ZMP
atat1
Ensembl ID:
ZFIN ID:
Description:
Alpha-tubulin N-acetyltransferase [Source:UniProtKB/Swiss-Prot;Acc:Q6PH17]
Human Orthologue:
ATAT1
Human Description:
alpha tubulin acetyltransferase 1 [Source:HGNC Symbol;Acc:21186]
Mouse Orthologue:
Atat1
Mouse Description:
alpha tubulin acetyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:1913869]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9581 | Nonsense | Available for shipment | Available now |
sa12225 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
This allele has been removed from public view.
Allele Name:
sa29221
Status:
Less stringent filtering
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:
n/a
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049368 | Essential Splice Site | 51 | 305 | 2 | 11 |
ENSDART00000103922 | Essential Splice Site | 51 | 297 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 27969748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27899860 |
GRCz11 | 19 | 27484083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACAGGTCACCACAGTTATAGACGAGCTAGGCAAAGCTTCCTCGAAGG[T/A]AATAATGGCTGTCTTTTGTCTCTTCTTGAGCTTGCAGATGTCAGTCAGTG
Long Flanking Sequence:
AAGAAAGGCGTAATCTACATCTTAGATTGCTAGAAGGTAGTAAGTTAACAGAAAACTTAAATCATTCAGAGAAATGTCTCTTTTAAAAATACACTGGAATGAGCATGTCCCTTCTCTTAGAACATATCAGCAAATCATGATTCATTAATATGATAGAACAAAGATCTATTGGCTTATTAGGAAAGTAGGACAAGCCATTTAATATGTTCCAAGCCCAATTCATTATGCAATATGTCAACACAGCAGAGAAATAAAAGAAAAGTTACCTTTTTTTCCATTCGATGACGTCAATATTTGCTAATGGAAAATTGCTCAAATATATTGCAAATCTTAATATAGTGTACACTGTGACCTACATAAATGTTATCTTAAGCACGCATTGTCATTTTAATCCTTCTGCCTGTGAAATTCCTAACATATCTGCTTTTTGTTCTCCAGACCAGATCCTCTTCCACAGGTCACCACAGTTATAGACGAGCTAGGCAAAGCTTCCTCGAAGG[T/A]AATAATGGCTGTCTTTTGTCTCTTCTTGAGCTTGCAGATGTCAGTCAGTGTCAGTTCAGTTTATCATCATGTTGTGTGTGTGTGTGTGTTTATCTTCTCAGGCCCAGCAGCTGCCTGCGCCTATTACCAGTGCTGCAAAGCTCCAGGCCAACAGACATCATCTCTACCTCCTGAAAGATGGAGAACAGAACGGGTAAAATAGCTTTCTCTTTCTCCCCCACCCCATGCTTCAGATTTAATCTATTTATAAGTCAATACAACTGACCTCTCTCCTTCCTGTTTTTCCGTTTCCATTACACATAAACACATCCACTTCTGCTAATAACAATCTTCGACTCCCTGTTCCTGTTTTTTGGTTTGTTGTTGTTTTTACCAGCGGGAGGGGTGTTATAGTTGGATTTCTGAAGGTTGGCTACAAGAAGCTCTTTTTACTTGTAAGTGTTCCCTCATTATCGACTTGGTAATTACATCTCACTTGATGCCTGACTCCACACTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9581
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 |
---|---|---|---|---|---|
ENSDART00000049368 | Nonsense | 80 | 305 | 3 | 11 |
ENSDART00000103922 | Nonsense | 80 | 297 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 27969934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27900046 |
GRCz11 | 19 | 27484269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGCTCCAGGCCAACAGACATCATCTCTACCTCCTGAAAGATGGAGAA[C/T]AGAACGGGTAMARTAGCTTTCTCTTTCTCCCCCACCCCATGCTTCAGATT
Long Flanking Sequence:
AGGACAAGCCATTTAATATGTTCCAAGCCCAATTCATTATGCAATATGTCAACACAGCAGAGAAATAAAAGAAAAGTTACCTTTTTTTCCATTCGATGACGTCAATATTTGCTAATGGAAAATTGCTCAAATATATTGCAAATCTTAATATAGTGTACACTGTGACCTACATAAATGTTATCTTAAGCACGCATTGTCATTTTAATCCTTCTGCCTGTGAAATTCCTAACATATCTGCTTTTTGTTCTCCAGACCAGATCCTCTTCCACAGGTCACCACAGTTATAGACGAGCTAGGCAAAGCTTCCTCGAAGGTAATAATGGCTGTCTTTTGTCTCTTCTTGAGCTTGCAGATGTCAGTCAGTGTCAGTTCAGTTTATCATCATGTTGTGTGTGTGTGTGTGTTTATCTTCTCAGGCCCAGCAGCTGCCTGCGCCTATTACCAGTGCTGCAAAGCTCCAGGCCAACAGACATCATCTCTACCTCCTGAAAGATGGAGAA[C/T]AGAACGGGTAAAATAGCTTTCTCTTTCTCCCCCACCCCATGCTTCAGATTTAATCTATTTATAAGTCAATACAACTGACCTCTCTCCTTCCTGTTTTTCCGTTTCCATTACACATAAACACATCCACTTCTGCTAATAACAATCTTCGACTCCCTGTTCCTGTTTTTTGGTTTGTTGTTGTTTTTACCAGCGGGAGGGGTGTTATAGTTGGATTTCTGAAGGTTGGCTACAAGAAGCTCTTTTTACTTGTAAGTGTTCCCTCATTATCGACTTGGTAATTACATCTCACTTGATGCCTGACTCCACACTTTTTAAAGCTGCTCTGTATGTTGTAATTGCTGATAGGACCAACGGGGGGCGCATTTGGAGACCGAGCCATTGTGTGTGCTGGATTTCTATGTGACAGAGACCCTACAAAGACATGGCTATGGCTCAGAGCTCTTCGACTTCATGCTAAAAGTGAGTCGTACGCATGATTTGTTGAATTACATGTGATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12225
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049368 | Essential Splice Site | 139 | 305 | 5 | 11 |
ENSDART00000103922 | Essential Splice Site | 139 | 297 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 27970395)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27900507 |
GRCz11 | 19 | 27484730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTACAAAGACATGGCTATGGCTCAGAGCTCTTCGACTTCATGCTRAAAG[T/C]GAGTYGTACGCATGATTTGTTGAATTACATGTGATTTTTACACAAWGTAR
Long Flanking Sequence:
GCCAACAGACATCATCTCTACCTCCTGAAAGATGGAGAACAGAACGGGTAAAATAGCTTTCTCTTTCTCCCCCACCCCATGCTTCAGATTTAATCTATTTATAAGTCAATACAACTGACCTCTCTCCTTCCTGTTTTTCCGTTTCCATTACACATAAACACATCCACTTCTGCTAATAACAATCTTCGACTCCCTGTTCCTGTTTTTTGGTTTGTTGTTGTTTTTACCAGCGGGAGGGGTGTTATAGTTGGATTTCTGAAGGTTGGCTACAAGAAGCTCTTTTTACTTGTAAGTGTTCCCTCATTATCGACTTGGTAATTACATCTCACTTGATGCCTGACTCCACACTTTTTAAAGCTGCTCTGTATGTTGTAATTGCTGATAGGACCAACGGGGGGCGCATTTGGAGACCGAGCCATTGTGTGTGCTGGATTTCTATGTGACAGAGACCCTACAAAGACATGGCTATGGCTCAGAGCTCTTCGACTTCATGCTAAAAG[T/C]GAGTCGTACGCATGATTTGTTGAATTACATGTGATTTTTACACAATGTAGGTTTTAAAGATTGCCCACATTGCTCTATTAGAACCATACACCAACCTGATTTCACCAGTTAAAGTAGGACATGCTCCTGGATTAACCTCTGTGTTGATCCTGGAACAACATTCCAATCAGCCAATCAGAATTAAGGAATATACTTATAGTTTATGTTCAGTTTAGGCTTACGGTTAGGTTTATGCACTTCTACATGATTGTTTACCAACTATTAATCCTTTCTGATTATGCAAATAATTTACAGTTATGGTTGGGTGTAGGGGTAGGGAATGTGTATGGATTTTGGATAGTATGGATGGACATTTCACATCAAAAATGATGTATAGGATCAACATAAATGGTAATCCAGGATCGCATATTACTTTGCAAAATCATGGCTAAAACCAGACTAGCATCAACATGCAGCATAAATTGCTATTGACCTTATTCTGCAATGCAGAAATGCGCTAG
Associated Phenotype:
Not determined