ZMP
ENSDARG00000075433
Ensembl ID:
Human Orthologue:
MYOM2
Human Description:
myomesin (M-protein) 2, 165kDa [Source:HGNC Symbol;Acc:7614]
Mouse Orthologue:
Myom2
Mouse Description:
myomesin 2 Gene [Source:MGI Symbol;Acc:MGI:1328358]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17101 | Nonsense | Available for shipment | Available now |
sa21858 | Nonsense | Available for shipment | Available now |
sa31817 | Nonsense | Available for shipment | Available now |
sa16728 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17101
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 |
---|---|---|---|---|---|
ENSDART00000087105 | Nonsense | 404 | 1366 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 11 (position 11346710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11241713 |
GRCz11 | 11 | 11225334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGGAACTAAGGACTGGGTCCAGTGCAATGACTCWCCTGTGAAAGTGTG[C/A]AAGCTGCCCGTCCACGGCCTGACYGACGGGGCWTCCTATCACTTCCGAGT
Long Flanking Sequence:
ATTTTTTTAAATAGAGGAAGTTATAATTGTTTGCCAATTACACTTACTGCCCAAGAAACTATGAATTGGAAAAGAAAATAATGACGATAGATGATATATTTAATATGTGTCATTACTTTGATGCATACAATGTTTCTCTTTCTATATATCTAATGTTTCACTTCACTGCAAATAATAAAATGATTTTATTTCTATTGCTTTTTAGGGAAATTAATTGGGAAATAATATTTATTGTCTTAGAAATATTGGTTTTTAATTAGTAATAAAATTTATTTTTAGACAAAGGGCTTATAAAAGTAATTCAAATACTTTTTAATGAGGTAATTAGGAATTAATAAATTAACTATAGTGCCTTGCATCCATTAATAAATAAATATATCTGGTGTGTGAATAATTTTTATCTTGACAGTATTTATTTTGTATTTTGTGTGTTCACTTTGCAGGCGTAAGTCAGGAACTAAGGACTGGGTCCAGTGCAATGACTCTCCTGTGAAAGTGTG[C/A]AAGCTGCCCGTCCACGGCCTGACCGACGGGGCATCCTATCACTTCCGAGTGAGGGCTGTGAACAAATCTGGCATCAGTCTGCCTTCCAGGATGTCCTCTGGAGTGACCACAGGAGAAGTGGAGAGCGATGTGGAAGGTAGGACTCATGCATTGAACCCAAACAACTTAATAGAGTTGTTTCATTAAACTGGGGCTAAACTGAAAGCTTAAAGGTCCAGAAGCGTCAAGGTAAGTTTACAGGATCAAGAGTCATGCTTTTTTTCTTCTTCTCCCGTTTCTGGATATTTGTGTGTTTTATGAATTTTTTCCAACACAATTTCACTCAGAAACTAGTGGATAAGTGGATTGTTAATATGAATTTGTACAAGCATATTCATAAGAAAATGTGTGTTTTATAGAACAAATGTCTACCCAAATCTCTCTCTATCTCTGCCTTTTAATGTAACCGTAACTGAAGTGTGAGCAGATTAAATAAAACATACATTTCAAATGCAGGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21858
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 |
---|---|---|---|---|---|
ENSDART00000087105 | Nonsense | 405 | 1366 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 11 (position 11346711)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11241714 |
GRCz11 | 11 | 11225335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAACTAAGGACTGGGTCCAGTGCAATGACTCTCCTGTGAAAGTGTGC[A/T]AGCTGCCCGTCCACGGCCTGACCGACGGGGCATCCTATCACTTCCGAGTG
Long Flanking Sequence:
TTTTTTTAAATAGAGGAAGTTATAATTGTTTGCCAATTACACTTACTGCCCAAGAAACTATGAATTGGAAAAGAAAATAATGACGATAGATGATATATTTAATATGTGTCATTACTTTGATGCATACAATGTTTCTCTTTCTATATATCTAATGTTTCACTTCACTGCAAATAATAAAATGATTTTATTTCTATTGCTTTTTAGGGAAATTAATTGGGAAATAATATTTATTGTCTTAGAAATATTGGTTTTTAATTAGTAATAAAATTTATTTTTAGACAAAGGGCTTATAAAAGTAATTCAAATACTTTTTAATGAGGTAATTAGGAATTAATAAATTAACTATAGTGCCTTGCATCCATTAATAAATAAATATATCTGGTGTGTGAATAATTTTTATCTTGACAGTATTTATTTTGTATTTTGTGTGTTCACTTTGCAGGCGTAAGTCAGGAACTAAGGACTGGGTCCAGTGCAATGACTCTCCTGTGAAAGTGTGC[A/T]AGCTGCCCGTCCACGGCCTGACCGACGGGGCATCCTATCACTTCCGAGTGAGGGCTGTGAACAAATCTGGCATCAGTCTGCCTTCCAGGATGTCCTCTGGAGTGACCACAGGAGAAGTGGAGAGCGATGTGGAAGGTAGGACTCATGCATTGAACCCAAACAACTTAATAGAGTTGTTTCATTAAACTGGGGCTAAACTGAAAGCTTAAAGGTCCAGAAGCGTCAAGGTAAGTTTACAGGATCAAGAGTCATGCTTTTTTTCTTCTTCTCCCGTTTCTGGATATTTGTGTGTTTTATGAATTTTTTCCAACACAATTTCACTCAGAAACTAGTGGATAAGTGGATTGTTAATATGAATTTGTACAAGCATATTCATAAGAAAATGTGTGTTTTATAGAACAAATGTCTACCCAAATCTCTCTCTATCTCTGCCTTTTAATGTAACCGTAACTGAAGTGTGAGCAGATTAAATAAAACATACATTTCAAATGCAGGGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31817
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087105 | Nonsense | 492 | 1366 | 12 | 33 |
Genomic Location (Zv9):
Chromosome 11 (position 11355018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11250021 |
GRCz11 | 11 | 11233642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAACATGCCACAAACCTCCTGGGTTACTATGTTGATGCCTCTGTGGTC[G/T]GATCCAAGGACTGGTTCCCCTGTAATCACAGGCCTTACAAACACACCAGG
Long Flanking Sequence:
TTCTTTTCTCAGCCTTGATGATAACTGCACAGCTCCATTTCGTCTTTATTATCATGAAACACGGCACACAATGTAAACAGCTTGTCCAGTTGAATTTTGTCTTCCATTCTACAGTTGTTGATTTTGTTAAATGGAGAGCTTGGGGTTGTTGTCCAACTGCTTATGTCACTTTACAATTTCTAGAAATGGTTTAATTGCAACCAGGAATATGGTTTGGTGGAAATTAGTTCTCAAAGAACCAGCCTGGTGGTTCCTGTATATGAAATGTGAAAGCCCCTATGGTCACCATCACTACAGCAGTTCACAGTTTCCACTCTTATTTTAGTCAATGACTGACAACATCTGATGATTAATTAAAATTTTTGGTTTGTGCAGGTGTTCCTTCTGCCCCGGGACAGGTGATTGCCTCCAGAAATACCAAAACGTCTGCTTTTGTGCAGTGGGATGCTCCGAAACATGCCACAAACCTCCTGGGTTACTATGTTGATGCCTCTGTGGTC[G/T]GATCCAAGGACTGGTTCCCCTGTAATCACAGGCCTTACAAACACACCAGGTAAAATGCGCACACACACAAAAAAAACCTCCCAAGTTGTTAGTCATGCGAGTCTTAGACTGAAATCGCCCCCTATACCCTTAAAGAGCCCTCATGATACATTGAAAAGGTCATATTTTGGTTTTACGGGTCTCCAACATCAGTCTGATATGCATGCAAGGTCAAAAAACACTTTCATTTGTCATATAGTATGAATTTATTTTTGCCTAATTATCCCAGCGACTCCCATATGAATCGTTCAGTGGTTCATTTGTTCCCAAACCCCTCTTTCGCACGATGCTAATCTGTGCTGTGCTGATTGGACCGATAACAGTCTGTTGCGATTGGACAGAGTGAAATGCCCACCATGGCTTATCAACTATATTGAAGTAGTCAGAGTGCATTGTGTGTGTGTGAGCATGCCCCCCTCAACTCCCACCCCCCCCCCCAACTCCACCAACTATACCTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16728
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087105 | Essential Splice Site | 654 | 1366 | 16 | 33 |
Genomic Location (Zv9):
Chromosome 11 (position 11364684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 11259687 |
GRCz11 | 11 | 11243308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATGTAATGCACATCTTGTYTAAACTGATACTTTCTCTATTTGTCATC[A/T]GGTCCAGCATATGACATYAGTTTCTGGGAAGTGCGYGACACCTCCMTTTT
Long Flanking Sequence:
CAGCTCCCAGCATGTGATTTGAGACTTAAATCTAATTACCTCAAAGTTTTTTTTTTTTTTTCAGTTCTCAGACCAGCCAAACAACTATTTAAAGTCAGTGTCCAGAAAGTATAGGCTGCACGTTCATGAGAGTGCTGCACTCTTTATGCTTGTCAAGCTGATAGATAGTCAACAGATAGATAGTTAAGCTGTTTTATAGGTGATACATATTAAAGCAACTCATAAGTATCTACAGTATATATATATATATTGTCAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATATGTATGTATATATGTATATATATATATATGTATGTAATGCACATCTTGTCTAAACTGATACTTTCTCTATTTGTCATC[A/T]GGTCCAGCATATGACATCAGTTTCTGGGAAGTGCGTGACACCTCCATTTTGGTGCAGTGGAAACCCCCTGTGTACACCGGACAGAGTCCCGTCACTGGTTATTTTGTGGACATGGCTAAGAAGGGCTCATCAGATTTTGCCACAGTAAATGCTGAAAAAGTTGAACATTGCTTCCTGAAGGTATAGCACCAGAATTCCCAAAACAAACACAACACTAAAGAAAAACAAAAACATACTCAGATGTTTGTACACTCATCTGTAGGTCACTGGACTTGAATCTGGAGCGTCATATGTGTTCAGAGTACGGGCTGTCAATGACAAAGGTGTTGGAAAAGCCTCAGACTTGTCTGATCCCATATGTGCAAAAGCACTGCCAGGTAACTACAACACAGCTCTACCACCAATTATAAGCACTCAATAACTATAATTTATTAAAGGGATAGTTTACCAAAAAAGACACTTCATTGCCATTTGTTTACACTCAAGTGGTTATAAACTTT
Associated Phenotype:
Not determined