ZMP
si:dkey-240a9.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myosin IE (MYO1E) [Source:UniProtKB/TrEMBL;Acc:B0S6F2]
Human Orthologue:
MYO1F
Human Description:
myosin IF [Source:HGNC Symbol;Acc:7600]
Mouse Orthologue:
Myo1f
Mouse Description:
myosin IF Gene [Source:MGI Symbol;Acc:MGI:107711]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12700 | Nonsense | Available for shipment | Available now |
| sa16214 | Essential Splice Site | Available for shipment | Available now |
| sa34373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14554 | Nonsense | Available for shipment | Available now |
| sa21261 | Essential Splice Site | Available for shipment | Available now |
| sa10240 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12700
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 |
|---|---|---|---|---|---|
| ENSDART00000113183 | Nonsense | 91 | 1096 | 3 | 27 |
| ENSDART00000148304 | Nonsense | 92 | 1095 | 4 | 28 |
Genomic Location (Zv9):
Chromosome 8 (position 20815316)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20245213 |
| GRCz11 | 8 | 20277298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCCAATATGAAAATCCACCACACATTTACGCTCTGACAGACAACATGTA[C/A]AGGAACATGATGATTGACAGTGAAAATCAGTGTGTCATTATCAGKTTTGT
Long Flanking Sequence:
ATCCATTTTAAACAAGTGACACACTTTTACAGGTTATCAACTAGGTTTTGCAGGTTGTACTAATTGTTTAAAGAAATGCATTAACTGTTGTGCAAATGTAAATAGTGTTGTGAGAAATACACCAAAGCGACTGAGAAAAAAATGTAAATACTTCACCATTTCAGTAATGTGACATGATTTGAACTGAAACGAACAGAATTTAAATTTAATTGAAGTAGATTGTTTAAATATCCTTAACTGTGGACATTGAAGACTTATATTGGGCCTGTGTTGATATCGGTGAATCCCTTCAAACAGATGCCATACTTCACTGACCGGGAGATTGAACTCTACCAGGGAGCTGTGAGTCAAATACACTGAACACCTGCCAATCAGTTAGCATTTGTATCATGCATTTTACTTTAGTATATCAGTTCTAACATTTTCCCCCTCTCTCTGCTTTCTTCTTAGGCCCAATATGAAAATCCACCACACATTTACGCTCTGACAGACAACATGTA[C/A]AGGAACATGATGATTGACAGTGAAAATCAGTGTGTCATTATCAGGTTTGTGATGCTCGTGTGATTTGCGCCAAACACGGATTTGGTGCTCTTCCTCTTCCTGTTATGTGGCACATTCGAAACCCAAACCCACATTTACATGAAAGCCACACTTCCAGGTTACCTATGAATGTTCCAAAATAAATCTGCCAGAGATCAACTTTTTCCTTTCCTTTTGTAGACTTTTTTTTGTATGCATTTTTACTTCACAGATCTTTACAACATTTAACATCTAGATAAATGCTTCATGATCATCAAGAGGCACTATGCGGAGATGCAAATATTTGATTATTTATCTGATAATCACCCTCTTTAGTCCTGTTCTCATTATTGGCAGTTCCTTCCTCCATTTTGTCATAACCACAAAAGGCTTCGCAGCAGCAGTGGTCACCATTCTTAGCATGGTTTCCTTCCTGATTTACACACGAAGAAGAGCTTGCAAATGTTGTTTCTTCGTTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16214
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 |
|---|---|---|---|---|---|
| ENSDART00000113183 | Essential Splice Site | 106 | 1096 | 3 | 27 |
| ENSDART00000148304 | Essential Splice Site | 107 | 1095 | 4 | 28 |
Genomic Location (Zv9):
Chromosome 8 (position 20815271)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20245168 |
| GRCz11 | 8 | 20277253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTAMAGGAACATGATGATTGACAGTGAAAATCAGTGTGTCATTATCAG[G/T]TTTGTGATGCTYGTGTGATTWGCGCCAAACAYGGATTTGGTGCTCTTCCT
Long Flanking Sequence:
TTTTGCAGGTTGTACTAATTGTTTAAAGAAATGCATTAACTGTTGTGCAAATGTAAATAGTGTTGTGAGAAATACACCAAAGCGACTGAGAAAAAAATGTAAATACTTCACCATTTCAGTAATGTGACATGATTTGAACTGAAACGAACAGAATTTAAATTTAATTGAAGTAGATTGTTTAAATATCCTTAACTGTGGACATTGAAGACTTATATTGGGCCTGTGTTGATATCGGTGAATCCCTTCAAACAGATGCCATACTTCACTGACCGGGAGATTGAACTCTACCAGGGAGCTGTGAGTCAAATACACTGAACACCTGCCAATCAGTTAGCATTTGTATCATGCATTTTACTTTAGTATATCAGTTCTAACATTTTCCCCCTCTCTCTGCTTTCTTCTTAGGCCCAATATGAAAATCCACCACACATTTACGCTCTGACAGACAACATGTACAGGAACATGATGATTGACAGTGAAAATCAGTGTGTCATTATCAG[G/T]TTTGTGATGCTCGTGTGATTTGCGCCAAACACGGATTTGGTGCTCTTCCTCTTCCTGTTATGTGGCACATTCGAAACCCAAACCCACATTTACATGAAAGCCACACTTCCAGGTTACCTATGAATGTTCCAAAATAAATCTGCCAGAGATCAACTTTTTCCTTTCCTTTTGTAGACTTTTTTTTGTATGCATTTTTACTTCACAGATCTTTACAACATTTAACATCTAGATAAATGCTTCATGATCATCAAGAGGCACTATGCGGAGATGCAAATATTTGATTATTTATCTGATAATCACCCTCTTTAGTCCTGTTCTCATTATTGGCAGTTCCTTCCTCCATTTTGTCATAACCACAAAAGGCTTCGCAGCAGCAGTGGTCACCATTCTTAGCATGGTTTCCTTCCTGATTTACACACGAAGAAGAGCTTGCAAATGTTGTTTCTTCGTTGCTTTCTGAATCTAAAAGCGGCTATTTTGCCACCTTTCTGCCTAGTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34373
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 |
|---|---|---|---|---|---|
| ENSDART00000113183 | Nonsense | 611 | 1096 | 17 | 27 |
| ENSDART00000148304 | Nonsense | 610 | 1095 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 8 (position 20802083)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20231980 |
| GRCz11 | 8 | 20264065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTCACGGCCCCAGAGCGAGACATCAAGTGGAATATCTCGGCTTAAGG[G/T]AAAATATTAGGGTACGACGTGCTGGATTTGCCTACCGTAGAATCTTCCCA
Long Flanking Sequence:
ACTGTTTTTCTCCTTCTGGAAAGCCCCAGCAAATTGACGTATCTCCTTTTCCCGTAACCTCAATCAACATGTTCCAAACAGCCAAAGTTATTTATTTCTTTGCCATTTCAGTGACTTCATCCAAAGCCTCTTCCCAGAAAACCTCAACACGGATAAGAAAGGTAGACCAACCACAGCTGGCTCCAAGATCAAAGTAAGAGCAGAGATCTCAATAACCTCAGCACACCTGTTAGATTTATTTCTATTTGGCGTCTTTTACTGACTGTCTGGTCCACAGAGGCAAGCCAATGAGCTGGTCAGTACACTGATGAAGTGCACACCGCACTACATACGCTGCATCAAACCCAACGAGACCAAGAGGCCCAAAGACTGGGAGGAGAGCAGGTATAATGTCATACTCGTGCAATATGATGACAGATATCATGCATGAAGCAAACCATCATGAATTTATTTTTCACGGCCCCAGAGCGAGACATCAAGTGGAATATCTCGGCTTAAGG[G/T]AAAATATTAGGGTACGACGTGCTGGATTTGCCTACCGTAGAATCTTCCCAAAGTTTTTACACAGGTGAGTAAGCTCGGAAAAAATATGTTTGGTTATAAAAATTCACAATCTTTGCAAATATGGACGTTTTAGTAGAAAAGCCGTCCAGGACTTGACTTAAGGCTCAATATATGTGTCAACAGGTTATTTGTGCAGTGAAATGTAGCTGTATTATGTGCTGCGCTCTTTCTACTGAAGATATAAAAGTGAACACAACAAAAATGGCAGCTGTTAAAAAAGCATCTGATTGTAGTGATGTGGATGTTTGCATTTCACCACTTTAAGGGATATTTCACTCAGAAATGAATATTCTGTCATCATTTACTCAGCCTTGACTTGCTTCAAACAAGATGGAGGTTTTTTTTTTTTTCAACACAAAAGAAGATATTGTGAAGAATGTTAGAAACCTATGACCATTGACATCAGTAGTAGTGTTATGATCACCAGCAATCTGCCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14554
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 |
|---|---|---|---|---|---|
| ENSDART00000113183 | Nonsense | 630 | 1096 | 17 | 27 |
| ENSDART00000148304 | Nonsense | 629 | 1095 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 8 (position 20802025)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20231922 |
| GRCz11 | 8 | 20264007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGGTACGACGTGCTGGATTTGCCTACCGTAGAMTCTTCCCAAAGTTTT[T/A]ACACAGGTGAGTAAGCTCGGAAAAAATATGWTTGGTYATAAAAATTCACA
Long Flanking Sequence:
CTCAATCAACATGTTCCAAACAGCCAAAGTTATTTATTTCTTTGCCATTTCAGTGACTTCATCCAAAGCCTCTTCCCAGAAAACCTCAACACGGATAAGAAAGGTAGACCAACCACAGCTGGCTCCAAGATCAAAGTAAGAGCAGAGATCTCAATAACCTCAGCACACCTGTTAGATTTATTTCTATTTGGCGTCTTTTACTGACTGTCTGGTCCACAGAGGCAAGCCAATGAGCTGGTCAGTACACTGATGAAGTGCACACCGCACTACATACGCTGCATCAAACCCAACGAGACCAAGAGGCCCAAAGACTGGGAGGAGAGCAGGTATAATGTCATACTCGTGCAATATGATGACAGATATCATGCATGAAGCAAACCATCATGAATTTATTTTTCACGGCCCCAGAGCGAGACATCAAGTGGAATATCTCGGCTTAAGGGAAAATATTAGGGTACGACGTGCTGGATTTGCCTACCGTAGAATCTTCCCAAAGTTTT[T/A]ACACAGGTGAGTAAGCTCGGAAAAAATATGTTTGGTTATAAAAATTCACAATCTTTGCAAATATGGACGTTTTAGTAGAAAAGCCGTCCAGGACTTGACTTAAGGCTCAATATATGTGTCAACAGGTTATTTGTGCAGTGAAATGTAGCTGTATTATGTGCTGCGCTCTTTCTACTGAAGATATAAAAGTGAACACAACAAAAATGGCAGCTGTTAAAAAAGCATCTGATTGTAGTGATGTGGATGTTTGCATTTCACCACTTTAAGGGATATTTCACTCAGAAATGAATATTCTGTCATCATTTACTCAGCCTTGACTTGCTTCAAACAAGATGGAGGTTTTTTTTTTTTTCAACACAAAAGAAGATATTGTGAAGAATGTTAGAAACCTATGACCATTGACATCAGTAGTAGTGTTATGATCACCAGCAATCTGCCAGGAGTGGATCGCTTGTAATCATAACATTACTACTGATTTCAACTACACATATTATACTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21261
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 |
|---|---|---|---|---|---|
| ENSDART00000113183 | Essential Splice Site | 873 | 1096 | 22 | 27 |
| ENSDART00000148304 | Essential Splice Site | 872 | 1095 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 8 (position 20792938)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20222835 |
| GRCz11 | 8 | 20254920 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTACGAGGAGCAAACCCGAAGCAAACTCACACTGTCTTTCAGCGACAG[G/A]TGCCCATTATCCTCCATCTCTCTCTCTCTCTCTCTCTCGTACCACTCAAG
Long Flanking Sequence:
GCCAAGTGTGATTTCGCCAAGTATAAGGCGATTCTGGATTAGCATCTATGTTGATCATTGCTCGAAAACGTAGTTCGAAACATAGTTAAATAGGGAATATATAGTTTAGAATTATATATATATATATACACAATGCTGGAAAGTTCATTCACATTCTCTTCAGTAACTGTAAATATGAATATTTACATTTAGTCATTTGGCAGACACTCATGTCCAAAGCGACCTCCATTGAGCAGACATTCAGCAAATCAACACGAAGAGGCCGTAAACACAGTGCTATTTACACAAAGGAGCTGTTGGTGCTCAGAGAATTAAATGCGTTTTATTGTAATAATCTTTTTTATTCCCTGCAGCACAAGGCAAGATGACTTCTTCATCCTGCACGAGACTGAGTACGACAGTCTGCTGGAGTCCATGTTCAAGACTGAGTTCCTGACACTGCTGTGCAAACGTTACGAGGAGCAAACCCGAAGCAAACTCACACTGTCTTTCAGCGACAG[G/A]TGCCCATTATCCTCCATCTCTCTCTCTCTCTCTCTCTCGTACCACTCAAGATGATGCTTATGTTTTGTGCAGGCTGCAGTTTAATGTGAAGAAAGAGGGATGGGGAGGAGGAAGCACACGAATGGTGGTGTTTCAGAGAGGACAGGCCGATGAAGCTGTCATCAAAGCCGGAGGAAAGACCCTCACCGTCAGTGTTGGAGATGGACTGCCAAAGACATCCAGTATGTGGGAGGCATGGATGAAGAGGGTATTCAGCATCTGTACATTGAGTTTACTACTCTTTTTGTTTCTCTACAGAGCCGACTAGGAAAGGCATGCCTCAGAGTCATGGAGGAAGAAGCCAGCCACAGCACAGAGGTAGGGAGACTCTGAATTTTAATAACTAATGTGCTTTTCACACTGCGTTCTTTGTCACTGATGGGAAGATTCATATTTGCAGTTGCGAAGTGTATTTGGAACTGTTTTACTTAGGGTTTCAACATGGATTATTAAACCCACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10240
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 |
|---|---|---|---|---|---|
| ENSDART00000113183 | Nonsense | 1038 | 1096 | 26 | 27 |
| ENSDART00000148304 | Nonsense | 1037 | 1095 | 27 | 28 |
Genomic Location (Zv9):
Chromosome 8 (position 20789145)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20219042 |
| GRCz11 | 8 | 20251127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGCCAGCGTCCTCCTCCGGCCCCCTCTAGCCGGCCCAAACCTCAGGCA[C/T]GACCACAGGGCCCACGRTGCCGAGCGCTTTATCAGTATTTTGGCCAAGAT
Long Flanking Sequence:
TAATTTGCTTTATTTTGGCTAGAATAAAAGCAGTTTTAAATATTTTTTTATATTTTCAATAGTCTACAGAACAAACCATCATTGTACAATAACTTGCCTAATTAACCTAACCTGTCTATTTAACCTAATTAACCCAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCATGAAAAAATTTAGTCAAATAATTTTTACTGTTATCATGGCGAAGATAAAATAAATCAGTTATTAGAAATAAGTTATTAAAACTATTATGCTTAAAAATGTGTTGAAAAAATCTCTTCGTTAAACAGAAATTGGGGATAAAAATAAACACAGGGGGAATAATTCAGGGGGCTAATAATTCAACTGTATGTACATTTAGAAACATCCCAAAATGTAGTTTGTCAAAATACTAAATGAAATGTAAAACTCCCCAGCATGCAGCGGAAAAAGAGTATCAGCCAGCGTCCTCCTCCGGCCCCCTCTAGCCGGCCCAAACCTCAGGCA[C/T]GACCACAGGGCCCACGATGCCGAGCGCTTTATCAGTATTTTGGCCAAGATGTAGATGAAATCAGTTTTGAAGTCAACGACATCATTGAACTCCTCAGTGAAGGTAAGAACTAGAAATGAGACTGTGAGAAGATTTTGTTTGAGACTGGTTGTACTTTCTCTAACATTCCTCCGGGTCTCCTGCAGATCAATCAGGATGGTGGCGAGGAAGAATTCGTGGGAAAGAAGGACTTTTTCCTGGAAACTATGTGGAGAAGATCTAAAGAGGTAGACCTGCACCCTAGATCCATGGTTCTAAACTGGTTTGGCCACAGGACCCACATTTTCTCATGGTCATTGAACACAAGCATCGCCCCTTATTGAAAGAATATTGTTAATAGTGATGAATCATAATTAAATAGCAGTTACAAACTAGCTTTTGCTGATGCAATAACATTAGTAAACTTTAGTAACAGAATAACAGCTGACAGGTCGAGAAAGATTATTGCCGCATCTCATCTG
Associated Phenotype:
Not determined