ZMP
myo10l3
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO10
Human Description:
myosin X [Source:HGNC Symbol;Acc:7593]
Mouse Orthologue:
Myo10
Mouse Description:
myosin X Gene [Source:MGI Symbol;Acc:MGI:107716]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17549 | Nonsense | Available for shipment | Available now |
sa17384 | Nonsense | Available for shipment | Available now |
sa31704 | Nonsense | Available for shipment | Available now |
sa21444 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17549
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 |
---|---|---|---|---|---|
ENSDART00000088042 | Nonsense | 213 | 2023 | 5 | 40 |
ENSDART00000138360 | None | None | 916 | None | 16 |
ENSDART00000146265 | Nonsense | 212 | 684 | 5 | 18 |
ENSDART00000088042 | Nonsense | 213 | 2023 | 5 | 40 |
ENSDART00000138360 | None | None | 916 | None | 16 |
ENSDART00000146265 | Nonsense | 212 | 684 | 5 | 18 |
The following transcripts of ENSDARG00000074143 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 13028744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 12781309 |
GRCz11 | 9 | 12752512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATACWGTTGCWTTAAATCCTTTAACATTTSTCTCCAGAATCGAGTTGTG[C/T]GACAAAATCCAGGAGAAAGAAACTATCATATTTTCTATGCCTTRTTGTCA
Long Flanking Sequence:
GTTGAACGTGAGTTATGGGATTAACTTTAAAGTGTAAACTAACAGTAAAGTGTTTTAAAGACCTGCCATGAGGTGTCATTATTCTCTTAATAGTTCTTCCATTGAATATTAAAAGAAGGAACAATTATTTAGAGGAATTCAAAAGAGTCTTGGCCACAGATATATGCTTGTGAGATAAATATGTAAAAAAAACAAGTGTATGTTATTTTCTTCTCATTTAGTTTTAGAAGATCTAGTAAATTGAAACTGACAGTCCAGTTTTCAGAGTTGAAGTTTAGTTCATGGTTTAATTTTCACTAGTGAAAGTCCATACATGTATACCTTGTATATGGTTTGATCATCATAGCACAACCCTATTAATTTATGTTTCAGCATTTATTATTGGAAGTTGGCTACCCATAATTTGAACTGCAGTAGTCACTAGTGGGAAATGGTAGATAGCCCTCTGTAAATACAGTTGCATTAAATCCTTTAACATTTGTCTCCAGAATCGAGTTGTG[C/T]GACAAAATCCAGGAGAAAGAAACTATCATATTTTCTATGCCTTGTTGTCAGGTGCCAAGTATGAACACAGAGGTGAGCTTTTATCATGATTTTTTGTTAAATTGGATTTAATTCATAGAGATTTTGAGGAAGCTTAATAATTTTGCCGACTGTAGTGCAGTACAGTATATTGAACCCTGTTTTCACCTTCAGAAATGTATGTGCTAGCTGACTCTCCTGAAGCTTATCATTACCTCAACCAGTCCGGCTGTGTAAAAGACAGAAGCCTAGATGACAAACACCTCTATGATAGTGTAATGGTGAGTCAAGAAATTGCTTTATTATCTTTGTGTGAAAGCATTGTTCTCGCACCTCAGACTGATACTGTTTTCATGAACACACAGATGCTGTTTTACTATGCTTTAATTGCCACTAGAGGGCACCACATCCTGACTTTTCTGTATACAGTTCATAGTTATAGAGATAGGTTTGTTTCTTTATTATTCAATCAAAAATATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17384
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 |
---|---|---|---|---|---|
ENSDART00000088042 | Nonsense | 213 | 2023 | 5 | 40 |
ENSDART00000138360 | None | None | 916 | None | 16 |
ENSDART00000146265 | Nonsense | 212 | 684 | 5 | 18 |
ENSDART00000088042 | Nonsense | 213 | 2023 | 5 | 40 |
ENSDART00000138360 | None | None | 916 | None | 16 |
ENSDART00000146265 | Nonsense | 212 | 684 | 5 | 18 |
The following transcripts of ENSDARG00000074143 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 13028744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 12781309 |
GRCz11 | 9 | 12752512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATACWGTTGCWTTAAATCCTTTAACATTTSTCTCCAGAATCGAGTTGTG[C/T]GACAAAATCCAGGAGAAAGAAACTATCATATTTTCTATGCCTTRTTGTCA
Long Flanking Sequence:
GTTGAACGTGAGTTATGGGATTAACTTTAAAGTGTAAACTAACAGTAAAGTGTTTTAAAGACCTGCCATGAGGTGTCATTATTCTCTTAATAGTTCTTCCATTGAATATTAAAAGAAGGAACAATTATTTAGAGGAATTCAAAAGAGTCTTGGCCACAGATATATGCTTGTGAGATAAATATGTAAAAAAAACAAGTGTATGTTATTTTCTTCTCATTTAGTTTTAGAAGATCTAGTAAATTGAAACTGACAGTCCAGTTTTCAGAGTTGAAGTTTAGTTCATGGTTTAATTTTCACTAGTGAAAGTCCATACATGTATACCTTGTATATGGTTTGATCATCATAGCACAACCCTATTAATTTATGTTTCAGCATTTATTATTGGAAGTTGGCTACCCATAATTTGAACTGCAGTAGTCACTAGTGGGAAATGGTAGATAGCCCTCTGTAAATACAGTTGCATTAAATCCTTTAACATTTGTCTCCAGAATCGAGTTGTG[C/T]GACAAAATCCAGGAGAAAGAAACTATCATATTTTCTATGCCTTGTTGTCAGGTGCCAAGTATGAACACAGAGGTGAGCTTTTATCATGATTTTTTGTTAAATTGGATTTAATTCATAGAGATTTTGAGGAAGCTTAATAATTTTGCCGACTGTAGTGCAGTACAGTATATTGAACCCTGTTTTCACCTTCAGAAATGTATGTGCTAGCTGACTCTCCTGAAGCTTATCATTACCTCAACCAGTCCGGCTGTGTAAAAGACAGAAGCCTAGATGACAAACACCTCTATGATAGTGTAATGGTGAGTCAAGAAATTGCTTTATTATCTTTGTGTGAAAGCATTGTTCTCGCACCTCAGACTGATACTGTTTTCATGAACACACAGATGCTGTTTTACTATGCTTTAATTGCCACTAGAGGGCACCACATCCTGACTTTTCTGTATACAGTTCATAGTTATAGAGATAGGTTTGTTTCTTTATTATTCAATCAAAAATATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31704
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 |
---|---|---|---|---|---|
ENSDART00000088042 | Nonsense | 436 | 2023 | 10 | 40 |
ENSDART00000138360 | None | None | 916 | None | 16 |
ENSDART00000146265 | Nonsense | 435 | 684 | 10 | 18 |
The following transcripts of ENSDARG00000074143 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 13019594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 12772159 |
GRCz11 | 9 | 12743362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGGAGTACTTCAACAAGCACATCTTCTCCCTGGAGCAGCTTGAATA[T/A]AACAGGTGAGTCCTGTCAATGGCCCTGGTTAGCACAGATCCAGATATCTA
Long Flanking Sequence:
TCACTGTATTTCCACGATGATGAAATTCAAATGGACATATTAGTGTTTCATAATGACCTCTTGAGACTTTTGCTTGTTGATGTTGTGGGTTTCAGTTGCACTGTTGGAGACTAACTAAAGGAAAATATCTCTGGATTATTATGTTTCTTGCTTTCCAAAGGCAATTGATTCCCGGGATTCTGTGGCGATGGCATTGTATTCCCAGTGTTTTTCTTGGATCATCGCCCGAATCAACCAGAAAATCAAAGGAAAGGACAACTTCAAGTCCATTGGCATTTTGGATATCTTTGGCTTCGAGAACTTCGAGGTGGGGGATTTGTTAAGTATTGAGGGGCGAAAATGTTCCAGACAGACTGTCTGTCATTGGCATGTTGTCATGTTTTTATGACTTATTTCCCCCTCCAGGTGAACCGGTTCGAGCAGTTCAACATTAACTACGCCAACGAGAAGCTCCAGGAGTACTTCAACAAGCACATCTTCTCCCTGGAGCAGCTTGAATA[T/A]AACAGGTGAGTCCTGTCAATGGCCCTGGTTAGCACAGATCCAGATATCTATCAGCAAAAAAAGCTGTATTTCTTAGATTTTAACTATGGATGCACTGATATGGAATGTTTGACAGAGACTAATAAGTCATGTATGCCCAAAAAATATGAATCTTGCTAGAGTTTTATTTTCAACCTGATTATAAAAGCAAAATACAAACAAATACAGTGGATAAATTAGAATTAATATAAGTTTTTTATTATTATTATCATCATTATTTTTTTTTATTTAAAACCCTACCTGCAAAAAATAAGTAAAACTTCAAGACAGCAACTGAATCTTTTTTTCCCAAAAATGACTTGGGACTGCAAATTGCATGCAAAAATTCCTATACCGCTGACATTTTGTGCGTCTGTGCATATGTCATATCATGTGGATGGCACCAATCAAAAATTAAAACCTAAAATCTATTAAAATAATAGGCCAACAATGATTACATTACAAAAATAAGCATTTGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21444
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 |
---|---|---|---|---|---|
ENSDART00000088042 | Essential Splice Site | 685 | 2023 | 18 | 40 |
ENSDART00000138360 | None | None | 916 | None | 16 |
ENSDART00000146265 | None | 684 | 684 | 18 | 18 |
The following transcripts of ENSDARG00000074143 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 12988022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 12740587 |
GRCz11 | 9 | 12711790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGAAGTACGACGTCACGAAGAAAGAGTGGCAGCTGGGGAAGACTAAG[G/A]TGTGGTTGCATGACCAGCACATGTTCACACACTGTTTTAAGTAGAAACAA
Long Flanking Sequence:
TTGACTCAGATGTGGTTCTGAACCAGCTCCGCTACTCTGGAATGCTGGAAACAGTGAAGATCCGAAGAGCTGGCTTTCCAGTACGCAGAACCTTCCAAGATTTCCTCAGCAGGTGAGACATGTGTCCAAAAAACCATTAAAAAAACCAGACAGTCTATCAAAATACAGTTTGACACACACAATCATTTCCAGATGCCCATATCTCTTCTATTTTTAAAAAGTTTGTCCCGTAAATGCCCCTGAACTCTTAATGAACAATACCAGGGGTTTTTACTTCTACTCTGAATCAGCGAACACTTAATCATTACATTGTTCTCTTACAGTAAAATATGTGAGGTGGAGAGTGTATGTGAGTGTTTTCAAGCTGTACCCACTTCCTGTGCAGATACACTATGATCCTGAGGGACAGAAACCACACGGCGGACGAGAGGAAGAAATGTGCGGATCTGCTGACGAAGTACGACGTCACGAAGAAAGAGTGGCAGCTGGGGAAGACTAAG[G/A]TGTGGTTGCATGACCAGCACATGTTCACACACTGTTTTAAGTAGAAACAAATAGTCTGTGCTGCAGGAATGAAAGACTTGACATGAAAGCTCTTTCTCTCTCAGACTGAACTGTTTAAACTTTATGTGGTGTGTGGGTTGATCCCTGACATTTATGCTTTACAGTGCTGAGAGGGCCATGTTTGATTAAAACAATCTGAAATGGAGAATTCACGGAGATGCACATTCTTAGGGTTTTTAACACTTTTAAATACTTCTTATTTTATTTTTTTCACTTTATTTTGATGGTCCATTTGTTGAATTTAAGTTACATTGCATCTACATGCCAACTAATACTTATTAGATTATAAGTAGACTGTTAGGTTGGGGTTAGTGTTGGGTTTAGGGTTAGGGTTAGTATAAGTTGACATGTACTACTAAAGTTTCTTATAGTCAGTAAAATGTCAGATGAAGGAGCATATCAACAGATATTAAGCAGACCATCAAGTGTTATCATTTTTT
Associated Phenotype:
Not determined