ZMP
MYH11 (2 of 2)
Ensembl ID:
Description:
myosin, heavy chain 11, smooth muscle [Source:HGNC Symbol;Acc:7569]
Human Orthologue:
MYH11
Human Description:
myosin, heavy chain 11, smooth muscle [Source:HGNC Symbol;Acc:7569]
Mouse Orthologue:
Myh11
Mouse Description:
myosin, heavy polypeptide 11, smooth muscle Gene [Source:MGI Symbol;Acc:MGI:102643]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38402 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20079 | Essential Splice Site | Available for shipment | Available now |
| sa33243 | Essential Splice Site | Available for shipment | Available now |
| sa33244 | Nonsense | Available for shipment | Available now |
| sa26113 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18760 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38402
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 |
|---|---|---|---|---|---|
| ENSDART00000004854 | Nonsense | 50 | 1961 | 1 | 40 |
Genomic Location (Zv9):
Chromosome 3 (position 36482606)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36566498 |
| GRCz11 | 3 | 36708356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGGTGTGGATTCCCTCAGAAAGGGATGGTTTTCAGTCAGCCAGCATT[A/T]AAGAAGAGACGGGGAATGAGGTGGTGGTGGAGCTGGACAACGGGCAGAAG
Long Flanking Sequence:
CTTAAAGGGGCTAATAATTTTGACCTTAAAATGATTTTTTTTTTTAATTAAAACTGCTTTTATTCCAAGTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTGGGGAATATTTAAAAAATAATAATAAAAGGGGGGCTAATTATTGTGACTTCAACTGCATGTTTCTAATATCGCCTGAATAACATAAGCTTGCTTCACACTGAAGAAATATCATTCTTGATTGAAATATTTTTTGTAAAAAAAGTCAAATAATGAATTGACTTTTAACCACAGAATAACTCACAGAAGTTCTTCAAGATGACCATGCAGGACAACGATGACAGCAACAAGTTCCTTTTCCTGGACAGTGAGTTCAAAAACAGTGGGGTGGCTCAGGCTGACTGGTCCACCAGAAAGATGGTGTGGATTCCCTCAGAAAGGGATGGTTTTCAGTCAGCCAGCATT[A/T]AAGAAGAGACGGGGAATGAGGTGGTGGTGGAGCTGGACAACGGGCAGAAGGTGACCGTCAGCAAAGACGACATTCAGAAGATGAACCCACCCAAATTCAACAAGGTTGAAGACATGGCTGCTCTGACCTGCCTGAACGAGGCTTCAGTGCTGCACAACCTCAGGGAGAGGTACTTCTCAGGCCTTATTTATGTAAGTGCATTCAATAATCACCATATACAGACAGATAAGTGATTACACAGGGTACATGAATTTAGCTTTTCTCTTTCTGCAATATGTGAAAACTGAAAAACATGGTTAGTATCAAATCTGATTTAAATGTTTTCCATTTAGTTTTAGAGATTTGGTTTAAAAATATAAAAGTGAATCTGTAAATGTCAAATATGAATGGATGGATTTGTTTGAAAAATTGAAGAAAAATTAAATGACTGATTTTTCTAAGTGTGTTTAAGTAAAATGGCAATATTGATTTTATTTATGAAGGTCTGATTACATTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20079
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 |
|---|---|---|---|---|---|
| ENSDART00000004854 | Essential Splice Site | 750 | 1961 | 18 | 40 |
Genomic Location (Zv9):
Chromosome 3 (position 36495429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36553675 |
| GRCz11 | 3 | 36695533 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAACCTATCTTACCCTTGATGACAATTTCTCCCTGTTTTATGAACATC[A/T]GATTAAACATCTAGACTTGGACCCAAACCTGTATCGGATTGGTCTGAGCA
Long Flanking Sequence:
TCTTAATTATTGATTTCAGGAATAAAATGTTTGATATCAAGAATTAAATAGATGATATCAACCATCAGCATTTTTGATATGAAGAATTGTATTTCTGCAAATGATGACATCATTGTTGATAGAAAATTAACATTGTTAATAGTTGACATGTAATTGTTTTATCTACAGTCAGCATTTTTGATATACTAAATCCTTGATATCTTGACATCATAAAAATGACGTGCCATAAAACTACTTTATATGTCAATAAACTTTAAACTTAGGGCATTAGTAGGCACTTAAGTTGAGGTTTGTAGAATAAATTGATATTAATAAATTTCTAGCTATGAGGTTCTTGCTGCCGGTTCCATTCCTAAAGGTTTCATGGATGGAAAACAATCCTGTACGCTTATGGTGAGTTGAGCAAAATATCTCATTTTACTCTACTGGCAGGGACAATTCAAATGCTATATTAACCTATCTTACCCTTGATGACAATTTCTCCCTGTTTTATGAACATC[A/T]GATTAAACATCTAGACTTGGACCCAAACCTGTATCGGATTGGTCTGAGCAAGATATTCTTCCGCACAGGAGTGTTGGCACAGCTGGAGGAAGAACGAGACCTGAAACTGACTGATATTATAATAGCCTTCCAGGCCCAGGCCCGTGGTTTTCTTGGCAGAAAGTGAGTTCTTGACATGCACATACAGGAGATCAAAATTGCAGAAAGATTTACATAAAAAAAAATAATAATAATAATATTAAGTAGTGTAATACCAGTTTTACCATGCTAGTTGTGTTTTCCACAATTGCACTGTAGTGGCTATTTTGAATGAGTTAGTTAATGTCATTGTAAATAATGAAATATTTTAGAAATCAGATTTGTAATTACCAAATTCTCTGTCTGGCTAGCTGTGAGTTTCTCACTCAGTTTGCCCTAGCCATATCACCAGGCAGCCTAGGGGAACCTATATGAGGTAAACACAAAACAAAACTTTCCATCCAGAGCTCCTTCATGGGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33243
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004854 | Essential Splice Site | 883 | 1961 | 20 | 40 |
Genomic Location (Zv9):
Chromosome 3 (position 36497847)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36551257 |
| GRCz11 | 3 | 36693115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAAGTCTGAAACGGAACTAAAGGAGATCACACAGAAACACGACCAG[G/A]TAAAGTCAGATCAAAAATGTGACACAAACTCAGCCGTAATTACTATTGTC
Long Flanking Sequence:
ATTAAAAAAAAGAGGACCAAAGCAGTAAGCTCAAAATGCATAGGCTGTTCTCCACACTGATCTTGACTTTAATCTTCACTGTACATCAGTCACCATCTACTTGAATTTTCTTACTGTATTAACAGTAATCATATTTATCAAAATGCCTCACAGTGGCCATTTTAAGTAAATCTAAAACCTCTAAATTTACAGGGCATTCAGCAACAAACAAAAGCAGTTGACAGCCATGAAAGTGCTACAGAGGAACTGTGCTGTTTATCTGACACTCAGGAACTGGCAGTGGTGGAGACTTTTCACTAAAGTAAGTGTAAAACCCAGCTACACATTATCCATGTATGCTCAAGTACTCAGTTTATTTTCTCCTTTAGGTCAAACCCCTGCTTCAGGTGACTCGTCAAGAAGAGGAGATGAATCAAATAGAAGAGGAGCTCCAGAAAGCCAAAGAAATTGCCCAGAAGTCTGAAACGGAACTAAAGGAGATCACACAGAAACACGACCAG[G/A]TAAAGTCAGATCAAAAATGTGACACAAACTCAGCCGTAATTACTATTGTCATTCATACAGATTAAATATGCACTTACCAGCTGAAGCATTTACTCAACAGGTTGTGGAGGAGAGGAATAAGCTGCAGGCGAAGCTCCAGGAGGAAGCAGAACTGTACGCAGAGTCTGAGGAGGTCAGGATACGACTGGAGACCAAGAAGCAAGAACTGGAGGAGGTGCTGCATGAGATGGAGGCTCGACTTGAGGAAGAGGAGGAGCGCAGTCAGGCTTTTCAGCAAGAGAAAGGGAATTTGCAACAAAAACTTAAGGTTAAATAGTGATTACTTATGGCAAACTATAGAACAAGTGGAATTTAATGAGACTGTAATTTGTCGAAAACATATCATCAAATTGTTATTTTTATTGTTGAAACTAAAAAAAGACAAACAATAGTAATAATGATGATAAAGCAATAGTAATACTGATACTTATTAGTAGTATAACTTTAATTCTGTAATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33244
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 |
|---|---|---|---|---|---|
| ENSDART00000004854 | Nonsense | 1643 | 1961 | 33 | 40 |
Genomic Location (Zv9):
Chromosome 3 (position 36503603)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36545501 |
| GRCz11 | 3 | 36687359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAGACCAGGTTGATGTAAACAGCAGAGCGAGGGATGAGGCCGTTAAA[C/T]AACTCCGAAAGATTCAGGTCAGAAAGATAACTCTTCAAATTCTTTCAGAA
Long Flanking Sequence:
AAAACATAACATTTATAAAAGGCCCATGAGCTGGAGAAGACCAAACGTGCACTGGAGGCTCAAGTGGAAGAAATGACAATTCAGATGGAGGAGCTTGAAGATGAATTACAGGCTGCGGAGGATGCTAAGCTCCATTTGGAAGTAAATATGCAGGCCCTCAAAGTCCAAATACAAAGAGACATCCAAGGCAGAGAGGAGCAAAGTGAAGAGAAGAGGAAACAACTCCTCAAGCAGGTGTAGATCAATTTCTTTCTGGGTCTTCTTGAATTTGAACTGCACTTGTAGATTATTTAACTTTATTCATAAAGCAATAGCAAGAAATCTTTTCTTTTATTATTTACTCACTTCATGCACAGGTCCGTGAGCTTGAGGCTGAGCTAGAAGATGAGCAGAAGATGAGAACGTCCTTGGCTGCTGCCAAAAAGAAACTGGAAGGGGATTTGCAGGACCTTGAAGACCAGGTTGATGTAAACAGCAGAGCGAGGGATGAGGCCGTTAAA[C/T]AACTCCGAAAGATTCAGGTCAGAAAGATAACTCTTCAAATTCTTTCAGAATTTCCCAAGCCATTCCCACCAGCCTTTATCTTCCCCATGACAGACTCAGATGAAAGACTACCAGAGGGAGCTGGAAGATGCTCGAGCATCCCACAAGGAAGTTCTTTCCGATGCTAGAGAATCTGAGCGAAAGGCCAGAGCTATGGAGGCCGAAATCTTACACTTGCATGAGGTAACATAATACCACATTTTTTTACTGCAATGTACTTAAATTACTTCCCATACAACGGCAATACCAATCCCTTTATAGGAACTTGCTTCAGCAGAGAAAGCTCGCAAACATGCTGAAAGAGAGAGGGATGAGATAGCAGGGGAGATGGCAAGTGGTTCCTTCGGAAAGTAAGTTGAGGGTTATTATTAGTGAAAGGAGAAAAATAAACAGGACAAGCCACTAAACATACAATTATTGCACACTGATAGATCTGGTACGTCTGATGAGAAACGTCGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26113
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 |
|---|---|---|---|---|---|
| ENSDART00000004854 | Nonsense | 1916 | 1961 | 39 | 40 |
Genomic Location (Zv9):
Chromosome 3 (position 36504891)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36544213 |
| GRCz11 | 3 | 36686071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTCAGAAAGAGCTGAATGAGGCCATCGAGGCCAACGATGCCCTGAGC[A/T]GAGAAGTTTCCTCACTCAGGAGCAAACTCAGGTTGTTCTGAAGTGACTCC
Long Flanking Sequence:
AGATGGAGGGACAAGTCAAGTCCAAGCAACGGTCCACTGTAGCTGCCCTAGAGTCGAAGTTACAACAAACAGAAGACCAGCTGGATCATGAAAGCAGGTGAGATCATCAGCATTAAGATGGATTTGGTTGTAAAGAAAAAGTAGGCCCGACTAAAATATTTTCTTGCTCTAGAGAGAGACAAGCAATTGCAAAGGCCATGCGCCAGAAAGACAAGAAACTAAAGGAGCTGATGAATCAGGTAGAGGATGAACGGAAACAGATGGAGCAATATAAGGACCAGGTATAAAGGGTTCATGTAAAGTATTTGACGTCCTATGTTCTATTCTGACAAATCTAATGGACGTTGCATATGTTTAAGGCTGAGAAAGCAAATCTTCGAGCAAGGCAGCTGAAGATGCAGATGGAAGAGAGCGATGAAGAATCTCAGCGTGCTACTGCTGCTCGGCGTAAACTTCAGAAAGAGCTGAATGAGGCCATCGAGGCCAACGATGCCCTGAGC[A/T]GAGAAGTTTCCTCACTCAGGAGCAAACTCAGGTTGTTCTGAAGTGACTCCTTTTTATTGTGTATGTGAAACCAGAATTCCACTGACATTCTCTGTATTGTACAAAGATATAAAATCAGTGGAATAGATAATCACTTTTGAAAATCGTGTTTGGAGACAAGTGGATTCTTAGTATCCTTTATGTTCCTCAGGCGTGGCAGTGATTCATCCTTCAGCACACCATTAAGGCGTAGCGCTGGTGGAAGCTTTAGACAAGCACGCAGAACCATGATGGAAACGTCAGAGATCCCAGAAGATGGGGGTCCATCTGCTACATCAGTGTGTCAACCTGGGGAACTTCAGATGGAGTCAATCAGCAACACCCAGGATAACAACTAAGAAAACGGATTTCCTTCTCGCTTCATGTTTTTTCCTATTTCTGTGTAATTTATACTTATTTAATCTTGATCATCTCCTACAAAGGAGGATTGGTACTTATGTTTGTTCTTTATGGGTAAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18760
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004854 | Essential Splice Site | 1926 | 1961 | 40 | 40 |
Genomic Location (Zv9):
Chromosome 3 (position 36505081)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36544023 |
| GRCz11 | 3 | 36685881 |
KASP Assay ID:
2259-3809.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAATCGTGTTTGGAGACAAGTGGATTCTTAGTATCCTTTATGTTCCTCA[G/T]GCGTGGCAGTGATTCATCCTTCAGCACACCATTAAGGCGTAGCGCTGGTG
Long Flanking Sequence:
AAAGGCCATGCGCCAGAAAGACAAGAAACTAAAGGAGCTGATGAATCAGGTAGAGGATGAACGGAAACAGATGGAGCAATATAAGGACCAGGTATAAAGGGTTCATGTAAAGTATTTGACGTCCTATGTTCTATTCTGACAAATCTAATGGACGTTGCATATGTTTAAGGCTGAGAAAGCAAATCTTCGAGCAAGGCAGCTGAAGATGCAGATGGAAGAGAGCGATGAAGAATCTCAGCGTGCTACTGCTGCTCGGCGTAAACTTCAGAAAGAGCTGAATGAGGCCATCGAGGCCAACGATGCCCTGAGCAGAGAAGTTTCCTCACTCAGGAGCAAACTCAGGTTGTTCTGAAGTGACTCCTTTTTATTGTGTATGTGAAACCAGAATTCCACTGACATTCTCTGTATTGTACAAAGATATAAAATCAGTGGAATAGATAATCACTTTTGAAAATCGTGTTTGGAGACAAGTGGATTCTTAGTATCCTTTATGTTCCTCA[G/T]GCGTGGCAGTGATTCATCCTTCAGCACACCATTAAGGCGTAGCGCTGGTGGAAGCTTTAGACAAGCACGCAGAACCATGATGGAAACGTCAGAGATCCCAGAAGATGGGGGTCCATCTGCTACATCAGTGTGTCAACCTGGGGAACTTCAGATGGAGTCAATCAGCAACACCCAGGATAACAACTAAGAAAACGGATTTCCTTCTCGCTTCATGTTTTTTCCTATTTCTGTGTAATTTATACTTATTTAATCTTGATCATCTCCTACAAAGGAGGATTGGTACTTATGTTTGTTCTTTATGGGTAAAAACTGACTAATTAAAAAGGGTGTGTATGCAGGGTTGTACAAGCAAGCAAATTTATTACCGAGTACCATGGTGCCTCCATGCATTTTGGGCATGAACATCATAAAATAATGGTTAATTAACTCTTTAGCACTAATGACCTTATTCTGCAATACGGAAGTGCACTTGTTTTTGCGATTGTTTTAGTATTAAATAT
Associated Phenotype:
Not determined