ZMP
myhz1.3
Ensembl ID:
ZFIN ID:
Description:
Novel myosin family protein [Source:UniProtKB/TrEMBL;Acc:B8A569]
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 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20463 | Nonsense | Available for shipment | Available now |
| sa10927 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20463
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000122889 | Nonsense | 409 | 1937 | 13 | 41 |
| ENSDART00000127125 | None | None | 423 | None | 9 |
| ENSDART00000130531 | Nonsense | 409 | 790 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 33909193)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31671425 |
| GRCz11 | 5 | 32271578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTTTGAACTCTGCTGATATGCTTAAGGCTTTGTGTTACCCCAGAGTC[A/T]AGGTCGGAAATGAGTTTGTGACCAAAGGACAGACTGTGCCACAGGTATGC
Long Flanking Sequence:
CTTCCCCATGTGCAGTCAGGGTCAGATCACAGTGGCAAGCATTGATGATAAAGAGGAGCTGGTTGCTACTGATGTGAGTCAATGTTTGATTATTGATATATTCTATATAGATATGACAGATCGTAGGTCTCATTCTTCTCTGTAATCTTCAGACTGCTATCGACATTCTGGGCTTCAATGCTGAAGAGAAAATGGGCATCTACAAGTTTACTGGAGCTGTGCTTCATCATGGTAACATGAAGTTCAAGCAGAAGCAGCGTGAGGAGCAGGCAGAGCCTGATGGCACAGAGGGTGAGACTCAGTTGCACTAATGTGTGTCATCACATATGATGCTTTTGACCGATCATTGTTTCTATTTACAATTAACAATGGTTAAATTTTCAAGTCAAGAAAATAAATGAATGTATGGTAATTTTTAAATCACAGAGGCTGACAAAATCGCATACCTTCTGGGTTTGAACTCTGCTGATATGCTTAAGGCTTTGTGTTACCCCAGAGTC[A/T]AGGTCGGAAATGAGTTTGTGACCAAAGGACAGACTGTGCCACAGGTATGCAGTAACATTTTCTGCATGTCCATGTGTTTCACCAGAAACCCCATATTGAATCTGACTGGTTATTGTTAAAAGCAAATAATTCTGTTACAATTGTACCTGTGTCTTACTTGCAGGTGTACAACTCTGTTAGCGCCTTGTCCAAATCTATCTATGAGAGGATGTTCTTGTGGATGGTCATTCGTATCAACCAGATGTTGGACACAAAACAACAAAGAAATTTCTTCATTGGTGTGCTGGATATTGCTGGCTTTGAGATCTTTGATGTAAGAAGGATTCTTTCAATTCTTTGTACTTTAAACTGAGACATATTCAGTAGTCAGTAAATAATCCTGTTTCTTCTCTAGTTCAACAGCATGGAGCAGCTGTGCATCAACTTCACTAATGAGAAACTGCAACAGTTTTTCAACCACCACATGTTTGTGCTGGAACAAGAGGAGTACAAGAAGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10927
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 |
|---|---|---|---|---|---|
| ENSDART00000122889 | Essential Splice Site | 723 | 1937 | 19 | 41 |
| ENSDART00000127125 | None | None | 423 | None | 9 |
| ENSDART00000130531 | Essential Splice Site | 723 | 790 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 33907635)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31669867 |
| GRCz11 | 5 | 32270020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGAAAGGGTTTCCCCAGCAGAATCCTCTATGGTGACTTCAAGCAGAG[G/T]TAAATGGGACTTTATGAAAATGTAATTTACTGTAAGAGTCAATTTAAAAA
Long Flanking Sequence:
AGAAGGGAGGAAAGAAGAAGGGTGGTTCCATGCAGACTGTGTCTTCCCAGTTCAGGGTAATTTTTATTTTTTTATTTTTGTTGGGACCAAATGTAAATACTGAAGCAACTGAAAACAGTGGCATGGCTTTGCTTGACTCTGTGAAAATGTGAATAAAAATCTAAAGCTTTTCATGACTAAACAGGAGAATTTAGGCAAGCTCATGACCAACTTGAGGAGCACTCACCCTCACTTTGTGCGTTGTCTGATTCCCAATGAGTCCAAGACTCCAGGTAAAGAAATACATATCTTACAGATGTACTGACATAAACACAATGTTTAATGTTTTTTCCAAAATAATGTTAATAACTACCAAGCTCATGCTGTATAATTTTACAAATAGGTCTTATGGAGAACTTCCTGGTTATCCACCAGCTGAGGTGTAACGGTGTACTGGAGGGTATCAGAATCTGCAGAAAGGGTTTCCCCAGCAGAATCCTCTATGGTGACTTCAAGCAGAG[G/T]TAAATGGGACTTTATGAAAATGTAATTTACTGTAAGAGTCAATTTAAAAAGTTATAAACCACTGTCCAATTTTCCACAGATACAAGGTGCTGAATGCCAGTGTTATCCCAGAGGGACAGTTCATTGACAACAAGAAGGCCAGCGAGAAACTCCTGGGATCTATTGATGTTAATCATGATGAGTACAGATTTGGACACACAAAGGTTCATATTTGAATTTACAATAACATTTTCAGGGATTCAGTGATCAGTGTAACATAGCTTAGAAATACATTTTTGTTTCTCTTCTCTATTTACATGTATTCAGGTGTTCTTCAAAGCTGGTCTTCTGGGTACTCTTGAGGAGATGCGTGATGAGAAACTGGCTAGTCTGGTCACAATGACTCAGGCTCTCTGCCGTGCTTACCTGATGAGGAGAGAGTTTGTGAAGATGATGGAGAGGAGGTGAGGAATTGCAAAAAATATCTTATGAGTAGTGTGTAAACAGTAATAAAGTTATGA
Associated Phenotype:
Not determined