ZMP
smyhc2
Ensembl ID:
ZFIN IDs:
Description:
slow myosin heavy chain 2 [Source:RefSeq peptide;Acc:NP_001096096]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11877 | Nonsense | Available for shipment | Available now |
sa24570 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11877
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 |
---|---|---|---|---|---|
ENSDART00000056849 | Nonsense | 18 | 1939 | 3 | 39 |
ENSDART00000124862 | Nonsense | 18 | 169 | 3 | 5 |
The following transcripts of ENSDARG00000071433 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 42283399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 891910 |
GRCz10 | 24 | 40999078 |
GRCz11 | 24 | 40698872 |
GRCz11 | KZ115969.1 | 6295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGGGATGCTGTGATKGCAGAGTTTGGGCCTGCGGCTCCGTTCTTACGT[A/T]AATCAGATAAGGAGCGTCTGGAGGCCCAAACTCGTCCTTTTGACATGAAG
Long Flanking Sequence:
ATATATTATTATATTATATGATGTTATATTAAATTATATTATAATATATTTTAATATATTATATAAATTAATATTTTATTATTTTATATTAACTTATATTAAATTAAATATTAAATTATAAAATATAAATTAATATATTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATACTAAAATAATATATAATATTACTGGTTGTCTTCATCACAGAAATATTACTTTTATCATTGCTGACTTTAGTATTATTATAATGATTATGAATGCTAAATATTATTTAAATATCACCAATAATATTCTGATTGTCTTGGCTTCATTTCTGTTGTTTTACTATTTATGTGTTCTGTGTTAATAAAACAGCATATTAATAAATCAGAGAATATCGTCATCTCTTCCGCAGATTGACTGAAAGATGGGGGATGCTGTGATGGCAGAGTTTGGGCCTGCGGCTCCGTTCTTACGT[A/T]AATCAGATAAGGAGCGTCTGGAGGCCCAAACTCGTCCTTTTGACATGAAGAAGGAGTGTTTCGTGCCTGATCCCGAGGTTGAGTATGTCAAAGCCTCCGTCACCAGTAGAGACGGTGATAAAGTCACTGTTGAGACTGAATTTGGGAAGGTAAGGTCTAATTTATGCACTTATATTTTACAATATTGAACGCTTATTCAGGTTTTTTACTGTCAAAACTTTGTTATCCACAGACCGTCACTGTGAAGGAGGTTGACTGTCACCCTCAGAACCCGCCAAAGTTTGATAAGATTGAGGACATGGCGATGTTCACCTTCCTGCACGAGCCTGCTGTGCTGTTTAACCTCAAAGAGCGTTACGCAGCCTGGATGATCTACGTGAGTGGAGTCTTAAAACACTCTCACACTCACTTTATGATGGAGGAGCAGATCTAAAGCTGCTGTCGATCTCTTCCAGACCTACTCTGGCCTCTTCTGTGTCACTGTCAACCCCTACAAGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24570
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056849 | Nonsense | 372 | 1939 | 12 | 39 |
ENSDART00000124862 | None | None | 169 | None | 5 |
The following transcripts of ENSDARG00000071433 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 42276408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40992087 |
GRCz11 | 24 | 40691881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCATGCACTACGGCAACATGAAGTTCAAGCAGAAGCAGAGAGAGGAA[C/T]AGGCCGAGGCTGATGGCACTGAGGGTCAGAACAATTTGAAACCTCAGCTT
Long Flanking Sequence:
CAATTAAGACTTTTTATTAACTTTTAAGGGCCCTAATTGTCTCATAATTGATTTATCAGCTTTCAATACTTTTTAAGACCCCGCGAACACCCTGTATTTTAGGCCGCAACAATCTAAAATATTTTGCACAAAATCCAGGAGGAACTGACTGATCACTGAGCAGACAAATACAGCCAAAGCATAGAAAACAATTGTACAATTTAAAATGGCAAATAAATTTCTCAGATACTCCATGGCACGGGCAAAGAATGAAAACTAATATTCAATAAATTGTAATATCTGGAATTGACTTTTACATTTCCATGACTTGTGGAATCCCAGATTTTAAATCCAAAATGCACAATTCTGTCATTCTAGCACCTTTGACCTTTGTGTATATGTTGCAGGAAGCGTTTGATGTGCTGGGCTTCACCCAAGAGGAGAAGAACAGCATCTACAAGCTGACTGGTGCCATCATGCACTACGGCAACATGAAGTTCAAGCAGAAGCAGAGAGAGGAA[C/T]AGGCCGAGGCTGATGGCACTGAGGGTCAGAACAATTTGAAACCTCAGCTTCATAAAATGAATATATGTTTTATCTGAAGTTGTAGCACTGTATTGCTACATTAACATTGCTGTATCAACATGTAGATGCTGACAAAGTCGCTTATCTGATGGGCCTGAACTCTGCTGACCTCATCAAGGGTTTGTGCCATCCAAGAGTCAAAGTAGGAAATGAGTGGGTCACCAAAGGACAGAATGTCCAACAGGTAAAGAGACATCACATTATTTACCACTGATACAGCCACCTAAATCATGCAATATATTATTACAGTGGTTCTCAAACTGTGGTACGCGTACCACTAGTGGTACGCGGGCTTCCTCCAAGTGGTACGCGGAGGAACCGCTGAATAATGAAAGAAACAATTAACACTTTTAATGCTTTAATGCGTAATATAACATCGATGTGATCAGCATTGGCTGTTTTGTGAAGCGTACGATCACAACGCTGTGCTTAGAATGTTT
Associated Phenotype:
Not determined