ZMP
myo1e
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO1E
Human Description:
myosin IE [Source:HGNC Symbol;Acc:7599]
Mouse Orthologue:
Myo1e
Mouse Description:
myosin IE Gene [Source:MGI Symbol;Acc:MGI:106621]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20980 | Essential Splice Site | Available for shipment | Available now |
| sa20979 | Nonsense | Available for shipment | Available now |
| sa26972 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30634 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40919 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20980
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052539 | Essential Splice Site | 1 | 1117 | 1 | 29 |
Genomic Location (Zv9):
Chromosome 7 (position 32059203)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30451545 |
| GRCz11 | 7 | 30722695 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGATTATAACAGAAGGTCGGCTGCAGTGTGATTAACCAATAAAAATGG[T/A]GAGTGAAAATACTTAACAGCACAGTCGCGTATCGCCTACGGAGAGAAACA
Long Flanking Sequence:
ATACAATTCTGTATTTGTTGCTTCAGCTCTTTGTGTCTTCAGTGTCTATGCTCTTTGGCGCAGTGATGCTGTAAAGTGTTTACGCAGCCTCGCTGCGCATATAGGACGCGCTTTAACACACCCGAAATCATCTGGTGGGATTCCCTTTGGAATGACGCGCCGAGCAGCGCTCCTATTGGCCAAAAGCAACTCACGAAATTCTCCATTTATGGGTTGTTTGCCTCTTTGATTCCGTCAACCAGCAGTCACAAAGTTTAACTTTGTGCAGCAGACGCTGAGTGAGTGCAGTGCAGTCAGTGCGCTCGAGCCGTTTACCGGTGCGGTCCACACTATTATGGAGCGGCGACACTGGTCCTGAGGAGACGTTTACAACAGCAGAGGCTAAAAGAGACCGTGACATCGCCACGGGGAAATAGAGAGGTTTATTATTTTACTATAAACAGTTACAAAACGGATTATAACAGAAGGTCGGCTGCAGTGTGATTAACCAATAAAAATGG[T/A]GAGTGAAAATACTTAACAGCACAGTCGCGTATCGCCTACGGAGAGAAACACAAGGGACACTGCTCTTGTTTTGGAAACAGTTTTACAGCATCCTTATCGACGTAATATAGGTTGTAATAACAGCTGCTTGGTGTTAATGTTTTCATCTGGTTTAATAATTTACAAGCCACAATTAGCAGCTAATAAATTGCTTTAACACTCTTTAAAATTATCTCACTCATAGTGACAAAACCATATACTACTGTACTGTATGCCATCCATTGTCATCAGAAATGTTAAATCGGGTAAATGACGTTTCAGTGTGGTCACATCAAGTTTAAACTTCTAGTAAGTTTTTGTTTTCATTCTAGACTAATTGCAGATACTTAAATTTACCAGAGATGCACGGTTTCAGATTACTTTTAGTTATTCTCTGGTCACTTTGTGTTATAAACATATCATACATGTTTCTTGCTATTTTTGGCACTATGTGTCTTCAGGCAGTTTAAATAGCCTGGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20979
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 |
|---|---|---|---|---|---|
| ENSDART00000052539 | Nonsense | 133 | 1117 | 5 | 29 |
Genomic Location (Zv9):
Chromosome 7 (position 32013590)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30405932 |
| GRCz11 | 7 | 30677082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGAAGACCGTAGCAGCAAAGTACATCATGGGCTACATCTCCAAAGTGT[C/A]AGGTGGAGGACCCAGAGTTCAGGTGGGTTGCACAGAGTACTTTAACAAAC
Long Flanking Sequence:
CCTAGTTCAGCATTTACTAAAGCATACATGAAAACCAAATTCATACTTGGTATCACTAGTCAATGCACAGTGAGGTAAGATGGATTAGCAATGTAACAACTGTATTTTCATTAATTAATGTTAGCAAAAATATACAAATACTTTGATAAATGTATTGTTCATTGTTTGTTCATGTTACACTCTTAAAAATAGCATATTTTTCAAACAACTTATTCAAATTGAGCTGAAAATTCACAATTGCTTTTTGATGAATCCACTTATATTTGTAAAAACAATAAAGTTAACTTAATCTATTTGTGTTTGGACAACATGAATGAATTGTGTGGAAGCCTGCATTTTTACAGTGTAATAACTACATTAACTAACGTGACTTAATGCAAGCTTATTGTGAAGTGTTACCAATTTGTGATCTTTCATTTTGCTTTGTATTTTCAGCGGTGAAAGTGGAGCAGGGAAGACCGTAGCAGCAAAGTACATCATGGGCTACATCTCCAAAGTGT[C/A]AGGTGGAGGACCCAGAGTTCAGGTGGGTTGCACAGAGTACTTTAACAAACATGAAAGCTTTTGGACGCGCATCAGGATTGTTTAATGTAAAAGTAAAAACAACATATAGTGGCTTTCTGGGCTGTTTTTGACCAATAACGTTAAGCAGAATCCTGATGCATGTTGAAGTTCGCCTCATCTGACATCATTCCTCCACCCCCATCTCTTACAATCTACCTTTCATCTGTTTCATCCTTCTACAAACCCCACCAGCAGCCATCTGTCCCCCACAATCCCCCTCTGATCTGTCCCGCGCGGCTCTCAGTGCCTTCAGGAGCCATGTGAGTGAGCTCAGAGTCAGAGGACTGACACTTTCTGATTCAACTAACCAGTTGACTGTATATACCATCTGAGAGCACTAGTGAAAATGCTTGAATTTGGCATAAGATTTTATTTTTGTTGCTTTAATATCAGCATTGTTTGAGCTGTACGAACTCTACAAGTGAATTAGATGATTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26972
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 |
|---|---|---|---|---|---|
| ENSDART00000052539 | Nonsense | 169 | 1117 | 6 | 29 |
Genomic Location (Zv9):
Chromosome 7 (position 32010404)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30402746 |
| GRCz11 | 7 | 30673896 |
KASP Assay ID:
2259-8999.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCGAGGCCTTTGGGAATGCTAAGACAGTGAGGAACAACAACTCCAGT[C/T]GATTTGTAAGCATTAGTCATCCTCCCGTTATTTTATATTTATTATTATTT
Long Flanking Sequence:
ACAGTTATATTACCTACTGAAACAAAGCTAAAATAAAATTATGCAACCTTTCTTTTATATTTGTGATATTACTCCACAAATCTTATGTCATAAAAAGTGATGGTTTTGGGATATCCCAGAACTGCCGCATGTGTCTGTCTGTCTCTTGGCTGCTTTGCTGACCGAGATGGCTCTAAGTAGACTGTGCTGTGTAAATTATGTGTGAAATATGCATGTGTACTGACATTGATATGTCTTCAGGGTAAATTAGGTCACCCATTTTGACATTGAGATGACCCGTGTTACTTTAGTTCACCCTACAGGCAGGATTTTATCTACTGATCTCGTCCATTTCAGATCCACATTGTTTCTGTGCTTATTATGCCAAATGTCAATGAAACATTACATCTCTCTCTTGTTTGTTTATTTTCACACAGCATGTCAAGGACATCATTCTTCAATCTAATCCACTTCTCGAGGCCTTTGGGAATGCTAAGACAGTGAGGAACAACAACTCCAGT[C/T]GATTTGTAAGCATTAGTCATCCTCCCGTTATTTTATATTTATTATTATTTCATTTGAAGAAAGCAGACGGCAGATGTATTGTGATGTGTTGGGCATAAGTTGCACTAAAACCAAAAAAAGGGGTGATCATCAATGTTAAAGGGACTAAGCTGAAAAGAAAATGAATGAATGAATGAATGAATCATCCATAGTAAAGGGATAGTACACCAAAGAATGATAATTCTGTCATCATTTACTCACCCTCGACTTGTTTCAAAATAGTCTTTTTTTTCTGCTGAATGCAAAAGAAGACATTTTGAAGAATGTTGAAAACCTGTAACCATTGACCTTCATACTAGGACAAAAAAAATACTTTATCGTATGATGGTTATAGACGATTACAGGTTTCCAACTTTTGTCAAAATATCTTCATGCGTGTTCAACTGAACAAAAAAACTCAAACTGGTTTTTAACAAGTCAATGGTGAGTAAATGATGACAGAATTTTTATTTGTAGCGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30634
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052539 | Essential Splice Site | 260 | 1117 | 9 | 29 |
Genomic Location (Zv9):
Chromosome 7 (position 32007057)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30399399 |
| GRCz11 | 7 | 30670549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGTAACTTCCCTCTTTTTCTTCTGTGTGTCTCTCTGTCTGACCCCA[G/A]CATGCCATGGACGTGATTGGTATCTCAGGGATTGACCGCACCATGGTGCT
Long Flanking Sequence:
AAAAACTTAAAATTGGTTGTTCATGTTAGTTCACGGTGCAATAACTACATTTACAAATGCAACTCTGGATTTATTTATTCATTTTAATTATATATTAATCATTGACCATTTTTTATGGTCTAAAACTCACCCAAATTCACCCAAGAACTTTTTGTGAATGTGTTATAACCTACATTCCTCTTCACAGCTAATAGAGGGAGCCAGTGGAGACCAGAAAAGCAGTCTGGGCATTACCAGCCTGGATTACTACACTTACCTCAACCAGTCCGGTTCCTACAAAGTGGACGATATCAACGACAAGCATGATTTCCAAGAAACCTTGGTGAGTATGATTAGGCAACTTGATATTTGCATGGAGCGCACTGGAGATCCTATATAGTAAATCCAATATAGTTCAATAGAGTTTGCCTGTTCAAATATGTGAACTGTTTTCCATATTGGCCGACACTGTTATTGTAACTTCCCTCTTTTTCTTCTGTGTGTCTCTCTGTCTGACCCCA[G/A]CATGCCATGGACGTGATTGGTATCTCAGGGATTGACCGCACCATGGTGCTGCAGATTGTGGCAGGAATTCTTCATCTTGGGAACATCAACTTCAGGGAAGCTGGGAATTATGCTGCTGTAGAGAATGACGAGTGTAAGTACACAGTCTCAATTTTGCATATTTCCTTTTAAGGAAATGAGGAATTACATATACTCAAATTAATGTGATTAAGTAGTTTTTCTCAGGTATTGTACTTCACTAAGCAGTTTTTAAAAATGTATACTTTTACTTGAGTATGTTTTATTGCTGTATCATTACTTTTATGTTTACTTGTCTATGTTGATTGGCTAAGTAGAAAAATCAGTCCAGTGATTTCAATCAAATCGAGCATAGTAAAGTCAGCACATCAGACTGAGCGACCTCCAGACATGGTTGCTATACAAATATGTACCATGTGGAAACATTGAAAATGTCTAAGAAGGCACAAAATAATTGCAGCTCGGGCTGAGCCTGATTAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40919
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052539 | Nonsense | 715 | 1117 | 20 | 29 |
Genomic Location (Zv9):
Chromosome 7 (position 31982646)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30374988 |
| GRCz11 | 7 | 30646138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGAACCATTCAGACTGCCTGGAGGAAATATTGTGCACGCAAGAAATA[T/G]GTTCAGATGAGAGAGGAAGGTAGGTTTAGACTTTAGATTTAGATAGATAG
Long Flanking Sequence:
TCTAGAGTGCAGCAAAACTCTGACTGTTCTGAGGACATACAGGAAGCACAGTGAAGCTACACAGTGCTTAGAGCATTATGGGAAGACCACGGAACATTTAGACAGCTGCTTGCTGAAAAAGTTGCCATATAGAAAGAGAGAAGTTACCACATGAAGGCCGGGATTAACTGATCCCACTTTGTGTCATAATAAGCCGTGTCTGTCCTCGGCTGTTTAATGTCTTAGATGAACAGTGACCTTTAGTGTAATGGACAACATTTCACAGCTCTATTCTCTGTTTTTATGCGGGCTATTAAATTTGAAGTCAGCAACAGCATGGTTTCAGTGCCTAATTCATTAGATTGATTCAAACCGACATGTTTGCGAGTTCGTTTGATTGATTCCTGCAATATTTTTTGTTTACAGCTATTCCTGCTGGAGGAGACGAGAGAGCGCAAATTCGATGGCTATGCCAGAACCATTCAGACTGCCTGGAGGAAATATTGTGCACGCAAGAAATA[T/G]GTTCAGATGAGAGAGGAAGGTAGGTTTAGACTTTAGATTTAGATAGATAGGTTTAGATGAGTTCAAATGGTGGATGTTATACAGTATACATGCACTCACACACTAAAACAAACTAATTATAGGAAAGTGGAAATCAATGTTATTTGACATGGCAAAAAATGTCAACTTCTGTGTTTTCCCTGTATATCTTTGGAATCTGACCTCAACTCCTGATCTAAGCTAAATTATTAAGTTTAAAAGTAATAATACACAAACAAAAGGCAAACAAAAAACCGGCACATATTTTCTGGGTGTTCACGTTTTGGTGGTAATTCAGTTTTGGAATATAAATAAATTTGTAAATAAAAATTTTGTTTTACAATATAACTTTTTATAGTTCTAATATAGTTCTAAATCTCAATGACCGCAGTTTTTTTTTAAAGCACAATAAACAAAATTGCAGATATTCAGTTAAATTCAGATTTTTTAACATTTTTTTTGCCAGAAATCAACTGACTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40918
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 |
|---|---|---|---|---|---|
| ENSDART00000052539 | Nonsense | 1069 | 1117 | 28 | 29 |
Genomic Location (Zv9):
Chromosome 7 (position 31972446)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30364788 |
| GRCz11 | 7 | 30635938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCTGCCCCCAAACCAAAGCCTCAGGTGCCTCAGTGTAAAGCTCTTTA[T/A]GCCTACGACGCTCAGGACACCGATGAGCTCAGTTTCAACGCAGATGACAT
Long Flanking Sequence:
GATTGGGCATTTTCTGGCATTTTCTCTGTTGTAGTCATGATGACGATCAACTCGGACACATCATGAAGGCTGAAAGGCTACTAAATGGCCCTTCGTAGCAACAGCTGAAAAATAAATTCTGGTTTTAAAACTGAGGTGAATGATCAACTAAACAAATCCGATTTTTGAAACTAGTTCCGACAGTTCCACCATAAATAAATGTGAATCTGTCGCCATCTTGTGGGAAACACGTGAACTAACATCACAAAATCAGCCTACTAACCCTCTCACAGCAGCTATAGGGTGCTAGCTGACTTCACACTTACCTTCACTTGTAGAAGCATGGTTGCAGGTTGCTGGAATGTTGGAATCATCACCTGAAATTCCACAAGTTCATGAGTTTGTGTGCTTTTTTTATGAAGGGCCCACAGACAGTCCACAAACAGGCCAGCTCCAGGAGGAGGACGACCCAAACCTGCCCCCAAACCAAAGCCTCAGGTGCCTCAGTGTAAAGCTCTTTA[T/A]GCCTACGACGCTCAGGACACCGATGAGCTCAGTTTCAACGCAGATGACATCATTGAGATCATTAAAGAAGGTAATATTACATAAAAATGACTTGTTTATCCAGAACATCAGTGTGTATTGTAAATCAGTTTGCTTCTCTTTGTTCTTTGCTGACATATTCACTGGCAGGGCAAGCTGTCAATCACATGACATCACAGTAATAGCAAATCAATCGATTACCAGTGAACTTAAACAAATCCTTCACCTTTTCTGCTCATTCCTGAAGAAGTTTCACACAGTTTAGTTTTCAATGATTTGATTGGTGTGGCGACTCAGAGGGCTAATCATCAGCAGAAATGCTGGACAGACCTGTTAAGCTTTCATTTGTATCAAACCACAAATATTTAGATCACCTCACGCCGACAAGTGTTTTGTACTTGTGATTCAATTACAACAGATGCCGCACTAATTTAATCACTAAAAACTGTGGGACATTCTATTAAGCAAGTTACAAATGGTTA
Associated Phenotype:
Not determined