Busch Lab

ZMP

ANK3 (2 of 2)

Ensembl ID:
ENSDARG00000061736
Description:
ankyrin 3, node of Ranvier (ankyrin G) [Source:HGNC Symbol;Acc:494]
Human Orthologue:
ANK3
Human Description:
ankyrin 3, node of Ranvier (ankyrin G) [Source:HGNC Symbol;Acc:494]
Mouse Orthologue:
Ank3
Mouse Description:
ankyrin 3, epithelial Gene [Source:MGI Symbol;Acc:MGI:88026]

Alleles

There are 15 alleles of this gene:

Allele Name Consequence Status Availability
sa17048 Essential Splice Site Available for shipment Available now
sa13397 Nonsense Available for shipment Available now
sa18498 Essential Splice Site Available for shipment Available now
sa42911 Nonsense Mutation detected in F1 DNA Not yet available
sa23050 Nonsense Available for shipment Available now
sa36387 Nonsense Mutation detected in F1 DNA Not yet available
sa36386 Nonsense Mutation detected in F1 DNA Not yet available
sa15975 Nonsense Available for shipment Available now
sa23049 Nonsense Available for shipment Available now
sa23048 Nonsense Available for shipment Available now
sa9548 Nonsense Available for shipment Available now
sa39159 Nonsense Mutation detected in F1 DNA Not yet available
sa36385 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17048
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Essential Splice Site 549 3980 14 43
Genomic Location (Zv9):
Chromosome 17 (position 20609488)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20759499
GRCz11 17 20779335
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCCAATCTTCTACTGCARAAGAAAGCYGCACCAGATGCTGCAGGCAAG[G/A]TTGGTGAACATATGCATGRTGTAATATTCAGTGCAAAAAACAACATGTAC
Long Flanking Sequence:
CAAATGATTAAAAAAAAACACTCAATACTTTTTTATTCATCGGCGATGCATTAACTGGAACTAATTGATAATTGATAGTAAAGACATTTTATAATGTTAAAAATATGTAATGTTTCTACAACAATATTAAGCGCCACAGTTGTTTTCACAATGTATGTTTTCTGAGAACCAAGTGGGCATATTAAAATGATTTCTGAAGGATTTTGTGACACTGAAGACTGAAGACTGAAGTAAAAGTAAAATATATGAAAAAGATTTAGGTGGTCACTGGACACCATTGTGTGCAATTTACATTCATAGTACCTTATCGTTCCAATCTTAAGTCATAATTAAATTGCATAAAACTCTGCATCTTTTTCACTCTTTTTTCATTTCTTTTATCCCTGTATATACCTCCACAGAAAGGGTTCACTCCTCTACATGTGGCTGCAAAGTACGGGCAGCTGGAAGTGGCCAATCTTCTACTGCAGAAGAAAGCTGCACCAGATGCTGCAGGCAAG[G/A]TTGGTGAACATATGCATGATGTAATATTCAGTGCAAAAAACAACATGTACTAGCACATCTTTTAACATACCCATTTATGCATGGCGGGTCACATTTTATAATGATGTAACATTTTAATGAGTCCCCTTGTGCTTTCCATAAGACTGCTCGGTTTTGTCCCAAATGAAGCGCTTAATGTAGAATTTACTTGTTCTTGATAAATTCCAAAAGATGGGACACTAGTAAAGCTATAACATAATTATTTTGTTGGATTGTTTGCACACACACAAAATAAGGTCAGAATACATGGATACTTCTGACTTACCGTGAAAACCAGATGGTGTAGTTACAACATCTACCAGCAGGGGTGAACTAGGCCACACTAACCAGCCAACCATGATGCCTTAGAGGTATAGTTCACCCAAAAAGGAATATTTACTCACTCCTAAGGTTATAAACCTTTATGACTTTTTTCTTCTGTTGAACACAAGATAACATATTTTGAAGAAAGCTGAAACATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13397
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
ENSDART00000088106 Nonsense 603 3980 16 43
Genomic Location (Zv9):
Chromosome 17 (position 20602962)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20752973
GRCz11 17 20772809
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTCTCCACATTGCAGCRAAGAAGAATCARTTGGAGATTGGGACGACGT[T/A]GCTGGAATATGGAGCGGAGTGTAACACAGTGACCCGCCAGGGCATCAGTC
Long Flanking Sequence:
GGATTTAATAATTCTGATTTCTACTGTAGTTGAGGAATTTATTGATAATTTTATGTTTTAAACCAATTGATTTTAATTAAAACAACTTAAACTTGCTGTTTCTGAAGTATTTTTTTTTTTTTATAAATAACAGTTTTTAGCATTACAAAACTATTAAAGCTGTTGTTTCAATTGGGCTGAGGACAAGGACAATGACAGGGTTTATACATTTGTAAAGTGTTTCTAAATAAAGAAAAACAACCTAAGAATCAAATGAAGGACATATTCCTTTGCAGAACTACTCATGGAAATCAACCATCAGCCCATTTTAGACATTTTTGGGATGAAACACTTTTCATTCACTGTTTTTCTGTTTTTATATCAGGGACAGTTTCTGGTAGAATGTCCCTCAATTTTTCAATTAAAAATGTCTGACTATTTCTCTCTTCTTTCTCTACAGAATGGCTACACGCCTCTCCACATTGCAGCAAAGAAGAATCAGTTGGAGATTGGGACGACGT[T/A]GCTGGAATATGGAGCGGAGTGTAACACAGTGACCCGCCAGGGCATCAGTCCACTCCACCTTGCCGCACAGGAGGGCAGTGTGGACCTCGTGTCTCTGCTGCTCACCAAACAAGCTAATGTGAACATGGGCAATAAGGTAAACACCTTTTAATATGACTCATACACAGAGCTCAATGTGGAGAATGAGGACTCAATGTGAATCTGTGTTTGTAAACAGAACGGTCTCACGCCGCTGCACCTCGCTGCACAGGATGACAAAGCAGGTGTTACTGAAGTGCTGTTGAACCATGGAGCAGAAATTGACGCCCAAACCAAGGTCAGGGTTCAGGTTTTGTAGAGTTTCCATTGGGTGAATCCATTATGTAAATTATAGGAGTAACTTTGATTAAAGCGTAACATTTTCTCTTGTCCTAATAGAGTGGCTATACTCCGCTGCATGTGGCGTGTCATTATGGCAATATGAAGATGGCCAACTTCCTGTTAGAGAATCAAGCCAAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18498
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Essential Splice Site 1134 3980 28 43
ENSDART00000088106 Essential Splice Site 1134 3980 28 43
Genomic Location (Zv9):
Chromosome 17 (position 20562908)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20712919
GRCz11 17 20732755
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCCTTCCCGCAGGGAGCGCTTACCAAGAAGATTCGTGTAGGACTACAG[G/A]TACATTTAAACAATAAACAKAAGGGCTCATCAAGATGGCTGTTGTGTGTG
Long Flanking Sequence:
ACATCTAGACTACTGAATATAAGGGTTAAATGCACATTTATGCATTGTGACATATCACTATCATATCACTGTCCTTTTTTCTGTAGTGAAGGGATGCCAGTACATTTCAAAAGCTCAACTGTTGATGCCGAGGTTGATATTAGTTCCTGTCTCTGTTTTTTAATATGTGTGACAACCACAAAACACAACTGTAAATACATGAATTTATGGCACATTTAATTAAATATTTATAGTTTAATATAATAATTTAATATAGTTTAATAGTTAAATTTTCATATTTGATTGCAGAGATGGACAGTCCAGCAGAACTGGAGAAGAAACGTATCTGCCGCATCATCACAAAAGATTTCCCACAGTACTTTGCAGTGGTGTCACGTATTAAGCAAGAAAGTGATCACATGGGCCCAGAGGGTGGAGTCTTGACCAGTGAAGCAGTTCCAATGGTGAAGGCTGCCTTCCCGCAGGGAGCGCTTACCAAGAAGATTCGTGTAGGACTACAG[G/A]TACATTTAAACAATAAACATAAGGGCTCATCAAGATGGCTGTTGTGTGTGATCAAACTTTGTAATTAAATCTTAGATGGAAAACATAGAAACATTCTGGAAATTATAAGGGCCAGATTTTTAATACCATTTTAAAGGTTTATAAATAAGTTTTACATTAGGTTTGCAGTACGTTTACATCCATCCAAGCTCAAAAATCACTTTCACATTCTCCTTTAACCATTCCTTCGAGAATTCTCTTTCTAAACTCATAGATACAATATTTTTAACATGTCAACAGCCCAAACCAGACCAAACTCTTTCAGCGTGGTGTTTATAGTCAAGTTAAAGTAGACATTTGCATTCTGTAAGTATGTATGTTTATGAAGGAAATGACTGTGATTATTGATTATTTAGACTTACTCATTTTTGGTAGTTCAGAATGCAGTAGGTTCTTTTTGGAGACAATAACTATTTATTGTGAATTGTGAAGTCTGAAACAAAGCAGACATTTTGCAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42911
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Nonsense 1324 3980 32 43
Genomic Location (Zv9):
Chromosome 17 (position 20558899)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20708910
GRCz11 17 20728746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATAAATTTTTTGTCAGATTTTGGAGGGAAAGCCTATCCATGGAGAATG[C/A]TACGGCAACATCTATCCTCTAGCAAAGAGTGGCCAGCAACTCATCTTCAA
Long Flanking Sequence:
AACATCTACCTGCAAACCTTTTTTCTCTTTAAATTAGGTTATATTCATACAAATACTTTATTCATTCATTCATTCATTCATTTTCTTTTTGGCTTAGTGACTTTATTAATCTGGGGTCACCACAGTGGAATGAACTGCCAATTTATCCAGCAAATGTTTTACACATTGGATGCTTTTCCAGCTGCAACCCATCACTAGGAAACACCCATACACTCTCATAGACACTCATACACTACACTAATTTAGCCTAATCAGTTCATCTGTACCACATGTCTTTGGACTTGTGGGGGAAACCGGAGCACCAGGAGGAAACCCACGCCAACACGGAGAGAACATGCAAACTCCACACAGAAATCCAACTGACTCAGCTGCATGTAAACACTTACACATTAATATTCACTCATATTCCAACACAATAACCTGTTTTGATCTGCCATCAACACAATTGAGACATAAATTTTTTGTCAGATTTTGGAGGGAAAGCCTATCCATGGAGAATG[C/A]TACGGCAACATCTATCCTCTAGCAAAGAGTGGCCAGCAACTCATCTTCAACTTCTATGCCTTCAAAGAGAACCGACTCCCATTCAACATCAAGGTTTGAGAGATTTGAATGGCTGACTCAAATGAAATCTTACAGCTGTTAAAGATACACACTCAGAACATCAGTTGCTTGTGTACAAGGCCTTGGTTAGTCTAGCTCCACAATATTTATCTGAGCTTTTAATCCCATACACTCCTAGACGTTCTTTTCGCTTGTTTTATACTGGTCTTGTAACTGCTCAGTCAATGCGGCTAAAATTTATGGTTTGACATTCGCAATGCAGAATCCAATGCAGAGTATTTTTAAATCATCTCTTATATCATCGTACTTTTTAGGGTAGAGTTTATTTGATTTTATTCAATTTTTAGATCTTTTACTCTTATTATTATTTTATGTTTTAAATTTGTTTTTTTTTGTATTACTTTTTTTAATTATCCTTATATGGATCTTTTACTGCTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23050
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
ENSDART00000088106 Nonsense 1411 3980 35 43
Genomic Location (Zv9):
Chromosome 17 (position 20557054)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20707065
GRCz11 17 20726901
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTACGTAGGTTTCTTAATTTTGTGTTATTGCAGAATGACAAAGATCGA[C/T]GACATACCTTTGCCTCATTAGCATTGCGAAAGCGCTACAGCTATCTGGCC
Long Flanking Sequence:
AAGTGCATGACTTCCTTTTGCGTTTATCAGTAGATTTAAAGCATTGTGTTATTTTGTGGCTTGGTGGAAACTTTTTTTTTTTACACATATCTCTTTTGCAGATTTGATTTTTAATTTATTTTATTTCAAAGTGAAGCAATTAGACCGTTTCACTGGAAAATACTAACCTCTCAAACTGTTAGCGAATGGCCTTTGTGTGTCTAGTTGACCCTTCTCTCAGGAGACCCCATTTTAAAGTGAACTATAGCACAGAAAGCTTACAGAAACTGAAGCAATTCAATTATTTTACTCACTACAGCAAATTCAATTCACCACTTAATGTTTTTCTTTAAAAGATGAAGTAAAAAAAATCTTAAACAATATAGATACAATGCTTTCCATTCGGTCAAAAGAAAGTGGTAGTAGCTGGCCACTTAAAAGATCATTGCTCTACGATTTTTGTCACTTTGTTCTTACGTAGGTTTCTTAATTTTGTGTTATTGCAGAATGACAAAGATCGA[C/T]GACATACCTTTGCCTCATTAGCATTGCGAAAGCGCTACAGCTATCTGGCCGATCCAGCATCCAGTGAGTCCCTATTTTTTCTTTATTCTTAAAACATCAGCATGACATAATCACCCATTTAACATCTACCATGTACATAGGCATCTGATACAGGCATCTATGAAGGAACAATAATTTTGTACCACTATTTCCTAAAACAGAATTGCCCATATGAAATGTCTATGTATAGTCATGAATACATTTGTTCGCTTGGTTTTTTGTTGCCTTTTCTGCTTAATTATTTGTCACTCATTGTTTTACATTTCATATGATTTGCTATCACATTGTCCACTCTGTTGTGCTGTTGAATAAATCCATCATGATGTCTTGTATTATTTTTAAAAGAATTTGCTCTCTTGACAGTTCTTAATGATGAAAAACCATGGAACTCAATGTCAGTCTTTTACAACATCATTTTTTTAACGTTTTTTAAATCTAGATGACTTTTACATTAAAATGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36387
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
ENSDART00000088106 Nonsense 1951 3980 36 43
Genomic Location (Zv9):
Chromosome 17 (position 20554302)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20704313
GRCz11 17 20724149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGGATGACATTGAAGATAATCCACAAAATGAATGGAGATGCCCCCCT[C/T]GATATGAAACAGTAGCTCCTCAAGTCAAAACAAAAGCTGTATCTGACAGA
Long Flanking Sequence:
CAGAACACCAGTTTAAAAAGCTTCCAGAAGTCTCCAAATCGACAGCCGCTCTTCTGTCTCCTAGAAAGGTCATGCCCCAAGAAGTAAATGCCCAGAATCAGTCCTCTTTTGCCAGAACTCTGTCTCCTGTCAAGACTCCCCTGCACATGTCCCCAGGAACACTAAAATCTGCTACCTCTTCATCCCCTCTGTCCAACAGTCAGGAGATACTAAAAGATGTGGCTGAAATGAAGGAGGACCTTATTAGAATGTCTGCAATTTTGCAAACTGATACAAATTCAAGCTCCAAAGGTTACCATTCTGACTCTAAGGAACATAAAGTGGAGGATGAGGAGCCTTTCAAGATTGTAGAGAAAGTAAAACAGGACCTGGTCAAAGTCAGTGAAATACTTAGCAAGGATGTTTTAAGAGAGAGTAAGGCAAATATTAAAAACCACAAAAAGGACGTCCTAGAGGATGACATTGAAGATAATCCACAAAATGAATGGAGATGCCCCCCT[C/T]GATATGAAACAGTAGCTCCTCAAGTCAAAACAAAAGCTGTATCTGACAGAGATTTTAACCTTGCAAAAGTTGTTGATTATCTAACCAATGACATTGGCACAAGTTCTCTTTCTAAAATAGCAGAGGCTAAACAAAGAACTGAGGAGGCAAGGAGAGATGGAGAGGAAAAACAGAAACGTGTCCTGAAACCTGCAATGGCATTACAGGAGCACAAACTCAAAATGCCTCCAACAAATATGCGTCCCTCACCTTCTGAAAAAGAACTTTCAAAACTAGCTGATGCATTATTTGGCCCTGAAATAGCACTGGACTCTCCTGATGATGTTTCTCATGACCAAGACAAGAGTCCGCTTTCAGATAGTGGATTTGAGACCCGCAGTGAGAGGACACCCTCAGCTCCCCAAAGTGCTGAGGGGATGGGGCCCAAAGGCCTCTTTCAGGAGATTCCCCCTGTCATCACTGAAACACGCACTGAGGTTGTACATGTCATACGTAGCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36386
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
ENSDART00000088106 Nonsense 1958 3980 36 43
Genomic Location (Zv9):
Chromosome 17 (position 20554281)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20704292
GRCz11 17 20724128
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCACAAAATGAATGGAGATGCCCCCCTCGATATGAAACAGTAGCTCCT[C/T]AAGTCAAAACAAAAGCTGTATCTGACAGAGATTTTAACCTTGCAAAAGTT
Long Flanking Sequence:
TTCCAGAAGTCTCCAAATCGACAGCCGCTCTTCTGTCTCCTAGAAAGGTCATGCCCCAAGAAGTAAATGCCCAGAATCAGTCCTCTTTTGCCAGAACTCTGTCTCCTGTCAAGACTCCCCTGCACATGTCCCCAGGAACACTAAAATCTGCTACCTCTTCATCCCCTCTGTCCAACAGTCAGGAGATACTAAAAGATGTGGCTGAAATGAAGGAGGACCTTATTAGAATGTCTGCAATTTTGCAAACTGATACAAATTCAAGCTCCAAAGGTTACCATTCTGACTCTAAGGAACATAAAGTGGAGGATGAGGAGCCTTTCAAGATTGTAGAGAAAGTAAAACAGGACCTGGTCAAAGTCAGTGAAATACTTAGCAAGGATGTTTTAAGAGAGAGTAAGGCAAATATTAAAAACCACAAAAAGGACGTCCTAGAGGATGACATTGAAGATAATCCACAAAATGAATGGAGATGCCCCCCTCGATATGAAACAGTAGCTCCT[C/T]AAGTCAAAACAAAAGCTGTATCTGACAGAGATTTTAACCTTGCAAAAGTTGTTGATTATCTAACCAATGACATTGGCACAAGTTCTCTTTCTAAAATAGCAGAGGCTAAACAAAGAACTGAGGAGGCAAGGAGAGATGGAGAGGAAAAACAGAAACGTGTCCTGAAACCTGCAATGGCATTACAGGAGCACAAACTCAAAATGCCTCCAACAAATATGCGTCCCTCACCTTCTGAAAAAGAACTTTCAAAACTAGCTGATGCATTATTTGGCCCTGAAATAGCACTGGACTCTCCTGATGATGTTTCTCATGACCAAGACAAGAGTCCGCTTTCAGATAGTGGATTTGAGACCCGCAGTGAGAGGACACCCTCAGCTCCCCAAAGTGCTGAGGGGATGGGGCCCAAAGGCCTCTTTCAGGAGATTCCCCCTGTCATCACTGAAACACGCACTGAGGTTGTACATGTCATACGTAGCTATGAACCTCCTGAAGATTCTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15975
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
ENSDART00000088106 Nonsense 2505 3980 36 43
Genomic Location (Zv9):
Chromosome 17 (position 20552639)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20702650
GRCz11 17 20722486
KASP Assay ID:
2261-0912.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGAAGCATCGTAGACAARATGCAAGGGAGACTCRATCTGGGCCCAGCT[C/A]AACTTGCAGTAGCCCAGAGAGATCAGGGCATAGAAATGGSGGGAGTGGAG
Long Flanking Sequence:
TCACCAATCATTGGAATACCAAGATGATGAGTCCTCTGAAACAAGGGGAGACTCATACAAGTTTGCAGATAAAATGCTTTTGTCAGAAAAATTTGACTCTTCCCATTCAGACTCAGATGAATCTGTTATTGACCGATCTCGATACTATGGCGAGGGCACACAAGGTGGATCGATTCGAGAATTCATGCTGAAGCCTGATAGGTCACGTAGATCATCAGACGATGATTATGATAAACTCACTTTGTTGCAGTATGCTTCTGATCCTGATAGTCCAAAAAAGTCAATTTGGATGAGAGTTTCTGAGGATGGGCAGAAAAAAGGCAGAGAAAAGCAGAAATATGAGGACAGAGTAGACAGAACTGTCAAAGAGGCAGAAGAAAAACTTACTGAAGTCTCACAATTCTTTCGAGATAAAACTGAAAAACTGAATGATGAGCTTCAGTCCCCCGAGAAGAAGCATCGTAGACAAGATGCAAGGGAGACTCGATCTGGGCCCAGCT[C/A]AACTTGCAGTAGCCCAGAGAGATCAGGGCATAGAAATGGGGGGAGTGGAGAAGACTGGAGTAGAGACAGGTTTAGAGATAAGTATGGTTCTCATGATAGAAAATCCGCTAGTTTGCCTAGTAGTCCTGAAAGAAGAGTCTTGCTTCAATACAGTGATGACCCAAAAAGGGGTGACTGTTCATCTGCCAGCAGTGCCAGTGAGTCATCTAAATATTTCCAACCCTCAACATCTAAGGTTAGCTCAGTAAGAATGAAGTTTGAGTCTGAGGCCCAGAAACAAGATAAAGGGCCGCAGTGGGGACAAACTTCTGCATCTCCAGTGAGGAAGTTGCAGGAAAGTAAGCTGCCTGTTTATCAAGTTTTTGCAGGGGGGAATCTCCCTAAATCAGGAGAGTCTTCAGATAATGAAAGAAGCTCCAAAAAAGATAATGAAGGTGGGCACAGTTACAATGTTAGAAAGGCTCAAGCATTTGCCAATAATCAGCAAAGTGACAGACAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23049
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Nonsense 2919 3980 37 43
Genomic Location (Zv9):
Chromosome 17 (position 20551380)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20701391
GRCz11 17 20721227
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACACGTGGAGCCTTTTATTCTGTAAAACAGAAGCAGCCACAATCACCT[C/T]AGGGAAGCCCTGAAGATGACACGTTAGAGCAGGTAACATTTATGGACAGT
Long Flanking Sequence:
TAATCCGAGAAGACCCAAGCAATACTGAAAAATGCAATGGTGCTCTAAAAAAAAACTCGGAATCACAAATTCCTGTTAGGGTGTCATCTAGTTTTATAGATCATCATCAAAGTAGTACTTTAAAGTTAGATTCCTCCATTAAATCTGAGAGAACAGGGTCTCACAAAGCAAGAAATACACAGCACCCCAGTTCAGGTGGTACCAAATCACATAGTGATGTGTCGTCTGTAGTGAACTCAGATTCTAATAGGCAGATTGTTAATATAGTCTGTAATGGAGTGGATGAAAACCAAGTTGAGTACGTTGAAAAAGTGACCCCAGGTGCAGATATAAAACCTCTTCCTGTGTATGTCAGCATTCAAGTAGGTAAACAGTATGAGAAGGAAACCGCTACTGGGCAGCTAAGCACTTACAAAAAAGTAGTAAGCCACGAGAGCAGGACAGTACATGAAACACGTGGAGCCTTTTATTCTGTAAAACAGAAGCAGCCACAATCACCT[C/T]AGGGAAGCCCTGAAGATGACACGTTAGAGCAGGTAACATTTATGGACAGTTCAGGGAGAAGTCCTGTAACCCCTGAGACACCTACCTCTGATGAGGTCAGCTATGACCTGAACTCCAGGGCTCCTGAGCCTGTCATTGGTTCCATGGCTGGCATGCCTAGCCCAATACCAGAGGAGTCTGAGGAAGAGGAGCAGCCCAAGACATTCATTTTTAAGGAAAAACCAACAGAAAATGTCAAACCTGCCAATCATTCACCAGAATCATCAAAAAGAAAGCAAGACTCGACTGGAAAAAGGTCAAAAGACAAACGTATAGCTTACATCGAGTTTCCACCACCACCACCATTAGAGACCGAGCATGCTGACCCTGAAAAGAGGGCGTCGTGCCCTTCCTCTGAAGCAGAAACAGAGATGATAGAGGTAAACCTTCAAGAAGAACATGACAGGCATCTCCTTGCAGAACCAGTAATCAGAGTGCAGCCTCCTTCCCCTCTTCCACCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23048
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Nonsense 3588 3980 37 43
Genomic Location (Zv9):
Chromosome 17 (position 20549373)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20699384
GRCz11 17 20719220
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAAGCTCAGTTCTGTAGGGAGTCTGTGGAGAAAGCTTCTCAAAGTCAT[C/T]AGAATAAAGTAGTCTTTGAGAACAGGCAGCCAAAGTCTAGGCTCCCAGTC
Long Flanking Sequence:
CAACTGCAGATTTAACACCATCCAGAGGCAGCACAGTGCAGGGCAGTGCTGACTGCCTGGAAGCACCTCCATCCGCTGACACCACCTCATGCACTGTCACAGCCTCCAAGGTTGATCCCAAATTACGCACCCCCATTAAGATGGGCATCGCAGCTTCCATTACTATAAAGAAAGACCCTGGCTCAGCTGAACTGACTGATGTAAAAGCTGAGTCCTCAGACAGTCAGATGCCGGAATACATTAGTTTGGAGTCTCAGTTAGCCGAAAGTCACTTTGATAGCAGATGCACTACCTCTCCCACAATGGGCAGAAAAGATTACCCCTCTGAAAACTACAATAACAACAATAATTTAGAGTCATCCAATGTGCAGGCCAACTACATCCAGTGTGGAAGTGTAGTGTTCAATTTGCAGTCATCTTCTGAACCCACCTTACAGAAAGCTAGTAGAATAGAAGCTCAGTTCTGTAGGGAGTCTGTGGAGAAAGCTTCTCAAAGTCAT[C/T]AGAATAAAGTAGTCTTTGAGAACAGGCAGCCAAAGTCTAGGCTCCCAGTCAAGGCAGCTGGATTCAGTTTTAACACACACAGTTCAGGAAAGCAAAAACCTAAGCAGGTTGTGAGGCCAGAGGCAAGGAAAGTGGACCCTGTCTCCATAACACCTGAGCACAAGTCTAGAATTCCTGTCAAAGACATGAAAAAAAATTGTGCCGTTAGTTTCCAAGTAGTACCAAGATCAAGTAAGCCTGAGTCAGAGAGATCAGTCAGACCAGTAGTTCCAACTAGGCTTCCTTTCAAAGACAGGTCATCTGGTGCTTCCAGATGTTCAGTTAGTGAGGCAGGTCGAGGCAACTTTAGCGAAGTGTGCAGGCAGTCAATTGAGTTCCTAAAGAATGTTAGTGGAGAAGCAATAAAGGTGGCCGAACGACTCTCAGATGAGGAGAAACAGACACAGGGAGAGCAGTCGCAATCGGAGGAGGACAGCAGCACATCACGAAGCACCTCACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9548
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
ENSDART00000088106 Nonsense 3723 3980 38 43
Genomic Location (Zv9):
Chromosome 17 (position 20548956)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20698967
GRCz11 17 20718803
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATTGAGTTCCTAAAGAATGTTAGTGGAGAAGCAATAAAGGTGGCCGAA[C/T]GACTCTCAGATGAGGAGAAACAGACACAGGGAGAGCAGTCGCAATCGGAG
Long Flanking Sequence:
CTTCTGAACCCACCTTACAGAAAGCTAGTAGAATAGAAGCTCAGTTCTGTAGGGAGTCTGTGGAGAAAGCTTCTCAAAGTCATCAGAATAAAGTAGTCTTTGAGAACAGGCAGCCAAAGTCTAGGCTCCCAGTCAAGGCAGCTGGATTCAGTTTTAACACACACAGTTCAGGAAAGCAAAAACCTAAGCAGGTTGTGAGGCCAGAGGCAAGGAAAGTGGACCCTGTCTCCATAACACCTGAGCACAAGTCTAGAATTCCTGTCAAAGACATGAAAAAAAATTGTGCCGTTAGTTTCCAAGTAGTACCAAGATCAAGTAAGCCTGAGTCAGAGAGATCAGTCAGACCAGTAGTTCCAACTAGGCTTCCTTTCAAAGACAGGTCATCTGGTGCTTCCAGATGTTCAGTTAGTGAGGCAGGTCGAGGCAACTTTAGCGAAGTGTGCAGGCAGTCAATTGAGTTCCTAAAGAATGTTAGTGGAGAAGCAATAAAGGTGGCCGAA[C/T]GACTCTCAGATGAGGAGAAACAGACACAGGGAGAGCAGTCGCAATCGGAGGAGGACAGCAGCACATCACGAAGCACCTCACTATCGGACCCCTCTCAGTCCCAGCCCTCCCTCTCCGCTGGCTCCTCCCGAGGGGTCACACCCTCGAAGACAAAGGCCAAAAGGGCGGCGGGCAGTGAGAGGAGGAGTAAGCGGACTGGAGGAGGGAAGGAGGGCAGTAAGAACGAAGGGGCTCGCAGGTCGCCCCCCGTCGCGGAGATCAAGCCTAGTTTGTAAAACTTTATTGAAAACTTTACTTGATCCTTAGTTGCATGAGCCGTTGTGACTGATTGGATTGCCTGTGGCGTGAATAATAGCTGTCATTCTTGTCATTCTCTCATCACTGTGCTGTGTGACTGTACCGTTCTGTATCTGTCCCTGTCAGATTTCCCCTTCTCTCTCCCTTACCTTCCAGAGAAAATAATGAGGGGTGGGGCACTGAACAGTCTATCTGTGTTGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39159
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Nonsense 3886 3980 41 43
Genomic Location (Zv9):
Chromosome 17 (position 20546671)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20696682
GRCz11 17 20716518
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAACCGGATGGATATTGTGACTCTGCTGGAAGGGCCCATATTTGACTA[T/G]GGTAACATTTCAGGCACCAGAAGTTTTGCAGATGATAGCGCTGTGTGCCA
Long Flanking Sequence:
ATTTTTATTATATTTTTAAAAGTTCAAAAACCAATTCTTCAACAAATGTATATGTATAGTACATGCATATGATATATGTATATGATATATGACTTCAGATTTAAAAAGCTTTTTATACTTTCTAGTTATAATGAAATGTGTTTTATTGTTTTATAGAGCTTGCTCGAGAGATGAATTTTTCTGTGGATGAAATTAACCACATTCGCACAGAGAACCCAAACTCTCTCACAGCCCAGAGCTTCATGCTCCTTAAGAAGTGGGTCAGTCGGGATGGGAAAAACGCCACAAGTGAGAATCTTTTTTTGTGTGTCTGTCCCTCCTGCTCTGTTCTATTCAGTTATATATCATTCTTTGATTTCTTTTATAAATGCTAAAGTTACAATGAATATAAGTTACTGTTATGTTGTTGTTTTTTTCATAGCGGATGCACTGACAGCGGTCCTGACTAAAGTGAACCGGATGGATATTGTGACTCTGCTGGAAGGGCCCATATTTGACTA[T/G]GGTAACATTTCAGGCACCAGAAGTTTTGCAGATGATAGCGCTGTGTGCCAGGAAAAGGCGGATGGTAAAGTTTAGCCCCATCTAGCTGAACCCCCCACCCAAACCTCGCCCTCTCCTCCCCAACTCATTCCTTTTTTTTGTTTTCCTCTACAACCTCCCTGCAGTTTGCCAAAGTGTTAATCACAGGTGGACTATTAATAGTTTTTTTTTTGTTTACTTGAAATCTACATCCAAACATTGCCTTTGGCACATTTATAGAACATCAGATCCTTTTCTGAGGCCCTGTTTACATCCATGTCGTGTTAAATCACTCACTACTTGTTTTAAAATTTTGATTTTAAAGACTTTCTTTATTCAGAGACTCTTCATTTCTGTTACCCCCTTCCCTTCCTCCCAACACCATATGCATGGACCTGGTTTGAACATGCATGTATATGGTCATGTGATGTGAAGCAATCACAGCATGATGCTTTGCCTCAACAAGTGTAGGAAGGGCCGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36385
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088106 Nonsense 3948 3980 43 43
Genomic Location (Zv9):
Chromosome 17 (position 20539502)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 20689513
GRCz11 17 20709349
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATTTGAACCCTCTTGTAGTCAGGAGAACTCCAGCGACTCTATAACGT[C/A]ATCATCCAAAGGGGATTCAGGAAAACCTCGACAAAACGGTGAGCACCCCA
Long Flanking Sequence:
ACATTGAGACTATTTTGACTGGACTATTGCACATTTATGTTCTGCCACTGCAGCAGTTAATTCAAACATATATTTAAATAGAAATAAGTTATATTAAATGGTTATAATATTTCATAATATCATATTTGTTTAATGAAGTTAAAGGGATAGTTAGGAACCCATAAAATAAAATTTGCCATCATTTACTTACTCTTTACTTGTTCCAAACCTGTTTGACTTTCTTTCCTCTGTTGAATACAAAGGAATATTTTTTGTTTTTGAAAAAGGTGAAAATATGTAACTACTGACATTCATAGTATTTGTTTTTTCTGCAATGGAAGTCAATGGTTACATGTTTTCAGCTTTCTATAAAATATTATACTATGGATGTCAATTGTTACAGGTCTAGAAAAATGAAACTCATGAAGGATTAAAAACTACACAAGTGTGAGTATATGGTAACTAAATTGTTACATTTGAACCCTCTTGTAGTCAGGAGAACTCCAGCGACTCTATAACGT[C/A]ATCATCCAAAGGGGATTCAGGAAAACCTCGACAAAACGGTGAGCACCCCAACGTCATGCCCCGCAGCTCAGCGTCTCAGGAATCAGCCAATGATATGAAAGCAGGGGCGGGCAAGCAAGAAGGAGCTCTGATCGCTGAGCACAAAGTCCAGGTGAGATAATCTCTGGATTACAGCATATAATAGCTGATAACACTGCCGATTCAAAGTTTAGAATCAGTTTAAAGGTCCCGTGAAGTGCTTTGAAATATGTGAGATTTTATTTGATGTCTGATGTAATCTAAGCTAAAACATGAAGAAAGGGTGGGACATACATTAGCTACTCCCTTTAAAAAAGAAATCATCAGCGTTTCGTTTTTATCACAGGTCTACCAGTAAGAGTAGTTGAGGTCAGGCTCATCAAATAAAAGCAAAACAAGATGCGTCTTGATGGGGTCGAGACAGGTCAGATACTAGAGTGCATTTTGAAGAGGAACTTCTGTTTTATAGCACACTAGAGTAC
Associated Phenotype:
Not determined