Busch Lab

ZMP

myh7b

Ensembl ID:
ENSDARG00000076075
Human Orthologue:
MYH7B
Human Description:
myosin, heavy chain 7B, cardiac muscle, beta [Source:HGNC Symbol;Acc:15906]
Mouse Orthologue:
Myh7b
Mouse Description:
myosin, heavy chain 7B, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:3710243]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa21910 Nonsense Available for shipment Available now
sa12629 Nonsense Available for shipment Available now
sa38843 Nonsense Mutation detected in F1 DNA Not yet available
sa8767 Nonsense Mutation detected in F1 DNA Not yet available
sa31830 Nonsense Available for shipment Available now
hu7861 Nonsense Available for shipment Available now
sa9233 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21910
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097316 Nonsense 3 1944 1 41
Genomic Location (Zv9):
Chromosome 11 (position 26147198)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24976023
GRCz11 11 25213639
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTTCAGTCTTCAGTGCGTAAAGCAGCGGTGGATTTATCATCATGTCG[C/T]GAATGTTGGATATGAAGGAGTTTGGAGAAGCTGCTCCGTTTCTGCGCAAA
Long Flanking Sequence:
GTAAAGATGAAAATATGGCTTGCCCTTTTGTGTCAGTTTGGGCACATGGTGAGCACCAATAGGCATTGGAGGAGGCGACACACGATAATTTCTGACCATGACCTTGGAGGAGATGATAAAAGGAGGTTAGCCACTCCAGCCATTCAGTCCCTGTTAAGGTCAGCTACCAAATTAACTAGACACTTAACACTAAATTGATCATTTATTTTTTAATAACAGGAATCATAAATGCCATTAAAACTATTTAGGTTAAAAATCTAATAATGTAATTAGTTTTGTTATATAAATGTATAGACCTACTGGAATATAGGCCTACATTAAATTTAAGTTAACTCGTTGTGTTTGTTTACTTGTCTGACTTGTTAATTTTGTCAACATAAAAGTATTTTTAATTTTAAGTTTAAAAGTTTTAAACAAAACAATTTGTCTATACTTTTAAGGCGTCAGGCAAGTTTTCAGTCTTCAGTGCGTAAAGCAGCGGTGGATTTATCATCATGTCG[C/T]GAATGTTGGATATGAAGGAGTTTGGAGAAGCTGCTCCGTTTCTGCGCAAATCCGACCTGGAGCTGCTGGCTGCGCAAACTGTGGCGTTTGATGGTACTTGAGAAACATTTCAAGCGTCTTCAACAAATGTTTTACAGCGGATACAAGCACTTTAGTTTCTCTTCAAAATAGCTAATTGTCATTTCTTTACGCGCCGGCTTTTAAAGGCAGTTCGTAATTCTGTGTTATAACTTGTTAACGTAAACACTGAAATAAAATTGGAATTGAATTACTGGATTTATTACAAACAAACCAACCAATGAGAAACTTTGTCAGCCTTTGGATATCGCTCTCTGACAGCCTCCCTTGTGCGCAGGAAAGAAACGCGCTTGGATACCAGATGACAAGGACGCGTATATTGAGGTGGAAATCAAGCAGATTGATGGTGACAGAGTCGAAGTTGAAACGAAGGATGGAAAGGTAAGGCTTAAGACTATTTATCATGTAGCTAAAAACGGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12629
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097316 Nonsense 743 1944 21 41
Genomic Location (Zv9):
Chromosome 11 (position 26136410)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24965235
GRCz11 11 25202851
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATTTCTACAGGTATCGCATTCTGAATCCTCACGCTATTCCCSATGAC[A/T]AGTTTGTGGATAGCAGGAAGGCTGCGGAGAAACTTCTGGCTTCACTGGAT
Long Flanking Sequence:
TCACTCATTGAGCAGTACAGAGTCCCCATCAATATACTGGGGCATTAGGACTCACACAGATCAAAGGTTGAGCACCCCCTGCTGGCCTCACTAACACCACTTCCAGCAGCAAACTAGCTGCCGGCTGAGTCGGTGGTTCATTCTGCTGTGGTGACCCCTTATGAATAATGGGGACAAAGCTGACAGAAAATTAATGAATAAATGAATATTTCTAAAATATTTGTCAAACATAGAGATTTATATGAAAGTTTTTTCATTTAAGCCATGGCTGTGACAATATTTTAACATTATAACCCTTTACCCTTCTGTAACTTGTTAGGAGTATGATGAAAACCCTGTCTAAACATACAGTATGTATCCATAAAATCAATAAACAATATAACAATATGTTTACCGTGAGATTTAGCTGCTATATGAAGAACAGCACAATGAATAAACATTAACCGTGTGTTTATTTCTACAGGTATCGCATTCTGAATCCTCACGCTATTCCCGATGAC[A/T]AGTTTGTGGATAGCAGGAAGGCTGCGGAGAAACTTCTGGCTTCACTGGATATTGACCACAATCAATATAGATTTGGACATACTAAGGCAAGTCAGACTTTTGCTAGAAAACGTTTGTTGCTTTGAGGCTCAAGCAGTGGGACATCATTCAGAGGTATGACTCTGAACACAAGACAAGATAGGCTAAATCAAGCCAAATCAAAGTGTTTCTGCAATACAGGTGTTCTTTAAGGCTGGTCTGCTGGGACAGCTGGAGGAGATGAGAGACGAGCGTCTGGCTAAAATTCTCACTCTGCTGCAGGCCGCCAGCCGCGGCAAGATCATGAGGATGGAGCTGAACAAGATGACGCAGAGGAAGTATGAGCTAAAGATGTTTTTAAGATTAAATCACAGCAGCCCCCATATATTTAGACATTCACTGCACACTTGAAAAAGAATGAAAGTCATTACATAAGATTGCATTTCAAACCAGCCTCCGTTCATTTTACAGAAAGCTATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38843
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
ENSDART00000097316 Nonsense 766 1944 21 41
Genomic Location (Zv9):
Chromosome 11 (position 26136341)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24965166
GRCz11 11 25202782
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGCGGAGAAACTTCTGGCTTCACTGGATATTGACCACAATCAATAT[A/T]GATTTGGACATACTAAGGCAAGTCAGACTTTTGCTAGAAAACGTTTGTTG
Long Flanking Sequence:
GAGCACCCCCTGCTGGCCTCACTAACACCACTTCCAGCAGCAAACTAGCTGCCGGCTGAGTCGGTGGTTCATTCTGCTGTGGTGACCCCTTATGAATAATGGGGACAAAGCTGACAGAAAATTAATGAATAAATGAATATTTCTAAAATATTTGTCAAACATAGAGATTTATATGAAAGTTTTTTCATTTAAGCCATGGCTGTGACAATATTTTAACATTATAACCCTTTACCCTTCTGTAACTTGTTAGGAGTATGATGAAAACCCTGTCTAAACATACAGTATGTATCCATAAAATCAATAAACAATATAACAATATGTTTACCGTGAGATTTAGCTGCTATATGAAGAACAGCACAATGAATAAACATTAACCGTGTGTTTATTTCTACAGGTATCGCATTCTGAATCCTCACGCTATTCCCGATGACAAGTTTGTGGATAGCAGGAAGGCTGCGGAGAAACTTCTGGCTTCACTGGATATTGACCACAATCAATAT[A/T]GATTTGGACATACTAAGGCAAGTCAGACTTTTGCTAGAAAACGTTTGTTGCTTTGAGGCTCAAGCAGTGGGACATCATTCAGAGGTATGACTCTGAACACAAGACAAGATAGGCTAAATCAAGCCAAATCAAAGTGTTTCTGCAATACAGGTGTTCTTTAAGGCTGGTCTGCTGGGACAGCTGGAGGAGATGAGAGACGAGCGTCTGGCTAAAATTCTCACTCTGCTGCAGGCCGCCAGCCGCGGCAAGATCATGAGGATGGAGCTGAACAAGATGACGCAGAGGAAGTATGAGCTAAAGATGTTTTTAAGATTAAATCACAGCAGCCCCCATATATTTAGACATTCACTGCACACTTGAAAAAGAATGAAAGTCATTACATAAGATTGCATTTCAAACCAGCCTCCGTTCATTTTACAGAAAGCTATATTTTAAGTATGCTTGAAAACTAAACTAATCTATAGATTTTTTTTTGCTCACATTGCTAGTTTTGTGGTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8767
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
ENSDART00000097316 Nonsense 846 1944 23 41
Genomic Location (Zv9):
Chromosome 11 (position 26132867)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24961692
GRCz11 11 25199308
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTCAACATTGTGAAGAACTGGCCATGGATGAAACTGTTCTTCAAWATC[A/T]AACCCCTGCTGAGGAGYGCAGCCACAGAAAAAGAGCTGGCYGCTCTGAAA
Long Flanking Sequence:
CACTAAGGATTAAGGCAGTTCTGAAGGCAAATAGGGGTCCAACCCTATACTAGTAAGTTGTACCTAATAAAGTGGCCATTGAGTATATGTCACTGTAACAATGAATGAAACGATAACTTCAGTGTTAAAAAACAACAACTATAACTTATTTTCTAAAAAAAAATAAAATAAAAAAAGAGGACTGGACAAGAGTCAAACCATCAAACCATCCATCGAAAAATATCTGGTTAAAGAAAAGTCATATTACGTTTTATAAAAGAAGCCCAAACTATTCATTTTTAAGCATGTTTAAGTATAAGTTGAGTTAAAAAAAGGTAAAACTTACTTATTTTGCCATTACAGTAGAAGAGCTACGTGTACAACCAAGATAATTATGAGACTTAATAAGACTAATTATACCTGTCTTTGTCATTAGGGAGGCTCTGATGATCATTCAGTGGAATATTCGGGCCTTCAACATTGTGAAGAACTGGCCATGGATGAAACTGTTCTTCAAAATC[A/T]AACCCCTGCTGAGGAGCGCAGCCACAGAAAAAGAGCTGGCCGCTCTGAAAGAGGAGTTCCTGAAGCTAAAGGAAGCACTAGAGAAATCTGAGGCCAAACGTAAGGAACTGGAGGAGAAACAGGTCAGCCTGATCCAAGAGAAGAATGACCTTTCTCTGCAGCTTCAGGCAGTAAGTATCATGCAATATTACTTTATCTTGTAAATATAACACAGGCTCATTGGAAATACATGCTTCAGACTACATTTTTGTGAACTGCAAAAAATTCACTTCATCATATGTTTGACTGCAGTTTCTAGGTTAAATGAATGCATTTTTCCTTTTCGAACAAATAATATTTACAGGGACATATTATCAACAAATAAAGGATTATTTTCTTGCAGTTATTTGCACAACACCAAAAAAATTATACAAAACAAATGACTGGCGTCTGTGGTTTGTGGAATAATATGTTTGCCTCTCTGATCTATCTCCTTTTGGACAACTTTTCCAGTGTGGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31830
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097316 Nonsense 1000 1944 25 41
Genomic Location (Zv9):
Chromosome 11 (position 26130326)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24959151
GRCz11 11 25196767
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGAAGAATCTGATAGAAGAGATGGCAGCTTTGGATGAAACTATACTG[A/T]AGCTCACCAAAGAGAAAAAAGCCCTACAGGAGAGTCACCAGCAGACCTTG
Long Flanking Sequence:
TATCAATGATCTATTGCAGCTTCAGGCAAGAATGATGGTGGAAAGCATATGGTTTTAATACTGCTACTCTGTAAACTATGAAATTGTCTTTGAAGGATTGAATAACTGTGCATATTCACGCTACAGGAACAAGATAACCTTGCAGATGCAGAGGACCGCTGTGATCTGCTCATTAAGACCAAGATCCAACTTGAAGCCAAAGTAAAGGAGATGACCGAACGCCTGGAAGACGAAGAGGAGATGAATGCTACAGTTCTGGCAAAGAAGCGTAAACTGGAAGATGAGTGCGCCGAGCTGAAAAAAGACATCGATGATCTGGAGATAACCTTGGCCAAGGTGGAGAAGGAGAAGCATGCCACTGAAAACAAGGTGAGGCCATTCTGTTGTTCTGAAGACAAATGAAGCTCTTGCTTTGTTGTTGAAGTCAAATAATCAAAGTTCCTTTTTTATAGGTGAAGAATCTGATAGAAGAGATGGCAGCTTTGGATGAAACTATACTG[A/T]AGCTCACCAAAGAGAAAAAAGCCCTACAGGAGAGTCACCAGCAGACCTTGGACGACTTGCAGACAGAGGAAGACAAAGTCAATACTCTGACTAAGGCCAAAGCCAAGTTGGAGCAGCAAGTTGATGATGTATGTTCATTTGCTGGATAAATAGTAACAGGACTGTTAATGGGTCTAGAATGAGTCAGGAATCAGTAATCCACTATAATGCCTTTGTTTTAGTTGGAGGGCTCCTTAGAACAGGAAAAGAAATTGCGAATGGATCTGGAACGTTCAAAACGCAAGCTGGAGGGCGATCTGAAGCTGTCAATGGAGTCTGTCATGGACCTCGAAAATGACAAGCAGCAATTAGAGGAAAAGCTAAAGAAGTAAGATTTATTATGTGCCAGGACGCTGTAAAAATATGACACCATTTTCATTCGGAAACAAGAAACGTTGTTGTGATTTTTGGCCATTTATTTACATGACAGCAACAATTCCATTACACTTCAACTTGAGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
hu7861
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097316 Nonsense 1052 1944 26 41
Genomic Location (Zv9):
Chromosome 11 (position 26130077)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24958902
GRCz11 11 25196518
KASP Assay ID:
554-2377.1 (used for ordering genotyping assays)
KASP Sequence:
CCACYATAATGCCTTTGTTTTAGTTGGAGGGCTCCTTAGAACAGGAAAAG[A/T]AATTGCGAATGGATCTGGAACGTTCAAAACGCAAGCTGGAGGGCGATCTG
Long Flanking Sequence:
ACAGTTCTGGCAAAGAAGCGTAAACTGGAAGATGAGTGCGCCGAGCTGAAAAAAGACATCGATGATCTGGAGATAACCTTGGCCAAGGTGGAGAAGGAGAAGCATGCCACTGAAAACAAGGTGAGGCCATTCTGTTGTTCTGAAGACAAATGAAGCTCTTGCTTTGTTGTTGAAGTCAAATAATCAAAGTTCCTTTTTTATAGGTGAAGAATCTGATAGAAGAGATGGCAGCTTTGGATGAAACTATACTGAAGCTCACCAAAGAGAAAAAAGCCCTACAGGAGAGTCACCAGCAGACCTTGGACGACTTGCAGACAGAGGAAGACAAAGTCAATACTCTGACTAAGGCCAAAGCCAAGTTGGAGCAGCAAGTTGATGATGTATGTTCATTTGCTGGATAAATAGTAACAGGACTGTTAATGGGTCTAGAATGAGTCAGGAATCAGTAATCCACTATAATGCCTTTGTTTTAGTTGGAGGGCTCCTTAGAACAGGAAAAG[A/T]AATTGCGAATGGATCTGGAACGTTCAAAACGCAAGCTGGAGGGCGATCTGAAGCTGTCAATGGAGTCTGTCATGGACCTCGAAAATGACAAGCAGCAATTAGAGGAAAAGCTAAAGAAGTAAGATTTATTATGTGCCAGGACGCTGTAAAAATATGACACCATTTTCATTCGGAAACAAGAAACGTTGTTGTGATTTTTGGCCATTTATTTACATGACAGCAACAATTCCATTACACTTCAACTTGAGAAAAATGAAATAAGGAATTAAAAATACACCTATTATAAAGATTGCTATCTATTTATAAAGATTTTCATACTTTATATAGACCTTTTTCTTCGTTGCTGCATGGAGGGCGCAATAGTGGCCAGTGTCTTCCAATAGGACGCTTAGAAATTCCATTTACAGTGTTTCTCAACTGGAATTATTTATCCCAAAGTAACATTTTGAGTGGCTTACTGATTGTTTTTGTGATGCACAACTTAATTTTGAAAGATGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9233
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
ENSDART00000097316 Nonsense 1150 1944 28 41
Genomic Location (Zv9):
Chromosome 11 (position 26128317)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 24957142
GRCz11 11 25194758
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGCGCTCYACCCGAGCCAAAATGGAGAAACATCGAAGYGATTCGTCC[A/T]AAGAGCTTGAAGAGCTCAGTGAGCGTCTCGAAGAAGCCGGAGGAGCCACA
Long Flanking Sequence:
ATGAAAAAAGTTTATAGTGCCTTACAAACAAATGATATGTGTTTTGTTTTTGAGGCACTTAATAAAGGATTTTTTGCTTGTGTTTAGGTAAGCTAGATACTTTATGAAAACAGATGTTTTGTGAAAAACTTTTCTTTTTGTAGACTGTTACAGTATATTGTTAACATACCAATGAATTGTTGATCTTTTATAGGAAAGATTTTGAAATGAACCAGATCAGTTCAAAAATCGAAGATGACCAAGTGCTAATCATCCAGCTTCAAAAGAAGATCAAGGAACTGCAAGTACGTCCAACTAGACCAAATATATATATATATATATATATATATATATATATATATATATATGTATGTATATGTATGTATGTGTCTCTTCATAAGAACATATTATTGTTTAATCTTCCACTGTGTTTTAAGGCTCGTATTGAGGAGCTTGAAGAGGAAATGGAAGCAGAGCGCTCTACCCGAGCCAAAATGGAGAAACATCGAAGCGATTCGTCC[A/T]AAGAGCTTGAAGAGCTCAGTGAGCGTCTCGAAGAAGCCGGAGGAGCCACATCGGCCCAAATTGAGATGAATAAGAAACGAGAGGCCGACTTTTTAAAACTACGCCGTGACCTTGAGGAGGCCATACTGCACCATGAGGCCATGACTGCCGCATTGCGCAAAAAGCATGCAGACAGCGTGGTTGAACTGAGTGAGCAGATTGACAGCCTTCAGCGAGTCAAACAGAAGCTGGAGAAGGAGAGAAGTGAGGCCAAGATGGAGGCCGATGACCTCACCTCCAATTTAGAGCAGCTGGCAAAGGGCAAGGTGGAAAATATGAGCTGTTGCATCACATGCTGATCTAATTTAACTAGCATTAACTTAGCGTAGACTTTAACACTAAAAAAAAACAAGGGCAGATTTCACTTCTCAGGGTTAAATTAGCTTTGCCTGATCAGCTTTGTATATATTATTCTTATTTTTGTTTAGTTTAAATTGCATTTATTTGAAAATATTTTTTGT
Associated Phenotype:
Not determined