Busch Lab

ZMP

myo10l3

Ensembl ID:
ENSDARG00000074143
ZFIN ID:
ZDB-GENE-070912-237
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.
Availability:
Order Allele From ZIRC
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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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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