ZMP
naa35
Ensembl ID:
ZFIN ID:
Description:
N-alpha-acetyltransferase 35, NatC auxiliary subunit [Source:UniProtKB/Swiss-Prot;Acc:Q7T322]
Human Orthologue:
NAA35
Human Description:
N(alpha)-acetyltransferase 35, NatC auxiliary subunit [Source:HGNC Symbol;Acc:24340]
Mouse Orthologue:
Naa35
Mouse Description:
N(alpha)-acetyltransferase 35, NatC auxiliary subunit Gene [Source:MGI Symbol;Acc:MGI:1925939]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12739 | Essential Splice Site | Available for shipment | Available now |
sa45340 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31684 | Essential Splice Site | Available for shipment | Available now |
sa10722 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12739
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098707 | Essential Splice Site | 208 | 724 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 52211481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49960333 |
GRCz11 | 8 | 49949102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAGGAATGCTGAAAGATGTTGAGGATGAACTTCAGAGGAAAGTRAAGG[T/A]ATGAGGACTCRAATKKAAACATTATTTAGTTGATTCTTYGATTATTTTTG
Long Flanking Sequence:
GTAAATGTGGATTTTTCTCTTTTGTTATTGCAGGAAGATTTTCAGGCCATGACTTACGGCTTTAAAATGGCCAACAACGTAACTGATCTGAGAGTGACGGGTAAGTGTGTGTTTTTTCAAGTGATTCATGTTAATTAGAATTAAACACAGTTTCTCTCTAATTGTTGTTATTTTAATGGCAAAATCAAGTAAGTTCATTAAAAAATGCACATTTTGTAGGAAGGATGCATTACATTTATTAAAAGTGACTGTAAAGATATTTATGATTTTTTTAATGTTACAAATTATTTTATTTATTTATTTGTTTTACTTTATCAAAGAATTATTCAAGAACTATGTTATTCAGTGGAAAACATAAAATTTTTAAAAATATTTTTTTATTATTAGATTTTTATTGTATAATTTTGATCATATGGCGTTCAGTCTTTTCATCCCTCTGTTAAATATTTCTGTAGGAATGCTGAAAGATGTTGAGGATGAACTTCAGAGGAAAGTGAAGG[T/A]ATGAGGACTCAAATGGAAACATTATTTAGTTGATTCTTTGATTATTTTTGGTCTTGTTAAATAAGCCTCCTTTCCTTTTACTCCCAGAGTACCCGCAGTCGACAGGGTGAACAGCGAAATCCTGAGGTGGAACTGGATGTAAGATAAATATATTTCTCTTCACTAGAGATTTAGCCATATAAAGACATTTTAATAGCTATGCTTCCATCCAAAGATGCGAATTAGATTTATGCGCAAAATCTGGAATATTACATAAAAGATTTGAGAATAAAGCTCTGTTTCCATCCAATGAGTCAAAAGAGACTTCCTGATAAACCGGTGTAAAATAAACCAAAAAAAAAAAAAAAAAAAATTTAGTAGTTTGAGAAACCACTGTGGGACTTCTTTCCTACGTAATTAATTACTCAGAAGTCGAAATGCAATGAGCCCTAGGTGAATTTTAGAGGTGTGAGACAGTTCTGAAGGTAATAATAATAATAATACTGAACCACTATGATGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45340
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098707 | Nonsense | 512 | 724 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 52222488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49971340 |
GRCz11 | 8 | 49960109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCGCATCATGATCCAGTACCTGCTCAGCGGCTTTGAGCTGGAGCTCTA[C/G]AGCATGCACGAATACTATTACATCTACTGGTACGACCACTAAACAGCTAC
Long Flanking Sequence:
CTGCCGGGACTCGAACCAGCGACCTTCTCGCTGTGAGGCGACAGTGCTAACCACTGAACCACCGTGCCGCCCTCAAACATTCTTACCATCTTACCATGTGCGTCTTTAATTCTGAGAACTATTTCCCTACATTTATTGCATGTGAAGTCCTCACTGTTGACAGAGAGACACACTAATCATGTGTCAGGCAGTCACTTGTGAGATGAACAGGAGAAGATATTACTCACCATGATCATTACTCATTTACTTTATATTGTATATATCTGTATATATCAGGCAGTGAGGATCGTTGATGTAATGACTTAATGGAAATTGTAGGTCATGATCGAGTGTGTTTTTGTTGTTGTTCAGGCAGAGAAGGTGGACGCTGCTCTTCACGGTCTGCTGATGAAGCTGGAGCCGCAGCGGCAGCATTTAGCCTGTCTGGGCACCTGGATCCTCTACCACAACCTGCGCATCATGATCCAGTACCTGCTCAGCGGCTTTGAGCTGGAGCTCTA[C/G]AGCATGCACGAATACTATTACATCTACTGGTACGACCACTAAACAGCTACAACAGTTTAAATATTACAGGCTGACCCAGAAGCGTGGGTACAGAACAAAACACACTGTATGCACAAACGTGAGCACCATTTTGTTAAAAAACATTTACATAAAAATATTTAAATGCTAAATCATATTTGAAACAGATGAGTTTAATCACTCTTGAGTCCATTCAGCAGATCTCCAGGTCTGGCGGGAGCACTTTTAGCTTAACTTAGCATAGATCGTTGAATCGGATTAGACCATTTGCATTTTGTTAAAAAATGACCAGTGAGTTTTGATTTAATTTTATTTTTTATTTAGAGCTTGACTCTTTTGTGGTTGCACTGTGTACTAAGACCGACAGAAAATGAAAAGCCTCTATTTTTCTAGGCCAATTTTAGATTTTGGCATAATTAATGACTGTCATCTAAATATTTATCAGTCATATTTTAATTGTTTGTCTTAAAATTTAGAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31684
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 |
---|---|---|---|---|---|
ENSDART00000098707 | Essential Splice Site | 637 | 724 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 52227231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49976083 |
GRCz11 | 8 | 49964852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAACAGTGTGGTCACGCCACCACCAGTTCACTACATCCAGTTTAAGG[T/C]ACATGACTTTTATTCAATATACGAAGGGGATGTGTACTGATACAATTCTC
Long Flanking Sequence:
TGGAACTTACTTGGTATTTTTGAGTAATGTGCTGGATTTCTGCTTCATCCGTGTGCATCTCTGTCACTGACTGATGTTTATATGACGTCATGCAGTTAAAGCAGACAAGCACTTGGGAAAGATGGGTGGGGAGAACCAGCTCATTTGCATTTAAAGGCATAGGCTACAAAAACAGCTAAAATGTCCTCTAACCTAATATCTAGATGTAATCTAGGAATCTGATGGGTACTTTTTGCAGAAACTTTTACAGGCACATTCTGGAGACGCCAAAAGACTTACTTAATGTTTTTATAAACAAATAGTTTCAGACAAAAAGATGTCTTTGATTCTGCTACTTTATCTACTGTCTCTCTGTCAGACGATGATCGCGCTGGATATGGATCGAAAGGTGCGCAAACCTCAGTTTGAGCTGGACAGTGAGCAGGTGCGCTACGAGCATCGCTTCGCCCCTTTCAACAGTGTGGTCACGCCACCACCAGTTCACTACATCCAGTTTAAGG[T/C]ACATGACTTTTATTCAATATACGAAGGGGATGTGTACTGATACAATTCTCTTACATTTTTGTTGTGATTTTATCAAGTATTCCCAAAGCATTGAATATTACATAAACAATGAATACAATATTAATACATGTATACATGCATAAAAAAACAATAAAAAATTTGATAAATCCATACAGAAAAAAAGACTAATATGATTATTAAAAAAGATGTATGTATCTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTGTATATGAATGTATGTATATATATATATATATTTATATATATATATATATATATATATATATATATATATATATATATATTATTATTATTATTACTCTATTATTAATTATGAATAGATAATTAAGTATATGATTAATTAATTGTAATGTATTAATTATTATTCATATTATTTCTCTCCATCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10722
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 |
---|---|---|---|---|---|
ENSDART00000098707 | Essential Splice Site | 705 | 724 | 22 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 52229510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49978362 |
GRCz11 | 8 | 49967131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTGTTGTAATGAAGCTGCTGGCTGGAGGACACAAGAAGGAGACCAAGG[T/C]ACNAAAAAATGTWTTWTGGTTATGTCCCTTGTTACAAGATGTAAWRTAACT
Long Flanking Sequence:
TCAGTTTTAGTCTCATTACACCAGAAAATTTAGTTTGTTATGTCTGAGAGTCCTTCAGATGCCTTTTGGCAAATTCCAGGCGGGGAGTGGCTTCCGTCTGGCCACTTTACTATACAGGCCTGATTGGTGGATTGCTGCACAGATGCTAGTCCTTCTGTAAAATTCTCCTCCCTCCACAGAAGAACATTGGAGCTCAGACAGAGTGACCATCGGGTTATTGATCACCTCCCTGACTAAGGCCCTTCTCCCCCAATCACTCAGCTTAACATAACATTTTTTTAGAAAAAGTGAAGCGCTATGAATACTTTTCAGATGCACTGTAAATCTATTTAAAACTCATTTATTTTATGTTAGAAGGAACATCTTTCTCAAGCAATTACTGCGCTAAAAATGATTTTGTTGCTGAATCTTGTTTTAGGTTAATCGTATCCTTAAAGTGGCCAAACCCAATATTGTTGTAATGAAGCTGCTGGCTGGAGGACACAAGAAGGAGACCAAGG[T/C]ACAAAAAATGTTTTTTGGTTATGTCCCTTGTTACAAGATGTAAAATAACTCTCTGATGTCTCTAGAGTGTGTATGTGAAGTTTCAGCTCAAAACACCACACAAGTAATATTTTATAACTCTTTGAAACTGACCCTTATAGACTTTATATTCAAATGAGATTGTGCTCTTTACAAATGAAGGCGGAGCATAGCATAGTGGCAGATTCAAAAACAAGAATAACGGCTGATTCACATGGGGCTTCAGCGTCAGTGCTTGACAGAGGGCGTGTCTGAAGTTGGGGCTGACGCGATCGTTATATCAGCGTCAGCCAATGACATTTGTCCACAATCGGCTACTGTCTGAGCTGGTGTATTTGCATACAGCAATCTCATTGGCTGCCGCTATTGGCTGCGGCATCGATGGACCCACAATTCAGTTCGGCAACGCTTGACGTCACCCATTCAAATTTAATGGGAAGCGTTGACGCTGATGCTCCGTGTAAATGAACCGTAACATCATA
Associated Phenotype:
Not determined