Busch Lab

ZMP

myo10l2

Ensembl ID:
ENSDARG00000017004
ZFIN ID:
ZDB-GENE-070912-277
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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