Busch Lab

ZMP

SYNE1 (1 of 2)

Ensembl ID:
ENSDARG00000063068
Description:
spectrin repeat containing, nuclear envelope 1 [Source:HGNC Symbol;Acc:17089]
Human Orthologue:
SYNE1
Human Description:
spectrin repeat containing, nuclear envelope 1 [Source:HGNC Symbol;Acc:17089]
Mouse Orthologue:
Syne1
Mouse Description:
synaptic nuclear envelope 1 Gene [Source:MGI Symbol;Acc:MGI:1927152]

Alleles

There are 36 alleles of this gene:

Allele Name Consequence Status Availability
sa14682 Nonsense Available for shipment Available now
sa16903 Nonsense Available for shipment Available now
sa9773 Nonsense Available for shipment Available now
sa12762 Nonsense Available for shipment Available now
sa36319 Nonsense Mutation detected in F1 DNA Not yet available
sa18036 Nonsense Available for shipment Available now
sa10324 Nonsense Available for shipment Available now
sa30694 Nonsense Mutation detected in F1 DNA Not yet available
sa32120 Nonsense Available for shipment Available now
sa28806 Nonsense Mutation detected in F1 DNA Not yet available
sa11808 Nonsense Available for shipment Available now
sa28805 Nonsense Mutation detected in F1 DNA Not yet available
sa36318 Nonsense Mutation detected in F1 DNA Not yet available
sa28804 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa28803 Nonsense Mutation detected in F1 DNA Not yet available
sa42869 Nonsense Mutation detected in F1 DNA Not yet available
sa11059 Nonsense Available for shipment Available now
sa9065 Nonsense Mutation detected in F1 DNA Not yet available
sa13399 Nonsense Available for shipment Available now
sa7444 Missense Mutation detected in F1 DNA Not yet available
sa11274 Nonsense Available for shipment Available now
sa36317 Nonsense Mutation detected in F1 DNA Not yet available
sa11252 Nonsense Available for shipment Available now
sa8519 Nonsense Mutation detected in F1 DNA Not yet available
sa32119 Essential Splice Site Available for shipment Available now
sa8895 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa7443 Missense Mutation detected in F1 DNA Not yet available
sa8603 Nonsense Mutation detected in F1 DNA Not yet available
sa10495 Nonsense Available for shipment Available now
sa13678 Nonsense Available for shipment Available now
sa45593 Nonsense Mutation detected in F1 DNA Not yet available
sa11189 Nonsense Available for shipment Available now
sa2927 Nonsense F2 line generated Not yet available
sa14747 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa14682
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
ENSDART00000091828 Nonsense 335 8759 9 143
Genomic Location (Zv9):
Chromosome 17 (position 7942610)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7945384
GRCz11 17 8102562
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGATGTACTGYGGGCACAGGGATCTGAAGAGAGTCTCACTGACAAATA[T/G]CAGGTCAACTTTGGAATTAAACAGGCTGTTTTGTCACTTTYAGTGCAAGA
Long Flanking Sequence:
ACAAATGGCATCATTTCCTGAGAATGGTCTATTAGCGATGGATGCTCTCTGCTTGTTTCCCCTTTTTCTCTGGCTTTAATCTTGCTAACGTCTTGACTGTGTTGTGTTTGCATCTCTTGATATGCTTTTGCTCTCCTGGACAGTATGATCCACAAGATATTGAGCTAATGCTTGAGGTATGTGTATATTAGTACATAGGATCATAACAGTAGCTTGTTATTGTAAGAAAATGCAGAGTAGTGAAAGATCTTCAGTCTTCTTTATCAGTGGACTTTTTCCTGTTGTTCAATTTTTCACACTGCTGTGTTACCTGCTGTGTGTTCTTGTTATATGGATTCTTGCTGAAAACCTGCTAAGCGAGTGATAAATGGGTGCTTTTTTGTCTGATGCGCACAGCGAGAGGAACGCAAGGTGCTGAGAGAGGTGAAGATCTGGCTGGATCAGCTGGAGAGAGATGTACTGCGGGCACAGGGATCTGAAGAGAGTCTCACTGACAAATA[T/G]CAGGTCAACTTTGGAATTAAACAGGCTGTTTTGTCACTTTTAGTGCAAGAAACTGCAGGCAAATAGGGAGAAAAAAATAATACTGTAGTTTTCACAATACTTTGTTAATGTGCTGGATTATTGTTCATTAAGAATGGCAACGGTTTCTGTATTACAACTTTTTAAAAAAGATATTTAAATATGCTAATTATCCATAATTTGTGTTTTTAATATGCACCAATTTGCATACAGTTATAAAACATAAAAACATTGGATGAAATCAGGTTTAAAATTAATTTCTTTTTTGACATTGTAGTGACAAAAGTGTTTTACAAGGGGATATTTATCTCTTTCCTCCATTATTCAGTGAAAAATATATTATATATTATTAAAATATATATAATATATAATATTAAAGGAAAAGAGATAAATATTCCCTTGTGAAATAATAATAATAAAAACACAGAGGCAAAATTCCCTAAAAATGTTGTTGAGAAAATAGAATAGCAAAAACGCTGACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16903
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
ENSDART00000091828 Nonsense 452 8759 12 143
Genomic Location (Zv9):
Chromosome 17 (position 7937432)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7940206
GRCz11 17 8097384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTGCAGGAGGTGTTAAAGAACTTGGAGGSACACAGACAGACATTTCAG[C/T]AGATTCACAGAGACCGATCRGTAAACGGTGTACCRGTACCACCAGAGCAG
Long Flanking Sequence:
GGAGCGGAGACCGTAGATACCGGCTTCATTACTAAAAAGAAAGAGGACAAACACACAGAGACTGTTTTGTTCGGAAGAACAGAGAAGCCCACAGAGCGAAAGCGGCAATCTGGCCAGACACTTGACAGCTTGAAGGGTCTTCACAAACACCGAAGAGCATTAAAAACACATCTCTCCTTTTGATATCTGCCATGCTTTTGTGTGGTTTGTGCAGCTCTTAGACTGGCACATCCATCTGGACAAATCTTTGCCTGGTCCTCTGGGAGTGATCGGGGCCTGGCTGCATCGGGCAGAACTTTCCCTGAGAGAGGACGTCCCGATTCAACAGGCCCACGAAGAGACGGCCAACATCATCCACAGAAAACTGGAGCAGCACAAGGTAGTTTTTCTTTCTTGATGGACTTGATTTGATCCATGTGCTCCAGGAATTTAATATATTGTCTGTGCTTTACTTGCAGGAGGTGTTAAAGAACTTGGAGGGACACAGACAGACATTTCAG[C/T]AGATTCACAGAGACCGATCGGTAAACGGTGTACCGGTACCACCAGAGCAGCTTCAGGACATGGCAGAAAGGTCAATTTCATTTTACTGTTTATGGACAAAGGGCAGCATGGTGGCTCAGTGGTTAGCACTGTCTCCTCACAGCAAGAAGGTCGCTGGTTCCAGTCCCGGCTGAGCCAGTTGGCATTTCTAAGTGGAGTTTGCATGTTCCATGTGTTCATGTGGGTTTCCTCTGCATGCTCTGGTTTCCCCCGGTTAAAAACCCCTGATGTTAGTCTAGGGCAGTGGTTCTCAAAGTGGGGGTCGGGACCCCCAGAGGGGTCGCGGGACAATGAAGGGGGGTCCCCTGGTGATTTCCAAAAATCGATTTAATTTTTATTAAACCACAAGATTTACCATATTTTATTCATAACCTACTGAAGAGAAAAAATATATACTATATAGATACTATAATAGCTTATATTTCTATTGCAGGGGTGCTCAACCCTGTTCCTGGAGATCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28807
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 687 8759 17 143
Genomic Location (Zv9):
Chromosome 17 (position 7922577)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7925351
GRCz11 17 8082529
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACATACATTGCGTATGTAATTCTAATGGCCTATTTATTCTTCACAGTA[T/A]GCAAGAGCAGACGAAGTGGACAAATTGAGGAAGGATTATGATGACGGGAT
Long Flanking Sequence:
TTGTTAACTCATTATTAGTTTGTCATGTTCACCTGTTTGTGTCAATTTACTTTTGCTTTAAAATCCCCTCATGTTTTCAGTCCTGTGCCAGTTCGTTGTATTAACTCCCCATGTGTTCCTGCTTTTGTTCTTGTCGTGCCAAGTTTGTTAGTGTTATAGTTATGTTTTTCCCCCTCGGGGTGGTTTTTGCTGTTCTTTTATTTTATTTCTATTATCAATAAATTGTCCTGCATTTGCACTTGAGTCCTCGCTCCCTCATCCTTCCTGAAACCCTGACATCACCGAACATTAGATTGAATTTTTCTTGCAAATAGTTTTTCTTTTCAGACCCTTTCTTACAGTCTGTCATCATTCTCATTAGCATAATAATTTGATGTTATAAAATGCATTATAATTGACATTTATGCATTTAACAGACACATTTATCAACCACTAATCTTAATGTTTATGTTACATACATTGCGTATGTAATTCTAATGGCCTATTTATTCTTCACAGTA[T/A]GCAAGAGCAGACGAAGTGGACAAATTGAGGAAGGATTATGATGACGGGATTGAAGCTTTAAAGGCGTTTATTGACACGGCCAATGAAAGGATGAACACTCCCGTTCAAGTGTCTTTTCTCAACATACGGACATATCTACAAGACGTTGAGGTAAAATCCATAGCATGAATCCACTTTAGAGTGATAAAATTACCTTTACTGACAAAATGATTACATTTATATGAGTCTGATAAAAAATAATAGGTAACACTTTTGTTACCTTTTTTAACTAGTGGCTTATTACCTGCTTATTATTAAGATACTGGCTGTTTATTTGTGCTTGTAAAATACATATTCTGCATGATCTTATTCTACACCCCTAACCCTACCCAATGCCTAAACCCAACTACTATATAATAATATTAATTGATTAGTTTATTGAGGCAAAGGTCAAAGGTAATGGTTTGTTTTTGAATTAAATTAAAGTGTGAGCAAATTATATTTAGAAATATAATTAGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9773
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
ENSDART00000091828 Nonsense 1034 8759 23 143
Genomic Location (Zv9):
Chromosome 17 (position 7915070)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7917844
GRCz11 17 8075022
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACATCMCTGCAGGAGTGTCAGGCCGAACTGGCCCGCGAAAACCGCAGTT[T/A]GCCCAGYGTCGGCAGCGAGAGGTTAATTAAAGAGCACCGRGTGAGAGCCA
Long Flanking Sequence:
TACGTGCATACATGTACCTAGGTATATGTATGCAAATATACAGTTGAAGTCAGAATTATTAGGCATGACTAGGCAAGTCATTTGACAACAGTGGTTTGTTTTGTAGCTAATTGGAGAAAATACGGGTTCCATAAAATAATATTGACTTATTTTATTATGATAAATATATGCTGGAATAGTTGGTGGTTCATTCTGCTGTGGTGACCTATGAAAAATTAGAGACCCAGCCGAAGGAAAATGAATGAATGAATTAATGAAGTTGCTTTTTTTGTATACGATGGACGAAATCCAAGTACATTTATTATGGGTCGTGTAAAAAGGTTGGATAGCTATAGTGTATCAGGGCAAAAAATCTATATAAATAAATGCATGATTCCTGCAGGACGTCCAGACAGAATTTCCCTATCACCTGCTGCATCTGAAGGTGGATCTGGAGAAGAGTCGCCTGATGACATCACTGCAGGAGTGTCAGGCCGAACTGGCCCGCGAAAACCGCAGTT[T/A]GCCCAGTGTCGGCAGCGAGAGGTTAATTAAAGAGCACCGAGTGAGAGCCAGCATCTGTAAACCCACTCTATATGTCCTGTTTATGGAGGAAATACTAATGCCGAATCTCTTTATGCAGATGTTTTTTAAGGAAAAGGGTCCACAGGCTCTTTGTGAGAAGCGGTTACAGCATATGGATGAACTGTGCTTGAAGCTCCCGGAAAGCCAACAGGCTCAACAAACCCTGGTGATCGCCAGAACAGCATTTGCAGAGGTCAAAGAGGAGATTGACAGCACACACCAGAGACTAATGCAGCACCCGGACAAGTGGAAGGAGTTTAACACCAGGTGAACCACTGACTTTTTGAATATAAACTGGTTTGGGGCTGTTGTTATTAAGTGAGAACCAAATTGAGTCAACAATGATAAAGTAAGCTGAATTATTATATGCTATATTTAGCTTACTTATAAATACAGTTGAAGTCAGAATTATTAGCCCCTCCCTGTATATTTTTTCCCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12762
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
ENSDART00000091828 Nonsense 1469 8759 31 143
Genomic Location (Zv9):
Chromosome 17 (position 7906145)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7908919
GRCz11 17 8066097
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAAAGAGAAATGGATGCCTTAAAAAGCTCCAGCATACCTTTGGACCAG[C/T]AGATCTGTACTGTACAGGTGCRAAAATGTATATTTTATTGCAAATTAAAA
Long Flanking Sequence:
GTTTTTTTATATGTGTTTAGTTTATTCTGCCTCACACAAAGAAAGCACGCTTCATTCTCCCTTCATTTGTTCCCGCAGGATCTCCTGAAACAGTGTGAAACGGAGGTCAGACAGGTGAACACACTTCTGAAAAGGGCCACAGAAATCCAACTGGGCCCCAAAAACCAGTCTCTTCTTCAGGATCAAGCACGAGCTTTGAGCGAACAAGTGGACAAAGTAGAGAAAGGACTCAAGCGAGAGTAATACCCTACTTTATCATATGGATTTTACATTAGGATTATTAAGATGAATGCATTAGAAGTCATACTCTAAGTGAATAAATAAAGCAGCTGTAAGAGAGTGTTTTGATGACTGTCTGGTTTTTCAGTGTGAAGACTTTGGAGGGAATGAAAAGTCAGTGGGATTTGTTCGGGAGTGAGTTTGAAGCGTTTTCCTCATGGATAATGGAGAGAGAAAGAGAAATGGATGCCTTAAAAAGCTCCAGCATACCTTTGGACCAG[C/T]AGATCTGTACTGTACAGGTGCAAAAATGTATATTTTATTGCAAATTAAAATTCTTTCTGATGTATATCTAATCATTTAGTTATTCATCATCATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTGCTTTTATATTATTGACTGCATGACTTTTTTTTTTCAAATATAGTTATATACAGTGTGACCCTGTGCCATAAACCATTTCAAAGTTTATTAAATACGCTAAATATTGAGAAAATCTCCATTAAAGTAAAAATAGTTCTTAGCAATGGATATTACCAATCAAAAAATAGGGTTTTGTCTTACAAAATAGAAATAATTATAAATCTATAAATAAATAATATAAAATAGATCTTTACATAATATTTTAATGCTTTAATAAGGCTGTAATGCTAATTTTAACTTTATCTCTTTGTATTTTTAGCTATTCCCACAAATATAATTAAGCAACATAATTTTAAAACAATAATTTTTATTATTTTTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36319
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 1682 8759 35 143
Genomic Location (Zv9):
Chromosome 17 (position 7897078)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7899852
GRCz11 17 8057030
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCCCTGACAGTCAGTCTCTGCCAGTCGACAAACTAAAGCTGGATGGA[G/T]AATTGCTGGAACTAAAAGTAATACGTTTTTAAAACATTATTCACAATGCA
Long Flanking Sequence:
TGTATTATTATTATTATTATTTTGGTTAATAATTAAGTAATTATAATATTAATACATACAATTAAGTAAATTTATATTTTCATTTTTTTTAAATATTAAAAAATGTATTAATTAAATTAATATTTTAAAGCAATACGTTTACACAAATGTTTTAAGTTTTCTGAGCTAAGCAGGTTTTACAGTCTGAAAGCATCCCATTTTATTGCATATGTGAGTAAAATGGCTTCTGAACAACATGTGTAGGACAAGCTTTTGTTTATGGGGAATTGATTGGATGCTAGTTTGCCATTGGTGGATCTCATGTAAGAGACAGGTTGTCCCCGCCCTCGCACCAGTAAACACGCCATCAGAGGACAGATGGAACAGACATCATTTTACATTTTGTTTTTTTCAGGTATGAAAAGGATTGGTCTGCACTGAAGTCATGTCTGGAGAGATGTGAAGCTGCGTGTGGCCCTGACAGTCAGTCTCTGCCAGTCGACAAACTAAAGCTGGATGGA[G/T]AATTGCTGGAACTAAAAGTAATACGTTTTTAAAACATTATTCACAATGCAATTCAGTTCTGGAATGTGTCATTTTTCTTTCGAAGTCAAGATGTAATAGGGGCTTATTTTATTTTTTATGTTAGCTCATTTTGGATGTACTGTACTGGAATTATGAAATATGAATAATTAAATGGATAGTTCATTGAATAAACTAACGAATGAGTGAACTAACGAATGAACTAACGAACGAACAATCAAACTAACTAACAAACTATCAAACTAACAAACTAAATAAATAAAAAACACAGAAATCAATAGTAGCTAGAAACTGTTTTAAGTTTAGGCTGAACTTACCTTAAATGTATTTATGTTATTTTTCATTTCTTTTCTTGAAATTCTAATAAATCTGGTTATTAAATGGGTAGTTCAGCAACCCCACCATGCCTTCAAGAATATACATACATAACAGTTCATTTTACACAATTTAAAAGTATATTTGAGCTCCTATTTACTTAAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18036
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
ENSDART00000091828 Nonsense 1813 8759 38 143
Genomic Location (Zv9):
Chromosome 17 (position 7892974)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7895748
GRCz11 17 8052926
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGAGAAGCTCTCCTRAAGCAAAGCATCGTCCGGCAGAATCTTCMGCAG[C/T]AAACTAAAACCCTGTGTGAYGTTTGTGAGCCAGCKGAAGTCCAGCATCTT
Long Flanking Sequence:
TTAACCTAATTACCTAATTAGTTAATTAGTAACCTAATTAGTTAAGCCTTTAAATTTGCCTTAAAATACTACTATCTTGCAAATAACTATTAAAATAGTACATACTGTCATCATGGCAAAACAAAAGAAATTAGTTATTAGAAATTAGTCCATGTTTGAAAAAAAATAAACATCATTTGTAGAAAGATTTGAAGGTTATGGAGGGCTAAGCATTTTGCCTTCAATTGTTTATAGGACATTACTGTGACACAAAAATGCATTTATCATAATCAAAAACAATATTTTTACTGACTTTTAAAACAGATTTATTGTTTAACATGTTAAGTTGAGAACCCTAAAGTCAACCCCCTGGGGTATGAATAATTTCAGGCTTGACTGTATATATAAACCAAGTAAAAGAGTGCTTATATTACAAGACAATAAAATTGTATCATTTTCCTCACCAGGAAAAAAGAGAAGCTCTCCTAAAGCAAAGCATCGTCCGGCAGAATCTTCAGCAG[C/T]AAACTAAAACCCTGTGTGACGTTTGTGAGCCAGCTGAAGTCCAGCATCTTCAGGGAAGGTGGGAGAGCTCCTTACAGCCGTACCTGGAGGCCCATCAGCTGGTTGAACTTCGAGGAGAGAGTTTGGAGAAACTGGAGGCCTTTCTACACACCCACAGTGTGGCAGCGGGCGTTCTCCAGGGCCTCAGACAGACCGTGGAGAGCGCTGGGAGTTGGGATAAAAGCCGGGTGGAAGAGCTGCAGAGAGAGCTGGAAGCCATCGTTCCGGATATCAGCCGCCTTGAAACGCTCGCCGTGAATTTGGACGGCAACCTGTGTAAATCTCACCTGCACTTAATGAGCGGGAAAGAGACACGGTCCTCGTGTCGTTCACTGGCTGACTCCTTGAGCGCTGAATTGGACGCCGTGAGAAACCTACTGGGCTCCAAACAAAGCGAAGCTGAGGCTCTCGGTGCTCTTTGGAGCTCCTTCAGACAGCGTAAAGAACAGCTGCTGAAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10324
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
ENSDART00000091828 Nonsense 1956 8759 38 143
Genomic Location (Zv9):
Chromosome 17 (position 7892545)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7895319
GRCz11 17 8052497
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCTTGAGCGCTGARTTGGAYGCCGTGAGRAACCTACTGGGCTCCAAA[C/T]AAAGCGAAGCTGAGGCTCTCGGTGCTCTTTGGAGCTCCTTYAGACAGCGT
Long Flanking Sequence:
ATCATTTTCCTCACCAGGAAAAAAGAGAAGCTCTCCTAAAGCAAAGCATCGTCCGGCAGAATCTTCAGCAGCAAACTAAAACCCTGTGTGACGTTTGTGAGCCAGCTGAAGTCCAGCATCTTCAGGGAAGGTGGGAGAGCTCCTTACAGCCGTACCTGGAGGCCCATCAGCTGGTTGAACTTCGAGGAGAGAGTTTGGAGAAACTGGAGGCCTTTCTACACACCCACAGTGTGGCAGCGGGCGTTCTCCAGGGCCTCAGACAGACCGTGGAGAGCGCTGGGAGTTGGGATAAAAGCCGGGTGGAAGAGCTGCAGAGAGAGCTGGAAGCCATCGTTCCGGATATCAGCCGCCTTGAAACGCTCGCCGTGAATTTGGACGGCAACCTGTGTAAATCTCACCTGCACTTAATGAGCGGGAAAGAGACACGGTCCTCGTGTCGTTCACTGGCTGACTCCTTGAGCGCTGAATTGGACGCCGTGAGAAACCTACTGGGCTCCAAA[C/T]AAAGCGAAGCTGAGGCTCTCGGTGCTCTTTGGAGCTCCTTCAGACAGCGTAAAGAACAGCTGCTGAAAACTGTGGAGGATATTGAGGAGAAGGCGGATCAACAGGGCCTGAAGGAGCCCAATGTGCTTACTCTACAGCAGAGGTATGGATTGTGATTATCAATGTGGTTGTTTATGTGAGGGATATTTAACAGATTGCCATGAGTTGTAAATGCATGACATTTAGGCAAAGAACTGCCCGATGCAAAGCAGAAGTGCATTTAAAGGTGTTGTATGTACATTTTTGACTCTTCTAAAACATAAAAAAGTTTGCAGATACAGCAGGGAAAATAAAAATTTAACACGTCACCATTTTTCTCAGAAAACATATTTCTTAAGGTGCCTTTGAAGTTTTTTTTCTGGGTGTTGGTAACAACCAAAGAAATCCATATATGCAAAGAAAAGGAATCGGATTAGTTTACAAATGAAGTTATGCATAATAAAAGGAAATAATGCTTGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30694
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
ENSDART00000091828 Nonsense 2029 8759 39 143
Genomic Location (Zv9):
Chromosome 17 (position 7889005)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7891779
GRCz11 17 8048957
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGCTCCAGTCTCACCAGCATGAGGAGCAGTGGCTCAGGGATAAAGGT[C/T]AACAGCTCGCTCACAGAGATGCTGAGCTGGGCAGTGAAGTGCTAAGAGAG
Long Flanking Sequence:
CCAAAAGGAACAGGTAGCAAGACAACATAAAACAATGACCAAAGCAAAGATCAATAATCACGAAAGGACAAGGCAAGGAAACCGCTTAGTAATGTTACAGGGGAACAAGTCTCAGAAAAGCCTGCATGCGTGTGTGCTGTTTATATGGTCTATCTGATTATAAGCTTCAAGGTGTGTGTGTGTAATCAGGGGGAATCAGGAACTGGTGTTTCTGAGGTGCATGATGGGAGTTGTAGTTTATTTAAATGGCATATGTGTTGTTCTCCAGCGATCTGCATAGGCTAGATTGCTGATGATTGTGACACCATGTGGTATCTGGCATCATGAGATAAGGCACAAAATGGCGGAAAATGTCAACTCTGTTATTGTCAACTCTGTTATGCTTTACTCTATAGAGGAAACTCTTTTCTTGTGATGTGTTTAGGCTTCGGTTTTTCAATCAGCTGGAAGATGAGCTCCAGTCTCACCAGCATGAGGAGCAGTGGCTCAGGGATAAAGGT[C/T]AACAGCTCGCTCACAGAGATGCTGAGCTGGGCAGTGAAGTGCTAAGAGAGATTAACCTGCTTCAGACTACCTGGGAGGACACTAAGAAACTCATTACTGAGAGGTGAGCTGGCAGAAATCGGCTCTTATACTGTTTTTTGGGATGTTTGGCTTTTAATCGTGTGATATATGATATATGTAGTAAATGTTTTAAAAAATAAAGTGTTCTTGGATCAACTCATATTAGAGGTTTTGACAAATGGGGTTTGTCATTGGCAAATTCTTACATTTATGTGAATGGTTTCCCCAGTGTTAGACATTAGATTCCATCTTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATCATTAATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACCGCCAACTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32120
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
ENSDART00000091828 Nonsense 2045 8759 39 143
Genomic Location (Zv9):
Chromosome 17 (position 7888957)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7891731
GRCz11 17 8048909
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAACAGCTCGCTCACAGAGATGCTGAGCTGGGCAGTGAAGTGCTAAGA[G/T]AGATTAACCTGCTTCAGACTACCTGGGAGGACACTAAGAAACTCATTACT
Long Flanking Sequence:
GATCAATAATCACGAAAGGACAAGGCAAGGAAACCGCTTAGTAATGTTACAGGGGAACAAGTCTCAGAAAAGCCTGCATGCGTGTGTGCTGTTTATATGGTCTATCTGATTATAAGCTTCAAGGTGTGTGTGTGTAATCAGGGGGAATCAGGAACTGGTGTTTCTGAGGTGCATGATGGGAGTTGTAGTTTATTTAAATGGCATATGTGTTGTTCTCCAGCGATCTGCATAGGCTAGATTGCTGATGATTGTGACACCATGTGGTATCTGGCATCATGAGATAAGGCACAAAATGGCGGAAAATGTCAACTCTGTTATTGTCAACTCTGTTATGCTTTACTCTATAGAGGAAACTCTTTTCTTGTGATGTGTTTAGGCTTCGGTTTTTCAATCAGCTGGAAGATGAGCTCCAGTCTCACCAGCATGAGGAGCAGTGGCTCAGGGATAAAGGTCAACAGCTCGCTCACAGAGATGCTGAGCTGGGCAGTGAAGTGCTAAGA[G/T]AGATTAACCTGCTTCAGACTACCTGGGAGGACACTAAGAAACTCATTACTGAGAGGTGAGCTGGCAGAAATCGGCTCTTATACTGTTTTTTGGGATGTTTGGCTTTTAATCGTGTGATATATGATATATGTAGTAAATGTTTTAAAAAATAAAGTGTTCTTGGATCAACTCATATTAGAGGTTTTGACAAATGGGGTTTGTCATTGGCAAATTCTTACATTTATGTGAATGGTTTCCCCAGTGTTAGACATTAGATTCCATCTTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTAAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATCATTAATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28806
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
ENSDART00000091828 Nonsense 2070 8759 40 143
Genomic Location (Zv9):
Chromosome 17 (position 7887813)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7890587
GRCz11 17 8047765
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGATGTTGCTACATGATTTTGTTGCAGACAAGAGCAAAGCAGTGCTT[T/A]AGTAGACCTCATGAAAGACTACCAGACTCTGAAGTCTTCAATAAACTCCA
Long Flanking Sequence:
CTCTACACAAAAACGCCATCTGAGCCGAGGTTCGAGCCAGCGACCCAGCGACCTTTTTGCCGTGAGGCGACAGCACTAGACTGCGCCACTGCGTCGCCCTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTTATTTTATTTTATTTTATTTTATTTTACTTTATTTTACTTTATTTTACTTTATTTTACTTTATTTTACTCAACATTTATTCTGTGATACATTATAGACCAGGACACAAAATAAAATGAGCTTTTTATAAAATATAAGTGGATTATTTTGCCTAATTTGATCAGGCTTGGTTGGTAACTCGATCTAAAATATTGAGCATCACTGCATGAGGATTTCATAGCTTTTTCATTTTCGTTTAGTTAGGCAAAAGTGATTTTCAGTGTCTAACTGATGTTGCTACATGATTTTGTTGCAGACAAGAGCAAAGCAGTGCTT[T/A]AGTAGACCTCATGAAAGACTACCAGACTCTGAAGTCTTCAATAAACTCCATTTTGGAAAGCGCTGATGCAATAGCCGATATTAAATCTGTCCTGAAAGATCAAGAGGACACGCGGAGATCCTTGTTGAAGGTAAAACCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTTTCATGCAAAATAAACAAATGCAAATAAACACTTGAATGTCGGTCTTCAATGATCTTTCTTTCTGTAGCATGAAGCTGTAAAAGCAGACATGGCCAGTCACCAGGATGTACTAGACCGATTCTCCAGTAAAGGGAAGAAGCTTTTAAGTGAATTAAACAAGATCCCTGATTGTGACACACAGATTGTGAAGACAGAAATAGATGCTACAGTGGACCAGTGGCTTGATGTGAGTTTACCTAAAAGCCAAATATTCATTAGTATAGTTTTCATTAGAAATATTGGTAACACTTTATACTAAGAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11808
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 2511 8759 48 143
Genomic Location (Zv9):
Chromosome 17 (position 7880530)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7883304
GRCz11 17 8040482
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAATCTAAATTAAAWCCTGTGTTKGTTTTGTAGGTTTGACGGCCGTCTG[C/T]AGAGACTGAGCCGCTGGCTGGAACGCATGGATGTGAARATGAGCACAGAG
Long Flanking Sequence:
CACACGCACCAAGCACACACTCAGGCAAAGCTCTCTCTCTCTCATTCGCAAAGCAATATCCGCGATATTGCTAGACAGCCCGCTCCCGTCCTAAATTAAACCCGTTACCGACCGCTCCCGCGATTTATTCGTAAATTTATTCCCGCGCCGCAGAAATCTGGTCGGGTCCCGCGGCTGTCCCACGGGCAGACCTTTAATGCAGACCTCTAGTCTGAGGACAGTGTAGCTGTTTTTTGTAGCCTGTGCCTTTAAATGCAAATGAACCTGTTGAAATGAAGCGTGTTTGGCTTCTTACATCAGATAAACGGCAGTCGGTGACCGACATTAATCCCAAAATCTAGGTGCTGTGTCTGTGGTGTCTCACCTTTAATATTAGTGCAACAAGTAATTTTGATGTGGAGGAAGCTGTGCACTTGACTCTCAGCTTGGCACGCAGTCGTTCGTCAACGAACAATCTAAATTAAATCCTGTGTTTGTTTTGTAGGTTTGACGGCCGTCTG[C/T]AGAGACTGAGCCGCTGGCTGGAACGCATGGATGTGAAGATGAGCACAGAGCTGCCAGAAGGAAGACATGGCGATCAGGAGAGAGTCACGCTGGAGCGGGTGGAAGAATTCCAGCATGAAGTGCTCAAAGAGAGGTACCGTGCTAATGTTATGTTATATCATTGCTTTGCCCTGTTGTGTGCACTGACTGACTCAATACACTTTAGGGATGCACCAATGTATCAGCTGTTGATATTTATCAGCTGATACTGGATTCATTTAAAGCTGTCGACAAATCAGCAATAATATGAAAAAGGCAGATGACTATGGCTACATATTGTAATTTGCAATAAACTCAAAATAATCAATCAGTCAATTAATCAATCAATCAATCAATAACTAAATAATTAAAGTCAATCAATAAATAAAATCTAAAATCAAACTTGCGCCTCTTAAAAATGTTGGACAGTTGAATGTTAAAAGGATTTAATAGATATTAAATAACATTAATTAAATGGAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28805
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
ENSDART00000091828 Nonsense 2746 8759 51 143
Genomic Location (Zv9):
Chromosome 17 (position 7872866)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7875640
GRCz11 17 8032818
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCAGTGGCTGGAGATGGTGGAGCAGGAGGCAGGAGTGGCTCTACCT[C/T]AGCAGCCCGGGCTGAAAGAGAAAGCCGCTCTGCTGGAGAGACTACGGGTC
Long Flanking Sequence:
GCTGATCTTGTTTCAGGACATCTTGCTGATGAAGGGTGAAGGGGAGGTGAAGCTAAACATGACGGTTGGGAAGGGCGAGCAGGTGCTGAAGAACTGCAGTCGAGACAAACAGGAAGTGATTCGCTCTCAGCTCAAGAGTCTGAAAGATTCCTGGGCCAATATTCTCATGACCGCCATGAGCTGCCACAGGTCAGATCCTGTCTCTGGTGTTTATATGCTAAAATTAAAATTTTTCTCAAAATGTGTGTACAGTTGTGGTGACACGGTGGCTCAGTGGTTAGCACTGTCGCCTCACAGTAAGAAGGTCGCTGGTTCGAGTCCCTGTTGGGCCAGCTGACATTTCTGTGTGGAGTTTGCATGTGTAAACGTGTGTGTGTGTGTGTGTGTGTTACAGTCGTCTGGAGTGGACCGTAGCTCAATGGAGCAGTTTTCAGGAGAGTAAAGCACAGCTCCAGCAGTGGCTGGAGATGGTGGAGCAGGAGGCAGGAGTGGCTCTACCT[C/T]AGCAGCCCGGGCTGAAAGAGAAAGCCGCTCTGCTGGAGAGACTACGGGTCATTCAGGCAGATGTGGAGGTCCATTCGACAGCACTGAGTCGCCTCAATGAGAAAGCCACAGAGCTGTATGAGAAGACAGGAGACCAGGCGTTTGCCGAGAGACCAAAATCTGACTTTAACACACAGTTTACCAACATCACTGCGGTCATTAAAGTAAGAATTTGTTTAATAACATTGTCTTACAATCAGCACACATCTCTAAAAAATAAATAAATAAATAAAATACATTGTGCAATTATGAAGTGACCTTCGCTCAGGTGAGTAGGCTTGACAAACCACATGTAGAAACACTCTTCTCTCTATAAATATCTAACAAACAAACTCCCCCTCCTTACTCTAACACTTAATTCTTTGAGGACAAACAGTTGCTCTGTATAATGCAACCCAGGCTCATTCTGGAAACGTAGCCCTGCGGACATTTCTGGAGACCGTGAAATACGTCCCCGGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36318
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
ENSDART00000091828 Nonsense 3089 8759 55 143
Genomic Location (Zv9):
Chromosome 17 (position 7864535)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7867309
GRCz11 17 8024487
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGTGTTTTGACGTGCCTCAGAATCTGGCTGAGGCATCGTCCAGCCTG[C/T]AGAAGATCCAGGTAACGTTTTATCGATTTCTCATTTTTGTTTGGTCCAGA
Long Flanking Sequence:
TTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTTATTTTATTTTATTTTCTGTTTATAAATGAAACAATAAGATATAAAGAGGGAGAAAAATATATATACATTCAAATACATACATACATATAAACTGTACATAAAAACATATAAATATGTACATACCTATGCATATTATAATTCATATTTGGTAAGATTAACACAAATAATCAATAGTAAAACAAATTGTATAATTTTGGATGCATGTAAAATGTTCTTTATCTGTGTGTGTAGTTTTTAACCTCTCTCTCTCTCCTCTTGGCTGTAGTCTCAGTCTCCAGGCGTCTCGAGAGTGTCAGGGAAAGGAAAAGCTGCTGGAGCAGAGGTTTCGTGCTGCTTTTCGAGACTTCCAGCAGTGGCTGGTCAATGCCAAAATCAATACAGCCAAGTGTTTTGACGTGCCTCAGAATCTGGCTGAGGCATCGTCCAGCCTG[C/T]AGAAGATCCAGGTAACGTTTTATCGATTTCTCATTTTTGTTTGGTCCAGATTCTAGCTGATAGCTGAGCCTGTTTCATTGCAGGAGTTTCTGAGTGACCGAGAGCAAGGCCAGGGTAAACTGAACACAGTGGCGGCAAGTGGAGAGCTGCTGATGAGCATCGCTGCTAAAGACAGAGTGGAGTCAGTCAGAGCTAAAATCAACTCAGCCAGAGAAGACTGGAAAACACTCATGACCAACCTGCACCAGAGAGAGAACGCCTTACAGGTGTCACCATTCACACACAACTGCTTATCTGTTCAACTAACACCCAAAACTAGAATACATGAATTTTAATTTAAAGGGATAGTTTACCCACATATGAAAATTCTGTCCTCGTATACTCATCCTTTACAGAGTTACTTTCTTCTGTTGAACACTAAAGAAGATATTTTGAAGAATGCTGAAAACCTGTAACCATTGACTTCCATAGTATTTCCTTTTCCTACTATGGAAGTCAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28804
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Essential Splice Site 4012 8759 71 143
Genomic Location (Zv9):
Chromosome 17 (position 7834480)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7837254
GRCz11 17 7994432
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTACCCTTTGTCACATAATCCAGAGTAATGTTTGCCCTTTGTCTCTTC[A/T]GGTGTATCAGAGTCTGGACCGTGAGCTCCAGAAGCACGTCAGCCATCAGG
Long Flanking Sequence:
AAGAGAGTACAAAGTCAAAAGTATTGTCCTGCCAATAGACGCTGCGTTACAAACACCTCACATAAGCCTTAGCTGTTGTTTTTGTAATTTGATGCGATATGATATAATATAAAATGTAGCTTTATAGATGTACATACGCTTTTAAAAATCAAATATTAAAAACTTTATTATTGTATTATTTAATATATATATTTTTTTCTTTCAAAGTGTATTACATTATTTTGAGTTTATATATTATTCTTGTTTTATTTTGTTATTATTTATTCATTTTTGCTAAACTGTAAATTTGAAACCTTTGTCAATTTGTATGACAATGTTTCAAATAAAAATAGTTGTTAAAAAAAAAACTTAAGCGGATTTAAGAAGCTGATGATCGTTAAATATATGATCACCGTCTTGTGAAAACGGTCCGCTATCAGTAATCGCATCTCATTTATTTCATCGTCTAATGTTTACCCTTTGTCACATAATCCAGAGTAATGTTTGCCCTTTGTCTCTTC[A/T]GGTGTATCAGAGTCTGGACCGTGAGCTCCAGAAGCACGTCAGCCATCAGGACACCCTCCAGCAGTGTCAGACATGGCTCTCCTCTGTTAAAGAGGAGATTCAGATGCAGCCGCAAACTCCCTATGGTCTGCAGGAGGCTCTGAAACAGGTAAATGTCAAAGTTCAGACGGATAAAACATTATCTGTCAGACCCGTAGAGAGCCACTCCTGCCAAATTGTAGCATTTCCTTTAAAGTCCGCATGAACTGGAAGCTCCAACCGTTTTTTTTTTATTGTGATGCAGTAGATAAACGGAATATTACATGAGAAAACAGTGGGTGTGGCTTGTTTTATTTCTACTTAGAGCTGATTGGATGTAGTAAAGTAGGCATTTCATTCATAAAGATAGGGAAAAGGGTTCGGGGAGAGTTATTAAAACCGACTCCTCCCCCTCACCATTTCTGTTTGTTGTCAAAACTGACAGTTAGAGGGGCGTGGCTAAGTGTGTTAGCTCCGCCCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28803
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
ENSDART00000091828 Nonsense 4070 8759 72 143
Genomic Location (Zv9):
Chromosome 17 (position 7831626)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7834400
GRCz11 17 7991578
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTGTAACGCTTTACTCCACAGGTGAAACACTTCAGGGCCCTACAGGAG[C/T]AGGCCAGCACGTACCTAGATCTGGTTTGTTCAGTGTGTGATTTATCTGAT
Long Flanking Sequence:
CCCGGGACAGCATGCCAAACACGCTTTATAATCAATCTTCAGCTAGGGGGCGAACTCTTGAATATGTAATAAGTGGCTGAAATAACCACGAATGTCAGGGCATGTCAAAACATCTTAGGAGCCCCAATCACCTCAGACCCCAGAGGGTTAGTTGGGCAAGTTCTTGTATAGACCATTTAAATGTGGTGATGTCATTGGCCAATGAACATTTTCTGCTTGTTATTAAACTATTTCATAGCTGTAACAAGAGGCAATCATAACTTAATGTTAAAAAGCGACCTTAGTCGACGCCAATAGCCTAGTGGTTGGTGCGTCAACGCATAGCACTGAGGTGCTTGATTTAATCATAATTTGGGAAATATTTGAAAAAGAAAACAAATTCACAGGAGGGTGAATAATTTTTGTAATTAAACATTTGTTTTTCCATTTGTTTGTAATTATATTTATTTACATTGTAACGCTTTACTCCACAGGTGAAACACTTCAGGGCCCTACAGGAG[C/T]AGGCCAGCACGTACCTAGATCTGGTTTGTTCAGTGTGTGATTTATCTGATGAGTCTGTGAGAGCCACAGCTGCCAAAATACAGCAGACCAAAACAATGGTGAGTTTGATGACTCAGGCTAATAGTGATTACTGCTTTGGGATGTAAAAACGTAATAATAATGTGAGTAATATTGTCAATTCTACAGATTGAGGAGAGGATGAGCACTTCTCAAGAGCTGTCAGATAGCTGGAGGGAGATCAAAGAGCAAAAGCAGGAACTCTCGACACTCTTTCAGGACATGGAGCAGCAGCTGCAAAGTCTCTCCAGAAGACCCGCTGAGCTGGAGACCAAGATTGCTCAAAACATGCTTGATCAAGCCAGGGTAAATAGAAGTCTTTTATTGGATGTAGAACTATGTATTATGTCTGAATACGCTATCATGGTGGCTTAAGAAAGCCAACATACTGTTTTGCTAAACTTCTTCTTCTTCTTCTTTTTTTTCTGAGACTAATTTCTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42869
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 4282 8759 75 143
Genomic Location (Zv9):
Chromosome 17 (position 7826460)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7829234
GRCz11 17 7986412
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCTCAGTTGTTCTTAAAGACAAGAAAAGCACACTTGAGGATCTCAAA[G/T]AGCAGAAGCAAAAAGTAATGTACCATCTAAACCTGGATGACAAAGAGCTG
Long Flanking Sequence:
GATCATGAACGACCCATCACTACTACTTAGTGTCATTGGGAATCCGCTTCTGTAGCTCCAAAGGCGCCTCTTACTAGCACAGAATGAATCTACTTATCTAGCACTTTGTTCTGAAAACACACACACAAGATACATGGGTGAAACTCACACCAGTGGGACACAATTGATTGAGATTTGTAATTTTTTAGGTTTCTTGATGACAGAATACACATTGTAGATGTCACCTGATGATTGCTCGCAAAACAACTTTTAGTCTGACGTATTTGGTACCCAACACACATCAAGATTTAATCTGGATAAAATCGCATAATCTTACACAGTGACTATTGTGATCAACAATTAAAATTGTGCAGTCTGAATGGGCCTTAGAAACTTTTGAGACGTATTATTCTTTGATGTTTTATAGAACTGATGCTGAAAGTTCATCTGATCATCTGGAGGCTCTTCGGAAGCTCTCAGTTGTTCTTAAAGACAAGAAAAGCACACTTGAGGATCTCAAA[G/T]AGCAGAAGCAAAAAGTAATGTACCATCTAAACCTGGATGACAAAGAGCTGGTAAAGGAGCAGATAGGCCACTTTGAGCAGCGATGGGCTCATCTAGAGAGCCTCATTGAGAGGAAGATCCAGGACTCCATTTTGACACTTGAAGACATGGGGCAAGTCGAGGCCTGTTTGAGGGAAGCTCGTGAATGGGCCGAGGAGCAGCAGCCGACTCTGTCTGAAGCCATGAAGATGAGTCCCCCACCGGAGCTAGCGCAAAGTTTCCTCTTTGACCATCTCAGTATATGCAGCGAGCTGGAAGCCAAGCAGCTTCTGCTGGCCCAGGCGATGGGTGATGCAGACAGAGTTTTAGCACATCTGGGGCTAAATGAAAGACAAAGACTGCAGCAGCTTATCTCAGAGACGCAAGCAGAAGTAGAGTGCTTGAGCGTCAAAGTAGCTCAGCGTAGGAAACACCTTAGCAAGGCTTTCACCGAGAGAACACAGTTCTTGTTGGCTGTGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11059
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 4337 8759 75 143
Genomic Location (Zv9):
Chromosome 17 (position 7826293)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7829067
GRCz11 17 7986245
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCAGGACTCCATTTTGACACTTGAAGACATGGGGCAAGTCGAGGCCYG[T/A]TTGAGGGAAGCTCGTGAATGGGCCGAGGAGCAGCAGCCGACTCTGTCTGA
Long Flanking Sequence:
TTGAGATTTGTAATTTTTTAGGTTTCTTGATGACAGAATACACATTGTAGATGTCACCTGATGATTGCTCGCAAAACAACTTTTAGTCTGACGTATTTGGTACCCAACACACATCAAGATTTAATCTGGATAAAATCGCATAATCTTACACAGTGACTATTGTGATCAACAATTAAAATTGTGCAGTCTGAATGGGCCTTAGAAACTTTTGAGACGTATTATTCTTTGATGTTTTATAGAACTGATGCTGAAAGTTCATCTGATCATCTGGAGGCTCTTCGGAAGCTCTCAGTTGTTCTTAAAGACAAGAAAAGCACACTTGAGGATCTCAAAGAGCAGAAGCAAAAAGTAATGTACCATCTAAACCTGGATGACAAAGAGCTGGTAAAGGAGCAGATAGGCCACTTTGAGCAGCGATGGGCTCATCTAGAGAGCCTCATTGAGAGGAAGATCCAGGACTCCATTTTGACACTTGAAGACATGGGGCAAGTCGAGGCCTG[T/A]TTGAGGGAAGCTCGTGAATGGGCCGAGGAGCAGCAGCCGACTCTGTCTGAAGCCATGAAGATGAGTCCCCCACCGGAGCTAGCGCAAAGTTTCCTCTTTGACCATCTCAGTATATGCAGCGAGCTGGAAGCCAAGCAGCTTCTGCTGGCCCAGGCGATGGGTGATGCAGACAGAGTTTTAGCACATCTGGGGCTAAATGAAAGACAAAGACTGCAGCAGCTTATCTCAGAGACGCAAGCAGAAGTAGAGTGCTTGAGCGTCAAAGTAGCTCAGCGTAGGAAACACCTTAGCAAGGCTTTCACCGAGAGAACACAGTTCTTGTTGGCTGTGAATCAAGCGATTACCTGGGTCCAGCAGAATGAGAAGAAAGCACAAGCAGAAGAGTACATAGCCCTTCTTCCTGACGACCTTTCAAAGCAGGTGAGAACATGCCGGAACATCCAGAGCAGTTTGAGAGCCTACCAGAGTGAGCTGACCTCCCTGTGGTCACAAGGCAGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9065
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 4499 8759 75 143
Genomic Location (Zv9):
Chromosome 17 (position 7825807)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7828581
GRCz11 17 7985759
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACATCCAGAGCAGTTTKAGAGCCTACCAGAGTGAGCTGACCTCCCTGTG[G/A]TCACAAGGCAGGGATCTGATGAAAGATGCTTCTGAAGARGAGAAGACAGA
Long Flanking Sequence:
CAAGTCGAGGCCTGTTTGAGGGAAGCTCGTGAATGGGCCGAGGAGCAGCAGCCGACTCTGTCTGAAGCCATGAAGATGAGTCCCCCACCGGAGCTAGCGCAAAGTTTCCTCTTTGACCATCTCAGTATATGCAGCGAGCTGGAAGCCAAGCAGCTTCTGCTGGCCCAGGCGATGGGTGATGCAGACAGAGTTTTAGCACATCTGGGGCTAAATGAAAGACAAAGACTGCAGCAGCTTATCTCAGAGACGCAAGCAGAAGTAGAGTGCTTGAGCGTCAAAGTAGCTCAGCGTAGGAAACACCTTAGCAAGGCTTTCACCGAGAGAACACAGTTCTTGTTGGCTGTGAATCAAGCGATTACCTGGGTCCAGCAGAATGAGAAGAAAGCACAAGCAGAAGAGTACATAGCCCTTCTTCCTGACGACCTTTCAAAGCAGGTGAGAACATGCCGGAACATCCAGAGCAGTTTGAGAGCCTACCAGAGTGAGCTGACCTCCCTGTG[G/A]TCACAAGGCAGGGATCTGATGAAAGATGCTTCTGAAGAGGAGAAGACAGAGATGCTTCATAAGCTCCAAGAACTGCAAAGTATCTTTGAGGTTGCCCTGCAGAAGTGTAGCCAGAGGCTTCAGGACCTGGAAAAAGTGTTGGTGACTAGAAAATACTTTAAGGCAGATTTGGAGAAGATATGCCAATGGTTGAAACAAGCCGATATTGTGACCTTTCCAGAGATAAACCTCATGAACGGAGATGCAGAATTATGCTCACAGCTTACAAAATACCAACAGATATTGGATCAAGCTATGGAATTTGAGAACCTCCTGCTAACTGTGCAAAGGACAGGTCAAGAGATACTTCCCACTCTCAATGAAGTAGACCACTGTTACTTGGATGAGAAATTGATTGCTCTTCCTCAACAGTACAATAATATCTTGGGACTAGCTAAAGAGAAACAGGAGAAAATACAGCAAGCCATTCTTGCCCGACAAGAATATGCCTCCTTCATTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13399
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 4608 8759 75 143
Genomic Location (Zv9):
Chromosome 17 (position 7825482)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7828256
GRCz11 17 7985434
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAGATATTGGATCAAGCTATGGAATTTGAGAACCTCCTGCTAACTGTG[C/T]AAAGGACAGGTCAAGAGATACTTCCCACTCTCAATGAAGTAGACCACTGT
Long Flanking Sequence:
CACAGTTCTTGTTGGCTGTGAATCAAGCGATTACCTGGGTCCAGCAGAATGAGAAGAAAGCACAAGCAGAAGAGTACATAGCCCTTCTTCCTGACGACCTTTCAAAGCAGGTGAGAACATGCCGGAACATCCAGAGCAGTTTGAGAGCCTACCAGAGTGAGCTGACCTCCCTGTGGTCACAAGGCAGGGATCTGATGAAAGATGCTTCTGAAGAGGAGAAGACAGAGATGCTTCATAAGCTCCAAGAACTGCAAAGTATCTTTGAGGTTGCCCTGCAGAAGTGTAGCCAGAGGCTTCAGGACCTGGAAAAAGTGTTGGTGACTAGAAAATACTTTAAGGCAGATTTGGAGAAGATATGCCAATGGTTGAAACAAGCCGATATTGTGACCTTTCCAGAGATAAACCTCATGAACGGAGATGCAGAATTATGCTCACAGCTTACAAAATACCAACAGATATTGGATCAAGCTATGGAATTTGAGAACCTCCTGCTAACTGTG[C/T]AAAGGACAGGTCAAGAGATACTTCCCACTCTCAATGAAGTAGACCACTGTTACTTGGATGAGAAATTGATTGCTCTTCCTCAACAGTACAATAATATCTTGGGACTAGCTAAAGAGAAACAGGAGAAAATACAGCAAGCCATTCTTGCCCGACAAGAATATGCCTCCTTCATTGATGTTACCCACAAAGCACTTAAAGAACTTGAGGAACAGTTTCACAGCTTGGGGACGCAGCCAATCGGCCTTAAGACTGAGGAAGTTGTAAGCCTTCAAGCTGACTACAAAGCCCTTCTGGAGGAGCTGACCAATCTTGGGCAAGCTGTCGGTGAACTTAACCAAAAGAAAGAAGGATTCCGAAGCACCGGTCAACCTTGGATGCCTGAAGAAATGACGCAACTGGTTAGCCTTTACAATGGACTCAAAAGATTAATTGAACAGAGGGTAGAACACCTTGACGACACTCTTGAATCTTTCGAGGACCATCAAGCCATGGCTATGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7444
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Missense 4813 8759 75 143
Genomic Location (Zv9):
Chromosome 17 (position 7824866)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7827640
GRCz11 17 7984818
KASP Assay ID:
554-4375.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGGAGAGGYTGAAGAATTATCATGCCCTAGCTGCTAGTCTTCAAGGTG[C/A]CAGCTCTCACCTCACTCGACTGATGGAGCAGATGGAHAACCTGGTATCCC
Long Flanking Sequence:
GAAACAGGAGAAAATACAGCAAGCCATTCTTGCCCGACAAGAATATGCCTCCTTCATTGATGTTACCCACAAAGCACTTAAAGAACTTGAGGAACAGTTTCACAGCTTGGGGACGCAGCCAATCGGCCTTAAGACTGAGGAAGTTGTAAGCCTTCAAGCTGACTACAAAGCCCTTCTGGAGGAGCTGACCAATCTTGGGCAAGCTGTCGGTGAACTTAACCAAAAGAAAGAAGGATTCCGAAGCACCGGTCAACCTTGGATGCCTGAAGAAATGACGCAACTGGTTAGCCTTTACAATGGACTCAAAAGATTAATTGAACAGAGGGTAGAACACCTTGACGACACTCTTGAATCTTTCGAGGACCATCAAGCCATGGCTATGCAGGTTGACTCAGAGCTGAAAGCCACCAAAGAGCAACTGGTGAAAGTCAATGCCGAGACACAGTCGGCTGAGGAGAGGTTGAAGAATTATCATGCCCTAGCTGCTAGTCTTCAAGGTG[C/A]CAGCTCTCACCTCACTCGACTGATGGAGCAGATGGATAACCTGGTATCCCACATGGATACTGCTGCACATGAGGTTTCAAAACAGCGGGTGACCTCTTGGCAGGAAGAGCTTCGGTCCTTACAGTCATCTGTTGGAGAGCTTATTGTGGAGTGTGAGAACAGGTTCGTGCAGAGTAAAGACTTTGAAACTGAAGTCAATCGGACCTTAACCTGGCTCCAACAAATCAAAGATGAACTTGGCTCTGAGGTGGTGGTAGATGTCAAAGTTGAGAAGGTCCAGGAAGAAATCCGAAAGCAACAGATCATGCAAGAGGAAGTACAATCAAGGCTGAGGATAGTGGCAGCTTTGAGTACAAGAGAGAAACAGAAATACACCAGTGCCAATGAGCTTGTCCCTGCTCATGTGGATTCGAGTCTACAAGAGATGGCCAAGCTGGAGGCTGATGTTCAGCGTGCCCTAAGCTCTAAACAGGCAAGTTCTAATGCAAACTATCAATGGA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28802
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 4819 8759 75 143
Genomic Location (Zv9):
Chromosome 17 (position 7824849)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7827623
GRCz11 17 7984801
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATCATGCCCTAGCTGCTAGTCTTCAAGGTGCCAGCTCTCACCTCACT[C/T]GACTGATGGAGCAGATGGATAACCTGGTATCCCACATGGATACTGCTGCA
Long Flanking Sequence:
AGCAAGCCATTCTTGCCCGACAAGAATATGCCTCCTTCATTGATGTTACCCACAAAGCACTTAAAGAACTTGAGGAACAGTTTCACAGCTTGGGGACGCAGCCAATCGGCCTTAAGACTGAGGAAGTTGTAAGCCTTCAAGCTGACTACAAAGCCCTTCTGGAGGAGCTGACCAATCTTGGGCAAGCTGTCGGTGAACTTAACCAAAAGAAAGAAGGATTCCGAAGCACCGGTCAACCTTGGATGCCTGAAGAAATGACGCAACTGGTTAGCCTTTACAATGGACTCAAAAGATTAATTGAACAGAGGGTAGAACACCTTGACGACACTCTTGAATCTTTCGAGGACCATCAAGCCATGGCTATGCAGGTTGACTCAGAGCTGAAAGCCACCAAAGAGCAACTGGTGAAAGTCAATGCCGAGACACAGTCGGCTGAGGAGAGGTTGAAGAATTATCATGCCCTAGCTGCTAGTCTTCAAGGTGCCAGCTCTCACCTCACT[C/T]GACTGATGGAGCAGATGGATAACCTGGTATCCCACATGGATACTGCTGCACATGAGGTTTCAAAACAGCGGGTGACCTCTTGGCAGGAAGAGCTTCGGTCCTTACAGTCATCTGTTGGAGAGCTTATTGTGGAGTGTGAGAACAGGTTCGTGCAGAGTAAAGACTTTGAAACTGAAGTCAATCGGACCTTAACCTGGCTCCAACAAATCAAAGATGAACTTGGCTCTGAGGTGGTGGTAGATGTCAAAGTTGAGAAGGTCCAGGAAGAAATCCGAAAGCAACAGATCATGCAAGAGGAAGTACAATCAAGGCTGAGGATAGTGGCAGCTTTGAGTACAAGAGAGAAACAGAAATACACCAGTGCCAATGAGCTTGTCCCTGCTCATGTGGATTCGAGTCTACAAGAGATGGCCAAGCTGGAGGCTGATGTTCAGCGTGCCCTAAGCTCTAAACAGGCAAGTTCTAATGCAAACTATCAATGGAACCAAAACTACTTGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11274
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 4981 8759 76 143
Genomic Location (Zv9):
Chromosome 17 (position 7823778)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7826552
GRCz11 17 7983730
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYCAATTGTTTCTTTTGTAGATTACAKTAGAGCAAGCTCTTGTCTTGTGC[C/T]AGAAGTACCACTCCAGAATGCAAGCAGCATGTGAGTGGCTTGAGGATGCT
Long Flanking Sequence:
ACCACCTATAGGACACTCCTCATCATATGCACTAGACATTGTCTTATAAAACTATTGTGATAAAAATATTGTGCAGGTCTGAGTGTACTTAATGCAATTGAGCGAGCTTGACACATCCCCTGTAGAAGGCACAGTCATTTCCTCTATATGTACCAGACTTTCTTATAAACACTGCATGTTTCTGGGAAAATGTAGTGCAATTCTAAGTGTACTTATTGCAGGTGAGTGGACTTGACAAACCACCTGTAGAAACAGTCTTTTCCTTTCCAAATGCTCTAGACACTTTCTTATAAACGTGTATATTTAAGTATGTGTACTAAAAAAATCAGTTAAAAAAACTAAGGCCTGTAGATGCATCGTCCAACGTGAAATGCCAGTGTGTTTACCAAGTGTTTAACTACCTAAGCCTGCAAAACTTCCTTATTCAGCCAATGCTAACTCACTAATGAATCCAATTGTTTCTTTTGTAGATTACATTAGAGCAAGCTCTTGTCTTGTGC[C/T]AGAAGTACCACTCCAGAATGCAAGCAGCATGTGAGTGGCTTGAGGATGCTGTGGGCTTTTTGCAGCAGGCCAGTCTTGGGGTGGATGTAGAGAACTACGAGGAGTGTCTGAGGCAACAAGAGGACATCATGGCCACTGAGCAAGAGTTCCTGGGGGTTCTCGAGGAGCTGGAATCTCTGCCACCGCAACTTGAAAACCTTGTCAACCCTACAGCCAAAGAGCAGCTTCGACTGAGTGTGGAGTCTGCACAGCAAAGAGGTGTGGAGGTCAGAGACCAGCTGCAGTGCCACCAAGACGTCTTAAACAGGTTCAGTTTGGTACAGATTTATTATATTGTATTGAATTAAGAATACGATGCTAACGAAGACCAATGTGATTTTTATAGCTGTGTTGCTCAGTGGAATTCTTACCAAGAAGCCAGACAGACAGTCATTGACCTGATGAATGAGGTGGAGAAGAAGTTAACAGAGTTTTCCACAGCCAAGGCTGCAACAAACCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36317
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
ENSDART00000091828 Nonsense 5016 8759 76 143
Genomic Location (Zv9):
Chromosome 17 (position 7823671)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7826445
GRCz11 17 7983623
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGCAGCAGGCCAGTCTTGGGGTGGATGTAGAGAACTACGAGGAGTG[T/A]CTGAGGCAACAAGAGGACATCATGGCCACTGAGCAAGAGTTCCTGGGGGT
Long Flanking Sequence:
TTGACACATCCCCTGTAGAAGGCACAGTCATTTCCTCTATATGTACCAGACTTTCTTATAAACACTGCATGTTTCTGGGAAAATGTAGTGCAATTCTAAGTGTACTTATTGCAGGTGAGTGGACTTGACAAACCACCTGTAGAAACAGTCTTTTCCTTTCCAAATGCTCTAGACACTTTCTTATAAACGTGTATATTTAAGTATGTGTACTAAAAAAATCAGTTAAAAAAACTAAGGCCTGTAGATGCATCGTCCAACGTGAAATGCCAGTGTGTTTACCAAGTGTTTAACTACCTAAGCCTGCAAAACTTCCTTATTCAGCCAATGCTAACTCACTAATGAATCCAATTGTTTCTTTTGTAGATTACATTAGAGCAAGCTCTTGTCTTGTGCCAGAAGTACCACTCCAGAATGCAAGCAGCATGTGAGTGGCTTGAGGATGCTGTGGGCTTTTTGCAGCAGGCCAGTCTTGGGGTGGATGTAGAGAACTACGAGGAGTG[T/A]CTGAGGCAACAAGAGGACATCATGGCCACTGAGCAAGAGTTCCTGGGGGTTCTCGAGGAGCTGGAATCTCTGCCACCGCAACTTGAAAACCTTGTCAACCCTACAGCCAAAGAGCAGCTTCGACTGAGTGTGGAGTCTGCACAGCAAAGAGGTGTGGAGGTCAGAGACCAGCTGCAGTGCCACCAAGACGTCTTAAACAGGTTCAGTTTGGTACAGATTTATTATATTGTATTGAATTAAGAATACGATGCTAACGAAGACCAATGTGATTTTTATAGCTGTGTTGCTCAGTGGAATTCTTACCAAGAAGCCAGACAGACAGTCATTGACCTGATGAATGAGGTGGAGAAGAAGTTAACAGAGTTTTCCACAGCCAAGGCTGCAACAAACCAGGAAGCTGAAGAGAAACTTAGGAGCCATAAGGTGAGCTTTGCATGCAGAATTGTGTCTCTGAGAAAAAGAAACAATCTACATGACCATATTAATCCAAGTAAAATGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11252
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 5087 8759 77 143
Genomic Location (Zv9):
Chromosome 17 (position 7823382)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7826156
GRCz11 17 7983334
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAATACGATGCTAAYRAAGACCAATGTGATTTTTATAGCTGTGTTGCT[C/T]AGTGGAATTCTTACCAAGAAGCCAGACAGACAGTCATTGASCTGATGAAT
Long Flanking Sequence:
ACTACCTAAGCCTGCAAAACTTCCTTATTCAGCCAATGCTAACTCACTAATGAATCCAATTGTTTCTTTTGTAGATTACATTAGAGCAAGCTCTTGTCTTGTGCCAGAAGTACCACTCCAGAATGCAAGCAGCATGTGAGTGGCTTGAGGATGCTGTGGGCTTTTTGCAGCAGGCCAGTCTTGGGGTGGATGTAGAGAACTACGAGGAGTGTCTGAGGCAACAAGAGGACATCATGGCCACTGAGCAAGAGTTCCTGGGGGTTCTCGAGGAGCTGGAATCTCTGCCACCGCAACTTGAAAACCTTGTCAACCCTACAGCCAAAGAGCAGCTTCGACTGAGTGTGGAGTCTGCACAGCAAAGAGGTGTGGAGGTCAGAGACCAGCTGCAGTGCCACCAAGACGTCTTAAACAGGTTCAGTTTGGTACAGATTTATTATATTGTATTGAATTAAGAATACGATGCTAACGAAGACCAATGTGATTTTTATAGCTGTGTTGCT[C/T]AGTGGAATTCTTACCAAGAAGCCAGACAGACAGTCATTGACCTGATGAATGAGGTGGAGAAGAAGTTAACAGAGTTTTCCACAGCCAAGGCTGCAACAAACCAGGAAGCTGAAGAGAAACTTAGGAGCCATAAGGTGAGCTTTGCATGCAGAATTGTGTCTCTGAGAAAAAGAAACAATCTACATGACCATATTAATCCAAGTAAAATGCTTTCATATATACCCCGCAGTCCTTAGTATCAATGGTGAACAGTTTCCAAGAAAAATTGACCGGTCTGGAGGAGCAAGCATCCCAGTTAGAGCAGATTGGAAGTGACGCCAGTAAAGCAACTATAAGTCGATCCATGACCACCGTGTGGCAGCGCTGGACCAGGTTACGCAGTGTAGCACGAGGCCAAGAAAGGGTGCTGGAGGACACGGCCCATGAATGGAGGACTTTCAGAGAAAAGGTGCAGTTCCTCTCTGTATGATGTTATGATGTTCTGGAAACTGAAGGTGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8519
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 5124 8759 77 143
Genomic Location (Zv9):
Chromosome 17 (position 7823271)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7826045
GRCz11 17 7983223
KASP Assay ID:
2261-0613.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGTTAACAGAGTTTTCCACAGCCAAGGCTGCAACAAACCAGGAAGCT[G/T]AAGAGAAACTTAGGAGCCATAAGGTGAGCTTTGCATGCARAATTGTGTCT
Long Flanking Sequence:
ACCACTCCAGAATGCAAGCAGCATGTGAGTGGCTTGAGGATGCTGTGGGCTTTTTGCAGCAGGCCAGTCTTGGGGTGGATGTAGAGAACTACGAGGAGTGTCTGAGGCAACAAGAGGACATCATGGCCACTGAGCAAGAGTTCCTGGGGGTTCTCGAGGAGCTGGAATCTCTGCCACCGCAACTTGAAAACCTTGTCAACCCTACAGCCAAAGAGCAGCTTCGACTGAGTGTGGAGTCTGCACAGCAAAGAGGTGTGGAGGTCAGAGACCAGCTGCAGTGCCACCAAGACGTCTTAAACAGGTTCAGTTTGGTACAGATTTATTATATTGTATTGAATTAAGAATACGATGCTAACGAAGACCAATGTGATTTTTATAGCTGTGTTGCTCAGTGGAATTCTTACCAAGAAGCCAGACAGACAGTCATTGACCTGATGAATGAGGTGGAGAAGAAGTTAACAGAGTTTTCCACAGCCAAGGCTGCAACAAACCAGGAAGCT[G/T]AAGAGAAACTTAGGAGCCATAAGGTGAGCTTTGCATGCAGAATTGTGTCTCTGAGAAAAAGAAACAATCTACATGACCATATTAATCCAAGTAAAATGCTTTCATATATACCCCGCAGTCCTTAGTATCAATGGTGAACAGTTTCCAAGAAAAATTGACCGGTCTGGAGGAGCAAGCATCCCAGTTAGAGCAGATTGGAAGTGACGCCAGTAAAGCAACTATAAGTCGATCCATGACCACCGTGTGGCAGCGCTGGACCAGGTTACGCAGTGTAGCACGAGGCCAAGAAAGGGTGCTGGAGGACACGGCCCATGAATGGAGGACTTTCAGAGAAAAGGTGCAGTTCCTCTCTGTATGATGTTATGATGTTCTGGAAACTGAAGGTGCCATAGAGTGCATTGATGTAATATGTTAAATTGTTTTCTGATATCTACATAGGCTTAGGTAAGTTAAAAATTCTCTAAAAATGGTTTTGCTCATTTATAACTATTGAAATCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32119
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Essential Splice Site 5131 8759 77 143
Genomic Location (Zv9):
Chromosome 17 (position 7823247)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7826021
GRCz11 17 7983199
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGGCTGCAACAAACCAGGAAGCTGAAGAGAAACTTAGGAGCCATAAG[G/A]TGAGCTTTGCATGCAGAATTGTGTCTCTGAGAAAAAGAAACAATCTACAT
Long Flanking Sequence:
GTGAGTGGCTTGAGGATGCTGTGGGCTTTTTGCAGCAGGCCAGTCTTGGGGTGGATGTAGAGAACTACGAGGAGTGTCTGAGGCAACAAGAGGACATCATGGCCACTGAGCAAGAGTTCCTGGGGGTTCTCGAGGAGCTGGAATCTCTGCCACCGCAACTTGAAAACCTTGTCAACCCTACAGCCAAAGAGCAGCTTCGACTGAGTGTGGAGTCTGCACAGCAAAGAGGTGTGGAGGTCAGAGACCAGCTGCAGTGCCACCAAGACGTCTTAAACAGGTTCAGTTTGGTACAGATTTATTATATTGTATTGAATTAAGAATACGATGCTAACGAAGACCAATGTGATTTTTATAGCTGTGTTGCTCAGTGGAATTCTTACCAAGAAGCCAGACAGACAGTCATTGACCTGATGAATGAGGTGGAGAAGAAGTTAACAGAGTTTTCCACAGCCAAGGCTGCAACAAACCAGGAAGCTGAAGAGAAACTTAGGAGCCATAAG[G/A]TGAGCTTTGCATGCAGAATTGTGTCTCTGAGAAAAAGAAACAATCTACATGACCATATTAATCCAAGTAAAATGCTTTCATATATACCCCGCAGTCCTTAGTATCAATGGTGAACAGTTTCCAAGAAAAATTGACCGGTCTGGAGGAGCAAGCATCCCAGTTAGAGCAGATTGGAAGTGACGCCAGTAAAGCAACTATAAGTCGATCCATGACCACCGTGTGGCAGCGCTGGACCAGGTTACGCAGTGTAGCACGAGGCCAAGAAAGGGTGCTGGAGGACACGGCCCATGAATGGAGGACTTTCAGAGAAAAGGTGCAGTTCCTCTCTGTATGATGTTATGATGTTCTGGAAACTGAAGGTGCCATAGAGTGCATTGATGTAATATGTTAAATTGTTTTCTGATATCTACATAGGCTTAGGTAAGTTAAAAATTCTCTAAAAATGGTTTTGCTCATTTATAACTATTGAAATCACCAATAAAATGAAAATATTGGTTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8895
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
ENSDART00000091828 Essential Splice Site 5919 8759 91 143
Genomic Location (Zv9):
Chromosome 17 (position 7795793)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7798567
GRCz11 17 7955745
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCCAGTTTAGATGATCTCCAGCGCTCATGGGAGACCCTGAAAAATGTG[G/A]TATGTTGATCTCRTTAAAAAYAMATTTTTGATTTGAGGTATTTGACTATT
Long Flanking Sequence:
AGTTATAGGATTACATTAACGTTATAGCCATTTTGCAAGCTAGTGCAGCGTGTGCCTGACTGGAGTAGTGTTTTGGAGGTGGGAGGGGAAGGCAGCATGTTGCCTGTCACGTCATTTGGGATGCCTTGAGCATTGTTGCACTGAAAACATTATATTTTGTACTCTTATTCTCTTTTATCTTTTTAGATATTAGTCTGAATTTTACGGTTTGTAATGCGTACTGAACCGAAAGTCTCGTACTGAACAGTTACGAACAGAATATGAATATGTGTATCGTTACACCCTTACTAAATTGTCATCTTATATTTTATAATTGTCTTTTTTTCTTGATTATTTCTTTTTAAATAACATTAACAATAACAACATTGTCCTAAATGTAGATGTCCATGGGAAGGTCAAGTCTCACCAGAGCGCCGGTCCAGGAGCTGTACAATCCTGCACTGGAGTCTGTGGCCAGTTTAGATGATCTCCAGCGCTCATGGGAGACCCTGAAAAATGTG[G/A]TATGTTGATCTCATTAAAAATAAATTTTTGATTTGAGGTATTTGACTATTTTAAAGGGGACCTATTATGCTCCTTTTTACAAGATGAAGTCTCTGATGTGCCTGGCATGTGTATGTGTTTCGGCTCAAAATATTTCACAAATATTGTTTTATAACTCTTTGAAACTGCTCCCTTTACGCCCCATTCACACGGGGCTTCAGCGTCATCGCTTGACTGAAGGCGTGTCTGGAGTTGGGGCTAACGCAATCGTCATAGTAGTGTCAACCAATAAAATTCATTCAGCAATAGGTCACTGTCTAGCTGTTGTATTTGCATACAGCGATCTGATTGGCTTACGCTTCCATCGGCGCTTAAAAAGTTTAGCTAGTCCCAACTTCTGCAGCGAGCAATGCCTCTGAATCGGCGCCGACGGATCCACAATTTAGTACGGCAACGCCTGACGTCACCCATTCAAAGTGAATGGGAAGCATTGACGCTGACGCCCCGTGTAAATGGGGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7443
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Missense 6383 8759 101 143
Genomic Location (Zv9):
Chromosome 17 (position 7776224)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7778998
GRCz11 17 7936176
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACATTATGTCAATAGTCAYGTWTTGTTTGGCRTTKTTGTCTYACAGACT[C/A]TGGGTAAAGAAGTGACGGAGRTGACGCAGGAGGTGGGACACACTCAGGGG
Long Flanking Sequence:
CTTTTAAATAATGGTCAGTTAGTTCATGTTAGTTAATGTAGTTAATTTACTATTGTAACATTGACAAAAAAATGAACAATGGATTTATTACAGTATTTTATTTTATTTTATGCAGTATAATGGTATTTTAAATATACCTTTGTTAATGTTAGTTAATGATAATAAAGTTGTTCGTTGTCAGTTCATATTATCTCACAGTGCATTACCTAATGGCAAAAAGCACAACTATGGCTTTGAATAATGCATTAGTGTATGGTGAATTATGATGAATAAATCCTGTAAGCAGTTCATGTGAGCACATAAATCAGCTGACATTAGTGCTACTGTTATAATTCAACTTTATTTCTGTAGCGATTTTCACAAATGTAGATTATGTCAAAGCAGCTTAACATAGTGTTAGTTATAGTAGTAACATTGATAATTATACTCCAGCTGCACTGTTAAATAAAGCACATTATGTCAATAGTCATGTTTTGTTTGGCGTTGTTGTCTTACAGACT[C/A]TGGGTAAAGAAGTGACGGAGGTGACGCAGGAGGTGGGACACACTCAGGGGTTGATCAAAGGATCTGTGGGTCTGTCTGAGGACGAGCAGAGCCTGATGAAGGACACTCTGGACTGCCTGACCCGACGCCTCGGAGCCCTGGACTCAGCTCTGGACCGCCGCTGTGACTCCATGCGGAGCAGAATGAGGGAACTCAGCGCTTTCCAGGTGCAGATCAGACTTGATGAGCTTAATTCAGTGTTGTATTGAGTGCAGCAGAATGAGCTTTTTTACTGTGTGTTCACAGACGGAGCTGCAGCGTCTCTTTACAGCTCTCAGTGAAAGCAAGTTTCAGATTATCCAGAAAATGGCAGGAGTTCTTGACCACACAACAACTAAACAGATTGAAGTAAGATTTTTTTTTTATCATCAAATATGTTTTTATTAGTGCTGGGCGAAGATTAATTGTGACCAATTACATGCAAAATAAAAGTTTGTTTTGGCATAATATATATATGCGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8603
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
ENSDART00000091828 Nonsense 6483 8759 102 143
Genomic Location (Zv9):
Chromosome 17 (position 7775845)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7778619
GRCz11 17 7935797
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGATTATCCAGAAAATGGCAGGAGTTCTTGACCACACAACAACTAAA[C/T]AGATTGAAGTAAGATTTTTTTTTTATCATCAAATATGTTTTTATTAGTGC
Long Flanking Sequence:
AGCAGCTTAACATAGTGTTAGTTATAGTAGTAACATTGATAATTATACTCCAGCTGCACTGTTAAATAAAGCACATTATGTCAATAGTCATGTTTTGTTTGGCGTTGTTGTCTTACAGACTCTGGGTAAAGAAGTGACGGAGGTGACGCAGGAGGTGGGACACACTCAGGGGTTGATCAAAGGATCTGTGGGTCTGTCTGAGGACGAGCAGAGCCTGATGAAGGACACTCTGGACTGCCTGACCCGACGCCTCGGAGCCCTGGACTCAGCTCTGGACCGCCGCTGTGACTCCATGCGGAGCAGAATGAGGGAACTCAGCGCTTTCCAGGTGCAGATCAGACTTGATGAGCTTAATTCAGTGTTGTATTGAGTGCAGCAGAATGAGCTTTTTTACTGTGTGTTCACAGACGGAGCTGCAGCGTCTCTTTACAGCTCTCAGTGAAAGCAAGTTTCAGATTATCCAGAAAATGGCAGGAGTTCTTGACCACACAACAACTAAA[C/T]AGATTGAAGTAAGATTTTTTTTTTATCATCAAATATGTTTTTATTAGTGCTGGGCGAAGATTAATTGTGACCAATTACATGCAAAATAAAAGTTTGTTTTGGCATAATATATATATGCGTGTATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTATTTATTTATTTATTTATTATGTATGATACACACATACATAGAAACAAAACTACGTTGTTACATAGATATTTAAATGTATCAATAATTTGTATCACATACAGTTGATATCAGAATTATTAGCACCCCTGTTTTTTTCCCCTAATTTCTGTTTAACGAAGAGAATATTTTTTCAGCACATTTTTGCACATAATAGTTTTAATAACTCATCTCTGATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTACTAGATATTTTTCAAGACCAAGGTTTCTTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10495
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 6925 8759 111 143
Genomic Location (Zv9):
Chromosome 17 (position 7764448)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7767222
GRCz11 17 7924400
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTGTGGTTTTCCTCCTGTAGGGCTTCAGGGTGGATGTGAACTGCAAA[C/T]AGCTCACTGTGGACTTTGTKAACCAGTCAGTGCTCCAGATCAGCGGTGCG
Long Flanking Sequence:
GCAATTTGAATGCTCAATTAGGCAAGTCATTGGACAGCGGTGGTTTGTTCTGTAGCCAATAAAAAATAACAGTTTCTTTAGGAGGATAACAATATTGACCTCAGCAGTTTAAAAAAAAAAAAGTTTTTCCATTTTAAAAAAAAGTAGAAGAAGAAAAATGAAATATTGCCTTGCAGACATCATTTGGCAAATGTTTGAATACTAATTTCAAAGGGGGGCTAATAATTTCAAGGATCTCTCGAGCTCAGGGCTCTCTCCCAGGACAGCGTTCCAGCAACTTTTGGAATCTCAAAAAAACTCTAAAACAGAAGAGGCGCTTTCCGAAGGAATCATAGACATATTAATCACAAGCTTGTAGCAAACAATTCAGCTTTTTTGCTCATTTTTTGAAGTTTGAACAACAAAGACATTTCCCCCTAGCCTTCATTGCTCATATTTACTCCTGGTTTCTTTCTGTGGTTTTCCTCCTGTAGGGCTTCAGGGTGGATGTGAACTGCAAA[C/T]AGCTCACTGTGGACTTTGTTAACCAGTCAGTGCTCCAGATCAGCGGTGCGGACGTCGAGAGCAAGCGCAGTGATAAAACTGATTTTGCTGAAAAACTGGGCGCCATGAACTGCCACTGGCAGATCCTGCAGACACGCATCACAGAGAGGGTAAGACTTCACATTACTGTGACTCTTCAAAGAGAGGATTTGTAGATAACTTCAGTATGAGCTGTGCTACCAAATTATTACTAATAGAAGTCTTCTTCATCATAAGTTTTTTATTATTAAAATACTAGTTGCACTGTATTTCGTAGTATTTGTGTACTTATAGTAATGTAAAATACTGGCTTTGGGCTTAGCTCCTATTTTTTACCTAGTTCATTGAATGACTATGATAAGCAAATCGTATCCACATATGAAACAGAACTGTGGAATAAAGAGCTACAAGAATACTTGAAGTCTATTGTTATACTTTATTAGTAGGTGTGCTTATATCAGTGGATTAAAAAGTAAATATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13678
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 7045 8759 113 143
Genomic Location (Zv9):
Chromosome 17 (position 7761339)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7764113
GRCz11 17 7921291
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAGGTGAYGGTGAARGAGAAAGAGAGAGAGCTGGAGAGAGTGGAGGAA[C/T]AGGCCTGTGCTCTCGTCCAAAACAAGACGGACGAGGCCTGTGCTGTCGTG
Long Flanking Sequence:
ATAATCTAACCATGATAGTTATAATAACTCATTTCTATTAAGTGATTTTTTTAAATCTTTGCCATGATGACAGTACATTATAATTTACTAGATATTTTTCAAGATACTAATATCAGCTTAAGGTGAAATTTAAAGGCTTAACTAGGTTAATTAGGCAAATCATATAGTATAATTATCGTTTGTTTTGTAGACTATCGAAAAGAAATATTGCTGTAGGGGGCTAATAATATTGACCTTAAATGGATTTTAAAAAAATTAAAAACTGCTTTTATTCAAGCTTAAATTAAGCAAATAAGACTTTTTCTAGAAGCAAAAATATTATAGGAAATACTGTGAAAAACTCCTTGCTTTGTTAAACATTATTTGGGAAATATTTAAAAAAGAAAAATTCACAGGAGGACGAATAATTTAGACTGTATTTGTCTTTATGTGATGTGTAACTGCAGGAGATGGAGGTGATGGTGAAGGAGAAAGAGAGAGAGCTGGAGAGAGTGGAGGAA[C/T]AGGCCTGTGCTCTCGTCCAAAACAAGACGGACGAGGCCTGTGCTGTCGTGATGGAGTCTCTACGAGCCCTCAACAACACATGGGCCAATCTGGACCACCTGGTATTTTGTTTAGACCTTCAGTATTGTATTACATTTCAAACAGAAAATATATATGGTTCTGTCTTATTTATTAAATGATATATATGGTGTATTTATTTATAACCTCGTGGTTAAGAATATTGAGGCTAAAGCATCAAACTGACATCATCAGAAAAGGACCGCCACTGCAAGCGCAGAAGCAAACTTTAATTGAAAATTACCACAACAAACAGTTTTTCAGTGGATTGGCTTGTACGGGTTAATTGTTTGCCTAAAGAATATCAATGTGTGCTAGCAAAATAAACATTGGCTGCGTCCGAAACCACCTACTACTCAGTAGGTACTGCATTTGAATGTAAACATACTACTCGGCCGTTAGAAAAGTACGTTCTATACAGTATGAATGTGAAGAGTACTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45593
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
ENSDART00000091828 Nonsense 7426 8759 120 143
Genomic Location (Zv9):
Chromosome 17 (position 7745599)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7748373
GRCz11 17 7905551
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAAACTTCAGGCGCTGCTTCTCCAGCAGCAGACATTTCTGGAGAAGTG[T/A]GAGACATGGATGGAGTTCTTGGTGCAGACGGAGGAGAAACTGGCCGTGGA
Long Flanking Sequence:
GAATAATTATATCAAATGAATCAGCATCTTCAAAAGTTTACTGAAAACCTGTTATACACCGCTATTTAGTCATAATTTAAAATCTTAGATTGGTTTAAAAGAATCATTGTTTAAGGTATTAATCAAATGTTGTATAATGTTGTAATCTAATCAAGAGGAATGAACAAACTCTTTGAATTAAGTCAATCCGATCTGACTTCCAGTCCAGCTTCGCTTTGGGCTTTAGCACCTAAACTAAATCCTAAACATGTGACGTGACAACCTAAATAAATATTTTCCTTTTTGTCTGCTTTATATAATGATAATCTCTAAAGATTCAGCATCTTCCTGAAAACCTACATAATCTACTACATGTCTTCTGCTGACTGATTGATAACTGCTTTAGTATGAATGTAAAAACCTGGTCATGGCTTAAATGTTTGCCTCCTAAAGGGTGTAAATTGTCTCCTCAGTAAACTTCAGGCGCTGCTTCTCCAGCAGCAGACATTTCTGGAGAAGTG[T/A]GAGACATGGATGGAGTTCTTGGTGCAGACGGAGGAGAAACTGGCCGTGGAGATTTCCGGAAACTTCCAGAGCCTGATGGAGCAGCAGAGAGCTCATGAGGTCAGATGCAACAAAGCAAATTAAGGCTGAATTATACTTCTGCGTTGAGTGAGCGCCGTAACCCATGGCACATGGCTCGCACATAGCTGTGCATTTATACTTGTGCCTTCTGTTTGTGAAGCTCTGCAATAACACTTTCAAAATGCTAGCAGGCAGGTTTTTTAATGATTTTCTGTGATGTTTCTTCTCAGATGTTTTGTCTACATTGTCCGTACAAGTAGCTCAAACTCGCTCATTCAGAGGCGGAACCGGCAAACATGCAATAACTTGTGAAGTTTATTCATAAACTAATTTCGAGAGGATCACGTGCTTATGATTTATCATGGCCGGTCTCGCATTTGCTAATCACTATCTTCCAATCATATGAGCCCTTAGCTACTATAAAAAACCACAGTTTTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11189
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 7527 8759 122 143
Genomic Location (Zv9):
Chromosome 17 (position 7741272)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7744046
GRCz11 17 7901224
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACGGGCACAGCAGCGACGGGGCATCATCGACAGTCTCCTGCGCCAGTGG[C/T]AGCGCTACCGGGAGATGGTGGARAAGCTYCGCAAGTGGCTGCTGGAGGTC
Long Flanking Sequence:
GACTGTCAAATTGTTTCAATTCAACTGAGATTGTGATCTTTTTAAAAGAGGGCGGAGCTACAAAGCCTATGTGTCAGCATGGTGGCAGATTTAAAAACAAGACTAACGTCGTATGCTAATGAGAGAGATATCATCACTAATGGGCGGGGCTTTCCAACTCTGATGACACGTATAAAGGAAGAATGTCAATCAAAGTGTTTCTGCAGACTGTTTTTATCAAGTGTGATTATAAACAAATAAAATGTATGCATTTTTACCATTAAAGGCTGATTATATTTACAGACTGTCACCACAATACTGTGTTTAAACCCCTTATAAAAGTGATTTTCGCATAATAGATCCCAAATACATGAACGGATTTGATGCTTCTGTTTGAAACTGTCCTTGTTTGCAGAGATGAGTTCAAGCTGAAGCTGGCTCTGCTCAGTAACCAGTGGCAGGGTGTGGTGAGACGGGCACAGCAGCGACGGGGCATCATCGACAGTCTCCTGCGCCAGTGG[C/T]AGCGCTACCGGGAGATGGTGGAAAAGCTTCGCAAGTGGCTGCTGGAGGTCAACCATCAGACCCAGAGCCTGCAGGCGGGGACACCAGTGCCACTGCAGCAGGCACGAGCCATGCTGGATGCAGTTCAGGTAGATAACCTCCCAGAACATCTTAAAGGGACAGTGAAATAAAAAACATGCTTTTTAGATGTTAGTATCAGTCTGTTGTGTTCTCCAAAACAATGACAAAATTTGCATTTAGAAGATATAGAACTGATATATACATGTAATTCATGTAGTCCGTCACTTCCGCCTAAATGGATCAACGTTTTTTTTTTACACCTCACCTAAAACTTCCGTTTTTTTTTTGCCAAACCTACCAAGTAGGTTTTTTGAAGCATCCTCGAGATGTTGCCAAAGTTGTTCTGGATTTAGTTTTTTCTCAGTTTGTTCTGTTTTTTCATGTCATTCCAGACAGACGGATCAGATAATGATCAGATCAGATCTCTGTGAGGAGCACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2927
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Nonsense 7615 8759 123 143
Genomic Location (Zv9):
Chromosome 17 (position 7736400)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7739174
GRCz11 17 7896352
KASP Assay ID:
554-3320.1 (used for ordering genotyping assays)
KASP Sequence:
CGAGCTGAAGCCRTTCTACAAGAGGAGCTGCTYAACATTCAGGAGCGCTG[G/A]AGAAATGCCAAYAWCCGCCTGGACGAGCAGAAGAAGGAACTGGCCGTCCT
Long Flanking Sequence:
GGATGGGATCATGTGAGCCTGTTCATCCCTTTCTGAAGTCCACAATGAGCTCCTTGGTCTTGTTTGTTGTTAAGGAGCATTATTTTTGTCATTAATTATAATTAATGACAAAAATAATGTTGGGAAATATAAATTGATATTTTAAACCGACATGCTACAAAAAACATATAGAATTAACCAGCTTTAAACCTTTTTTAATGAAAATACTAGTGACGTTAGACTTTTGCACAGTACTGTACATCCGAGGGAACGAGACCGAGGGAATTTAGTAATTGTAGGACATAAAAAAGTGTCAGTATCTGCAGGTCTGTGTGACTTTTGCCCCAGGTTATGGGTTGTGATGGGTTGTTCGATGCTCTGCAGCTCAGAGAGAAGGTTCTGCTGAGACAGCAGGGAAGTTACATTTTGACAGTGGAGGCCGGCCGACAACTGCTTCTGTCTGCTGATTCTCGAGCTGAAGCCGTTCTACAAGAGGAGCTGCTCAACATTCAGGAGCGCTG[G/A]AGAAATGCCAACATCCGCCTGGACGAGCAGAAGAAGGAACTGGCCGTCCTGCTCAGGGTACAGTTAATGGATCCACACATTTATTTCATTTACAGCCCTTATTGCTATATGTCTGGATAATTTGAGTTATTCTTTACTATTATAAAAATATAGGTAACACTGTACAATAAGGTTGTATTAGTTCATTTTAGTTAATGCAATATCTTACAGGAACAAACAATGAACAATGCACTCATTACTGTATTTATTCATGTTTGTAAACATTAGTTAATGGTAATAAAGTTGTTCATTGTTAGTTTATGTTAAATCACCGTGCATTAACTAATGTAAACAGGCATAAATTCAAATTTTAATAATGCATTAGTAATTGATGGATTATTAACAATAAATGCTGTACACGTATTGTTCATTATTAGTTCATGTTAATAAATGGATTAACTAGCATTACCTAATAATAACCTTATATACACTATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14747
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091828 Essential Splice Site 8065 8759 131 143
Genomic Location (Zv9):
Chromosome 17 (position 7719364)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7722138
GRCz11 17 7879316
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGGATAACCTGCAGAGRAGAGTGTCATCCGTCCTCCGSAGACTGAAGG[T/C]ACAGRGACTATCAATAAGATGGTAGTTAATCAGTCTTGAGTTCAACACAT
Long Flanking Sequence:
GAAGTGCAGAAGGGTTACTAAAGAACTACTGAGAGATTTCAGCTGCTGCCTGGGCTTTCACTGCCTTTCTACACCTCCCTTTCTACATGTGTTCATTAATTTTTCCCTGCGTCTTTTTATTTTATCATGCATATTATTATGCATAACTTAATTTGTTAACTAATTAGATTTGTTTTCTTATATATTGGTTGTTACCAACATCTGGTGAACATTTCAAGTCAACAACACCACTGTTATACCATACAATCATACACTGAATCAACATAGCGTCAGTGTAAAGTCTGATAGTATTAACACTCTTTAATCTACTTTATAGACGTTCCAGCGGCATGTGCATGAAAGTTTGACACAGTTGGAGCTGATCAACAAACAGTATCAGCGACTGGCACGTGAGAATCGCACCGATGCAGCCTGTAGTCTGAGAGAAATGGCCCACAATGCCAATCAGCGCTGGGATAACCTGCAGAGAAGAGTGTCATCCGTCCTCCGGAGACTGAAGG[T/C]ACAGAGACTATCAATAAGATGGTAGTTAATCAGTCTTGAGTTCAACACATGTTTTAATAGCACAAAACTGTGAATGTGTCTTATTTTACATTTGTACTAAACCAACAGAAATTAAAGGTGCAGTAGGTGATCTAACCGGTTAGCATAATATCTTTGAAACACAGTCCCTCCCCTGCCATCCAAAGCCACGCCTCCTGAAGTCATGAAGGCACGTTAAAGATGACAGAAACCCACTAGGTCAGGGGTGTCCAAACTCGGTCCTGGAGGGCCAGTGTCCTGCAGATTTTAGCTCCAACTTGCTTCTACACACCTGCCAGGAATCTTCAAGTTAGGTCATGTCATTCACCAGTTAAAAAACGTTATAGTACTTTATAATACTACAAATGTTAACGAAAAACTGTATTATATCTAGCATATTTACAGTTGTGTAGCAAGCAAAACTTAATAATAGCATAATGTGCAATATTTCATGCATGCAACGATCACTGGTCTCACTCTCT
Associated Phenotype:
Not determined