ZMP
smyhc1
Ensembl ID:
Description:
slow myosin heavy chain 1 [Source:RefSeq peptide;Acc:NP_001018343]
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 |
---|---|---|---|
sa12384 | Nonsense | Available for shipment | Available now |
sa24569 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12384
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 |
---|---|---|---|---|---|
ENSDART00000004536 | None | None | 943 | None | 21 |
ENSDART00000045928 | None | None | 939 | None | 21 |
ENSDART00000056853 | Nonsense | 1581 | 1939 | 31 | 37 |
Genomic Location (Zv9):
Chromosome 24 (position 42242729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40958408 |
GRCz11 | 24 | 40658202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAGTTGGAGTTCAATCAGGTMAAAGCTGACATTGAGCGTAAGCTGTCT[G/T]AGAAAGATGAAGAGATGGAGCAGGCCAAGAGRAACCAGCAGAGAGTGGTG
Long Flanking Sequence:
AAAGTGCCCAGAAAGAGTCCAGATCTCTGAGCACTGAACTGTTCAAGCTGAAGAACTCGTATGAAGAGGTCCTGGATCAACTTGAGACTATGAAGAGAGAGAACAAGAACCTTCAAGGTATGTATTTTGGTTAACTACAAGATTAACAGATGCTACCATCAGCAAATGTTTGCTTAACAGTTATTCTTCTGTTTAACAGAGGAAATCTCTGACCTTACTGAGCAACTCGGAGAAACCGGAAAGAGCATCCATGAGTTGGAGAAAATCAGAAAGCAGTTGGAGCAAGAAAAAGCAGAGATCCAGACAGCCTTGGAAGAGGCTGAGGTAACCGTGAATGATCATTTCCTATTATGTTATTTACATTAGATTAATTTAAGACTAATGACTTAAAATGCTTTCCTTCATACTTAAAGGGTTCTCTTGAACACGAGGAAGGCAAGATCTTGAGAGCTCAGTTGGAGTTCAATCAGGTCAAAGCTGACATTGAGCGTAAGCTGTCT[G/T]AGAAAGATGAAGAGATGGAGCAGGCCAAGAGAAACCAGCAGAGAGTGGTGGATACCCTGCAGAGTTCACTGGAATCAGAGACTCGCAGCAGGAATGAAGCTCTCAGACTGAAGAAGAAGATGGAGGGAGACCTCAATGAGATGGAGATTCAGCTCAGCCAGGCTAACAGGCAGGCATCAGAAGCCCAGAAGCAACTCAAGGGTCTTCATGGACATCTCAAAGTATGAAGTGTCTTCATATCAAGATCTTATGATCCCTAACCCTAAAATTCAGAATAGCATTAATTTGTAAGCTTGTATTTTGTAGGATGCCCAACTGCAGCTGGATGACGCTCTGCGTGGCAATGATGATCTCAAAGAGAACATCGCCATTGTGGAGAGACGCAACAATCTGCTGCAGGCTGAACTGGATGAGCTGAGATCCCTGGTGGAACAGACTGAGAGAGGAAGGAAACTGGCTGAGCAGGAACTGATGGACGTCAGTGAGAGAGTTCAGCTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24569
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 |
---|---|---|---|---|---|
ENSDART00000004536 | None | None | 943 | None | 21 |
ENSDART00000045928 | None | None | 939 | None | 21 |
ENSDART00000056853 | Nonsense | 1616 | 1939 | 31 | 37 |
Genomic Location (Zv9):
Chromosome 24 (position 42242624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40958303 |
GRCz11 | 24 | 40658097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTGCAGAGTTCACTGGAATCAGAGACTCGCAGCAGGAATGAAGCTCTC[A/T]GACTGAAGAAGAAGATGGAGGGAGACCTCAATGAGATGGAGATTCAGCTC
Long Flanking Sequence:
AGAACCTTCAAGGTATGTATTTTGGTTAACTACAAGATTAACAGATGCTACCATCAGCAAATGTTTGCTTAACAGTTATTCTTCTGTTTAACAGAGGAAATCTCTGACCTTACTGAGCAACTCGGAGAAACCGGAAAGAGCATCCATGAGTTGGAGAAAATCAGAAAGCAGTTGGAGCAAGAAAAAGCAGAGATCCAGACAGCCTTGGAAGAGGCTGAGGTAACCGTGAATGATCATTTCCTATTATGTTATTTACATTAGATTAATTTAAGACTAATGACTTAAAATGCTTTCCTTCATACTTAAAGGGTTCTCTTGAACACGAGGAAGGCAAGATCTTGAGAGCTCAGTTGGAGTTCAATCAGGTCAAAGCTGACATTGAGCGTAAGCTGTCTGAGAAAGATGAAGAGATGGAGCAGGCCAAGAGAAACCAGCAGAGAGTGGTGGATACCCTGCAGAGTTCACTGGAATCAGAGACTCGCAGCAGGAATGAAGCTCTC[A/T]GACTGAAGAAGAAGATGGAGGGAGACCTCAATGAGATGGAGATTCAGCTCAGCCAGGCTAACAGGCAGGCATCAGAAGCCCAGAAGCAACTCAAGGGTCTTCATGGACATCTCAAAGTATGAAGTGTCTTCATATCAAGATCTTATGATCCCTAACCCTAAAATTCAGAATAGCATTAATTTGTAAGCTTGTATTTTGTAGGATGCCCAACTGCAGCTGGATGACGCTCTGCGTGGCAATGATGATCTCAAAGAGAACATCGCCATTGTGGAGAGACGCAACAATCTGCTGCAGGCTGAACTGGATGAGCTGAGATCCCTGGTGGAACAGACTGAGAGAGGAAGGAAACTGGCTGAGCAGGAACTGATGGACGTCAGTGAGAGAGTTCAGCTCCTGCATTCTCAGGTATGACACACCTGTATTAGTAAACTTCTTCTATTACACATGATCATCTGCAGACTTAATGAATGTCAACACTGTCCATGTTCAGAACACCAGCC
Associated Phenotype:
Not determined