Busch Lab

ZMP

myh6

Ensembl ID:
ENSDARG00000090637
ZFIN ID:
ZDB-GENE-031112-1
Description:
myosin-7 [Source:RefSeq peptide;Acc:NP_942118]
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 6 alleles of this gene:

Allele Name Consequence Status Availability
sa37186 Nonsense Mutation detected in F1 DNA Not yet available
sa37187 Nonsense Mutation detected in F1 DNA Not yet available
sa6659 Nonsense Mutation detected in F1 DNA Not yet available
sa25148 Nonsense Mutation detected in F1 DNA Not yet available
sa37188 Nonsense Mutation detected in F1 DNA Not yet available
sa12893 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa37186
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126983 Nonsense 259 1936 1 1
Genomic Location (Zv9):
Chromosome 20 (position 53928138)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53772917
GRCz11 20 53578334
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCGGGAAATTCATCCGCATTCATTTCGGGACGAGCGGAAAACTGTCAT[C/A]GGCTGATATCGAAACGTACCTGTTGGAGAAGTCAAGAGTGACCTTCCAGC
Long Flanking Sequence:
GCTGACGTTTCTTCATGAACCTGCGGTGCTGTTCAATCTAAAGGAGAGATACACCGCATGGATGATCTACACCTATTCTGGGCTGTTTTGTGTCACCGTAAACCCTTATAAGTGGTTACCGGTGTATGATGCAGATGTAGTCGCTGCTTACCGTGGTAAGAAGAGGACAGAAGCGCCTCCTCACATCTTCTCCATCTCAGATAATGCTTATCAATACATGCTGACCGACCGGGAGAATCAGTCTGTGCTCATCACCGGAGAATCCGGCGCTGGGAAGACTGTAAACACTAAGAGGGTCATCCAGTATTTTGCTAGCATCGCTGCCGCTGGGGGATCCGCTGGAAAAAAGGACTCGAGCAAGGGAACGTTGGAGGATCAGATTATTCAAGCTAACCCTGCGCTGGAGGCTTTCGGCAATGCGAAAACGCTCCGAAACGACAACTCGTCTCGCTTCGGGAAATTCATCCGCATTCATTTCGGGACGAGCGGAAAACTGTCAT[C/A]GGCTGATATCGAAACGTACCTGTTGGAGAAGTCAAGAGTGACCTTCCAGCTGAAGTCTGAGAGAAACTACCATATCTTCTTCCAGATATTATCCAACGAGAAGCCCGAGCTTCTGGACATGCTATTGATCACCAATAATCCATACGACTACTCGTACATCTCACAAGGAGAAGTGACCGTCTCATCTATCAATGATAATGAGGAGCTGATAGCGACCGATAAGGCTTTTGATGTGCTTGGCTTCACGTCTGAGGAGAAGATGGGAGTCTATAAGCTGACCGGCGCTATCATGCATTACGGAAACATGAAATTCAAGCAGAAGCAGCGCGAGGAGCAGGCCGAGCCCGACGGCACTGAAGACGCAGATAAAGCAGCTTATCTAATGGGGCTGAACTCTGCCGACCTGCTCAAAGGACTCTGCCATCCAAGGGTTAAGGTGGGCAATGAATATGTTACAAAAGGACAAAGTGTGGACCAGGTGTATTACTCAATCGGCGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37187
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126983 Nonsense 815 1936 1 1
Genomic Location (Zv9):
Chromosome 20 (position 53929805)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53774584
GRCz11 20 53580001
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCGAGTATCAGAAACTGGTGGAGCGTAGAGATGCGCTGATGGTGGTG[C/T]AGTGGAACCTGCGCTCCTTCCTCGGTGTGAAAAACTGGCCGTGGATGAAA
Long Flanking Sequence:
CTGCCCTGCATAGAGAAAACCTTAACAAATTAATGACCAATCTGAAAACCACTCACCCACACTTTGTCCGCTGTTTAATTCCAAATGAGAGCAAGATTCCGGGAATCATGGACAACTGTTTGGTCATGCACCAGCTCCGCTGCAATGGTGTACTAGAGGGAATCAGGATTTGCAGGAAAGGTTTCCCCAACAGGATTCTTTATGGAGATTTCAAACAAAGATACAGAATCCTGAACGCATCAGCCATCCCAGAAGGACAGTTCATAGAGAACAAGAAGAGTGCAGAGAAGCTGTTGGGGTCTCTAGATATTGACCACACGCAATACAAATTTGGCCACACAAAGGTCTTTTTTAAAGCAGGTCTACTCGGTACCTTGGAGGAGATGCGAGATGACCAACTCGCTCGTATCCTCACTGGAATCCAAGCATTCGCTCGTGGACTTCTGATGAGAGTCGAGTATCAGAAACTGGTGGAGCGTAGAGATGCGCTGATGGTGGTG[C/T]AGTGGAACCTGCGCTCCTTCCTCGGTGTGAAAAACTGGCCGTGGATGAAACTCTTCTTCAAGATAAAACCCTTGCTGAAGAGCGCCGAGTCTGAAAAGGAGATGGCAAACATGAAAGATGAATTCAATAAGTTGAAGGAAGCCTTGGAAAAATCTGACGCCAGAAGGAAAGAGTTGGAGGAAAAAATGGTGTCGTTGCTTCAAGAGAAGAATGATTTGCTCCTTCAGGTGCAATCGGAGCAGGACACGCTAACGGACGCAGAGGAACGATGTGAGCAGCTCATAAAAAGCAAGATCCAGCTAGAAGCTAAAGTTAAAGAGCTGTCGGAGAGAATTGAGGATGAGGAAGAAATAAATGCAGATCTCACAGCCAAGAGACGCAAGCTAGAAGACGAATGCTCTGAGCTCAAGAAAGACATCGATGACCTGGAACTGACACTGGCTAAGGTAGAAAAGGAAAAGCATGCTACTGAGAACAAAGTGAAGAATATTACCGAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6659
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126983 Nonsense 980 1936 1 1
Genomic Location (Zv9):
Chromosome 20 (position 53930300)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53775079
GRCz11 20 53580496
KASP Assay ID:
554-4662.1 (used for ordering genotyping assays)
KASP Sequence:
AGGTAGAAAAGGAAAAGCATGCTACTGAGAACAAAGTGAAGAATATTACC[G/T]AAGAAATGGCATCTCTTGATGAAAAYATAATGAAACTCACCAAGGAGAAA
Long Flanking Sequence:
TGGTGCAGTGGAACCTGCGCTCCTTCCTCGGTGTGAAAAACTGGCCGTGGATGAAACTCTTCTTCAAGATAAAACCCTTGCTGAAGAGCGCCGAGTCTGAAAAGGAGATGGCAAACATGAAAGATGAATTCAATAAGTTGAAGGAAGCCTTGGAAAAATCTGACGCCAGAAGGAAAGAGTTGGAGGAAAAAATGGTGTCGTTGCTTCAAGAGAAGAATGATTTGCTCCTTCAGGTGCAATCGGAGCAGGACACGCTAACGGACGCAGAGGAACGATGTGAGCAGCTCATAAAAAGCAAGATCCAGCTAGAAGCTAAAGTTAAAGAGCTGTCGGAGAGAATTGAGGATGAGGAAGAAATAAATGCAGATCTCACAGCCAAGAGACGCAAGCTAGAAGACGAATGCTCTGAGCTCAAGAAAGACATCGATGACCTGGAACTGACACTGGCTAAGGTAGAAAAGGAAAAGCATGCTACTGAGAACAAAGTGAAGAATATTACC[G/T]AAGAAATGGCATCTCTTGATGAAAATATAATGAAACTCACCAAGGAGAAAAAAGCACTGCAGGAGGCTCACCAGCAGACACTGGATGACCTTCAAAGTGAGGAGGACAAAGTGAACACACTAACAAAAGCCAAAGTTAAGCTTGAACAACAGGTGGATGATCTTGAGGGCTCGCTGGAGCAGGAGAAAAAAGTCAGAATGGACTTGGAGCGCAGCAAGAGGAAGCTGGAAGGAGATGTCAAACTGACTCAAGAAAATGTAATGGACTTAGAAAACGACAAACAGCAACTGGAGGACAAGCTCAAGAAGAAAGACTTTGAGATCAATCAGCTGAATCAAAGAATCGAAGATGAGCAAATGGCTTCGGTGCAGTTGCAGAAGAAATTAAAAGAAAACCAAGCTCGGATTGAAGAACTCGAAGAGGAGCTGGATGCAGAGCGAGCTGCTCGTGCAAAAGTGGAGAAGCAGCGATCTGACATTTCCAGAGAACTGGAGGACATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25148
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126983 Nonsense 1074 1936 1 1
Genomic Location (Zv9):
Chromosome 20 (position 53930582)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53775361
GRCz11 20 53580778
KASP Assay ID:
554-7582.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATGTCAAACTGACTCAAGAAAATGTAATGGACTTAGAAAACGACAAA[C/T]AGCAACTGGAGGACAAGCTCAAGAAGAAAGACTTTGAGATCAATCAGCTG
Long Flanking Sequence:
AGCTCATAAAAAGCAAGATCCAGCTAGAAGCTAAAGTTAAAGAGCTGTCGGAGAGAATTGAGGATGAGGAAGAAATAAATGCAGATCTCACAGCCAAGAGACGCAAGCTAGAAGACGAATGCTCTGAGCTCAAGAAAGACATCGATGACCTGGAACTGACACTGGCTAAGGTAGAAAAGGAAAAGCATGCTACTGAGAACAAAGTGAAGAATATTACCGAAGAAATGGCATCTCTTGATGAAAATATAATGAAACTCACCAAGGAGAAAAAAGCACTGCAGGAGGCTCACCAGCAGACACTGGATGACCTTCAAAGTGAGGAGGACAAAGTGAACACACTAACAAAAGCCAAAGTTAAGCTTGAACAACAGGTGGATGATCTTGAGGGCTCGCTGGAGCAGGAGAAAAAAGTCAGAATGGACTTGGAGCGCAGCAAGAGGAAGCTGGAAGGAGATGTCAAACTGACTCAAGAAAATGTAATGGACTTAGAAAACGACAAA[C/T]AGCAACTGGAGGACAAGCTCAAGAAGAAAGACTTTGAGATCAATCAGCTGAATCAAAGAATCGAAGATGAGCAAATGGCTTCGGTGCAGTTGCAGAAGAAATTAAAAGAAAACCAAGCTCGGATTGAAGAACTCGAAGAGGAGCTGGATGCAGAGCGAGCTGCTCGTGCAAAAGTGGAGAAGCAGCGATCTGACATTTCCAGAGAACTGGAGGACATCAGCGAGCGCCTGGAGGAGGCAGGGGGAGCCACGTCTGCTCAGGTGGAGCTCAATAAAAAAAGAGATGCAGAGTTTCAGAAGATCCGCAGGGATCTTGAGGAATCCACCCTTCAGCATGAAGCCACTACCGCCTCTCTACGGAAGAAGCACGCAGACAGTGTTGCTGAACTCGGGGAACAGATTGACAACTTGCAAAGAGTCAAACAAAAGCTAGAGAAGGAAAAAGTAGAGTTAAAGTTGGAATTGGACGACCTTGCCTCAAACATGGAGAGTATTGTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37188
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126983 Nonsense 1233 1936 1 1
Genomic Location (Zv9):
Chromosome 20 (position 53931060)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53775839
GRCz11 20 53581256
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTAGAGAAGGAAAAAGTAGAGTTAAAGTTGGAATTGGACGACCTTGCCT[C/A]AAACATGGAGAGTATTGTAAAAGCCAAGGTCAATCTAGAAAAGATGTGCC
Long Flanking Sequence:
AATGGACTTAGAAAACGACAAACAGCAACTGGAGGACAAGCTCAAGAAGAAAGACTTTGAGATCAATCAGCTGAATCAAAGAATCGAAGATGAGCAAATGGCTTCGGTGCAGTTGCAGAAGAAATTAAAAGAAAACCAAGCTCGGATTGAAGAACTCGAAGAGGAGCTGGATGCAGAGCGAGCTGCTCGTGCAAAAGTGGAGAAGCAGCGATCTGACATTTCCAGAGAACTGGAGGACATCAGCGAGCGCCTGGAGGAGGCAGGGGGAGCCACGTCTGCTCAGGTGGAGCTCAATAAAAAAAGAGATGCAGAGTTTCAGAAGATCCGCAGGGATCTTGAGGAATCCACCCTTCAGCATGAAGCCACTACCGCCTCTCTACGGAAGAAGCACGCAGACAGTGTTGCTGAACTCGGGGAACAGATTGACAACTTGCAAAGAGTCAAACAAAAGCTAGAGAAGGAAAAAGTAGAGTTAAAGTTGGAATTGGACGACCTTGCCT[C/A]AAACATGGAGAGTATTGTAAAAGCCAAGGTCAATCTAGAAAAGATGTGCCGATCACTTGAAGATCAGATGAATGAGCACAGGTCAAAAGCTGAAGAAGCCCAAAGAGCTCTTAATGACGTGTCAACACAGAAAGCGAAGCTTCTGACTGAAAATGGTGAACTTGGACGTCAGCTGGAGGAGAAAGAATGTTTGATTTCCCAACTTACCCGAGGAAAGACTTCCTACACGCAACAACTTGAAGACCTGAGAAGGCAACTTGAGGAAGAAGTAAAAGCAAAGAACGCTCTGGCTCATGCCGTACAGTCAGCACGTCATGATTGTGATTTACTCAGAGAGCAATTTGAAGAGGAACAAGAAGCAAAAGCCGAGCTCCAGCGAGCATTATCAAAGGCTAATACAGAGGTGGCAACATGGAGGGCGAGATATGAGACTGATGGCATTCAGAGAACCGAGGAACTGGAGGACGCAAAGAAGAAACTTGTTCAGAAACTGCAAGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12893
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126983 Nonsense 1585 1936 1 1
Genomic Location (Zv9):
Chromosome 20 (position 53932115)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53776894
GRCz11 20 53582311
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCRAGRCAGATTTCGAGCGCAAGATGTCTGAGAAGGATGAAGAAATGGAG[C/T]AAGCGAGGAGAAACTATCAGCGTATGATTGAATCCTTGCAAGCCTCTCTT
Long Flanking Sequence:
AACATCGCCTGCAAAATGAGATTGAAGATTTGATGCTGGATCTTGAGCGGTCCAATGCGGCGTCCGCAGCTCTGGATAAGAAACAGAGATCTTTCGATAAAGTCATGGCAGAGTGGAAGCAGAAATATGAAGAGTCACAATGTGAGCTTGAAGGAGCGCAAAAAGAGGCTCGCAGTTTAAGCACTGAACTCTTCAAGCTGAAGAACTCCTATGAAGAAACTCTCGATCACCTAGAGACCATCAAAAGAGAAAACAAGAATCTACAGGAGGAGATCTCTGACTTGACGGATCAAGTAAGCGAAGGGCGAAAGAGTGTCCATGAGTTGGAAAAACTGAGGAAGCAATTGGAACAGGAGAAAACGGAGTTGCAGTCGGCACTAGAAGAAGCTGATGCTTCAGTCGAGCATGAAGAAGGTAAAATCTTACGGGCTCAGCTAGAGTTTAATCAACTCAAGGCAGATTTCGAGCGCAAGATGTCTGAGAAGGATGAAGAAATGGAG[C/T]AAGCGAGGAGAAACTATCAGCGTATGATTGAATCCTTGCAAGCCTCTCTTGAGGCAGAGACGAGAAGCCGTAATGAAGCCTTACGAGTGAAGAAGAAAATGGAGGGAGATCTTAACGAAATGGAAATTCAGTTAAGCCAAGCCAACAGACAGGCAGCTGATGCTCAAAAGCAGCTCAAGATGGTCCAATCATGCTTGAAAGAAACCCAACTCCAGATGGACGACACTCTCCACAGTAATGATGACCTCAAAGAAAACATAACTCTACTGGAGCGTCGAAACAATCTCATGCAAACCGAATTAGAAGAACTCAGAGGCATTCTGGAGCAAACCGAAAGAGTTCGCAAACTTGCCGAGCAAGAACTCACCGATGCAACCGAACGGATGCAACTCCTGCACTCACAAAACACAGGCCTCATCAATCAAAAGAAGAAGCAAGAGTCGGATCTTCTCCAGCTGCAAAACGAACTGGAGGAACTTGTGCAAGAGAACCGCAATGCT
Associated Phenotype:
Not determined