ZMP
si:ch73-149o12.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
NAA25
Human Description:
N(alpha)-acetyltransferase 25, NatB auxiliary subunit [Source:HGNC Symbol;Acc:25783]
Mouse Orthologue:
Naa25
Mouse Description:
N(alpha)-acetyltransferase 25, NatB auxiliary subunit Gene [Source:MGI Symbol;Acc:MGI:2442563]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41574 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34814 | Essential Splice Site | Available for shipment | Available now |
| sa21640 | Nonsense | Available for shipment | Available now |
| sa38772 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21639 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41574
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111241 | Essential Splice Site | 20 | 975 | 1 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 3401699)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 3393893 |
| GRCz11 | 10 | 3394197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGGCCATGTGCAAGACCCTAACGACAGGAGGCTACGACCTATCTACGG[T/A]AAGATAAAAACCGCACCGTGGGGCTGATGGAGACCCTGCTGGTCTCGCTA
Long Flanking Sequence:
TCGTTGAGTTTTTTTTTTTCATTATTATTATTTCAAAGCATTTTCTTAAAATATGTGTCAAAATAAGATTTGTAACCAAAGATCATTCTGCTAGCTGAAACAGAGAGAGCTGTGGCCAAATTAAGCCTCAAAATCGCGACAGAGTGGATGAAAACATCCCCAACTCGACACAACGGTTAAGTTCGTTCCGGAAATGTTCAAAGCATGGAGGAGAGTCTTCCTGCATACAGCAGTGTTTGTAATATTTAGCAATTAGGAAAACAATATTCACAATGTCTGATAATGACTTGTCTGAACCATAAACATAAAGCAGAATACATCGGGAGATGTGTCTTTTACAGTGACACTGAACGACACGCATGACTCCCAGGTTCCCGTTTAAAGTCTTTCCGGAGTGCTCGCTCTGCGCATGCGCATCAATTAATCCTGCTCAGCTCCATCATGGCGGCGAGGGGCCATGTGCAAGACCCTAACGACAGGAGGCTACGACCTATCTACGG[T/A]AAGATAAAAACCGCACCGTGGGGCTGATGGAGACCCTGCTGGTCTCGCTAGTGTTGCAAGACCGACCAGTGCGTTGTTGTGTTTATCAAATGGCTGCAGGAGCTGTGGAGAGCCGGTGAGGCCTGTGGAGCTGAAGCCGCGGTCTCAGTTCGGCTGCGGTGCCCTATGACAGTGCGTCTTTATGCGGTCACAGTCTGACCCTTATATCGATGCAAAACACCTTTGCGTTTAGCCCCTTTATCACAGAAATGCGCTTTAAATATCCGGACATAAGTGACAATGTCATCTGATGATCCAGCTCCTAACCTGTGAGAGATGTCAAAGAGATTAACTGCCACATATGAGCCTTTTGTGCTTTAATATTTCATGTTCTTTCTGTGTTGTTATGCTTGTAGACTGCGAGACTTGTGCTTTGCATGCCTTTAGATATGTTTAGGTTAGTATAACCTTTGTAATTATGTTACAGATTCATAAAGCTGCACTTTATGTCTAAATGAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34814
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111241 | Essential Splice Site | 95 | 975 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 3393533)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 3385727 |
| GRCz11 | 10 | 3386031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAACTCTCTACAGGCACTGACCATCCTCTACAGAGAGATGCACCGACG[T/G]AAGTGATCACGGACCATCAAGGCATGTTTTGCATTGTATAACAGTGCTTA
Long Flanking Sequence:
TATATATATATATATATATATATATTGTTATTATTATTATTATTATTATTAAAAATATATTTAATGTTTTTTTTCCTACAGTGGCTTGAATTATTTTGATCATTTTTTTGAATTATTATTATCATCACTAACATTGATTGCATTTGAAAATGATTACAACGTTTTCCGAATCTGATGTTCGTATCAGCCTAATTGTCACAAAGTGTCCGCAGAACTGCTGCATTTACACTACTTCACATGACGCTGTGGACGGAGATCAACACAAAAGATCTTTTTTTCAGAAAAGGTCAAATAAAAGCCATGAACATGCCCTTATCTATTGATAAATTAGTTCTGGATTCATTTATTGTCATGCTGCAGGTCCTGAAGGCAATCGGTCTGCAGCGAACAGGAAAACAGGATGAAGCCTTTACGTTAGCACAGGAAGTGGCGGTTCTCGAACCCACTGATGACAACTCTCTACAGGCACTGACCATCCTCTACAGAGAGATGCACCGACG[T/G]AAGTGATCACGGACCATCAAGGCATGTTTTGCATTGTATAACAGTGCTTATATTTGCAAAAAAAATGTAATCAAATGAAATTTTTCTTCCTGTAGCCGAGTTAGTGACCAAGCTTTATGAAGCTGCAGTTCGGAAGGTTCCAGCAAGCGAAGAGTACCACTCTCACCTCTTCATGGCCTATGCTCGGGTTGGAGAATACAAGAAGATGCAACAGGTTCGAATTGGACTGTGTTGGCTCTTATTTATTTAGGGGTGGCAATCTTTAGGGACTTTGCGATCCGATCCTATTTCGATTCTGGGAATCACAAATCTATTCCAATTCTTTCATCCTATTTAAAAATCAGTTGTGCAGATGCATCTTTCCAACTGTTTATTTTAACCAGAATTGTTTTGTTTCTATGCTTTTATAATAGTTTTTTATGAATCTTAGTATGATAACTAAATTTAGTTTTATTTTATTAAAGTTATATTCTGAATACAAAGATATATTCTTATACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21640
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111241 | Nonsense | 550 | 975 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 3379678)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 3371872 |
| GRCz11 | 10 | 3372176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTTAAATATTATCCATTCTGTGTTTCCAGGTATTTATTGACCCGCTA[T/A]GCAGAGTCTTTGGGCCAGTTTGCTGCTGCTTCCCAATCTTGTAACTTCTC
Long Flanking Sequence:
CCAAGCCCAGTTTGATGATTTGTTGTCCTTGTCACCCGGAGGATTTCCCCTGGGACAGCATTAACAGGTTCTACGTCACAATCACGCCCCCACAAGAGCAAGCAACTGATTGGTTAACGCGGCGCGAATGTCCGCTATAGTTCAGATTTTCGAACTCGAGAGATTCACACGAAACGCTCGTCAAGCGCGTCAAACGCGCAAAACGCTCAATTTGCCCCGCGCCTTTCGCGCGTATTGCGCTATTCGCACCGCGCCATTCGCTTCATACACGCCGCGCCATTCGCGTGTATTGCGCCGCAGGATGTCTATTCGCACGTTTGCATTGACTTAACATGTAAATCACTCACGCTTGACGCGCGTTCCGCGTCTGGTGTGAACACAGCATTACATTGTAATTTGCAGACATTTATGTCAAATTAAATGTAGTGTATTTGCAGTTAAAACGTGTTACTTGTTAAATATTATCCATTCTGTGTTTCCAGGTATTTATTGACCCGCTA[T/A]GCAGAGTCTTTGGGCCAGTTTGCTGCTGCTTCCCAATCTTGTAACTTCTCCCTCAGGTTTTTTCACTCGAACCAGAAAGATGTATGCTTATTTTCTGTTTTAAATGCTTTCATCTGTATGGCAAATCTCCAAAGAATAACCGGTCGTGCATTTGTTCCTGCAGACCTCAGAATACATTATTCAAGCATATAAGTACGGTGCTTTTGAGAAAATCCCGGAGTTCATCGCCTTCAGGAACCGACTCAATCACTCGCTGCACTTTGCTCAAGTGCGCACGGAGCGGATGCTGCTGGACCTCTTCCTAGAAGCCGACATGTTAGTGCTTTTTCATCATTACCTGCCTGTTTTTTATGTCACAGGTGGTGTTATTTTCACTGCAAAAAAGCTTTTCTTATTAAGATTTTTTTGTCTTGTTTCTTGTCCAAATATCTTACAATTCTTAAACCATAAAGCATATCCTAGACTGGTCTTTTTTTTTTAAATAATAAGCCAAAATTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38772
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111241 | Essential Splice Site | 577 | 975 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 3379595)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 3371789 |
| GRCz11 | 10 | 3372093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATCTTGTAACTTCTCCCTCAGGTTTTTTCACTCGAACCAGAAAGATG[T/A]ATGCTTATTTTCTGTTTTAAATGCTTTCATCTGTATGGCAAATCTCCAAA
Long Flanking Sequence:
ACGCCCCCACAAGAGCAAGCAACTGATTGGTTAACGCGGCGCGAATGTCCGCTATAGTTCAGATTTTCGAACTCGAGAGATTCACACGAAACGCTCGTCAAGCGCGTCAAACGCGCAAAACGCTCAATTTGCCCCGCGCCTTTCGCGCGTATTGCGCTATTCGCACCGCGCCATTCGCTTCATACACGCCGCGCCATTCGCGTGTATTGCGCCGCAGGATGTCTATTCGCACGTTTGCATTGACTTAACATGTAAATCACTCACGCTTGACGCGCGTTCCGCGTCTGGTGTGAACACAGCATTACATTGTAATTTGCAGACATTTATGTCAAATTAAATGTAGTGTATTTGCAGTTAAAACGTGTTACTTGTTAAATATTATCCATTCTGTGTTTCCAGGTATTTATTGACCCGCTATGCAGAGTCTTTGGGCCAGTTTGCTGCTGCTTCCCAATCTTGTAACTTCTCCCTCAGGTTTTTTCACTCGAACCAGAAAGATG[T/A]ATGCTTATTTTCTGTTTTAAATGCTTTCATCTGTATGGCAAATCTCCAAAGAATAACCGGTCGTGCATTTGTTCCTGCAGACCTCAGAATACATTATTCAAGCATATAAGTACGGTGCTTTTGAGAAAATCCCGGAGTTCATCGCCTTCAGGAACCGACTCAATCACTCGCTGCACTTTGCTCAAGTGCGCACGGAGCGGATGCTGCTGGACCTCTTCCTAGAAGCCGACATGTTAGTGCTTTTTCATCATTACCTGCCTGTTTTTTATGTCACAGGTGGTGTTATTTTCACTGCAAAAAAGCTTTTCTTATTAAGATTTTTTTGTCTTGTTTCTTGTCCAAATATCTTACAATTCTTAAACCATAAAGCATATCCTAGACTGGTCTTTTTTTTTTAAATAATAAGCCAAAATTAAGTGAGTTTTTCCTTAAAACCAGCAAAATAATCTGCCAATCAGGCAAAAAAAATAATAATATTGCTTTCCTTTCGATATAAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21639
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111241 | Nonsense | 963 | 975 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 3373645)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 3365839 |
| GRCz11 | 10 | 3366143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGTGCAGAGCAGCTACCTGCGTTCGCTGCAAGAGATCGGGGAACTGT[T/A]GAAGAAGAGAGCGGACTCGTTGAAATCCCTCAAAATCTGAGCGCTCCGTC
Long Flanking Sequence:
AAGCTCACTCTTGATCACGTCTGATGATGATTGATGATCCTAGCTAACTGAACAGACCTTTAATTTCCAGTTTCTTTGCGCTCGTCCTGTCTTGTTGATATAATTATATGCGTTACTACGGAGACATGTTAATGCGCGCAGCTGTCAATCAATATTGGTGGGCGGGGGGACCGCACTCCTACGTCAAGTTGCGGTCGATCTGAAAACCACTCCAATTGGTCCACCGTTTTTGTTGTTAAATTGAAAAAAAACCACTGTGTGTGTTTATATCACCCCAAAATGACAGTATATACACTATACTTACACACACGTCTGTCCAAACAGCTTTAAAAGTAGATTTTTCACCTTAGGTGCCTTTTAAAACCGTCTGAGAATTGGTTGTGCTTGTTTTTGACTCTATTTTTCCCTTCTCATCCAGGCGGAAGGGACCTTCACAAAGACCGCGATGGAGAAGGTGCAGAGCAGCTACCTGCGTTCGCTGCAAGAGATCGGGGAACTGT[T/A]GAAGAAGAGAGCGGACTCGTTGAAATCCCTCAAAATCTGAGCGCTCCGTCAATCCATCCATCCAGCATCCAGTCCAGTCCCCGACCCGCACGGCATCTTTGCTCCCAAACTCAGTCTGTGATCTCAGCCGGTCTCTTCCTTCCTATTTATCCGTCTCATTACTCACGTACAGATGAACAGGCACACTGTAACAAAAACAAACCCCAAAACTTCGGCTTCAGCACAAACCTCTACAGTGCTCCGTGCGGCACTTTTAAGTGGAAACGTAAACGTCATACCCCTAGCGAAACCACATAGGCGAGCGAAATTAAGCAATTTTAGAAGTACTGCTATAAATTATTGTACATAGTGTGAAGATAAACCGATATCATCGAGAACTCCTTGGCGAATTAAAGTGAACTGCTTTGTCTTTTTTTTTTTTTTGTCGATGTCTTGCGTTATTGTCTCACTTCTTTCCCTGCCGTATAAACCCCTCCTGACGATTTGTTGACGGTGCCACT
Associated Phenotype:
Not determined