Busch Lab

ZMP

mll3b

Ensembl ID:
ENSDARG00000075560
ZFIN ID:
ZDB-GENE-070705-340
Description:
Novel protein similar to human and mouse myeloid/lymphoid or mixed-lineage leukemia 3 (MLL3) [Source
Human Orthologue:
MLL3
Human Description:
myeloid/lymphoid or mixed-lineage leukemia 3 [Source:HGNC Symbol;Acc:13726]
Mouse Orthologue:
Mll3
Mouse Description:
myeloid/lymphoid or mixed-lineage leukemia 3 Gene [Source:MGI Symbol;Acc:MGI:2444959]

Alleles

There are 23 alleles of this gene:

Allele Name Consequence Status Availability
sa5126 Essential Splice Site F2 line generated Not yet available
sa11689 Nonsense Available for shipment Available now
sa32861 Nonsense Mutation detected in F1 DNA Not yet available
sa19694 Nonsense Available for shipment Available now
sa39784 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25777 Nonsense Mutation detected in F1 DNA Not yet available
sa38316 Nonsense Mutation detected in F1 DNA Not yet available
sa39785 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa5127 Nonsense F2 line generated Not yet available
sa6827 Nonsense Mutation detected in F1 DNA Not yet available
sa38317 Nonsense Mutation detected in F1 DNA Not yet available
sa17591 Nonsense Available for shipment Available now
sa39786 Nonsense Mutation detected in F1 DNA Not yet available
sa15663 Nonsense Available for shipment Available now
sa10821 Nonsense Available for shipment Available now
sa25101 Nonsense Mutation detected in F1 DNA Not yet available
sa17423 Essential Splice Site Available for shipment Available now
sa1802 Missense F2 line generated Not yet available
sa38318 Nonsense Mutation detected in F1 DNA Not yet available
sa19695 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa5126
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Essential Splice Site 204 4879 4 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12694384)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13219609
GRCz11 2 12902395
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAAGACCGGGGCTGCCAGCCAATCAGGGAGGCAAAGGGGCCTAGAGAG[G/A]TAAGCTGATTGGCTGGGGCAATTGAGTCTGTGACATATTATAATATGTCA
Long Flanking Sequence:
CCTTAGTTTTTATCCTTGTGTAATTCAAAAATTTCATTCATAATGCCCTGCTGAAAAATCCAGCATAAACCAGCCTAGGTTGGTTGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGGTTTTGGCCACTTCCAGGCTGGTTTCCAGCCATTTCCAGCCTGGTCTTAGCTGGTCAGGCTGGGAGATGAAACCTGTAGAAACCCTGATTTAACCACAAATGTCTTTAAAGCTCATTATGTTGCATGTTTAGAATTGTAAAATAATCCATGATTTCTTTGGCTAAAGACATTCCTCTGGTTTTCTCACAGCGAACAGCTCTGTGCCTTCTGTTACTGTGGTGGCCGAAGTCTGTTGGGCCAGGGAGATTTGAAGCCATTCAGGGTCACGCCCGGATACGACCCTCCACCCCGACAGTCCTCGACAGAGGAGGTCCACGACCATAGCGACAAGACCGGGGCTGCCAGCCAATCAGGGAGGCAAAGGGGCCTAGAGAG[G/A]TAAGCTGATTGGCTGGGGCAATTGAGTCTGTGACATATTATAATATGTCATGTGTAGCTTAATGTTAAGATGAGCTCAGCTAAATGGGGCATCTCTCGTGACAACACAGCTGTTTTTTCCTTGTTTGTTGGCTTCTGTGAAATAGATCAGACAGTATTGGCCATTGTTAGAGAGAGGAAAGCAGTACATGAGCCAAAGGATGTGTGTGCGTGTGTGTTATGGTGTGTGAACGGTAGGCCTGTTACAGGCAGCAGGGAGCACTGAAACATGACGTCACTGGTTGAATCATCCTCATCTGGATGAAATTTCAGGCTGTTTGAATACTGATCATTCCATTTGAAAATTACACTCATTGCTCTAGTATGTGTGTGTTTTTGCTTGATATCCTGGAGACAAACTTGTGTGCAGCAAACAGTGTTTGTCCTAAAGTGACCCTTTGCATTTGCTTGATAGCTATTCAGTGTCTCCTAATTATATGACTGTAGTATGCTTTTTTTACT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3422
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Essential Splice Site 480 4879 None 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None 280 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12731205)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13256430
GRCz11 2 12939216
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGTTCCCGATATCCAAAAAGACTTGCTTTCATGCCATCAATGCAAAAGG[T/C]ACATATCCAGAGCAGATCTGCACTTTGAATTGAATTGTCAGCTGTTCCTT
Long Flanking Sequence:
AGCACATGCTAATATCAGGTGTAAACAGGCCAGAGATGTGTTATAAATGTTATGCATCAATGGAATTAGTTGTAGGAAAGGACAAATTGATTGTGTTTCTGTATTTTTCAGGGAGCCTGGAGAAGACACTAAAATGCTAGTGTGTGATGTATGCGACAAAGGTTATCACACTTTCTGCTTGAAGCCAGCTATGGATTCTATCCCCACCAATGGCTGGAGGTGTAAGGTATGGGCAGCTCTAGATTTTATTGTTCTCATGTTAAATTATGAAATGAAATAAAAATGTATTTAATGAATTATAACTAATTGTTGCTGTATTTTTATAGAACTGTCGGATGTGTGTTCAATGTGGCACAAGGAGCAGTGAACAATGGCACCACAATAGCCTACTGTGCCAAAACTGTGGCGATCAACAGGACACCACCCTCTCCTGCTTATGTCCTAGCAATGTAGTTCCCGATATCCAAAAAGACTTGCTTTCATGCCATCAATGCAAAAGG[T/C]ACATATCCAGAGCAGATCTGCACTTTGAATTGAATTGTCAGCTGTTCCTTTAAGCAGATTCAAAAAGTTCATCTTTTGAGCCTAGTTATAGATGCAGTGAATTAGATGCAGTTATTAGCAATCTCTTTTTATTCAGGTGGTTCAACCCAGAGTGTGAACGACCGAGTGAAGGTCACACACATCCCCAGCCCAAAGAAGATCACATATGTTCCACCTGTAGAACCACTGGCATTGAATCGGGTCATGTGTGCACGGAAGCAGATGGAGTTCAGGCGGAGATTCAATCAGATGTGGGTGCTGAAGAATCAACACAACTAGTTCCATCAAATAATGATTCTGAGCCTGCCAAAGTTCAAGATATAGAACCTCATCAGCCTGTTCGAGAGATGCAGAATGAAGAGAAGCAAACAACAAATGAGAAACAAATGATGGGTAAGACCAAATTTATTTTCTTATAGGCCATAACTCGATTGCTGGAGGGCCGCAGCTCTGCACAGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11689
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Nonsense 551 4879 11 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12731553)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13256778
GRCz11 2 12939564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAAGAATCAACACAACTAGWTCCATCAAATAATGATTCTGAGCCTGCC[A/T]AAGTTCAAGATATAGAAMCTCATCAGCCTGTTCGAGAGATGCAGAATGAA
Long Flanking Sequence:
GTGGCACAAGGAGCAGTGAACAATGGCACCACAATAGCCTACTGTGCCAAAACTGTGGCGATCAACAGGACACCACCCTCTCCTGCTTATGTCCTAGCAATGTAGTTCCCGATATCCAAAAAGACTTGCTTTCATGCCATCAATGCAAAAGGTACATATCCAGAGCAGATCTGCACTTTGAATTGAATTGTCAGCTGTTCCTTTAAGCAGATTCAAAAAGTTCATCTTTTGAGCCTAGTTATAGATGCAGTGAATTAGATGCAGTTATTAGCAATCTCTTTTTATTCAGGTGGTTCAACCCAGAGTGTGAACGACCGAGTGAAGGTCACACACATCCCCAGCCCAAAGAAGATCACATATGTTCCACCTGTAGAACCACTGGCATTGAATCGGGTCATGTGTGCACGGAAGCAGATGGAGTTCAGGCGGAGATTCAATCAGATGTGGGTGCTGAAGAATCAACACAACTAGTTCCATCAAATAATGATTCTGAGCCTGCC[A/T]AAGTTCAAGATATAGAACCTCATCAGCCTGTTCGAGAGATGCAGAATGAAGAGAAGCAAACAACAAATGAGAAACAAATGATGGGTAAGACCAAATTTATTTTCTTATAGGCCATAACTCGATTGCTGGAGGGCCGCAGCTCTGCACAGTTTTGCTCCAACCCTAAACAACACAGCTGTTCCAACTAATCAAGGTGTTCAAGACTACTAACGACTTTTAAGCAGGTTTGAGTTGGAGGTGATTGGAGCTATACTTTGCAACTCAATTCATCTTTATTTCTATAGCACTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATAGAAGTTCAAGTAAAACATAACTGTCAGTCCAGTTTTCAGAGTTGAAGTTCAGTTTAGTTCAGTGTGGTTCAATTTTCCCTTTGGAATGTCCAAACACTGAAGTGGCGAGGAAGAACTTTTTACCAATTGATAAAAGTGAAGGAAAAAAAAAACTTAAAAGAAACCAGGCTAAGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32861
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
ENSDART00000112279 Nonsense 1203 4879 22 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 Nonsense 34 601 1 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12768329)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13293554
GRCz11 2 12976340
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTCAGAGTCTTGCCAACGCAGCATCTCGCCGGAGACGCTCTAAACCT[A/T]AACTCAAGCTGAAGATCATAAACCAGAACAGTGTAGCTGTGCTGCAGACA
Long Flanking Sequence:
TAAAGATGCCCTTAGTGCATCTGGACCATGCGCTTTAGACTTTGCACTTATTGATCATTAAAATAGAGCTAATTGTCATGCTAGAAAAGAACTGCTCTATTAATAAGGTTTTAAAACATTGTATCTGTTATTAAATGCTATCGCTGTTAATACTATTTGACAGACCTAATCTAACATGAAAATTAGAGTATTTAATACTGTTAGTTAATGTTAATCAATGCGTTAACTACTGAGAAATAACCGAAATTTCTATATAAATGTTTCTTGCAAAAAAAAAAAAAAAACACAAACAAACAAAAAAAAGCAGCTAATGCAATTTGTGAATAAAATCTTGTCATGAAAAAATTCTTCATAGACTTCTTTTTTTTTGTGTGTGTGTCTTCTACTCCACAGACCTGATGAGGACTTACACCCAGGATGGTGTATGTCTAACAGAGTCTGGTCTGTCACAGCTTCAGAGTCTTGCCAACGCAGCATCTCGCCGGAGACGCTCTAAACCT[A/T]AACTCAAGCTGAAGATCATAAACCAGAACAGTGTAGCTGTGCTGCAGACACCTCCAGACCCTCAGACTGAACTCTCCAGAGACGGAGACCTTGAAGACACCAAAAGTAACGCTTCTCACATCTTCACTGATTATAGGCCCTTTTCACATCCAAGGGATGTGTATAATCACATAACTTCAGTTCTGACTCAAAGCAGTGTATACCTGTTTCTGACAACACAGAGCTAGCAACAGGGAGTTTACCAAGACACTTGTATATTTGCTACAGATATGATTAGATGACAACTATGGCTATATTCTGTTGTCACCATTCCAATCGAGATATCTGGCGTCTCAAACAAACTTACCAATTGGCAAGATTTCTGCTTAAACTGAGAAAGTGGGAGTTTAAAATGGAGCGCCGAAATTGTACTGAAGTAAAAAAAAAATTGACTTGTCAGCATTTTTCAAATAACAATTTCAATTATTTACATTGGTGCTGTACATTTTTAAAGCCAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19694
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
ENSDART00000112279 Nonsense 1586 4879 32 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 Nonsense 387 601 10 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12786865)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13312090
GRCz11 2 12994876
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGTATCCACTGTGTATTGGTATGTTTTTTTATGCAGGATTGTCTTCA[C/T]GAATGCCAGTGATGAATGGTTTAATGGAATCCAAACAGCAGTTTTCACAG
Long Flanking Sequence:
ATCAGCATACTGCTTTCTGAAGTAACTTATTAAATAAAGAAAAAATTCACAAAGCTTCCCCTACCGCATCAAATTCCATTTTTACTGTTATTGATATTTGGCGCCAGTCAATCTGGAAGTGACGGTTTTGTTTTCTTTGACTACTTGGATGGAAACCCTGCTTTATTCGCATGTCTTATATGCGATATTCCAGTTATGCGCATACATTTAATTTGCATCTTTAGATGGAAACATAGCTACTGACTAAATCAATGGGACTTTTTGATTGATTACAGATAGGGGAATTCAAGAATGCGGAGGGGAAATTTTGTGGTGATGGCGGTGATGAGAATGTTCTTTATACAAGCTCTGTCAGTAACATTTATATGAGCATGTTTTTGTATATTTTTACAAAGTGAGGGTTTCCTGAGGTTTTTGATTCTACTTTGTTCATAAATCTTCATAAGTGATTGTTGTATCCACTGTGTATTGGTATGTTTTTTTATGCAGGATTGTCTTCA[C/T]GAATGCCAGTGATGAATGGTTTAATGGAATCCAAACAGCAGTTTTCACAGGCTCGCATAGGTCCGGGAGCAGGACCAGAAATGGCCCAAAATATTCCCCCAATGCAGCGTATACCTTTCTCAGACAATCTTAGGTAAGTCATTAGTAAACTTTCTTCGACATATCCACATTTCTCACACCCAAGAAATATATTTTTTTACTCGGTCAAACTACTTATTTAAAATGAGCTAAAACCACACAATTCTTGAGAGTTCATTGGGACAACTTAATTTTTTATGTTCAATCCACATAAATTTGTTAAAAGTACCAAGTTAACTTAATCAATTTGTGTTGGGACTACATGAATGAATTGTGTGGAACCCTGCATTTTTTACAGTGCAGCATAATTGAGTACATCCCATTTTGAAATTGAATATTTTTATCCATTTCTCAGTCAATGTAGGCAATGCATTTTGGTGCATTTAAACAAAACAGATTTATTAAACAGATATATTTATTAA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25776
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Nonsense 1731 4879 34 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 Nonsense 532 601 12 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12788419)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13313644
GRCz11 2 12996430
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATTGCAAAACTATGGAGAAAAGCAAGTTCACAGGACCGGGCTCCATA[T/A]GTGGTAAGTTCACCTATGTAATAAATGTCAAACAATACATCATGTCATAA
Long Flanking Sequence:
AGGAGACTGCTGGACCATGGTCTGCTACAGGGTCAGCTTCTTCCTCTGCTCCAGCTGCTGTTTCGGAAATGGAAGGAGACTCCATGTCTACCGCACAGAAAAGCACTTTGAAGTGGGAGAAAGAGGAAACTCTTGGAGAACTTGCCACTGTTGCACCAGTTTTGTACACTAATGTCAATTTTCCAAACCTCAAAGAAGAATACCCAGGTCCGCTAAGTTTCTTTAAAGTGATCTGTCATATGCAGCTTTGTAAATCAATGTTGAAATCAGCATGAACTGCATGCATTGTTAACAACCCTTTGTACTATAATAAGCATGCAATCAGACATGATTTTAACTTGACTGTTTAACGTAAAAGTTAAACGTTCTTAATAACTCTTATTGTTATTCTTTTAATTGACATATTGTTTTTTATGTTATGACTTTATAGACTGGTCAACACGAGTAAAGCAAATTGCAAAACTATGGAGAAAAGCAAGTTCACAGGACCGGGCTCCATA[T/A]GTGGTAAGTTCACCTATGTAATAAATGTCAAACAATACATCATGTCATAATATGATTTATCTTGGAAGCACAGTCTTTCTTCGATGTTTTATGTAGTTAAAAATACAGGTAGAAGTTTCTGGAAAGAGCAGTCAGGTGCAGGTCACAGTTAATATTGTGTTTTAAACAACAGTGTGCCAGCTCATCAACCTTCTATACCTGCATCACACCACCACTAAACAACGTAAATCAGCATGGCATTTATTTCTTCAATCTTCCTCTTTAATGTTGCTCAAAGTCAAAGGAATAAATTGAGCTCAAGAAGCTCAATTAATTTCTATGAGATAAACACATTTCAAAAGATATGATTAAAGGGAACATTACCTTGACATGAAGGGAATTCACTTAAAAAAGCTTTCAGACAATTAGTCTAAATAGCATGCAATTTTAACAGATTTAAACAACCTTTGAATGTTCATGATCGTTCTTTGATATAAACTGCATGACCACTCTACCATTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39784
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
ENSDART00000112279 Essential Splice Site 1800 4879 None 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None 601 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12789128)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13314353
GRCz11 2 12997139
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAAGCACAAGGAGTCAGAGCATGAACAAGAATGGAAGTTTAGACAAG[T/A]AAGTCTACAATAGTTATTTGTTTGCAAATGGGCTAAATGACAAATGTGTC
Long Flanking Sequence:
CCACCACTAAACAACGTAAATCAGCATGGCATTTATTTCTTCAATCTTCCTCTTTAATGTTGCTCAAAGTCAAAGGAATAAATTGAGCTCAAGAAGCTCAATTAATTTCTATGAGATAAACACATTTCAAAAGATATGATTAAAGGGAACATTACCTTGACATGAAGGGAATTCACTTAAAAAAGCTTTCAGACAATTAGTCTAAATAGCATGCAATTTTAACAGATTTAAACAACCTTTGAATGTTCATGATCGTTCTTTGATATAAACTGCATGACCACTCTACCATTCACAGCAAAAGGCCAGAGATAACAGGGCAGCCCTGCGCATTAACAAAGTCCAAATATCCAATGAGCCTATTAAGCGGCAACCACCCCAGCCTCAGCAGCCTTTAGAAGTGTTTGATCCTGCTATTCCACCTCTGGACCCGGAATTACTGTTCAAAGATCCATTGAAGCACAAGGAGTCAGAGCATGAACAAGAATGGAAGTTTAGACAAG[T/A]AAGTCTACAATAGTTATTTGTTTGCAAATGGGCTAAATGACAAATGTGTCACAACTGCATTTAGATGTTTGCTGTTTTTAATTGTTGATATATTTTGCAAAAGCAGCCTTTAGAATAAATTCCACTAAATCATATTTGTTGACTATAGGGCAGAAAAGAATTTGAAATATTTGACAGAATACGTGTAAGTAAACTTATCAACTGACACAAAAATGTACATTTTTTGTTGTTTTATATGAAGACATTTTGATATTTTTAATAATTACTCTTCTATTGTATTTTCTAAATGTGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTTTTAGACAAATTGCACATTGTACATTTACCTGCTGTTTAATCATTAAATTATATATGTTTATATCAATTTATTTTTCCAGCAAATGAGACAGAAAAGTAAGCAGCAAGCAAAAATTGAAGCTACACAGAAACTTGAGCAGGTGAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25777
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
ENSDART00000112279 Nonsense 2298 4879 36 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12791052)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13316277
GRCz11 2 12999063
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAGGAAGGTCCCAGTCATTACGAAATGATTCATGTTCACATATCCCA[C/T]GAACACCTCATCACGGAGTTGTAGGACAGGTATTGGTATCTGGGCCCTTG
Long Flanking Sequence:
AGCCTGGGCCAATGACACGACAACCATCATGTAACTCCTATGCTCGAGCACCTTCTACCCCTCGGCCAGACTATTCGCAGTGTGATCCATATGTACAGCAACCTGGGACTCCAAGACCTTCAAGTGACCCTTTTGCCCAGTCTCCATTTTCTAATCCATATGCTAGAATGCCAGGCACACCTAGACCTCATGATCCTGAACCCTATTCTCAGCAATCTGCATCTCGGCATCCAGCTATGATGAATCAACCCTCTCAGCAGTCTCAGCAGCAGACTCATAACCGTATAATGTCCCCTATATCAATGGACCCTTACACACAACACCCTAACACCCCACGGTCAGGAATAGTAGACCCATTTCCTAAGTCTCCAAGTAACCAAAGGACCCCAGATCCTTTTTGTCAACCTCCTGGACTGCCACGCTGTGTGGGCCCTGATCTTCATATACAGTCAATAGGAAGGTCCCAGTCATTACGAAATGATTCATGTTCACATATCCCA[C/T]GAACACCTCATCACGGAGTTGTAGGACAGGTATTGGTATCTGGGCCCTTGTCCAGTCAGGATCCATTCTCTCCTCCACAAGTTTTGATGCAAGAATCTTTTTCCAGTCCAACAAAACATGGACCTCAGACCCTTAAACATCTGAGCATGACAGATGATTCAGGATCTCAGCCACTATCAAATCGACCTAATCAGACTCCTATTCATGATCCATTTGAGCAGACCGCTATGCTTGGTCAGTGTGGAGAAAATAAAGACCAACAAAGTTTAGTACAAATTATCAGTTCCCACACCATGGGGCAACCTGGCAGTGGAACACAAACAATACCTCTTGCCGAAGCTGAGGAAAGACTGAGACAGGTGTTTATTTTGTTACTACTATATTTTAAATGGTTATTTTTTTCAGAGAATTTTTTTCATCTTATGATACAGCAATGTATCACTTAAAATATATAATCTGTACAACACCAGATATTTTAATATATTTTAATAATATTTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38316
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
ENSDART00000112279 Nonsense 2357 4879 36 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12791230)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13316455
GRCz11 2 12999241
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCTTAAACATCTGAGCATGACAGATGATTCAGGATCTCAGCCACTAT[C/A]AAATCGACCTAATCAGACTCCTATTCATGATCCATTTGAGCAGACCGCTA
Long Flanking Sequence:
ACCTAGACCTCATGATCCTGAACCCTATTCTCAGCAATCTGCATCTCGGCATCCAGCTATGATGAATCAACCCTCTCAGCAGTCTCAGCAGCAGACTCATAACCGTATAATGTCCCCTATATCAATGGACCCTTACACACAACACCCTAACACCCCACGGTCAGGAATAGTAGACCCATTTCCTAAGTCTCCAAGTAACCAAAGGACCCCAGATCCTTTTTGTCAACCTCCTGGACTGCCACGCTGTGTGGGCCCTGATCTTCATATACAGTCAATAGGAAGGTCCCAGTCATTACGAAATGATTCATGTTCACATATCCCACGAACACCTCATCACGGAGTTGTAGGACAGGTATTGGTATCTGGGCCCTTGTCCAGTCAGGATCCATTCTCTCCTCCACAAGTTTTGATGCAAGAATCTTTTTCCAGTCCAACAAAACATGGACCTCAGACCCTTAAACATCTGAGCATGACAGATGATTCAGGATCTCAGCCACTAT[C/A]AAATCGACCTAATCAGACTCCTATTCATGATCCATTTGAGCAGACCGCTATGCTTGGTCAGTGTGGAGAAAATAAAGACCAACAAAGTTTAGTACAAATTATCAGTTCCCACACCATGGGGCAACCTGGCAGTGGAACACAAACAATACCTCTTGCCGAAGCTGAGGAAAGACTGAGACAGGTGTTTATTTTGTTACTACTATATTTTAAATGGTTATTTTTTTCAGAGAATTTTTTTCATCTTATGATACAGCAATGTATCACTTAAAATATATAATCTGTACAACACCAGATATTTTAATATATTTTAATAATATTTTAATAATATTTTGTTTACAGCGTCAACGTATTCGAGAGCTGATTCTTAAGCAGCAACAGCAGAAAAGTGCCATACGTCAAGACAAGGTTGTGCAAGATCATACTCTAACCATGTCTCCAGCAACTCCTCAACACTGGAATCTGGAGTCTACAGGCCAACAAAGTGAAATTTTTAATCACCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39785
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Splice Site, Nonsense 2417 4879 36 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12791409)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13316634
GRCz11 2 12999420
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTGGAACACAAACAATACCTCTTGCCGAAGCTGAGGAAAGACTGAGA[C/T]AGGTGTTTATTTTGTTACTACTATATTTTAAATGGTTATTTTTTTCAGAG
Long Flanking Sequence:
TTCCTAAGTCTCCAAGTAACCAAAGGACCCCAGATCCTTTTTGTCAACCTCCTGGACTGCCACGCTGTGTGGGCCCTGATCTTCATATACAGTCAATAGGAAGGTCCCAGTCATTACGAAATGATTCATGTTCACATATCCCACGAACACCTCATCACGGAGTTGTAGGACAGGTATTGGTATCTGGGCCCTTGTCCAGTCAGGATCCATTCTCTCCTCCACAAGTTTTGATGCAAGAATCTTTTTCCAGTCCAACAAAACATGGACCTCAGACCCTTAAACATCTGAGCATGACAGATGATTCAGGATCTCAGCCACTATCAAATCGACCTAATCAGACTCCTATTCATGATCCATTTGAGCAGACCGCTATGCTTGGTCAGTGTGGAGAAAATAAAGACCAACAAAGTTTAGTACAAATTATCAGTTCCCACACCATGGGGCAACCTGGCAGTGGAACACAAACAATACCTCTTGCCGAAGCTGAGGAAAGACTGAGA[C/T]AGGTGTTTATTTTGTTACTACTATATTTTAAATGGTTATTTTTTTCAGAGAATTTTTTTCATCTTATGATACAGCAATGTATCACTTAAAATATATAATCTGTACAACACCAGATATTTTAATATATTTTAATAATATTTTAATAATATTTTGTTTACAGCGTCAACGTATTCGAGAGCTGATTCTTAAGCAGCAACAGCAGAAAAGTGCCATACGTCAAGACAAGGTTGTGCAAGATCATACTCTAACCATGTCTCCAGCAACTCCTCAACACTGGAATCTGGAGTCTACAGGCCAACAAAGTGAAATTTTTAATCACCCACCACCACCATATCCTGGCCCAGGAGCTGTAAGAGCACCTCAGAGATTCTATGCGACAAGAGATAGACAAGGACAGTTTCCTGAAGGCCAGTTACCCAGACCACAGTTTCCTGGGGATGCTGACTCAAATACAAGGCAGCTTGGTGCTAGGTAGGTGAATTCACACACTACAAAAAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5127
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Nonsense 2488 4879 37 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12791782)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13317007
GRCz11 2 12999793
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACCACCATATCCTGGCCCAGGAGCTGTAAGAGCACCTCAGAGATTCTA[T/A]GCGACAAGAGATAGACAAGGACAGTTTCCTGAAGGCCAGTTACCCAGACC
Long Flanking Sequence:
GCTTGGTCAGTGTGGAGAAAATAAAGACCAACAAAGTTTAGTACAAATTATCAGTTCCCACACCATGGGGCAACCTGGCAGTGGAACACAAACAATACCTCTTGCCGAAGCTGAGGAAAGACTGAGACAGGTGTTTATTTTGTTACTACTATATTTTAAATGGTTATTTTTTTCAGAGAATTTTTTTCATCTTATGATACAGCAATGTATCACTTAAAATATATAATCTGTACAACACCAGATATTTTAATATATTTTAATAATATTTTAATAATATTTTGTTTACAGCGTCAACGTATTCGAGAGCTGATTCTTAAGCAGCAACAGCAGAAAAGTGCCATACGTCAAGACAAGGTTGTGCAAGATCATACTCTAACCATGTCTCCAGCAACTCCTCAACACTGGAATCTGGAGTCTACAGGCCAACAAAGTGAAATTTTTAATCACCCACCACCACCATATCCTGGCCCAGGAGCTGTAAGAGCACCTCAGAGATTCTA[T/A]GCGACAAGAGATAGACAAGGACAGTTTCCTGAAGGCCAGTTACCCAGACCACAGTTTCCTGGGGATGCTGACTCAAATACAAGGCAGCTTGGTGCTAGGTAGGTGAATTCACACACTACAAAAAATGTAAATGTTATAGAAAATGTTTGTTTTCCAAATAATGCAAAAATTGTAATGTTGTTTTGTTGATTTTAGGATGCCTTTGACTCCTGGCATCCAAGGTCCTTTAGGAGCTATAAGACCTCATCAAATGCAGGACTCAATTGAAGCTCATCCACAAATGAGAAGATCCATGTCTATGGATCTAGGAAAGTCAATAGAGGGCAGCCCTTTAGGAACCCCACATATGCCTCCTCGTGGTATGCATGTTCAACAGCATAACATCATGGGACAGCCTTTTATTGAACTGAGACACAGAACACCAGATAGCAGACTTCGTCTTTCCTTTGGACCTCCTGGTATGCAGGGTAATCGAATGGAATCACCCTTACAGCAACATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6827
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
ENSDART00000112279 Nonsense 2595 4879 38 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12792198)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13317423
GRCz11 2 13000209
KASP Assay ID:
554-4846.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTTCAACAGCATAACATCATGGGACAGCCTTTTATTGAACTGAGACAC[A/T]GAACACCAGATAGCAGACTTCGTCTTTCCTTTGGACCTCCTGGTATGCAG
Long Flanking Sequence:
TACAGGCCAACAAAGTGAAATTTTTAATCACCCACCACCACCATATCCTGGCCCAGGAGCTGTAAGAGCACCTCAGAGATTCTATGCGACAAGAGATAGACAAGGACAGTTTCCTGAAGGCCAGTTACCCAGACCACAGTTTCCTGGGGATGCTGACTCAAATACAAGGCAGCTTGGTGCTAGGTAGGTGAATTCACACACTACAAAAAATGTAAATGTTATAGAAAATGTTTGTTTTCCAAATAATGCAAAAATTGTAATGTTGTTTTGTTGATTTTAGGATGCCTTTGACTCCTGGCATCCAAGGTCCTTTAGGAGCTATAAGACCTCATCAAATGCAGGACTCAATTGAAGCTCATCCACAAATGAGAAGATCCATGTCTATGGATCTAGGAAAGTCAATAGAGGGCAGCCCTTTAGGAACCCCACATATGCCTCCTCGTGGTATGCATGTTCAACAGCATAACATCATGGGACAGCCTTTTATTGAACTGAGACAC[A/T]GAACACCAGATAGCAGACTTCGTCTTTCCTTTGGACCTCCTGGTATGCAGGGTAATCGAATGGAATCACCCTTACAGCAACATGCCCCAGGTTTCTTGAGTGGCCAAGAACTGGTATTCCCCTTCAATCAGATTACAAAAGCAGTGGACACACCATTAAACCAGCCTCAGGTAGCTTTTACACAGATGCAGACATCTCTGAGCTTAGGGAATTTACAACAGCCCAATATTTCACTGAGAGCTGGACATACACAAATCCCCTTGACAAGATCTATAAGTCAACCTGCTTCCAATGAGACTCTCAGTTCTCCCTTACACACAGATATTGCTGCTGTTTCAGCTGTACAAAATGATGAGGTCCCTTTACCCACAAATGAAGTACCTGAGGAGAAAATCGATACTGTTGAATCTGCTGTGAAAGAACTTGAAGATGTTGAAGTGAAGGACCTTGTTGATGCTGACTTAGAGAACCTAAATCTTGACCCAGACGATGGAAAGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38317
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
ENSDART00000112279 Nonsense 2627 4879 38 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12792295)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13317520
GRCz11 2 13000306
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGGTAATCGAATGGAATCACCCTTACAGCAACATGCCCCAGGTTTCT[T/A]GAGTGGCCAAGAACTGGTATTCCCCTTCAATCAGATTACAAAAGCAGTGG
Long Flanking Sequence:
AGACAAGGACAGTTTCCTGAAGGCCAGTTACCCAGACCACAGTTTCCTGGGGATGCTGACTCAAATACAAGGCAGCTTGGTGCTAGGTAGGTGAATTCACACACTACAAAAAATGTAAATGTTATAGAAAATGTTTGTTTTCCAAATAATGCAAAAATTGTAATGTTGTTTTGTTGATTTTAGGATGCCTTTGACTCCTGGCATCCAAGGTCCTTTAGGAGCTATAAGACCTCATCAAATGCAGGACTCAATTGAAGCTCATCCACAAATGAGAAGATCCATGTCTATGGATCTAGGAAAGTCAATAGAGGGCAGCCCTTTAGGAACCCCACATATGCCTCCTCGTGGTATGCATGTTCAACAGCATAACATCATGGGACAGCCTTTTATTGAACTGAGACACAGAACACCAGATAGCAGACTTCGTCTTTCCTTTGGACCTCCTGGTATGCAGGGTAATCGAATGGAATCACCCTTACAGCAACATGCCCCAGGTTTCT[T/A]GAGTGGCCAAGAACTGGTATTCCCCTTCAATCAGATTACAAAAGCAGTGGACACACCATTAAACCAGCCTCAGGTAGCTTTTACACAGATGCAGACATCTCTGAGCTTAGGGAATTTACAACAGCCCAATATTTCACTGAGAGCTGGACATACACAAATCCCCTTGACAAGATCTATAAGTCAACCTGCTTCCAATGAGACTCTCAGTTCTCCCTTACACACAGATATTGCTGCTGTTTCAGCTGTACAAAATGATGAGGTCCCTTTACCCACAAATGAAGTACCTGAGGAGAAAATCGATACTGTTGAATCTGCTGTGAAAGAACTTGAAGATGTTGAAGTGAAGGACCTTGTTGATGCTGACTTAGAGAACCTAAATCTTGACCCAGACGATGGAAAGGACTTGGATCTTGAAACAAATGACTTGCATCTTGATGACTTCTTAAAATCTGGGAAATTTGATATTATCGCCTATACAGATGCTGATTTAGATCTTAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17591
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
ENSDART00000112279 Nonsense 2931 4879 38 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12793206)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13318431
GRCz11 2 13001217
KASP Assay ID:
2259-1708.1 (used for ordering genotyping assays)
KASP Sequence:
CAAGCATGCTGGTCAGTGTACCACCAGAAGGTAAARAACTGAAGCAAGAA[C/T]AATGTGGAAAGTCAACAGAACAAAACAACCTTTCAAATCAGGAAACTGCA
Long Flanking Sequence:
TTGAAACAAATGACTTGCATCTTGATGACTTCTTAAAATCTGGGAAATTTGATATTATCGCCTATACAGATGCTGATTTAGATCTTAGTGAGGACCTGGATCTCAGTGATACTATGGAAGACAACACTGAGATATCTGAGAAAAAAGCTGAGAAAAAGACTGAAAGTTTTAATGCCACATCCTCAGCATCATGTTCTACATCGGCAGTGACGGAAGCAGTAGACAAAACTGCTCTGTCTCAAGATGACACCAATCAAGAAATTCCTCAGGATCAGGTGTTGGTTTCCTTGAAAAAAGAGGATGATAACAAAAATGGATTTAAAGATTGCTTGTCCCAAGACTCTTCTTGTAGCAATCAGATAAGTGATAGCGCTGCCAATAATCAGGCTAGCTTTAAAAGAGATGTTGAATCCAGTTTACAAGTTCATCCCGATACTACTCCAGTGCTTTCAAGCATGCTGGTCAGTGTACCACCAGAAGGTAAAGAACTGAAGCAAGAA[C/T]AATGTGGAAAGTCAACAGAACAAAACAACCTTTCAAATCAGGAAACTGCAATGTCTCTCAGTAACACTATGCTCGGGCAAGAAAACTTCTCAGTTCAGGGAATTGATACTGGCCTCAATATTGACCAGTCACTGGTGTCTTCTCATGATGAAAGTGCATTAGAAGTCTCAAGCTCCATTCAGGAACAGCAACAAAGCCATATTTTTGGTATTGATCAAAAGGATGCTGTACTCTCAGGGGAACAAAACAGCATTCTTACTCAACAGGCAGTCTTATCACAGCAAGGCCATCAAAACAGACCACTGCTTCTGGAGGAGCAACCACTCCTTCTTCAAGACCTCCTGGATCAGGAGAGACAAGAGCAGCAGCAGCAGAAGCAAATGCAAGCTATGATAAGACAGCGTTCCAGCGACTCATTTTTCCCCAACATAGGTAAGTGGTAGCTAATATACAAATATAGAATTTTGTTCTTCCATGATATATTTATATGTGGCAAACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39786
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
ENSDART00000112279 Nonsense 2993 4879 38 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12793392)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13318617
GRCz11 2 13001403
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTTCTCATGATGAAAGTGCATTAGAAGTCTCAAGCTCCATTCAGGAA[C/T]AGCAACAAAGCCATATTTTTGGTATTGATCAAAAGGATGCTGTACTCTCA
Long Flanking Sequence:
CATCATGTTCTACATCGGCAGTGACGGAAGCAGTAGACAAAACTGCTCTGTCTCAAGATGACACCAATCAAGAAATTCCTCAGGATCAGGTGTTGGTTTCCTTGAAAAAAGAGGATGATAACAAAAATGGATTTAAAGATTGCTTGTCCCAAGACTCTTCTTGTAGCAATCAGATAAGTGATAGCGCTGCCAATAATCAGGCTAGCTTTAAAAGAGATGTTGAATCCAGTTTACAAGTTCATCCCGATACTACTCCAGTGCTTTCAAGCATGCTGGTCAGTGTACCACCAGAAGGTAAAGAACTGAAGCAAGAACAATGTGGAAAGTCAACAGAACAAAACAACCTTTCAAATCAGGAAACTGCAATGTCTCTCAGTAACACTATGCTCGGGCAAGAAAACTTCTCAGTTCAGGGAATTGATACTGGCCTCAATATTGACCAGTCACTGGTGTCTTCTCATGATGAAAGTGCATTAGAAGTCTCAAGCTCCATTCAGGAA[C/T]AGCAACAAAGCCATATTTTTGGTATTGATCAAAAGGATGCTGTACTCTCAGGGGAACAAAACAGCATTCTTACTCAACAGGCAGTCTTATCACAGCAAGGCCATCAAAACAGACCACTGCTTCTGGAGGAGCAACCACTCCTTCTTCAAGACCTCCTGGATCAGGAGAGACAAGAGCAGCAGCAGCAGAAGCAAATGCAAGCTATGATAAGACAGCGTTCCAGCGACTCATTTTTCCCCAACATAGGTAAGTGGTAGCTAATATACAAATATAGAATTTTGTTCTTCCATGATATATTTATATGTGGCAAACAGCTGGCCAGGGACTAAAAAGATACTCATCTCAATTTCCTTTTTTTGTTAAAACGTAGATCTTCACTATAAATGTGGGATTTAACAGATAGCTAAATATGCAGTTTTGCCCAACTGTTTCATTAACTGCAAATAATAACATGTATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15663
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
ENSDART00000112279 Nonsense 3375 4879 43 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12799359)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13324584
GRCz11 2 13007370
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAACCCATTTAGCGAAGGCTTCCAGGAGCGAGAACGCAAGGAGAGAKTA[C/T]GAGAGCAGCAGGAGCGGCAAMGAATRCAGATCATAAAGGAGGTGGAGAGG
Long Flanking Sequence:
TTTTTGAGGTCAAGGAAATGTAATGTTTCAGTCCAATATAGGATGAATGTAATTTGAGTTTGTTTGTTTTTTTCCAGATTCGAAAACAGCAGAAGGAACATGCAGAGCTAATAGAGGAGTACAGGGTTAAACAGCAGCAACAAGGTGCACTACAGCCCCCGATTATGCCAGGAATGCAGCCTCCTGCTGGCATGATGCAAGTTGGTCCCCCCATAAACCAATCTATGGTGGGTCCCATGATGCCCATTCGCCTTCACTCCAATCAACCAGATGTCACTAAAATGCCCAACACAGCGGGCTGGCACCCTGGTGCACCTGTTCCTACTGGACCTCGAATGCCAGGAGTTATGCCTGCTCAAGTGGTGCAACCACAGCCTCTGCAGCCAGCAGCGGCTAGGCCCACTCAGGTGCAAGCAGGTGGTGAGTCTCCTCATGTGAACTTTGATGATACCAACCCATTTAGCGAAGGCTTCCAGGAGCGAGAACGCAAGGAGAGATTA[C/T]GAGAGCAGCAGGAGCGGCAAAGAATGCAGATCATAAAGGAGGTGGAGAGGCAGCATGTGAAGCACTGCGTAGAACAACAGCAAGTTTCTAACTGCCAAGATGGTACCATGAGGGGTCTGTCCCAGATGCCTTTTTACAACCAGGAGCTACCGCAGGACTTCATGCAGCCACCCAGATTGCAGCAACAGATCCAAGGGCCCACTTTTCCACAGCAGCAAGGCACACAACAAGGGTACATTGGAGGACCACCCAGACCATTATTGGGAAATGGTCCATTTCCTCAGGAAATGGGATCAGGTTTTGCTCCTCAGAATCTAGCAGTTCATGGGCCTAACTTGATCCAGGCACAAACTAGACCTCAAAGATATTCTGTGCCGCATATGATGGCTCAAAATCCACCTCAAGGGCACCCATTTCCAATGGAAGGGCCTACACCCTTACCTCCAAACTTTCCAGGTCCTGGTCCATCCCTTATTCAGTTGTACTCTAACATCATCCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10821
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
ENSDART00000112279 Nonsense 3437 4879 43 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12799545)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13324770
GRCz11 2 13007556
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACCAGGAGCTACCRCAGGACTTCATGCAGCCACCCAGATTGCAGCAA[C/T]AGAWCCAAGGGCCCACWTTTCCACAGCAGCAAGGCACACAACAAGGGTAC
Long Flanking Sequence:
CTGGCATGATGCAAGTTGGTCCCCCCATAAACCAATCTATGGTGGGTCCCATGATGCCCATTCGCCTTCACTCCAATCAACCAGATGTCACTAAAATGCCCAACACAGCGGGCTGGCACCCTGGTGCACCTGTTCCTACTGGACCTCGAATGCCAGGAGTTATGCCTGCTCAAGTGGTGCAACCACAGCCTCTGCAGCCAGCAGCGGCTAGGCCCACTCAGGTGCAAGCAGGTGGTGAGTCTCCTCATGTGAACTTTGATGATACCAACCCATTTAGCGAAGGCTTCCAGGAGCGAGAACGCAAGGAGAGATTACGAGAGCAGCAGGAGCGGCAAAGAATGCAGATCATAAAGGAGGTGGAGAGGCAGCATGTGAAGCACTGCGTAGAACAACAGCAAGTTTCTAACTGCCAAGATGGTACCATGAGGGGTCTGTCCCAGATGCCTTTTTACAACCAGGAGCTACCGCAGGACTTCATGCAGCCACCCAGATTGCAGCAA[C/T]AGATCCAAGGGCCCACTTTTCCACAGCAGCAAGGCACACAACAAGGGTACATTGGAGGACCACCCAGACCATTATTGGGAAATGGTCCATTTCCTCAGGAAATGGGATCAGGTTTTGCTCCTCAGAATCTAGCAGTTCATGGGCCTAACTTGATCCAGGCACAAACTAGACCTCAAAGATATTCTGTGCCGCATATGATGGCTCAAAATCCACCTCAAGGGCACCCATTTCCAATGGAAGGGCCTACACCCTTACCTCCAAACTTTCCAGGTCCTGGTCCATCCCTTATTCAGTTGTACTCTAACATCATCCCAGAGGAGAAAGGCAAGAAAAAAAGAAACCAGAAGAAGAAGAAAGATGAAGATTGTGAGTCGCTGCGAGCTCCATCTACACCTCATACACCTCACTCAGACATGACTGCTCCATTAACACCCTGCGTGTCAGACACATCATCCACACCGACAAGGAACCCAATGGTCTTTGGTGACCATGAGTTCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25101
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
ENSDART00000112279 Nonsense 3582 4879 43 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12799982)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13325207
GRCz11 2 13007993
KASP Assay ID:
554-7545.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACACCTCATACACCTCACTCAGACATGACTGCTCCATTAACACCCTG[C/A]GTGTCAGACACATCATCCACACCGACAAGGAACCCAATGGTCTTTGGTGA
Long Flanking Sequence:
CAGATGCCTTTTTACAACCAGGAGCTACCGCAGGACTTCATGCAGCCACCCAGATTGCAGCAACAGATCCAAGGGCCCACTTTTCCACAGCAGCAAGGCACACAACAAGGGTACATTGGAGGACCACCCAGACCATTATTGGGAAATGGTCCATTTCCTCAGGAAATGGGATCAGGTTTTGCTCCTCAGAATCTAGCAGTTCATGGGCCTAACTTGATCCAGGCACAAACTAGACCTCAAAGATATTCTGTGCCGCATATGATGGCTCAAAATCCACCTCAAGGGCACCCATTTCCAATGGAAGGGCCTACACCCTTACCTCCAAACTTTCCAGGTCCTGGTCCATCCCTTATTCAGTTGTACTCTAACATCATCCCAGAGGAGAAAGGCAAGAAAAAAAGAAACCAGAAGAAGAAGAAAGATGAAGATTGTGAGTCGCTGCGAGCTCCATCTACACCTCATACACCTCACTCAGACATGACTGCTCCATTAACACCCTG[C/A]GTGTCAGACACATCATCCACACCGACAAGGAACCCAATGGTCTTTGGTGACCATGAGTTCTGTGAGACATCCCAACCTGGATCATCAACACCAGGCTCCATGAGCAGCCAACCACACTCTGAATTGGAGCGGCAGCTCTCTGAAGGCAGCTGTGGTGGGGGGCCAGAGTCAGCCATGGGACATGAAGAAATGCATGACAGGATCCTATCCAACATCAAATTGGAGAAGGTGGAGGCAAATGATTGCCATGGACATAAGCCTATAGATATGGAAATAAGAATAGGAATGGTCAAGGTGGAGAGAGAAATAATGTTGCATCATCCTTCAAGCCAAAGTCCAGCCAATAGCTCAAAAGAAGAAGGTGGTAATGAACTCCTCAAGCACCTCCTAAAGAATAAGAGGACTCCACCTCATGCACTGCCTCACCAGAGGTCTGAAGACAGCCTGAGATCGGAGGAAGAGGGATCCACAGAAAGCAAAGCGTTTTTTCGGCAGAACTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17423
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Essential Splice Site 3922 4879 46 60
ENSDART00000131780 None None 734 None 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 Essential Splice Site 208 383 4 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12802595)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13327820
GRCz11 2 13010606
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACAGAGGAGCTTGCCAGAAAAGGTGGCCTCATTGCTGGACACGAWGG[T/C]GAGTAGYAGCTGATGTAGACTGAGCGGGTGATTTYGATCTATATTWGAGC
Long Flanking Sequence:
TTTCATTGTTTCTTTTCAGCAGCATCTTTCTCTCTTGCCTCTAATGGAGCCACTGGTGGGGGTGAACTTTGCCCATTTAATGCCCTATGGGGGGGGACAGCTGGATGGAGAGAATCGCCTTTCTGGTACATTTGGGAGTGCCTCATTGGATGGTGTATCAGACTATTATTCCCAGCTAATTTACAAGGTACTAACGAGCTACTAATTAAAATACTGACTGTTCATTTGCTGCTGAAGCATCAAGCAATCGCTTTTATTCCTAACCAGGAATCTTGCTCAGCTGTAAATTCCACTGACTGTAAAAGATTTTGGTTATGAGATAAACAAATGGTCACTTGTGTTTTCATTCTTTTACAGCAGAATAACTTAAGCAACCCGCCCACCCCACCTGCTTCCCTGCCCCCGACCCCTCCTCCAGTGGCACGACAGAAGTTGCTTAATGGCTTTGCCACAACAGAGGAGCTTGCCAGAAAAGGTGGCCTCATTGCTGGACACGATGG[T/C]GAGTAGTAGCTGATGTAGACTGAGCGGGTGATTTCGATCTATATTTGAGCGTGCGTAAATTCTAGAAGAAGTCATACATGTTTATTCATTTGGCCAGAAGAGAATTGGTTATCTGATTTCTAATAGTTTTTTTTTATTATTATTGAATAAAGTCAGTAAACTTCACCCTTACGACCTCAAGTGGCACCCACTAACTTGAAATGTTTGTTTTAATCTTACCCTGAATATCTGGAAAGCTGCCTAAAGAAAATATTTTTATTTTTACATTTTTATTTATTCTGTAAATAGGAGGTGTAATGGTTCATCTGGTGTTATGGAATTTGTTAATTTCTCAATTTTCAGAGTCACTGGTCAGCTCAATTTCTATACAATTACGAAGAAGAAAAACCTAGAATAAAACTGCTTGTATTTTTTATTATTTACTATTGGTATGTGTGTACACCAACAGATATTTAAACAATTTACATAAAATGCCTTTTATATATAAAGAAATACACATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1802
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Missense 4278 4879 53 60
ENSDART00000131780 Missense 133 734 3 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12812281)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13337506
GRCz11 2 13020292
KASP Assay ID:
554-1794.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTTCTCCTGCTCCGTACCTCCACATGGCTTTTGCACCAGCSAAAGCAA[T/A]CAAGACAGAATCCAAACCTAGAAGCATATCAGAGGGCCATCTTAAAGTCA
Long Flanking Sequence:
TGGAATCAGGTTGGACTTTATCTTAGTGATTGGGTCATTGTTGGCATTCTGCATCAGAAAATGTTTAAACCCATAATCTTGTCCTGTGTTCAGGAGTCTCGGTTATGTTCAGATGGTGGTTTGGTGTTCTGCAGCCACAGCTGTCTCATTCTGCATTCATCATCATCTCAGTCCAACGGGAATGCTGACAACAAGGTTTGCTTTCTCTGTCATAATCCATATGCAAACAGTTTTGAGATTTGGAGTTTTGAGTGTGGTTGATTTTATTTGAATAATGGTGAACTACTTTTAAATATGCATGTTATATGTATCCACATTGTATTTCCAGGCTTCTGTTCCTCTACTTTCTGAAAGTGCTTTGAAACAGAGCTTTTCTAAAGTCCAGCACCAGTACAGCAACAACATGTCCTCACTGGATGTCCATTGCCTGGCCCAACTCCAGCCCAAGCCATCTTCTCCTGCTCCGTACCTCCACATGGCTTTTGCACCAGCGAAAGCAA[T/A]CAAGACAGAATCCAAACCTAGAAGCATATCAGAGGGCCATCTTAAAGTCACAGTCAAGCTAAAACCACGTTTGCACAGTCACTTAGAAGACAAACAATGGCATCACGGCAAACGCTGGAAAGGCCTGCGCTGGCGAAAGTGGACTATAGACATTGCAATGCCAAAAGTAGCCCCTCAATCTTCAGAGTCAGAATTGGAGGAGCGCTTGAAACAGCTCACCACATCTTTGCGGCCATGCTTAACCATCCGCGATCAGCGCCGCTGTTGTTTCTGCCAGCAGATTGGGGATGGGATGACGGATGGCCCTGCTAGGCTGCTCAACCTGGACTTGGACACATGGGTGCACCTCAACTGTGCCCTTTGGTCCTCAGAGGTCTATGAGACCCAAGCAGGTGCTTTGATCAATGTTGGTTTGGCCCGTCAGCGTGGACAAACTGTGGTTTGTGCATTTTGTCAACGCTTAGGTGCCACCAGTGGCTGCCATCGCCTGCGGTGCCTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38318
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
ENSDART00000112279 Nonsense 4293 4879 53 60
ENSDART00000131780 Nonsense 148 734 3 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12812325)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13337550
GRCz11 2 13020336
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAATCAAGACAGAATCCAAACCTAGAAGCATATCAGAGGGCCATCTT[A/T]AAGTCACAGTCAAGCTAAAACCACGTTTGCACAGTCACTTAGAAGACAAA
Long Flanking Sequence:
CATTCTGCATCAGAAAATGTTTAAACCCATAATCTTGTCCTGTGTTCAGGAGTCTCGGTTATGTTCAGATGGTGGTTTGGTGTTCTGCAGCCACAGCTGTCTCATTCTGCATTCATCATCATCTCAGTCCAACGGGAATGCTGACAACAAGGTTTGCTTTCTCTGTCATAATCCATATGCAAACAGTTTTGAGATTTGGAGTTTTGAGTGTGGTTGATTTTATTTGAATAATGGTGAACTACTTTTAAATATGCATGTTATATGTATCCACATTGTATTTCCAGGCTTCTGTTCCTCTACTTTCTGAAAGTGCTTTGAAACAGAGCTTTTCTAAAGTCCAGCACCAGTACAGCAACAACATGTCCTCACTGGATGTCCATTGCCTGGCCCAACTCCAGCCCAAGCCATCTTCTCCTGCTCCGTACCTCCACATGGCTTTTGCACCAGCGAAAGCAATCAAGACAGAATCCAAACCTAGAAGCATATCAGAGGGCCATCTT[A/T]AAGTCACAGTCAAGCTAAAACCACGTTTGCACAGTCACTTAGAAGACAAACAATGGCATCACGGCAAACGCTGGAAAGGCCTGCGCTGGCGAAAGTGGACTATAGACATTGCAATGCCAAAAGTAGCCCCTCAATCTTCAGAGTCAGAATTGGAGGAGCGCTTGAAACAGCTCACCACATCTTTGCGGCCATGCTTAACCATCCGCGATCAGCGCCGCTGTTGTTTCTGCCAGCAGATTGGGGATGGGATGACGGATGGCCCTGCTAGGCTGCTCAACCTGGACTTGGACACATGGGTGCACCTCAACTGTGCCCTTTGGTCCTCAGAGGTCTATGAGACCCAAGCAGGTGCTTTGATCAATGTTGGTTTGGCCCGTCAGCGTGGACAAACTGTGGTTTGTGCATTTTGTCAACGCTTAGGTGCCACCAGTGGCTGCCATCGCCTGCGGTGCCTTAACATCTACCACTTTACTTGCGCCCTACAGGCTGGCTGTACATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19695
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
ENSDART00000112279 Essential Splice Site 4603 4879 53 60
ENSDART00000131780 Essential Splice Site 458 734 3 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12813257)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13338482
GRCz11 2 13021268
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAGCAGGGATATGAGGATCTGGTTCTGACTGATACCTCTGCTAAAGG[T/C]ACATCGTCATTAGACTCTTTCCTAATTGTATTATGTTTGTTAATGACAGA
Long Flanking Sequence:
GGCTGCCATCGCCTGCGGTGCCTTAACATCTACCACTTTACTTGCGCCCTACAGGCTGGCTGTACATTTTTCAAGGATAAGACAATGCTCTGCCACCAGCACCGTCCACGCGGAGCTGGTGCTGCTGCTGGTTTACATGTAGAACATCAGCTGCGCTGTTTCTCAGTGTTCCGTCGCGTTTATGTACAGCGTGATGAACTGCGTCAGTTGGCGGCAGCCGTGCAGCAGCCGGAGCGTGGCCATACTTTCCGTGTGGGTAGTTTGCTTTTCCATGCAATGGGTCAGCTGCCTCCTGCCCTGATGCCCACATTTCACTCATCTACAGCCATCTTTCCACCTGGCTATGAAGCGACTCGCCTTTACTGGAGCATGCGACATGGTCAGAAGCGTTGCCGATATGTCTGCTCTGTAGAAGAGCATGAAGGGCGTGCCGAATTCAGCATTCGTGTCATTGAGCAGGGATATGAGGATCTGGTTCTGACTGATACCTCTGCTAAAGG[T/C]ACATCGTCATTAGACTCTTTCCTAATTGTATTATGTTTGTTAATGACAGAGTTCCTGTTTCTCCTTAACAGAGTCTTATGTTTAATTTGATCATTTACTACATGTAAAGTCATTACGAGAAGACTGAATGTTCAAAGTAAAAATGCAGTGTTGTTGTGCATTCTCCAGACTCCTGGTTTTACAGCACTTTGCAATCAATGAGCATTGCACATCAGTGTCAAGCAATTGCTTATGATCTATAGTTTAATCACTTTAGTTTACCCTGTCTAAGGAATAAATCGACTGTAAAAATATTTCTTAACACATTCGATATAGAGATTTTACAAGTATCTTCTGTGTCATTTTTTGTAATCACATTGGCGAAAACCATTTATTGGTCATTATCCAATTTTCCAGTAGCTAAACTTAAAGAGCCCCTATTATGCATTTAAAAAGGTCATATTTTGGTTTAGGGGGTCTCCAACAACAGGCTGAAATGCATGCAAGGTCAAAAAAAACTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25778
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112279 Nonsense 4831 4879 59 60
ENSDART00000131780 Nonsense 686 734 9 10
ENSDART00000132574 None None 90 None 2
ENSDART00000133043 None None 383 None 8
ENSDART00000137621 None None 293 None 4
ENSDART00000143400 None None 279 None 6
ENSDART00000145384 None None 328 None 8
ENSDART00000146674 None None 601 None 13

The following transcripts of ENSDARG00000075560 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 12825521)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 13350746
GRCz11 2 13033532
KASP Assay ID:
2259-1714.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATAAATCATTCATGCTCACCAAATTGTGTGGCTGAGGTTGTGACGTTT[G/T]AGCGGGGCTACAAGATCATCATCAGTGCTGCCTGCAGGATTGAGAGAGGA
Long Flanking Sequence:
TTTGATTCAAAGCTTATTTTTTGTCATCATTACTCCAACTCTCAGCATCAAGTGATCCTTCTGAAATCATTCTAAAATGTAGAAATGTTTCTAATTATATTGAAATCAGTAGATAAAATCATGATATTTTTATTTTATTATTTTTCGCTGAATAGAAGGTTTATTTGTAAAAAAGAATACAGCTATGTGAAATATTTTGTAACATTGAAAATGTATTTTCTGTCATTTGTAAACAGTTTAATGCATCCTTAGTAAAGTAAAAAATTCATATTAAATAAAAAAATAAGAATAGTGTTGAATAGTGTAATAAGTTAAACTAGTATATACATTTTCTTGCACTGTTTCTGCTACAGGAGTCTTTTCTGTGCAGTTTGAAGTACAGTTATGCTCACTGAATAACTACAACCGCTTTAATAATGATTTAAGATTTATTTCATTTATTTTTTAGGTACATAAATCATTCATGCTCACCAAATTGTGTGGCTGAGGTTGTGACGTTT[G/T]AGCGGGGCTACAAGATCATCATCAGTGCTGCCTGCAGGATTGAGAGAGGAGAAGAGGTGAGATTTTATCTGTCATTTATTGTCATGCACACTAAATAAAATAACTTCATTTGCTAATGCCACAAACACAACCGATACTTTTTCTGTTTGTTTTCTTATATATTCATATATTGATATCGGATTGTATAGGACATTTAGTTGTACATTAGTTTTGCATTTAGTTTTTGTTTATTGTTACCTGACTTACAATCTCATGTTAGGTCAATAGGTGGTCTTTAGCAACTCAAACACATCAACCACATGAGCAGTTACACTCTGAAAGCAATATTAATAAATGTGTGGTTGACTACTTCTGAAAGGGGTCAACAGTTGAAAAGCTTCTAACTTTTTAGACTTTGTTTAAACATGTAACATCATCCACCTATGATCAAACTAACTGCAATGTATCATAGTACCTGGTATCAAAATAGCATTAAAGAGATGAAACGAGATTTGACAATG
Associated Phenotype:
Not determined