ZMP
myo1ha
Ensembl ID:
ZFIN ID:
Description:
Novel myosin head motor domain containing protein [Source:UniProtKB/TrEMBL;Acc:A2BGM6]
Mouse Orthologue:
Myo1h
Mouse Description:
myosin 1H Gene [Source:MGI Symbol;Acc:MGI:1914674]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31422 | Nonsense | Available for shipment | Available now |
| sa40386 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40387 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa990 | Essential Splice Site | Available for shipment | Available now |
| sa40388 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33563 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20375 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31422
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 |
|---|---|---|---|---|---|
| ENSDART00000089014 | Nonsense | 192 | 1036 | 5 | 31 |
| ENSDART00000146215 | Nonsense | 185 | 1027 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21198126)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18910998 |
| GRCz11 | 5 | 19414798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGATTCTAATACACAGGGAGATGCTGTCGGTGGCCACATACTCAGTTA[C/A]CTGCTGGAAAAGTCGAGAGTGGTTCACCAAAACCATGGTGAGAGAAACTT
Long Flanking Sequence:
AAACATTTTAAAATAAATGTTTTTGTCCGTTTTTTAGTTATGCATTAGCAGATAATGCCTACCACACCATGCTATCTGAAGCCAACAACCACTTCATTTTAATATCTGGGGAGAGTGGAGCAGGCAAAACTGAGGCCTCCAAGAAGATCTTGCAGTACTATGCTGTCAGCTGCCCTAGTTCCACCTTACTGGACACTGTGCGGGACCGCATGCTCATGTCTAACCCTGTGTTAGAGGTTGGTCCAACAAAAATACTCCCAGAATAGATTTGAACATTCCCTACATATACAATGCATTCATCAAATCTGCTTTTAGGCATTTGGAAATGCAAAGACTATGAAAAACGACAACTCTAGCCGTTTTGGAAAGTATATGGACATCCAGTTTGATATCCAGGTATGAACAGATGCTAGCTTCATTCCATCGCATAATACTGCATACAGATAAACACTTGATTCTAATACACAGGGAGATGCTGTCGGTGGCCACATACTCAGTTA[C/A]CTGCTGGAAAAGTCGAGAGTGGTTCACCAAAACCATGGTGAGAGAAACTTTCATATCTTCTACCAGCTGGTGGAAGGAGGGGAGGAAGACCTGCTGCGGCAGCTAGGCTTGGAGAGGGACACTAAACGCTATTGTTATTTAGTTCAGGTATGGTTTAAATCGAAATCTGGTGTCAATATGACTACAAGCATGAACAGTTTTTCTTTTATACATTTGCTTTCTCAATAGGGAGAGTGTTCCAATGTGAGCTCCATCAATGACAAGAATGACTGGAAAACTGTTAAAAATGCGTTATCGGTCATTGACTTTGATGCTAGTGACACTGAGGTAAGGAGAGGTGATTTTTTTTTAATGCACTTTTTTTGTGTGCATGTGTATATGTGTATACAATCAAGCCTGAAACTATTCATACCCCTGACAAATTGTGACTTAAAGCTATTTTATTCAACCAGCATTTTTTGACACAGGTTTCTCCCAAAAGACCATAAGAGGCATCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40386
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089014 | Essential Splice Site | 313 | 1036 | 8 | 31 |
| ENSDART00000146215 | Essential Splice Site | 306 | 1027 | 8 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21199969)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18912841 |
| GRCz11 | 5 | 19416641 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTTATTTTTAAATATCCGTGTAACATTCCTGTTTAATGTTGATGCTC[A/C]GCTGTTAGGTGTCCATGTTCAAGTCCTTCATGGAGCTCTTACATTTAGGA
Long Flanking Sequence:
CTATCTGCAAAGTCAGACCTTACTGTCTTAATTGAATAATTAAAAATCATATTTTATTTAGGTAAAATAAGTGTAATCTAGAGGCCTCTGCCTTTCATATAAGACACTTCTGATTACAAATAATCAACTTAAAGTCAAGTTATTACTTGTTGTCCGTAAAACTTGCATAGGCAATCTGACTTTTGTCTGGTAGTGTATGCTGGATTGCTAACAGCTTTGATCATAAGGTGATCTTTTTTCTTTACCACCCTAGCATCTCTTTGGGATCATATCTAGCGTGCTTCATCTGGGGAATGTGCACTTTGATAGAGACACCAAAGGTTATGCTATTTTAAACTCTAATGCAGCGCTGAGATGGGTATCCAAGGTCAGTTTCTATTTAATATTGACTTATGACAAACAGCTTGCACTGATAGAATAGTGATTTTTTAAAGTTGCTTCAGAATGATCACACTTATTTTTAAATATCCGTGTAACATTCCTGTTTAATGTTGATGCTC[A/C]GCTGTTAGGTGTCCATGTTCAAGTCCTTCATGGAGCTCTTACATTTAGGAAGATTGAAGCCAAATCAGAGGAGGTAAAACTGGGTCATGTGTGTAATGTTTTGTCTTTTGTAAAACAGTCACTCTCCAATCAGGTGATCTTTCTGTCTTTCTGGCCCCTAGGTTCTCAGTCCATACACTGTGGATCATGCTATCTATGCCAGAGATGCTTTGGCCAAAGCCATCTATGACCGTGCTTTCACGTGGCTGGTCAACAGGATCAATGAGTCTCTAGAGAATAAAGTAAGTAAAAGTTAAATAATAATACTATTAATAACAACAAACCTGGGCGTCATGGTGGTGCAGTGGGTAGCATGATCGCCTCACAGCAAGAAGGTCACTGTTTCGAGCCCCAGCCCATAAAAAACCTGTACGTTTGATAACTTTGTAAATCTCTTGGTACAATTATGACGAATATGTTTGGTTTCATTTTAAAGAAATGGAGGTGTTGTTTCGTTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40387
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089014 | Nonsense | 389 | 1036 | 10 | 31 |
| ENSDART00000146215 | Nonsense | 378 | 1027 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21200514)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18913386 |
| GRCz11 | 5 | 19417186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTCACCACTTTTTTTGTGTTTAGGATTCTGAAAGGAAGACTGTCATT[G/T]GATTGCTTGACATCTATGGATTTGAGGTATTCACTGCTAACAGGTATGTG
Long Flanking Sequence:
TTAGGAAGATTGAAGCCAAATCAGAGGAGGTAAAACTGGGTCATGTGTGTAATGTTTTGTCTTTTGTAAAACAGTCACTCTCCAATCAGGTGATCTTTCTGTCTTTCTGGCCCCTAGGTTCTCAGTCCATACACTGTGGATCATGCTATCTATGCCAGAGATGCTTTGGCCAAAGCCATCTATGACCGTGCTTTCACGTGGCTGGTCAACAGGATCAATGAGTCTCTAGAGAATAAAGTAAGTAAAAGTTAAATAATAATACTATTAATAACAACAAACCTGGGCGTCATGGTGGTGCAGTGGGTAGCATGATCGCCTCACAGCAAGAAGGTCACTGTTTCGAGCCCCAGCCCATAAAAAACCTGTACGTTTGATAACTTTGTAAATCTCTTGGTACAATTATGACGAATATGTTTGGTTTCATTTTAAAGAAATGGAGGTGTTGTTTCGTTCTTCACCACTTTTTTTGTGTTTAGGATTCTGAAAGGAAGACTGTCATT[G/T]GATTGCTTGACATCTATGGATTTGAGGTATTCACTGCTAACAGGTATGTGTTTAGAAATATGAGCGAGAAGACAGTTTGAGATGATTTGAACCTTATGATAGCACTGTATACTGCTGGAAGTAGCCTTCACAAGATTGGGTACTCTGTTGTCATAAAAGGATGGAAATGGTCAGCAGCGATGTTCAAGTAAGTTTTGTCATGTTAAACAATGTTATTAAGGGACTAGAGCTTGGCAAGAAAAACAAGGCATTGTAAGTTGATACAAAGCAGTATGCATCAATGCTTTCACGTTTAACCAAATTCTGACCCAACCATCTAAATATTGATGAAAATAAGATACATCAGATGAGCCAGTGGTTTTTGTTCTGCTGCTGTAGCTCATCTGCTTCAAGGATTCACTTGTTGTGGATTCAAATATAGTATTTTGCATAGCTTAGTTGGAATGCTTATCTGAGTAGCCTTTTTTTCTCACACCAGTCTGGCCACTCTCATCTGACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa990
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 |
|---|---|---|---|---|---|
| ENSDART00000089014 | Essential Splice Site | 438 | 1036 | 11 | 31 |
| ENSDART00000146215 | Essential Splice Site | 427 | 1027 | 11 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21202685)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18915557 |
| GRCz11 | 5 | 19419357 |
KASP Assay ID:
554-0894.1 (used for ordering genotyping assays)
KASP Sequence:
AGTTGACGCTGAAGGCTGAACAGGAGGAGTATGAAGCAGAAGGAATCGGG[G/T]TGAGTTTATCAGTCATTCAGTAATCACGTATGCAATGAYATTCAAAGTTT
Long Flanking Sequence:
TGTTCCAATTTACATTGGATTTACTTACTTTTTAAAGTAAATTCAACTTGTTCATTTTTTTGGCAACGGTTTTACTCACTTTTTTGAGGAAACTAACTGCTGTTACAGTGTGCTTTTTAAGGTATGAAAATCTGGCAGGATAGGAAAAATCGACAATACATCGGGCTTTACTTTGACCAGCCCATCAGGCACCAACCACGCCACATTTAAACATTCTGATGCTCAATTTGAACTTAATCATGTCTACATGCCTAAATGCATTGTGTGATTGTCTGATTAGAAATTTGTATTGACAAGCTGTTAAACTTGTGTACGTAATAAAGTGGCTGATGAGTGTAGAATTTTTGTTCAATGAGTGCATATTTTTGTTAATTTTATTTCTATGTGTGTTTAGTTTTGAGCAGTTTTGTATAAACTACTGCAATGAGAAGCTACAGCAGCTCTTCATTCAGTTGACGCTGAAGGCTGAACAGGAGGAGTATGAAGCAGAAGGAATCGGG[G/T]TGAGTTTATCAGTCATTCAGTAATCACGTATGCAATGATATTCAAAGTTTATAAATCAGAGAATAACGCTCTTCACACTTTGTTAAATTGGGTTTCAGTGGGAGCCTGTTCAATTCTTCAACAATAAAATCATATGTGATCTGGTGGAGGAGAAGCACAGAGGAATCATCTCTGTGTTGGTATGAAGTTATACACGTACAATGCATTTCTCTGGCACATTTTGAATTGAAAATTATGCTGCAAAAATGTTGTTGGTACTTAGAGCTTTTGCCTTTTTTCTAGTCTAAACTTTTTTAAAAACTTAAATTAAGAAGTATATTTTAGGCCAGTGGTTCCCAAAGTGGGGGCCGGGACAATCAGGCGAGGTCGCTTGGTGATTTCCTAAAGTCAAATTTATTTTATTGAATTACAATCACCATATTTTATCCAAAACCTACAGAAGAAAAAATAGTAGTTAGTAGTTAAAAAACAACTTGCAAATAAAAAGCCATTAGTCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40388
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089014 | Nonsense | 635 | 1036 | 18 | 31 |
| ENSDART00000146215 | Nonsense | 624 | 1027 | 18 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21208820)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18921692 |
| GRCz11 | 5 | 19425492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTAGGGTTGATGGAGCACCTGAGGGTCAGGCGAGCTGGATTTGCATA[T/A]CGCCGTAAATATGAGGTCTTTCTAAAGAGGTAAACTTAAATTAATAACAT
Long Flanking Sequence:
TATTAATTGCTGCAAAGGTATAGAGTAATAATTTTCATCAAGTAATGTAATTTAAATAACAGATAAAAAAAAAATAAATAAAATACTGCTGCTGTCTCATTTAATCAGAACTGCTCTATGAAATGTGTAGGTGGCCACTCAGTTCAAGAACAGTCTCCTGCGGCTGACAGAGATTCTCACAGCTAAAGAAGCTTGGTACGTGCGCTGCCTCAAGTCCAACGACAATAAACAACAAGGTGAGGACCTCATGTAAGAATGAGAATGCATAGACTTAAATTGAACACAGCATAATTTGATGATACAGCTGGTACCAGTATAATTAAAACACATTCATTTACTTGTGTTGTCAAATGTGTTTTTATTTCGGGCAGTTAAAATTATGTTAGATTTTCCTGCGTTCTATTTAATACAGGGAAGTTTGATGAAGTTCTGGTCAGGCACCAGGTGAAGTATCTAGGGTTGATGGAGCACCTGAGGGTCAGGCGAGCTGGATTTGCATA[T/A]CGCCGTAAATATGAGGTCTTTCTAAAGAGGTAAACTTAAATTAATAACATGTAGAAGCTGTAGCAGTAAAATTCATGCACTTACAAAAATCATGTTTCTTAGGTATAAACCACTTTGTCCTGCCACTTGGCCCCATTGGAGAGGTGTACCTTCTGAAGGTGTGGAAAAGCTGGTGCAACATCTGGGCTACCAGCCTGATGAGTATAAAATGGGCAGGTGAGCTGTTCTGCTCTTTTAACTTTAGAATTTTCTACTAAACAATTGTCTTTAATTTTTTGACCACACACCCATTGTGTTCGATCTTATTAAAAGGACAAAGATATTTATACGATATGCCAGGACACTTTTTGCCACAGAAGATGCCTTTGAAATCTGCAAACATGAGCTGGGTAAGCAGCAATGAACTCGAGAGACATTTTTCTGAAATATTTATTTTTATTTGAAACTTGTGTCAATTATGTTTTATAGCTACAAAATTACAAGCCAAGTATAAAGGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33563
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089014 | None | None | 1036 | None | 31 |
| ENSDART00000146215 | Nonsense | 1020 | 1027 | 30 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21217752)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18930624 |
| GRCz11 | 5 | 19434424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCATGATTTATAAAGGCCCAAATGGACACCTGATGGTGGTGAGTGATT[T/A]AGTTTTGTATTTGTACTTGATTTAATATTATCGTTCCTATTCTTACACTA
Long Flanking Sequence:
TGTCAGTAATCTGGGCGACTCTGTGATGATCCTCCACGTTGCCTTCAATGATCCAAAACAGAAGGTGAACAAACCAGGATTCACAATAGCACTATACTCGCTACGTCGTAGCCAATAGGCTGCATGTCAGCTCCAAACTGTTTCACGGGTGCCACATTACACAATTTCATGCATAATTTGCGAGAACTAAAGTAGTTTCCTTTGTACAAGGGGGACTTGGTGCTTCAGTGTGACCATCTGTTTGAAGCTTTGACTAAGCTGGCGATGATTGCAAACAAGCAGAATAACATCACTGTTGTTCAGGGAAGGTAAATAAATAAACAAACACATTTCCAACCTGAGATGTGATGTTTTATTGCTGTGAAACATTAACATCTGATCTTTCCGCAGCATAAAGTTTGAGATCCAGGCGGGAAAACAGAATGCAGTGGACTTCAGCACTGGCCAAGAGCCCATGATTTATAAAGGCCCAAATGGACACCTGATGGTGGTGAGTGATT[T/A]AGTTTTGTATTTGTACTTGATTTAATATTATCGTTCCTATTCTTACACTATTTCATTATCAAAGGTGGCTCCACGGATCAAGTCACGATGATCTGAAGGAGGTCAGCAAGTCTGTGTATATTTCATGAGGGAAACCCTTATGGAAGAGGATATCTTTCTTCAACCCCCTATAAGGCAACACACACACATGACCAGTTTGGTATCTTTGCGGGGACTTTTAAAACTGTGAAATATTTATATATAAACCCCTTACAGGGAACATTCTGCATTTTTACATTTTGAAAGGACTTATTTTCTGTATGACGCATACAGTGTTCAGCATATATGAGTGCACCCCTCACTAATTTATCTTTTAAATTCATATTTTTAATTGGAAGCTAATATTATATTTGTGCAAATACTGTACATTAGATTAGTCAGTACTGAAGCCAAATCTAGAGCTTATCTTGCAAAATAACTTACGATAATGGTCCAAAAATTAGTACACCCAAATTTAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20375
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 |
|---|---|---|---|---|---|
| ENSDART00000089014 | Nonsense | 1036 | 1036 | 31 | 31 |
| ENSDART00000146215 | None | None | 1027 | None | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 21217838)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 18930710 |
| GRCz11 | 5 | 19434510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTATTCTTACACTATTTCATTATCAAAGGTGGCTCCACGGATCAAGTCA[C/T]GATGATCTGAAGGAGGTCAGCAAGTCTGTGTATATTTCATGAGGGAAACC
Long Flanking Sequence:
TAGCACTATACTCGCTACGTCGTAGCCAATAGGCTGCATGTCAGCTCCAAACTGTTTCACGGGTGCCACATTACACAATTTCATGCATAATTTGCGAGAACTAAAGTAGTTTCCTTTGTACAAGGGGGACTTGGTGCTTCAGTGTGACCATCTGTTTGAAGCTTTGACTAAGCTGGCGATGATTGCAAACAAGCAGAATAACATCACTGTTGTTCAGGGAAGGTAAATAAATAAACAAACACATTTCCAACCTGAGATGTGATGTTTTATTGCTGTGAAACATTAACATCTGATCTTTCCGCAGCATAAAGTTTGAGATCCAGGCGGGAAAACAGAATGCAGTGGACTTCAGCACTGGCCAAGAGCCCATGATTTATAAAGGCCCAAATGGACACCTGATGGTGGTGAGTGATTTAGTTTTGTATTTGTACTTGATTTAATATTATCGTTCCTATTCTTACACTATTTCATTATCAAAGGTGGCTCCACGGATCAAGTCA[C/T]GATGATCTGAAGGAGGTCAGCAAGTCTGTGTATATTTCATGAGGGAAACCCTTATGGAAGAGGATATCTTTCTTCAACCCCCTATAAGGCAACACACACACATGACCAGTTTGGTATCTTTGCGGGGACTTTTAAAACTGTGAAATATTTATATATAAACCCCTTACAGGGAACATTCTGCATTTTTACATTTTGAAAGGACTTATTTTCTGTATGACGCATACAGTGTTCAGCATATATGAGTGCACCCCTCACTAATTTATCTTTTAAATTCATATTTTTAATTGGAAGCTAATATTATATTTGTGCAAATACTGTACATTAGATTAGTCAGTACTGAAGCCAAATCTAGAGCTTATCTTGCAAAATAACTTACGATAATGGTCCAAAAATTAGTACACCCAAATTTAAAAGGTTATAGAAAATATTAAATACAAATTAAAAAAATAAGAAAAATCAAGAGAAAAAAAATTGAAAAATTAAGTTGAAATTTTGTAGTT
Associated Phenotype:
Not determined