ZMP
ENSDARG00000074723
Ensembl 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 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.
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.
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.
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 |
---|---|---|---|---|---|
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
---|---|---|---|---|---|
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.
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 |
---|---|---|---|---|---|
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
---|---|---|---|---|---|
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
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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 |
---|---|---|---|---|---|
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