ZMP
myo10l2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myosin X (MYO10) [Source:UniProtKB/TrEMBL;Acc:B0S541]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39909 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38351 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11921 | Nonsense | Available for shipment | Available now |
sa19845 | Essential Splice Site | Available for shipment | Available now |
sa19844 | Nonsense | Available for shipment | Available now |
sa19843 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39909
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 |
---|---|---|---|---|---|
ENSDART00000043201 | Essential Splice Site | 39 | 1753 | 2 | 32 |
ENSDART00000124493 | None | None | 243 | None | 6 |
ENSDART00000139515 | None | None | 107 | None | 3 |
ENSDART00000140159 | Essential Splice Site | 355 | 2069 | 11 | 41 |
The following transcripts of ENSDARG00000017004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42748476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42797940 |
GRCz11 | 2 | 42647358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGATGTTAATTGCATGGTGTTCATACGAATGAGCTCTGTGTATGTGTA[G/A]CGCTCAGTAAAGCTGCAGATCTGCTGGGTTTGGATTGTGCTCAGCTGGCT
Long Flanking Sequence:
GTGTTGAAGCAGGGTTGGAACTTAACTGTGCAGAGCTGCGGCCCATCAGGAACTGGAATTGACACCTGTGTGCTAGACCAGCTATAATAGCAATTTAAAAAATACATTTCCCATTAAAAATGCATACATCATAATTATCATCATCATGCGGAAATTGCAGTTTAAAAGCAAATGTGTTAAATAATTATTAGTTCTTTTCTTGTTTTACATATTTCATAATATATATCACAACCATATTTTGGTGTTTATTTGTTTTTGTTTAAAGAATGCACTCAGGACAATGCAGTTTGGAGAGGAGAACATTAAAGAGGTGTTGAGGCTCCTTTCAGGAATCCTACATGTGGGAAACATTGAGTTTTTAACAGCAGGCGGAGCACAAGTTTGCTCCAAAACAGGTAAATACTTCTCTCCGTTCTCTCTCTTTCACATTGTCTTGAATTGCTTAATATTACTGATGTTAATTGCATGGTGTTCATACGAATGAGCTCTGTGTATGTGTA[G/A]CGCTCAGTAAAGCTGCAGATCTGCTGGGTTTGGATTGTGCTCAGCTGGCTGAAGTGTTGACCCACAGATCAATGATCCTCAGAGGAGAAGAGATCAGCACACCGCTCACAGTAGAGCAGGTAAACTCTTTCAACACACACACATTCATGGTATGGAGAAAAAAAATTTATGAAAGTCATTATGAAACACCAATCCACTATTTCTTTCAGATATATTTACACATTTACAAAATATCTCAGTTCAATAGCAGGGCATTACTCTTAGGCGTTAGAAACATTACAAAAGTAAAGCAGAAATCAAGTCCATCCTATAACAGAAAATATATAAAAACTTGTATGGTAAGAAATAGTACAACATTTTATTATATTTGTTACATTTGAAAGTTACTGCAAATGAGTTCAGAAACTCTCACTCCCTCTAGTGGACTTAACAAGTAATTACATTTCTTCAATAAACATTTTTCTCACTTTACTGGAACGTTTTATGACTATGTATGGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38351
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 |
---|---|---|---|---|---|
ENSDART00000043201 | Nonsense | 105 | 1753 | 3 | 32 |
ENSDART00000124493 | None | None | 243 | None | 6 |
ENSDART00000139515 | None | None | 107 | None | 3 |
ENSDART00000140159 | Nonsense | 421 | 2069 | 12 | 41 |
The following transcripts of ENSDARG00000017004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42746992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42796456 |
GRCz11 | 2 | 42645874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTTTGTACTCTCAGTGCTTCACTTGGATCATTCGCAAACTGAACAAC[C/T]GAATCAACGGCAGTGAAGACTTCAGATCCATCGGCATCCTGGACATCTTT
Long Flanking Sequence:
TATTCAGGTATATTTAATTAATACAGATATTTTAAATTTGTTCAGTCACGTGGTTATAATAATAACTGATAAAAGTTTGTTGGCTCTGACTTAAAAAAAATTTTAACTAATAATAAATTTCACAATTTTGAAAGATATCCCCCAAAACTTTATTCTGTCCAATTTACTTGCTTATCTCTATTCTCTAACTTCTGAAAATTAAATTAACCTTTTTAATGTTATAATTTCATATTAACACTGATGTTAGATGCTTTTCTTTACCTTTATTTTTTATTTGACAACATATAATTTACTATAGGTATACCAAAGTGCAGAAAATGTATTTTATTTGCAAAAACCAAATATTATTGCATGATACATTCGTTCATCTTTAATAAATCATACATTAAAGATGTGTGTGTGTGTTTTTGTTTGTGTGTCAGGCGGTGGACTCGCGAGACTCAATGGCGATGGCTTTGTACTCTCAGTGCTTCACTTGGATCATTCGCAAACTGAACAAC[C/T]GAATCAACGGCAGTGAAGACTTCAGATCCATCGGCATCCTGGACATCTTTGGCTTTGAGAACTTTGAGGTGGGAGTTAACTAGGCTTTTTACTATTGTTTTTGTGGTTGTTTTTTTTTTTGAGTTTTGTTTATAGTTTGAATTTGTATTTTGATTGGTGTAGGTCTTTAACATCTGACAAAGAGACTATCAATGAAAACTAGTCTTTGGGCTAATTTGCGTAAATTTATGTTCTTGATGAACGTTAAATAATGTACACTGTCCCTTGTTATGAAATAAATAAATTGAAAAAATTTAAACTGGTAAGATTTACAGACACCGGTTTGAATCAAGTGGTAATGTTAGTCCCAAACAATTAAAACAATTTTCAAATCTAAATTTTAGACCTTAAAAAAACTTAAATTCACTGAAATATGAAGTTGTAGGTCTTAAATATTTATAAACAGGTCTTCATTTTCTTTTATCCATATAAAGCTCCCCAATACAACCAACAATCCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11921
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043201 | Nonsense | 344 | 1753 | 11 | 32 |
ENSDART00000124493 | None | None | 243 | None | 6 |
ENSDART00000139515 | None | None | 107 | None | 3 |
ENSDART00000140159 | Nonsense | 660 | 2069 | 20 | 41 |
The following transcripts of ENSDARG00000017004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42731710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42781174 |
GRCz11 | 2 | 42630592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATGCCCGGTCAGTTTGAGCAGACTGTGGTCCTCAATCAGCTCAGATA[T/G]TCTGGGATGTTGGAAACRGTGAAAATCAGACGTTCTGGGTTTCCCATCAG
Long Flanking Sequence:
CATCCACCTCCCCCATCAAGCTCAATGACATTGATCCTGTCTGCTTTCTGTTACTCTCGCTGCATGTATCAGTATGTTAATGTACCACTGACTAGAATGAATGATTGTGTGTGTGTGTTGTGTGTGTATGTGTGCTGACCTTGCTCTCACAGAGCTCATTCAGCACTCATCTCTTCATCTCACTTTCATTCGCCAATTTCTCTGGTTCAGTCCTGCTTCCAAAGAGATGACATTTAGAAGCGGGGATCACAGCGCCCCGTTTCCGACCTCACCCCCACACAGGGTCAGAGGTCATCGGGAGAGGGGGTGATAATGACCCACTTAATGTGTTTGAAGAATGAGTCCACTCAAAACTCTACTCGGCTATATTTGAAAGCAGAATTAATGCGGCTAATTTAGATCTGACTTTTCATTCTTTATTTTTTTAAATGTCCCCGTCTCTGTTTTTCACAGATGCCCGGTCAGTTTGAGCAGACTGTGGTCCTCAATCAGCTCAGATA[T/G]TCTGGGATGTTGGAAACAGTGAAAATCAGACGTTCTGGGTTTCCCATCAGGAGGACGTTTAAGGATTTCTGTTCCAGGTTTGTACGCCTAAGACAGTGTGCTCTCAGTTTACTGAAGTAAAAACTAAAGCACACTACAGTATTTATTACAGTTTATCAGTTCAGGATATTTAAAAGCAAAGCTTGATGTAGCAATAATTAAGTTGTAAGTGCTATAATATACAGGTGAAGTCATAAAATTGTGAATTTTTTTTTCTTTTTTAAAAATTTCCCAAATTATGTTTAACAGAGGAAAGAATTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAATGCAGTTTTTAGTTAAAAAAATGTTTTAAGGAAAAAATAAGTGTTATTGGCAACAGCATGAGTTGAATCACTCTTTTGTGTTGTGTTTTTGTCAGGTACTATGTGTTGATGAGGGCTTTGGCTTTGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19845
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043201 | Essential Splice Site | 409 | 1753 | 13 | 32 |
ENSDART00000124493 | None | None | 243 | None | 6 |
ENSDART00000139515 | None | None | 107 | None | 3 |
ENSDART00000140159 | Essential Splice Site | 725 | 2069 | 22 | 41 |
The following transcripts of ENSDARG00000017004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42730046)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42779510 |
GRCz11 | 2 | 42628928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAATCAGGCTTGAATGATGGGCTGCATTTGTTGTCTTTTCATTTTGC[A/T]GGTGTTTATGAGAGAGAGTTTGGAGCTGCGGTTAGAAAAACAAAGAGAAA
Long Flanking Sequence:
TGCTCAAAACACACCCATAACTCATTAAGAGAATAAACACAGCTCTGTTAGACCACTGCCAGGGCGCAGAGCACATTTTTTCTGTCCTTAAAATAGCAAAAGTGGATTCGGACACACCCTAATGCTTTTGCACCATGCGCTTTAGACCCTGCGCTTAGATCATTAAAATAGAGCCCACTGTGTAAGTTTTATTTGCTCGCGCACTCATGATTGAGTATTATGAATTATGAGTACAACATCTTTTGATAACACAATTTTCATGGAAATTCAACAGACATCAATAAGTTTAACACTTAAGTACATAAAAAATGCTTTTGTAATTTTTTTCTTAGTAATATTTTTAAGTAATGCTGTAAATGGAGGCTTTTACTACAGTAATATTCATAAGGACCTTAACTCCAGTCCCTGATTTGTGTACTTCGCCACCAGTTTTTTTATATACTTCTAGAACAGTAATCAGGCTTGAATGATGGGCTGCATTTGTTGTCTTTTCATTTTGC[A/T]GGTGTTTATGAGAGAGAGTTTGGAGCTGCGGTTAGAAAAACAAAGAGAAACAGAAGTTCTCAAAGCAGCATCAATTATCCAAGCTCATATACTGGGCTACAGAGCACGGTAAACACACTGGCACGTGCATATACACAAACAAACACTAAAGTACTAAACTCTAATGTAGTCACTGTGTTTTTGCTCTCTGCTGGTCACAGGAGGCAGTACAGACGCCTGTTGCTGTGCATTGTTGTCATTCAGAAAAATTACCGTGCTCTATATTGGCGCCGACGCTTTCAGACAATGCGATGGGCCACCGTCACCTTACAGAAGAGGCTCAGAGGTCAAAGGGCACGAAGGCTCTATGTTCACCTTTTAGAGGAGAAGAGGAAGAGGGAAGAGGAAGAAAGGAGACACAGAGAAGAACAGGAGGCACTGGAGAGGTGGGCAGTTTGTGTGAAAGTTGCCTTTATTAATAAAGTTAGATTGTTGTATAATAATGCTTTCTAAGTTTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19844
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 |
---|---|---|---|---|---|
ENSDART00000043201 | Nonsense | 490 | 1753 | 14 | 32 |
ENSDART00000124493 | None | None | 243 | None | 6 |
ENSDART00000139515 | None | None | 107 | None | 3 |
ENSDART00000140159 | Nonsense | 806 | 2069 | 23 | 41 |
The following transcripts of ENSDARG00000017004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42729709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42779173 |
GRCz11 | 2 | 42628591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGATGGGCCACCGTCACCTTACAGAAGAGGCTCAGAGGTCAAAGGGCA[C/T]GAAGGCTCTATGTTCACCTTTTAGAGGAGAAGAGGAAGAGGGAAGAGGAA
Long Flanking Sequence:
TTTTTAAGTAATGCTGTAAATGGAGGCTTTTACTACAGTAATATTCATAAGGACCTTAACTCCAGTCCCTGATTTGTGTACTTCGCCACCAGTTTTTTTATATACTTCTAGAACAGTAATCAGGCTTGAATGATGGGCTGCATTTGTTGTCTTTTCATTTTGCAGGTGTTTATGAGAGAGAGTTTGGAGCTGCGGTTAGAAAAACAAAGAGAAACAGAAGTTCTCAAAGCAGCATCAATTATCCAAGCTCATATACTGGGCTACAGAGCACGGTAAACACACTGGCACGTGCATATACACAAACAAACACTAAAGTACTAAACTCTAATGTAGTCACTGTGTTTTTGCTCTCTGCTGGTCACAGGAGGCAGTACAGACGCCTGTTGCTGTGCATTGTTGTCATTCAGAAAAATTACCGTGCTCTATATTGGCGCCGACGCTTTCAGACAATGCGATGGGCCACCGTCACCTTACAGAAGAGGCTCAGAGGTCAAAGGGCA[C/T]GAAGGCTCTATGTTCACCTTTTAGAGGAGAAGAGGAAGAGGGAAGAGGAAGAAAGGAGACACAGAGAAGAACAGGAGGCACTGGAGAGGTGGGCAGTTTGTGTGAAAGTTGCCTTTATTAATAAAGTTAGATTGTTGTATAATAATGCTTTCTAAGTTTCTGATCTTCTTGATGTTGCTGCTTTAATTGTTAGAGAGAGACATCGCTTGTTGGAGTTGGAGCTTTTAGCACAAGCAGTAAGTGAATGATATATATATTTATTGTCTGTCTTCATCTATCTTCTGTCTATCTGTTGTCTGTTTGCCTGTCTGTCTGTCTGCCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19843
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043201 | Essential Splice Site | 1465 | 1753 | None | 32 |
ENSDART00000124493 | None | None | 243 | None | 6 |
ENSDART00000139515 | None | None | 107 | None | 3 |
ENSDART00000140159 | Essential Splice Site | 1781 | 2069 | None | 41 |
The following transcripts of ENSDARG00000017004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42713378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42762842 |
GRCz11 | 2 | 42612260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATAGAGAGCAGGACTGTGGTGGCCGACATCCTCGCCAAGTTTGAGAAG[T/C]GAGTCTCACCTTTTACACACCAGCTTCAGTCTGTCCAAAACCACAAATAT
Long Flanking Sequence:
TAAAAGGATGATAGTATTAGTAAAAAAAAAAAAAAATGTGTCATTTAATATATGGCTGTTAATATTCCTAGGTGGCCCGCCCAAGTAAAATCTGTGTGTGAAGCACTGCATATAGCTTGAGCATCAAAGGGTTAAAAGGTGCATGAAGCGAATTTTGCCAAACAGTGTTGATATTTGAAAGCAACAAAACAAACATGCCCATAACCCAACAGGACCTCGCCCATTTTTTGATATCTCTCCCTTAGTTACAAGACACGCCTCTTACTGCTTATTGGCTGCAAATGTGTTTTGGCACTTGGTCTGACACTGTGTTCAAAAGCTATCTGACCTGTATATGTGTGTGTGTGTCTGATGGTGTGCAGGTGGTGGAGAAGCTGCTGAAGGGTCTGTCTATGGAGGACTGCAGGAACATGTTTGCTTTGTTTGAACACAACGACAACACAGACAGAGCCATAGAGAGCAGGACTGTGGTGGCCGACATCCTCGCCAAGTTTGAGAAG[T/C]GAGTCTCACCTTTTACACACCAGCTTCAGTCTGTCCAAAACCACAAATATTTTAATATTTAAATTTAATATGATATAAATATATTACAACAATTTTAATACTGTAGGTTGCATAAACTAATTTATAACTCTCTAAAAGGCTTCTGAAGACATAGCATCAAATGTAAACAAATGAGATGAAAGACCATGAGAGAATTTTGATTAAAAAAAAAAAATTTATTAAATGGGTTGTTCCTTACAATATAAAAGGCTCTTTCACGCTAAGGACCAGAAATTTTTCCATCACAGCGGAAACAACAACAGCATTCTTGAAATCAGATATTATAGGAATATTTGCTGTATCTTGATACAAAAACAAATTTCATAGCACATTCTATGAGTTGTTTGAATTATATGGAACAACTTTCTCTCTCTCTATTTCTTTCAGGTTGGCCAATAAAGAGCAGGACGGAGAGAGCTGGAAGTTTTATTTCAAGCTGTTCTGTTTCTCTGAACCTGAGA
Associated Phenotype:
Not determined