ZMP
zgc:162939
Ensembl ID:
ZFIN ID:
Description:
aminopeptidase O [Source:RefSeq peptide;Acc:NP_001116730]
Human Orthologue:
C9orf3
Human Description:
chromosome 9 open reading frame 3 [Source:HGNC Symbol;Acc:1361]
Mouse Orthologue:
2010111I01Rik
Mouse Description:
RIKEN cDNA 2010111I01 gene Gene [Source:MGI Symbol;Acc:MGI:1919311]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41235 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21324 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41235
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111358 | Essential Splice Site | 483 | 787 | 5 | 16 |
ENSDART00000133209 | None | None | 45 | None | 4 |
ENSDART00000139864 | None | None | 45 | None | 6 |
ENSDART00000143809 | None | None | 45 | None | 7 |
The following transcripts of ENSDARG00000068461 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31132075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30274801 |
GRCz11 | 8 | 30284033 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCTTCGCTACTTACTTAGAGGATGTTTTCTGGAGCCACGTTCAGAAG[G/A]TATTATGATATGGTTGAATCTTTGAGTGCTTGTCTGAGGCCCTGTTTCCT
Long Flanking Sequence:
CCACTGGCAGCGAACAGGCCTCATTTTGGCTGAGAGCTCCACCTCCTTAACGACAGTCTGTCGACGGGAGAGAAAATCCCACACTTTGATGTTCTTTCAGGGTGGCTGAGTTTTATAACATGTTATAACTAGATCAGAGCTGAATGCAGAGCTCTGAACGCTCAGCACCCGCTGCAACATTATAACCACTGATTTGCTAGTTAACCAAATACAACTGTGATGTTCAATCCTAGTCTGTTTTCTTTTTTTGTTAATTCTTTTTTTAAATGCTAAAATAAATCAATCAACTGTGATTTCACTTGTTTTCCAGTCCACATATCGTGTTCCTGTCTCAAAGTGTGCTAACTGGTGAGAGGAACCTCTGTGGGGCAAGGTTATGCCATGAAATTGCCCATTCCTGGTTCGGGCTGGCCATTGGAGCACGGGATTGGACAGAAGAATGGATCAGCGAGGGCTTCGCTACTTACTTAGAGGATGTTTTCTGGAGCCACGTTCAGAAG[G/A]TATTATGATATGGTTGAATCTTTGAGTGCTTGTCTGAGGCCCTGTTTCCTGCTGGTGTTAACATGCGTTTTTTAGTAGTCTGCCGAGACGCATTACTGTTAACACCTGGTAATATCATCTGTTCAAATTTATCTTGTATGACCACTTTTGTTCAGATTTGATCTAAACCTTTCCATTTAATTTTGTGACACTCTACATCACAAGTGGTCAGTACGACCCATGAGTACTATTGAATAATAAAAAGTTTTTTAAACAGCTTATGACTGGAAAGCAAGCGAATGGAAAGCATGGGAAATGACATCTATGACTTAATCCTGATTCATACTTCTGTGTCGATTGATCAGCATACCCCACACCACATACATGATCAGTTTGTGCAGCTCTAGCAGGAACACTTCCGAAACACTAGTAGGCAGTGGGGTTTCTATAGCCATTTCACACAGGGATACCAGTAAATATCTGGAAAATTTCCGGAACGACTTTACCGGTATTTTCAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21324
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111358 | Nonsense | 575 | 787 | 8 | 16 |
ENSDART00000133209 | None | None | 45 | None | 4 |
ENSDART00000139864 | None | None | 45 | None | 6 |
ENSDART00000143809 | None | None | 45 | None | 7 |
The following transcripts of ENSDARG00000068461 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31110449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30253175 |
GRCz11 | 8 | 30262407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGTTTCTGGCTGATCAGATCGGCGAGGAGAAGTTCCTGCAATTCTTC[A/T]AAGTGTTTGTTGGAAAATTCCACGGGCAGCTAATTCTGTCTCAGGTGATC
Long Flanking Sequence:
CTTACTCAACAAAGAGCCATAAAAACACAGCATTACTGTAATCTATGGTGCTCTAGACAGAGAGGCAATCAAGGACATAATGCTTTCATGAATGCAATTGTTTATACACTTAGCAAACTGTTAGCAGCTCCTAATGTATGCTGATGTAAGTGTATTCCTGTAGATGCAGCACTTTACCTTATCAGACCACAGTATGATTGATGTGCTGTTTGTGTGTTTGCATATGTTTGTATATTTGCACACAGGCCCAATAAAGAGAACACAGGGGAAGTGAGCGAGTCCGGTGCGTCAGTTGTGAAGCATGCCCTCAACCCAGAAAAACCCTTCATGCAGGTGCACTATTTGAAGGTACGTTTGAAAGCTCAAAGTGCAGCGTCTTCTGGGCCATCTGGGAGATTTGGCTGGTGTAGATCTGGCTTTCTGTCTTTTTCTCCCAGGGCTACTTCCTCTTGAAGTTTCTGGCTGATCAGATCGGCGAGGAGAAGTTCCTGCAATTCTTC[A/T]AAGTGTTTGTTGGAAAATTCCACGGGCAGCTAATTCTGTCTCAGGTGATCTTGCCCTGCATTGAATGGATCTGTTCATTCAATCTGTATGCAAATGTTGCTGTTGGATGGGGCGTGCATATTTTGGACACTGTTTCAGTTTCATTTTCATTCTTTCAGCCTGTTAAGAATGTAGGTAAAAAGTGGAAACGTTAGATTACAGATTATTTCAAATTGTTAAAGGTGCAGTATGCAGGAGTGACATATTGCACTCCACATTCAAAACCATAGAGGGTTTTTTTTCACCCGGCCCTTCCTCATTCAATAAAAACTCAGGTTGCCAGATTGCCATTAAGTACAGTTGAAGTCAGAATTATTAGCCCCCCTGAATTATTCACCCCCTTGTTTATTTTCTTCCCCAATTTCTGTTTAACGGAGAGCAGATTTTTTCAACACATTTCTAAACATAATAGATTTAATAATTCAGTTCTAATAACTGATTTATTTTATCTTTGCCATGAT
Associated Phenotype:
Not determined