Busch Lab

ZMP

LOC100331557

Ensembl ID:
ENSDARG00000089850
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa35427 Nonsense Mutation detected in F1 DNA Not yet available
sa13314 Nonsense Available for shipment Available now
sa42146 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35427
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125593 Nonsense 3 391 1 8
Genomic Location (Zv9):
Chromosome 13 (position 9580253)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 9691358
GRCz11 13 7015777
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACACTGGACATGAAAGATAATTTGTAATCTTTCCTTAATGCTCGTG[G/A]TTGCCAAAAGCATGGTCCTCTCAATGCTCAATATTGTGTTTTGCTGGCTC
Long Flanking Sequence:
TGCATTCATTCTTTTTAACAAAATGTTCCAAACAGTTGTTTTGGCCATGCCTATAGTTTTTGCCATCTCTCAGATGGGTTCGTTTTGTTTTTCAGCCTAATGATGGCTTGCTTGACTGATAGTGACAGCTCTTTAGATCTCATCTTGAGAGTTATAATTGGGATAATGAGAGAATAACACACCTGCTCATGGAACAGATTTTTGAAGCCAATTGTCCAATTGCTTTTGGACCCTTAACAAGTGGGAGGCACATATGCAAACTGTTGTAAATCCTACAGAGTTCACCTGATTTGGATGTAAATACCCTTGAATAAAAGCTGTCAGTCTGCAGTTAAAGCACATCTTGTTCATTTCAAATAAATTATGTTGGTGTATAGAGCCAAAAACACTAGAATTGTGTCTATGTATATAATTTAAACATGAAAATCAATGATTTCCAAATAAATTTTTAACAACACTGGACATGAAAGATAATTTGTAATCTTTCCTTAATGCTCGTG[G/A]TTGCCAAAAGCATGGTCCTCTCAATGCTCAATATTGTGTTTTGCTGGCTCTGCTATCATACAGCTTCAGGTCGGAGCAGGATCTTGGCAGAGAGTGAACACTAAAGTGCCCATCAGATCCCCTCGCTATGCTGTCTTCGACCTGTCTGAAGGAAAGGACTATCTCTTCCGTGTTCTGTCTGCTAATATATATGGCATCAGTGAACCCTCGGAGCCCACCAGCACTATAACTACCTTGCAACTAAAGGGTAAAAAATGCATGTCAAAGGCCACCACTCTTCCGATATATTCAGTTAAGCTATTGAAATGGTGAATCTTCTGCATATAAAATTGCATATACATCTTTGAAGCTTTGGTCAGGCTGTGACTTTGATGTTGTTATTAAGGCAGTAATGAATTTTATATGCCTTTCTGTAGTGGAACTAATTCATGCATGATAGGTCATCAAGAAATTGATTGGGCTGGTTGGTGAAATCAGCCTTGAAATGAAGTTCTTTGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13314
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125593 Nonsense 209 391 4 8
Genomic Location (Zv9):
Chromosome 13 (position 9571760)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 9699851
GRCz11 13 7007228
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCTCTCTTCTGTATTGTGACGGGGAATCCATGGTGCTCAACTGGAAG[C/T]AGCCCATCCATTCTGGAGGAGCAGAGGTCACCGATTATTACATTGACAAA
Long Flanking Sequence:
AATTAGTTGTCATGTAGATGCAATGTACCTTGAATTAAACAAACGGACCATCAAAATAAAGTGTGACCCAGTATTCTAAAATAAAGCTCTTACATGTTCAATATTCTAAATGCGTATCCATTTCCTTTACACTGCTTCTTCAGAAGGCAGCTGTTTATGTAGGCAGTAGACAGAAAGCAGCTCATTCTGTTTTCACTGTGAGTCCTACATTCTCTTGCTGAAAGCATTGCTATAATTTGAGCCTTATATTTATGTGCAACATTAAGATGCATTTCATCCTATTATATTACACCTCCAGGCGCAACATTTCCCTATGAAATGTGCATATTATAAGCCAGAGATGTGCCTTGCACGTCATTGCATGTTGCCCCGTGTAGAAGACATTGAGTAATGGCTACATCCAACTGAAGCAATCTGTCTTCTCCACAGAGTTGCCCTCTTCCCCTTATGACATCTCTCTTCTGTATTGTGACGGGGAATCCATGGTGCTCAACTGGAAG[C/T]AGCCCATCCATTCTGGAGGAGCAGAGGTCACCGATTATTACATTGACAAATGCAACGTGGCCAAGAAGACGTGGAAGGAGGTCAACATCCCGCCTGTTAAGGAAAGACTGCACAAGGTGGCCATGTATTGGTATTGCAGCATCCTGTGCATGCTGTTGTTGTATCAGCTAATGTTAATGGGTTTCTAATAAAATAGTGTGGTGTTATAATACTGTAATTGCTCAGATGAAATGTTCTTTCTGAAGGTTGGAGGTCTGACTGCTGGCTCAGTGTATCAGTTTAGGGTCTATGGTGCTAATGTGGTTGGAGTTGGTGATCCCTCGACCGCTAGCCCTTCCTTCAGATGTGACGCTTGGACCATGTCTGAACCCGGTAATGTGAAGTCTGCTAACACATTTAATGCTTAATGATTTGTTTTGTTCATTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42146
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125593 Nonsense 359 391 7 8
Genomic Location (Zv9):
Chromosome 13 (position 9564705)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 9706906
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGTTTGAATCTTTTGCAGGTCAAGGGTCTCGAGACAGGCACGTCTTA[T/A]CTGTTTCGCGTGCGGGCAGAGAATGCCAAGGACGTTGGCATGGCTTCAAC
Long Flanking Sequence:
TTGTCAACACCAGCCTCCACAAGAACACAAGTCCATTCTCTGCATTCTTGGAATTGAGAAACAACCAGAATTTCACAATTATATGTTTTGTTATCATGAAAATTGTCCAAAAACATGACTGAAAGCATTGGGAACCTTGAGCCCTAATGGCCAATTTTTTTGGGGTTTGTCTTTGGTAGGTCCAGCCTATGACCTGACCTTCACTGAGGTGAGGGATGACTCTTTGGTGGTGGAGTGGAAGCCTCCCGTCTACAATGGGGCTAGTGCTGTCACCGGATACTTCATTGAGAAGTGCAAGAAAGGCTCTGATTCTTGGAGCAAAGTCAACGAAAGTTCAGTCGACCACTGCTATCTCAAGGTATTGATTTATGAGTGCTGACAAGTACATGTTCTCAGCTATTCTGCTCTATTATCTCAGAACACTGTATATAGAAATATTATTTATTAAATATATGTTTGAATCTTTTGCAGGTCAAGGGTCTCGAGACAGGCACGTCTTA[T/A]CTGTTTCGCGTGCGGGCAGAGAATGCCAAGGACGTTGGCATGGCTTCAACCCCGTCTGATCCTGTGTGTGTCAGAGCATTGCCAGGTAAACTGTGCACTGTAGAACAGATAGTTTAATGTTGTAATGTGTGTGTGTGTGTATGTATAGATATATATGTATATATATATATATATATATATATATATATATATATATATATATATCCTGTTTAAATAGTCAAAATTATTAGCCCAATTGTGATCTTTTCTATAATATGTTTTTTCTTCTGGAGAAAGTCCCGGCTAGAATAAAAGCAGTTTTAGACAGAAACAGACCAAACCATCATTATACAATGACTTGCCTATTTATCCTAACTTGTCAAGTTAACCTATTCAACCTAGTAAAGCCTTTAAATTGCACATTATTGCTGAATATTAGTATCTTGAAAAGATGTTAAAAATAAAATAAAATAATGTTCCGTCATCATGGAAAAGATAAAAGAAAACGGTTATTAAAACAA
Associated Phenotype:
Not determined