ZMP
si:ch211-158m24.10
Ensembl ID:
ZFIN ID:
Description:
Novel myosin family protein [Source:UniProtKB/TrEMBL;Acc:B8A559]
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 |
---|---|---|---|
sa12688 | Nonsense | Available for shipment | Available now |
sa14985 | Nonsense | Available for shipment | Available now |
sa31459 | Nonsense | Available for shipment | Available now |
sa20462 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12688
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098111 | None | None | 232 | None | 7 |
ENSDART00000139917 | Nonsense | 664 | 1222 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 33892127)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31654359 |
GRCz11 | 5 | 32254512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGGAATGTCAAAGGCAAACAGTGAGGTTGCTCAGTGGAGAACCAAATA[T/A]GAAACTGMTGCCATCCAGCGCACWGAAGARCTTGAAGAATCCAAGTATGA
Long Flanking Sequence:
AAACTGATAAAATCTTACTTCCAAAGAATGTTTGTTACAACTTACAAAAACAAATTATTTTTTAATCAAAAATATAACCTAAAAAATATCTGAAAAGGTGAGTTTGGCCGTCAGCTGGAGGAGAAAGAAGCTCTGGTTTCTCAGCTCACAAGAGGAAAACAGGCTTTCACTCAGCAAATTGAGGAGCTTAAGAGGCAGATTGAAGAGGAGGTCAAGGTAATAATAATAATAATAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCACATTTACTATAGAGTCGGGTTAATAGTATCTGACTTGTTTCCTAGGCTAAGAACGCACTGGCCCATGCTGTACAATCAGCCCGTCATGACTGCGACCTGCTTCGTGAGCAGTTTGAGGAGGAGCAGGAAGCAAAGGCTGAGCTGCAGCGGGGAATGTCAAAGGCAAACAGTGAGGTTGCTCAGTGGAGAACCAAATA[T/A]GAAACTGATGCCATCCAGCGCACAGAAGAACTTGAAGAATCCAAGTATGAACTTTAAAAGAACTGTGTGGTTTTACTTTGGGTGACTGCATGCATTTTTATTGATGACGATGAAATATTTAACAGGAAGAAACTGGCTCAGCGTCTGCAAGAGGCAGAGGAACAAATTGAGGCAGTGAACTCCAAATGTGCATCTCTGGAGAAGACCAAACAGAGACTCCAGGGTGAAGTGGAGGACCTCATGATTGATGTGGAGAGAGCCAATTCTTTGGCTGCCAACCTTGACAAAAAGCAGAGAAACTTTGACAAGGTAAAATATGTAGTCATGTTGTGATGTGATGTTCTTTTTCAGAAAGTAGTATGAGCTTTATTCTAGAGAATACACGTTGAACAAACCTCATAGTGATATATTCCACCCTAAAGGTCCTGGCAGAATGGAAACAGAAATATGAGGAAGGTCAGGCAGAGCTGGAAGGTGCCCAGAAAGAAGCTCGTTCACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14985
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 |
---|---|---|---|---|---|
ENSDART00000098111 | None | None | 232 | None | 7 |
ENSDART00000139917 | Nonsense | 736 | 1222 | 13 | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 33892422)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31654654 |
GRCz11 | 5 | 32254807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGATGTGGAGAGAGCCAATTCTTTGGCTGCCAACCTTGACAAAAAGCAG[A/T]GRAACTTTGACAAGGTAAAATATGTAGTCATGTTGTGATGTGATGTTCNT
Long Flanking Sequence:
ATATACCACATTTACTATAGAGTCGGGTTAATAGTATCTGACTTGTTTCCTAGGCTAAGAACGCACTGGCCCATGCTGTACAATCAGCCCGTCATGACTGCGACCTGCTTCGTGAGCAGTTTGAGGAGGAGCAGGAAGCAAAGGCTGAGCTGCAGCGGGGAATGTCAAAGGCAAACAGTGAGGTTGCTCAGTGGAGAACCAAATATGAAACTGATGCCATCCAGCGCACAGAAGAACTTGAAGAATCCAAGTATGAACTTTAAAAGAACTGTGTGGTTTTACTTTGGGTGACTGCATGCATTTTTATTGATGACGATGAAATATTTAACAGGAAGAAACTGGCTCAGCGTCTGCAAGAGGCAGAGGAACAAATTGAGGCAGTGAACTCCAAATGTGCATCTCTGGAGAAGACCAAACAGAGACTCCAGGGTGAAGTGGAGGACCTCATGATTGATGTGGAGAGAGCCAATTCTTTGGCTGCCAACCTTGACAAAAAGCAG[A/T]GAAACTTTGACAAGGTAAAATATGTAGTCATGTTGTGATGTGATGTTCTTTTTCAGAAAGTAGTATGAGCTTTATTCTAGAGAATACACGTTGAACAAACCTCATAGTGATATATTCCACCCTAAAGGTCCTGGCAGAATGGAAACAGAAATATGAGGAAGGTCAGGCAGAGCTGGAAGGTGCCCAGAAAGAAGCTCGTTCACTCAGCACTGAGCTGTTCAAGATGAAGAACTCCTATGAGGAGACTCTGGATCAGCTGGAGACCCTCAAGAGAGAGAACAAGAATCTGCAGCGTAAGAATCAAACATTAAGAATAAAAATATGTGATGAATGAATGTTCTTTATGATACAGAGGATGATTTTTCTTTTTACAGAGGAGATTTCAGATCTGACAGAGCAGATAGGTGAGACTGGTAAGAGCATCCATGAGCTGGAAAAGGCCAAGAAGACAGTGGAGACTGAGAAGGCAGAGATTCAGACCGCCCTAGAAGAGGCTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31459
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 |
---|---|---|---|---|---|
ENSDART00000098111 | None | None | 232 | None | 7 |
ENSDART00000139917 | Nonsense | 983 | 1222 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 33893585)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31655817 |
GRCz11 | 5 | 32255970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACACTCTGATGCAGTCTGAGATCGAAGAGCTGAGAGCTGCTCTGGAG[C/T]AGACAGAGAGAGGACGCAAAGTGGCTGAACAAGAGCTGGTGGATGCCAGT
Long Flanking Sequence:
CCAGGTCAAGGGTGAGATTGACAGGAAGCTTGCAGAGAAGGATGAGGAGATAGAGCAGATCAAGAGGAACAGTCAGAGAGTTACTGAAGCCATGCAGAGCACTCTGGACTCTGAAGTCAGAAGCAGGAATGATGCTCTCAGAATCAAGAAGAAGATGGAGGGAGACCTTAATGAAATGGAGATTCAGCTGAGCCATGCCAACCGCCAGGCTGCTGAGGCCCAGAAACAGCTCAGGAATGTTCAGTCACAACTCAAGGTATGACTTTGTTGTGTCATTGGGGCACATATATGTGTTTGTTTAAGCTAAACTATGTTAAGTAAAAGTCAACTGAAACCAGATAAAAATTTGCTTACAAAGATGTTGTTGTGTTCAGGATGCCCAGCTGCACCTTGATGATGCTGTGAGAGCACAGGAAGACATGAAGGAGCAGGTGGCCATGGTGGAGCGCAGAAACACTCTGATGCAGTCTGAGATCGAAGAGCTGAGAGCTGCTCTGGAG[C/T]AGACAGAGAGAGGACGCAAAGTGGCTGAACAAGAGCTGGTGGATGCCAGTGAGCGTGTTGGACTTTTGCACTCTCAGGTAAAAGAACAATGTTTATGTTTTTGGACATTAAGATAACTGAAAGCATTTTTCAAGACTTTTATTGTTGCTTTACATGTTGTAGAACACAAGTCTTCTGAACACGAAGAAGAAGCTTGAGTCTGACCTTGTTCAGATCCAAAGTGAAGTTGAAGACACTGTACAGGAAGCCAGAAATGCTGAGGAGAAGGCCAAGAAGGCCATCACTGATGTGAGCAACAAAACATAGCAAATATACCACAAAGAACGGATAAACTTAAAAATGTGAAACAAATGCATTTCTGTATGTTTGCAAAAGGCTGCAATGATGGCAGAGGAGCTGAAGAAGGAGCAGGACACCAGTGCTCACCTTGAGAGGATGAAGAAGAATCTGGAGATCACAGTGAAAGACCTGCAGCACCGTCTGGATGAAGCTGAGAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20462
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 |
---|---|---|---|---|---|
ENSDART00000098111 | Nonsense | 146 | 232 | 4 | 7 |
ENSDART00000139917 | Nonsense | 1135 | 1222 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 5 (position 33894339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31656571 |
GRCz11 | 5 | 32256724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGAGACGTGGAGCTGATGCTGTTAAAGGCGTCCGCAAATATGAGAGG[A/T]GAGTCAAGGAGCTCACCTACCAGGTAAAGACATCAGAGCACAAATTTTTA
Long Flanking Sequence:
ATGCTGAGGAGAAGGCCAAGAAGGCCATCACTGATGTGAGCAACAAAACATAGCAAATATACCACAAAGAACGGATAAACTTAAAAATGTGAAACAAATGCATTTCTGTATGTTTGCAAAAGGCTGCAATGATGGCAGAGGAGCTGAAGAAGGAGCAGGACACCAGTGCTCACCTTGAGAGGATGAAGAAGAATCTGGAGATCACAGTGAAAGACCTGCAGCACCGTCTGGATGAAGCTGAGAATCTGGCCATGAAGGGAGGAAAGAAACAACTCCAGAAACTGGAGTCCAGAGTAAGCAGGATTTGTTTCCCGTGTTAATCATTAATATCTAAATAGTATGTCAAGTTGAACACCTTTTTTGAGAAAATTCAGGAAAGCAACATATTTGGGTAAGGTTCAGCAAAGTATCTCCATTAGGTTCGTGAGCTTGAGAGCGAAATCGATGCAGAGCAGAGACGTGGAGCTGATGCTGTTAAAGGCGTCCGCAAATATGAGAGG[A/T]GAGTCAAGGAGCTCACCTACCAGGTAAAGACATCAGAGCACAAATTTTTATCAAATGAATATAAAATAATTTATGTTCGCTTTATGCAGACTGAGGAGGACAAGAAGAACATCAACAGGCTGCAGGATCTGGTTGATAAGCTTCAGCTGAAGGTCAAGGCTTACAAGAGACAGTCTGAAGAAGCTGTGAGTTCCTCTTTTGAGAACTTAGACACCTGTGAACTTTCAAGATGTTCTTTTACTGATACAGTTGAATGTGACTTTGCAGGAGGAACAAGCCAACTCTCACCTGTCCAAGTTGAGGAAGGTGCAGCATGAGCTGGAGGAGGCTGAGGAGCGCGCTGACATTTCTGAATCCCAGGTCAACAAGCTCAGAGCCAAGAGCCGTGACGCTGGAAAGGTCAGTTGCATATTACTAGATTCTGTACATTTACTCAGAAGAAAAATGAATTCTTGAATATACACTGATTATTTACATGATTTACATGATATGATTTTTTT
Associated Phenotype:
Not determined