Busch Lab

ZMP

ENSDARG00000075433

Ensembl ID:
ENSDARG00000075433
Human Orthologue:
MYOM2
Human Description:
myomesin (M-protein) 2, 165kDa [Source:HGNC Symbol;Acc:7614]
Mouse Orthologue:
Myom2
Mouse Description:
myomesin 2 Gene [Source:MGI Symbol;Acc:MGI:1328358]

Alleles

There are 13 alleles of this gene:

Allele Name Consequence Status Availability
sa35034 Nonsense Mutation detected in F1 DNA Not yet available
sa41789 Nonsense Mutation detected in F1 DNA Not yet available
sa17101 Nonsense Available for shipment Available now
sa21858 Nonsense Available for shipment Available now
sa31817 Nonsense Available for shipment Available now
sa41790 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16728 Essential Splice Site Available for shipment Available now
sa35035 Nonsense Mutation detected in F1 DNA Not yet available
sa5837 Nonsense Mutation detected in F1 DNA Not yet available
sa41791 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35036 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9372 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35034
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 66 1366 3 33
ENSDART00000087105 Nonsense 66 1366 3 33
Genomic Location (Zv9):
Chromosome 11 (position 11331246)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11226249
GRCz11 11 11209870
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAATGTGTATTTCTGTGTATTCAGGGCTCCTGAGGGCATGCAGGAGTA[T/A]CAGAGGATGGCGGCTCACTTTGGAAGAGATTTGGTTCAAATTCAACAGGA
Long Flanking Sequence:
TCCATACGTGCAAACTGAATGTTTGATCCTTTAATGCTTTGCCTGAATTGTAAAACCTACATCTTCATTCAAAATTGTGATACATTTTTTTTGGACATGGAGATAAATCCATATATACATGTACTACACAAATAAAATGTAATAGTCTGTCATTCAGAACACTGAAATCAAACCAATCTTCTCACACCTAATTTCGCCCTATGATTCTGATTGTGTCTGGCAGGAAATCAAGCTCTCAGGTTGTAAAGAAGGAGCAGGTCCAGGCCACGGAGGTGATGGTGGAACCAGCCTACACAGTGCCAAACTTCAGGGAGAGGTGAGATCTATTGGCTCCTGCATCTATTACAGTTCAGAAGGCTATTTAAAGATGGCGTAAGACAAAACCAGGAGAGCGCTTCCATATTTACAGATGAGGAAAATCAGTGTCACTGCATGTACTCCTCGGTGCATTTGAATGTGTATTTCTGTGTATTCAGGGCTCCTGAGGGCATGCAGGAGTA[T/A]CAGAGGATGGCGGCTCACTTTGGAAGAGATTTGGTTCAAATTCAACAGGAGCTGCACAGGATGAAAGTGGCCACAAAGGAGCAAGTGCAGAACATTGAGATTACTAGAGAGGTGAACACATACTTTTGCACTTAAATGTCTCTTTCATGAAAAATATCTCCCTAAAATGCTGTTGATGTATGCTTTATACATACAGTATACTTGTGTTTAGTGATGTAGGTGTATAGTTGATTGCATAGACAAACACAGACTCTCACTACAATTCACTCAAACAAGCATTTTGGTTTAATGTCTGCAATATAACTGTGTTTGTAGTGATTTAAAACAGTTGTGGATTTTAGCACAAAATAATAATAAAAAAAACTCCTAAACCATTTTCCACAGACTTTAATGTCTTCTCCTTAGCTTCTATACTGATCAAATTATCTGGATTCTGAAAGTCAAAACTAATCCAAAAAAAGTTTCCATTTCAATCAATGTTCAATACGATGAAACGTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41789
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
ENSDART00000087105 Nonsense 82 1366 3 33
Genomic Location (Zv9):
Chromosome 11 (position 11331292)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11226295
GRCz11 11 11209916
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATCAGAGGATGGCGGCTCACTTTGGAAGAGATTTGGTTCAAATTCAA[C/T]AGGAGCTGCACAGGATGAAAGTGGCCACAAAGGAGCAAGTGCAGAACATT
Long Flanking Sequence:
ATTGTAAAACCTACATCTTCATTCAAAATTGTGATACATTTTTTTTGGACATGGAGATAAATCCATATATACATGTACTACACAAATAAAATGTAATAGTCTGTCATTCAGAACACTGAAATCAAACCAATCTTCTCACACCTAATTTCGCCCTATGATTCTGATTGTGTCTGGCAGGAAATCAAGCTCTCAGGTTGTAAAGAAGGAGCAGGTCCAGGCCACGGAGGTGATGGTGGAACCAGCCTACACAGTGCCAAACTTCAGGGAGAGGTGAGATCTATTGGCTCCTGCATCTATTACAGTTCAGAAGGCTATTTAAAGATGGCGTAAGACAAAACCAGGAGAGCGCTTCCATATTTACAGATGAGGAAAATCAGTGTCACTGCATGTACTCCTCGGTGCATTTGAATGTGTATTTCTGTGTATTCAGGGCTCCTGAGGGCATGCAGGAGTATCAGAGGATGGCGGCTCACTTTGGAAGAGATTTGGTTCAAATTCAA[C/T]AGGAGCTGCACAGGATGAAAGTGGCCACAAAGGAGCAAGTGCAGAACATTGAGATTACTAGAGAGGTGAACACATACTTTTGCACTTAAATGTCTCTTTCATGAAAAATATCTCCCTAAAATGCTGTTGATGTATGCTTTATACATACAGTATACTTGTGTTTAGTGATGTAGGTGTATAGTTGATTGCATAGACAAACACAGACTCTCACTACAATTCACTCAAACAAGCATTTTGGTTTAATGTCTGCAATATAACTGTGTTTGTAGTGATTTAAAACAGTTGTGGATTTTAGCACAAAATAATAATAAAAAAAACTCCTAAACCATTTTCCACAGACTTTAATGTCTTCTCCTTAGCTTCTATACTGATCAAATTATCTGGATTCTGAAAGTCAAAACTAATCCAAAAAAAGTTTCCATTTCAATCAATGTTCAATACGATGAAACGTTTGAAATAGTAGCCATTTTAATAAAAGGTGTTTCACCAATAATATGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17101
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 404 1366 11 33
Genomic Location (Zv9):
Chromosome 11 (position 11346710)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11241713
GRCz11 11 11225334
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGGAACTAAGGACTGGGTCCAGTGCAATGACTCWCCTGTGAAAGTGTG[C/A]AAGCTGCCCGTCCACGGCCTGACYGACGGGGCWTCCTATCACTTCCGAGT
Long Flanking Sequence:
ATTTTTTTAAATAGAGGAAGTTATAATTGTTTGCCAATTACACTTACTGCCCAAGAAACTATGAATTGGAAAAGAAAATAATGACGATAGATGATATATTTAATATGTGTCATTACTTTGATGCATACAATGTTTCTCTTTCTATATATCTAATGTTTCACTTCACTGCAAATAATAAAATGATTTTATTTCTATTGCTTTTTAGGGAAATTAATTGGGAAATAATATTTATTGTCTTAGAAATATTGGTTTTTAATTAGTAATAAAATTTATTTTTAGACAAAGGGCTTATAAAAGTAATTCAAATACTTTTTAATGAGGTAATTAGGAATTAATAAATTAACTATAGTGCCTTGCATCCATTAATAAATAAATATATCTGGTGTGTGAATAATTTTTATCTTGACAGTATTTATTTTGTATTTTGTGTGTTCACTTTGCAGGCGTAAGTCAGGAACTAAGGACTGGGTCCAGTGCAATGACTCTCCTGTGAAAGTGTG[C/A]AAGCTGCCCGTCCACGGCCTGACCGACGGGGCATCCTATCACTTCCGAGTGAGGGCTGTGAACAAATCTGGCATCAGTCTGCCTTCCAGGATGTCCTCTGGAGTGACCACAGGAGAAGTGGAGAGCGATGTGGAAGGTAGGACTCATGCATTGAACCCAAACAACTTAATAGAGTTGTTTCATTAAACTGGGGCTAAACTGAAAGCTTAAAGGTCCAGAAGCGTCAAGGTAAGTTTACAGGATCAAGAGTCATGCTTTTTTTCTTCTTCTCCCGTTTCTGGATATTTGTGTGTTTTATGAATTTTTTCCAACACAATTTCACTCAGAAACTAGTGGATAAGTGGATTGTTAATATGAATTTGTACAAGCATATTCATAAGAAAATGTGTGTTTTATAGAACAAATGTCTACCCAAATCTCTCTCTATCTCTGCCTTTTAATGTAACCGTAACTGAAGTGTGAGCAGATTAAATAAAACATACATTTCAAATGCAGGGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21858
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 405 1366 11 33
Genomic Location (Zv9):
Chromosome 11 (position 11346711)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11241714
GRCz11 11 11225335
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAACTAAGGACTGGGTCCAGTGCAATGACTCTCCTGTGAAAGTGTGC[A/T]AGCTGCCCGTCCACGGCCTGACCGACGGGGCATCCTATCACTTCCGAGTG
Long Flanking Sequence:
TTTTTTTAAATAGAGGAAGTTATAATTGTTTGCCAATTACACTTACTGCCCAAGAAACTATGAATTGGAAAAGAAAATAATGACGATAGATGATATATTTAATATGTGTCATTACTTTGATGCATACAATGTTTCTCTTTCTATATATCTAATGTTTCACTTCACTGCAAATAATAAAATGATTTTATTTCTATTGCTTTTTAGGGAAATTAATTGGGAAATAATATTTATTGTCTTAGAAATATTGGTTTTTAATTAGTAATAAAATTTATTTTTAGACAAAGGGCTTATAAAAGTAATTCAAATACTTTTTAATGAGGTAATTAGGAATTAATAAATTAACTATAGTGCCTTGCATCCATTAATAAATAAATATATCTGGTGTGTGAATAATTTTTATCTTGACAGTATTTATTTTGTATTTTGTGTGTTCACTTTGCAGGCGTAAGTCAGGAACTAAGGACTGGGTCCAGTGCAATGACTCTCCTGTGAAAGTGTGC[A/T]AGCTGCCCGTCCACGGCCTGACCGACGGGGCATCCTATCACTTCCGAGTGAGGGCTGTGAACAAATCTGGCATCAGTCTGCCTTCCAGGATGTCCTCTGGAGTGACCACAGGAGAAGTGGAGAGCGATGTGGAAGGTAGGACTCATGCATTGAACCCAAACAACTTAATAGAGTTGTTTCATTAAACTGGGGCTAAACTGAAAGCTTAAAGGTCCAGAAGCGTCAAGGTAAGTTTACAGGATCAAGAGTCATGCTTTTTTTCTTCTTCTCCCGTTTCTGGATATTTGTGTGTTTTATGAATTTTTTCCAACACAATTTCACTCAGAAACTAGTGGATAAGTGGATTGTTAATATGAATTTGTACAAGCATATTCATAAGAAAATGTGTGTTTTATAGAACAAATGTCTACCCAAATCTCTCTCTATCTCTGCCTTTTAATGTAACCGTAACTGAAGTGTGAGCAGATTAAATAAAACATACATTTCAAATGCAGGGTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31817
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 492 1366 12 33
Genomic Location (Zv9):
Chromosome 11 (position 11355018)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11250021
GRCz11 11 11233642
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAACATGCCACAAACCTCCTGGGTTACTATGTTGATGCCTCTGTGGTC[G/T]GATCCAAGGACTGGTTCCCCTGTAATCACAGGCCTTACAAACACACCAGG
Long Flanking Sequence:
TTCTTTTCTCAGCCTTGATGATAACTGCACAGCTCCATTTCGTCTTTATTATCATGAAACACGGCACACAATGTAAACAGCTTGTCCAGTTGAATTTTGTCTTCCATTCTACAGTTGTTGATTTTGTTAAATGGAGAGCTTGGGGTTGTTGTCCAACTGCTTATGTCACTTTACAATTTCTAGAAATGGTTTAATTGCAACCAGGAATATGGTTTGGTGGAAATTAGTTCTCAAAGAACCAGCCTGGTGGTTCCTGTATATGAAATGTGAAAGCCCCTATGGTCACCATCACTACAGCAGTTCACAGTTTCCACTCTTATTTTAGTCAATGACTGACAACATCTGATGATTAATTAAAATTTTTGGTTTGTGCAGGTGTTCCTTCTGCCCCGGGACAGGTGATTGCCTCCAGAAATACCAAAACGTCTGCTTTTGTGCAGTGGGATGCTCCGAAACATGCCACAAACCTCCTGGGTTACTATGTTGATGCCTCTGTGGTC[G/T]GATCCAAGGACTGGTTCCCCTGTAATCACAGGCCTTACAAACACACCAGGTAAAATGCGCACACACACAAAAAAAACCTCCCAAGTTGTTAGTCATGCGAGTCTTAGACTGAAATCGCCCCCTATACCCTTAAAGAGCCCTCATGATACATTGAAAAGGTCATATTTTGGTTTTACGGGTCTCCAACATCAGTCTGATATGCATGCAAGGTCAAAAAACACTTTCATTTGTCATATAGTATGAATTTATTTTTGCCTAATTATCCCAGCGACTCCCATATGAATCGTTCAGTGGTTCATTTGTTCCCAAACCCCTCTTTCGCACGATGCTAATCTGTGCTGTGCTGATTGGACCGATAACAGTCTGTTGCGATTGGACAGAGTGAAATGCCCACCATGGCTTATCAACTATATTGAAGTAGTCAGAGTGCATTGTGTGTGTGTGAGCATGCCCCCCTCAACTCCCACCCCCCCCCCCAACTCCACCAACTATACCTCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41790
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Essential Splice Site 549 1366 13 33
Genomic Location (Zv9):
Chromosome 11 (position 11358379)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11253382
GRCz11 11 11237003
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGAGGAGTCGCAGGAATCTGCTCCTCTCTTCATTGATGCTGCGCTTAG[T/A]AAGTGTACAACTTTGCTGACTTCTGTAGCAATGTCTCTGGAATGTCCTCA
Long Flanking Sequence:
GGAAGGTGGCTCTCCAGGATGGCCACCCCTGTTCTAAATAATATACTGCTAAATGGTTAAAGAATACATAAGAAATCACAATCCTTTGTTTCATTACTAATAGAAAGTTTGCTTAGTGTTAAAAAAAACTTTTACAGGGTCTGATCAATAAGTTTATTTTATTTTTATCAACCAGCGACACACAAACAAAATGGCATCCCTTCTGTTGCTTAAATTAACTCACTAATTTTTATTTACTCCTTTGAGTGGACTATGTTAGTGGACTAATTCAGGAAATAGTGAATGAGTGTATAGAGGCCGATTTCAGATACAGCCTTAGACTAGATTCTATAAGTAAGTTTACATTGGGCTTGACTATCTGGAGTTGCATTTTTCAGGTTTGTAGTCCATGGTTTGACCCCAGGAGATACCTATGTGTTCCGGGTGCAAGCTGTGAATGCATACGGATTGAGTGAGGAGTCGCAGGAATCTGCTCCTCTCTTCATTGATGCTGCGCTTAG[T/A]AAGTGTACAACTTTGCTGACTTCTGTAGCAATGTCTCTGGAATGTCCTCAGGAAAGCAGTGATAAATGGAATCGTTAGGAAAATGTATTATAATTAAATTATCCAACATTACAATGGACATGCAGTTAGAATATTAAATGTGCAAAAATATTAACCCTCGTGATGCATTCAAAATCTCTAATTCCAGACTGGAATGTTTTTTTTTATTATTAAACAGTCATAGGTTAATATTTTTCTACACATTCTTTTAACTAAAACTATATAGTGTCTGATTATAATGGATCTCATTGGGTAGTATGCAACTTGTGGTTCATATTGACACCTACTGGTGTGGCTGTAGAATGTGAAAATTCACTTCACCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATAAAAGACCATAGTAAATTGAAATAGTGTAGTTCAGTCTTAAAGTTTAAGTTTAGTTCAGTTTAGCTTAGTTCAGTTTGATTTAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16728
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Essential Splice Site 654 1366 16 33
Genomic Location (Zv9):
Chromosome 11 (position 11364684)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11259687
GRCz11 11 11243308
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATGTAATGCACATCTTGTYTAAACTGATACTTTCTCTATTTGTCATC[A/T]GGTCCAGCATATGACATYAGTTTCTGGGAAGTGCGYGACACCTCCMTTTT
Long Flanking Sequence:
CAGCTCCCAGCATGTGATTTGAGACTTAAATCTAATTACCTCAAAGTTTTTTTTTTTTTTTCAGTTCTCAGACCAGCCAAACAACTATTTAAAGTCAGTGTCCAGAAAGTATAGGCTGCACGTTCATGAGAGTGCTGCACTCTTTATGCTTGTCAAGCTGATAGATAGTCAACAGATAGATAGTTAAGCTGTTTTATAGGTGATACATATTAAAGCAACTCATAAGTATCTACAGTATATATATATATATTGTCAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATATGTATGTATATATGTATATATATATATATGTATGTAATGCACATCTTGTCTAAACTGATACTTTCTCTATTTGTCATC[A/T]GGTCCAGCATATGACATCAGTTTCTGGGAAGTGCGTGACACCTCCATTTTGGTGCAGTGGAAACCCCCTGTGTACACCGGACAGAGTCCCGTCACTGGTTATTTTGTGGACATGGCTAAGAAGGGCTCATCAGATTTTGCCACAGTAAATGCTGAAAAAGTTGAACATTGCTTCCTGAAGGTATAGCACCAGAATTCCCAAAACAAACACAACACTAAAGAAAAACAAAAACATACTCAGATGTTTGTACACTCATCTGTAGGTCACTGGACTTGAATCTGGAGCGTCATATGTGTTCAGAGTACGGGCTGTCAATGACAAAGGTGTTGGAAAAGCCTCAGACTTGTCTGATCCCATATGTGCAAAAGCACTGCCAGGTAACTACAACACAGCTCTACCACCAATTATAAGCACTCAATAACTATAATTTATTAAAGGGATAGTTTACCAAAAAAGACACTTCATTGCCATTTGTTTACACTCAAGTGGTTATAAACTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35035
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 710 1366 16 33
Genomic Location (Zv9):
Chromosome 11 (position 11364855)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11259858
GRCz11 11 11243479
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGGCTCATCAGATTTTGCCACAGTAAATGCTGAAAAAGTTGAACATTG[C/A]TTCCTGAAGGTATAGCACCAGAATTCCCAAAACAAACACAACACTAAAGA
Long Flanking Sequence:
ACAGATAGATAGTTAAGCTGTTTTATAGGTGATACATATTAAAGCAACTCATAAGTATCTACAGTATATATATATATATTGTCAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATATGTATGTATATATGTATATATATATATATGTATGTAATGCACATCTTGTCTAAACTGATACTTTCTCTATTTGTCATCAGGTCCAGCATATGACATCAGTTTCTGGGAAGTGCGTGACACCTCCATTTTGGTGCAGTGGAAACCCCCTGTGTACACCGGACAGAGTCCCGTCACTGGTTATTTTGTGGACATGGCTAAGAAGGGCTCATCAGATTTTGCCACAGTAAATGCTGAAAAAGTTGAACATTG[C/A]TTCCTGAAGGTATAGCACCAGAATTCCCAAAACAAACACAACACTAAAGAAAAACAAAAACATACTCAGATGTTTGTACACTCATCTGTAGGTCACTGGACTTGAATCTGGAGCGTCATATGTGTTCAGAGTACGGGCTGTCAATGACAAAGGTGTTGGAAAAGCCTCAGACTTGTCTGATCCCATATGTGCAAAAGCACTGCCAGGTAACTACAACACAGCTCTACCACCAATTATAAGCACTCAATAACTATAATTTATTAAAGGGATAGTTTACCAAAAAAGACACTTCATTGCCATTTGTTTACACTCAAGTGGTTATAAACTTTTATGATTTGTTTTTCTTCTGTTAAACACAAAACAAGATATTCTGAAGAATGTTTTAGCAGCTATTGACATCCATAATACTAGTAATAGTACATAGTTAAAAAAAAATGTTCAAATTACTTATTTAGAATTAGCTGCATCATTGAAATTTTTGGGACAACTTAATTTTTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5837
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 723 1366 17 33
Genomic Location (Zv9):
Chromosome 11 (position 11364976)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11259979
GRCz11 11 11243600
KASP Assay ID:
554-3660.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTTGTACACTCATCTGTAGGTCACTGGACTTGAATCTGGAGCGTCATA[T/A]GTGTTCAGAGTMCGGGCTGTCAATGACAAAGGTGTTGGAAAAGCCTCAGA
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATATGTATGTATATATGTATATATATATATATGTATGTAATGCACATCTTGTCTAAACTGATACTTTCTCTATTTGTCATCAGGTCCAGCATATGACATCAGTTTCTGGGAAGTGCGTGACACCTCCATTTTGGTGCAGTGGAAACCCCCTGTGTACACCGGACAGAGTCCCGTCACTGGTTATTTTGTGGACATGGCTAAGAAGGGCTCATCAGATTTTGCCACAGTAAATGCTGAAAAAGTTGAACATTGCTTCCTGAAGGTATAGCACCAGAATTCCCAAAACAAACACAACACTAAAGAAAAACAAAAACATACTCAGATGTTTGTACACTCATCTGTAGGTCACTGGACTTGAATCTGGAGCGTCATA[T/A]GTGTTCAGAGTACGGGCTGTCAATGACAAAGGTGTTGGAAAAGCCTCAGACTTGTCTGATCCCATATGTGCAAAAGCACTGCCAGGTAACTACAACACAGCTCTACCACCAATTATAAGCACTCAATAACTATAATTTATTAAAGGGATAGTTTACCAAAAAAGACACTTCATTGCCATTTGTTTACACTCAAGTGGTTATAAACTTTTATGATTTGTTTTTCTTCTGTTAAACACAAAACAAGATATTCTGAAGAATGTTTTAGCAGCTATTGACATCCATAATACTAGTAATAGTACATAGTTAAAAAAAAATGTTCAAATTACTTATTTAGAATTAGCTGCATCATTGAAATTTTTGGGACAACTTAATTTTTTATGTTTAATCCACTAAAATTTATCAAAACAATTAGCTTAACTTAATTCAATTGTGTTTGGACAATGTGAATGAATTGTGTGGACTCCTTTTTAACAGTGTAGGAACAAAATAAACCATTGACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41791
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
ENSDART00000087105 Essential Splice Site 840 1366 19 33
Genomic Location (Zv9):
Chromosome 11 (position 11369425)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11264428
GRCz11 11 11248049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGACTGACACAGATGGAGTTTCATCCAGTTACTCTGTCAATGAAGAAG[G/A]TCAGAGATTTGGGTGTGAATTTCCCTTCCTTTGTTTACTTACAACGGAGG
Long Flanking Sequence:
CTTTTACCGTCAGAATCGGCAGGATAGCGCAGAAGCTCCATTGAATATACTGGGGTAAAATAAATGCTCATTTTATAAAGACATGGCAGGAAAAAATATGGTTTGATGCAGTGCTTCTTGTACAATCTGAGACTCACGTTATATCGGATATCACTCAGCTAGTGGAGATCTCTGATTTTTAAAGAAATCTGACCTCAAATGCACCAATTTTTGCATTGGCATACAGTTGACCAGATGCGCTTAACCCAGGTTACTGGCAAATTCAAAGACCTGTTAGCATGCTTCAGCATATACTCTATTAAATTATTGCTACAGCTTCATAATATACTGAAGTGTTACTCAAGAGTGAAGTGGTGTAAACTGACTAAAGCTGTCATGTGTTATTTCAACAAGCTCAAAGCTGACATTCGTGAACCCCGAGAAGGAGGATCTGGGAATCTACTCTGTTGCAGTGACTGACACAGATGGAGTTTCATCCAGTTACTCTGTCAATGAAGAAG[G/A]TCAGAGATTTGGGTGTGAATTTCCCTTCCTTTGTTTACTTACAACGGAGGAGCTCAGTGAAAATAATCCCTGTTTTTCTTTACAGAGTTAAAAAAAATGCTTGATCTGAGCTACAACATCAGACACCCCAGTAAGTTGCTAGTGGGTTTTTCATTCATGCGTCGGGCTATTTCGTAGAAGTGATTTATTTAATGGCTTTCGACTTTTTCATCAGTTGTTCCACTGAAGACGGAGCTGAACTATGAGATTCTGGAGAAGGGTCATGTGCGTTTTTGGGTTCAGGCTCTGAAGCTGTCCTCCTCTGTCAACTATAGGTTCATTGTCAACGATAAAGCCATCTCAAGCACTGAGGTACAGCCCATCTCTACACCAAAACCAAAATCACACATGATATTTATTAGATTTTTAAAGATATTTCCCTAGTAACCCCTTTACTTATTTACTATAATAGGCAATTAATAAGTATTGGTGGTTGCCAAGATGTTGCTTTTTATTTGCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35036
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
ENSDART00000087105 Essential Splice Site 1175 1366 30 33
Genomic Location (Zv9):
Chromosome 11 (position 11379446)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11274449
GRCz11 11 11258070
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGTTCAACAGCATACACTGATGCCTATGCAGAATTCCAGAGACTGAA[G/A]TAAGAGAAAGTTCATTGTTAATTTTCAACACAATCATGATTCTTCTGAAG
Long Flanking Sequence:
TTCCCCCACAGTCCAAAGACATGCGGTACTGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTGTAAATGTGTGTGGATGTTTTCCAGAGATGGGTTGCGGCTGGAAGGGCATCCCCATCTCCTGCAACTTGCTGGATAAGTTGGCGGTTTATTCTGCTGTGGCGACCCCGAATTAATAAAGGGACTAAGCCGACAAGAAAATGAATAAATGAATGAATGAACATAAACTGCTTGAACATCTTATTTTTTTTGACTATTGATATACTGTTAACGTTATCAATTGTTAGCTAATAGATATCATTGTAAAATGTTAACAACAACTTTGGTATATAATTGTAAAATGTATGTAAATGGTAACAGTTCTAAACCATTTCAACGGCTAATATTGGCAGAAATAAACAGAATTTCTCATGTATGTTTCTTTTGTAATGTGTTTTTTACTGTTTTAATTTGGTTCAACAGCATACACTGATGCCTATGCAGAATTCCAGAGACTGAA[G/A]TAAGAGAAAGTTCATTGTTAATTTTCAACACAATCATGATTCTTCTGAAGAATCAGCTCAAAAACTGAGCCAGACACACTGACATTTCTCTACTTCTTTCCTCAGAGCGGCTGCCTTTGCTGAAAAGAGTGAGTATTTCTGGGAACTGCTTAAATGCAACATTAATGAGGGTCTAATCCGATATTCATGCATACTTGAACTCAGGAAGTATAAAGCTTTGTACAAGTACAATAATCCCATTTAATAAGCTTAGGAATGTGTTCATATTTCAGAATTATGACCCAGATTTTTATATGTGAAAATAACCCATTTATTATTAAATTGACTTTTGTAAGACTCAAAACTATGATTTTAAAAATATTCCATTGGAAACAGTGTCCAAATGTGTTAAATTACTTATTTGCCCTTTGTAGATCGTGGTAGAGTGATGGGTGGTCTGCCAGATGTTGTCACCATTATGGAAAAGAAGGTAATGTGTCTTTTACTTTTCCCATCCTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9372
Status:
Mutation detected in F1 DNA
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Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087105 Nonsense 1219 1366 33 33
Genomic Location (Zv9):
Chromosome 11 (position 11381376)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11276379
GRCz11 11 11260000
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAGTCTGACWTGTACAGTGTGGGGTGACCCCAGCCCAGAGGTCACCTG[G/A]TTTAAGAATGAGCAGGAAGTGGTGTCCGACGACCGCTACAAGAKCACCTT
Long Flanking Sequence:
TTTGGCACTTCCGTGTTGGTGTTGCTGGGAATCTTTAGATCAGGGGTGCCCATACTCGGTCCTGGAGGGATGATGTTCGGTAGAGTTTTGCTCCAACCTCAATTACACACACCTGCACCAGCTATACTCAAGGACTTTCTAGGTATACTAGAAACTAGATACTAGAAATAAAGCAAGTTGGAACTTAACTCCGCAGCCTTCCAGGATCGAGTTTGGGCACCCCTGGATTAGACATAAGGAGTAATGTCAGACTTGGCTCTGAGGTGTTTCTTTAGCTTCTGGCTAAAGTTGTTAGAAGGCTGTCCTGATGAGCCAGCTCTTGCGATAGCACTGACTCCAAACCAGCACCTGGTTTGTACTGATGGAAAATAGGTATAAATTAGTTCTTGTAAAAGCCTCTATAGTGTAACTAATATACTTATACGTTGTAACCTTTTGCCTTTGCAGAGCCTGAGTCTGACTTGTACAGTGTGGGGTGACCCCAGCCCAGAGGTCACCTG[G/A]TTTAAGAATGAGCAGGAAGTGGTGTCCGACGACCGCTACAAGATCACCTTCGAAAGTGGCAAGTTTGCCAGCCTCACTATCAAGAGTGTGTATGTGGAAGATTCTGGAAAGTACAGCATCAATGTACGGAACAAGTATGGAGGTGAATTTGTGGAGATAACAGTCAGTGTCTACAAACAAGGCGAAGATATCCCCGAGCCTAAACTGGGACAGATGTCCAGACCTGCCGCTACCCCAAAGCCAGCTACACCTGTTCCACAGTCTGTGAAAACCCCATCTCCTGCAACTCCTACACCCTCTATCAAGTCCCCAACCCCTACTCCACCGTCCTCTGTCAAGTCTCCCACCCCCACTCCAGCTTCTAAATCACCCACCCCACCCAGATCCATGAGGTCCCCCACCCCACCAAGATCCATGAGATCCCCCACCCCAACTAAGAAGTAACTTCTAAACTATGGCTTATTGAACCTGAAGATACACACAGTATTAATAGTGTTGGT
Associated Phenotype:
Not determined