Busch Lab

ZMP

si:ch211-165e15.1

Ensembl ID:
ENSDARG00000024748
ZFIN ID:
ZDB-GENE-081028-59
Description:
Novel protein similar to vertebrate dystonin (DST) [Source:UniProtKB/TrEMBL;Acc:B8A457]
Human Orthologue:
DST
Human Description:
dystonin [Source:HGNC Symbol;Acc:1090]
Mouse Orthologue:
Dst
Mouse Description:
dystonin Gene [Source:MGI Symbol;Acc:MGI:104627]

Alleles

There are 22 alleles of this gene:

Allele Name Consequence Status Availability
sa42113 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38913 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42114 Nonsense Mutation detected in F1 DNA Not yet available
sa15356 Nonsense Available for shipment Available now
sa35396 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42115 Nonsense Mutation detected in F1 DNA Not yet available
sa14777 Nonsense Available for shipment Available now
sa12257 Nonsense Available for shipment Available now
sa16177 Essential Splice Site Available for shipment Available now
sa35397 Nonsense Mutation detected in F1 DNA Not yet available
sa10442 Essential Splice Site Available for shipment Available now
sa11822 Nonsense Available for shipment Available now
sa22196 Nonsense Mutation detected in F1 DNA Not yet available
sa42116 Nonsense Mutation detected in F1 DNA Not yet available
sa11890 Nonsense Available for shipment Available now
sa22197 Essential Splice Site Available for shipment Available now
sa35398 Nonsense Mutation detected in F1 DNA Not yet available
sa42117 Nonsense Mutation detected in F1 DNA Not yet available
sa42118 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42113
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Essential Splice Site 22 7146 None 125
ENSDART00000133961 Essential Splice Site 223 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1355956)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1353308
GRCz11 13 1483599
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCCAGAAGAAGACTTTCACCAAATGGATCAATCAGCACCTCTTAAAGG[T/C]ACAGTACATCCGATTTGCTTGTTAATGTGGAAGAGTGAAGAGTGTAAAGA
Long Flanking Sequence:
TAATGGAGACTGTGATTTTCAGTGATTTGCTTCACATCCTGTGCAGAATCCCAGATTAGCAACATGACATTACAGCTTGACATAGTTAATAACACTAGTGCTCATTCATCAGATAACTTCAGTGTTTATTCAGGGCCGCAGGACTAAAATGAACACAAGAAACTGCTTAAAAATATACACATATATTATTAATTAAAATATGTATACCTTTGGGTATAAGTGTATCTTTGGTGGCTCAGTGGTTGGCACTGTGGTCTCAAAGCAATAAGAACGCTGATTCAAGTCTCGGCTGGGTTAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCATGTTGGCATGGGTTTCAATATTTCAAAAATAGTACAAATATCACAGGATGAGAATCATTTTTTCCTTCAAACGTGTATATTAATGCAGATCTTCTTGTTTTTCAGATGAAAGAGACCGAGTCCAGAAGAAGACTTTCACCAAATGGATCAATCAGCACCTCTTAAAGG[T/C]ACAGTACATCCGATTTGCTTGTTAATGTGGAAGAGTGAAGAGTGTAAAGAAGGCAGAAAGAGGACATTCCCAAAATACAGGGATCTACGTGATATTAACATGCACGCACAGCCATACACATGCACACACACTAACACAAACACACACACATACTGCACAGCCATACACATGCACACACACTAACACAAACACACACACATACTGCACAGCCATACACATGCACACACACTAACACAAACACACACACATACTGCACAGCCATACACATGCACACACACTAACACAAACACACACACATACTATCATTCATTAATCAGTCCCTTCATTAATCTGGGGTCGCCACAGTGGAATGAACCGCCAACTAATCCAGCATGTTTTCTGCAGTGGATGCCCTTCGAGCTGCAACCCGTCACTGGGAAACATCCATACTCACTCATTCACACTCATTACACCACGATCAATATAGTTCATCAGTTCCCCTATAGCGCATGTGTTTGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38913
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
ENSDART00000092780 Essential Splice Site 78 7146 3 125
ENSDART00000133961 Essential Splice Site 279 310 7 8
Genomic Location (Zv9):
Chromosome 13 (position 1365843)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1363195
GRCz11 13 1493486
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGACTCCAGAATGTACAGATCGCACTCGACTACTTAAAAAGACGCCAG[G/A]TAAGAAGAATAATCAACGCTGCAGTCTGATTTCATGCCTTTAAAGGGCAC
Long Flanking Sequence:
AGAAAAAACATTATAGGAAATACTGTGGAAATTTCCTGAATCTGTTCAACATCATTTGGGAAATATTTAGAAAATAAAACAAAATAAGTCACTGGAGGTTGAATAATTCTGTCGTCAACTGTATCTGTGAAATGCAAAATGAACTGTGCATGTAATTTGCATATATTACCATATATAATGTTTCCTCTCACTGCTTTATTGCTTTGCGTCTCTGACCCTGCGTTTGGCTTTGTGTTCTTCTCTCTGTAAACTGATCTCAGAGCTGTGTGAAGGTATAGTCAGACAGCAGTAGAGATGCAGATGTGAGTTTCTCTCCTGCAGCAGATGTTTCTCTCTGTGTGTTTCTGCTGGCCGTAAGTCTTCTCTGTCTGATAAATCTGTACTGATGATTTTTTTATTCTGCATCTCTGTCATCTTCACAGCCGCGGGAGAAGGGCCGCATGCGCTTCCACAGACTCCAGAATGTACAGATCGCACTCGACTACTTAAAAAGACGCCAG[G/A]TAAGAAGAATAATCAACGCTGCAGTCTGATTTCATGCCTTTAAAGGGCACCTGTTATGCAAAAATCACTTTTATAAGGGGTTCAAACATAGTCATGTGGTAAGAGTGTGTGAATAAATCCAGCTTCTAATAGTAAACATGTATTAATTCGATTGTTTATAATCAGGCTTGATGAAGTCAGTTTGCAGAAACACTTTGATTGACATTCTTCTTTTGTACGTGTCATCAGAGGGGGAAAGCCCCGCCCACTAGTGACCATCTCTCCCTCATTAGCATATGACGTTAGTCTTGTTTTTGAATCTGCCACTATGCTGATGTATATTCATTTGTAGCTCCGCCTTATTTTGAAAAGAGCACACTCTCATTTGAATTTAAAGCGACAGCCCCCAAAACATCACACAATTAGAATCAAAGCCTAACAGGGTCAGTTTCAGAGAGTTATAAATAATATCTGTGTGGTATTTCGAGCTTGAACTTCACATACACACTCTAGAGACATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42114
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
ENSDART00000092780 Nonsense 99 7146 4 125
ENSDART00000133961 Nonsense 300 310 8 8
Genomic Location (Zv9):
Chromosome 13 (position 1369312)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1366664
GRCz11 13 1496955
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACATCAGGAACGACGACATAACAGATGGAAACCCAAAGCTGACACTG[G/T]GATTAATATGGACCATAATTCTGCACTTTCAGGTGAGTCTGGACTTCTCC
Long Flanking Sequence:
ATGATAGCATGTCATGTTATAAGGTGTTTTCACAAGCGAAGAGTATTAAATAGTAGTAAATATGCTGCAAAATGTGGCCAATGTTACCGGCTGAATCCTAAAGTGGCGATAAGGTCTTAAAATGTTTGGAAAGAGGCTTTAAACAAGTGTTGATTTTCACTCTCTGATTCCTGTATTGCACCTGAAGGAACATTACAAATGCATGAAAAAAAGCTTCATTGCAGATTGTTGCAAAGGGCTGAGTTTAACCAAACAAATGAAGTTGAACATGACTGCATTTAATTTGTTTGTTTAAATTCAGCCCATGTAAAATGTTTGCAACCACTTACCTTAACATTTTTCAGTGTAGAGCCTTGTGCATTATGTCTTCATGATTGTGCATGATCGTGTTATGATATATCACTCATCAGTATTTAACCATGACCATATTATTTATCCAGGTCAAACTGGTGAACATCAGGAACGACGACATAACAGATGGAAACCCAAAGCTGACACTG[G/T]GATTAATATGGACCATAATTCTGCACTTTCAGGTGAGTCTGGACTTCTCCTGTGTGATTTAAAGTCAGCTGCTTATATCAGATGCTTACTGGAGATACATCCGACTGCTTATTTCTCAGTATATGTGAAAGCCTAAAAATGTTGGGTAATTTTTGCTGGACTAGTGTTTGTGTGCAGTGTTTTAGCTCAGATATAAAAGCTTAGATTAGCTTAGAAACTCCAGTGCAACTGATGCCTTGGTTTTGGAGTTCATCGTGTGACCACTAGAGGTCAGACTTGTATCTGTAAAGCCACAATTGCTCAAGTTTGCTCAGCACTGCTTTTTATTTGACCTTTTTTATTTAAAGAGGATGGAAAGCACACATACAGTTGTATATATGATTTTAAAAAATTATCAAAAATACACACTGTCTTTGTACAAAGCAGCATCTTTAACTGTGATTTCTACAGAATTCAAAGTACAGCCACAGGGCTCGAAATTGCGACCATTGCGGCATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15356
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Nonsense 829 7146 23 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1408764)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1405934
GRCz11 13 1537457
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTCAGATCACCATCGGCAAAGAGGACGAGTGTGTTCTGGTGAGCAACT[C/A]GCACAGAGCCAAGTGGAAAGTCATCAGTMCGTCTGGAAATGAGGCCATGG
Long Flanking Sequence:
GGACTACCTGAAGAGCCTCCAAGATGCCATTCACAGGAAGTACAGCTGTGACAGAAGCAGCAGTCTACACCGGCTGGAGGATCTCATTCAGGAGTCGATGGTGGGTCACACGTGCACACGCTAAACGTCTCGTTCCGGAGGCTTCTCCGTATATCTTGTGTGTATCGTGCACTTGAGTGGATCACTACTCCAGCGCTGATGCATGACTGATGTTTCTCCACAGGATGAGAAGGAGCAGCTCCTGAAGTACAGCAGTACTGTGGGTGGGTTAGTGGGCCGAGCAAAAGCCATCGTTCAGCTCAAGGCTAGAAACCCAGAGAATCCCATCAGGACGTCCATACCTGTCAAAGCCATCTGTGACTACCGGCAGATAGAGGTGCGCTCACTATAGGATCTGCTTCTGCTGTTCATGTTTACAGAGATGCAGTAATGCATTGTGTGACCTGTCTGTCCTCAGATCACCATCGGCAAAGAGGACGAGTGTGTTCTGGTGAGCAACT[C/A]GCACAGAGCCAAGTGGAAAGTCATCAGTACGTCTGGAAATGAGGCCATGGTGCCTTCAGTCTGCTTCAGTGTTCCTCCACCCAATAAAGAAGCCACTGAAATGGCAAGCAGGTGAAGAAATCCCCACTCACTCACTCACTCACTCACTCACTCACTCACTCAATCATTTCACTCATTCATTCATTCATTCATTCATTCTCTCACTCACTCATTCACTCATTCATTCACCTACTCATTCATTCACTCACTCACTCACTCACCCACTCATTCACTCATTCACTTATTCATTCACCTCACTCACTCACTCACTCACCTACTCATTCACTCACTCACCCATTCACTCATTCAATCATTTCACTCATTAACTAATTAATTAATTCCTTCATTCATTCATTCATTCATTCATTCATTCATTCATTGTCAATCTGTCATTCACTCTTTCATTCACTCACTCATTCACTCACCCACTAATTCATTCATTCATTCATTTTTTCATTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35396
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Essential Splice Site 1131 7146 28 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1414911)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1412081
GRCz11 13 1543604
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAAATGCCAACATCAAGTCTATCGATGGAGTCGTGAGCACTCTTAAGG[T/C]AATACACTCCCGTTATCATGGTAAACATGCATTTCTTTAATGACCTGACT
Long Flanking Sequence:
CAAGCCTTACTCATGCATTAATGCATCACACTGTAAGACGTAATAAGACACACTCTGGCACAGACGTCCAGTCTGCACGCTGGAATACACGCTATTATGTCATGACCGTGACGCAGCTTCAAAAATTAGTTTCAAACCGGAAGTACGAATTTGCTTGAAATAACGCAAAAACAACCAATTTACACTTTTTAGTGAAATATAGGTGTCCTAATAGTGTTTTCAGCAGTGTGGGACACATATACGACTGTCAACAGCTCAAAAAATGTGTTTTGGTGTTTCGTGACCCTTTAATTATTTTCATGTCTGATCAAAAGCTGAGCCGACTGAGCTGTTAATGTGTTGATTTTCTGGTTGACTCAGGCTGAAGACGGTGAGTTTGGTGGTGAAACACAGTCAAAGCGCTGAAGCTCTGGTCAAACTATATGAGGCCAAGCTGAGCGAGGAGGATTCAGTAAATGCCAACATCAAGTCTATCGATGGAGTCGTGAGCACTCTTAAGG[T/C]AATACACTCCCGTTATCATGGTAAACATGCATTTCTTTAATGACCTGACTGAACGTTGCTGATCCATTTTTAGCAATGGAGGTCTGAAATTGACGAGAAGCGAGAGGTTTTCCATGACCTGGAGGACGAGCTGCAGAAGGCGCGGGTGGTCAGCGAACGCATGTTTAAAACGCACAACGAGAGAGACTTTGATTTGGACTGGCACAAGGAGAAGGCAGACCAGCTGAAAGAAAGATGGCAGAACATCCACTCTCAGATTGAAAACAGGTCATTATGTTGATCCTTTAGCTCCGTCTAGTGCTGTGCTGCAGGATTCAGCCTGCTTTATTTGCAGTAAAAGACAACACTTATTAGAAATGGTGGCTCAGTGGTTAGCACTGTGGTCTCACAGCAAGAAGGTCGCTGGTTCGAGTCCCGGCTGGGTCGGTTGACATTTCTGTGTGGAGTTTGCCTGTTCTCCCCATGTTGGCATGAGTTTCCTTTGGGTGCTTCGGTTTCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42115
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
ENSDART00000092780 Nonsense 2028 7146 41 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1433371)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1430541
GRCz11 13 1562064
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCAATGCACACAGTGAACCCTGAATGTAAAGATGTCATTCAAGACCAA[G/T]AATCCTCATCAATATTTCCTTCTGAGGCAATTAGCTATACAGAAATGCCT
Long Flanking Sequence:
CTTCTTACCTCATGATGAACAGTTATATGGATCCAGAGTCAGGTCAAAGGCTGCTAATTTTTGATTTGCAGCTTAACAAAATGGCTGAGATACTCTTTGAATGTTTACAATCAGAAAGCTCAGATGAGATAAGTATGGATGATATTTCAGAAGAATCTCCACTTAGCATTGTGGACACTGACAATGACTGCCTGGAAGCCAAGTATTGTGCTTTGGGAGAATTGCAAATATGTGAACCATTGGAAAGCAGAACGGAAGAGTGCGAAGCAATGGATGCCAACGTACGACAACATTACCTTGCTTTAAACACCCTACCAACAGATCAAAAATGTGGTATTTCCCTAGGTAGTAATGATCATGTGACTGTAAGTGAAGCTGATGAACTGCAAAAGGATTCTGCATGTTCAATCATAGATGAATACCAAGCAGACACAAATGTACCCCTGTCAAAGGCAATGCACACAGTGAACCCTGAATGTAAAGATGTCATTCAAGACCAA[G/T]AATCCTCATCAATATTTCCTTCTGAGGCAATTAGCTATACAGAAATGCCTTCTGAATTCACCTTTACGGAGGTTGTGTGGGATGACAAACTTGAGAGAGATTATGCCATTCATCTTTTAAAGGCACAAGTAGAGGAAGGCGGGATTTTAGATGTCACCTCTGGAAAACGGTACGACCTTGAGGCCGCCCTTGGTAAGGGACTTATTGATGAAGAGACTGTCTTAGAAGTACTTGCATTACGGCTTAATGAGGACAGTTTTAAAGATAAAGAAAGGGCTGCATTGTCAGTTCTAAACACTTCCGCTAATAAAGGATGGATCTCAAATAAGGTAGCACTACAGATCATGGTAAAGCAGAACCTTCTGGGTGGTTTCTATGATGCAGCGGTTGGAAAAACCGTTAGCATTTGTGAAGCTTTGGAGACGGGTCTGATTACTGATGATATTAGCAGAAGTGTTCTTTGTTCAGAGCCAATCACGAAAGCCATTATCGATCCAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14777
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
ENSDART00000092780 Nonsense 2380 7146 43 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1434776)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1431946
GRCz11 13 1563469
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGATATTAAGCATGCATCTACCGAAAAAGCAAGTGTAAGCAGTAGTT[T/A]GGAGCTCTATTTAMAGTCCAATTCTGAYATTCACTCTAAAACTTCTTCTA
Long Flanking Sequence:
CAATGTGTTTGATAAAGTTTCCAAGACAAGCCAGGGATCAGATAAAGCCATGCAGGTCTCTAGTGACGTGGGAAGTCTGAGCTCTAGTTCGGAGCTGCCATTAACCATAATTTCTGACATTCAACCTAAAGCAATTTCAACACAAGCCAATGTGTTTGATGACGTTTCTAAGACAAGGCAGGGATCAGATGAAGCCATTGAGGTATCTACCGACACAGAAGCAGTAAGAGGTAGTCAGGATCTTTATTTACCATCCATTTGTGACATTCAACCTGAAGCTATTTCTACAAAAGATAAAATGTCACATGATGTTTCTAGGACAAGACAGGGATCCGATGAACCCATGCAGATATCTGCTGACATAGCAAGTAAGAACAGTAATCAGGAACCCCCTTTACCTATCATTTCTGACAATATGTTAAATATTGTTTCTGAGGCAAGTCAGGCATCAGATGATATTAAGCATGCATCTACCGAAAAAGCAAGTGTAAGCAGTAGTT[T/A]GGAGCTCTATTTACAGTCCAATTCTGACATTCACTCTAAAACTTCTTCTACAAATATGTTTGATAACGTTTCTGAGATGAGCCGAGTATCGGATGAACCCATGAAGATATCTACTGGCATAGCAAGTTTGAGCAGTAGTCAGGAACCCTCTTTACCCATCATTTGTGACTTTCAACCTAAAGGTATTTCGACAAACAGTGTGATGGATAATGTTTCTAAGACTAATGGAATGGTGGATGATTGTGATGTAAAGTGTGCTAGTTCTCCATCTTATGTTAGGCAGGTGACATATTTCGGGACCTCAGCGAGTCAAGTTGTAAGCCCTGTACAGAGTGATTCTGGGATATCCTGTTCCTCACAAAGTGACATCTGTTCAGATGAAAGAAAATCAGAGAGTGTACTTAATCCTGGACAGGAATTCAAAGAGTCTGAAATAACACATGTGAATTTAGACAAAGGATCCTCTGGGAACTCAAGTACTTTGCTACCATTGGTAGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12257
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
ENSDART00000092780 Nonsense 2464 7146 46 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1435325)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1432495
GRCz11 13 1564018
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGTTRCACAAGTTAGTTCACTCACCGAACCACAGTCAGACYTGTCTT[T/A]GTGTGGTGCAAATSCTCAGCCAMMAATTGAGACAACAGAGGTCAGTTTAA
Long Flanking Sequence:
TACAAATATGTTTGATAACGTTTCTGAGATGAGCCGAGTATCGGATGAACCCATGAAGATATCTACTGGCATAGCAAGTTTGAGCAGTAGTCAGGAACCCTCTTTACCCATCATTTGTGACTTTCAACCTAAAGGTATTTCGACAAACAGTGTGATGGATAATGTTTCTAAGACTAATGGAATGGTGGATGATTGTGATGTAAAGTGTGCTAGTTCTCCATCTTATGTTAGGCAGGTGACATATTTCGGGACCTCAGCGAGTCAAGTTGTAAGCCCTGTACAGAGTGATTCTGGGATATCCTGTTCCTCACAAAGTGACATCTGTTCAGATGAAAGAAAATCAGAGAGTGTACTTAATCCTGGACAGGAATTCAAAGAGTCTGAAATAACACATGTGAATTTAGACAAAGGATCCTCTGGGAACTCAAGTACTTTGCTACCATTGGTAGAAGATGTTGCACAAGTTAGTTCACTCACCGAACCACAGTCAGACTTGTCTT[T/A]GTGTGGTGCAAATGCTCAGCCACCAATTGAGACAACAGAGGTCAGTTTAAGTGCCGACGGTCATCCTACATTTGTTCAAAATTTGCTGAATGATAAAAAGTATATGTCATCTCAGACCAATGCATTGTGTACTGCTAAATACCCAAGTCATATAAGAAAGAACCTAGATGTCAAACATTGCAATGAAGATCCAAGTGTGGATGACCCAAGTACAGAGAATACAGTTAAAGAGTTGTCTGACATACAAGGAATGTTCAGAAATTCCTCTGAATTGCAACCAGGCCACGATAGTCCAAGTCCTTCTGTAAGTGTTATGCTTGACAAGAAAAATGAACAAACTGCAGGCATATTCACACAGTCTCAAGGTGGAGATACAGTAGTTAATGAAGTTGCTCACCAGGGTGACCTTGATTTACCTCATATATCAAAGGCCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGTTTTAAGATCTACCTTAAATGAGTTAAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16177
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Essential Splice Site 2478 7146 47 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1435746)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1432916
GRCz11 13 1564439
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KATACAGYAGTTAATGAAGTTGCTYACCAGGGYGACCTTGATTTACCTCA[T/A]AWATCAAAGGYCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGT
Long Flanking Sequence:
AACTCAAGTACTTTGCTACCATTGGTAGAAGATGTTGCACAAGTTAGTTCACTCACCGAACCACAGTCAGACTTGTCTTTGTGTGGTGCAAATGCTCAGCCACCAATTGAGACAACAGAGGTCAGTTTAAGTGCCGACGGTCATCCTACATTTGTTCAAAATTTGCTGAATGATAAAAAGTATATGTCATCTCAGACCAATGCATTGTGTACTGCTAAATACCCAAGTCATATAAGAAAGAACCTAGATGTCAAACATTGCAATGAAGATCCAAGTGTGGATGACCCAAGTACAGAGAATACAGTTAAAGAGTTGTCTGACATACAAGGAATGTTCAGAAATTCCTCTGAATTGCAACCAGGCCACGATAGTCCAAGTCCTTCTGTAAGTGTTATGCTTGACAAGAAAAATGAACAAACTGCAGGCATATTCACACAGTCTCAAGGTGGAGATACAGTAGTTAATGAAGTTGCTCACCAGGGTGACCTTGATTTACCTCA[T/A]ATATCAAAGGCCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGTTTTAAGATCTACCTTAAATGAGTTAAGCCTAATGAAGTTGGATGTTGGAAGTGTGGATGATACTCAAAAACAAAAAGTGGAGTTTGGAATAATGAATGTATATTTCAACAAAGGGATATCTGAGAGCTTAAGTACTTCACTACCAATGGTAGAAGATGTTGCACAAGTTAGTTCACTCACAGAATCACAGTCAACCTCATGTGGTGCAAATGCCCAGTCACCAATCAGGATGGGAACAGAGGTCAGTTTAAGGACTGATGGTCATCCCACATCAGCTCAAAATTTGCTAAATGGTAAAGAGTATATGTCATCTGAAACAAATGCATTGCATACATATAAATGCCCTAGTGGTATAAGTGAGAACCCAGATTTCAAGCCTTGGAATGAAGATCCAAATGTGGATGATCCAAGTATACAAAATACAGTTAAACAGTTGGCTAAGTGTGAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35397
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
ENSDART00000092780 Nonsense 2507 7146 47 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1435835)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1433005
GRCz11 13 1564528
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGGAAGTGTTTTAAGATCTACCTTAAATGAGTTAAGCCTAATGAAGT[T/A]GGATGTTGGAAGTGTGGATGATACTCAAAAACAAAAAGTGGAGTTTGGAA
Long Flanking Sequence:
AAATGCTCAGCCACCAATTGAGACAACAGAGGTCAGTTTAAGTGCCGACGGTCATCCTACATTTGTTCAAAATTTGCTGAATGATAAAAAGTATATGTCATCTCAGACCAATGCATTGTGTACTGCTAAATACCCAAGTCATATAAGAAAGAACCTAGATGTCAAACATTGCAATGAAGATCCAAGTGTGGATGACCCAAGTACAGAGAATACAGTTAAAGAGTTGTCTGACATACAAGGAATGTTCAGAAATTCCTCTGAATTGCAACCAGGCCACGATAGTCCAAGTCCTTCTGTAAGTGTTATGCTTGACAAGAAAAATGAACAAACTGCAGGCATATTCACACAGTCTCAAGGTGGAGATACAGTAGTTAATGAAGTTGCTCACCAGGGTGACCTTGATTTACCTCATATATCAAAGGCCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGTTTTAAGATCTACCTTAAATGAGTTAAGCCTAATGAAGT[T/A]GGATGTTGGAAGTGTGGATGATACTCAAAAACAAAAAGTGGAGTTTGGAATAATGAATGTATATTTCAACAAAGGGATATCTGAGAGCTTAAGTACTTCACTACCAATGGTAGAAGATGTTGCACAAGTTAGTTCACTCACAGAATCACAGTCAACCTCATGTGGTGCAAATGCCCAGTCACCAATCAGGATGGGAACAGAGGTCAGTTTAAGGACTGATGGTCATCCCACATCAGCTCAAAATTTGCTAAATGGTAAAGAGTATATGTCATCTGAAACAAATGCATTGCATACATATAAATGCCCTAGTGGTATAAGTGAGAACCCAGATTTCAAGCCTTGGAATGAAGATCCAAATGTGGATGATCCAAGTATACAAAATACAGTTAAACAGTTGGCTAAGTGTGAGGGCATACAAGGAATGTTCAGAAATCAAATGCCAAATGCCAAAGATGAATTTTCTCCAAAATCATTGGGAAGAAGAGATTCGAGATCTATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10442
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Essential Splice Site 3410 7146 58 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1444038)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1441208
GRCz11 13 1572731
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACGCCATTCATTTGTGCTTATTTGYGCCCCAAAWATGAACATTTGTGC[T/A]GGATTGGTGATATGAAACCTTAKTTTYTGGACTGTGTGAYGTYACTCTTC
Long Flanking Sequence:
CTGGAAAACATCCATACACTCTCTCATTCACACACACTCATACACTATGGCCAATTTAGTTCATCGATTCCCCTATAGCGCATGTGTTTGGACTGACTATGCTTGAACTGCTTGATCAAAGTAAGCACAGAGTAAACAGGGTGTTCGCAGGGGTCTTAAAAAGCCTTAAATTCACTCAAATATTGCATTGTAGGTATTAAATCATTTTTAAACGGGTCTTAATTTTCCTATTTACATGTGAAGCTTTCTAATTAGGGCAACACCCAATCACCAAAAAAAACAACACAAAAAATCTCAATAGAACCTTTAACAAAACTCTATTTTAAACTCCATTTACCAATATGGTTTAGTTGTGATTTTAATTATTATTAGGGATGCACTGAATTCTGAAAAAATATGAAAAGAGCTCAAAATATATATTTTAAAAATAAAAATAAACAATCCCCAAAACTACGCCATTCATTTGTGCTTATTTGCGCCCCAAAAATGAACATTTGTGC[T/A]GGATTGGTGATATGAAACCTTATTTTTTGGACTGTGTGACGTCACTCTTCACCCCACGTTGCTCAAAGAGTTTGTTTGTGCTCGAGTTTGTGCTCGTTTAGATTCTGCCATTAATCATTTTTGACATCGCACAGTCAAAAAGATAACATAATTAAGTTTATTGTAGTTTTTAAAGAGTTTTTGTCTTGTTTCTAGCTTAAATTTCTACAAATTTTTAAACCAAGAAGCTTTTTCTTGACAAGCGAAACATATGGTCTTGTTTTCAGAAATAATATGCCAAAATTAAGTGAGGTTTTCTTTAAAACAAGTAAAATAATCTGCCAATGGGATAAGTAAAATGATCTTATGACAAAAGGCAAAACTAGATTATTTTGCTTACCCCATTGTCAGATTATTTAGCTTTAATCTTAATGACTTTAATCTTTGAGCTTAAACGCTTAATTTTAACATATTTTGTTTTAAAACAAGACATTATATTTTACTTGTCTAGAAAATGCTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11822
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Nonsense 3417 7146 58 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1444061)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1441231
GRCz11 13 1572754
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGYGCCCCAAAWATGAACATTTGTGCWGGATTGGTGATATGAAACCTTA[T/G]TTTYTGGACTGTGTGAYGTYACTCTTCACCCCACGTTGCTCWAAGAGTTT
Long Flanking Sequence:
TCATTCACACACACTCATACACTATGGCCAATTTAGTTCATCGATTCCCCTATAGCGCATGTGTTTGGACTGACTATGCTTGAACTGCTTGATCAAAGTAAGCACAGAGTAAACAGGGTGTTCGCAGGGGTCTTAAAAAGCCTTAAATTCACTCAAATATTGCATTGTAGGTATTAAATCATTTTTAAACGGGTCTTAATTTTCCTATTTACATGTGAAGCTTTCTAATTAGGGCAACACCCAATCACCAAAAAAAACAACACAAAAAATCTCAATAGAACCTTTAACAAAACTCTATTTTAAACTCCATTTACCAATATGGTTTAGTTGTGATTTTAATTATTATTAGGGATGCACTGAATTCTGAAAAAATATGAAAAGAGCTCAAAATATATATTTTAAAAATAAAAATAAACAATCCCCAAAACTACGCCATTCATTTGTGCTTATTTGCGCCCCAAAAATGAACATTTGTGCTGGATTGGTGATATGAAACCTTA[T/G]TTTTTGGACTGTGTGACGTCACTCTTCACCCCACGTTGCTCAAAGAGTTTGTTTGTGCTCGAGTTTGTGCTCGTTTAGATTCTGCCATTAATCATTTTTGACATCGCACAGTCAAAAAGATAACATAATTAAGTTTATTGTAGTTTTTAAAGAGTTTTTGTCTTGTTTCTAGCTTAAATTTCTACAAATTTTTAAACCAAGAAGCTTTTTCTTGACAAGCGAAACATATGGTCTTGTTTTCAGAAATAATATGCCAAAATTAAGTGAGGTTTTCTTTAAAACAAGTAAAATAATCTGCCAATGGGATAAGTAAAATGATCTTATGACAAAAGGCAAAACTAGATTATTTTGCTTACCCCATTGTCAGATTATTTAGCTTTAATCTTAATGACTTTAATCTTTGAGCTTAAACGCTTAATTTTAACATATTTTGTTTTAAAACAAGACATTATATTTTACTTGTCTAGAAAATGCTTCTTAATTCAAGAATTTGTAGCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22196
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
ENSDART00000092780 Nonsense 4120 7146 70 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1462914)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1460084
GRCz11 13 1591607
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGTTCTTAAAAGACATTTGCTGGTCTTTTCCTTCTGTCTGCAGGACT[T/A]GCTGGACGCCTGGACCTCCAAATCTCCCGCGGTCCAGGATATAAATAGCA
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATATATAATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTACAGTATTGTACGATACAGGTCAGTACGGGTCACTTTTATCAGGCTTGCGTTTCCACTGCATAAAGGATACCAAGGGTGCGACAAAGTCTCTACTGTTAAACAGAAATTGGGAAATATACAGGAGGGCGAATAATTAAGACTGCAACTGTATGTTGTAGAGTTCTTAAAAGACATTTGCTGGTCTTTTCCTTCTGTCTGCAGGACT[T/A]GCTGGACGCCTGGACCTCCAAATCTCCCGCGGTCCAGGATATAAATAGCAAGGGATCTGCTCTGTGTAGCCTAATCAGTGTTTTGACATCGCCAGCCAAAGCCAAGATACATCACAACTCAGGTATTGCCACGGCGTATTTTAAGATTGGAGCGAAACATTCATCACACGTCTGTGTTCTGCATGATCACTCATTCAGTCCGTCTCTGGAGAATGCAAACAGACGGGATATCGGTGTTTTTTTTCTGTAGGATCGGTTGTCAGCAATGGTTCTGGTCCAGGAAATCATGCCTTTCTGACAAACCAAGGTGAAAGTTCATGCTAATGATGGATTAGTTTTGGGTTTACTTCAAGGGGGTGTTCATAAGACTGTCATGACGTCTTTATAATCATAATCAGCTTGCTTATGACAGCTGCTATTAAGTGTGATATTTTACAGTGCATGATTATAAAGGGCTTATAAACACCCCTTCAGGTAAAGTGTTACCAATATTAGTAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42116
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
ENSDART00000092780 Nonsense 4535 7146 76 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1470596)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1467766
GRCz11 13 1599289
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAATGTAACAATGTTATATTTCATCTTGTGTTCGCCAGCTAAGCGGATC[G/T]AGCAGCTCAACTCGGCTTTCGCCAGCTCTCAGCAGTTCCACCAGACATCG
Long Flanking Sequence:
TAAGCAGCAAATTATCAGTTTATTAAGGCAAAAGTCATAGTTATTGGTTTGTTAATACCAAGAATTGTACCATAAAATGAAGTCTGACCTAGATTTATTATGTAACAAATGCTAAATTTTACCTTGTGTTCACCAGACGAGCTGCCTAAACCCAACTATTACCTTAATAACTATTAATAAGCATCTAATTATTAGTTTACTGATGCAAAAATTGTAGTTATTGGTTTGTTAATACAAAAAAATTGTACCATAAAATGAATCCTGACCAAGAATTTTTATGTAACAATGTTATATTTTACCTAGTGTTCACCAGGCAAGCTGCCTAAACCCAACTATTACCTTAATAACTATTATTAAGCAGCAAATAAGATGTCTATTGAAGCAAAAGTCATAGTTATTGGGTTGTTAACAACTAAAATCTTATCTTAAAATGACGTCTGACCAAGATTTCTAATGTAACAATGTTATATTTCATCTTGTGTTCGCCAGCTAAGCGGATC[G/T]AGCAGCTCAACTCGGCTTTCGCCAGCTCTCAGCAGTTCCACCAGACATCGAAAGACTTCCAATCCTGGCTGAATCAAACTCTACAAGACCAATGCAATCCACAACCCATCTCTGCTGATGTGCAGAAGCTCAAACAGAGTCTCAAAGACAACAGCGCTGTTCAGAAAACCATTAATGACCACGAAGAACCTTACAGAACCATCATGAAAGAGGGAGAAGCTCTCCTCCAGAGCACCGAAGGCGCAGAAAAGGTGGCTCTTCAAGGACAGCTCTCTGCTTTAAAGTCCAACTGGGAAGATGTGAAGAAAAGCAACGCGGAACAAGCAGAAAAGCTTCAGACGGCAATGCAGAGGGCACTGAAATACAAGGAGAACGCTGAGAAGCTGAACTCGTGGTTGCAGGAGTGTGAAGACACGGAGAACACGGTGAAGCTCAGCGTAAGCTCGGTCGAGATTGAAGGATCGCTCTCGCAATTAAAGGCCATCCAGAAGGACATCGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11890
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
ENSDART00000092780 Nonsense 4667 7146 76 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1470993)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1468163
GRCz11 13 1599686
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGAGGGCACTGAAATACAAGGAGAACGCTGAGAAGCTGAACTCGTGGT[T/A]GCAGGAGTGTGAAGACACGGAGAASACGGTGAAGCTCAGCGTAAGCTCGG
Long Flanking Sequence:
TTGGGTTGTTAACAACTAAAATCTTATCTTAAAATGACGTCTGACCAAGATTTCTAATGTAACAATGTTATATTTCATCTTGTGTTCGCCAGCTAAGCGGATCGAGCAGCTCAACTCGGCTTTCGCCAGCTCTCAGCAGTTCCACCAGACATCGAAAGACTTCCAATCCTGGCTGAATCAAACTCTACAAGACCAATGCAATCCACAACCCATCTCTGCTGATGTGCAGAAGCTCAAACAGAGTCTCAAAGACAACAGCGCTGTTCAGAAAACCATTAATGACCACGAAGAACCTTACAGAACCATCATGAAAGAGGGAGAAGCTCTCCTCCAGAGCACCGAAGGCGCAGAAAAGGTGGCTCTTCAAGGACAGCTCTCTGCTTTAAAGTCCAACTGGGAAGATGTGAAGAAAAGCAACGCGGAACAAGCAGAAAAGCTTCAGACGGCAATGCAGAGGGCACTGAAATACAAGGAGAACGCTGAGAAGCTGAACTCGTGGT[T/A]GCAGGAGTGTGAAGACACGGAGAACACGGTGAAGCTCAGCGTAAGCTCGGTCGAGATTGAAGGATCGCTCTCGCAATTAAAGGCCATCCAGAAGGACATCGATAAGCATAGAGGACACATAGAAATGATGAACAGTGCGGCAGACGGCCTCCTGGAGGTCATCACAACAGATGGAGATGCAATTAAGGAGGACAAGCTATCAATTGGTAAAAGAGCTGATAAGCTGACGGAAGATCTGACGCTCAAGCGAGAGGCGTTAGAAAGCATCTCGCAGAAGCTGAAAGAGTTCAATGACCTCCAGAAGGAAGCTAAAGGACAATTGGAGAGCGCAAGGAAAGTGCTGGATGTTCACTCCTCATTGGGTGTCCAGGCTTTCAGCAATAAAAGCCTGAGCAATATGAAGGCTCAGCAGAACGCTTTGGAGAGCGTCCACAAGCAGATCGAGCATCTCAAAAGTATCGCACAAGGACTCGTTGTTGATGCATGCGAGGCCGAAGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22197
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092780 Essential Splice Site 5020 7146 76 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1472055)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1469225
GRCz11 13 1600748
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCGGATTGGAAACAGAAGTCATTAATCAGCAACTGGAGTCCTTCAAGG[T/A]AAGATTTGATGTGTTGTAGCGATCTGACTGGGTAGAGGTGCCAACCTATA
Long Flanking Sequence:
GGTGGACGATGCTTGCTCCAGTTTGGAGAGCAAACTTCTTGGAATCGGACAGTTCCAGAACAGCATTCGGGAGATGTTTGCAAGCTTCGCAGACTTGGACGATGAGCTAGATGGCATGGCTCCTGTGGGACGAGATCTTGAGATCTTGAGAGATCAGAAAAGTGCCATCGAAGCGTTCGTAGCCAAGCTTCAGGATCTGACGCGCAACACATCCAACGGGAGAGACAGTTGCAGGAAGATGCTGGAGTCGGAGGCTTCGCCGGATCTGCTGGGTCTGAGGAGAGACTTGGAGACGCTTGGAAAACAGTGTGGAAAGCTGATGGACAGAGCCACCGCGAGAAAGGAGCAGGTTGAGGAGACGCTCGGTCATCTGGAGGAGTTTTACAGCAAGACGCAGGAGTTTACCAGCAACCTGAGCACTGCGGAAAGGCAAGAGGAGTCCCAGGGGTCTGTCGGATTGGAAACAGAAGTCATTAATCAGCAACTGGAGTCCTTCAAGG[T/A]AAGATTTGATGTGTTGTAGCGATCTGACTGGGTAGAGGTGCCAACCTATACATTTATAGGTACAAATTAAAACATTTCTGCTGCTGTAGCCCATCCGCCTCAAGGTTGGCCGTGTTGTTTGTTCAGAGATGCTCTTCTGCAGACCTCGGCTGTAACGAGTGCTTATTTGAGTTACTGTTGCCTTTCTATCAGCTGGAACCAGTCTGGCCATTCTCCTCTGACCACAACAAGGCATTTGCACCCACAGAACTGCCGCTCACTGGATATTTCCTCTTTGTTGGACCATTCTCTGTAAATCCTAGAGATGGTTGTGCGTGAAAATCCTAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCCGTCTGGTACCAACAACCATGCCACATTCGAAGTTACTTAAATCCCCTTTCTTATCCATTCTGATGCTCAGTTTGAACTGCAGCAGATCGTCTTGACCATGTCTGCATGTCTAAATGCATTGAGTTGCTGCCATGCGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35398
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
ENSDART00000092780 Nonsense 5560 7146 86 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1517264)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1514729
GRCz11 13 1646252
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAACATTCACACAGCTTTCACAGCCCGCTATTGAGTATGAAGCCCTG[C/T]GACAGCAACAGGAGGAGCTCAGGGTAAGACACACACATGTGGCAAAACAT
Long Flanking Sequence:
GTGGATGACATCGTGAAGACCGGCGAAGCCATTATGAACAGCAAAGATGAGGCAGAGAAGCAGGCGCTCAAGGTAAATGCTGGAAAAATCGATGCGATTGGCTGTTTTTGAAAAGGGGGAGGAGCTACTCTGTCTTTGTTTTTCTGTTTCAAGATTAAAAATATGCAAATAAATAATGAAATTAGACACAGATTGTAATGGCATTCATTACAAGACCACAGGACAACACACGCTTCATAATAGCTAATCAAACATCTCTCATTCGGTTACACCTAAAGCACATTTTACTGTGCGCTGTCCTGCAGGTGAAGCTCCAGGCGCTGCTGGAGAAGTATACCGTGGTGAGCCAGCTGAACTCGGAGCGCTGCCTGCAGCTGGAGAGAGCTCATTCTCTGGCCTGTCAGTTCTGGGAGACCCATGATGAGCTGTGGCCGTGGCTGCAGGACACCAGAGCAACATTCACACAGCTTTCACAGCCCGCTATTGAGTATGAAGCCCTG[C/T]GACAGCAACAGGAGGAGCTCAGGGTAAGACACACACATGTGGCAAAACATTTAAAGTCCACATCAACTGGAAGCTGTGACCCTTTTTTGTTCCTTATTGTGACACAGTTCCTAGAGAAATGGAATATTAAATGAGAAAACAGTGGGTGTGGCTTGTTTTTTTTCTACTGCGAGCTGATTGGGTGTAGTACAGTAGGCGTTTCATTCAGAAAGATAAGGGGGAAAGGGTTTGGGGAGAGTTATTACAACCTAACAGACTCCTCCTCCTCTTCACTATTTCTGTTTGATGTCAAAACTGACAGCTAAATTGGGCGTGGTTAAGTATGATAGCCCCGCCCAATACCTCAGACAGACCTAATCTGAGAATTTACCTGAAAACTCAGGATTTTCTAGACTTTAATTTTAGATTACGAAAGCAAATTTTGAGTTTTGCTGTTGATCATTAGTTACAGTGCAAAAAAAGCTTAGTTTATGGCCTTTGCACACTTACCTTGATATGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42117
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
ENSDART00000092780 Nonsense 6330 7146 102 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1540236)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1536378
GRCz11 13 1667901
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGGACACTGAGTTGGAGATCGCCAACGACCCAGACAAGATCAAGACA[C/T]AGTTGACCCAGCACAAGGTGACTGACTGACACACAGAGTCTGTTTAGATG
Long Flanking Sequence:
TTTTTTCTTCTGGAGAAAGTCTCATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTTAATTGTTTTAAAGCCATTTTAAGCTCAATATTATTCGACCCCTTAAGCAATATTAGTGTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAACATTATGTGCTGTCATCATGACAAAGAGAAAAGAAATCAGCTATCAGAGATGAGGCATTAAAACTATTAAGTGCAGAAATGATAGCAATAGCAAATGTTTAGCAGTAATATAATGAGTGCAACACTAATGGATTGTCCTCTGCAGTTCCATGAGTCCTGGAGCAAACTGATGGAGTGGCTGGAGGAGTCAGAGCGAGCGCTGGACACTGAGTTGGAGATCGCCAACGACCCAGACAAGATCAAGACA[C/T]AGTTGACCCAGCACAAGGTGACTGACTGACACACAGAGTCTGTTTAGATGTGTTTCCAGTGATCTGATCATAGGTGGCAGTGTTTCCTCTTTTTTACTCAGATCTACCAACTACCTGTGGCGTTATTTATTTCAATGACAGATGTCGTGTGCGCAGTATTACAAGTCGAGATCGCATTTGTGTAATAGAATACGAGCATGCGAATCTCTTTGCTCGCTAGCCGATTTCCTCTGCTTGCGCACACAGCTTAATGCCCCCTCAATTATACGCTGCTCAAGCGCAGATCTTCTTGTGCGCCCTCAAATCAATGCTGCTGAAGTGCGGTTTATTGCATTTTAGCGTACTATATAGTAGGCTTGGGCGGTAATTCGGTAAAATGGTATACCGCGAGATCTAAAAATAGCAACGGTGTCAGTTTCGATACCGTTATACCGTCATAGAAACAATTCACTTAAGTTGGAGACAAGTATTATATAATAAATATTATTTATTTAATGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42118
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
ENSDART00000092780 Essential Splice Site 6504 7146 105 125
ENSDART00000133961 None None 310 None 8
Genomic Location (Zv9):
Chromosome 13 (position 1555268)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 1551408
GRCz11 13 1682931
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCGCTGGGAGACGGTCTGCAGCCTCTCCGTGTCCAAACAGACACGCCT[G/A]GAGCAGGCCCTCAGTCAGGTAACACTGGTCACAATCACTTACTATTTAGC
Long Flanking Sequence:
TCTGTGGTGCTTATATAGTGTCAGTAATCAGTGATGATGAGCTGCAGCTGTGTGTCAGTGTCCAGATTGTTATCAGCTGTGGCACAAAGTGCAATGGGAGGTGTAGTCCGGGCGAATGCCTGGTGGAGTGTTCGTATAGCTGGAGTGCCCTCTAGTGAGCCTGTTGAACACTCCAGCTAATGACTCGAAACAGCACCATAGGCAATGCAAAAGCTTCTACATAAGCACTTGGATTAAATGCTTTGATTGACATTATAAACACGGCTCATGTGTAGATTAAACGCAGACTGGTTGAATGTTTTGATCAATGCATGTGTGCTGCAGGTGTTCCAGAAGGAGCTGGGCAAGAGGACGGGCAGCGTTCAGGCTTTGAAGCGTTCGGCACGGGACTTGATTGAGAGCAGTCATGATGACTCCTCCTGGGTTAAAGTTCAGATGCAGGAGCTGAGCACCCGCTGGGAGACGGTCTGCAGCCTCTCCGTGTCCAAACAGACACGCCT[G/A]GAGCAGGCCCTCAGTCAGGTAACACTGGTCACAATCACTTACTATTTAGCTAGTTTTATATATATATATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGGATGCCACGGTTCTCAATATAATATTTAACAGTACAGTACGACCTCCACGGTTCAATACGAGCTTGTGAGTTGTGCGTTTAAATAATTTATGTGCATTTTATATCTCCCCGAATTGACTGTGTTTGCCTGTAAATCCATGAGCTGAGATAAGGAAACTCCTCCCTGCGAGTAAATATCCAATAACTAAGGTCTAAAGTTAGGGGGCGCTTGACCATCATTCCACACTTTAACATGGCGAGCGGCAGTGAAGTGAGGCTGAGGCAACAGTACCAGGAAGTGCCGGCGAAGTGAGGCAACAGTAACAGAATGTGCCGGCGTCTTTCAAATCTGCGGTTTGAGGACATTTCGGAATTGCCATTAAGTATAACGC
Associated Phenotype:
Not determined