Busch Lab

ZMP

myhz1.2

Ensembl ID:
ENSDARG00000067995
ZFIN ID:
ZDB-GENE-070705-73
Description:
myosin, heavy polypeptide 1.2, skeletal muscle [Source:RefSeq peptide;Acc:NP_001154918]
Human Orthologues:
MYH6, MYH7
Human Descriptions:
myosin, heavy chain 6, cardiac muscle, alpha [Source:HGNC Symbol;Acc:7576]
myosin, heavy chain 7, cardiac muscle, beta [Source:HGNC Symbol;Acc:7577]
Mouse Orthologues:
Myh6, Myh7
Mouse Descriptions:
myosin, heavy polypeptide 6, cardiac muscle, alpha Gene [Source:MGI Symbol;Acc:MGI:97255]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa16809 Essential Splice Site Available for shipment Available now
sa11919 Essential Splice Site Available for shipment Available now
sa15463 Nonsense Available for shipment Available now
sa31460 Nonsense Available for shipment Available now
sa10023 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16809
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098066 None None 446 None 11
ENSDART00000098067 Essential Splice Site 117 1937 2 39
ENSDART00000110726 Essential Splice Site 117 945 4 24
ENSDART00000131983 Essential Splice Site 117 1937 4 41
Genomic Location (Zv9):
Chromosome 5 (position 33928923)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31691155
GRCz11 5 32291308
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTGTGCTGTATAACCTCAAAGAGCGTTATGCAGCATGGATGATCTAC[G/T]TAAGCTCTAAAACAACCTAAAGCAGCACTTCCACACATTTACATCTGTAT
Long Flanking Sequence:
AAAACATATGACAGTCTGACTTTTTTTTCTAATTGTCATTTACTTTTAGAAGTAAGCCGCCACCATGAGTACGGACGCGGAGATGGCCGTTTATGGCAAGGCTGCCATTTACCTCCGTAAGCCTGAGAAGGAGAGAATTGAAGCTCAGAACAAACCTTTTGATGCCAAAACCGCTTGTTACGTGGTTGATGACAAAGAGCTGTACGTCAAGGGAACAATCAAGAGCAGAGACGGTGGCAAAGTCACCGTTATTACACTTGACACTAAGGAGGTGAATTTTTACATTTCATAAAGATTAAATTAATTACAATTATACAGTCTTAATGAATAGATTATTGACTAGATGACTTTTATAGGAGAGAGTTGCTAAGGAGGATGACGTCCATCCAATGAATCCTCCCAAGTTTGACAAGATTGAGGACATGGCCATGATGACCCATCTCAATGAACCCTCTGTGCTGTATAACCTCAAAGAGCGTTATGCAGCATGGATGATCTAC[G/T]TAAGCTCTAAAACAACCTAAAGCAGCACTTCCACACATTTACATCTGTATTTTTGCCATTGTTGGAATTTCAAGCCAATTCCATGCATGTTCAATAAGAAAAGGTCTGGAGAGGGTTTTCTTTAATGCCAAAAATATTAGTAATTTGACCATTTCTTTCCTCATTTTAGACCTACTCTGGGCTGTTCTGCGCCACTGTGAACCCCTACAAGTGGCTCCCAGTGTATGACGCAGAAGTGGTTGCTGCCTACAGAGGCAAGAAGCGTATGGAGGCTCCACCCCACATCTTCTCTGTCTCTGACAACGCCTATCAGTTCATGTTGACTGGTGAGATCTCATTTACAAGATCTGAATTACACACAAGTTCACATTCATCATTTTAACAAAACAATTGCTAAAACATTATTACATTTGCATTTACAGACAGAGAGAACCAGTCTGTCCTGATTACGTATGTATCTACTCTAATAGAGATGCTGAGAACAGGTTTATTTTCCTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11919
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098066 None None 446 None 11
ENSDART00000098067 Essential Splice Site 654 1937 15 39
ENSDART00000110726 Essential Splice Site 654 945 17 24
ENSDART00000131983 Essential Splice Site 654 1937 17 41
Genomic Location (Zv9):
Chromosome 5 (position 33925972)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31688204
GRCz11 5 32288357
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAAAGAAGAAGGGTGGTTCCATGCAGACTGTGTCTTCCCAGTTCAGG[G/A]TRTTTRTTTTGTTTTTGTTTTGAGACCAAATGTAAACAGTTATCAAAACT
Long Flanking Sequence:
CTTATTAACAAACAACCTTCTTTTATAAACAGCCCTTAGGTATCTTCTCCATCCTTGAAGAGGAGTGCATGTTCCCCAAGGCTACAGACACTTCCTTCAAGAACAAGCTGTATGATCAGCATCTTGGCAAGTGCAATGCTTTCCAGAAACCAAAGCCTGCCAAAGGCAAGGCTGAGGCCCACTTCTCCCTGGTCCACTATGCTGGAACTGTGGACTACAACATTTCTGGCTGGCTGGACAAGAACAAGGATCCACTGAACGAGTCTGTTGTGCAGCTTTACCAGAAGTCTTCAGTCAAACTGCTGGCTACTCTCTACCCACCTGTTGTTGAGGGTAATTAGGCAACATCAGTTTAACTTTGAGTCAAATTTACAATTGTTACTCTTTCTGTTAATTACAATACATGCTTTTTTCCCATTAAATTAATAGAGACTGGCGGTGGAAAGAAGGGAGGAAAGAAGAAGGGTGGTTCCATGCAGACTGTGTCTTCCCAGTTCAGG[G/A]TATTTGTTTTGTTTTTGTTTTGAGACCAAATGTAAACAGTTATCAAAACTGAAATCAATGACATGATTTTGCCTGAAGTTAGACAAACAATACAAAGAAAAATTAAGAATGTGAAAAAAAATCTGAATTTTTTTATGACTAAACAGGAGAACTTGGGCAAGCTCATGACCAACTTGAGGAGCACTCACCCTCACTTTGTGCGTTGTCTGATTCCCAATGAGTCCAAGACTCCAGGTAAATAAATAAAGGGACATATGTGTTGACATGAACACAGCATGTAATGTAATTTTGATTATCATTATAATATAATCTTTACCAAAATCATAGAGTAAACTGTTTCTTATAGGTCTTATGGAGAACTTCCTGGTTATCCACCAGCTGAGGTGTAACGGTGTACTGGAGGGTATCAGAATCTGCAGAAAGGGTTTCCCCAGCAGAATCCTCTATGCTGACTTCAAGCAGAGGTAAATGTGACTTCATAAAAATGTAATTTACTGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15463
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
ENSDART00000098066 None None 446 None 11
ENSDART00000098067 Nonsense 1257 1937 26 39
ENSDART00000110726 None None 945 None 24
ENSDART00000131983 Nonsense 1257 1937 28 41
Genomic Location (Zv9):
Chromosome 5 (position 33922889)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31685121
GRCz11 5 32285274
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTRTTTTTACAGGCCAATCTAGAGAAGATGTGCCGCACACTTGAGGAC[C/T]AACTTAGTGAAATTAAGTCTAAGAATGATGAGAACCTTCGCCAGTTGAAT
Long Flanking Sequence:
ACTGGAGGAAGAGATTGAGGCTGAGCGTGCTGCTCGTGCCAAGGTTGAGAAGCAGAGAGCCGATCTCTCCAGGGAACTTGAGGAGATCAGTGAGAGGCTTGAGGAGGCTGGAGGAGCCACTGCTGCTCAAATCGAGATGAATAAGAAGCGTGAAGCTGAATTCCAGAAGCTGCGTCGTGATCTTGAAGAGTCCACCCTTCAGCATGAAGCTACTGCTGCTGCCCTGCGCAAGAAGCAGGCAGACAGTGTGGCCGAGCTGGGAGAGCAAATCGACAACCTCCAGCGTGTCAAGCAGAAGCTTGAGAAAGAGAAGAGTGAATACAAAATGGAGATTGATGATCTCTCCAGCAACATGGAGGCTGTTGCCAAAGCAAAGGTTTGAGAATTGTTCAAGAATTGTAAAATAAGTATATTTTTATTGTTTGGTTAAAATTCATAATAATCAAATGACTTTGTTTTTACAGGCCAATCTAGAGAAGATGTGCCGCACACTTGAGGAC[C/T]AACTTAGTGAAATTAAGTCTAAGAATGATGAGAACCTTCGCCAGTTGAATGATCTCAGTGCTCAAAGAGCAAGACTTCAAACTGAAAATGGTAACTTATGATGAAAATGAACAACATCTATTTTACTACAAAGTTTTTTGTCAATGATTAATCAAGAATAAGGATGATTCACCAGTTTGACAAAGTCATATTTCAGCAAATACAATATTAAACAATTCAGAAGTCAACTGATAAAATATAACAAAGGATATGCTTGATATTTGATGATAGAGTTACTTAACCAATCGAAACAACAATATAATATCTCAATAATATCTCAAAAGGTGAGTTTGGCCGTCAGCTTGAGGAGAAGGAAGCTCTGGTTTCTCAGCTCACACGAGGAAAACAGGCTTTCACTCAGCAAATTGAGGAGCTTAAGAGGCAGATTGAAGAGGAGGTTAAGGTAATACAATATAAAATATACATTTATATATCCCACATTTACTATAGAGCCAGGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31460
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
ENSDART00000098066 Nonsense 33 446 2 11
ENSDART00000098067 Nonsense 1523 1937 31 39
ENSDART00000110726 None None 945 None 24
ENSDART00000131983 Nonsense 1523 1937 33 41
Genomic Location (Zv9):
Chromosome 5 (position 33921511)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31683743
GRCz11 5 32283896
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTACAGAGGAGATTTCAGATCTGACAGAGCAGATAGGTGAGACTGGT[A/T]AGAGCATCCATGAGCTGGAAAAGTCCAAGAAGGCAGTGGAGACTGAGAAG
Long Flanking Sequence:
AGACCAAACAGAGACTCCAGGGTGAAGTGGAGGACCTCATGATTGATGTGGAGAGAGCCAACGCTTTGGCTGCCAACCTTGACAAAAAGCAGAGGAACTTTGACAAGGTAAAATTTGGAGTCATGTTGTGATGTGATGTTCTATTTCAGAAAGTAGTATTAGCTTTCTTCTGGAGAATACAAGTTGAACAAACCTGATATATTCCACCCTAAAGGTCCTGGCAGAATGGAAGCAGAAATATGAGGAAGGTCAGGCAGAGCTGGAAGGTGCCCAGAAAGAAGCTCGTTCACTCAGCACTGAGCTGTTCAAGATGAAGAACTCCTATGAGGAGACTCTGGATCAGCTGGAGACCCTCAAGAGAGAGAACAAGAATCTGCAGCGTAAGAATCAAAAAATAATAAAACCTGATGAATAACCGTCTTTATGATATGATACAGATAATATTTTTTCTTTCTACAGAGGAGATTTCAGATCTGACAGAGCAGATAGGTGAGACTGGT[A/T]AGAGCATCCATGAGCTGGAAAAGTCCAAGAAGGCAGTGGAGACTGAGAAGGCAGAGATTCAGACCGCTCTGGAGGAGGCTGAAGTGAGTGGAGATGGAGATTTATATGGCGTTATCTGTAGAACATTTTATACTATAAATTATTTATCTTTGTCATAGGGCACTCTGGAGCATGAGGAGTCCAAGATTCTTCGTGTCCAGCTTGAGCTAAACCAGGTCAAAAGTGAGATCGACAGGAAGCTTGCAGAGAAGGATGAGGAGATAGAGCAGATCAAGAGGAACAGTCAGAGAATTACTGATTCCATGCAGAGCACTCTGGACTCTGAAGTCAGAAGCAGGAATGATGCTCTCAGAATCAAGAAGAAGATGGAGGGAGACCTTAATGAGATGGAGATTCAGCTGAGCCATGCCAATCGCCAGGCTGCTGAGGCTCAGAAACAGCTCAGAAATGTTCAGGCACAACTCAAGGTATGACTTCTCGTCAGCTTTAGGTGCATTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10023
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
ENSDART00000098066 Nonsense 176 446 4 11
ENSDART00000098067 Nonsense 1666 1937 33 39
ENSDART00000110726 None None 945 None 24
ENSDART00000131983 Nonsense 1666 1937 35 41
Genomic Location (Zv9):
Chromosome 5 (position 33920902)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31683134
GRCz11 5 32283287
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTTRTGTTCAGGATGCCCAGCTGCACCTTGATGATGCCGTGAGAGGA[C/T]AGGAAGACATGAAGGAGCAGGTGGCCATGGTGGAGCGCAGAAATACTCTG
Long Flanking Sequence:
GCGTTATCTGTAGAACATTTTATACTATAAATTATTTATCTTTGTCATAGGGCACTCTGGAGCATGAGGAGTCCAAGATTCTTCGTGTCCAGCTTGAGCTAAACCAGGTCAAAAGTGAGATCGACAGGAAGCTTGCAGAGAAGGATGAGGAGATAGAGCAGATCAAGAGGAACAGTCAGAGAATTACTGATTCCATGCAGAGCACTCTGGACTCTGAAGTCAGAAGCAGGAATGATGCTCTCAGAATCAAGAAGAAGATGGAGGGAGACCTTAATGAGATGGAGATTCAGCTGAGCCATGCCAATCGCCAGGCTGCTGAGGCTCAGAAACAGCTCAGAAATGTTCAGGCACAACTCAAGGTATGACTTCTCGTCAGCTTTAGGTGCATTCATATGTTTTTCAAATTAAAACTATGTGCTAACACACAGCACTCAAAAAGCTTACTGTAAAGCTGTTATGTTCAGGATGCCCAGCTGCACCTTGATGATGCCGTGAGAGGA[C/T]AGGAAGACATGAAGGAGCAGGTGGCCATGGTGGAGCGCAGAAATACTCTGATGCAGTCTGAGATTGAAGAGCTGAGAGCTGCTCTGGAGCAGACAGAGAGAGGACGCAAAGTGGCTGAACAAGAGCTGGTGGATGCCAGTGAGCGTGTTGGGCTGCTGCACTCTCAGGTAAAAAAGCATAATGGCTTTGTTTTTGCTTTCTGTTGCGCAATGTCATTAAGATAGTTGAAAGCATTTTTCAATACATTTATCTTGTTGCTTTCCATGTTGTAGAACACAAGTCTTCTGAACACCAAGAAGAAGCTTGAGGCTGACCTTGTTCAGATCCAGAGTGAAGTTGAAGACACTGTACAGGAAGCCAGAAATGCAGAGGACAAGGCCAAGAAGGCCATCACTGATGTGAGCAACAGAACAAAAGTTTCAAAGTGTATTTTAAAAAAAAAGTCTAATGGAGATTTGTGTTCATGTAAAAGGCTGCAATGATGGCAGAGGAGCTGAAGA
Associated Phenotype:
Not determined