Busch Lab

ZMP

ENSDARG00000074723

Ensembl ID:
ENSDARG00000074723
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 15 alleles of this gene:

Allele Name Consequence Status Availability
sa45244 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33822 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10569 Essential Splice Site Available for shipment Available now
sa20661 Essential Splice Site Available for shipment Available now
sa728 Nonsense Available for shipment Available now
sa11662 Essential Splice Site Available for shipment Available now
sa15852 Nonsense Available for shipment Available now
sa20660 Nonsense Available for shipment Available now
sa17425 Nonsense Available for shipment Available now
sa13802 Nonsense Available for shipment Available now
sa14730 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa45244
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
ENSDART00000113347 Essential Splice Site 208 1997 5 44
Genomic Location (Zv9):
Chromosome 6 (position 11057714)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10911340
GRCz11 6 11146767
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGTCTGCATTTCCCTTAATTTTTGCCCCTTCAGATTTACTTGAAAAG[G/A]TAAACCTTGCTGTCTGACTCACGTCTAACTACCAGAAACCAATATTCTGT
Long Flanking Sequence:
CTAACGATGTTTAAGAGAGCAATGAAATTTTAACAGCATGTCTGATAATATTTTTTCTTCTGGCGAAGGTCTTATTTGTTTTATTTTGTTTTTATTTCGTATTTTGTAAACACTTTTTTAAGGACAATTTTATTCGCCCCTTAAATTTTTTCCCCTATACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTTGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTATTGAAAAAGATCTAGTCAAATATTATTTACTGTCATCAAGGCAAAGATAAAATATACCAGTTATTAGAAATGAGTTATGAAACTATTATGCTTAGGATTTTGTTGAAAAAAATCTTCTCTGTTAAACATAAAATGGGGAAAAATAAAAAAGGGGGTCTAATAATTCAGCTCATCTGTTTCATGTGTCTGCATTTCCCTTAATTTTTGCCCCTTCAGATTTACTTGAAAAG[G/A]TAAACCTTGCTGTCTGACTCACGTCTAACTACCAGAAACCAATATTCTGTGCTAAAGTGCTAAGAGCATAAATCCTACTGTTGTTCTGATAATACAGTTTGGCACTGGATATATTGTAAAAGGCAGAATCACTCCACCATTTTGTAGAGAAAGTGTCTTTATGCCAAAGTGAGAATTTCGCCCACTCAGCATCTGTGATCTGATCTCTTCTTCCAGAATCGAGTGGTAAGGCAGAATCCAGGAGAGAGGAACTACCATATATTTTATGCTTTGCTGGCTGGGGCTAGTAAAAGCGAAAAGGGTGAATGAATAAACAGTGCAAATAAATACACACAGTGCTGATTTATCAAATAAAAACACGAAGCCATTTTGAAGGACTGAATGATAAGATATGTCTCTGTGGTTTTAGAAACATATTTTCTGGAAGACTCCCCGGAGTTATTTCATTACTTGAGTCAGTCAGGATGTGTGAAGGACCGCAGTCTCGATGACAAGAAGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33822
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
ENSDART00000113347 Essential Splice Site 514 1997 14 44
Genomic Location (Zv9):
Chromosome 6 (position 11051657)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10905283
GRCz11 6 11140710
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCAGACTGGCAGACCATCAGTTTGGGATAAAACATTACGCTGGAGAG[G/A]TACATGAAGAGTCTCTCTCTGTCTATCCCTCTGTCTCTTTATGTATCTCT
Long Flanking Sequence:
CCTAAGAGTTACCTAAACATTTTAAAAGAATGAACAATGAGTTGTGTTGTGCAGGGAAGGAATTCATTGGGAAGCCATTGACTGGATGGACAATGCAGAATGTCTGGATCTGATCGAGAAGGTAATTCAAACATGGTCAGCAGTGTGATTATGATTCATTTAGTCATATTATTATACTTGTATTCAACCAGAAGTCAGCTTTATCATTACAGTCGTTCAGTTATGCCCTTATTAATTATATGTTTTTTATGCAGAAATTGGGCATGTTAGCTTTGGTTAATGAGGAGAGCAGATTTCCCAAAGGCACTGACTTCACCTTGCTGGAGAAACTACACGGCAGACACTCTGTGAGTTATATTCTCATTAGAAAGACACAATGAAATTAATCTACGAATGTAAAAAACTGAACACTTGAGGTTGTTTTTCCACAGACTAATCCATACTATGTGAAACCCAGACTGGCAGACCATCAGTTTGGGATAAAACATTACGCTGGAGAG[G/A]TACATGAAGAGTCTCTCTCTGTCTATCCCTCTGTCTCTTTATGTATCTCTTCGCATATTTATAGTTAGTGCTTGACATATATTGTTTATGATAATATAGTAATTGTTTTAACAATGTGCGAGCCTGTGCTCCTGTTTCCCCCACAGACCAAAGACATGCGGTACAGGTGAATTGGGTTAGCTAAATAGTCCCTAGTGTATGAGTGTGAATGAGTGTGTGTGGATGTTTCTCAGGAATGGGTTGCGGCTGGAAGGGCATGAGCTGCGTAAAAACGTGCTGGATAAGTTGGCGGTTTATTCCGCTGTTGTGACCCCGGATTAATAAAGGGGCTTAGCCGAAAAGACAGTGAATGAATGAATAAATACCACAAAACTACTTGATGGTGTGTATTATTTAAAAAAATGAATAAGTTTGCTTTACATTCCTATCTCTAAATGGACAACTCTGGACAACTTTTATGGTTTAGTCATTTTGCTCGATAGTGAACAGTAATATTCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10569
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Essential Splice Site 605 1997 17 44
Genomic Location (Zv9):
Chromosome 6 (position 11049150)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10902776
GRCz11 6 11138203
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTCCAAYCCCTTCTTTGTGCGTTGCATCAAACCAAACATGGACAAA[G/A]TGAGAGCAGTTACAKCACCCAATAACAACYGCATGCCATTMAACACRANNNGT
Long Flanking Sequence:
CTTGTATGATGTAAGGGGGATTTTAGAGAAAAACAGAGACACATTTAGAGATGATATATTGAACATGCTGAAGGATAGCAGGTAGGACATAAATGCACAACGCACACACACACACACATGCTTGTGTATGCAGTTTATCCGACACATTATTTAACCTGTGCGTTATTCTGAATGTGTGCAGGCTGGATTTCATCTATGACTTGTTTGAGCAAGTGAGCAGCAGAAATAACGAGGAGACCTTGAAGATGGGCACGGCCAGAAAAAAGCCCACCGTCAGCTCTCAGTTCAGAGTGAGAAATAACTCCCATAATAAGACATTTACCTTAATAATACACCTACAATTAAAAGCTGCATTTCAAACAATCAGTCATTCACTGTCTGTTCTGTTTTGTCAGTGATTTGATTTTTCTGCTCCTCAGGACTCTCTTCATTCCCTAATGGCCACTCTCAGTGTGTCCAATCCCTTCTTTGTGCGTTGCATCAAACCAAACATGGACAAA[G/A]TGAGAGCAGTTACATCACCCAATAACAACCGCATGCCATTAAACACGAGTCATACAGTACATTTTATGCCCTTGGTATTTGCTCTTTAATAGACACCAAACAAGTTTGACCCAGAAGTGGTTCTTAATCAGCTGCGGTACTCTGGCATGCTGGAGACAGTGAAGATTCGCAGAGCCGGATTCCCTGTCAGACGCACATTTAAAGACTTCTTCACCAGGTGAGTGTTCTAAAACATGGACTGTTGACATGATGTTGCATTTTTACTGTCGCACATGACAAGAATGAATATATTTTGTGTCATCATCATTTACCACAGAACTGCCACTCAATGGATATTCTCTTTTTTTCGGATCATTCTCTGTAAACACTAGAGATGGTTGTGCATGAAAATCCCAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCGTGTATGGCACCAACAACCATGCCACATTCAAAGTCACTTAGGGTGCTTTCACACCTACACTTTTGTTTCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20661
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Essential Splice Site 778 1997 21 44
Genomic Location (Zv9):
Chromosome 6 (position 11044188)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10897814
GRCz11 6 11133241
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCAGAAGCACAGGAGAGGGCAAGTGGCAAGAGGAGTCTGCCGTAAACT[A/G]CGAGACGAGAAGAAGAAGAGAGAGGAGGAGGAAAGGAAAAAGAAAGAGGA
Long Flanking Sequence:
AGCTGAGACCCACTGTGCCTCCGTGTCGCCAATAATGGTTCCAATATGTTAACATATAGGTTGAATAAATGGCATAATATTTTTAAAAATCCAAACTTGAATATCATATACTGTGTGTGATTTGCACAAATTAGCTTATATCAGATTTCTGTATGAGCCGTCACACATCCTAATTTGCACTAGGCAGTGTTTAAAAGAATAAAATCTTTAGTTTTACACTAGCAGATGCACAGTATACCAAGGAATTTATGAAAACACAACTTATGATTACAGACCCTTTCTATTATATGTGTAAATGCTTAATATTTACCTATTGGCTGACAATGACATGACACTCATTACAGAAAGGACTTTAAGAAGGCTCTGGAGAGCATTGTGACCATCCAGAAGAACTACCGCACTCATCTCTATCGACGGAGGTTTCAGCGGAAACGCTCTGCTGCGCTGGTCCTTCAGAAGCACAGGAGAGGGCAAGTGGCAAGAGGAGTCTGCCGTAAACT[A/G]CGAGACGAGAAGAAGAAGAGAGAGGAGGAGGAAAGGAAAAAGAAAGAGGAGCAGGAGAAGAAAACAGAGGGAGATCGTGAAAAGAAAAATGAAGAGGAAGACGAGGCTGAGGTAAGTGATTTTAATGTTTCTTTTAAAGGGCACCTATGATGAAAATCGTCATTAGGAAGCTGTTTGGACAGAACTGTGTGTAGGTACAGTGTGTCCGCAGTCTTATTGGAGTGATAGAAACACTATAAGTGTCTTTTTGTTAGAATAGGATCCCCAAATTGATTGACAGCCGTGCTTTAACATGTCTCCATAGTAACTCTTATAATTATATGTACAAGACAGGACATGTGCAAAGCAACCGGGATTAAAAGATCTGTTCAGCTCTCTGTGTTCAGCAGCACCTCAAGAATGAGTTTTACAAGTTTAAAATGTTTCTAAAACAGTGCATGTTTGTAATAAAGACAGTAAAATTGCTGTAATTCATCACCACTGCTGCTTGTCATTACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa728
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Nonsense 805 1997 23 44
Genomic Location (Zv9):
Chromosome 6 (position 11042940)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10896566
GRCz11 6 11131993
KASP Assay ID:
554-0635.1 (used for ordering genotyping assays)
KASP Sequence:
ATRGGTGCCCTTTAAATTCCATGYATGCCAGCTGTTTRTGTATTTTAAGG[C/T]AAAATAACCTTGAAGTCACCATTACTGTATGTAATTAGTGTTNNGTTTGG
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAATTCTATAACTACATTTTGTGTGACTCATCTTTGCAGAAAGGCTTGAATTAACTCAAATCAAATACATCAAATAACCATTGGGAAAGTTCTTAATGCAGTAAAGTAGATTGCTTCATTGTTGTCTGTCACTGTGCTACTTATATACGAGACACAGCAGGAGGAGCTACACCCATCATAGCAATAGTGAGAAATCTCTTTAGCTCTGACATGCACGTCGGAACTGTGGCTGGGAGAACCAGCTCATGTCCATGAAAGGCACAGGTAACAAATATAGCTACATCAGTCATAACAGCTCAAATTTCCAATATACACAAAGGTATAATAAATAATCTGATGGGTATTTTGAGCTGAAAATTTACAGGCACATTCTGGAGACACAAAAGACAAAATTTTTAAAAGGAGTAAAATAGGTGCCCTTTAAATTCCATGCATGCCAGCTGTTTATGTATTTTAAGG[C/T]AAAATAACCTTGAAGTCACCATTACTGTATGTAATTAGTGTTCTGTTTGGTAAGGTGTTATTTTTTCAAAGTAGATTTAGCAAGTGATCATCATTTTTTAAGTTTGTCTCAGCTTTCTTCAAACTTTGAAACTAAATATGCGATATATTTGTTCACCTAAGCTAGAGCTGCACGATTAATGGAAAAAGATCTCAATTCATCCCCCTAGACAATCTTAATCCAGCATTTCTATGATTCTGCCAATCATATTTTCAAGTTCAGGAGAGAAGCAAAGGCGGCTGCACGAGTCTTTTCATTGTTTCACATACGTGGCTCAGTGACATGGACACCTCCAAATGGTGTTAAAAGAGTCACATACTGTATTGATAAGATACAATTCACCTAATATTGTCATTTTTATCCTCATATAATGCTGTATTCGCGGTCGGGAAATCACACGTGACGTGAACTGCTGACCATGAGCTGTTACCACAGAGAGGGTGGGCACACCCTACTTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11662
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Essential Splice Site 1069 1997 27 44
Genomic Location (Zv9):
Chromosome 6 (position 11039810)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10893436
GRCz11 6 11128863
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAATCCTACAACCGCAGCTCAGATTCAGTACGKTACWCAAAGACTRTGG[G/A]TCTGACAACAATCATTCTTAAAGCTTAAGGTGGACGYAATATGTGMATTT
Long Flanking Sequence:
AGAGGAAGAGTGCATACCACTTCCAGAGTTCCCTCCGCCAGCAGAAGGTCCAGTGGATCAGGAGATCTTAGCCACTTTACCGCCTCCTCCTGCTGCATTCGCTGAGGGCACGGTGGCTCCATCAGCACCCAACGTTCCACCTGGAGCTCCTCCTCCACCTTCTCCTCCTCCACCTCCTCCTCTTCCTGGCGAAACCAAAAAGGAAGAGGGCAAGCCTGAGGAGGCTAAAACAGATAAAGAGGTGGATGGGAAAAAGGAGGGTGAGGATGTGGACCGCACCAGCAGGCTGACGGCAGCAGAGTCTCTGCCGGACACTGAGGAACCCATCTACAGTGTACCAGGGGATGGAGAGTCGGACTACGACCAAGATGATCTGGAGGATGGGCAGAGCAGCATTGCAGCGACGGACGGAGAACATGCACGCAAGTCCACCTGCACCAACGCAAGCCAGGAATCCTACAACCGCAGCTCAGATTCAGTACGTTACACAAAGACTATGG[G/A]TCTGACAACAATCATTCTTAAAGCTTAAGGTGGACGTAATATGTGAATTTTCAAACTTATAAGATTGTTTGCACTTTTGGCTTAAAAGCTGCTTGCGAATTCGCAAACTAGCTGAGTAGGTACTGCAATTTAATTTAAGTTTACTTCACGACAGGTAGATATGTATGTTCTATAGCAGGAGTGCCAAACCCTGTTCCTGGAGATCTTTCTTTCTGCAGAGTTCTTGATTAAACACACCTTTCTGTAATTACCAAGAACTCCTTCAGATCTGAATTAGTTGGTAAGTTGTTTCTTAACAGGGTTGGAGCTGAATTCTGCTGGAAGAAAGATCTCCAGGAACAGAGTTGGGCACCCCTGCTATAGAACATACTTATCTAACAGTCGTGAAGTAAACTTAAATTAAAATGCAGTACCTACTCAGCTAGTAAGTAGATCTCCAGGAATAGGATTGGGCAACCCTGTTCCTGTATTGCTGCCTCCGAAATCTAATACTTCCATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15852
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Nonsense 1265 1997 33 44
Genomic Location (Zv9):
Chromosome 6 (position 11033525)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10887151
GRCz11 6 11122578
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTTGACAGCTGGTTCTGCTCTCCTTCCCTCAGGGCACACTGGATGTY[G/T]GATTGATCGATTCGGTTTGTGCTTCAGACAATCCTGACCGGTGAGTGTGA
Long Flanking Sequence:
TATTAGTTGTTAATACTTCCAGATTTAAGAGAGTACCCAATCAATGACTGAAGCCTCAAAAATTAGAGGGTCTGTTAAATGGCATGACCTATTTTCGGCTGATAAATTCATTATAGTGAAACATTTGGTACATCTCTAATGTCAACACACTTCTTCCCACTTGATTCCCATTGTTGCACATTACTGCTGTGTGATTGGCTCCTAAATCAATAAAGAGTAAAAAAGTCCAGAGCTTATCATTGTTATTTTTTTGTAACTGCACCAAATGTCTCTCCTTAATCTCCGATCTTTCTTCTGCTCCTTTTTTTTTCTTAGCGGCTGGTTCACCATGTTGAGTCGGGTCCACAATGCCTCCCCAGAGCAGCTGCTGGAGATGTCCCATGAGCAGGCCAACCCAAAGAACGCTGTGGTCAGTGTTCTGATATCTCATGCTCTCTTATTATTAAAACACCTGTTGACAGCTGGTTCTGCTCTCCTTCCCTCAGGGCACACTGGATGTT[G/T]GATTGATCGATTCGGTTTGTGCTTCAGACAATCCTGACCGGTGAGTGTGAGAAGATGCCAAATGCAGAAAATGATTGAATAAAAAGAATACAGTCCCCAGGGAATACAATTTTACTATGCTAACCTTGAGCGACACGGTGGCTCAGTGGTTAGCACTGTCCCCTCACAGCAAGAAGGTCACTGGTCCCACAGTCCCCCAGGTTTGAGAACTGGGTAGCAGCTGGAAGGGCATCTGCTGTGCAAAACATATACTGGATAAATTGGCGGGTCATTCCGCTGTGGTGACCGCTTATGAATAAAGGGACTAAGCCGAAGGAAAATGAATGAATGAATATACTAGCCCTTGGGTTATCTAAATATAAGCTAGTGTGCTTCAAAACTATGACAAGATTAACTTGTAAGATATATGCAAAATTCAAAACTGAGGGCTTTATTTTGACGGTCCATGTGCAGAGCGCAAAACGCAGGGCGCAAATGCTTTCAGGGCGTGTCAGGATGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20660
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Nonsense 1359 1997 35 44
Genomic Location (Zv9):
Chromosome 6 (position 11031363)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10884989
GRCz11 6 11120416
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGAAAAAGCGCTGGTTTGTCTTGACGCATAATTCTCTGGACTACTAC[A/T]AGTCTTCTGAACGCAATGCATCCAAGATGGGGACTCTGGTTCTAAACAGC
Long Flanking Sequence:
AAACAGTGGTAAGGATAGACTGCCCAACTGTTATGGTTACTGCCCAAACCCTAAATATAACCATTTTTTGTGATGCTAACACTGTTTTCCTCCAATCAGGCCCAACTCCTTTGTCATCATCACAGCCAATCGTGTGATCCACTGTAACTCAGACCTGCCAGAAGAGATGCATCACTGGATCAGCCTGCTGCAAAAACCCAAAGGAGACTCGAAGAGCGATGGACAAGAGTTCCTGGTCAGAGGTGTGACAGTCATCTTCAAGTTTGAAACTTTTAGAAACCAAACCTAAATGTAAACTGTGTTTGATTTAGTTCTGAAAGATTCCCATATGAGCATTTAGATTGAACTCAATATGATTGTGTGTATATTTTAGATGCTGTAAATGTTGCTTTTGTGACACAGGATGGCTCCACAAGGAGATGAAGGCGGGAGCCAAGAGTTCTGCTCTTAAACTGAAAAAGCGCTGGTTTGTCTTGACGCATAATTCTCTGGACTACTAC[A/T]AGTCTTCTGAACGCAATGCATCCAAGATGGGGACTCTGGTTCTAAACAGCCTGTGCTCTGTGGTCCAACCTGAGGAGAAGAAGTTTAAAGAGACTGGTATGGCTACTTATTAAGTCTGTTACAAGATGTATGGTATATGGTTTACAGTACTGTATGTATACATTACATATACAATATAATAAACAGTATATCATTGAATATAGACTATAGAGTATAGTGATTTTAAACATTATTTATTTAAAAAAACTAAACAGTTATTTTATTAAACAATTATAATCATTAAAATAAGAGTGTGATCACTTAACATCTTTAGGACTAGAAAGATAAAACATTTAAATTCAAATGAGAAGTTGCAAAATATATTATAATTTACTAAATTTAAACTAAATTATATTTATTTTCGATTCTCTTGATTTTTCTGCTTTATTAAAATTGTATTTAATATTTCTCCCTAACATACAGTATATTTGGTCCCACTTTATATTAAGTGTCCTTAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17425
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Nonsense 1454 1997 37 44
Genomic Location (Zv9):
Chromosome 6 (position 11028620)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10882246
GRCz11 6 11117673
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTTTNGYGATTTTGTGTAGGAAAACAGTGTTAATTCTGAAGCTGTGGAA[C/T]AAATGTATAGAAGAAACCCTATCCTGAGATACACCCAGCAWCCCTTGCAC
Long Flanking Sequence:
GGTCAGCAGAGTATTTACAAATGTAATTATAGAAGTTAATTACAGATGTAATTACATACAGGTATTTAATCAAGTATAAGTATTCATCCAACATTAAAAAAAACAAATAAGTACAATATGTGTAAATAAATGAGTGAATGCAGTACTATAACCATGAGAATACATTATGCAATTGTTTCTTTCATTGAACATACAGTAACATGTCCATGCTGATGTGTGGTTCGACTGCAGGTTACTGGAACATCATAGTTCACGGACGTAAACATTCATATCGTCTGTACACCAAGCTGCTGAATGAGGCCATGCGCTGGGTTTCTGCCATTCAGGGTGTCATTGACAACAAGGTGCCCATTGAAACGCCCACCCAGCAGCTCATCAGAGACATCAAGGTAATTCAGCTTAAACACATATGTTTAGTCTTTGCAATCAAGAATAAAACTCGAACTTGACATTTTTGTGATTTTGTGTAGGAAAACAGTGTTAATTCTGAAGCTGTGGAA[C/T]AAATGTATAGAAGAAACCCTATCCTGAGATACACCCAGCATCCCTTGCACTCGCCTCTTCTGCCACTGCCCTATGGAGAGGTCAGCGACAGCCGTGAGTATCTCTGATTGGCTAAATCCCTCACAAATGAGAAACAAAGGAAAGGTTTTTGAAAAATTGACTGACCGTCCGAATGAGCCACCGTGTCGGGCTGGGTAGCGCTAACCAGGCTGATAGAGCCCGCGCTAATGGCATCAACGGAGTGTTCACAGACGTGCCAGCTCTGGAGGGGAGTGCTCACCGAAAAAGAGCTGAAAATAAAAGATTGTCTCTTACCTTCCTCCCTGGATCCCGCGATGAGGCTGGAGTGAGAGAAAGGAGACTTCTCTTGCACCCTGGAAGCGAGCTGGGGGGGTGGGGTTTGAACACCTGAAGAGAGTGCACCTGTTCAAAACAATATCATCACATTCATTCAATTTCCTTCGGCTTAGTCCCTTTTTTCATCAGGGGTCGCCACAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13802
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Nonsense 1595 1997 39 44
Genomic Location (Zv9):
Chromosome 6 (position 11024010)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10877636
GRCz11 6 11113063
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTRAATAATCTCTCAGGGTYAGAGAGCGCTACCCTGGCACTGAGATT[G/T]AGAAGTATGCCCACTTTATTGGTGAGTCCCTGAARAAGACGAAGGCCAGG
Long Flanking Sequence:
CAAAATTGTACCTTGAAAGTATCAATGTGCACCTGTAAGATACAAAATTGTACCTTTCAATTAAATTAAATTCAATTCAATTAAATTCAATTCAATTTAATAAACTTTATTGTCTATCCCACAGGGTTAAAAAAATTCTTTGTCATCAGACATAGGCTCACACACAACAACAAAACATAATACACTTACATTATTATTTTTAAAAAATCGTATTTTAAAAATCCTATTTAAAAGGCACTGCCCCATAAGGCAGCGTTTTTGTAATTTTGTTTCTGAGAGTATCCTAAAGATATCTGGCAACATGGAAATCCGTAATGTGTCTGTTTGGTAATATTGCATTATCATAGCAAATGGAATGATTCATTCAGCCCTACTTGGAACCCAGTAATGGTCTAATTAACATTCTCATTTCATTTCTGGTAACAAAAGCTACTTTTTTTTTTATCTGTTTCTGTGAATAATCTCTCAGGGTTAGAGAGCGCTACCCTGGCACTGAGATT[G/T]AGAAGTATGCCCACTTTATTGGTGAGTCCCTGAAGAAGACGAAGGCCAGGGAGTATGTGCCCTCTCAGGAGGAGATCGCCGCCCTGCTGATTAGACAAGAGATGACCACTACTGTGTACTGCCATGGAGGAGGGTCCTGCAAGATATCCATCAACTCACACACCACGGCTGGAGAGGTCAGAGAAGGAGAGAGAGATGATCAATTTTATTTACAACCACAATCCTGAAAAAGTTGGAATGTTATATAAAATGTGATAAAGAATCTGTGATTTCTACTTTTATTTAATTGACAAAAGTACAAAAAATAATTTTCAATTTTTTTACTGGAATACGATTTTATTGTCTGAGATAAATTTTGTAAATCCTAAAAGATTCATTTGATCCTATGAAGACACTTTCCTGCAGTTTGGCTTTTCTTATGACAAGCAACAAATCAAGAACCAGTGAGCACACTGATCCTGATTGCGCTATCAAATGTAGTTTAATTTTAAAGTTTTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14730
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113347 Nonsense 1924 1997 43 44
Genomic Location (Zv9):
Chromosome 6 (position 11017202)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 10870828
GRCz11 6 11106255
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACATGATCTGTGGCTGGGYGTCAGTGCTGAAAATGTCKCGGTGTACAAA[C/T]GAGGTGAACCCAAACCCCTTGAAAYTTTCCAGTATGAGCACATTGTATTC
Long Flanking Sequence:
AAATCCGATGTGATCAATTTTTCAAAGATCAGATCAGTGTATTAAGACTTGAATTCTAAAATGCGAATGAGCCTGCATATGAAGCATTTAATTAATCATTTAATTAAAAAATGAAAACACATATAACAACAGAATTTCTGTGGAAAAAAGTCATCAAACAAAACAAACTTTAATAAACTAGCACTCAGGAACAAAAATATAAACATAGTTGAGCTAAGGGTTTACAAACTGACGGATAATCCATCATAAGCTTAGATTCATAAAATTCAGACTGGTCTAAGCTGCTTTTTCAGCAGTCATATAATCAGATCTCCTACAGTATTATTAGTGTAGCTATAATGTTATGATACAGTAAATCTCAGTGCTTAACCACTAATATTATTTGAATTCATTAGTAATGTGTGTTTGTGTATGTTTTTGTGTCTCTACAGTGTAAGGAAGGGGGCTTCCCACATGATCTGTGGCTGGGCGTCAGTGCTGAAAATGTCTCGGTGTACAAA[C/T]GAGGTGAACCCAAACCCCTTGAAACTTTCCAGTATGAGCACATTGTATTCTTTGGAGCACCTCAGCCCAGCACTTACAAAATCATAGTTGATGAAAGAGAGATGTTCTTCGAAACGTCACAGGTAACAAACTTTTGTGCCTTTGCTATCAGTGCATAATTTGGTTTTGTATTTCTTTTCGCTAGTTTAATATGTTAATGTAATTTATTCCTGCAATGCAAAGCTGAATTTTCAGTGAAGTCTTGTCACAGAATTCTTCAGAAATCAGTATAATATGCTAATTTGGTGTTTAATAATCTTTTTTTTTTTATTACACTGTAAATAGCGACCAGTTAAAATGTTTAATTAAACCAAGTACCTGCTGCCTTAAAAGTGACAATTTAACTTAAAAAAATTATATAAACAACTTATAAAAGTATATAAATGTGTTGTAACTTAAATTAGGGATAAAGTACATCCAGAAGGTTGTTATCGCAGAATAAAGCTTGACAGGCTTATCAG
Associated Phenotype:
Not determined