ZMP
myo18l1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO18A
Human Description:
myosin XVIIIA [Source:HGNC Symbol;Acc:31104]
Mouse Orthologue:
Myo18a
Mouse Description:
myosin XVIIIA Gene [Source:MGI Symbol;Acc:MGI:2667185]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18136 | Essential Splice Site | Available for shipment | Available now |
sa42546 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22645 | Splice Site, Nonsense | Available for shipment | Available now |
sa22646 | Nonsense | Available for shipment | Available now |
sa2798 | Nonsense | F2 line generated | Not yet available |
sa42547 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18136
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088648 | Essential Splice Site | 411 | 2057 | 3 | 41 |
Genomic Location (Zv9):
Chromosome 15 (position 23370851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24082038 |
GRCz11 | 15 | 24017303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGCACGATGGGACTGTACTGGATGTRGATGAGGATGAYGTAGAAAAGG[T/G]CAGTCTTGCGATGCTCATCACATTACTGGCATTTCAGTATGCACACATAA
Long Flanking Sequence:
GCGAAATGATATCTATATTACTAGAACGCTGTTATTTTAAGTTGAAGACAACATGAAATAGCATTCCCTGCTCATTTAACTTATAAAATTTGACACATTTCTGTGTAAAAAAAGAACATTGAGCCAGAGTGGAATATAACGTCGTCTGGAGATGGAGAACGTTATTACATTTTGATGAAAGATTACGGAAACGTTTTCTTCTTTGGAATATTGTGCACTTATGTTTCACACAAAATAATACTGGGGACATTTATTATCAAAAGAAAATGGGGTCGATTTTGATTCTAACATAATGTGGGCTTCAATGGCAGGAGTATATTAAAAGACTATTACAATTCTGTTTCATTTTGATATTGTGTGCATTTCCTCAATGTTCTCTGTTGTCCTCGCAGCCACTGTGGTGAAGACAGAAGCTGGCAGTCTACCCGAGGGGAAAGTGAAAATCAAACTGGAGCACGATGGGACTGTACTGGATGTGGATGAGGATGACGTAGAAAAGG[T/G]CAGTCTTGCGATGCTCATCACATTACTGGCATTTCAGTATGCACACATAACATATTTTATTCAAGGGTTGTTATTAGATTGAAATGGATTCTATTTTAATGCATGTCATAGATTTCATTGTTTTTTTGTTCCCTGCAGGTTTTGACCTCATTAAAATAGCATAACTGAATGGAACCTTCAGTAACCTTATTACCAAAACAATTAAGATTTGTGTGTGTAAAAAAAAAAAAGTTATTTTCTGCACTGTTTTGAACTGCTTCTTCGAATCGCACAATTTAAATAGTCATGGTATAGGCTTAGAAGTAAACAACCTCTGATATCAGTGTCTAACAGTTTGGAAATGTAAAATAATTTAAAAGGGTCACTGTTTTTACATGCTGTTGTAAACCACTGTATGGATGTTTGACAACCTACTATCTTTTTAGACAGACGCTGCAATGATTTAGGGTAAAACTGCATAAATACCAAGTACACACATACCAAATGATCTTTAATAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42546
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088648 | Essential Splice Site | 927 | 2057 | 15 | 41 |
Genomic Location (Zv9):
Chromosome 15 (position 23400799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24111986 |
GRCz11 | 15 | 24047251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAAAGACTCTTCAGTTATTACAGTCCTGCGGATGGAGAGAGCAAAGG[T/A]CAACACACATCCCACATGCTCACACACACACGTCATTGCATGTAGATGTA
Long Flanking Sequence:
ATACTGGTTATATACTGCTGTTTTGGCTTTATACTGTACTGAATTTAACAATTGCAAGACAATTACATGATTTAATTTATCATAATTGTAGATACAAATAGTACTGTTAACATTTGGAACTAGCTTCCCAACTATTAAAAAAAAGAAAAAATATAAGCAAATTTGAATATAATAATTAAAGGTAGACATACTGCATCTGCTCTGTTGTCATTATGACATGAATTGCCTGGATTCCTTACTCGCTTCCATTCAATACCATGATTTCAGACATACCACACTACTCAGATAGTCTTTTCACACACTGCATATTCAATTTCAAAGGTAGCCTATGTGTCCTCATATGTCATTGTGCTTCAGGTACGGACTCTGGCCAGGACGGATGAGGCGAGGGGCCTGCTGTGGCTGATGGAGGAAGAAGCTCTTCAGCCTGGGGGCTCGGAGGAAACTCTGCTGGAAAGACTCTTCAGTTATTACAGTCCTGCGGATGGAGAGAGCAAAGG[T/A]CAACACACATCCCACATGCTCACACACACACGTCATTGCATGTAGATGTATGCAGAGTTCATGCTCAATGTCTCCCACAGGCCCCGCCCTGCTCCTGAAGAGTGACAAGCCGCATCACTTCCTATTGGGTCACAGCCATGGCACTGACTGGGTGGAGTATGATGCTGGGGGCTGGTTGAGCCATGCCAAACAAAACCCTGCCTCTCAGAATGCTGCCATTTTGCTGCAAGACTCTCAGAAGTAAGTAGTGTTTGCTTAATGCCATCAACCATCTTCTCAAATTTGTTGGTAGAATTATTTATAGATCTGTTGGGATTATCAGTAGAAATATTTTATGACCTGTACTGGTTTTCTTTTGGCTTGGGGTTTGATGACCATGTAATAACACAAAACACATACCATGGTAAATATTACAAAATACAAACAAACTAAATAAACATAAACAGCTTCCGATTAGAATCAACATGCAAATCAGCCAGCAGATTATCAGTAACGTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22645
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088648 | Splice Site, Nonsense | 1329 | 2057 | 24 | 41 |
Genomic Location (Zv9):
Chromosome 15 (position 23429467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24140654 |
GRCz11 | 15 | 24075919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCCGAGACCTCGGAGAGACTGAGGCTGGAGAAAGACATGAAGGATCTA[C/T]AGGTACAACACACCCACACACTTCAGAACAGATTCAGAGTTTTGACTTTT
Long Flanking Sequence:
ACGCAAAATAACAGTCATCATTGCATACATGTAGACAATAATATAAAAATAATATCTTTATCCTTTAATCTTTAATCAATTTTCTAATCCTGACTATTGCGGATACATTGCAATATCGATGCTCAAACACTATATTGTTCAGCCCTAGTTCACAGTATATACAAAATCACACCATTACACCCAAACACAGTCACAGAAACCCACATCTCTCACTATCAGCATTGGACTGTTACCAAAATACCATCATCTCTGTGTGAAATATGTGAGCGATGATATAGATGTGAAGTGTTGCATGTGGATGCGAGATGAGCTCATACACTACACTGAAGTTTGCATCTAGTACACACACACCTCATGTTTGCCTCATTATTTTTATATTTCAGATCACAGAACTGTCATCAGAGCTTGCCGATGAGAGGAACACTGGCGAATCTGCCTCGCAGCTGCTGGAGTCCGAGACCTCGGAGAGACTGAGGCTGGAGAAAGACATGAAGGATCTA[C/T]AGGTACAACACACCCACACACTTCAGAACAGATTCAGAGTTTTGACTTTTCTGTAAGGAATCTCCTCATGCCTGAAATAGATATTTTCTGGCAATGCAGTCCAAGCAGCAGAGCATGAGCCGTATACAAATTTTGTCATCTTGCATTAAATATCTATGCGAAAGATGTAGTGTGTGAGCGAGTGTCTGCAGGTATTTGTCTGTGTGTGGTGTGTTTTATGTGTCTTCTAGGCTCAGAGTTGCCTGTGTGAGCAGATGGTCTGGGTATTTCCCTGTAGAACAGTGAGCTGATGTGCTTTGCGTCCCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGGCCAAGTTTGACGCTATGAAGAAGCAGACAGAGTCTATGGAGATGGAGGTAATGGAGGCACGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22646
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 |
---|---|---|---|---|---|
ENSDART00000088648 | Nonsense | 1682 | 2057 | 32 | 41 |
Genomic Location (Zv9):
Chromosome 15 (position 23450041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24161228 |
GRCz11 | 15 | 24096493 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGATGCTCAGATCATGCTGGATCACCTGAAGAACAATGCACCCAGC[A/T]AGAGAGAGATCGCCCAGCTCAAGAACCAGGTCTGTTGTTCATCTCCCTGT
Long Flanking Sequence:
GACACTAAAGAAGTGCTTATAAATGCTCAGTCCCTCATAGCAAACTAATGGTAAGAGTGTTATGGTTAAAAATGTTATTTCTGAAGCTGTCAAACTGACGTCAACAGAGTAGGTGCCACTTTAATCACGGAAGCAAATGGTCAGACTTTGGCTGAAGATTAATAAAAAAAAAAAAATTAGGAAAATATCTTGCAAGGATTAATTGTTACCTAAATAATAACAATGTGCACTAGTTTTACATTTTTATTTTCACAAAAAACAACTTTGCTCTAAGTGTCAAGAACAATCAGTAGCAGTTGCTAAAATCCAACCAAAATCACCTTCTTAATCACTGAATGTGTAAAACTTTAAGGATCATCTAAAACCATGCTTGTTATTTTCAGGTGAGCCACAGAGATGTGGAGGCAGAGAAGCGTCTGAGGAAAGATCTGAAGCGCACCAAGGCCCTGCTGGCTGATGCTCAGATCATGCTGGATCACCTGAAGAACAATGCACCCAGC[A/T]AGAGAGAGATCGCCCAGCTCAAGAACCAGGTCTGTTGTTCATCTCCCTGTGCGCTCAACATCGCATCCAGCAGTAAACATACATTTTATTTATGAGCGTTTGTGTTTACGTTCCCTGTACAGCTTGAGGAATCCGAGTTCACATGCGCTGCTGCAGTCAAAGCCCGAAAGTCGATGGAAGTGGAGATCGAGGACCTCCACGTCCAAATGGATGACATATCCAAATCCAAACAGGCTGTAAGTCTAACTGCGCTTGGGGGTAAAAGTAGAATGAAGCTGAAATTATTTTTATTTCTTTTAAATGAGAATCCACCATAGGTGTCAATTCAATTATTTGCTACAGAGAAATGATTTCCACCCTTAATGGCACATTTCCGATTCTGCCTCTAATTTGAACAAGATGTATCGCTCTGAAATGCATCACACTTTAATAATTCTATCATTGGTACAGTATTATTTGAGCGTGTAGAGAATTGTGTAATTGTGTCCTCGCTGTAGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2798
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088648 | Nonsense | 1770 | 2057 | 35 | 41 |
Genomic Location (Zv9):
Chromosome 15 (position 23456175)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24167362 |
GRCz11 | 15 | 24102627 |
KASP Assay ID:
554-2826.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGAATTCAGAATGWTTGACCCCWGTCTGGTGCATTCTTTTGCAGTCCT[C/A]ACAGAACTTGGCCCAGATCAGTGACCTACAGGCCCAGCTGGAGGAGGCTA
Long Flanking Sequence:
TTCATTTATGTGCAGGTTTTAAAACACACATTCATACTTGAGGCATTCAGATAGTCTCAACTATCTCCCCGCTTCATTTCACTCATGTTTCTGTTAAGATGCCATTTATTACTGCCATTTTTTGAGCGATGTCATTAGCAGGCAAAATGATAGTTTCTCTCTGCAGCTAAATGGAATATTTAAATAAAAAAGTGTCATCATAGTACACATTCCTCAGCTTGTGCAATGCATGTTGTTTTAATGGTACAGTAGTATGCTGTGAAGGATAATATTCTGTTTTTCATATGATTTTAAATTAATATGCATCCTTTTAAATAATGAAATGGATTGTTGTGTGGCAGTTTAGATGATACAGGTATCTTGAATAATTCATGCATACTAGAAAATGTGTACACATATGGAAATCATGTACACCAAAGCATAACAAATGACTTCTGGGAGATAGAAATGGAGGAATTCAGAATGATTGACCCCTGTCTGGTGCATTCTTTTGCAGTCCT[C/A]ACAGAACTTGGCCCAGATCAGTGACCTACAGGCCCAGCTGGAGGAGGCTATGAAGGAGAAACAGGACGTCCAGGAGAAGGTGAGTTCACTTTGGCATCAAGACAAAAACTGCATAATCACTGTCAACAATGTTACTTGCATTTTTATTGAACATTAAAGATTATTTTCGTTTAAGGTGGGAAAAGGACAGATTATTTGGAGTTCTAGTTGTCCATTGAACTCGAAAGTTACCAGACAATGCTTTAGACTCTTTGAGTTGATTGTGTTATATCAAGATCAAGCTTCAGACTTTCCTTTTTATGAGATTAACATTATACTCCACCCACTAAAGTTCTCATATTTGAATAGGTAACCTTTAAACCCTGCACCTCTTGGTACTTGAATTTTTATTGGTTGAATCTGGCTCTGCTCACTCACAGTTTGCATCTTTATTTGTAAGATCTTAACCCCGCTCAGCTTTTGACTTTAAAATAAAATCTGACTACACCAAAGTATTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42547
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 |
---|---|---|---|---|---|
ENSDART00000088648 | Nonsense | 1775 | 2057 | 35 | 41 |
Genomic Location (Zv9):
Chromosome 15 (position 23456189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24167376 |
GRCz11 | 15 | 24102641 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGACCCCTGTCTGGTGCATTCTTTTGCAGTCCTCACAGAACTTGGCC[C/T]AGATCAGTGACCTACAGGCCCAGCTGGAGGAGGCTATGAAGGAGAAACAG
Long Flanking Sequence:
GGTTTTAAAACACACATTCATACTTGAGGCATTCAGATAGTCTCAACTATCTCCCCGCTTCATTTCACTCATGTTTCTGTTAAGATGCCATTTATTACTGCCATTTTTTGAGCGATGTCATTAGCAGGCAAAATGATAGTTTCTCTCTGCAGCTAAATGGAATATTTAAATAAAAAAGTGTCATCATAGTACACATTCCTCAGCTTGTGCAATGCATGTTGTTTTAATGGTACAGTAGTATGCTGTGAAGGATAATATTCTGTTTTTCATATGATTTTAAATTAATATGCATCCTTTTAAATAATGAAATGGATTGTTGTGTGGCAGTTTAGATGATACAGGTATCTTGAATAATTCATGCATACTAGAAAATGTGTACACATATGGAAATCATGTACACCAAAGCATAACAAATGACTTCTGGGAGATAGAAATGGAGGAATTCAGAATGATTGACCCCTGTCTGGTGCATTCTTTTGCAGTCCTCACAGAACTTGGCC[C/T]AGATCAGTGACCTACAGGCCCAGCTGGAGGAGGCTATGAAGGAGAAACAGGACGTCCAGGAGAAGGTGAGTTCACTTTGGCATCAAGACAAAAACTGCATAATCACTGTCAACAATGTTACTTGCATTTTTATTGAACATTAAAGATTATTTTCGTTTAAGGTGGGAAAAGGACAGATTATTTGGAGTTCTAGTTGTCCATTGAACTCGAAAGTTACCAGACAATGCTTTAGACTCTTTGAGTTGATTGTGTTATATCAAGATCAAGCTTCAGACTTTCCTTTTTATGAGATTAACATTATACTCCACCCACTAAAGTTCTCATATTTGAATAGGTAACCTTTAAACCCTGCACCTCTTGGTACTTGAATTTTTATTGGTTGAATCTGGCTCTGCTCACTCACAGTTTGCATCTTTATTTGTAAGATCTTAACCCCGCTCAGCTTTTGACTTTAAAATAAAATCTGACTACACCAAAGTATTTTAATCTCAATTGTATGA
Associated Phenotype:
Not determined