Busch Lab

ZMP

MYOM3

Ensembl ID:
ENSDARG00000059838
Description:
myomesin family, member 3 [Source:HGNC Symbol;Acc:26679]
Human Orthologue:
MYOM3
Human Description:
myomesin family, member 3 [Source:HGNC Symbol;Acc:26679]
Mouse Orthologue:
Myom3
Mouse Description:
myomesin family, member 3 Gene [Source:MGI Symbol;Acc:MGI:2685280]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa36263 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa13988 Nonsense Available for shipment Available now
sa42829 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42830 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36263
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083571 Essential Splice Site 659 1285 15 35
Genomic Location (Zv9):
Chromosome 16 (position 56072840)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52581430
GRCz11 16 52467264
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCCAGTGAACTACTCTTATGTGAGCCCTGGACCATGCCTGAGCCGGG[T/C]GAGTCACAGTCAACTATGGACAATATTAGAGATTTGACATGCTTTATGTT
Long Flanking Sequence:
AAGGTCACTGGTTCGAGCCTTGGCTAGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTTTCTGCGTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTACCCCACAGTCCAAACACATGCAGTACAGGTGAATTGGGAAGGTTAAATTGTCCGTAGTGTATTAGTGTGAATGAGTGTGTTTGGATGTTTCTCAGAAATGGGTTGTGGCTGGAAGGGCATCCACTGCGTAAAAACATGCTGGATAAGTTGGCGGGTCATTCCACTGTGGAGACCCCGGATTAATAAAGGGACAAAGCCGACAAGACAATTAATGAATGAATTTCGTTTTGTCTTCTATTTTAGCTTAATTTTTGTCTGTTTTGTTTTAGCTGACGGGTCTTCAGGAAGGACATTTTTACCAGTTTCGAGTTTTTGCAGCCAATATTATAGGAGTGGGCAAACCTTCTGAACCCAGTGAACTACTCTTATGTGAGCCCTGGACCATGCCTGAGCCGGG[T/C]GAGTCACAGTCAACTATGGACAATATTAGAGATTTGACATGCTTTATGTTTAATAAATGACAGGTAGATTCAGGGCTTCATCTGCAATTGTTGATTATGACTTGGTTTTCATTTATGTGAAAAGATTGAATATCCACTCATATTACAGCATGTTCTTATACAGTTATCATTGACTTTGGGTTTCAGAGATGCGTTTCTTACAATAGATTGATTACAGCATTGAATAACAGGCTGTTCTTATGTTATCCCCCTTTATTTTAGATTAGACTGCATTATTTCACTGACTGCACATTCATTTAACAAGAAATTAGATAAATTGCTTGTCTTGTTTGTGATTCCTCATATGCAAAATACTATAGTAATATATAGTACATACTACAGTGTTTTTGAACCATACTGTACAATTGATATGTTGTGGTGATACTATAGTTGCTATGTTGTGGTGATTCTATAGTTGCTATGGTAATACGGAAATGCTTGAAGTTTCTGCCAACTCGACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13988
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083571 Nonsense 800 1285 18 35
Genomic Location (Zv9):
Chromosome 16 (position 56080491)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52588991
GRCz11 16 52474734
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATRAAGGAGTCTTWAGKTGGAATAAAAACWATGGAAAAGCCATTGATGCC[G/T]GACGAGCCCGACTGGAGAACAAAAACAACAGGTCTTYTTTTATTGTCATT
Long Flanking Sequence:
TCCGCCCTCTTTTGAAGAAAGCACAACCTCATTTGAATTTAAAGTGACAGTCACCAATACCGCATCAAGCCTAAAAGGGTCAAGTTTCAAAAAGTTATAAAACATTGTGTGTGATATTTTGAGCTGAAACTTCACACACACACACTTTAAGCACATCATAGACGCATTTTACATCTTGTAAAAAGGGGCATAATAGGTCACCTTTAACTTAATTTAATACATTAATCAGGTTTCAATAACCTTTTTTTAAGCTATACATGGTTTAACATAATATAATTAGGTAGTTTGACTGATTTAACTTGAGATGACTAGAAAAGTTAATGTAATCCAAATGCAGGAAGATTTTTTTACAGTGCAGCACATGTCTGCCAACAGGAACCAAAGAGATGGAGATCGGGGTTGATAATGACGGCTTCATATTCCTGAGTTTTGAAGCTCCTGATGGCACTGATGAAGGAGTCTTTAGTTGGAATAAAAACTATGGAAAAGCCATTGATGCC[G/T]GACGAGCCCGACTGGAGAACAAAAACAACAGGTCTTCTTTTATTGTCATTCATTCATTTTCAATCGGCTTAGTCCCTTTTTTTGTCAGCGGTCGCCACAGCGGAATGAACCGCCAACTATTCCAGCATATGTTTTGCATATGTTTTCCGCAACCCAGTTCTGGGAAACACCCATACACACTTATTCACACACACACAGACACTCACTACGGCCAATTTAGTTAATCAATTCACCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGAAGCACCCGGAGGAAACCCATGCCAACATGGGGAGAACATGCAAACTCCACACAGAAAGGTCAACTGACCCAGTTGGGACTCGAACCAGCAACCTTCTTGCTGTGAGACGACAGTGTTAACCACTGAACCACATTTTTTTAAATATTGTGATTATGATTATTATTCTTTTCCCAGAGATGGGTTGCTGCGTAAAAATGTGCTGGATAAGTTGGCGGTTCATTCCGTTGTGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42829
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083571 Essential Splice Site 861 1285 21 35
Genomic Location (Zv9):
Chromosome 16 (position 56094607)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52603107
GRCz11 16 52488850
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTCATCATCAGTTATTCCTCACTGTTGTGTCGTGTGTTCGTGTGTGTC[A/C]GTGATCGGTTTGCGCTCTGAGGGCTGGCAGGTGGAGGTGTCAGAGCAGGG
Long Flanking Sequence:
ATTGCATAGGAGGGGCGATGGCACCTGTAATGGAAAGGAAGGGAATCCCGCCATTTTTATATTTATTTCAATGTGTTTTCATGCCTAAATAAAATGAAAGCTCAAAGCATTGTGAATCACTGCCTGATAGATATATTTTAAAAAGTAATTCTCAGACTGTTCACATTTTTCCAAGCATGACATTTTATTTCACCACAGTATTTTCAGTGAGTTTTTGCACTCGCCTGCTGATTCTGACAACACTTGTGTTTAAACGGTGTTTCCTCTCATTTAATGCTTCAACAAATAATTGAACACTTAAGTCTGTTTAACTGATTATATTTTAATTACATTACAGCATCCATGCTGTAAAAAGGAACCTTATGAAAGTAAAAATACTCACATAAACCTTTCACCAGAAGTTTATCGTCGGCTGAAAACACTAGCTGTGCATAAAGCCCATTGAACAGCTAGTCATCATCAGTTATTCCTCACTGTTGTGTCGTGTGTTCGTGTGTGTC[A/C]GTGATCGGTTTGCGCTCTGAGGGCTGGCAGGTGGAGGTGTCAGAGCAGGGATCGGTGCGTCTGTGGCTGCAGACTGAAGCTCTTAGCAGTGCTGCGGTGCTTCGGCTCATCCTGAATGACAGAGAGATCTCCAGCACACCGGTGACTTTCACACACTTCTGCTATTGTGCCTAAGGGCCAGAGCTTGCTTGCATGAAAGTCCTTAAAGTCTGCATCCAGGCTGCAACCATTTTAATTTTCATATTGTGATGCAGTTCCTATAGAGAAACAGAATATTAAATGAGGAAACAGTGGGTGTGGCTTGATTTTCCTACTGCAAGCTGATTGGATGTAGTAAAGTAGGCGTTTAATTCAGAAAGATGGGGAAAGGGTTTGGGGAGAGTTTTTACAACCTAACAGACTCCTCCTGCTCACCATTTCTGTTTGTTGTCTAAACAGACAGATGAAGGGGCGTGGTTAGGTATGTTAGCCACGCCCAATGCCCTTAGACAGACCTAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42830
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083571 Nonsense 1009 1285 27 35
Genomic Location (Zv9):
Chromosome 16 (position 56099893)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 52608393
GRCz11 16 52494136
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTGTGTTCGCCTGCAGGTCACCAACACGAGTAAAGACACACGTCTG[A/T]AGTGGTTTAAGGATGGAGTGGAGCTTCCTCAGGCTGTGTTTGAGCCCTCG
Long Flanking Sequence:
ATGAGTATTTTTAAATAATATTAAATGATTGTGTAGAATGTGTGTAGTTTGTTGTGAGGACCGATTGTCCCTTCAAGTAAAGTAATGATAGTAACTTCTGACATTGTGGGGACCTTTTACAGCAGCGGTGGCCAATCCTGTTCCTGGAGATCTACCTTCCTGCAGATTTCAGTTGCAACCCTTATCAAACACACCTGTCTGTAATTATCAAGTGGATTTCAGGTCCTAATTAATTGGTTCAGGTGGGTTTGATCAGGGTAGGAACTAAACTGTACAAGAAGGTAGATCTCCAGGAACAGGATTGAGCACCCCTGTTTTACAGTATGTGTACAGTAGAACTCTCTATTTCTAAAGCGCTTTTACAATGTAGATTGTGTTAAAGCAGCTTAACATAGCCGTAGAAAAACATCCCTATAAAACATGAAAACTTAATGTGTAATGTGTGTGTGTGTGTGTGTGTTCGCCTGCAGGTCACCAACACGAGTAAAGACACACGTCTG[A/T]AGTGGTTTAAGGATGGAGTGGAGCTTCCTCAGGCTGTGTTTGAGCCCTCGGGTGTCAGTACACTCACCATATCACAGGTACATTCAAACCAAAGACACGCACACTAGACCTCAGATCACATGCAGGACACAAACACTCAAAACAGACCCTCTATTATTGACTTGTTTCTGGTAACAGTCTGGTAGATCCTTTTCTTCTTTGGTCTGGAGCACATGGCATCCATTTCTCCCCCAAAATTCATCTGACCACAGTAAACGTTTCCACTGTGTGATGGTTTATCCCGGATGCCTCAGAGCCCAGAGAAGTTGAAGGCACTTCTGGACACTGTTAACATAGGGCTTCCTTTTGGCACAATAGAGTTTTCACTGGCATTTGTGGATATAACTACATATTGTGGTACTTACAAAGGTTTGCCAAAGTAGTCCTAAGCCCATGTGGGGATCTGGCTTGTAGATGAATGAGGATTCTTGATGCAGCGCCACCTGAGGAGTCAGAGATCA
Associated Phenotype:
Not determined