ZMP
myh9a
Ensembl ID:
ZFIN IDs:
Description:
myosin, heavy chain 9, non-muscle, like-2 [Source:RefSeq peptide;Acc:NP_001091647]
Human Orthologue:
MYH9
Human Description:
myosin, heavy chain 9, non-muscle [Source:HGNC Symbol;Acc:7579]
Mouse Orthologue:
Myh9
Mouse Description:
myosin, heavy polypeptide 9, non-muscle Gene [Source:MGI Symbol;Acc:MGI:107717]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33805 | Essential Splice Site | Available for shipment | Available now |
sa20632 | Nonsense | Available for shipment | Available now |
sa2301 | Nonsense | Available for shipment | Available now |
sa18153 | Nonsense | Available for shipment | Available now |
sa33804 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5350 | Nonsense | F2 line generated | Not yet available |
sa15720 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33805
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011353 | Essential Splice Site | 171 | 1046 | 4 | 25 |
ENSDART00000105232 | Essential Splice Site | 175 | 1960 | 3 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7682045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7608061 |
GRCz11 | 6 | 7765230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTTCTTTTTCATCTTTAGATCGTGAGGATCAGTCCATATTGTGCAC[G/A]TAAGCTTGACGACCTCCTTTTTGTTCTTTGTTTAATTAAAAAAAGTCACA
Long Flanking Sequence:
TCAAATGCTAAATGTAGCTTGTGATGACTAGGAATGTATATTTGATTCGACCAAATTTTAAGGCAGCAAGAATTTTTACAATTTTTAATAAATTTTTTTAAAAGTGCATGTTTCTCCATTAGTCTCATCATTAAACTGAGAATCATGCAAACTTGAGCTTTGTGTTCGAGAAGAGTGGCTTTATACAAATGTGCGTTTTGTCTAATGACTGCTTGTAAACGACTGTTTCAGACATATTCTGGGCTCTTCTGTGTGGTAATAAACCCATACAAGTACCTGCCCATTTACACAGAAGAGATCGTGGAGATGTACAAAGGCAAAAAGAGGCACGAAATGCCCCCTCATATCTACGCCATCACAGACACGGCCTACAGGAGCATGATGCAGGGTGAAGACATGAACCATGACATAATGACAGACTTCCGTTCATGTGATGCAGTCACTTAAATATGTTTTTCTTTTTCATCTTTAGATCGTGAGGATCAGTCCATATTGTGCAC[G/A]TAAGCTTGACGACCTCCTTTTTGTTCTTTGTTTAATTAAAAAAAGTCACATATCTTTAAGTACATTTTAAATATGGAAATTTAATATTTATTTTGAGCTACAAGGGTTTGCATAAAAGTGAAATGAAGTCCTGGGGTCTGCATAGTCTTTATATTAGGAGTTACTGGTGATGATATTAAATCCATATAAAGTGAAATGGGTTCAAGCTTGGCATGGCACGGCACTTAAGCATTAAAATGTCACTTTCCATTATTTCCTCAGGGGTGAATCTGGTGCTGGAAAAACCGAAAACACCAAAAAAGTCATTCAGTACCTCGCTTATGTTGCATCATCCTTCAAAACAAAGAAAGATCAAGTGAGTACAGACTTACTTTTTCCCTCTGTGTTGGATTGATGGTGTGTGCATGACATGCAGTAGTATATTCACAGGATTTCAGTTTTGAATCTGTCATGCTCTTGTGTGCAAGGTGGATTTAGAGTCAATGTTGATTTGTGTGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20632
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 |
---|---|---|---|---|---|
ENSDART00000011353 | Nonsense | 360 | 1046 | 11 | 25 |
ENSDART00000105232 | Nonsense | 357 | 1960 | 9 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7676631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7602647 |
GRCz11 | 6 | 7759816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCTGAAGGTGGTGTCTGCTGTATTACAGCTGGGAAACATGAGTTTT[A/T]AAAAGGAACGCAACTCTGACCAAGCCTCCATGCCCGATGATACAGGTTTC
Long Flanking Sequence:
TAATAGCCATAGGAAGAATTAAACAGACAATTCACTCTGTATTCTAAGGCTGATCTATACAGAACGTTTTCAAGTTTGTTTTGTACTCTACAGCTGAGCTGTGCCTAGAGGACTACAATAAGTACCGTTTCCTGTCAAATGGAAATGTAACTATCCCTGGACAACAGGATAGAGAACTGTTTGCAGAAACCATAGATGCCTTCAGGATTATGGGCATCCCGGAGGATGAGCAGACAGGTATAGAGATTCAAACAAGGCACTTTTTCATCTGTAGTCTACAGTGTTTGTAATCACCTAAAGCCATGATTCTGAAAAAAAATTCTACTCAGAACTGTATTGGCTTTATATTAACTGAACCTGAAGATAAGATTTTCATTCACTAGCGGCTGATGTGTTGGTTACTGCCTCTTATGTAAGAGGAAATGTAATGTGTGTTTTGTTTTGTCCCAGGACTTCTGAAGGTGGTGTCTGCTGTATTACAGCTGGGAAACATGAGTTTT[A/T]AAAAGGAACGCAACTCTGACCAAGCCTCCATGCCCGATGATACAGGTTTCGTTTTCCTTAAGATGCGCTACTTGTCCCAATTGAACTTCATTACAACTAGAGATTGACTTTTTTTTTTTTTGACCTGTTGATGCTGGTTTTTATTGATTCCTATCTTTTTTGTAATTGATAGTGTATACATGCAACACATTTTTTTTGTTGCACTTTGTCATAATAAAGGATTGATTACAGAAATGGTTAATTTTAAAATTAATTACCTTTTTTATATTCATTGTTAAAATAAATTAGTTGTCCCAAAACTTTTCTGTTTTCACAAAGGTCCAAAGATATATGCTAAAGAAATTGACATTTTATATTTGAATTAACATTTGTTATAGTTTTGTTCTATTTTATAGATGCTATTTTTTCCCCTAATGCTTTTAATCTGGTTCCGGTAAAACTTTACCATGATTAATGATTTCTCTCTCTAATAGTTCTGACCGTTTTTAGCAGATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2301
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 |
---|---|---|---|---|---|
ENSDART00000011353 | None | None | 1046 | None | 25 |
ENSDART00000105232 | Nonsense | 1055 | 1960 | 23 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7669394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7595410 |
GRCz11 | 6 | 7752579 |
KASP Assay ID:
554-2806.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAAAGGAAGAGAAAATGAGGCAGGAGTTGGAGAAGAACAGGAGGAAGT[T/A]GGAGGGCGACTCTACAGAGCTGCATGATCAGATCGCAGAGCTGCAGGCTC
Long Flanking Sequence:
TTGTTTTTAGTTGTACATTTATTGAAATGTTCTTGCCATGAAAATATCCTTGGTTGCTGACATGTTATTAAATAAAATGCATCCATTTATCTGCTGCAGAAACGCTTTTTTCTTAGTCAGGATGGTGATGTTTGTTTGTGGGTTTCTGTATTAACAGGAGAAAAAACAGATGGAGGAGAGAATCTCCGAATTCACCACTAACCTGGCTGAAGAGGAGGAGAAATCAAAGAGTCTGCAGAAACTGAAGACCAAACATGAGACCATGATTACTGACCTGGAGGGTAAATATATTTGCATTCCTGAAATAATGCAGTACTTTTTTTGGAAACGCTCTTTCATTTAAAGACAGCCCAAGAGTCCTAGGAATAAACTTGGCTATACAGTATGTTCATATATCTTTCAGGTTTTGTTACTTTGTCATACTTTGTTGTTCTTGCTCTCAGATCGTTTAAGAAAGGAAGAGAAAATGAGGCAGGAGTTGGAGAAGAACAGGAGGAAGT[T/A]GGAGGGCGACTCTACAGAGCTGCATGATCAGATCGCAGAGCTGCAGGCTCAGATTGCAGAGCTCCGGGCCCAGCTGGCCAAGAAAGAGGAAGAGCTCCAGGCTGCATTAGCAAGGTGACAATGTTTTGGTGATGTTAGTTGCAACATTAGATTGCAACAAGTTTTTTTTGTTTTTTTTTAACTACATATTGATGTGTCAATCACTTTAATTTTTACCATGTAATGAGTTCACTTAACAGGGTAGGGTTGAAATTATTAATTGAGTATGAAATTTAAAGGATTAGTCAGCATCAGCAATAGAAAGTTTACATGTTTATCCATAATCCACTCATTCATTCTTTTCATCCCTCATCCATCCACCCATTTATCCATTGATTACTCCCATCTTTCCATCCACCAATAATTCCATCCATTCATTATTTCTTTCATAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTACTTCTATCCTCAATTCCTTATCCAGCCATCCAGCCTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18153
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011353 | None | None | 1046 | None | 25 |
ENSDART00000105232 | Nonsense | 1411 | 1960 | 29 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7664846)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7590862 |
GRCz11 | 6 | 7748031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGAGGTGGAAAGTGTCCKGCAGCAGTTGGAGGAGAGAAATGCCAGCTA[C/A]GATAAACTGGATAAGACCAAGACACGTCTGCAGCGGGAGCTTGATGATGT
Long Flanking Sequence:
AGTCCACAGCAAGAAGTTTTTTTGGGTTGGTGATTATGGGTTTATTGTCTTGCTTTTTTGTGTGTCAAAGGCATTGTATAGAAGTTAGAAACTGCAATATTGTGACATTTGCCATTGTGTGTTGTTAAGGCATTGCTAGAGGAAGAGACCAGGCAGAAGCTGGCGATCTCCACTCGTCTTCGGCAACTGGAGGATGAACAGAACAATCTCAAAGAGATGCTGGAGGAGGAAGAGGAGAGCAAGAAAAATGTTGAAAAGCAGCTGCACACCGCTCAAGCTCAGGTGTGTGCTTTTTTTGTTTTATAACGCTCCACTAAAAGCATTAGATTTTTTTGATTATATATTTTCTAAGCTGCTTCCTTTGTTTTTAAGTTGGCAGAGATGAAGAAAAAGATTGAGCAAGAGGCACAGAGCCTGGAAAGCATGGAGGATGGGAAGAAGAAATTGCAGAGGGAGGTGGAAAGTGTCCTGCAGCAGTTGGAGGAGAGAAATGCCAGCTA[C/A]GATAAACTGGATAAGACCAAGACACGTCTGCAGCGGGAGCTTGATGATGTCCTGGTTGACCAGGGTCACCTCCGGCAGACAGTGCAGGAACTTGAACGCAAACAGAAGAAGTTTGACCAGGTAGAGGACTTATTTTCAGAAAATTGCTTTTTTGCGAGTGAAAAAGAGCATAGAAGTAGGCTTGTGAAGGTTTTGCACACATACACTTTGAAATTTAACATTGTTATACAAAATAAATAAAACAATATATTGTATTCCACATACAAAAATACATAAGTACACATCAATCAATCAGTAGAGAGAGAGGGATTTGCTTGTGCCAGTGTATGGTTTTGTTCCAGAAACTGTATAAACAGATCCCAAATTTGATAGTACTCTTTTAATTGGCCCTTATACTGTAGGTAATTCTTTCCAGAGTAATGTAATGTCAAATCTTTCAGCCAGTGGTCAATGGATTGACTTTCTATTTTCTTCCAACGAAGTTCTATCAAACCTCTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33804
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011353 | None | None | 1046 | None | 25 |
ENSDART00000105232 | Nonsense | 1670 | 1960 | 33 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7659672)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7585688 |
GRCz11 | 6 | 7742857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGAGAGAGTTTGAGGATCTCCGTCTGTCCAGAGATGAGTCTCTTAAC[C/T]AGGCCAAAGAAAACGAGCGCAAGATCAAGAGCATGGAAGCCGAGATCATG
Long Flanking Sequence:
TTGTGTGGGTTTCCCTCGGGTTCTCTGGTTTTCTCCCACAGTCGAATAACATTCGACTGGTTAATTGACCAAACCACATTGGCGCTATAGATGAGCTCTTAATCAGCAGTATATCTCTACATTGCAATCTCTAATTTGTCATTGGCCATAAATAAGCAGGGGCGTTCTCGAGGCTTACCTGAGCTCAAACTCCCCTCTGACCCTGCAAATAGGAGGGAGCCCCGGGCTCCAGGATTTTATAAGCTCAGAGCTTGCTCCCAGGACAGCATGTCAAACAAGCTTTTATAATCAATCATGAGCTAAGTGTGAACTCTTGAAATAAATCACATATTTACTGATGTGAGACATTGAAAAATTGACCCTTTGAATAATAGAAGGGTAAACCGTCTGTTAGGTATAGATCTAACATTGCAAGTCCCTCCCTTGTGTTTCAGGCTCAGATGAAAGAACAGATGAGAGAGTTTGAGGATCTCCGTCTGTCCAGAGATGAGTCTCTTAAC[C/T]AGGCCAAAGAAAACGAGCGCAAGATCAAGAGCATGGAAGCCGAGATCATGCAACTACATGAGGTTTGTCTTGCATTTTTTTAAGGATGTATCTGAATTGCACTGCAGCTTAAACTTTAAGTACTTTAGGGTCAATTCAATTTTAAGGATGTCAGTGTCCTGTTTTTTCTCCTGGAAGGTCATCCTTCACAGTTTAGCTTCAGAATCCATCAGAAACTGATTTAAGCACTCCTTGTTTAAAGGGAGTTTTTCAGGAAAACTCAGTCATGTGTAAAATGTTTGCTTTTCTATCTCTGTAGGATCTGGCTGCTGCTGACAGAGCAAAGAGACAAATCCAGCAAGAGCGAGATGAGTTACAGGATGAGATCAATAGCCAGAATGCCAAGAAGTGAGTTTACCTGCTGTTATTGTGATGTATCGTCTGGTAGGGTGTCCTGCATCACACTCCTACAAAATCAAAGTGCATCTTACCCTGTTGACTAATGTTGTTGTATTTCTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5350
Status:
F2 line generated
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011353 | None | None | 1046 | None | 25 |
ENSDART00000105232 | Nonsense | 1684 | 1960 | 33 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7659630)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7585646 |
GRCz11 | 6 | 7742815 |
KASP Assay ID:
554-3483.1 (used for ordering genotyping assays)
KASP Sequence:
CTCTTAACCAGGCCAAAGAAAACGAGCGCAAGATCAAGAGCATGGAAGCC[G/T]AGATCATGCAACTACATGAGGTTTGTCTTGCATTTTTNNAAGGATGTATC
Long Flanking Sequence:
CGAATAACATTCGACTGGTTAATTGACCAAACCACATTGGCGCTATAGATGAGCTCTTAATCAGCAGTATATCTCTACATTGCAATCTCTAATTTGTCATTGGCCATAAATAAGCAGGGGCGTTCTCGAGGCTTACCTGAGCTCAAACTCCCCTCTGACCCTGCAAATAGGAGGGAGCCCCGGGCTCCAGGATTTTATAAGCTCAGAGCTTGCTCCCAGGACAGCATGTCAAACAAGCTTTTATAATCAATCATGAGCTAAGTGTGAACTCTTGAAATAAATCACATATTTACTGATGTGAGACATTGAAAAATTGACCCTTTGAATAATAGAAGGGTAAACCGTCTGTTAGGTATAGATCTAACATTGCAAGTCCCTCCCTTGTGTTTCAGGCTCAGATGAAAGAACAGATGAGAGAGTTTGAGGATCTCCGTCTGTCCAGAGATGAGTCTCTTAACCAGGCCAAAGAAAACGAGCGCAAGATCAAGAGCATGGAAGCC[G/T]AGATCATGCAACTACATGAGGTTTGTCTTGCATTTTTTTAAGGATGTATCTGAATTGCACTGCAGCTTAAACTTTAAGTACTTTAGGGTCAATTCAATTTTAAGGATGTCAGTGTCCTGTTTTTTCTCCTGGAAGGTCATCCTTCACAGTTTAGCTTCAGAATCCATCAGAAACTGATTTAAGCACTCCTTGTTTAAAGGGAGTTTTTCAGGAAAACTCAGTCATGTGTAAAATGTTTGCTTTTCTATCTCTGTAGGATCTGGCTGCTGCTGACAGAGCAAAGAGACAAATCCAGCAAGAGCGAGATGAGTTACAGGATGAGATCAATAGCCAGAATGCCAAGAAGTGAGTTTACCTGCTGTTATTGTGATGTATCGTCTGGTAGGGTGTCCTGCATCACACTCCTACAAAATCAAAGTGCATCTTACCCTGTTGACTAATGTTGTTGTATTTCTCACTAAGCTCACTGAGCAGCGACGAGAGGAGGAGATTGGAAGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15720
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 |
---|---|---|---|---|---|
ENSDART00000011353 | None | None | 1046 | None | 25 |
ENSDART00000105232 | Nonsense | 1891 | 1960 | 38 | 39 |
Genomic Location (Zv9):
Chromosome 6 (position 7656045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 7582061 |
GRCz11 | 6 | 7739230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTGAAGCAGATGAAGAGGCAGCTGGAGGAGACTGAGGAGGAAGCGGCT[C/T]GAGCAAACGCCTCCTGCAGGAAACTGCGGAGAGAGCTGGAGGAYGCCACT
Long Flanking Sequence:
TAGCATGTGTGGTGCACTTAAAATAGAAAATACTTTAAGCTAGTTAAAGTGGAAATAATAAATGCATACTTAAATAAAAGATGGAGTGGGTTCAGTCAGTGTTCAATCAACAAATCATTACATGAACACCATGTCTGCTACTACTGGGGTAGGGTGGGGGGGAGGGGGTTTGTAGCCTAAATGTTTGTATTAAATTTAAAATAATTCTTTCTAAAGCTAATTTCTATCAAGGAGTTCTTATTATTTATGGTTTGATTGGGAGAAAAAATTAACATCTCAAAATTAAAGGCCTGTCTTGTCTTTACTCCTAGTAATTTTATTTAAGTCTTATTCATGCATTTTAAGAGGTCTGCGAATTTGTTTGATTTTTCATATTATTTATAACCCTGTACCTGGAGTTCCTTTCCTAATGAACTGTTGCTCTTTGTCAGACTGAGAAGGCGAACATTCGTCTGAAGCAGATGAAGAGGCAGCTGGAGGAGACTGAGGAGGAAGCGGCT[C/T]GAGCAAACGCCTCCTGCAGGAAACTGCGGAGAGAGCTGGAGGACGCCACTGAATCTGCTAGTGCCATGAACCGGGAGGTCAGCACCCTCAAGAACAAACTCAGGTACTGGGACACGGATGATCATCCTTCAGGAAATATCACTTGAAAATCTGCAATTAATAGCAACAAATCAGTCTAAAATGTTTTGTATTTTCTTCCGGAAACGATTATAATATTTTTGTGTTGTATTCAGTCTATACATGCCGAATTAGTCACGTCCGGCAGATTTATTCCTATTTATTGAAGATGATGCAAGTCCAATGTGTAACCTCGATCAAGCCTTTCACCATAAAACATGTTTTATTTGAATGTGACATTTTAAAGACTCCTAGAAAAGATTTTTATACCGAGTGAGAGCATTTAAAAGTATAAACTCACAGGCCACTTTATTAGGCACACCTGTCCAACTGCTTGTACTGGTATTTCCACGCACAACCATCTCTAGGGTTTACAGAGAATA
Associated Phenotype:
Not determined