ZMP
myhb
Ensembl ID:
ZFIN ID:
Description:
LOC100002040 protein [Source:UniProtKB/TrEMBL;Acc:A7E2L9]
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]
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]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31534 | Essential Splice Site | Available for shipment | Available now |
sa25345 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18118 | Nonsense | Available for shipment | Available now |
sa17247 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31534
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026257 | Essential Splice Site | 684 | 1939 | 17 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 40682742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 40754342 |
GRCz11 | 6 | 40751878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGATCATCCTCTCTAAAACAATGATTTATTATTAACTCTCTTTATTTT[A/G]GGTCTTATGGAGAACTTTCTGGTCATCCACCAGTTGCGTTGTAATGGTGT
Long Flanking Sequence:
CATACTGTTACGATTACAACATTAGGATTCAAATATTTTTTTTGTTATGTATAAATTTCTGTTAAAGATAATTTCTGCTTGATTTCGGTACATGGTATTGTTTACCAAGATTATTTACTTATTTCTTTATCGACAGCTGAATCTGGTGGCAAAAAGGGTGGAAAAAAGAAGGGAGGCTCCTTCCAGACTGTGTCTGCTTTGTTCAGAGTAATGAAATGATTCACTTTTAGCCTTGAAATATTTAAGGTGCACTGTGTGTTTATAGTTTAACTGTTTATTCTACAATTAACAGGAAAATTTGGGCAAATTGATGACCAACCTGAGAAGCACTCATCCACATTTTGTGCGCTGCTTGATTCCAAATGAGTCAAAGACTCCAGGTCAAATTTTTGACACAACTTTTTTTAAAATACAGAAAAGCATGTGACATATACTCTTTGTTAAAATAACAATGATCATCCTCTCTAAAACAATGATTTATTATTAACTCTCTTTATTTT[A/G]GGTCTTATGGAGAACTTTCTGGTCATCCACCAGTTGCGTTGTAATGGTGTGCTGGAGGGAATCAGAATTTGCAGAAAGGGTTTCCCCAGCAGAATCCTCTATGGTGACTTTAAGCAGAGGTAATTAATGTGCATGACTTGTATTTCACTTGTCTTTGGTGAATTTAATATGTAAAATTGTGTGCATGGGCATTACCTGGATTATTGTACAGTGAATGTTGAGCATGTGCCCAACTCTATTAATCTTGATAAAATATCTCGGCTTTCTTTAATACACATGTCTGTCTAAATAAATGGAAACACACACAGTATGCAGATTGTGTGTACAAAGGCATGTGGATCTTCACAAGTATAGTGAATAAGACTGAGTCATATCTTCACTTTAGATACAAAGTATTGAATGCTAGTGTCATCCCTGAGGGTCAGTTCATTGACAACAAGAAGGCTTCAGAGAAGCTTCTTGGCTCTATTGATGTGGATCATACCCAGTACAAGTTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25345
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 |
---|---|---|---|---|---|
ENSDART00000026257 | Nonsense | 1579 | 1939 | 32 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 40678338)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 40749938 |
GRCz11 | 6 | 40747474 |
KASP Assay ID:
554-7299.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTCGCGTTCAGCTTGAACTGAACCAAGTGAAAGGAGAGATTGATCGG[A/T]AATTGGCCGAGAAGGATGAGGAGATTGAACAGATTAAGCGAAACAGCCAG
Long Flanking Sequence:
ACTTAGCACGGAACTTTTCAAAATGAAAAATTCTTATGAGGAGACTTTGGATCATCTAGAAACTCTTAAGAGAGAGAACAAGAACCTTCAGCGTATGTACAATTAAGTGCAGAACTATATGTTGTTGTTTTTTTTTTTGCTTTTTAGACGTAAATAGTGCATTTCACCCAATTGTTGGTCATGTTTTTGCATATACAGAGGAAATCACAGATTTAACCGAACAGCTTGGCGAGACTGGAAAGACCATCCATGAGCTGGAAAAAGGAAAGAAAACTGCAGAAATCGAAAAATCTGAAATCCAAGCTGCTCTTGAAGAAGCTGAGGTAACACCTAGGCCCTAGTGCTTAAAGTTTTTTTTTTATTCCCAATATCACCACTAAACTTCCAGCGAACAATACACTACACACCATCCTATTTTTCAGGCCACCTTAGAGCATGAGGAATCCAAGATTCTTCGCGTTCAGCTTGAACTGAACCAAGTGAAAGGAGAGATTGATCGG[A/T]AATTGGCCGAGAAGGATGAGGAGATTGAACAGATTAAGCGAAACAGCCAGAGGATCATCGACTCTATGCAGAGCACTCTGGATGCGGAAGTCAGAAGCAGAAACGATGCTCTGAGAATCAAAAAGAAGATGGAAGGAGACCTGAACGAGATGGAGATTCAGCTAAGCCATGCAAACCGGCAGGCAGCTGAAGCTCAGAAGCAGCTCAGGAACGTCCAAGGGCAACTCAAGGTTTGTTCCTTTAGAGTAGTATAGCAGTATATCTTGATTTGACTAACTAGATCAAACAATCTAATTGAAACTTGATTGCTTCAGGATGCTCAACTCCATCTTGATGAGGCTCTGAGGGCTCAAGAGGACATGAAAGAACAAGTTGCAATGGTTGAACGCAGGAATAACCTGATGCAGGCAGAGATCGAGGAGCTGAGAGTTGCTCTGGAGCAGACCGAGAGAGGCCGCAAAGTGGCTGAGCAGGAACTGGTGGATGCCAGTGAGCGAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18118
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026257 | Nonsense | 1624 | 1939 | 32 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 40678203)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 40749803 |
GRCz11 | 6 | 40747339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CKGAAGTCAGAAGCAGAAACGATGCTCTGAGAATCAAAAAGAAGATGGAA[G/T]GAGACCTGAACGAGATGGAGATTCAGCTAAGCCATGCAAAYCGGCAGGCA
Long Flanking Sequence:
TTTGCTTTTTAGACGTAAATAGTGCATTTCACCCAATTGTTGGTCATGTTTTTGCATATACAGAGGAAATCACAGATTTAACCGAACAGCTTGGCGAGACTGGAAAGACCATCCATGAGCTGGAAAAAGGAAAGAAAACTGCAGAAATCGAAAAATCTGAAATCCAAGCTGCTCTTGAAGAAGCTGAGGTAACACCTAGGCCCTAGTGCTTAAAGTTTTTTTTTTATTCCCAATATCACCACTAAACTTCCAGCGAACAATACACTACACACCATCCTATTTTTCAGGCCACCTTAGAGCATGAGGAATCCAAGATTCTTCGCGTTCAGCTTGAACTGAACCAAGTGAAAGGAGAGATTGATCGGAAATTGGCCGAGAAGGATGAGGAGATTGAACAGATTAAGCGAAACAGCCAGAGGATCATCGACTCTATGCAGAGCACTCTGGATGCGGAAGTCAGAAGCAGAAACGATGCTCTGAGAATCAAAAAGAAGATGGAA[G/T]GAGACCTGAACGAGATGGAGATTCAGCTAAGCCATGCAAACCGGCAGGCAGCTGAAGCTCAGAAGCAGCTCAGGAACGTCCAAGGGCAACTCAAGGTTTGTTCCTTTAGAGTAGTATAGCAGTATATCTTGATTTGACTAACTAGATCAAACAATCTAATTGAAACTTGATTGCTTCAGGATGCTCAACTCCATCTTGATGAGGCTCTGAGGGCTCAAGAGGACATGAAAGAACAAGTTGCAATGGTTGAACGCAGGAATAACCTGATGCAGGCAGAGATCGAGGAGCTGAGAGTTGCTCTGGAGCAGACCGAGAGAGGCCGCAAAGTGGCTGAGCAGGAACTGGTGGATGCCAGTGAGCGAGTGACTCTCTTACACTCCCAAGTAAGAAGAATGATTTATTTTGAAGAATGTTTTAAAGAATAACTGTTAAACAACATTACCTTTAACTTGATCTCAATGTCCGCAGAACACCAGTCTTATTAACACCAAGAAAAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17247
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026257 | Essential Splice Site | 1765 | 1939 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 40677608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 40749208 |
GRCz11 | 6 | 40746744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGGAAGCTCRAAATGCTGAAGAGAAGGCAAAGAAAGCTATAACTGAT[G/T]TAAGTAAATCTGTTCATGGATAATTNNNNNNNAAGTTTTCAAGATGTTGCATGTAAA
Long Flanking Sequence:
GGTTTGTTCCTTTAGAGTAGTATAGCAGTATATCTTGATTTGACTAACTAGATCAAACAATCTAATTGAAACTTGATTGCTTCAGGATGCTCAACTCCATCTTGATGAGGCTCTGAGGGCTCAAGAGGACATGAAAGAACAAGTTGCAATGGTTGAACGCAGGAATAACCTGATGCAGGCAGAGATCGAGGAGCTGAGAGTTGCTCTGGAGCAGACCGAGAGAGGCCGCAAAGTGGCTGAGCAGGAACTGGTGGATGCCAGTGAGCGAGTGACTCTCTTACACTCCCAAGTAAGAAGAATGATTTATTTTGAAGAATGTTTTAAAGAATAACTGTTAAACAACATTACCTTTAACTTGATCTCAATGTCCGCAGAACACCAGTCTTATTAACACCAAGAAAAAGCTGGAAGCAGATCTTGTTCAGATTCAAGGTGAGATGGAGGACGTGGTCCAGGAAGCTCGAAATGCTGAAGAGAAGGCAAAGAAAGCTATAACTGAT[G/T]TAAGTAAATCTGTTCATGGATAATTAAGTTTTCAAGATGTTGCATGTAAACTAAAAACTGGGTTAAAAAAATATATCAGGCCGCCATGATGGCAGAGGAGCTGAAGAAGGAGCAGGACACAAGCGCTCACCTTGAGAGGATGAAGAAGAATCTGGAGGTTACAGTCAAAGACCTGCAGCACCGTCTGGATGAGGCTGAGAGTCTGGCTATGAAGGGTGGAAAGAAGCAGCTCCAGAAGCTGGAGGCCAGAGTATGTGACTGCTCACACTGTTCATTGATTTACCTCACCGTAAGTCAGGAATAACCTCAGTTAAACTTGTGCGTCAGGTTCGTGAACTGGAGAGTGAAGTCGAAGCTGAACAGAGACGTGGTGCTGATGCTGTGAAAGGAGTCCGCAAATATGAAAGAAGAGTGAAGGAACTGACTTATCAGGTAATAATAATCACACAAATAAACGTATATAGGTGTTATAAGTCAAATACAGTCAAATCAAAATGGTT
Associated Phenotype:
Not determined