ZMP
myh7b
Ensembl ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
---|---|---|---|---|---|
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.
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.
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.
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 |
---|---|---|---|---|---|
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.
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 |
---|---|---|---|---|---|
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.
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