myh11a

Ensembl ID:
ENSDARG00000009782
ZFIN ID:
ZDB-GENE-050531-1
Description:
myosin-11 [Source:RefSeq peptide;Acc:NP_001019619]
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 9 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa20640 Nonsense Available for shipment Available now
sa11268 Nonsense Available for shipment Available now
sa15692 Essential Splice Site Available for shipment Available now
sa7029 Nonsense Mutation detected in F1 DNA During 2018
sa20641 Nonsense Available for shipment Available now
sa16962 Nonsense Available for shipment Available now
sa40634 Nonsense Mutation detected in F1 DNA During 2018
sa16661 Essential Splice Site Available for shipment Available now
sa20642 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa20640
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 29 1974 2 41
ENSDART00000138858 Nonsense 29 133 2 3
Genomic Location (Zv9):
Chromosome 6 (position 9227144)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8333520
GRCz11 6 8569059
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTTTTCACGGACAAAGACTTCATCAACAGCCCCGTGGCCCAGGCCGATTG[G/A]TCAGCCAAAAAGCTGGTGTGGGTCCCCTCCGAAAAGCACGGCTTCGAGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11268
Current 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 > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 427 1974 12 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9260748)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8299916
GRCz11 6 8535455
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CTMCCATTACAGGCTGATTTTGCCATTGAAGCTTTAGCTAAAGCTATGTA[C/A]GAACGCTTGTTYCGTTGGATCCTTCTAAGAGTCAACAAAGCGTTAGACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15692
Current 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:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Essential Splice Site 684 1974 16 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9263120)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8297544
GRCz11 6 8533083
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ACACACAGCCAAACTTTGTCCGCTGTATTATCCCCAACCATGAGAAACGG[G/A]TATATTGCCATCRTATTAGAWACCAAAAGTGGTGGTACAAANTCTTTTTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7029
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 726 1974 18 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9264573)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8296091
GRCz11 6 8531630
KASP Assay ID:
554-4668.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAAATAGTAAGGTTAAAAACNAKTTTGCATTTACATATTGACATACAGATA[T/A]GAGATCCTGGCAGCGAATGCTATTCCAAAAGGCTTCATGGATGGCAAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20641
Current 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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 1197 1974 27 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9272369)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8288295
GRCz11 6 8523834
KASP Assay ID:
2259-7167.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTATAGAGGACGAGAGCCGCGTCCATGAGGCTCAGGTGCAGGAGATGAGA[C/T]AGAAACACACCCAAGCTTTGGAGGAGCTCACAGAGCAACTGGAGCAGTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16962
Current 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
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 1316 1974 29 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9274360)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8286304
GRCz11 6 8521843
KASP Assay ID:
2259-7168.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GAAAGAACATAAAGCTTAGYAAGGATGTGGCTAGCTTGAGTTCTCAAGTT[C/T]AAGACACWCAGGTATGAGGGTCAAAAACGAGACATCTTATTTTGGTGTCW
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40634
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 1434 1974 31 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9276121)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8284543
GRCz11 6 8520082
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GAAGACCAAGAACAGACTGCAGCAGGAGCTTGAGGACACGCTGATGGATT[T/A]GGACAACCAGAGACAGCTGGTGTCCAACCTTGAGAAGAAACAGAAGAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16661
Current 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:
T > G
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Essential Splice Site 1524 1974 32 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9277233)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8283431
GRCz11 6 8518970
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TGCTGAAATGGAGGATCTAGTCAGCTCCAAAGACGAYGTRGGCAAAAACG[T/G]AAGTTCAGYAGTGTAARGGAAAATTTGAAACATTCCTTGCATTGGAATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20642
Current 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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041142 Nonsense 1762 1974 37 41
ENSDART00000138858   None 133 None 3
Genomic Location (Zv9):
Chromosome 6 (position 9282272)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 8278392
GRCz11 6 8513931
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGGAGCAAGGCAACATGGAGATGCTCAATGACAGGCTGAGAAAGAGCGCA[C/T]AGCAGGTACATGCGTTACAGTACATCAAATAGACATTAATATTAGGGATG
Associated Phenotype:
Not determined

OMIM

More OMIM information for MYH11

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