Busch Lab

ZMP

COL12A1 (1 of 2)

Ensembl ID:
ENSDARG00000019601
Description:
collagen, type XII, alpha 1 [Source:HGNC Symbol;Acc:2188]
Human Orthologue:
COL12A1
Human Description:
collagen, type XII, alpha 1 [Source:HGNC Symbol;Acc:2188]
Mouse Orthologue:
Col12a1
Mouse Description:
collagen, type XII, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:88448]

Alleles

There are 29 alleles of this gene:

Allele Name Consequence Status Availability
sa32318 Essential Splice Site Available for shipment Available now
sa23815 Essential Splice Site Available for shipment Available now
sa23814 Nonsense Available for shipment Available now
sa37166 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6653 Nonsense Mutation detected in F1 DNA Not yet available
sa13062 Essential Splice Site Available for shipment Available now
sa37165 Nonsense Mutation detected in F1 DNA Not yet available
sa43540 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10128 Essential Splice Site Available for shipment Available now
sa12086 Essential Splice Site Available for shipment Available now
sa37164 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23813 Nonsense Available for shipment Available now
sa23812 Nonsense Available for shipment Available now
sa11564 Nonsense Available for shipment Available now
sa16630 Nonsense Available for shipment Available now
sa43539 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43538 Nonsense Mutation detected in F1 DNA Not yet available
sa17277 Essential Splice Site Available for shipment Available now
sa12359 Nonsense Available for shipment Available now
sa6652 Nonsense Mutation detected in F1 DNA Not yet available
sa14083 Essential Splice Site Available for shipment Available now
sa10401 Essential Splice Site Available for shipment Available now
sa19245 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa32318
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 331 3643 8 76
Genomic Location (Zv9):
Chromosome 20 (position 49972022)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49857055
GRCz11 20 49660615
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACACAACCCCACGCATTAAACATGGCTCCTTTTTCTGTTTATTTTGC[A/T]GTCGTTGAACCAGCGTCAAACTTGCAAGTCACAGAGGTCGCGTCCAAGTC
Long Flanking Sequence:
GATTCCCCAGAGTAGCTGTTGTTATCACAGACGGGAAATCTCAGGACCCCGTGGAGGGTTACGCCAAGAAGTTAAAGAACGCTGGAGTGGAACTCTTCACATTGGGTATGTGGTCGTTCATCATTGCTTATCCTGCTTTCTCACAGAACTGGGAAGCTTACTAAAAAAATCCATCTGCCCCGAAGAAATCCTTGAAAGGAATCTCATGCTCTTATTTATTATTTTCATTCAGGGATCAAAGAAGCAGATGAGGAAGAGTTAAAACAAATGTCTTCAACGCCCTACAGAACGCACGTGTACACGGTGCCAAACTTCGACATGATCAAAGCTGTGGAGAAATCATTCATCGCGCAGGTGTGCAGCAGTGTGGACGACCAGCTCAACTCGCTGGCTAGTGGAGAGGAAGGTAAACAAACAATAACAAGTGTAAACCTGCCGCAGCGGGTTTACTAAACACAACCCCACGCATTAAACATGGCTCCTTTTTCTGTTTATTTTGC[A/T]GTCGTTGAACCAGCGTCAAACTTGCAAGTCACAGAGGTCGCGTCCAAGTCAATGCGGGTGACTTGGGATGCGTCTATTGGGGAAGTGACTGGATACAAGGTGCAGATGGTTCCCATGTTGGCCGGCAGCAAGCGCCAGGAGCTGTATGTTGGGCCGACTCAGACCTCCGTGAATGTGAGGGATTTGTCTCCTGATACAGAGTATGAGATTAGCTTGTTTGCACTTAAAGGTCTGACGCCCAGCGAGGCAGTTATGGCAATGGAGAAAACTCAACCCTTGAAGGTATCATTAGGTAAGAAAGAGTCTACAACGTTGATCTTGTAATGACTGGATTGCTCATTGCGTTATAAACTGCTGAGATGCTATGAAGGTATTTGATCCGCCATCTTACTATTCCCTACTGATAGAGGGCTACAACGTCTGCGCTACAGGGATCATTCAAAAATGGCTTGCGGTACAGCTTGAAAACAAGACAAGATGTTCCCTAAAGTGTATGGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23815
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
ENSDART00000025926 Essential Splice Site 722 3643 10 76
Genomic Location (Zv9):
Chromosome 20 (position 49961907)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49847040
GRCz11 20 49650600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAAGGAGAAAGCTTTCCGCTATCAGGCTACGAGACCACACTTGACGG[T/C]ACGTGTCTGTATTATTCACATTCATTTTAGCACTTGAGTTTCTACAGAGA
Long Flanking Sequence:
TTAAGGTAGTGGTTCGGTTTAGGTATTGAATAGGGGATGTAAAATAAGATCCTGCAAAACATGCACTTTATAAGCACTAATAATCAGACAATATCTAAATAACAGACTTGTATAAAGAACTAATAGTCAGAATTGGCACTCAAACTCATTTAGTATCAACATTTCTTTATAGAAACCAAAGGAGAAAGCCTCATATCTTCAATTCTGCTTTGCCTTTCAGGTCTGGTTGCTCCCAGGTCTCTGACGTTATCAGAGGTGACTTCCAGGAGCTTCAGAGCTTCTTGGGAAATAGATGCTGTGGATGTTCAGGCCTATCTGGTGCAGTACAAACCCGACGCAGACGCAGAAGCTAGTTATACCTCGGTGTCCATTCCAGGAGACTCTACCACTACCGTTTTATATCACCTTACTCCAGTCACAAAGTACGAGGTTAAGGTTTACGCCCAATATGAGAAAGGAGAAAGCTTTCCGCTATCAGGCTACGAGACCACACTTGACGG[T/C]ACGTGTCTGTATTATTCACATTCATTTTAGCACTTGAGTTTCTACAGAGAGATCTTTATGACCTATATTTTGTGCAGAATTAGGATCTGTTACCAACCTGAAGGTTTCAGAAGAGACCAGCAGCAGTTTTCGGGTGTCGTGGAGGGAGGCTCCTGGTCCAGTGGTGCGGTATAGACTCACATACGTCCCAGTCCAAGGGGATAGTGGCTTGCTGGAAACTGCAACAGTCGGCCCTGAAACCACCATCGTTCTTCAGCAGCTTTACCCAGTTACTACCTACCGTGTCTCTGTGGCAGCTGAATACCCATCAGGCGTTGGGCCTCAAATGCAGATTGATGGAACAACCAAAGAAGGTGAGTGGAAGCATTTTAAGAATTACTTTGAAGGCATGACACTGTAGGGTTATTACAATAGGATATAAGTGTTTACATTGATCTATCCAGGGCTGAGCAATATGACAAAAATCTCATATAGAGTTAAGTGGTGTGCAGGGACGGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23814
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
ENSDART00000025926 Nonsense 1117 3643 15 76
Genomic Location (Zv9):
Chromosome 20 (position 49926540)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49811673
GRCz11 20 49615233
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGTTTCCGAGTGACGTGGGACCCCGCTCCCGGTGATGTGCGGGGATA[C/A]AAAGTCACCTTTCATCCCAGCGAAAATGATATTGATTTGGGAGAACTTCT
Long Flanking Sequence:
AAAGTCCAAACATCAGGAAGCATTTTCTTCTCAATCAAACATTAGCTTTAGGTGGCATTTAAAGGCTTAATTGTGTTAATTAGGCAAGTTAAGGTAATTAGGCAAGTCATTGTATCGCGACTGTTTGTTCTATAGGCAATCAAAAACAAATATTGCTTAAGGGAGTTTATAATATTGACCTTAGAATGGTCTTTAAAAAATTAAAAACTGCTTTTACTCTAGCCGAAAATAAAACAAAAAAGACTTTCTCCAGAAGAAAAAATATTATCGGAAATACTGTGAAAAATTCCTTACTACGTTAAACATCATTTGGGAAATATTTGAAAAAGAAAGACTAATAATTCTGACTTCTGCATTATATCGCATTAGCTGATATTCCTGCTTTCTGTTTGTCCTGCAGTGTCTCCATATAAAGCCCCAAGAAACCTACAGACCTCCGAACCCACCAAAACCAGTTTCCGAGTGACGTGGGACCCCGCTCCCGGTGATGTGCGGGGATA[C/A]AAAGTCACCTTTCATCCCAGCGAAAATGATATTGATTTGGGAGAACTTCTTGTTGGACCATACGACAACACGGTTGTCCTTGAGGAACTCAGGTAATGCTTAGAGTAAACTTCAGATGTTTCTCTCAACATGACGAGGCTAATTGTTGTTCTTGTTTTGAGTTGTCACATGTGGTTTCAGTTTGGTGTCTTTGTTTGCAGAGCTGGAACCAAATACTCCGTGGCTGTTTTTGGCATGTTTGACGGAGGTCAGAGTATGCCGCTGGCTGGAGAGGAGAAGACCACCCTCTCTGATGCACCTGATAGCCCTCCTGTTAAATACTCCGGTATAATTTTAGCACGTCATACCAAAGACATCGCATTTACAGTTTGGTTTTAGCAATCGCTTTCAGTTAAGGAAACAAAAATAGTAAAATACTAAAGTTTGGAATCAGGAGTTATAAAGAAACCCAGAAATAAAGATCACTGTATAATTTCAGCACAACATACCAAAGATTTCGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37166
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 1383 3643 20 76
Genomic Location (Zv9):
Chromosome 20 (position 49911867)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49797000
GRCz11 20 49600560
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTGTGGACGACCTCACTGAAAATCTCTGTAACAGCGTTAAAGGCCCAG[G/T]TACAGTCACACACTTGACTAGTGTACAATTGAAGTTAGAATTATTCGCCG
Long Flanking Sequence:
AATCATCGACTAAACTAACCAAATTTACTGTGTTTTTAAAGGTATGGCCTTGAACTACATCCTCCAGAACAACTTCAGGCCGAATGTGGGCATGAGACCGGATTCCCGCAAGATTGGTGTCCTTGTTACTGACGGCAAATCCCAGGATGAGATTGTAGTGAATTCACAGAGACTGCGTGACTCTGGCATTGAGCTTTACGCCATCGGTGAGTTCTTCTCTTCTTGACACTCTATATTCAGTCACAATTGAATGCAAACATCTGCACGCCGGTAAAAGCTTTTCATCCTGATCTACTGTACGTCTCATTAACCCAGCTGAAGAAATTGAGATCTTTTATTAACTTGGCTCCTAGGTGTGAAGAATGCTGATGAAAATGAGTTGCGATCCATTGCTACCGACCCTGATGAAATCCACATGTACAACGTCAACGACTTCTCCTTCCTGTTGGATATTGTGGACGACCTCACTGAAAATCTCTGTAACAGCGTTAAAGGCCCAG[G/T]TACAGTCACACACTTGACTAGTGTACAATTGAAGTTAGAATTATTCGCCGTCTCGTGAATTGTTTTCAAATCTTTCCCAAATGATGTTTAACAGAGGAAGGAATTTTTCACAGTATTTCCTATAATATTTTTTTCTTCTGGAGAAAGTCTGATTTGTTTTAGATCAGCTGAAAACTTTTTAAGTTTAAGGTCAATAATAATAGCCCCTTAAGTAATCTGTTTTAGATTGTCTACAGAACAAATCTTCGTTATATACTCTCCGGCCACTTTATTAGGTACACCTGTCCAGCTGCTTGTTAGCGCAAAGTTTTAATCAGCCAATCACATGGTAGCAACTCAATGCTCTTGACATGGTCAAGATGATCTGCTGCAGTTCAAACTTTCTTTAAATGGGAAAGAAAGGTGATTTAAGTGACTTTGAACCTTGTATGGTTGTTGGTGCCAGATGGGCTGGTCTGAGTATTTCAGAAACTGCTACTGGGATTTTCACGCAGAACCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6653
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
ENSDART00000025926 Nonsense 1452 3643 22 76
Genomic Location (Zv9):
Chromosome 20 (position 49903892)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49789025
GRCz11 20 49592585
KASP Assay ID:
554-5114.1 (used for ordering genotyping assays)
KASP Sequence:
GGYGAGGAAAACACACTTGTCCTGGTCAACCTGAACCCCATGACCGAGTA[T/A]ATCGTCAGGGTCTATGGAGTGATCGGGGAGGAGAGCAGCGAACCTTTGAA
Long Flanking Sequence:
AATTAGGCTGTGTGATAATCTGTGCAAATAATCTGGTCACCATTACTGTGCCCGTTGCTATAAAAGTCAGGTTTGATGAAGTACAACATTTGACATTTAATTTCCACATCTCTGCATACCTCTGTATAATCTTAATGACTTCAATAAAACAGGGCAGCTTTAACGTCACATTCCTTCAGAGCTATGCAGTTCTCATATATTATTGTAATGTCAACATTGTGTGCATTGGGGAAAGTCTATATGTTTTAAAGGTATTGTGTATCAGTATGAGCTGATCTAGATACCATAAATCCCACAACCTGCCCTGCGTGTTTTGAGCTGAATTCCGACCTCTTAGAAGCAGCAACTTCAGAGAGAAGATTTCAGATGGCTTCACCCCTCCGCTTGTATAATACCCCTCTCAGCAGACAATCACCGCTCTCTGATGATGTTTTGCAGCTGTTCGTTGACGGTGAGGAAAACACACTTGTCCTGGTCAACCTGAACCCCATGACCGAGTA[T/A]ATCGTCAGGGTCTATGGAGTGATCGGGGAGGAGAGCAGCGAACCTTTGAAAGGAACCGAAACCACATGTAAGTCAAGCAGATCAACCCTTCTCCTGCTGTTTATTGCAACTGTTTAGTCTCATTGTCTGAACTAAACATTAACCACTGGAAACAGCTGTTTCCCTGCACACTACAGCTGTTTTCACAGACTTGATATCTGTCGCTTTGTACATATGGAACTACCTTTAAGGAAAGACTACACTTTGTTTCAACACAGGCTCATTGTGAGAATGTACTTCCATATACATTTCTGGAGAGCGCAAATTATGTAGCCAGAGCTATCTTATTTTTAAAACTCTACAGGGCAGTAAGACGTCGTAGATGACTTCAGTTTTGTTTTCCGCTCTACCAGCTGACCGCTTACCTCGGTGTGGATGTCTTTACCGTCAGTTTGCCCAGTGGCTCGCCGCATACATCAGCAGACTTGAGACGCAGTTGACCGCAACAACGCTGTTCGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13062
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 1566 3643 24 76
Genomic Location (Zv9):
Chromosome 20 (position 49896651)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49781784
GRCz11 20 49585344
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGCAYGGAGWGGCGGCCAGCCAACCGCTCATTGACAGAGGAGTCACTC[G/A]TATGCTAGTCTTCYYAATGCTTTCWGATGGTTTCCATTTGTYATTGTCAA
Long Flanking Sequence:
TTCTTTGTTAATTTTTTTTAATTGTAATATTGGCGGCGCAGTGGGTAGTGCTGTTGCCTCACAACAAGAAGGTCGCTGGTTCGAGCCTCGGCTGGGTCAGTTGGTATTTCTGTATAGAGTTTGTATGTTGTCCCGGTGTAAAACAAAACAAACATCATGGATATCTTGTTACAATACTTTTGCATAATTCTATTTCTATTTTAAAAGTAAGTAAATTTAAATGAACTTTTAAGTCATTACAAAGGTATGTAAGCTTTGGTTGTTTTTATCTTCCAAATGTGAAAGTTGTAGCACGCAAGCTTGGATACCCTGATAGACTTACATACTGATGCCAACTTTATTTAATTTGACGTGGACTTCCCTCTTGCAGATGCGAGTCGGTGCAGATGTGAATGACGTCCAGCTACTGCAGCTGCTTCCAAACACGGCGTACTCGATCTCCCTGTTCGCCCTGCACGGAGAGGCGGCCAGCCAACCGCTCATTGACAGAGGAGTCACTC[G/A]TATGCTAGTCTTCTTAATGCTTTCAGATGGTTTCCATTTGTTATTGTCAATATGTATTATATGTGCTTGTTAATCTGTCTGTCCGATGTAGTGCCTCTCCCTCCAGCCGGTAAGTTGAAAATCACAGAAGTGACCCACAGCTCTATGCGTTTGACCTGGGATGCGGCTCCTGGGAATGTCAGGAAATACATCATCACGTACAAGCGTGAGGACGGGGAACTGAAAGAGGTGAGTGAAATGTGCAATTCGCATTCTACACAATTGATTTGGGTTGGGACAACATGAAGGATTTAAGATAGCTTATTAGCTTTTACAAATTTAAGTTGATTGAACATAAAACAATTAAGTTGTCCCCCATAAATACACCAAGAGTTGTGTTGTTTCAGCTTATTTTAAAGAAGTAGTTTGAACAATGTTTTTTGAGTGTAGTAAGATCATCAAAAGCAATGTGCTTACATTAAAATATAAATACAATGTGCTTGATGTGTTCGTAATGTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37165
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
ENSDART00000025926 Nonsense 1641 3643 26 76
Genomic Location (Zv9):
Chromosome 20 (position 49893356)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49778489
GRCz11 20 49582049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAACCTGCGCTCTCAGACCGAGTATGATGTTGCCGTCACTCCAGTTTA[C/A]GACGAGGGTTCAGGAAATCCCATGCTTGGCACTGCAATAACTGGTGAGCT
Long Flanking Sequence:
TCAGCTGCAGATGTGCATGAATGGCGGAAGAAAGTAGTTCCTAGTACAAAAGGGTTTTAGACTCTCTGTGTTAGATTTTATTTTTTTATGTACAAGACTTTGCCGTCGAACTGTTGTATAAATGCAATATCACACTCGTAGCAGTGTGCAATGGCTGTATATCAGCACTGGTGGGGCACTAAGACACTCGGCCTGCAGCCTCGTGCCCACGCACGCTGATATACAGCCATAGCACACTGCTACTCGTGTGATATTGCTCATATATTAAATATATATTCAGTGTTGGAAACATTCATTTAAAAAGTAATTAGTTAAGTAACTTATGAATTATAGCCGAGTTGGTAAGTGAATTACATCCAGGGCTTAACATTAACACCCGCCAAACGCGTTCATGTCGATTCTGTTGTTTGACAGTTGGAGGTCAACGGTGACATCACCACCATGGTTCTTACCAACCTGCGCTCTCAGACCGAGTATGATGTTGCCGTCACTCCAGTTTA[C/A]GACGAGGGTTCAGGAAATCCCATGCTTGGCACTGCAATAACTGGTGAGCTTCAAATCCGCAATTGATTCTCCGAGTCGACTCTATTGACTGATGATGTTGGTTTGGCAGCAGCGTTGCTTCACTGCTGCTGGTTTTTGTTTGTGCTACGCTGGTGTTCAACTGTGTGACTTGCTGGTTACAAGACCTGCTATTTCAGCAAGTCTTTTCAAGCTCCCCTCCGTCTGCATAATGGCTGCCATGTGTGACGCCACCCTTACCCAAGCCACGTGCATACTGTATGTTCATAACTTGACTTTATCAGTCCCACGGGTGAATCATTTATTAGTTCCAGATGATCCACAAGTAGCTCCCCTTTACATAGGAACGTGCAGTAACATTTCAGTATAGGGACCAATTTCTTATTATTAACTAGTGACTTAGTACCTGCCTATTATTAAGATTTTGGCTGATTATTAGTACTTTTAAAGCACATATTCTGCATGTTTTTATTCTATATTCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43540
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
ENSDART00000025926 Essential Splice Site 1794 3643 29 76
Genomic Location (Zv9):
Chromosome 20 (position 49883155)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49768288
GRCz11 20 49571848
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTACAAAGTCACCCACCAGCCCGTCGCTGGAGGAAAACCATTATCT[G/A]TAAGTTCAGCTGCCCCCAAATCTCCCTCCAGTGAGATCTTTTGAAGCCAG
Long Flanking Sequence:
CCCTTTAGAACAGGAGTGTCAAACTCAATTCCTGGAGGGCCGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTAGGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTTTTGGAACTGAGTTTGACACCTGTGCTCTAGAAGGACAGAAATGATTATTAACCATATTCATAATATGAAATCAGATCCTGAATCAATAACATTCCTCATGATTCCCAACCCTAATACTCTGAAAGTATGATTTTTTTCATTTTTATTTCATTTGGCTAATTGAGTTTCCGTCTGCTCCCAGTGCCCACTGGACCCCCACAAAACCTCCAGGTCTTCAACGCCACCACAACAACCCTAACTGTGAAATGGGACCACGCACCAGGCCCTGTCCAGAGCTACAAAGTCACCCACCAGCCCGTCGCTGGAGGAAAACCATTATCT[G/A]TAAGTTCAGCTGCCCCCAAATCTCCCTCCAGTGAGATCTTTTGAAGCCAGGCACGGTTAATCTTTCACTTATGATGACCATGATGAGTCGCAGGATCTGTTTTTTTGAAGTTTGAGGACCTTGTGTTAGTCATTATAGCGAGCTTGCCGCTGTAAGCGAGATGAAAACATCATGACAGGAAGTCATTACAAACAGACTCATCTCATGCAAACCATATCAACATGTCTGCCATGTAGCCCTCGCTATCAATCAACATACAAAACCATCATTGTTATATATTTAATGTGAAGTGCGCCCGAGGTGAACATCCTAGCAAACTGTTGTTGTTCGTTTAGGGATTGTTTGGCTAACAATATTCAAATTGAACAATGGGGCTGTCAGTAGTTTGTTTATTAATTGAAGATCAACTGCTGCAAAACTATCGGATTTTGTCATATTTACTAAGTAATACAAAGTTCAAATATGGAAATCTGATATATGGCCATATATAAACGCACGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10128
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 2108 3643 37 76
Genomic Location (Zv9):
Chromosome 20 (position 49867651)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49752784
GRCz11 20 49556344
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAYGCATTGCAAAAAGACGATGTTGATWKAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTWACAGATCCTACTATMAG
Long Flanking Sequence:
GTGAAGTCGAGTTAATAAAGCATTTATTAACATACATAGTAACCATTAATATATGCCTGAATAATAAGACATATAAACATTAATTTCAATAGTTTATCAATCATTTACTAACTCATTCTGAATGATCCTAAAAACCCTCAACTACTCTTAAATACAACTGTTTTGTAAATAATGCAATACTTGATTTAGTAATGAAAAATTAATCATTTACTAAGTATGAAAATACAATTATTAAGCACATTTTAAATGTGGTTATAAGTCAAGAATAGAGCATTTGATGCTGCAGTTATAAACTGCTTACTAACGTTTATTAATGTAGAGTTAATGCTTAGCGGATAATGAATTCACTATTTGCTAATGCCTAATAAATGATTTATAGTGTGTAGTTATTATAAAGTGTTACCGCATTTTCTCACACTCAAGGATCATATATAAATAAATGAAGAATGTCTGGACGCATTGCAAAAAGACGATGTTGATTGAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTTACAGATCCTACTATAAGCACCTTGAATGTACGCTGGGAGCCAGCAGAAGGCAATGTGCGGGAATACATAGTCATTTACGTTCCTGCTGGTAGTCAAGATCAAGAAGTGGTAAGAACGATTTCCGTTTTTGAAGAATTTCGAGGGGATCACATGCTTATGATTGCTTGCAGCTTCCCCTGCATTATCCAATTGATTATTCACCAACCACACGATTCCTAGGCCACTATAAGAGCCCTGGGTTTCATACCACAGGCATCTTCGTTTTGAAGAATCCCCCCTTCCACCCCTACTCCTCCTCCTCTTTCCAGATGGGTGGCACGGTGGCCCAGTGGTTAGCACTGTTGCCTCACAGCAAGAACGTCGTTGGTTCTGGTCATCATCAAAACCAGCAGACGTTTCTGTGCAGAGTTTGCACGTTCTCCCTGTGCTCGCGTGGGTTTCCCCCGGGTCACCTTTTTCCTCCCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12086
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 2108 3643 37 76
Genomic Location (Zv9):
Chromosome 20 (position 49867651)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49752784
GRCz11 20 49556344
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAYGCATTGCAAAAAGACGATGTTGATWKAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTWACAGATCCTACTATMAG
Long Flanking Sequence:
GTGAAGTCGAGTTAATAAAGCATTTATTAACATACATAGTAACCATTAATATATGCCTGAATAATAAGACATATAAACATTAATTTCAATAGTTTATCAATCATTTACTAACTCATTCTGAATGATCCTAAAAACCCTCAACTACTCTTAAATACAACTGTTTTGTAAATAATGCAATACTTGATTTAGTAATGAAAAATTAATCATTTACTAAGTATGAAAATACAATTATTAAGCACATTTTAAATGTGGTTATAAGTCAAGAATAGAGCATTTGATGCTGCAGTTATAAACTGCTTACTAACGTTTATTAATGTAGAGTTAATGCTTAGCGGATAATGAATTCACTATTTGCTAATGCCTAATAAATGATTTATAGTGTGTAGTTATTATAAAGTGTTACCGCATTTTCTCACACTCAAGGATCATATATAAATAAATGAAGAATGTCTGGACGCATTGCAAAAAGACGATGTTGATTGAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTTACAGATCCTACTATAAGCACCTTGAATGTACGCTGGGAGCCAGCAGAAGGCAATGTGCGGGAATACATAGTCATTTACGTTCCTGCTGGTAGTCAAGATCAAGAAGTGGTAAGAACGATTTCCGTTTTTGAAGAATTTCGAGGGGATCACATGCTTATGATTGCTTGCAGCTTCCCCTGCATTATCCAATTGATTATTCACCAACCACACGATTCCTAGGCCACTATAAGAGCCCTGGGTTTCATACCACAGGCATCTTCGTTTTGAAGAATCCCCCCTTCCACCCCTACTCCTCCTCCTCTTTCCAGATGGGTGGCACGGTGGCCCAGTGGTTAGCACTGTTGCCTCACAGCAAGAACGTCGTTGGTTCTGGTCATCATCAAAACCAGCAGACGTTTCTGTGCAGAGTTTGCACGTTCTCCCTGTGCTCGCGTGGGTTTCCCCCGGGTCACCTTTTTCCTCCCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37164
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 2244 3643 39 76
Genomic Location (Zv9):
Chromosome 20 (position 49863428)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49748561
GRCz11 20 49552121
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATTACAAAGTGTTCTACATCCCGCAACCAGGAGATGCTGAGATGATGG[T/A]AGGATCTGAAGAACTAACTTCTAATGGCTTATATTAAGGTCCTTCCACAT
Long Flanking Sequence:
ATTTGCTCTTCAGTGTTTGGACTCTCAGTAACGATTTTAAACCACACTGAACTGAGCTAAACTGAATTGAACCTAAACACTAAAAACTGAACTACCCTGATCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCCTCACAAATAAAGCTGAATTGAATTGAATAGAATATATTTAGACCAATAGCAAAAGTGGATTCCAACACACCCTGCATTGTGCGCTTTATACTATGAGCTTATGTTGTTAAAATGGAGCCCACAGTGTAATACATCTTCTGATAAACAAGACTACTGGCAATTACTTCTTTAACAGTGACTGAGTATCTTTGTTTTTAGAACCACTGGGTGGAGTTCGCAACCTTCAGGTTACCGATCCCACCAGCAGCACCCTAAATGTGCGATGGGAGCATGCCGACGGAAACCCACGCAATTACAAAGTGTTCTACATCCCGCAACCAGGAGATGCTGAGATGATGG[T/A]AGGATCTGAAGAACTAACTTCTAATGGCTTATATTAAGGTCCTTCCACATTATGTGAGCCTCTTTTCTGATTTGCTGTGAACAGGAACTAGTGTCCGGTGGCACGACAAGTACCGTCCTACGTAATCTCAACGCGAACACCATGTACAAGGTCACATTGTTGCCCATGTATGAAAATGATGTGGAAGGAAAACGTCAGTCAGAGAATGGAAAGACAAGTGAGTGCAGTCCTTTGCAACTTCTACATTTCAGATGGAGAACTGATCTACTGTACTTCTGAGGGATCACTGACTACATTGAGGCACAGGTTATGTGTGTTCAGGTATGTTTTTTTTATTGACGCAGAACCTTTGGGAAGTGTGAAGAACCTTCAGGTGACTGACCCGACTGTCAACTCTTTGAGAGTGAGATGGGATGCTGCAGATGGGGATGTTCGCCAATACAACGTCATTTATGTTCCTGTTGCCGGAGGTGCTGCAGGCCAGGTAATGACCTAAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23813
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
ENSDART00000025926 Nonsense 2372 3643 42 76
Genomic Location (Zv9):
Chromosome 20 (position 49862747)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49747880
GRCz11 20 49551440
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACAAGGTCACTGTAGTACCAGTATATGCAGATGCTGAAGGAAAGAGA[C/T]AGTCAGCGAATGGAAAAACAAGTGTGTACCTCTAGTCAACACTTTGAATG
Long Flanking Sequence:
GTGGAAGGAAAACGTCAGTCAGAGAATGGAAAGACAAGTGAGTGCAGTCCTTTGCAACTTCTACATTTCAGATGGAGAACTGATCTACTGTACTTCTGAGGGATCACTGACTACATTGAGGCACAGGTTATGTGTGTTCAGGTATGTTTTTTTTATTGACGCAGAACCTTTGGGAAGTGTGAAGAACCTTCAGGTGACTGACCCGACTGTCAACTCTTTGAGAGTGAGATGGGATGCTGCAGATGGGGATGTTCGCCAATACAACGTCATTTATGTTCCTGTTGCCGGAGGTGCTGCAGGCCAGGTAATGACCTAAATCTTAATCATCTCAAATTGTCATTTTAATGAGTTAGTTGCTAAATGATATGTGCTCACACTGATGTGCTCTACAGACCCAAGTGTCTGGAATGTCCACCAACACTATTCTAAGAAACCTGCAACCAAATACGGAGTACAAGGTCACTGTAGTACCAGTATATGCAGATGCTGAAGGAAAGAGA[C/T]AGTCAGCGAATGGAAAAACAAGTGTGTACCTCTAGTCAACACTTTGAATGTAATTCGTTAGCATGCAAGATACTTCATTTCAGTTTTACCAATTTTCAGAGCCTCTGGGTGGAGTGAAGAACTTGCAGGTCACCGATCCCACAACCAGCTCACTGAAGGTGCGCTGGGAGCCTGCGGAGGGAAACGTCCGACAGTACAGAATCTTCTACGTTCCAGCATCTGGTGGTGCAGAGGACATGGTAGGAGATGCTCAACAGAAGAAGCTCTACTGTAATTCTTGACAACCTTTGATCTTCTATAACCATTTCAACTTCACATCAACAGGAGCAAGTTTCTGGAGGCACCACCAACACCATACTGAGGAACCTTCTGTCAGACACAGTCTACACAGTGACGGTGGTTCCTGTTTACCCTGAGGGGGAGGGTCTCCGTCAGTCTGAAAAGGGAAAGACTCGTAAGTTGTGCTTGGAAATTATATGCATGCTTGAATGAATGCGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23812
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
ENSDART00000025926 Nonsense 2387 3643 43 76
Genomic Location (Zv9):
Chromosome 20 (position 49862623)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49747756
GRCz11 20 49551316
KASP Assay ID:
2261-4959.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTTCAGTTTTACCAATTTTCAGAGCCTCTGGGTGGAGTGAAGAACT[T/A]GCAGGTCACCGATCCCACAACCAGCTCACTGAAGGTGCGCTGGGAGCCTG
Long Flanking Sequence:
AGGTTATGTGTGTTCAGGTATGTTTTTTTTATTGACGCAGAACCTTTGGGAAGTGTGAAGAACCTTCAGGTGACTGACCCGACTGTCAACTCTTTGAGAGTGAGATGGGATGCTGCAGATGGGGATGTTCGCCAATACAACGTCATTTATGTTCCTGTTGCCGGAGGTGCTGCAGGCCAGGTAATGACCTAAATCTTAATCATCTCAAATTGTCATTTTAATGAGTTAGTTGCTAAATGATATGTGCTCACACTGATGTGCTCTACAGACCCAAGTGTCTGGAATGTCCACCAACACTATTCTAAGAAACCTGCAACCAAATACGGAGTACAAGGTCACTGTAGTACCAGTATATGCAGATGCTGAAGGAAAGAGACAGTCAGCGAATGGAAAAACAAGTGTGTACCTCTAGTCAACACTTTGAATGTAATTCGTTAGCATGCAAGATACTTCATTTCAGTTTTACCAATTTTCAGAGCCTCTGGGTGGAGTGAAGAACT[T/A]GCAGGTCACCGATCCCACAACCAGCTCACTGAAGGTGCGCTGGGAGCCTGCGGAGGGAAACGTCCGACAGTACAGAATCTTCTACGTTCCAGCATCTGGTGGTGCAGAGGACATGGTAGGAGATGCTCAACAGAAGAAGCTCTACTGTAATTCTTGACAACCTTTGATCTTCTATAACCATTTCAACTTCACATCAACAGGAGCAAGTTTCTGGAGGCACCACCAACACCATACTGAGGAACCTTCTGTCAGACACAGTCTACACAGTGACGGTGGTTCCTGTTTACCCTGAGGGGGAGGGTCTCCGTCAGTCTGAAAAGGGAAAGACTCGTAAGTTGTGCTTGGAAATTATATGCATGCTTGAATGAATGCGGAATATAAGCTCAGAATTAGCATGCAACAATAGCTATGCTTTCATCCACCTATTGTCATGTGCATTTTGGAATATTGCATACGCTATGACAACATCTTGTCACGGTTTCAGGAAGGGAATGAGAGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11564
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Nonsense 2537 3643 46 76
Genomic Location (Zv9):
Chromosome 20 (position 49852492)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49737625
GRCz11 20 49541185
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCAACCTCAACAATGCTTTCCTGGATCAGCTCGTTCCAGATACTCCGTA[T/G]TCGGTGAATGTGATGGCGGTGTATGCTGAWGGAGAAGGCCCAGGGATTGA
Long Flanking Sequence:
TGTGTGCTGACCCATATTAGTCGAACACATCAGTTTGAGCCGGAGCTAATTCTGTCATGAGCTTTAGTGTATGAAAGGAATGCAGCAGCCTCTAAATGAACACATGCACAGATGTGGTGATAATCCCGCAGGGTGTTGACAGGTTACTGATGGGGTTTCCCTGTCACCTCCGATCCAGTCTCTCTTCAGCTCTAGCCGCCCCCGAGGGAAATTACACGCATTTGACAGTATTTATGTAGCATTTAACCCTGTGAGCACATCTGTTTGCATTACTTATCTGTTTGGAAATGTTATCTAGCCCTGCTAATCTAAACATGGGGCTTAACCAGTGACGTAATTCTGTATGTTCACTTTGCCAAACTCTTAAGGGTTGTAATACAGTGGATGTTTGTAAATATATTCTCCTCCATGTTATCTAAACCACGGGCTTCTCCTCAGGTTCTCGTTCCTGGCAACCTCAACAATGCTTTCCTGGATCAGCTCGTTCCAGATACTCCGTA[T/G]TCGGTGAATGTGATGGCGGTGTATGCTGATGGAGAAGGCCCAGGGATTGACGGAAATGGAAAAACATGTGAGCTAAATGATTAAATATGATGTTTTTTGCATGTACTGTGCAAAAAAAGTTTGTTTTTTTAATTATTGTACAGTTGAAGTCAGATTAATAAGCCCCCCTGGATATTTTCCATCAATTTCGGTTTGATTAAAAGAATATTCAACCATGATATCCTTCCATGATAACTGAAAGGTGGATAAAAGCATGACTTTTTCACCTATGCTTATGTTTATAAACAATTGCTGCCATTTTTTTCTTTGTCAATAAGCCACTTAAATTGGACACACATCACAGTATGCATGAAAAGATCTTTCAATACTTTCATTTCATTGCAACTTCACAACACTCACAGCATCCACATGGCAGCACAACCACTTATAATAACTTGGCTTTCGTAAATGTTGTCTGTTTCAGTACCACGAGCTGGACCCAGGAATATGAGGGTCTTCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16630
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
ENSDART00000025926 Nonsense 2562 3643 47 76
Genomic Location (Zv9):
Chromosome 20 (position 49852023)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49737156
GRCz11 20 49540716
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCACTTATAATAACTTGGCTTTNCGTAAATGTTGTCTGTTTCARTACCA[C/T]GAGCTGGAYCCAGGAATATGAGGGTCTTCGAAAYCACCACAAGCACCRTC
Long Flanking Sequence:
TCCTGGATCAGCTCGTTCCAGATACTCCGTATTCGGTGAATGTGATGGCGGTGTATGCTGATGGAGAAGGCCCAGGGATTGACGGAAATGGAAAAACATGTGAGCTAAATGATTAAATATGATGTTTTTTGCATGTACTGTGCAAAAAAAGTTTGTTTTTTTAATTATTGTACAGTTGAAGTCAGATTAATAAGCCCCCCTGGATATTTTCCATCAATTTCGGTTTGATTAAAAGAATATTCAACCATGATATCCTTCCATGATAACTGAAAGGTGGATAAAAGCATGACTTTTTCACCTATGCTTATGTTTATAAACAATTGCTGCCATTTTTTTCTTTGTCAATAAGCCACTTAAATTGGACACACATCACAGTATGCATGAAAAGATCTTTCAATACTTTCATTTCATTGCAACTTCACAACACTCACAGCATCCACATGGCAGCACAACCACTTATAATAACTTGGCTTTCGTAAATGTTGTCTGTTTCAGTACCA[C/T]GAGCTGGACCCAGGAATATGAGGGTCTTCGAAACCACCACAAGCACCATCAGCATTGGCTGGGATCATGCGGAGGGTCCTGTACAGCAATACAAGATTTCATATGCTTCGTTGACGGGAGATCCCATCACAGAATTTGTGAGTAAAAGTCTATAGCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACACCTGCCTGTAATTATCACGTGGTGTTCAGGCCCTAATTAATAGGTTCAGGTGTGTTTGATATGGGTTGCAACTGAAATCTGAAGGAAGGTGGTTCTCCAGGAACCGGGTTGGCCACCCCTGGTCTATAGTGATTATTGCTACCGTACATTTGCACGTTTAGTTAGTTTCTAATGCAGCCCAGCTTTCAGGGAACATTTACAGAACGTTCCTTAAAAGTTGTAAATGTGATCACAGAACATTAGTACTACTTTCTACTAACTTTTCTCGAACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43539
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 2651 3643 49 76
Genomic Location (Zv9):
Chromosome 20 (position 49847607)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49732740
GRCz11 20 49536300
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACACAAGCCTCTAGCTGATATTTTGCTCTTACTTTGCATTTTCTGTTC[A/G]GTCGGTCTACTGGCACCTCAGAACCTGCGAGTCTCAGACGAGTGGTACAC
Long Flanking Sequence:
CCTTTTTACAAGTCTGATGTGCCTAAAGTGTGTATGTGAAGTTTAAGCTCAAAATACCACACAACTAATGCTTTATAACTGCCCCTTTTTGGATTTGATCTTAATTGTGGTATTTTGGTGACTGTCACTTTAAATTTAAATGAGATTGTGCGCTTTCGAAAGAGGGCGGAGTTATATGTACCTGTGCCAGCATAGTGGCAGATTCAAAAACAAGACTAACGTCCTATGCTATAGTGGGCGGGGCTTTCCCCCTCTGATGACACGTATAACAGGAGAACGTCAATCAAAGTGTTTCTGCAAACTGTTTTGATCAAATCTGATTACATTATATTATTATTTATATATTTTTACCATTTAAAGCCGGTTATATTCACAGACTGTTGCCACACAACTGTGTTAAGACAGGTACTTTTGGATAGTATGTCTCCTTTAATGCACTTCTCAGTACTATGACACAAGCCTCTAGCTGATATTTTGCTCTTACTTTGCATTTTCTGTTC[A/G]GTCGGTCTACTGGCACCTCAGAACCTGCGAGTCTCAGACGAGTGGTACACGCGCTTCCGTGTGTCCTGGGATCCTGCTCCCTCTCCAGTCATGGGCTACAAACTGGTCTACCAACCAACAAGTACGAAACATTGCAGTATTATGACTGGTAACACTTTACAATAAGGATGTATTAGTTAATATATGTATTAACATGAACAAACAATGAATAATGCATTATTACAGTATTTATTCATGTTAGGTAATGAACATATAGTCATTCATTGTCTGTTGATGTTTCTGTCACGATCACATAAAAGAAGACTTGGAACCCAACTGCAAGTAAAAATAGACTTTTAATGAAGATCTCACAAAAACAGGTAAGAAGGTGACTGGAAGTAATAAAGATCCGTGTAGAGGAAATAATCAGAATAGAGCTGGATCAGCGGCGCCGATTAAATGTTCATGATAAACATCAACAGAGAGGATCAATCATTCATCTTCGATGAAAGCAGGAAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43538
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
ENSDART00000025926 Nonsense 2660 3643 49 76
Genomic Location (Zv9):
Chromosome 20 (position 49847579)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49732712
GRCz11 20 49536272
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTACTTTGCATTTTCTGTTCAGTCGGTCTACTGGCACCTCAGAACCTG[C/T]GAGTCTCAGACGAGTGGTACACGCGCTTCCGTGTGTCCTGGGATCCTGCT
Long Flanking Sequence:
TGTGTATGTGAAGTTTAAGCTCAAAATACCACACAACTAATGCTTTATAACTGCCCCTTTTTGGATTTGATCTTAATTGTGGTATTTTGGTGACTGTCACTTTAAATTTAAATGAGATTGTGCGCTTTCGAAAGAGGGCGGAGTTATATGTACCTGTGCCAGCATAGTGGCAGATTCAAAAACAAGACTAACGTCCTATGCTATAGTGGGCGGGGCTTTCCCCCTCTGATGACACGTATAACAGGAGAACGTCAATCAAAGTGTTTCTGCAAACTGTTTTGATCAAATCTGATTACATTATATTATTATTTATATATTTTTACCATTTAAAGCCGGTTATATTCACAGACTGTTGCCACACAACTGTGTTAAGACAGGTACTTTTGGATAGTATGTCTCCTTTAATGCACTTCTCAGTACTATGACACAAGCCTCTAGCTGATATTTTGCTCTTACTTTGCATTTTCTGTTCAGTCGGTCTACTGGCACCTCAGAACCTG[C/T]GAGTCTCAGACGAGTGGTACACGCGCTTCCGTGTGTCCTGGGATCCTGCTCCCTCTCCAGTCATGGGCTACAAACTGGTCTACCAACCAACAAGTACGAAACATTGCAGTATTATGACTGGTAACACTTTACAATAAGGATGTATTAGTTAATATATGTATTAACATGAACAAACAATGAATAATGCATTATTACAGTATTTATTCATGTTAGGTAATGAACATATAGTCATTCATTGTCTGTTGATGTTTCTGTCACGATCACATAAAAGAAGACTTGGAACCCAACTGCAAGTAAAAATAGACTTTTAATGAAGATCTCACAAAAACAGGTAAGAAGGTGACTGGAAGTAATAAAGATCCGTGTAGAGGAAATAATCAGAATAGAGCTGGATCAGCGGCGCCGATTAAATGTTCATGATAAACATCAACAGAGAGGATCAATCATTCATCTTCGATGAAAGCAGGAAGCATTAAGAAACTGCAACAAGGTATCAACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17277
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
ENSDART00000025926 Essential Splice Site 2739 3643 50 76
Genomic Location (Zv9):
Chromosome 20 (position 49845028)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49730161
GRCz11 20 49533721
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAATATGATGGCGGWGTCAGCAAACCTCTCATCGGACAAGGAACAACAT[G/A]TATGTAAAGAAACAAAGCTCRTCTGATTTCATYGGACGTATCCCWTCCTC
Long Flanking Sequence:
GGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGTTGAGGTTCGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCCTCGCCCTTAGCTAATGTTAACAAGCATAAATACGTACTTTAATAATGCATTAATAAATACTGAACTATGATTAATAAAGGCAGTACATGATTTGTTAAGTATAAGTTAATATTAGTAAATACATTAACTAATGAAACCTTATTGTAAAGTGTGACCTTATGACCCAAGACACTGCAAGCCCTCATGACAATTCAATTACAATTCATCACAGCTCTTTATTTGCTAAATGTGTCTTTTTGTGTTTTTCTTTAGCTAAAGATGAATCTTTGGAGGTGTTTGTTGGTGACGTCACCAGCTATACCCTTCACAATCTGCTACCCGGAACAACGTATGACGTTCAAGTTTACGCCCAATATGATGGCGGTGTCAGCAAACCTCTCATCGGACAAGGAACAACAT[G/A]TATGTAAAGAAACAAAGCTCGTCTGATTTCATTGGACGTATCCCATCCTCTGATTCATTTCAAACACTTCCCTCAGGATATCAGAATAGGCTTTCTTTGGCAGGGACCAACAGATTTCAATTTTCATTTGGTTTTAGTGCTATCGATCAGCTGAGTTTTAATGCATTGAAAAAGATGATGTCCGCAAAATTGTTGCAAACAATTCATTTGTGGTTAATTTAAACTAACCAATTCAATTTAGTCGAACTTGATGTTCAACTTAATTTGTTTGTTTAAATTCAGCCCAAATATATTGTTTAGTAAATCCAAGGAATCACCATAGTGTGGGAAGAGGTAGCCGCTGTTTTTAGTACTATTAATGTTGTGTAATGTTCGACGTTAGTATATTGTGTGGTATAATAACCTGATCTTTCGAGGAGATGTAACTGTTTTACATTTGGTCTGTTTCGTGGCAAATTTTTATGAATTGTACGATTTTAAAAGGAGGTGTGGCACACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12359
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Nonsense 2857 3643 54 76
Genomic Location (Zv9):
Chromosome 20 (position 49833713)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49718846
GRCz11 20 49522406
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTSAGCCRTTCTGTGCYTCAYGRAGCTGTTTTGTGTGTGCTCAGTGTGC[A/T]AAGGAGCAAAGGCAGATGTGGTTTTCCTCATCGATGGCTCCTGGAGTATC
Long Flanking Sequence:
TGCTAAGCTGAGGTAAAAGTGCTCCCTCTAGACCTCGTGATCATCTGAATGGGTTCATTAATGGTAAAACTAAACCATTTAACTCAAGGGAATTGCTAATAGTCTAATCCCATTCAATAATCTATGCTAAGCTAAGCTAAATGGGCTCCCTCCAGATCAGAGATCATTGAAATGGATTCAGAAATGCTAAAACATAACTGTTTAACTCTAGTGGAGTAGTAAAATAAGCTTATTTTACAAAAAGAAGTGGAGTGTTATTTAAGACCTTCTGGATTAAACAAGTTTCTCATTCCTATGTATTTTCTCTAGAACGTGTGACTGATTATTGCAGTAATTACAACATGGAGGTTCATTAAGCTGCAGTTTTTTTCAGTAACTGTGTTTGCTAATGAGACTTCATTACCCTCTTCAGCTCTTGTGTAAAAGTTTCATTGTAAATGAATGGTTTGGCTTCAGCCGTTCTGTGCTTCATGGAGCTGTTTTGTGTGTGCTCAGTGTGC[A/T]AAGGAGCAAAGGCAGATGTGGTTTTCCTCATCGATGGCTCCTGGAGTATCGGAGATGAGAGTTTCAGTAAAGTCATCCAGTTCGTCTTCAGCGTTGTTGGTGCTTTTGACGTTATCGGACCAACAGGAATGCAGGTAACGTGCTAGCAATGGCATAACAACCTTAGCAGCTACAGTACTGGATTTTAAAGGTCCCGTGAAGTGCTTTGAAATGTTTGTTGGAGGTTTGACGAAATCTCAAATGTAAATTAAAGAGAGGGTGAGACATACACTCTCAGAAATAAAGGTAGGCGAGCTGTCACTGGGGTGGTACCTTTTCAAAAGGTACAAGTTTCTACATAAAAGGCCCATCCCTGCTGAAAAATCCAGCTTAAACCAGGCTAGGCTGCTGGTTGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGGTTTTGGCCACTTCCAGGCTGGTCTTAGCTGGTCAGGCTGGGAGATGACCAGCTAAAACCAGCTTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6652
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
ENSDART00000025926 Nonsense 2988 3643 56 76
Genomic Location (Zv9):
Chromosome 20 (position 49829818)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49714951
GRCz11 20 49518511
KASP Assay ID:
554-5399.1 (used for ordering genotyping assays)
KASP Sequence:
TAACAGATGGACGCTCYCAGGACGACGTGCATAAGAACGCTGCCAAGTTG[C/T]AGCACGCKGGTATATATGATCCACTTYCACACGTTAAAAGATGTGACAAA
Long Flanking Sequence:
AATATACATTATCTGAAAGTTAAATAGTAAAACAATTCCTTTGGGGTATAGTTTGTTGAGCTATGATAATATTTTGTTGATAGTATTTTGTAAAAATATTTATAAATCTTTAATATAATATATAATATTATATTTAGTTAATATATATTGATATATAGTTAATAGTTTAAATGTGTATTTCATATACTGTTATATACAATATATTTTGACTATTCCCACATATATACCCACACAGCATAAGATCTTGTGGTCCAGAATCAAACTTTCTTTTTTTAATCTATTTTAAATTTCTATACATTTCATGATGAGTTGGCAGCGTGAAAGTAGATGGGTTTTGCTGATGATGTTTCCTCTGTGTTGTCGCAGGAGTGGCTCTGAAGCATGTTTATGAGAAGGTCATCACTGTAGAAAATGGGATGAGAAGAAACGTGCCCAAGGTGGTGGTGGCTGTAACAGATGGACGCTCTCAGGACGACGTGCATAAGAACGCTGCCAAGTTG[C/T]AGCACGCGGGTATATATGATCCACTTCCACACGTTAAAAGATGTGACAAAAGCGTTACTAACTTTATAGTCAATTGTAAGTCGCTTTGGACAAGAGCATCTGCTAAGTGACTAAAAATAAATGTAAATGTATATTCATCAACACCTATTTAAAAAAGTCATCTCCTGAATTGCAGTATTGTGCAGAGCTTTAACAATTATTGTACAGTTGAAGGGAAAATTACAACCCAAGCTTATTCTTGAAACGTAGCCCTGCGGACGTTTTTGGAGACCGCGATTTACGTGGCCAGAGGTACGTACGGCCGCGTTTAGTTTTTTTCGAGCGTACGCTGCGGGGTGGTGTGGCGTCGCTCCGCTCCTCCTCTTCGCGCTCGCCGGTTGACGGCTCGCCTCCGAGTGGAGGGCTTTCCCGATGCAACCAGTTTGTCCGCTTAGCTCACAGCGTTGCGTCAGCGGAGCGGAGGCCCCGGAGGAGGATGAAGAGCCTGCCGCGGGGACGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14083
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
ENSDART00000025926 Essential Splice Site 3297 3643 64 76
Genomic Location (Zv9):
Chromosome 20 (position 49800960)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49686183
GRCz11 20 49490030
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACATGCACGTCAGACAGTTCTGGACCCCCGGGCCCACAGGGGCCAGTGG[T/A]AAGTCAAATAAAGGAGGAATCTTTCTTATGGACCCTTTCACAAKACTGCT
Long Flanking Sequence:
GTGACGTCACACTTAACAAGCGGATAAGTGAATTGAATGCGCTAAATTGGCTGTAGTGTATGTGTGTGAATGCGGGTGTAAATGGGTGTTTACCAGTGCTGGGTTGTGGCTGGAAGGGCATCTGCTCTGTAAAACTAATTTTGGAATAGTTGGCGGTTCATTCCGCTATGGCGACCCCAGATAAATAAAGAGACTAAGCTGAAGGAAAATATAATGATATAGAACCTCTACATTTTTGGTTTATTTGCAGCTAAAGATATCAGTCTGGTTATGTAATTGACTTCCTTTCGATTAACTGTACCTGCTGTAAAGAATTTTTTTTTTTTTCTTCGGGATTATAAGTTCACAGTTAATTTATGGTTGCCATTTGTTCTCATGTTTTGTTGTTGTTGTTTTTCTTGATGTTATTCAGAGAGATGAATCCAAGTGTCCAGCTCTTCCCAACGCATGTACATGCACGTCAGACAGTTCTGGACCCCCGGGCCCACAGGGGCCAGTGG[T/A]AAGTCAAATAAAGGAGGAATCTTTCTTATGGACCCTTTCACAAGACTGCTATGTATATTGAGATTTTTAAAAAACTTATGAACATATATATGGGTTTACCTATGTATTATATGATCTTTGCATAAAATTACAAAAAAATAAGATAAAATAAATAAATAATAATAATAATAATAATAATAATAATAATAATAATAATAGATATTCAAGGTGTTTCCAATGCAGTGTCTTTAGGGCTTTGGTGTTGTTCTCTTCTCTGGGTGCCATCGTCAGTCTCACACAATTTTTCTCTTTTTCTGAGCGTCTTGATAACACCATCGTAGAGTTTTTCTTTTATTATTTCAGCAAATAGGATTGCAAAAAGAATGATTTGTTGTACTCTCCAATTTACTGCAAGTTTATCCAGCCATGACGCTTTCCGCTACTGAGAAACCTAGAAATGTGAAAAGAGCCCATAGAGTTCATAATATTATTGAATCCTTATTGTGTGTAATGAGTTACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10401
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 3348 3643 67 76
ENSDART00000025926 Essential Splice Site 3348 3643 67 76
Genomic Location (Zv9):
Chromosome 20 (position 49791216)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49676439
GRCz11 20 49480286
KASP Assay ID:
2261-4951.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTYTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGAC
Long Flanking Sequence:
TGATTAGACAAGTCATCGTATAACGATAGTTTATTCCGTAGACAATTTAAATTTAAAAAACGAATATTGCTTTAGGGGGCTAGTAATATTCACCTTAAAATGTTTTTTTTTTTAAATTAAAATTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACCTTCTCCAGAAGCAAAAATATTATTGGAAATACTGTGCAAATTTCCTTGCTCTGTTAAACATCGTTTAGGAAATATTCTTAATATTCGAAAAAAATCACAGGAGGGCGAAGAATTTTGACTTTAACTGTGTCTCAATTATATACCAATACCTTGGCATCCTCTATACATATACTTATTTTTTCAACTTTTTTGCTTTGTTTTTAGAGTAAGAAAATCTCTCAGATCACTCATGCCTTGTTCTCTGACTTGATATATAGTTTCAATTTTGTTTTGTTCTCATTGAAGCTCCTTATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTTTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGACAGAAAGTAAGTGTTTCTCTGGAGAGCCGCCGAGTGTTAGAGGGAAACAGGAGGATTATTCCTCTCTCTGCTACCTCTCTGGACCCGCTCCATGTGGCAAACGTTAGATCATAACTCAGGAGGGGGGAATGCTGGGAGAACAACAGTTGTAGATCACGCCACCAGATAAAATGTAGGCTGTGGCTGTAATTTAACCCAGTTCCTAATCAGTGCCACTTAGTGGTTCTCCAATAAAATCGTTTTTGTTGGACTGTTTGGAGCTGGAGCTTCTCTGGAAAGGGAATTAAGTCATTGAGTTTTGGCTTGTAGAGGTAGCACGTACAATTTAAAAAGCCCTTAGTTGAATTTAATTTAAATAAAAAACTGAGTTAAGCTATTGTTTCAAAAGTGATTAGTTGATTTGATCTAATAAAAGTGAGAACTCTGCGGACCCGGTACCATCATCGACTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19245
Status:
Mutation detected in F1 DNA
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Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025926 Essential Splice Site 3348 3643 67 76
ENSDART00000025926 Essential Splice Site 3348 3643 67 76
Genomic Location (Zv9):
Chromosome 20 (position 49791216)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 49676439
GRCz11 20 49480286
KASP Assay ID:
2261-4951.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTTTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGAC
Long Flanking Sequence:
TGATTAGACAAGTCATCGTATAACGATAGTTTATTCCGTAGACAATTTAAATTTAAAAAACGAATATTGCTTTAGGGGGCTAGTAATATTCACCTTAAAATGTTTTTTTTTTTAAATTAAAATTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACCTTCTCCAGAAGCAAAAATATTATTGGAAATACTGTGCAAATTTCCTTGCTCTGTTAAACATCGTTTAGGAAATATTCTTAATATTCGAAAAAAATCACAGGAGGGCGAAGAATTTTGACTTTAACTGTGTCTCAATTATATACCAATACCTTGGCATCCTCTATACATATACTTATTTTTTCAACTTTTTTGCTTTGTTTTTAGAGTAAGAAAATCTCTCAGATCACTCATGCCTTGTTCTCTGACTTGATATATAGTTTCAATTTTGTTTTGTTCTCATTGAAGCTCCTTATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTTTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGACAGAAAGTAAGTGTTTCTCTGGAGAGCCGCCGAGTGTTAGAGGGAAACAGGAGGATTATTCCTCTCTCTGCTACCTCTCTGGACCCGCTCCATGTGGCAAACGTTAGATCATAACTCAGGAGGGGGGAATGCTGGGAGAACAACAGTTGTAGATCACGCCACCAGATAAAATGTAGGCTGTGGCTGTAATTTAACCCAGTTCCTAATCAGTGCCACTTAGTGGTTCTCCAATAAAATCGTTTTTGTTGGACTGTTTGGAGCTGGAGCTTCTCTGGAAAGGGAATTAAGTCATTGAGTTTTGGCTTGTAGAGGTAGCACGTACAATTTAAAAAGCCCTTAGTTGAATTTAATTTAAATAAAAAACTGAGTTAAGCTATTGTTTCAAAAGTGATTAGTTGATTTGATCTAATAAAAGTGAGAACTCTGCGGACCCGGTACCATCATCGACTTT
Associated Phenotype:
Not determined