Busch Lab

ZMP

BSN (2 of 2)

Ensembl ID:
ENSDARG00000079822
Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Human Orthologue:
BSN
Human Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Mouse Orthologue:
Bsn
Mouse Description:
bassoon Gene [Source:MGI Symbol;Acc:MGI:1277955]

Alleles

There are 26 alleles of this gene:

Allele Name Consequence Status Availability
sa21405 Nonsense Available for shipment Available now
sa14012 Nonsense Available for shipment Available now
sa16623 Nonsense Available for shipment Available now
sa13749 Nonsense Available for shipment Available now
sa11540 Nonsense Available for shipment Available now
sa9997 Nonsense Available for shipment Available now
sa21404 Nonsense Available for shipment Available now
sa21403 Nonsense Available for shipment Available now
sa21402 Nonsense Available for shipment Available now
sa11595 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21405
Status:
Available for shipment
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Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 20 3782 1 18
ENSDART00000114444 None None 3719 None 19
ENSDART00000122421 None None 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55824557)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53943145
GRCz11 8 53811639
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGAT[C/T]GAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAAC
Long Flanking Sequence:
AGCACCCAGAGAAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAACACCAACTGAGCTGAGGTTCGAACCAGCGACCTTCTTGCTGTGGGGCGACAGCACTACCTACTGCGCCACGGCCTCGCCTTCCACTGCATTATGTGATTACCATTTTAAAATGTTTAAAAATTCAGTGTTTGTCCACTGGGGGGCGATCTGTGTAATCCAATAAAACCCAGATGAATCATGCAAGCTCACTGAGATCACCACCTAAGTGGCAAACAGGTTTCTTAGGTGTTTAATCTGATTGCAGATCATATATATTAGTTTGTAGACTTTCTAATGACACATTTATGAAATGAAAAGGAATAATAGTTAGGAGTCTCTTGTTTAAAAAATCCCCACTGGCAATACTCATGTGTTCTCATCTTCTTGTTTTGTCTTATTTAGGTTGGCTGGAGCGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGAT[C/T]GAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGATGGACCCAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCTTCAGCAGGGGGCATGGGAGCCAACCAGAGCCCGGGCCAGCACGCCTCCAGACGCAACCTCCAAGTGGACTTCAGCAGTAGCAGCAGAACGGGACGCTCCCCGTCAGCGTCTCCTGACAGAACTAGTGCACCGACTTCACCATACTCCGTACCCCAGATCGCACCGATGCCTAGCAGTAAACTCTGTCCAGTCTGCAATACAACAGAGCTGACCAATTTTGACGGGTCGCCGAACTTCAACAAGTGCACACAGTGCCACACTACAGTGTGCAACCAGTGCGGCTTCAACCCCAACCCACACCTTACAGGGGTAAGACTTCTGCAGAAATGGGATCTATTTATCAACATCTGTATGACTTGGCATGATGTGAATTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14012
Status:
Available for shipment
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Availability:
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55824482)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53943220
GRCz11 8 53811564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCMAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCT
Long Flanking Sequence:
TCGAACCAGCGACCTTCTTGCTGTGGGGCGACAGCACTACCTACTGCGCCACGGCCTCGCCTTCCACTGCATTATGTGATTACCATTTTAAAATGTTTAAAAATTCAGTGTTTGTCCACTGGGGGGCGATCTGTGTAATCCAATAAAACCCAGATGAATCATGCAAGCTCACTGAGATCACCACCTAAGTGGCAAACAGGTTTCTTAGGTGTTTAATCTGATTGCAGATCATATATATTAGTTTGTAGACTTTCTAATGACACATTTATGAAATGAAAAGGAATAATAGTTAGGAGTCTCTTGTTTAAAAAATCCCCACTGGCAATACTCATGTGTTCTCATCTTCTTGTTTTGTCTTATTTAGGTTGGCTGGAGCGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGATCGAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCCAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCTTCAGCAGGGGGCATGGGAGCCAACCAGAGCCCGGGCCAGCACGCCTCCAGACGCAACCTCCAAGTGGACTTCAGCAGTAGCAGCAGAACGGGACGCTCCCCGTCAGCGTCTCCTGACAGAACTAGTGCACCGACTTCACCATACTCCGTACCCCAGATCGCACCGATGCCTAGCAGTAAACTCTGTCCAGTCTGCAATACAACAGAGCTGACCAATTTTGACGGGTCGCCGAACTTCAACAAGTGCACACAGTGCCACACTACAGTGTGCAACCAGTGCGGCTTCAACCCCAACCCACACCTTACAGGGGTAAGACTTCTGCAGAAATGGGATCTATTTATCAACATCTGTATGACTTGGCATGATGTGAATTTGCCTTGGCAGTAGATATTCGATCATTGTTGCAGATATAGAATGCCAGTCAGAGCTCGGTAGATCATTTAGGAGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16623
Status:
Available for shipment
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Availability:
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55824482)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53943220
GRCz11 8 53811564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCMAGACATTCCCAGACTACRCCTACGCATCAGTCTCAAATTCAAGCT
Long Flanking Sequence:
TCGAACCAGCGACCTTCTTGCTGTGGGGCGACAGCACTACCTACTGCGCCACGGCCTCGCCTTCCACTGCATTATGTGATTACCATTTTAAAATGTTTAAAAATTCAGTGTTTGTCCACTGGGGGGCGATCTGTGTAATCCAATAAAACCCAGATGAATCATGCAAGCTCACTGAGATCACCACCTAAGTGGCAAACAGGTTTCTTAGGTGTTTAATCTGATTGCAGATCATATATATTAGTTTGTAGACTTTCTAATGACACATTTATGAAATGAAAAGGAATAATAGTTAGGAGTCTCTTGTTTAAAAAATCCCCACTGGCAATACTCATGTGTTCTCATCTTCTTGTTTTGTCTTATTTAGGTTGGCTGGAGCGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGATCGAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCCAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCTTCAGCAGGGGGCATGGGAGCCAACCAGAGCCCGGGCCAGCACGCCTCCAGACGCAACCTCCAAGTGGACTTCAGCAGTAGCAGCAGAACGGGACGCTCCCCGTCAGCGTCTCCTGACAGAACTAGTGCACCGACTTCACCATACTCCGTACCCCAGATCGCACCGATGCCTAGCAGTAAACTCTGTCCAGTCTGCAATACAACAGAGCTGACCAATTTTGACGGGTCGCCGAACTTCAACAAGTGCACACAGTGCCACACTACAGTGTGCAACCAGTGCGGCTTCAACCCCAACCCACACCTTACAGGGGTAAGACTTCTGCAGAAATGGGATCTATTTATCAACATCTGTATGACTTGGCATGATGTGAATTTGCCTTGGCAGTAGATATTCGATCATTGTTGCAGATATAGAATGCCAGTCAGAGCTCGGTAGATCATTTAGGAGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13749
Status:
Available for shipment
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Availability:
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Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1077 3782 8 18
ENSDART00000114444 Nonsense 1021 3719 9 19
ENSDART00000122421 Nonsense 1006 3727 9 19
Genomic Location (Zv9):
Chromosome 8 (position 55812197)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53955505
GRCz11 8 53799279
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCAAGCTGTACAAATCTGGTAGTGAGTACAACCTGCCCACCTTTATGT[C/A]ACYTTATTCTCCTACTGAAAAGCCAGAAACTACATCATCTACTGCTGCTG
Long Flanking Sequence:
CACCTCTGGAATATCCCCTACCTCCATATCCTCAATGGAAGATGATAGTGACAGTAGTCCTAGTCGGAGGCAGCGACTGGAGGAGGCGAAGCAGCAGAGGAAAGCGAGGCATCGCTCCCATGGCCCTCTCCTACCCACCATCGAGGATTCATCAGAAGAAGACGAATTGAGAGAGGAAGAAGAACTCCTAAGGGAGCAGGAAAAGATGAGAGAAGTCGAGCAACAGAGAATACGAAGCACAGTCCGGAAAACAAAACGCGATAAAGAAGAGTTAAGAGCACAAAGACGAAGAGAACGATCGAAGACTCCACCTAGTAATCTATCACCCATCGAGGATGCTTCTCCGACCGAGGAGTTGAGGCAGGCAGCTGAGATGGAGGAACTCCACCGGTCCTCCTGTTCAGAGTATTCTCCTTCAGCTGACTCAGATGCTGAGGGCTATGAAATTTCAACCAAGCTGTACAAATCTGGTAGTGAGTACAACCTGCCCACCTTTATGT[C/A]ACTTTATTCTCCTACTGAAAAGCCAGAAACTACATCATCTACTGCTGCTGTAACTACCTCCTCGAGTGGCAAGAAATTAAAAAGCGCAGAAGAAGTCTACGAGGAGATGATGAGGAAAGCGGAGATGTTGCAGAAGCAGCAAAAGCAGCAGACACAGCAGCAATCAAGCTCAAGTTTGATTTTACAGCAGTACAGCTCTGCCACCTATCAAGAGTCAGACATTAGAAATAGACAAGATATTGAAGATGAATATGATTATAATGAGCAAGATGATATGCATTACGAGAATGAGGAGACGGTTGATATTTATGAAGAGATCCGTCAGACCTCACAAAACATCTCAAAGCAGCTCGATGACCAAATGGAGATGGATGTTTCCTACAATGAAAAGCAGTTACTAGATACAGGCTCAGCTTTTGCTAAGTTGCTGGAACAAAGCAATGCTTTACTGACTCCTGGAACAAGCCCCACCCAGCTCTCAGCACCTGTATCGTTTTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11540
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1458 3782 8 18
ENSDART00000114444 Nonsense 1402 3719 9 19
ENSDART00000122421 Nonsense 1387 3727 9 19
Genomic Location (Zv9):
Chromosome 8 (position 55811053)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53956649
GRCz11 8 53798135
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTTGTTACACCAGGYCTTTTTAGGCAGCAGTCCACTCAAGAYACCTA[T/G]TATAYGATTAGAACAGAGGAGCCTGAGCYCACAAGTCCATCCAAACCAGT
Long Flanking Sequence:
GTATATGCCAGGGAAACGGTCACTGTCTCTCAAACTACTGCCAGTCAAACAATATCCACTACACAGCCCAGTTTATATGGTCGGCAAACCACCACAACCACTACTGTTTCAAACGTGTCTCATAAAATTGCTGCAATCACTCAGGCTTACAACCAGAGGGAAAGTGCGGCACGGAAAATGGCAATAAGCAGAGGAGTGCAGATGAGGGATAGTTCAACATCCTCAGACACTAGAATTGAATCTGGCCCAAGTTCAATCAGGTCTTATGCTTACCATGAAAGGAGCCCACCCCTTTCTCCAACCTCATCTCCTACACACAGTCCAACACGATCTCCTTCTAGGAGAACAGCTGAGTTTTCAACACAGACAGTTAGCCCTTCAGTGTTAGCTTCCTCTGGGAACGCTTCTCACACCTCTCCAGTTATGGCACAGGGCACTCAGACCTCACATGGAGTTGTTACACCAGGTCTTTTTAGGCAGCAGTCCACTCAAGATACCTA[T/G]TATATGATTAGAACAGAGGAGCCTGAGCCCACAAGTCCATCCAAACCAGTTACAGTTAACACGGCTACATCTCCGTTGTCTTCGCCGACAAGGTTTAGCCGCCAGTCAACATTTGATGCCTACTCACCTCCTTTCAGCCCTCCTGATACACCACCACATGAACAGTCTCCTCAGCATAGCTTATACAGGAACTATAGAGCTAAAAAAGTTAATGTTGGAACTAGCATGGCCACTACTGCGAGCATGTACTCACGTGGATCAATGTCAATGGAAAACATATCACTTTGTCGCATTTCAACGGTTCCTGGTACTTCAAGAATAGAGCAAGGACATCGATTTCAAAGTGCAAGTGTAGTAGATCTACGAACTGGCATAAAGCCAACACCAATTATCATGACTGACCAAGGAATGGATTTGACATCCTTAGCGACAGAATCTCGAAAATATTCTGGGTCCCTTGAAGGAAGTCCCATTCGTCAATCCACAACTATTCAGCCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9997
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1849 3782 9 18
ENSDART00000114444 Nonsense 1793 3719 10 19
ENSDART00000122421 Nonsense 1778 3727 10 19
Genomic Location (Zv9):
Chromosome 8 (position 55809776)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53957926
GRCz11 8 53796858
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCAT[C/A]AATAGCACCGAYCACATTACCACARCATTATCAGCAGTTTGATTTACGAC
Long Flanking Sequence:
GCAAAAGCTTCAGCAACAACAACAACTTCTTGAGCAACAGCTTCAGCAACATCATCAGCTTCAGCAACAACAAGCTGCCTCTTTTGCCAATCTGAATATATCTAGCCAACTACCTCTATTCAAAAAAGACATGCTAGTCACTCAGACGAGTACTGCCACAGAAGTTAATGTCATCTCACCAGCTATGGCTTCTGATGTGTATGGTGTTGGTGGTCCTCTTGAGTTTAGGGCAAAACAAGCCGAGGCAGGTGTCATGAATCTAGCAAATGTCAAGCCTCAAGTGATGATGGTGCAAATTGATGGTGCTGCACAAGGAGCTACGATCACACAACTCGTCAAGCCTGACGAAGGCCAGGATTCAATGAATTTAACAGGGCAAATAAAATCAGAAAACCAAGCGACTTGTTGTGACATGGTTTACAATCTTCCTTTTGGTGGCAGCTGTGTGGGTGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCAT[C/A]AATAGCACCGACCACATTACCACAACATTATCAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGTTAAATCTTACACATTGCCCCTCCCTGGGCGGCTTCAGCCATCAATGTCTGAAACTAACCTTTCAGAGGCAGGGTTGTCATCATATTCAGCAAAGCATGATCCACATTTTCATTCCTCTGGAGAATTATACACAGACACCATGAAGGATGGCTATGACGGAGGCTACCTTGGAATGGGGCTTCAGTATGGTTCTTTCACTGACCTTCGTCAGGGTGATATTGGAGATTTACCAATTAGAAGGTATAGCTCCCTGACCAACATTAACTCAGATTATGGATATTTCTCAAGTGATTTTGCAGAGTCTAATCTTGCCCAGTACAGTGCTACAACTGCCAGGGAGATAAGTCGCATGTGTGCAGCCCTTAACTCAATAGATAGATACAGTAGTAACCCTGATATACTACAGCTAGGCACTGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21404
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1859 3782 9 18
ENSDART00000114444 Nonsense 1803 3719 10 19
ENSDART00000122421 Nonsense 1788 3727 10 19
Genomic Location (Zv9):
Chromosome 8 (position 55809745)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53957957
GRCz11 8 53796827
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCTTCCAAGCAATCATCAATAGCACCGACCACATTACCACAACATTA[T/A]CAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGT
Long Flanking Sequence:
GAGCAACAGCTTCAGCAACATCATCAGCTTCAGCAACAACAAGCTGCCTCTTTTGCCAATCTGAATATATCTAGCCAACTACCTCTATTCAAAAAAGACATGCTAGTCACTCAGACGAGTACTGCCACAGAAGTTAATGTCATCTCACCAGCTATGGCTTCTGATGTGTATGGTGTTGGTGGTCCTCTTGAGTTTAGGGCAAAACAAGCCGAGGCAGGTGTCATGAATCTAGCAAATGTCAAGCCTCAAGTGATGATGGTGCAAATTGATGGTGCTGCACAAGGAGCTACGATCACACAACTCGTCAAGCCTGACGAAGGCCAGGATTCAATGAATTTAACAGGGCAAATAAAATCAGAAAACCAAGCGACTTGTTGTGACATGGTTTACAATCTTCCTTTTGGTGGCAGCTGTGTGGGTGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCATCAATAGCACCGACCACATTACCACAACATTA[T/A]CAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGTTAAATCTTACACATTGCCCCTCCCTGGGCGGCTTCAGCCATCAATGTCTGAAACTAACCTTTCAGAGGCAGGGTTGTCATCATATTCAGCAAAGCATGATCCACATTTTCATTCCTCTGGAGAATTATACACAGACACCATGAAGGATGGCTATGACGGAGGCTACCTTGGAATGGGGCTTCAGTATGGTTCTTTCACTGACCTTCGTCAGGGTGATATTGGAGATTTACCAATTAGAAGGTATAGCTCCCTGACCAACATTAACTCAGATTATGGATATTTCTCAAGTGATTTTGCAGAGTCTAATCTTGCCCAGTACAGTGCTACAACTGCCAGGGAGATAAGTCGCATGTGTGCAGCCCTTAACTCAATAGATAGATACAGTAGTAACCCTGATATACTACAGCTAGGCACTGGAAGAAGCAGTGGTCCACCAAGTAGGGTTAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21403
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
ENSDART00000111967 Nonsense 2280 3782 10 18
ENSDART00000114444 Nonsense 2224 3719 11 19
ENSDART00000122421 Nonsense 2209 3727 11 19
Genomic Location (Zv9):
Chromosome 8 (position 55808442)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53959260
GRCz11 8 53795524
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACTTTTGCAAATTGAGAGAGAGAGAGTGGAACTGGAAAAGTTGCGT[C/T]AGCTAAGGCTTCAGGAAGAGCTTGAGCGTGAGCGTGCAGAGTTGCAGAGG
Long Flanking Sequence:
CTCCAAGGACTGGGCAGGCACCTTTCCAATGTCCTACACCTAATCCTCTCCCTGTTACAACATCTACAAAAGTACCCGAGTCTCCAGCTATCACAACAGTCCAAGATGCACCATTGTATCTTGGCAAGTCTCCAGTTAGCATAACAGCAGCTGGAACTTTTGCGCAGCCAATTCAGCCCTCTTCTGTGCCTATTTCAACACCAATGAACTTGGCAATGAGCCAACCTGAGGTCCAAGCTCAACCAATAAATCTATCTCAGTCCCATCTTCAGGCGAATACCCAACCTACTTTACAACATCAACTACCACAATCTAACTCATCTGCTCAATCACACCCTCCAGTGCAAGGTCACCCGATTGCAACTCAAGGAGGTCGGACTACTCTTACTGCTGTTAGAAATATCGCAAGTCAAGAAAACGAAACTGAGGAAAAAGTCCATCAACAGCAGGAACAACTTTTGCAAATTGAGAGAGAGAGAGTGGAACTGGAAAAGTTGCGT[C/T]AGCTAAGGCTTCAGGAAGAGCTTGAGCGTGAGCGTGCAGAGTTGCAGAGGCATAGAGAAAAGGAGCAGATACTTGTACAGCGTGAGATTCAGGAACTGCAGAGTATAAAGCAACAAGTGTTGCAGCAGCAGCAAGCTGAGAGAGAAAGCCAGCTGATTCTACAGAGAGAGCAACTAGCTCAACAGAAACAGCAGCTTGATCAGATACAATCTTTGCAACATCAGTTGCAGCAGCAACTTGAGGAACAAAAGAGACAAAAGACAGTCAGTGGAAGCACCCAAGTCATCAGTGATCAATCTGGAAGAATTATTCAGCCACAGGAATTAGCCTCCGATGTATTATATAATGACGTTCAGGTTTTTGTTAGATCAATGCCAAATTCCACATCAGAAATATGCTTGAGAAGTACTGAAGATCAGGCAGAAATTAGGTCCATGCGTAAACAAAGATCTATGCCAAGATTGCAAGATGGAAATGAGGGTGAAGTGACGATGTTCCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21402
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
ENSDART00000111967 Nonsense 2629 3782 10 18
ENSDART00000114444 Nonsense 2573 3719 11 19
ENSDART00000122421 Nonsense 2558 3727 11 19
Genomic Location (Zv9):
Chromosome 8 (position 55807395)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53960307
GRCz11 8 53794477
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCGGTGTCCATTTAGTTGGTTCTGCAGATCCACTCTCACCAAGTCAT[C/T]AGAATGCCGTGAAGTTTGGAAGGCGGAGGCCCGATCCTTTGGAGTTTGGC
Long Flanking Sequence:
ATGGAGAGGAGAGATACCTAGTATCAAGAAGACGACGGACTAGGCGTAGTGTTGACTGCAGCGTTCAGACAGATGATGACGAAGACAAGGCAGAATGGGAGCAGCCAGTTAGACGTAGACGTTCCCGTTACTCAAGGCATTCTGCTGAATCTAACACAGACCATAAATCTGAATCACATTTTACACCTTCATCTGTTAAGACAGCATCCTCCAGTATTGCCATACAGACCATTCGAGATTGTTCTTGCCAAACAGAGACAGAGCAGCTGGTTAGAGTATCCCCAAGCATACATGCCACCATACCAGATCCTAGCAAGGTTGAAATTGTCCACTATATTTCTGGTCCTGAGAGAACACAGAAGGGTCAAAGTTTAGCTTGCCAAACTGAACCTGAGACTCAGTCTCAAAGCATAGTCATTCCACAGATAAGCATCGCTACCACGGTCAGCCCCACCGGTGTCCATTTAGTTGGTTCTGCAGATCCACTCTCACCAAGTCAT[C/T]AGAATGCCGTGAAGTTTGGAAGGCGGAGGCCCGATCCTTTGGAGTTTGGCTACCAGCAGCATCACCTGCATAACGAGTCTCTATCCAGCTTGATCCGGCAACAACCTAAATCTCCACAGGTGCTGTATTCCCCTGTTTCTCCTCTTTCTTCTCCACAACGCATCATAGACACATCATTCTCTTCTAGTGAGAGGCTGAATAAAGCACATGTCACCCCGCAGCAGAAATCCTGTATTGCCGAGCCATCCCAGAGACATCAGGCCATTCCTCGTCCAATGAAGAATATCCAGAGATCTATGTCAGACCCTAAGCCACTTAGTCCCACTACAGATGAACATACCAAGGCTAGGATTTCACTTTATCAACAGCAAGCCCTTCAGAGTCAGGTATGGGTAATTCATTTTTTGATTCTTAACTTGCACTTGCTTTGCACAAAGGACAAACTGAACTTGTGAATAATACAACAGTAGTGGAGCTTTATTTATGTTGTTTGTGTGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11595
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
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 3621 3782 15 18
ENSDART00000114444 Nonsense 3566 3719 16 19
ENSDART00000122421 Nonsense 3564 3727 15 19
Genomic Location (Zv9):
Chromosome 8 (position 55802872)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53964830
GRCz11 8 53789954
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTYAGGTTCCAGTAGGCAAGGTGTCTCCCAGCCTCCAGTTGATGGGCAG[C/T]AAGGGCAGCGAACGCAACTTCAACAGCAGGCACAGACTTCAGCAGCCAGG
Long Flanking Sequence:
GTCATTCTGGGAGACGAGGCCATGTCAAGCACACATACCATGATTATGATGAGCCACCAGAAGATCTGTGGCCGCAAGATGATTACGGTCACACCCGCCACATTTCTTCTCGTGAGCACCGTCATCATAGCAGCGGGAGTTCTGGTCGGCACTCTACACGCCACTCTGATGAGCCTCGTTCCTCTCGATCATCTCGTTCCTCAAAGGATCCGTCCATCCGGCATGACTCCCGCTCCTTGTCATCTTCAGGGAGGAGGGGAGACTCTCGTTCTCAGGGCTACCACTCCTCAGATTATTCCCGCGACACCTCAGGCCATCATCACAGCTCCCGTTCTGGAAAACAATCATCTTCCCACCATCAAGGATCATCTAGTAGGAAGCAACAGGATCATCCCTCGTCATCTAGGCAGCCAGGATCTCTTGGGGCTGGACAGAAAGGTCCTAGTGGACCTTCAGGTTCCAGTAGGCAAGGTGTCTCCCAGCCTCCAGTTGATGGGCAG[C/T]AAGGGCAGCGAACGCAACTTCAACAGCAGGCACAGACTTCAGCAGCCAGGCCCGGGTCTCAGACGTCCACCGCAGGTGCAGTGCAGCCACAGTTAGTGCAAGCCCAGCAACTGCAAGCCAAACCTGGCCAAACTGGTCCAATGCCCCGACAGCCCACCTCAGCAGCGCAGACATCCCCAGCTGCAGTAAGTGAATATATTAGCTTGATGTCATGGTTTGGTTCCTTTGGCCAATGTGAACAATGTCGTCCTAGACCCTAAACTGCAAACCGTGCCCCATAAGTAGGCCTACATATTAAGGCCTACATATTATCTTGACATATTAAGTGTTGTGAGATAAGAGTAGTATTTTAAATAATATGTATTTATTTGTCTTTTGTTTCCAGCCGATTAAACCAGAGCCCACACCTGCCACTGCTATTGGAGCAAAAGCAGTCCCCGGACAGCCTGCCAAAACAGCCCAGCCTCCACTCACCGGGATAGGTAATTATGCCATATAAA
Associated Phenotype:
Not determined