Busch Lab

ZMP

ENSDARG00000007906

Ensembl ID:
ENSDARG00000007906
Human Orthologue:
LRP2
Human Description:
low density lipoprotein receptor-related protein 2 [Source:HGNC Symbol;Acc:6694]
Mouse Orthologue:
Lrp2
Mouse Description:
low density lipoprotein receptor-related protein 2 Gene [Source:MGI Symbol;Acc:MGI:95794]

Alleles

There are 22 alleles of this gene:

Allele Name Consequence Status Availability
sa9938 Essential Splice Site Available for shipment Available now
sa35239 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41996 Nonsense Mutation detected in F1 DNA Not yet available
sa9724 Nonsense Available for shipment Available now
sa41997 Nonsense Mutation detected in F1 DNA Not yet available
sa22063 Nonsense Available for shipment Available now
sa14439 Nonsense Available for shipment Available now
sa35240 Nonsense Available for shipment Available now
sa2638 Nonsense Available for shipment Available now
sa22064 Essential Splice Site Available for shipment Available now
sa38877 Nonsense Mutation detected in F1 DNA Not yet available
sa41998 Nonsense Mutation detected in F1 DNA Not yet available
sa22065 Nonsense Available for shipment Available now
sa18454 Essential Splice Site Available for shipment Available now
sa17806 Essential Splice Site Available for shipment Available now
sa44753 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa1015 Splice Site, Nonsense Available for shipment Available now
sa35241 Nonsense Mutation detected in F1 DNA Not yet available
sa30666 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9938
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Essential Splice Site 117 4409 3 73
Genomic Location (Zv9):
Chromosome 12 (position 17207378)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16087088
GRCz11 12 16135898
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGACCATGTGCCAGACTGTGTGGATAACTCTGATGAGAACAACTGCAG[T/A]ARGAACYTTTCTTCCCATTTACTATTCCTCTGTARCAATGTGGATTTTAA
Long Flanking Sequence:
GGAACAAAGGACTGCACGGACAACTCTGACGAACTCAACTGCCGTGAGTATCTCTTGATGAACACTGACCCATAATGTGATGATGTGATGTCAAAGCATTTGTTTAATGCAAATACATTTATTATTATAATTATTTACCTCGTTCTTTTAGCATTACCCACCTGTAGCTCTCAGGAGTTCAAGTGTCTGACAGGAGGAGAGTGCATTCCTCTTGAGTTTGTATGTGATGGAGAAGCAGACTGCGCTGATGGCTCTGATGAGCAAAGGACCTGTAGTATGTCTACATAATTAAAATTTGGTTAATTCCGTTAAAAATAAGAAATAATATATATAACACATATAACACAGACAGTCTATGACCCCACCTTTTTTATTTTTTAAGGTGGTCAGACGTGTAGTCCAGACCAGTTCACATGTAGAGAAGGGCAGTGTATTCCCAAACAATACAACTGTGACCATGTGCCAGACTGTGTGGATAACTCTGATGAGAACAACTGCAG[T/A]AAGAACCTTTCTTCCCATTTACTATTCCTCTGTAGCAATGTGGATTTTAAACAACAGAATGTAGTAATTATCAAATCAGGCAAGTCTAACATATTTTGTAATTATTTAATTTTATGACTGTAATGAAACTCATGACTTATAGGGGTCTTTAGTAGATATGTGCTTTGTGAATTTTTAATTACTTTCAAACATTTAAATTAGGTGTTGTTTAACTGAGCAAGCACATTTTCACAGTATTTTACAGATTTTCCCCCATTGGCCACAGAACAGGCTCTGGTTGTTGAATGACTTAATCTAACTTGCCTAATTTACACCTTGTTGTACCCTTAAGCTAAATGCTTGTATCTTGATAATTTACTTGTAATATATTATGTATACTGTCATCAGAGCAAAGACAAAAGTAATTAGCTATTAAAAAATTATTTAACTATGTTTAAAAATGTGTTGAAAACTATGTTTGCTCCATTAACCTCATGTCGTGTTCACATCCCGGCGCTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35239
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
ENSDART00000079326 Essential Splice Site 154 4409 5 73
Genomic Location (Zv9):
Chromosome 12 (position 17209889)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16089599
GRCz11 12 16138409
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTGCTGTCATTTCCTTTCATATATGTTTTTGTCCTTCATCTCTGAAAC[A/T]GCAAGGCATTGTCAGTCACATCAATTTGAATGTGCTAATGGATTCTGCAT
Long Flanking Sequence:
AATCTTTTACACCTAAACTAAATTGCAACATGTCTGTCACAAAGGTTAAAATACTGTAAAGTAACCTTTACCTTAATGGTTAAAGTAAAGTAACGTTATCTTTACAAGAAAAAAGCATATGACTACTAGCCATGGTCCAGTACACATAAAAATCTCAAGATAAATCAGCTACCAAAATGACACGAGAACACTGTTGGGTGACGTAAAATTCATTCATATTCAGATTTTGTAATTGCAATAAAATGCATCAAATTTCTTCTCATTTATTCCAGATTACCCAGCCTGCACAGAGAAGACATGTGCTAATGGCGCTTGTTACAACAATGCTCAACACTGTAATGGGATACTAGATTGTCGAGATGGATCAGATGAATCCAACTGCAGTGAGTTGTAATAGTTATTAATTAGAGATGCCAGTGAATAGAGTTAAGATGTATATTTAGGATTTTACGTTGCTGTCATTTCCTTTCATATATGTTTTTGTCCTTCATCTCTGAAAC[A/T]GCAAGGCATTGTCAGTCACATCAATTTGAATGTGCTAATGGATTCTGCATCCCAATGCCCTTTGTCTGTGATCACTGGGATGACTGTGGAGACAATAGTGATGAGCAAAACTGTGGTGGGTTCCATATTTTTTTTAACATATTCGACCAAAGCTGCTGATGTTACACTGAGATTATTTTTCAGGAAAATGAATGTTCATTAAAGGAGTCAAAATATCCTGATATGATTTAAAACTGTGTCACAAAAATGAGGTGGGACTGGATAGAAATGCATTTATTGATAATAATTATAATTTATTGATTTAGATACAAACCACTAATACAAACCACATTAATCTTTAGTAATATGTGATTTTGAAACATTGCTTTGTAAAGCTTCATAATTTTGCAAATCTTTTGTTTGAATCCCGTGATTCAATTCCAGGTAAATGGATTCACATCTCTGTATTTTTCAGTTAAATATATTCAAGTGTGATGTTTGATGATCAAATTTTGGGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41996
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
ENSDART00000079326 Nonsense 297 4409 8 73
Genomic Location (Zv9):
Chromosome 12 (position 17215198)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16094908
GRCz11 12 16143718
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACCAGTGTTCTGCTTTGAGCTGTGAGTACCGCTGTCATCCCACCCCA[C/T]AGGGAGGAGCATGCTACTGTCCTGATGGCTTCACTGTGGCCAATGATAGT
Long Flanking Sequence:
TACACTTCAACACTTTTCAAAATATGTCTCCTACTGAGCTTGGTGAGGCCTCCTGTTGAGCCAGGACCCTCCCCTGTTGGGAACCAATGAATTTAACTTTCATTAAAACATTTAAATCACAAAGCTTGCAGCAGGAAAAGTATTCACTAGAAGCCAGTATAGCTATAATGACCTGATATGCTGTGAACATGAATTTAACTGTACACTCAGTATTACTGGACAAATAAGAGTACATAATGTGTTTTATGGAGTTTTATGTGGATTGAGTTTTTACCTCAAGCACATGTGAGCAGGTGATTCACGTTTTATTATAACACAGATGATGACCGGATGGCCTTTGGTGCAAGACTCATGTCACGTTATGCATGTGACAGACATGCTGTGATTGCCCAGGTGCTTCAGATATTTACAATAGCTAACTGCCACTGGTATCTGTTTCTCGTGTAGATTTACACCAGTGTTCTGCTTTGAGCTGTGAGTACCGCTGTCATCCCACCCCA[C/T]AGGGAGGAGCATGCTACTGTCCTGATGGCTTCACTGTGGCCAATGATAGTCGCACTTGTGTGGGTAAGTGCTTTTTATTCTTTTATTATAGTTATCAATAATTTACATTTGTTTTCTTTGTTACAATCTCTGAATATTTCTGCCATGCAACTAGACATGACTATAATGACTAAATTTAAAAATGTATAATGTATTCAGGTCATTGCATATGTGGGTACATTTAAATAAACTAAACAGATCTGAACAACAGAAATGAGTCATGTCATTAACCAAAGTATGTGGTTTATTCTTAGACTATGATGACTGTAAAATTTGGGGTATCTGTGATCATTTCTGTGAGGATCGTCCAGGCACACATCATTGCAGCTGTGCTGATGGATACTTCCTGGAGCAAGGTCATGTCTGCAAGGCCAATATTTCAGGTAAGTGGAAACTAGAACTGAATATATGGTAAACATGAGTATTTATGAATACAATGTTAATTTTTTTACTTTCCTTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9724
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Nonsense 978 4409 20 73
Genomic Location (Zv9):
Chromosome 12 (position 17226140)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16105850
GRCz11 12 16154660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACACCTGCATCCAGCCGTGTGTGTGGATGTCCCTTTGGCATGAAGCTG[C/T]AGGAGAACCAGAGAGACTGTGTGAAAGATGACTCTGAGCCCCCTCCAGAT
Long Flanking Sequence:
GAAATAAGTTATTAAAACTTATTATGTTCAGAAGTGTGTTCAAAAAATCTTCTCTCCGTTAAACAGAAATTGGGGAAAAATCTTCTCTCCGTTAAACAGAAATTGGGGAAAAATCTTCTCTCCGTTAAACAGAAATTGGGGAAAAATCTTCTCTCCGTTAAACAGAAATTTATTTAATATACATAAACATTATTTCTTCATTGATGCCACAAGAGCTTTCTCACTCTGATATATTTGACTTTATGCACACCAAAGCAATATCAAAATTGATTTAGATTAATTCTCATATTACAAGTTTTTATTTAGTTTTTTTTTTAATGTTCAAAGTGATAATGAATTGCTGTGATCTGTACTGTAAAGTGATACTGTACTAAATTATTGTACTTTTTACAGTATTTAAAAGCAGATGCAATATGATTCCAAACGGACGCTGCAGCCACTTTTGTTTTCCTACACCTGCATCCAGCCGTGTGTGTGGATGTCCCTTTGGCATGAAGCTG[C/T]AGGAGAACCAGAGAGACTGTGTGAAAGATGACTCTGAGCCCCCTCCAGATGATAACTGCGGAGACTATGCCTTTCCTTGTGACGGAGGTCGCTGTGTGCCCAATACTTATCGATGTGATGGTGTAAACGACTGCGTTGACAAGACTGATGAAGTCAACTGCACTCTTCCAGGTATGTACTGTATGTACCAAAACCTTGCATAGGGGGAAACTTAACTTAAACCAAAGATTTGTAAATACACTGTTTGCAGCATCTTCAGATGAAATTATTACAGAAGTGTGAAGGGTTATTTAACCTATGACATGCATAAAAGTCACATCTCGTGCACTTAAAAGGCTACTTTTTGAATTAAACAAACTTAAATGAAGTTATTACAGTAGAAAATATAAACAATCCTTAATATAAAACAATTAAGTTCAATGCCAAACACTCAACACTAAGCTGTACCTCCCTTTGGCTTGATTTTTGACTGATGTCTTGTGCCTTGTCCTCTATCTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41997
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Nonsense 1048 4409 21 73
Genomic Location (Zv9):
Chromosome 12 (position 17227010)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16106720
GRCz11 12 16155530
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTAATCAGGTGCAACCTGCTCCCCATATGCATTCACTTGTGGTAAC[A/T]AGCACTGCATCCCTGCTAGATGGCGCTGTGATGGGCATGATGACTGTGGC
Long Flanking Sequence:
TATTACAGTAGAAAATATAAACAATCCTTAATATAAAACAATTAAGTTCAATGCCAAACACTCAACACTAAGCTGTACCTCCCTTTGGCTTGATTTTTGACTGATGTCTTGTGCCTTGTCCTCTATCTGTGGTGTAACAGAATGTACAATGTTTTTTTTTTTTTGTACAATACAAAAAAGATTCATTGACAACATTTAATTTAAACATCTCAGTTGAAATTGTTGTAGTTTAAAAATAAAACAATCAAAAACCAAAAACATGTTATATTAAATTTGAAATTATGGTCTCTGTCAAAGGTAATTTTCCCTGACCCCCTTCTTCCCCTCTCTTTCTCCTCCTGGAAGTGCCCTATTATTAACAAGTGTTCTTATTTTGGGGCATGGGCATATCTAATTTATACATTTTTTGACCTAGACTGTAACATTTTTATGAACATCTTTTTCCTCCTCTTTTTTAATCAGGTGCAACCTGCTCCCCATATGCATTCACTTGTGGTAAC[A/T]AGCACTGCATCCCTGCTAGATGGCGCTGTGATGGGCATGATGACTGTGGCGATGGATCCGACGAGACTAACTGTCCAACACGTGGTCCAACCACCTGCTCATCTAGCCAGTTTGCTTGCACCAATGGAAACTGCATCCCGAAAACGTGGGTCTGCGATGCCTTTAATGACTGTGGTGATGGTTCTGATGAGAGACATTGCAGTGAGTATTGAAGAGGAGTTTTTTAAAACAGAAGTTTAAGTTCACTCAAAAATACAAATTAGTTTTTTCCAATCCCCTGAAATCTTCATTCATTCACTCGTTCATTTTCCTTTGGGTTAGTCCCTTATTTATCAGGGGTCACCACAGTCGAATGAACCGCCAACTATTCCTGCATATGTTTTAAGCAGCGGATGCCCTTCCAGCTGCAACCCAGTACTGGGAAACACCCATACACTCATATAACTGCCAATTTAGTTAATTCAATTTACCATATAGCACATGTCTATGTACTGTGGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22063
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Nonsense 1615 4409 29 73
Genomic Location (Zv9):
Chromosome 12 (position 17236294)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16116004
GRCz11 12 16164814
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGTTGAATTTTTCACTCTGTTCTATCTGTACCTGCAGGTGCTTCAA[C/T]AACCCCATGGCATTACCATCTTCGAAGACAACATCTTCTGGAGTGACAGT
Long Flanking Sequence:
CTGGTTCTAGACCCCCGCAACCAGTATGCACTTTGGATATACATATTTATTTGTTGCTATTGTTTGTACAAAAAATAACGTTGAGATACTGCAAAAGTAGTTTTGCTGTATATAGTCATATAATAATTATATAATGATAATTCCTTTCTGTTTTCTTTTCAGTACTAATTTAATGTTCTGGTCAGACTGGGGTCAGAACCCTCGTATAGAACAGGCTAGTATGGATGGACTCGGAAGAAGAGCAATTGTGACTAGCAAAGTATACTGGCCTAATGGACTTACACTGGATTACACAACTAGAAGAGTATATTTTGTTGATGCCTACCTAAAATACATTGACTACTGTGACTATGATGGCAAAAACAGGCATCAAGTCTTTGCGAGTGACATAGTAAGAGTTCGGATCTACCTATATTTTACTATCAGATACAAGGTCACAGACTAAATTCATCTGTGTTGAATTTTTCACTCTGTTCTATCTGTACCTGCAGGTGCTTCAA[C/T]AACCCCATGGCATTACCATCTTCGAAGACAACATCTTCTGGAGTGACAGTTACACAAGCCAAATCATGAGGACTAATAAATTTCATGGGGGAAACATAACCACTCTTCTGACCGGTGTTTATCAGTGCATGGGAATTGTAATGGATCACCCCATTAAACAGCCTATAGGTTAACCTTTTATGCCAGTTCTTAATTAAAAGACGTCTTGCTGTTTTATTTGTTAGTTTTTCACTTGACTAACATAGTCTGTTGATTTCCATATAGCATTTAATCCTTGCGAGAACAATCCATGCAGTCAGCTGTGTCTGCTATCAACCTTAAGACCCAGATACTACAGATGTGACTGCCAGTCTGGCTGGATCCTTGCCAGTGATGGTCGTACTTGCACTAAAGGTACTAAAGGAGTTTTGACAAATTGACTGCACCAAACGAGTTCTACATAGCATTTTACATGACTCAACGATGCTTTTTGCCTAGATGAAACACCATTCTTGATGGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14439
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Nonsense 2105 4409 37 73
Genomic Location (Zv9):
Chromosome 12 (position 17239993)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16119703
GRCz11 12 16168513
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTCATCATACCGAGGCATTTACAGAACAAAGACGGATGGCTCACGCTA[T/G]TCTACAGTCATCAGTCAATTGGGCAATGGAAGAATTCAGGGCTTAGCGGT
Long Flanking Sequence:
AAAAGTTATCAAAATGACTTATTTTATCAAATAAATTGTTAAAGACAATAAAAATACTTTAAAATCTTTTATTTTTAATTTTTAATCACATCCATTCAATGAAAGAATATTGCAATAATTGGCAAAAAACACATTTCAAAATACTTATAATTCTACCTGCATATGTGTAAAGATTTTAACAATTCTATTAAAACATCAGAATTTCATTATTTTGTATTATGTTGTTTATAAAGGACTGATTCAATCTTGTAGGACATCAAAGGCACTTTATTGTGATAATTAACCAAATAGTATAATTAGTTGCAAGTAGGTCCTGTGATATAACATTGTGAACTGTATTGTCAACAACAAAATATCATGTACTTTCATTATGTAGATACATACTCGATTATTGACAAGCTGGACATGCACATTGCTTCTGGATTCCTGTACTGGACTGATAACAGCACCTACTCATCATACCGAGGCATTTACAGAACAAAGACGGATGGCTCACGCTA[T/G]TCTACAGTCATCAGTCAATTGGGCAATGGAAGAATTCAGGGCTTAGCGGTAGACTGGATTGCAGGTAAGTTGCAACAAATTGCAGTAAATAGTGAAATTGATGTACACCTTGAAGAATGTGGCTTTCTGTGTTTATATGTATTGAACTATTTGTTTTTTATGTCAGGAAACTTGTACTTCACTAACAAATTCACCACTCAGACATACATTGAGGTGCTACGTTTGAACACAAGCATTCAACTGATCCTCCTGAAAAGTTCAGCAGATCGTCCCCAAGATCTTGCTGTGAGCCCCAAGTTACGTCTTCTCTTCTGGACTGATGCTGGTCAGTCCCCTAAGATTGAAAGTGCTCTTTTGGATGGTACCAATCGCACAGTTCTTGCTTCTGAGAGCCTTTCATCCCCCCGAGGCCTTACAATTGATTACACCAATGACTTTCTGTACTGGGTTGATGACACACTGGATATGATTTCTCGAATGGCTCCTGATGGTTCTCAACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35240
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Nonsense 2112 4409 37 73
Genomic Location (Zv9):
Chromosome 12 (position 17240013)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16119723
GRCz11 12 16168533
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACAGAACAAAGACGGATGGCTCACGCTATTCTACAGTCATCAGTCAAT[T/A]GGGCAATGGAAGAATTCAGGGCTTAGCGGTAGACTGGATTGCAGGTAAGT
Long Flanking Sequence:
ATTTTATCAAATAAATTGTTAAAGACAATAAAAATACTTTAAAATCTTTTATTTTTAATTTTTAATCACATCCATTCAATGAAAGAATATTGCAATAATTGGCAAAAAACACATTTCAAAATACTTATAATTCTACCTGCATATGTGTAAAGATTTTAACAATTCTATTAAAACATCAGAATTTCATTATTTTGTATTATGTTGTTTATAAAGGACTGATTCAATCTTGTAGGACATCAAAGGCACTTTATTGTGATAATTAACCAAATAGTATAATTAGTTGCAAGTAGGTCCTGTGATATAACATTGTGAACTGTATTGTCAACAACAAAATATCATGTACTTTCATTATGTAGATACATACTCGATTATTGACAAGCTGGACATGCACATTGCTTCTGGATTCCTGTACTGGACTGATAACAGCACCTACTCATCATACCGAGGCATTTACAGAACAAAGACGGATGGCTCACGCTATTCTACAGTCATCAGTCAAT[T/A]GGGCAATGGAAGAATTCAGGGCTTAGCGGTAGACTGGATTGCAGGTAAGTTGCAACAAATTGCAGTAAATAGTGAAATTGATGTACACCTTGAAGAATGTGGCTTTCTGTGTTTATATGTATTGAACTATTTGTTTTTTATGTCAGGAAACTTGTACTTCACTAACAAATTCACCACTCAGACATACATTGAGGTGCTACGTTTGAACACAAGCATTCAACTGATCCTCCTGAAAAGTTCAGCAGATCGTCCCCAAGATCTTGCTGTGAGCCCCAAGTTACGTCTTCTCTTCTGGACTGATGCTGGTCAGTCCCCTAAGATTGAAAGTGCTCTTTTGGATGGTACCAATCGCACAGTTCTTGCTTCTGAGAGCCTTTCATCCCCCCGAGGCCTTACAATTGATTACACCAATGACTTTCTGTACTGGGTTGATGACACACTGGATATGATTTCTCGAATGGCTCCTGATGGTTCTCAACGGGAGATTGTACGCTTCGGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2638
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
ENSDART00000079326 Nonsense 2704 4409 42 73
Genomic Location (Zv9):
Chromosome 12 (position 17244421)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16124131
GRCz11 12 16172941
KASP Assay ID:
554-2810.1 (used for ordering genotyping assays)
KASP Sequence:
TCAAGTGTGATGGCTACAGGGACTGCCTTGATGGGTCTGATGAGCTTGAA[C/T]GAGTTTGTGGTAAGTGACTTTAGCAATTTAACAGTTGTTTCATTTAGTTT
Long Flanking Sequence:
TGTGGCTGTAAGTGTCAGCGTCAACAGGAAATGAGTGGATCCTTGCACCTGTTTGTTGTAGGAGCTGTGTCTGTGGTGTGTACTGTGGCTTCTGAGATTAGATAATAGTCCGTATTCAGTGTTAAAGGGGATCCAAACTAAGGAAAGTTATTGTATGTTGATCAGTAAAATTATAATACAACATATTAACAGTGTAAGAGTGTAAATATATACATTTTATTTTGCCATTTTACTAACTCCCAAACTTTTGGACATCATTTGCCTTTTGATAAGCTTCTCATGGTTTCATTTATGACTTAATCTCAGGTCCAGCTGGTCCAGAGTGTCAGTGTCCCAGCACTGGTAACTGGTATCTGGCCAACGAAGGGAAAGACTGCATCCCTGACAATGGGCAACGTTGTCATGCAGATCAGTTCACCTGTCTGGATGGAAGATGTTTGTCTCAGAATTTCAAGTGTGATGGCTACAGGGACTGCCTTGATGGGTCTGATGAGCTTGAA[C/T]GAGTTTGTGGTAAGTGACTTTAGCAATTTAACAGTTGTTTCATTTAGTTTGCATATGTTTTGTCTTTATTGATTAAAAATATAACCATTAATGTTTCCTCTATAGCTTTTCACACCTGTTCACCAACTGAATTCACCTGCGATAATGGAGGCTGTGTGCCTCTGTACTATGTGTGCGACTACACTAATGACTGTGGAGATAACAGCGACGAGCATGGTTGTCCCTTCCCTACTTGTAACCCTTCCACAGAATTCACCTGTGCTAACGGACGCTGCATCAGTGCAGCTTACGTGTGTGATGGGATCAATGACTGCCGAGACAATGGCACCACAGATGAAGTTAACTGCCGTGAGTACAGTTCAATCTTTTTTTTATTAATTATATATTATTTTGGTATTAAACCTAAACGCTTGATTCTGACTGGAAAAGGAACATTCTAAGGTGTGTAATTTTCTTTAGAGAGGCACACACAAAAAGAAGTTCAAGACATATCTTTTCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22064
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Essential Splice Site 2707 4409 42 73
Genomic Location (Zv9):
Chromosome 12 (position 17244432)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16124142
GRCz11 12 16172952
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTACAGGGACTGCCTTGATGGGTCTGATGAGCTTGAACGAGTTTGTGG[T/C]AAGTGACTTTAGCAATTTAACAGTTGTTTCATTTAGTTTGCATATGTTTT
Long Flanking Sequence:
GTGTCAGCGTCAACAGGAAATGAGTGGATCCTTGCACCTGTTTGTTGTAGGAGCTGTGTCTGTGGTGTGTACTGTGGCTTCTGAGATTAGATAATAGTCCGTATTCAGTGTTAAAGGGGATCCAAACTAAGGAAAGTTATTGTATGTTGATCAGTAAAATTATAATACAACATATTAACAGTGTAAGAGTGTAAATATATACATTTTATTTTGCCATTTTACTAACTCCCAAACTTTTGGACATCATTTGCCTTTTGATAAGCTTCTCATGGTTTCATTTATGACTTAATCTCAGGTCCAGCTGGTCCAGAGTGTCAGTGTCCCAGCACTGGTAACTGGTATCTGGCCAACGAAGGGAAAGACTGCATCCCTGACAATGGGCAACGTTGTCATGCAGATCAGTTCACCTGTCTGGATGGAAGATGTTTGTCTCAGAATTTCAAGTGTGATGGCTACAGGGACTGCCTTGATGGGTCTGATGAGCTTGAACGAGTTTGTGG[T/C]AAGTGACTTTAGCAATTTAACAGTTGTTTCATTTAGTTTGCATATGTTTTGTCTTTATTGATTAAAAATATAACCATTAATGTTTCCTCTATAGCTTTTCACACCTGTTCACCAACTGAATTCACCTGCGATAATGGAGGCTGTGTGCCTCTGTACTATGTGTGCGACTACACTAATGACTGTGGAGATAACAGCGACGAGCATGGTTGTCCCTTCCCTACTTGTAACCCTTCCACAGAATTCACCTGTGCTAACGGACGCTGCATCAGTGCAGCTTACGTGTGTGATGGGATCAATGACTGCCGAGACAATGGCACCACAGATGAAGTTAACTGCCGTGAGTACAGTTCAATCTTTTTTTTATTAATTATATATTATTTTGGTATTAAACCTAAACGCTTGATTCTGACTGGAAAAGGAACATTCTAAGGTGTGTAATTTTCTTTAGAGAGGCACACACAAAAAGAAGTTCAAGACATATCTTTTCCGCATTACTTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38877
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
ENSDART00000079326 Nonsense 2750 4409 43 73
Genomic Location (Zv9):
Chromosome 12 (position 17244657)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16124367
GRCz11 12 16173177
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGACTGTGGAGATAACAGCGACGAGCATGGTTGTCCCTTCCCTACTTG[T/A]AACCCTTCCACAGAATTCACCTGTGCTAACGGACGCTGCATCAGTGCAGC
Long Flanking Sequence:
CTCCCAAACTTTTGGACATCATTTGCCTTTTGATAAGCTTCTCATGGTTTCATTTATGACTTAATCTCAGGTCCAGCTGGTCCAGAGTGTCAGTGTCCCAGCACTGGTAACTGGTATCTGGCCAACGAAGGGAAAGACTGCATCCCTGACAATGGGCAACGTTGTCATGCAGATCAGTTCACCTGTCTGGATGGAAGATGTTTGTCTCAGAATTTCAAGTGTGATGGCTACAGGGACTGCCTTGATGGGTCTGATGAGCTTGAACGAGTTTGTGGTAAGTGACTTTAGCAATTTAACAGTTGTTTCATTTAGTTTGCATATGTTTTGTCTTTATTGATTAAAAATATAACCATTAATGTTTCCTCTATAGCTTTTCACACCTGTTCACCAACTGAATTCACCTGCGATAATGGAGGCTGTGTGCCTCTGTACTATGTGTGCGACTACACTAATGACTGTGGAGATAACAGCGACGAGCATGGTTGTCCCTTCCCTACTTG[T/A]AACCCTTCCACAGAATTCACCTGTGCTAACGGACGCTGCATCAGTGCAGCTTACGTGTGTGATGGGATCAATGACTGCCGAGACAATGGCACCACAGATGAAGTTAACTGCCGTGAGTACAGTTCAATCTTTTTTTTATTAATTATATATTATTTTGGTATTAAACCTAAACGCTTGATTCTGACTGGAAAAGGAACATTCTAAGGTGTGTAATTTTCTTTAGAGAGGCACACACAAAAAGAAGTTCAAGACATATCTTTTCCGCATTACTTAGAGAAATTAATTTATACCACCTGTGATGGGCGACACAGTGACGTAGTAGGCAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCAAGCCTCGGCTGGGTCAGTTGGCGTTTCTGTGTGGAGTTTGTACCACTCCGGGTACTCTAGTTTCGCCCACAAGTCCTAAGACATGCGTTACAGGTAAATTGGGTAGGCTAAATTGTCTGTAGTGTATGTGTGTGAATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41998
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
ENSDART00000079326 Nonsense 2796 4409 44 73
Genomic Location (Zv9):
Chromosome 12 (position 17247377)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16127087
GRCz11 12 16175897
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAACATATTTCATCTAATTTATTAGCGGATCGAACCTGTGCACCTGGCT[T/A]AGTGAAATGTGACACCACCAACATCTGCATTCCTTCGAGCAGCCTGTGTG
Long Flanking Sequence:
GATAAAAATCTGACAAATATCTTAGAATAAGAATAAATTAAATATCTCGTCATCAAGTATATGGTTCTTTTTGTGTTAATTAATATTTTGGACTAGCATTAATCTTTATATTTTACAAGTTTTGTCACTTACTGTATTGTCACTTAATAATGCTATTTGGCTTGTCATTTGTGTATATTTTGTATTATTGTATTTTTGTTAAATCATACCGATGTAATTTGAGGTCAAATAAGGAAAAAGCTTTTTTTTTTTCATTTAAAATGTATGTTATTTGAGTAGTATATATACAGTAGTGTGCTTTACCATAGGACAAAAGTAACAAAGTGGCTTTTCTTGAAGCCCTGGCAACGTTTAATGTCCAGGCTAAAAAAAAAAAAAAAAAAAAAAAAATCTTTTATAATTAGGTTTTTATGAAAAATGTTACTTTTGTTCCCGCTCTCTCCTGTGTATTTAACATATTTCATCTAATTTATTAGCGGATCGAACCTGTGCACCTGGCT[T/A]AGTGAAATGTGACACCACCAACATCTGCATTCCTTCGAGCAGCCTGTGTGATGGCCATAACAACTGTGGGGATAACAGTGATGAAAATCCACTCTTTTGTGGTGAGTTACAAATTCTCTATTGTTTGCAGACTTCATGATGACAGAAGGTTCAACTCTGATTCAATATTCTCTTTAACATGTCCTGTGCTGTCTGTGGTCAACAGCTGGACGAACGTGCTCTGCAGATGAGTTCCGCTGTGATAGTGGGAAGTGTATTCCCCAGTTTTGGGTGTGTGATCGCATCTCAGATTGTTTGGATGGCACAGATGAGCCTCCCACTTGCGGTACATGTTCCACTTACTTAAATCTGGAAAGTGATGACTGGACTCACTGTTTAATACTCCTCCTTTTTTTTATTTCACAGAGGATCACATTTATACTTGTAGCCCTCAGCAGTTCAACTGCGCGAATGGAAACTGTATTCAGCAATCATGGGTATGTGATGGCAACAATGACTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22065
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Nonsense 3369 4409 52 73
Genomic Location (Zv9):
Chromosome 12 (position 17256406)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16136116
GRCz11 12 16184926
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTAATATTTGTTTTGCTACAGTTATGCTGATATGGATGGTCAAAAC[A/T]GACACAGAGCTATAACAGGCTCCTTGCCCCATGCTTACGCTCTGACTCTG
Long Flanking Sequence:
AAAAAAACTTTTTAAACTAATTAATTTTAAATAAAACCAGTGTTGCTATGGTAGAATAATGTCTGCTTTCCAAATAAATAAATTCTGTCATAATTTGGAAAAATCTTTGAGTCAATTCAGCTGCCCTTAGAAGCTCTGGTTCCCATGTAGACTTGACACTTTCACATTGACTGACCCAAAACACTTTTTATGTAATTTAAGCATAAGAAATAGCATTTATTAGGCAGTTAATGTCAATTATTATGTTCATCAGAAAATTTCTGATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTAGCGATTTTACTTTTCCCTCATTCAAATTGGTCTTGTATGCTGTTAATAGCTGTCCAGAGACAGTGCAATTGTAGCCTTGTTTAACCTTAATATGTTATGTGTTGTGTATTCTTAAAAGCTGTTCTTCTAATATTTGTTTTGCTACAGTTATGCTGATATGGATGGTCAAAAC[A/T]GACACAGAGCTATAACAGGCTCCTTGCCCCATGCTTACGCTCTGACTCTGTTTGAGGATTTGGTGTACTGGACTGACTGGAATACCCACACCATAGAGCGAGCTCACAAGTACACAGGCGCTAACCGTGTTGTAATGGGCAACAACACACATCGCCCTAATGACATTCATATCTATCACCCTTACAGACAGCCACACAGTAAGACAGCATATTATTTAGTTCACCATTAACTTCAATTGTTTGATAGCTGTTTGGATAATTAATTAATATATTCTTAGGTGAAAATCCATGCAATGACCATTACCTGACCTGTAGTCACCTGTGTCTGATTGGTCCGGGTGGGACGGAGGCCAGATGTGAATGTCCGGACCACTTCATTGGTCTGGCTATCGGATTTAAGATTCAGTGTGTGGCCGACTGCTCCAGCACTCAGTTCCGCTGTGGAGACAATGAGAAGTATGTGAATTAATTATCTCATGATTTCCCAGGGTATTTAATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18454
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
ENSDART00000079326 Essential Splice Site 3435 4409 52 73
Genomic Location (Zv9):
Chromosome 12 (position 17256606)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16136316
GRCz11 12 16185126
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCGCCCTAATGACATTCATAYCTATCACCCYTACAGACAGCCACACAG[T/A]AAGACAGCATATTATTTAKTTCACYATTAACTTCAATTGTTTGATAGCTG
Long Flanking Sequence:
GCATAAGAAATAGCATTTATTAGGCAGTTAATGTCAATTATTATGTTCATCAGAAAATTTCTGATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTAGCGATTTTACTTTTCCCTCATTCAAATTGGTCTTGTATGCTGTTAATAGCTGTCCAGAGACAGTGCAATTGTAGCCTTGTTTAACCTTAATATGTTATGTGTTGTGTATTCTTAAAAGCTGTTCTTCTAATATTTGTTTTGCTACAGTTATGCTGATATGGATGGTCAAAACAGACACAGAGCTATAACAGGCTCCTTGCCCCATGCTTACGCTCTGACTCTGTTTGAGGATTTGGTGTACTGGACTGACTGGAATACCCACACCATAGAGCGAGCTCACAAGTACACAGGCGCTAACCGTGTTGTAATGGGCAACAACACACATCGCCCTAATGACATTCATATCTATCACCCTTACAGACAGCCACACAG[T/A]AAGACAGCATATTATTTAGTTCACCATTAACTTCAATTGTTTGATAGCTGTTTGGATAATTAATTAATATATTCTTAGGTGAAAATCCATGCAATGACCATTACCTGACCTGTAGTCACCTGTGTCTGATTGGTCCGGGTGGGACGGAGGCCAGATGTGAATGTCCGGACCACTTCATTGGTCTGGCTATCGGATTTAAGATTCAGTGTGTGGCCGACTGCTCCAGCACTCAGTTCCGCTGTGGAGACAATGAGAAGTATGTGAATTAATTATCTCATGATTTCCCAGGGTATTTAATTAATCTTATAAAAATGCTAGTGTAAGAATGGTGTTTTAACTACTGCGGTTCCAACTGTAATTCTTCCGAATGACTAAAAAGTAATCAGTATGATGGTGAAAAACTGTACATTTCTAGTCAAACCATGCTTCTGGAATTAATAGCTTAAAATGTGGGAGAGTGTTGCTATTAAGTGATTGTTTTGTATTGGAATATGGAGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17806
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Essential Splice Site 3494 4409 53 73
Genomic Location (Zv9):
Chromosome 12 (position 17256863)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16136573
GRCz11 12 16185383
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGGCCGACTGCTCCAGCACTCAGTTCCGCTGTGGAGACAATGAGAA[G/T]TATGTGAATTMATTMTCTCATGATTTCCCAGGGTATTTAATTAATCTWAT
Long Flanking Sequence:
ATATTTGTTTTGCTACAGTTATGCTGATATGGATGGTCAAAACAGACACAGAGCTATAACAGGCTCCTTGCCCCATGCTTACGCTCTGACTCTGTTTGAGGATTTGGTGTACTGGACTGACTGGAATACCCACACCATAGAGCGAGCTCACAAGTACACAGGCGCTAACCGTGTTGTAATGGGCAACAACACACATCGCCCTAATGACATTCATATCTATCACCCTTACAGACAGCCACACAGTAAGACAGCATATTATTTAGTTCACCATTAACTTCAATTGTTTGATAGCTGTTTGGATAATTAATTAATATATTCTTAGGTGAAAATCCATGCAATGACCATTACCTGACCTGTAGTCACCTGTGTCTGATTGGTCCGGGTGGGACGGAGGCCAGATGTGAATGTCCGGACCACTTCATTGGTCTGGCTATCGGATTTAAGATTCAGTGTGTGGCCGACTGCTCCAGCACTCAGTTCCGCTGTGGAGACAATGAGAA[G/T]TATGTGAATTAATTATCTCATGATTTCCCAGGGTATTTAATTAATCTTATAAAAATGCTAGTGTAAGAATGGTGTTTTAACTACTGCGGTTCCAACTGTAATTCTTCCGAATGACTAAAAAGTAATCAGTATGATGGTGAAAAACTGTACATTTCTAGTCAAACCATGCTTCTGGAATTAATAGCTTAAAATGTGGGAGAGTGTTGCTATTAAGTGATTGTTTTGTATTGGAATATGGAGCAATTAAGTGTTGATGTTAAATCAAAAGTCATTCACAAATACTTGAAAATGAAATGGTTTGATGACAATAATTATCTATGGTTACAACTGAATTAATTACAAAATAACAGTATAAAATAATTAAATATGAAGTGATAAAAACATGCAATAATAATTGTACTCGGCTTGAATGTAAAATAAAGTTACCAGAGAGGGAAGAAGAGTCTAAGCCTGATAGTAGTACAGCCAGATAAGATCTGGAGTGGTGCAGAACTGGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44753
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
ENSDART00000079326 Essential Splice Site 3494 4409 54 73
Genomic Location (Zv9):
Chromosome 12 (position 17260977)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16140687
GRCz11 12 16189497
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTGGCACACAAGATGATATTTTAAGATGTCTCTGCCTTTTGTCTCC[A/T]GGTGCATTCCTATATGGTGGAAGTGTGATGGCCAGTCAGATTGTGGTGAT
Long Flanking Sequence:
ATTGAGCTTACATTTCACCCTTTGAAGACAAAACTGAAAGGAAAATGCCCCAAGAGCAGGAACTGAAGGCAGTTGCTGTAGAGGCCTGGCAGAGCACCACCAGGAATGAAACCCAGTGTCTGGTGATGTTGTGTGTTCCAGACTTCAGGCTGTAATTGACTGCAAAGGATTTGTAACCAAGTTTGATTTATTTTGATTATTTTGTCCAATAACTTTTAGACTCTTAACAAGTGGGAGGCACATATGCAAACTACTGTAATTCCTACAGGGTTTACCTGATTTAGGTATGCCATAAATACCCTTAAATTAAAGCTGACAGTCTGCAGTTAAAATACATCTTGTTTGTTTTTTATTTCAAATCCATTGTGTTGGTGTATAGAGCCAAAAATATTTATGGGCTTAACTGTATTATGAGAAAATGTATTTCAATTAGTTTTGCTTTAATGTGAATATTTTGGCACACAAGATGATATTTTAAGATGTCTCTGCCTTTTGTCTCC[A/T]GGTGCATTCCTATATGGTGGAAGTGTGATGGCCAGTCAGATTGTGGTGATGGCTCTGATGAGCCTCAGACGTGTCCTCCACATTACTGCAAAACTGGGCAGTTTCAGTGCCAGGATGGGAACTGCACTAACCCATTTTTCCTATGTGATGGCCACAAGGATTGCTTTGATGGATCTGATGAAGACGCTGCACTTTGCAGTATGAAACACTTAGAGTCTAGAATATCTCAACCAAGGGTGTGTTATACTGTAGTAGGGGCTTTCTCTTAAAAGGAATGTTTTTATAGTCCTTTGGACTACTGCTCTACATTCTTTCTCTGTTATTATAAAATTTATGATACAGCTTCGATCACAGCACCATCCTTCTTTCAGTGGTTAATTTGCTGAATGCCACATTTGATGTCACATCTGTCAATGTCACCTAGTTCCTACCAGGAAAATGTCCTGACGAAACATTCTGTTTTTGGGAGTGGCTAGCTTCCTGTAACTGAATTCTAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1015
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079326 Splice Site, Nonsense 3684 4409 56 73
Genomic Location (Zv9):
Chromosome 12 (position 17262033)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16141743
GRCz11 12 16190553
KASP Assay ID:
554-0919.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTGTGATGGCACCAATGATTGTCTAGACAACAGTGATGAGAACACCTG[T/A]CGTGAGTCCTATAGAATGATTTCAATTGATTCAAAAAAGGTTGGACAGAA
Long Flanking Sequence:
TTCTTGGATTAACAGTTGTTTCTCTAAAAACTTCTTTCATTATCCAGGTGACCACCGTTGCACTGAGAACCAGTTCCAGTGTAAAAATAAGCATTGTATTCCCATAACTTGGCACTGTGATGGTGTGGTGGACTGTTCAGATGGCAGTGATGAGGAAACGGACAGTTGCATAGACAAGACCTGTAAACCTGGACAGTTTCAATGCAAAAAAGGAGGCTGCATACCACAAAGTTATGTGTGTGATGCACAGAACGACTGTGGAGATAATTCAGATGAGCCATATGAAGTGTGCAGTGAGTGTCTCTTTAGAAAAAATTACTTTTCTTTAGCTACTTGGAGTTAACTGATCTTTTTTCTCAATCTGTTTTTGTAGTGGGTCCTGACTATAAGTGTGATCCAGACACCGAGTTCCCCTGCAAAGGAAACTATCGTTGTATACCTCTATGGGCTGTGTGTGATGGCACCAATGATTGTCTAGACAACAGTGATGAGAACACCTG[T/A]CGTGAGTCCTATAGAATGATTTCAATTGATTCAAAAAAGGTTGGACAGAAACATTAACAGAAACAAATACAGAAATGAACATCTAAAGAAGAAGAATACGAACTATACTCTACGAACATACCTTCAAATGTTTTCTTGTTAACGGGATAGTTCACACAAAAATGAAAAATTACTCACTATTTTCTCACCCTGAAGTGGTTTAAAACCTTTGAGTGTCTTTACTCTGTTGAACACAGAAGAAAATATTTTGAAGAAAGTTCAAACCTGTATCCATTGACTTCCATAGTAGGGAAAACTAATTTAATGTTTACAGATGGCTTTTTAAAATATCTGCTATTGTGTTCAGTAGGATAAAGAATCTCTGTTTGAAACAAGTAAAGGGTGAGTATATAATGGCAGAATTTTCAGTTTGGTTGAACTATTTGTTTAATCAACAGGGCTTGACCTTAACACCCACCATCCCGCCAAATAGGGGTAGATTTTAGCTGTGGCGGGCTAGA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa35241
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
ENSDART00000079326 Nonsense 3965 4409 63 73
Genomic Location (Zv9):
Chromosome 12 (position 17267130)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16146840
GRCz11 12 16195650
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACAAACCTGAATGGCACTGGCTTTATCTGTTCTTGTCGTCCTGGCTA[T/A]GCAGTAGATCCTGATAACACCTTTCTTTGCAACGGTACACACAAATGCAC
Long Flanking Sequence:
TACAAACACTCAAAGCTTCCTGAATATACTGTTGTGTAATACATTTAAATATTTATAGTATATACAATAAATATAAATATATAAAACTATATAAAAATAAATAAAATTATATATAGTGCTCTGGTGCTTCATAGAGCATGACAGTATGATTGTTTTGTTTAAATCAGGCCAAGAACCCACTCTCGCCCCCTGCACACCAAATGAGTTTAAATGCTCAAATGGCCACTGTGTTCCTCTGCCTTACGTGTGCGACCACAATAACAACTGTGGAGACCTAACTGATGAGCTGGGCTGCAGTAAGCCAACAAATACCCTATTTCATCATTATTTTTCTTAAAATAGAACTCTAAAGTAACTGCATTAGATTTCGTCTGTCAGGTTGCTGATGAGCTCATCTTTTCAGATTTTGGCCATGATCGCAACTGTGATGAGAAGTTATGCAAGCATGAGTGTACAAACCTGAATGGCACTGGCTTTATCTGTTCTTGTCGTCCTGGCTA[T/A]GCAGTAGATCCTGATAACACCTTTCTTTGCAACGGTACACACAAATGCACATCTCGCATCTGATTGGAGAATATTTCTTTTGCTGAAAGAATGAATTTCAAAGTCTCTGAATATAATGTAACACTTAATGCATTTACATCTTATTCTTACTTCGGTTGGTGATTCATTTGACTCTAAGCCTATGTCTATTGTGCTCCCTACAGATATAGATGAGTGTTTAGAATATGGCACATGCCCACAAGCCTGCATGAACACTAAAGGAAGCTATCACTGTGATTGTGCCCAGGGCTACAGGAAAGCTGGCACAGGCAATCAGTGTGAGGCCGAAGGTAGGACAGAAATTTCAAAGTACAAAGTCAAGACATTTTGGAAATGTATATCATCCTAAATCATCTTTTTCTTAGGTCCTGGACCACTGCTTCTGTTGCCAGAGAACATTCGCATTCGCCGATACAATCTTCAGACAGAGGAGTATCATGACTTCTTGCAGGAAGAGGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30666
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
ENSDART00000079326 Essential Splice Site 4165 4409 67 73
Genomic Location (Zv9):
Chromosome 12 (position 17269163)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 16148873
GRCz11 12 16197683
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACTGACCTGGAAGCACCTAATTCTGTGGCATTGAACCCTCGCTTGGG[G/A]TGAGATTTACTTGCTCTTACTGTCTGTTTAAAGGGAAAGTTCACTCCTAA
Long Flanking Sequence:
CACTTTGAATGTAAAATAATGAATAATGATTTATTTGTGCTTAATATGTGACTCCTCTGGTGTGTTTTAGGTGTGGTGTATTTTACAGTAGAAGGGAGGGGTGCATTGCCTGGTGCTATTAAAAGAGCTTTTCTGCCAGATGTGGATGATCATAATAATAACATTGCTGCAGCTGTGGAGCTGGATATAAAGTACATCACTAAGCCTTATGGAATTGCAGTGGACTGGGTTGGCAGGTAAAGCAATCACAGTACATTTTAAATAATATTTGCCAAAAAAAAACATAACTTACTTGAATAAAACTGAAAAATAATAAATAGGTTTGTGTTAATGAGTCAGTAATAGCTCATGAGACTTTATTATTCTTGTAGGAATTTGTATTGGGCTGATGCACAGCTGAAGCGTCTAGAAGTGGCCATGTTAGATGGCCGTTACAGGAAGCACCTGATTAAAACTGACCTGGAAGCACCTAATTCTGTGGCATTGAACCCTCGCTTGGG[G/A]TGAGATTTACTTGCTCTTACTGTCTGTTTAAAGGGAAAGTTCACTCCTAAAAGAAAACAATCTGACATTATCTTCATGCCATTCTATATCCATACAATTAAGCAATTACATTTTCTCTGCAACGTACCTAAATCTCCAAAAGGAAGCAGATCGTAAAATGAAAAAAAATGATCACCATGTATGTTGGAGCTGTACATTTAAATACCAATATTTTCACTTTTTGTCATCATGTGGTCCAGCATGCTTTACTGGATTGACAATGGAAACACACCTCGTATTGAATGCTCCTGGTTGGATGGTCAAGAGAGAAAGGTTCTGGTAAACAATGGTTTGGGATGGCCAACGGGCCTGTCGATTGACTTCACAAATGGTGACCGGATTTATTGGTCAGATGCAAAAGAGAGTCGCATTGAGTCCATCCTGCCAGATGGACAGAACAGAAAGACATCGGTTTTCATAGGTAAGAGTTTGATGATTTACTCACTTAAAATATGAGTAGA
Associated Phenotype:
Not determined