Busch Lab

ZMP

wu:fd14a01

Ensembl ID:
ENSDARG00000035437
ZFIN ID:
ZDB-GENE-030131-5336
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 5 alleles of this gene:

Allele Name Consequence Status Availability
sa37392 Splice Site, Nonsense Available for shipment Available now
sa24042 Nonsense Available for shipment Available now
sa29676 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37392
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 > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051360 Splice Site, Nonsense 269 1936 8 39
Genomic Location (Zv9):
Chromosome 22 (position 284509)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 293593
GRCz11 22 280714
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTAATCAAGACTAGTCCATGTCTTACTATGTTTTTTTCTTTGAAAGA[C/A]CTGCTGGAAAAGTCAAGAGTAACATTCCAGCTGTCTGCTGAGAGGAGTTA
Long Flanking Sequence:
AGAACACCTATTTTAGACACCTATTTTTGTTATTAATTACAGCATTTGTAGTTATAACTATGCTCTGTCTTGCAACTACATTTAGGGGTCACTGGAGGACCAGATTGTGGCAGCAAACCCTCTGCTGGAGGCTTATGGTAATGCCAAGACTGTGAGGAATGACAACTCCTCTCGTTTTGTAAGTTGCAAGTGAGAATTATTATAAAATGTAATAATTTAAAAATGTTTTCAAAGCTTCCATACAGTTTTACTTTAAGAACAAAAATTATTTAAATCTTTATAGGGTAAATTCATCAGGATTCATTTTGGGACCACTGGAAAACTGGCCTCAGCTGACATTGAAACCTGTGAGCGAACATTGTTTTAATTATTAATGAATTCATGTTATGATTAAAAGTTTATTCCACAGTCTACATCAGAAGGGTATAATTGTGAGCCATATTTGCAGACATGTTAATCAAGACTAGTCCATGTCTTACTATGTTTTTTTCTTTGAAAGA[C/A]CTGCTGGAAAAGTCAAGAGTAACATTCCAGCTGTCTGCTGAGAGGAGTTACCACATCTTCTACCAGCTCATGACTGGACACAAGCCAGAGCTGCTGGGTGAGAAACCTACAGGATCATATTTAAATATGGATTTTATGATTCACGATGTGATGCGATTCATTATACTAATCTCATGAGTCATGATTTAGTCACATTTTTTCTAAAAATATTTTAGATTAATTTAAGGTGAACAAGAGTCCTTTCATTTTCCTCAAATGCTGCACAATTTCTTCATTCATTCATTTTCTTTTCGGCTTAAGCCTGGTTTATACTTCTGCGTCAAGTGACTGGCGTAACCCACAGCGCATGCAACGCGCATAGGTGTGCATTTATACTTCTGCGCGCTGTCTCTAATGGTCTGCATTTACACTTTCGAAACGCTAGTTGGCAATGAGGTGTTAATGTTCCTCTGTTTTGCTTTTCCTGAACACTTCCGGGATGTACAAGTGGCTCAAACTCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24042
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
ENSDART00000051360 Nonsense 1615 1936 32 39
Genomic Location (Zv9):
Chromosome 22 (position 293430)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 284672
GRCz11 22 271793
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGCAGAGCACTCTGGACTCTGAGGTCAGGAGCAGAAATGATGCCCTG[A/T]GAGTCAAAAAGAAGATGGAGGGAGATCTGAATGAGATGGAGATCCAGCTG
Long Flanking Sequence:
TTTTTTAAACCCATTTAGAGGAGATTTCTGACCTCACTGAGCAGCTTGGAGAGACTGGAAAGAGCATTCATGAGTTAGAGAAAGCCAAGAAGACTGTGGAGTCTGAGAAAGTAGAGATCCAGACTGCACTTGAAGAAGCCGAGGTACTATTTCTTTACTACTTCGTAAAAGTATGATTTGAAACATTGTTTTGGATATAATTCAAAACTTTGATAAATTACAAATATTTCATACTCGTATAAATGTACAGATTTGAGATAGCATTAACAAAAACTTAAAAATTCATTTTGCTTTATTTTCTCCTGTAGGGCACCCTGGAGCATGAGGAGTCCAAGATTCTGCGTGTGCAGCTGGAGCTGAACCAGGTGAAGAGTGAGATTGACAGGAAGCTTGCTGAGAAGGATGAAGAGATAGAACAGATCAAGAGGAACAGCCAAAGAGTGCTTGATGCCATGCAGAGCACTCTGGACTCTGAGGTCAGGAGCAGAAATGATGCCCTG[A/T]GAGTCAAAAAGAAGATGGAGGGAGATCTGAATGAGATGGAGATCCAGCTGAGTCATGCCAATCGCCAGGCTGCTGAAGCCCAGAAACAGCTCAGGAACGTTCAAGGCCAACTCAAGGTGTTTATTATTATTATTATTATTATTATTATTATTATTATTATTGTTGTTGTTATTGTCTTTATTTTACCAGAAAAACGCACATTGAAATTAAAAATCTTTTTTACAAGAGTATCCTGGCCAAAATGAAGCTGTATACAGTTGCATGTAGGTTTAACAAAAAACAGACGAAATCATTCATCCATCAAAACATGCATACAAGACAATTAAATCTACAGGTCAATGTTTCACAATCCAAATCATTTAAAATCTTTTCAAAAGTAGTGAAACCAACTCTTTAAACTGCAACTCTGTTTGCATGTAATTCTATGCAAAAGGTGCTGCGTATTTAAAAGCCACTTTCCCATTTCAGTCCGCACCACTGGTACAAACAATAAATACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29676
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051360 Essential Splice Site 1763 1936 34 39
Genomic Location (Zv9):
Chromosome 22 (position 295983)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 282119
GRCz11 22 269240
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGGAGGCCAGAAACGCAGAGGAGAAGGCCAAGAAGGCCATCACTGAT[G/A]TGAGTGTTTACATTCTGTTGCTCTATTCTCTCGTAAACTCTTTTACTGAG
Long Flanking Sequence:
CTTGATCCGATGGTAAAGAATAAGAAACGTTTGACATTTTAAATGAATGTAAGATAATTAACAAAGATAGAACATTATCACAGGATGCCCAACTGCACCTTGATGAAGCCGTCAGAGGACAAGAGGACATGAAGGAGCAGGTGGCCATGGTGGAGCGCAGGAATAACCTGATGCAAGCAGAGATTGAGGAGCTGAGAGCCGCACTGGAGCAAACAGAGAGAGGCCGCAAAGTAGCAGAGCAGGAGCTGGTGGATGCCAGTGAGCGTGTGGGACTGCTGCACTCACAAGTACAGAAACTCATCACGAATGCATTTAAAAACACATGCAAGGCTGCTTGAAAACAGGCAGACACTAAAACTATCTATAACTTGCAGAATACAAGTCTTATTAACACCAAGAAGAAGCTTGAGGCTGATCTGGTCCAAATTCAAGGTGAGGTGGATGATGCAGTTCAGGAGGCCAGAAACGCAGAGGAGAAGGCCAAGAAGGCCATCACTGAT[G/A]TGAGTGTTTACATTCTGTTGCTCTATTCTCTCGTAAACTCTTTTACTGAGCTGCCTGTGGTTACAAAGGAAAGCTTCATGGAAGGTTCTTCTACAAACTCTGATCATTCAAACTTTATTGGCTGATATTTCAGGCTGCCATGATGGCTGAGGAGCTGAAGAAGGAGCAGGACACCAGTGCTCACCTGGAGAGGATGAAGAAGAACCTGGAGGTGACTGTCAAAGACCTGCAGCACCGTCTGGATGAGGCAGAGAATCTGGCCATGAAGGGTGGAAAGAAACAGCTCCAGAAACTGGAGTCCAGGGTAAGGTTGTGCGGCTAAGAACAATTAACACTTAGATTTAAAGGCTAGAGCTGATTTTCTTACTAACTTTACTGAAGGTTCGTGAGTTGGAGAGTGAAGTTGAAGCTGAACAGAGACGCGGTGCAGATGCTGTTAAAGGAGTGCGTAAATATGAAAGGAGGGTGAAGGAGCTCACCTACCAGGTAAAGCAGCACAG
Associated Phenotype:
Not determined