ZMP
naa15b
Ensembl ID:
ZFIN ID:
Description:
N(alpha)-acetyltransferase 15, NatA auxiliary subunit b [Source:RefSeq peptide;Acc:NP_976066]
Human Orthologue:
NAA15
Human Description:
N(alpha)-acetyltransferase 15, NatA auxiliary subunit [Source:HGNC Symbol;Acc:30782]
Mouse Orthologue:
Naa15
Mouse Description:
N(alpha)-acetyltransferase 15, NatA auxiliary subunit Gene [Source:MGI Symbol;Acc:MGI:1922088]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17329 | Essential Splice Site | Available for shipment | Available now |
sa30585 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19540 | Nonsense | Available for shipment | Available now |
sa14582 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17329
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 |
---|---|---|---|---|---|
ENSDART00000040798 | Essential Splice Site | 46 | 800 | 2 | 19 |
ENSDART00000123873 | Essential Splice Site | 46 | 685 | 2 | 16 |
ENSDART00000130490 | None | None | 559 | None | 14 |
ENSDART00000133343 | Essential Splice Site | 29 | 208 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 41011405)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39900814 |
GRCz11 | 1 | 40618887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAATTCTGCAAACAGATCCTCTCYAAYTCAAAGTTCTCAGAACATGGAG[G/A]TAAGAACCACAGGTGGAAGTGTTTGTGACGGCTACAACCAGACATCACTA
Long Flanking Sequence:
TTTCCACATATAATATTTTTACTCCAACTTAATATCTTCAGTTGATCGTTTGAAATAAATGCATCTGTGGGATTATTTCCTAATCGTGTGATTTGATGCATTAAATCAATGAAAGCAGGAAAATCTTCTGTTTATTGATCAAAGTTGTTTCTTTGTGGGTATTATGGAGTTCGTGCACAAGAGCACCCTCTGGCCTTTGAAATAGATTTACTACTATTACAGAAATGCGCTTCCCTGGCAAGATGTGCATGACTTTATCGTGCATGACTTTATCATGTCTAAGATTTAATTTTAATGAATCAACCATCCTTATATGCTGTCAGTGCATAGTTAGTCTAGATTACCTTATTACAAAAGATTTATAATGTTAATATTTATTTATTTTTTAAAATTTCTTCTCTGTTTTTGTCCTCAGAGATGTTACGAACATAAGCAGTACAGAAATGGGCTGAAATTCTGCAAACAGATCCTCTCCAATTCAAAGTTCTCAGAACATGGAG[G/A]TAAGAACCACAGGTGGAAGTGTTTGTGACGGCTACAACCAGACATCACTAATACAAAGTTAATTGTGATATAAACAATGTTAATTAAGTGAGAAAAATGTGTTCTAAAAAACTTCAACATGCATAAATTTACGTCAACATTTATTTTTGTTTTGAAATATTTAGTCATTGGGAACAATTTCTGATGTCATTTTAAAATAGCACAGCATTAAATTAATATTAAAGGCACAGTTTGTAAATTTTCACAGCTAGAGGGTGCATATTCACAACAAACAAATGCAAAGTTTGGTTATGCCATGACTGAGTGTGGAACCATGGGAGTTGTCATCTTCACTACATCCTTCATGTCTCCTGCAGAAACCATGTAAACTACGACACCTGGCTTGCATGTAGCAGTGCATTTATTCTTCTGCCTTCTATTTGTGTTGCTCTGACAATAACTCATTGGAAATGCTAGCTGGCAATGGGATTTCTATGTTCTTCTGTGTCGAGTTTCTTCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30585
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 |
---|---|---|---|---|---|
ENSDART00000040798 | Nonsense | 71 | 800 | 3 | 19 |
ENSDART00000123873 | Nonsense | 71 | 685 | 3 | 16 |
ENSDART00000130490 | None | None | 559 | None | 14 |
ENSDART00000133343 | Nonsense | 54 | 208 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 41012377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39901786 |
GRCz11 | 1 | 40619859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGCTAAACTGCCTGGGGAAGAAAGAAGAAGCCTATGAACTAGTCCGC[C/T]GAGGGCTCCGAAATGACCTGAAGAGCCACGTCTGTATCCTTGGAGCTTGA
Long Flanking Sequence:
CTATGTTCTTCTGTGTCGAGTTTCTTCGTAGGTGTTTTGTTTACATCAGACATGCCTGTTATTCTAACTTGCTGTACAAGTAGTTCAAACTCGCTAATTCGGGGGCAAGAACCTGCAGACATGCAACAACTTTAATCATAAAGTAAATACAAAACAAAAAGATCTAGTACCTTACAGCCTTATTCTGAAATGGATTAAATTCGTTTGTTTCCTCAAAATTCTACACGCAATACCCCATAATGACAATGTGAAAAAAGATACTTTCCAGATGAACTGAATTTTAATAAAAAGCCATACATGTACACACTGTGCCTTTTAATAAAGCATTGCTGATTTAAAAAAAAAAAACAGGTTTTATCTCTATCATTTATCCTCTTTGAGTTTACTTTAGGTCTATGAGTGAAAGGTTAAAGATTATGCTCATTGTAGAGACGCTGGCGATGAAGGGCTTGACGCTAAACTGCCTGGGGAAGAAAGAAGAAGCCTATGAACTAGTCCGC[C/T]GAGGGCTCCGAAATGACCTGAAGAGCCACGTCTGTATCCTTGGAGCTTGAGACCATTACACGCTTATGAATGCTTTCAGTTTGATATTTAAATGCATTAACCCATCAGTATTCAGAACAGAGTGTGGTAATGGTCCATGTGTTGGAATGAGTTTGTTTCCTCATGTTCACAGCACCAGAATTAACACTCGTCTCAGTTTGAAGCCTGTCGCTGGCGGTGGGATGCTGGATGTCCGCCAAGATTCCTGCCCTGTGTCTGACCATGATGCGCAGTGACACCATGAACTGTTTGGAGAGCTAAACACATAGTGCAGTGTTTCCTCGCTGACAGCCAAATGCTTCACATCCCAGAGGTTCATGTTAGACACAGAAAATTACCATTTTATAATAGAATAGGCCACTTCAGGACTTTAATATGTTGTTTTATTGGCTTTCTGTGTTTTCAGAATACCAAAAAATGAACAAGCAGACCCTGTACTTTCCATTGAGCCATCCAATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19540
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040798 | Nonsense | 247 | 800 | 7 | 19 |
ENSDART00000123873 | Nonsense | 247 | 685 | 7 | 16 |
ENSDART00000130490 | Nonsense | 121 | 559 | 5 | 14 |
ENSDART00000133343 | None | None | 208 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 41019743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39909152 |
GRCz11 | 1 | 40627225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGAGCTTCTGTTGAATCTGGAGCGGTTTGAGGAGGCGGCAGATGTGTA[C/A]AGAAGACTGCAGGAGAGGAATCCGGAGAACTGGTTGTATTACCATGGCCT
Long Flanking Sequence:
AGGTTGCAGGAAATTCTGATCAATATTACCCTTCTGGCTAAAGCATAGCAAAGCATGTTTTTCTTACAACTCCATTCTCTATTAATGTGTGTCTATTTTATGGTTTTCTTGAATATTTGTTTTGCTCTTGTTTTTTTTTTTTCTCCAGACGTCACCTGATAAGGTGGATTATGAGTACAGTGAGCTGCTGTTGTATCAGAATCAGGTGCTGAGAGAAGCAGGACTCTTGAGAGAAGCTCTGGAGCATCTCACCACCTACGAGAAGCAGATCTGCGATAAACTGGCTGTGGAGGAAACCAAAGGTACGTCAGCACAATTTTTCGCATTTGTCTTGCTTCCTTATGTCTGCAGTTGCATTATCATTTCGCTTTTCCAGTTCACAGTTTGCTTGTCTAGCAGATTGACTTCCTGTTTGTGAATGCCTGTGGAAAATGCTCTTTCTCGTGTGTAGGTGAGCTTCTGTTGAATCTGGAGCGGTTTGAGGAGGCGGCAGATGTGTA[C/A]AGAAGACTGCAGGAGAGGAATCCGGAGAACTGGTTGTATTACCATGGCCTGGAGAGAGCCCTCAAGCCTGGTATGCAAGAAAACTGATTCGCTGGGAAAGTTTTCAACTATTTGTAGGCCCTGTGATTTCTGCAAAGCTGAAAAGGGCAGACTGAGTCACAGACTTCAGGAAAACCATGTTATTCTAGTGTTAGGATTGATCGGATTTTGGATGTATAAAACCAAAGTAATGCTACGCTATATGAATAATTAAATATTAAAGGGATGGTTCACCCAAAACTAAAAATTGTCATGTCACCTTCTTGTCACAAACCTAGATTCTTTTTTTATGTTGAACACAAAAGAAGATATTTTGAAAAAATGCTTTAAACCTGTAACCATTGACTTCCATAGTGGGAAAAACAAATATTACGTATTTCAATAGTTACAGGATTCATTTTTCAAAATTTATGTTTTGTCTTCAACAAAAAAGGAAACAAGTGTTTGGAGAGAAGAGGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14582
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 |
---|---|---|---|---|---|
ENSDART00000040798 | Nonsense | 451 | 800 | 12 | 19 |
ENSDART00000123873 | Nonsense | 451 | 685 | 12 | 16 |
ENSDART00000130490 | Nonsense | 325 | 559 | 10 | 14 |
ENSDART00000133343 | None | None | 208 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 41024707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 39914116 |
GRCz11 | 1 | 40632189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGCTTTGGACACCGCCGACCGCTTTATTAACTCCAAATGCGCCAAGTA[T/A]CTTCTTAAAGCTGGCCTGGTCARAGAGGCTGAGGAAATGTGCGCCAAATT
Long Flanking Sequence:
ATATCACCTGATTTGTTTCAATGTAGATGATGGTAAAGAGGAGCCACCCACCACGTTACTGTGGGTGCAGTATTTCCTAGCCCAACATTATGATCAGATCGGCCAGCACAGCATGGCTCTGGAAAACATCAATGCTGCCATCGAGAGCACACCTACTCTCATAGAGCTCTTCCTCATTAAAGCCAAGATATACAAGGTAAAGTATTAAACACTGCATGCTCGCTAACTTTTCTTATTTAGTTATTCATTTATGTATGCATGTTTGCATGTATGGCTTGCATTATCTCAGTTGTGTCACTAAAAGTTGTGACTGATTATAAGAACATTTGAATATTAAACATTTAGTTTGTCAAATATCTCTTAGCTTCATTGTTTTTTTCATTTATGTGTGTTTTCTTGGCTCAGCATGCTGGGAACATCCGAGAAGCAGCTCGCTGGATGGATGAAGCTCAAGCTTTGGACACCGCCGACCGCTTTATTAACTCCAAATGCGCCAAGTA[T/A]CTTCTTAAAGCTGGCCTGGTCAAAGAGGCTGAGGAAATGTGCGCCAAATTCACAAGGGTAAGGAAAATTTGAGAACACATGCAGAGGTTCATTCATTCATTTCCTTCAGCTTAGTTCCTTTATTAATCTGGGATCACCATAGCGGAATGAACCACCAACTTATCCTGCATGTGTTTTACATAGTGGATGCCCTTCCAGCTGCAACCCAGTACTGGAAAACATCCACACACACACACACACACACACACACACTACGGCCATTTTAGTTTATTCAGTTCACCTATACTGCATGCCTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCTAACACAGAGAGCAAACATGCAAACTCCACACAAAGATGCACACTCACCCAGCTAGGACTCTTTCTGTGAGGCCATGCGGAGGATATTGTTTGTTGGTGTTTCTTTAACTGTGGTGTTTTTCTCTGTTATAGGAGGGAGCGTCTGCAGTGGAGAATCTGAAT
Associated Phenotype:
Not determined