATTTACAGTGCAAAACAGACAGATCAAAAAAGAAACAATAATTCACTTTTTATTTACAGTATATTTTTGTCGCATTTGCACTAAAAGTGTATGTGTTTTTGTCATCAGGTATGAAGTAATGCAGTTTTGTTGGCTTCAGCCTGACCAAAGGCCCAATGCAGAAGAAGTTCATCTTTTGCTTAGTTACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42084
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 |
---|---|---|---|---|---|
ENSDART00000111560 | Nonsense | 688 | 1657 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 12 (position 38065546)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 36013122 |
GRCz11 | 12 | 35707377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTATTACTTTGAACCATCACCTCCTAAGGTTATGGGCCGCTATATGATA[C/T]GAGACTCAACAGAAACTCTACAAGAAAGCTGGGGCTCTCGAAGTCTGAGA
Long Flanking Sequence:
CAGGAGGAATAGTGGGGGGATGTGCTGTTGATGGACTTGCCCTAGGGGTTTCTCCTTCATATTATGAGCCCAAACAATTACACACCCCTGGTGTGGTGCCTGTGCTGAGTGCTCATAGTCCATCAGTGAGTAACGAGTACTATATTCGCATTGAGGAGCCAGTACAAAGCAATATTGATATGAACTTTACCATGTGTGCTTACAGCCCAGAGTTTGGTGGCAGTAATGGAAGCTTTTTAACCGGTAGTGGAGACTCTGGTGAGTGTATGAACTGTCCCCCTGAGGCTAAACCAGACATTTACTGGTCAGCTGAAGTTCACAAAAGTGGTGCTTATGATTCTGACTCCAGCCCTGCTATGTCTTTAACTATGGAGCCTCTTTTGGGCCACGGTAGCCCCCTTAGAGCATGGGAATCAGGCCACTATGTCTCATACAAAGACAGGGATGGAGGTTATTACTTTGAACCATCACCTCCTAAGGTTATGGGCCGCTATATGATA[C/T]GAGACTCAACAGAAACTCTACAAGAAAGCTGGGGCTCTCGAAGTCTGAGACAAGCACTTGGGGAACTGGAGGACCCTTTAGGCATCTCACCATCACTTGGAAGTCCTCCACAAGGCTATGCTGATCCTTATTTGGAGAGCATTCAAGGCTCCATTATAGGAAAGAATGTAACGGGTGGATACTATGATATGATGGGCTCTTTGAGAAAGACTATGCCAGGTGGCCACTCTGTTTGTACTGACATAGCATCAGGTGGTGCTGTATTTGTAGGTCGAGATGACAGCGAGTCTGATGAAGAGGAAGACATCTTTGTGGAGAGGCGAGGAAGAAGCTGGTCTGCCAGCAATCCACCAAATACAAACCCAAGGACCTTGCGTCAGAGGCAGGGGTCTTGTATCCAGGATTCCTATGCAGACTTCCACTACACTATGCCAATGACTGATATTGAGGATACATGGCCAGAGCAGCAGACCCTGTCATACCATATGACCAAACCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45475
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 |
---|---|---|---|---|---|
ENSDART00000111560 | Nonsense | 795 | 1657 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 12 (position 38065867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 36012801 |
GRCz11 | 12 | 35707056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGAGATGACAGCGAGTCTGATGAAGAGGAAGACATCTTTGTGGAGAGG[C/T]GAGGAAGAAGCTGGTCTGCCAGCAATCCACCAAATACAAACCCAAGGACC
Long Flanking Sequence:
AAAGTGGTGCTTATGATTCTGACTCCAGCCCTGCTATGTCTTTAACTATGGAGCCTCTTTTGGGCCACGGTAGCCCCCTTAGAGCATGGGAATCAGGCCACTATGTCTCATACAAAGACAGGGATGGAGGTTATTACTTTGAACCATCACCTCCTAAGGTTATGGGCCGCTATATGATACGAGACTCAACAGAAACTCTACAAGAAAGCTGGGGCTCTCGAAGTCTGAGACAAGCACTTGGGGAACTGGAGGACCCTTTAGGCATCTCACCATCACTTGGAAGTCCTCCACAAGGCTATGCTGATCCTTATTTGGAGAGCATTCAAGGCTCCATTATAGGAAAGAATGTAACGGGTGGATACTATGATATGATGGGCTCTTTGAGAAAGACTATGCCAGGTGGCCACTCTGTTTGTACTGACATAGCATCAGGTGGTGCTGTATTTGTAGGTCGAGATGACAGCGAGTCTGATGAAGAGGAAGACATCTTTGTGGAGAGG[C/T]GAGGAAGAAGCTGGTCTGCCAGCAATCCACCAAATACAAACCCAAGGACCTTGCGTCAGAGGCAGGGGTCTTGTATCCAGGATTCCTATGCAGACTTCCACTACACTATGCCAATGACTGATATTGAGGATACATGGCCAGAGCAGCAGACCCTGTCATACCATATGACCAAACCTGTTGACTACTTGGAGGCACCGATTAAAAGCAATACTTGCTTGGTACATGGAAGACATGTACCTTCAAACCCTTCACCTGAGTGCAACTCATACATCCATATGTGCCACGAACCTAGAGAGGCTGAAGTATACCCTGTGCCATGTTGTCAAGCTTTGAGCAGTTCACATTTTGTAGACCCTTTAACAGGAACACTTGTGAGGAACTGCTTCATGATTGACTGTATTCCAGGGAAAACCATGACCTTGCCCAACAGAGACCAACATCTACCTTTATCTGCTGGACATATAATCTCCAAAATAGAAGCATCAAGGGAAGGAGCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11207
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 |
---|---|---|---|---|---|
ENSDART00000111560 | Nonsense | 981 | 1657 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 12 (position 38066425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 36012243 |
GRCz11 | 12 | 35706498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCTCGGAGCAATTTGTGGATAYTGCAGWAGGAGAAACAAACTTAAAA[C/T]AAGAAAAAACRTTGCATCAAGATATATCTACAGCAGATCCAAAAACTGAA
Long Flanking Sequence:
AGAGGCAGGGGTCTTGTATCCAGGATTCCTATGCAGACTTCCACTACACTATGCCAATGACTGATATTGAGGATACATGGCCAGAGCAGCAGACCCTGTCATACCATATGACCAAACCTGTTGACTACTTGGAGGCACCGATTAAAAGCAATACTTGCTTGGTACATGGAAGACATGTACCTTCAAACCCTTCACCTGAGTGCAACTCATACATCCATATGTGCCACGAACCTAGAGAGGCTGAAGTATACCCTGTGCCATGTTGTCAAGCTTTGAGCAGTTCACATTTTGTAGACCCTTTAACAGGAACACTTGTGAGGAACTGCTTCATGATTGACTGTATTCCAGGGAAAACCATGACCTTGCCCAACAGAGACCAACATCTACCTTTATCTGCTGGACATATAATCTCCAAAATAGAAGCATCAAGGGAAGGAGCCAAACAGTTTGACATCTCGGAGCAATTTGTGGATACTGCAGTAGGAGAAACAAACTTAAAA[C/T]AAGAAAAAACGTTGCATCAAGATATATCTACAGCAGATCCAAAAACTGAAATTATCGCCATATACCCACAGTTGGAAAAATCCCCAGCAGAATTATCCAAACCAGAACCAGAGTCTGAGCTGAGTAAGACTGCAGACAGTGGTATGGACCGTGGACACTCTAGTATCAGCCTGGTTGAGATAGATGACTGCAGTGATGATGACATCACTGACGTAACCTCAGGCATTTTTGGTGATTTTGCAATTGAAGTGGAAACTGTTGACTACCCCAGTCCAGCATTCAAGTCATTACAAAAACAAGTTGGTACTCCAGACTCCATGGACTCTATTGACATACCGTCTACTGCATGTTCCAGTGAGACTCTCAGTCCGGCTTCCATCCATCCATCAAGCTCTCCTAAGACTGTGGATAGTGGCTATGACACAGAAAACAATGAATCTCCAGAGTTTGTCTTAAAGGAACCTCATGAGGTACAAGATTCCAAGACTTTCATTCAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19043
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111560 | Nonsense | 1262 | 1657 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 12 (position 38067268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 36011400 |
GRCz11 | 12 | 35705655 |
KASP Assay ID:
2260-5686.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGGAGACAGATGTAGATGAATATCTTATGCCATCTACAAAGAAGAGT[G/T]AAAAAATCCCTGAACTGTCTGATCATTCAATCTCAAACCTTCCATCAATG
Long Flanking Sequence:
CTGCATGTTCCAGTGAGACTCTCAGTCCGGCTTCCATCCATCCATCAAGCTCTCCTAAGACTGTGGATAGTGGCTATGACACAGAAAACAATGAATCTCCAGAGTTTGTCTTAAAGGAACCTCATGAGGTACAAGATTCCAAGACTTTCATTCAACCTTTGGGAAAGGTAACATCTGGGACAAGTTTTGTCAGTGAAGACCAAGAGATTACAACAACAGAATGTGAGAAGCTTGAGGGTGATTTTTATACTGCAGTGGCCTTGACAGCATCTGAGAGCAGTGATGGAGAGCTGAAAGCACTGAGTGATAAAACACCATACAGAGATTCTGCCTACTTTTCTGATTATGATGCTGGCAAAGATAAAGAAAGCGAAGAGGACATCAATGAACTTGAAGATCAGAAAGACAGACCAGGGGAAATTATATATAAAGAGGAACAACTTCCTCCACAAAAGGAGACAGATGTAGATGAATATCTTATGCCATCTACAAAGAAGAGT[G/T]AAAAAATCCCTGAACTGTCTGATCATTCAATCTCAAACCTTCCATCAATGACAGATGAAAGTTTGTCTGTGTGTGGCACAATCTGTAGCGTGTCTCTCTCACCTCTTAAAGACGTTTCTACCATAAAAAGTAGTTTTGAAGATAATGAAAATATTGGTGTTGTTTCAGATCTCTCTGCAGAACTTTTAGCATCTGAAGAACTTGGTACTGATGGAAAGCAAGAGGAATCTTTCAAACAAGTAGAAAGTGAAGATAGTCTGTCTCATGACCAAGTTACTTTTGAAGGCGATCTTGTAAACAAGCCCAATCCAGAGGTACTTACTGATGAGAACGAAGAGGACATAGTCAAAGATGTCAGCTGTGCCATTTTGTCCGAAGAGGAACTACAGTCTCAAAAGGAAAAAGCAGAAAAGAATGACTCTCCTACACATGAGGAGCTAAAATCCAAGAGTAAGGACTGTGAAGGAGAAGGACGGAAAAGAATCTCCGCACGATCTGGC
Associated Phenotype:
Not determined