ZMP
myoz2
Ensembl ID:
ZFIN IDs:
Description:
myozenin 2 [Source:RefSeq peptide;Acc:NP_957193]
Human Orthologue:
MYOZ2
Human Description:
myozenin 2 [Source:HGNC Symbol;Acc:1330]
Mouse Orthologue:
Myoz2
Mouse Description:
myozenin 2 Gene [Source:MGI Symbol;Acc:MGI:1913063]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1608 | Nonsense | Available for shipment | Available now |
| sa14169 | Nonsense | Available for shipment | Available now |
| sa31620 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1608
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 |
|---|---|---|---|---|---|
| ENSDART00000049928 | Nonsense | 21 | 264 | 2 | 6 |
| ENSDART00000124764 | Nonsense | 21 | 264 | 2 | 7 |
| ENSDART00000049928 | Nonsense | 21 | 264 | 2 | 6 |
| ENSDART00000124764 | Nonsense | 21 | 264 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 72557209)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 69599722 |
| GRCz10 | 7 | 69612033 |
| GRCz11 | 7 | 69841077 |
| GRCz11 | 7 | 69853388 |
KASP Assay ID:
554-1549.1 (used for ordering genotyping assays)
KASP Sequence:
ATAGTCTGATGTCAACACAGGAGAGGAAAATGCAGGCAGCGGCTATTTGT[A/T]GAGAGATCCACGCCAACGAAGGTACAAACACTGATTTATTACCATTGAGT
Long Flanking Sequence:
CCCCCAAAAAATAAAGAATTGTGTTGATTCAGCTCATTTTAAAATCATAGTTTAAACAAGGAGCAAAATGACTTTTTTTAGGGTCTGGTCAGTAGTGTATGCCAGCTGGACTGGTTTGGTGTGACGTCACATCCTGGGCCGCTCTGTTTTTGTCCTGAATAGTCTGAATGAGACGTATGGATTCTCCGTCTCTGCTGAAGCACACAGAAGCGCCTCTTTGCTCTTACGTCATGTTTAAATGCTGCTGGTTATTTAAAGGGATCTGCTTGTGTCAGCCTTCCAGCAGCTGTACTGTAATAAATGTCACCACTCCACTGTCAGTGTGATCATGAGTGTGTGTTTGCTGTGTTGTGTTGAAGTAAGTGTGAGATTGCGAGGGGCAAATTGGAGATTCGCATTCCCAAACTGTGTGTTTTTTGTTTGTTTTATCCACAGACAGCATGTCTCAGCATAGTCTGATGTCAACACAGGAGAGGAAAATGCAGGCAGCGGCTATTTGT[A/T]GAGAGATCCACGCCAACGAAGGTACAAACACTGATTTATTACCATTGAGTTGGGCTAGGCAGAATCTGAATCAGAATCTGAATTTTTTTTTTTTTTTTGCGCAGAATTGTGTACAAAATCAGCAGATTTATGCAGATGATTTGGAGAGTCTTAACACATGAAATTAAAAATAATAACTTTGTAACATTTATTTAAGATTTACAATGCAAATTCAATTAGAAGTCAGTCTCTCATATAATATATCTATTAAAAGACAAAGTCTGACTCGCTGTATTGTACATAAATCGGTAACACTTTACAATAAGGTTCATTAGTTAATGCATTAACTAACATGAACTAATCATGAACAACACATGTACAGCATTTATTAATCATAATTGAACATTTACTAATGCATTATTTACATCCAAGTCCGTGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACAACTGTATTTTCATTAACTAACGTTAACTAAC
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa14169
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 |
|---|---|---|---|---|---|
| ENSDART00000049928 | Nonsense | 21 | 264 | 2 | 6 |
| ENSDART00000124764 | Nonsense | 21 | 264 | 2 | 7 |
| ENSDART00000049928 | Nonsense | 21 | 264 | 2 | 6 |
| ENSDART00000124764 | Nonsense | 21 | 264 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 72557209)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 69599722 |
| GRCz10 | 7 | 69612033 |
| GRCz11 | 7 | 69841077 |
| GRCz11 | 7 | 69853388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGTCTGATGTCAACACAGGAGAGGAAAATGCAGGCAGCGGCTATTTGT[A/T]GAGAGATCCACGCCAAYGAWGGTACAAACACTGATTTATTACCATTGAGT
Long Flanking Sequence:
CCCCCAAAAAATAAAGAATTGTGTTGATTCAGCTCATTTTAAAATCATAGTTTAAACAAGGAGCAAAATGACTTTTTTTAGGGTCTGGTCAGTAGTGTATGCCAGCTGGACTGGTTTGGTGTGACGTCACATCCTGGGCCGCTCTGTTTTTGTCCTGAATAGTCTGAATGAGACGTATGGATTCTCCGTCTCTGCTGAAGCACACAGAAGCGCCTCTTTGCTCTTACGTCATGTTTAAATGCTGCTGGTTATTTAAAGGGATCTGCTTGTGTCAGCCTTCCAGCAGCTGTACTGTAATAAATGTCACCACTCCACTGTCAGTGTGATCATGAGTGTGTGTTTGCTGTGTTGTGTTGAAGTAAGTGTGAGATTGCGAGGGGCAAATTGGAGATTCGCATTCCCAAACTGTGTGTTTTTTGTTTGTTTTATCCACAGACAGCATGTCTCAGCATAGTCTGATGTCAACACAGGAGAGGAAAATGCAGGCAGCGGCTATTTGT[A/T]GAGAGATCCACGCCAACGAAGGTACAAACACTGATTTATTACCATTGAGTTGGGCTAGGCAGAATCTGAATCAGAATCTGAATTTTTTTTTTTTTTTTGCGCAGAATTGTGTACAAAATCAGCAGATTTATGCAGATGATTTGGAGAGTCTTAACACATGAAATTAAAAATAATAACTTTGTAACATTTATTTAAGATTTACAATGCAAATTCAATTAGAAGTCAGTCTCTCATATAATATATCTATTAAAAGACAAAGTCTGACTCGCTGTATTGTACATAAATCGGTAACACTTTACAATAAGGTTCATTAGTTAATGCATTAACTAACATGAACTAATCATGAACAACACATGTACAGCATTTATTAATCATAATTGAACATTTACTAATGCATTATTTACATCCAAGTCCGTGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACAACTGTATTTTCATTAACTAACGTTAACTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31620
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 |
|---|---|---|---|---|---|
| ENSDART00000049928 | Essential Splice Site | 27 | 264 | 2 | 6 |
| ENSDART00000124764 | Essential Splice Site | 27 | 264 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 72557187)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 69599744 |
| GRCz10 | 7 | 69612011 |
| GRCz11 | 7 | 69841099 |
| GRCz11 | 7 | 69853366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAAAATGCAGGCAGCGGCTATTTGTAGAGAGATCCACGCCAACGAAG[G/A]TACAAACACTGATTTATTACCATTGAGTTGGGCTAGGCAGAATCTGAATC
Long Flanking Sequence:
GTTGATTCAGCTCATTTTAAAATCATAGTTTAAACAAGGAGCAAAATGACTTTTTTTAGGGTCTGGTCAGTAGTGTATGCCAGCTGGACTGGTTTGGTGTGACGTCACATCCTGGGCCGCTCTGTTTTTGTCCTGAATAGTCTGAATGAGACGTATGGATTCTCCGTCTCTGCTGAAGCACACAGAAGCGCCTCTTTGCTCTTACGTCATGTTTAAATGCTGCTGGTTATTTAAAGGGATCTGCTTGTGTCAGCCTTCCAGCAGCTGTACTGTAATAAATGTCACCACTCCACTGTCAGTGTGATCATGAGTGTGTGTTTGCTGTGTTGTGTTGAAGTAAGTGTGAGATTGCGAGGGGCAAATTGGAGATTCGCATTCCCAAACTGTGTGTTTTTTGTTTGTTTTATCCACAGACAGCATGTCTCAGCATAGTCTGATGTCAACACAGGAGAGGAAAATGCAGGCAGCGGCTATTTGTAGAGAGATCCACGCCAACGAAG[G/A]TACAAACACTGATTTATTACCATTGAGTTGGGCTAGGCAGAATCTGAATCAGAATCTGAATTTTTTTTTTTTTTTTGCGCAGAATTGTGTACAAAATCAGCAGATTTATGCAGATGATTTGGAGAGTCTTAACACATGAAATTAAAAATAATAACTTTGTAACATTTATTTAAGATTTACAATGCAAATTCAATTAGAAGTCAGTCTCTCATATAATATATCTATTAAAAGACAAAGTCTGACTCGCTGTATTGTACATAAATCGGTAACACTTTACAATAAGGTTCATTAGTTAATGCATTAACTAACATGAACTAATCATGAACAACACATGTACAGCATTTATTAATCATAATTGAACATTTACTAATGCATTATTTACATCCAAGTCCGTGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACAACTGTATTTTCATTAACTAACGTTAACTAACAAGAACAAATACAGTAGTAAAT
Associated Phenotype:
Not determined