Busch Lab

ZMP

wu:fl04e06

Ensembl ID:
ENSDARG00000076867
ZFIN ID:
ZDB-GENE-030619-16
Human Orthologue:
MKL2
Human Description:
MKL/myocardin-like 2 [Source:HGNC Symbol;Acc:29819]
Mouse Orthologue:
Mkl2
Mouse Description:
MKL/myocardin-like 2 Gene [Source:MGI Symbol;Acc:MGI:3050795]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa18765 Nonsense Mutation detected in F1 DNA Not yet available
sa10413 Nonsense Available for shipment Available now
sa10883 Essential Splice Site Available for shipment Available now
sa10111 Essential Splice Site Available for shipment Available now
sa20120 Essential Splice Site Available for shipment Available now
sa44573 Nonsense Mutation detected in F1 DNA Not yet available
sa17904 Essential Splice Site Available for shipment Available now
sa9339 Nonsense Mutation detected in F1 DNA Not yet available
sa18766 Nonsense Mutation detected in F1 DNA Not yet available
sa15353 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa18765
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
ENSDART00000113531 Nonsense 50 926 1 15
ENSDART00000113531 Nonsense 50 926 1 15
Genomic Location (Zv9):
Chromosome 3 (position 46342679)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48352232
GRCz11 3 46304566
KASP Assay ID:
2259-4007.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAACTGTCTCTTCAGCCCACTCAAAGCCTTCCACCCATTAAAGAGCGC[A/T]AGAACGGTGAGTGAGACCATTCGGTCAGACCCCTCAGGCCATAACTCTGC
Long Flanking Sequence:
TAAATGTATTTATTTTGAGACAGAGTTTTTTCATTTTGTGGTGTGCTAAGTTTACTATCATCAGTGAATGTAATGCAATACAAATGAATGCATTAACCTCATCCGCATTTCTGGCCCAGTTAAAGTTCATTAACAAAGAACCACACACAAGTAAATTAGTTTTGCCACCACACCCCAGCAACAACAACAACATAAAGCTCCATTAAGGCTTTCTAATGTTTACAAGTGCTGCAAAACACTTAAAAGCCTTTTGTTTTTCTGGCAGGCTGCAGTCTGAGCTTCCCGCTAGTCGTCTGTGCCGCTGTGGTACTTTTCAGAGAGAGAGAGACCCGTTCCTCTCCCCCCGAGGAGAGATGGAGCCCCGGGGGAGTCTGGGAGTGGAGGGTGACGCGAGTGCTCTAGGGGTGCTGGTGCCGAGCCCACGGAGCGAAGCGGTGACCCATGACCTGGAGGAACTGTCTCTTCAGCCCACTCAAAGCCTTCCACCCATTAAAGAGCGC[A/T]AGAACGGTGAGTGAGACCATTCGGTCAGACCCCTCAGGCCATAACTCTGCTCCCAAGCTCCTATTTCCTCCTCATTCGCTCAACTACCGCCCCGATTTGACAGTGAGAAAATAAGGCTTGCCAGAAGGTTGAGAAATTTGTTTGTGGTAAGACGTGGGGAATTACACAGGAATTGCATGCGAACGCCAGCATGTAATCATGTCTTAAGTGCTGCCTTTAACTCTTTTCCAAAGTGTTTTTGGCTCAGGTTCGAGTGCGCGACTGCTAATCTAATGTGATAGATTTTTGTGTCGAACGCGATTGCAGAAAGTCTCCGATATAGAGGGGTTTTTTTAGACTCGCAGTCATAATGTGGCTTTGGTTTGGCAGTAACTCAAAGGCACAGTCGATCATTCAGAAATGATCATCCTGTCAGAATTTATACACCATCATCATGTTTTAAAGCAGTAGGACTTTGATTCTTTTGTCAAAGACATTTTTGTTCGAATGTCTCAGCCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10413
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
ENSDART00000113531 Nonsense 50 926 1 15
ENSDART00000113531 Nonsense 50 926 1 15
Genomic Location (Zv9):
Chromosome 3 (position 46342679)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48352232
GRCz11 3 46304566
KASP Assay ID:
2259-4007.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAAYTGTCTCTTCAGCCCACTCAAAGCCTTCCACCCATTAAAGAGCGC[A/T]AGAACGGTGAGTGAGACCATTCGGTCAGACCCCTYAGGCCATAACTCTGC
Long Flanking Sequence:
TAAATGTATTTATTTTGAGACAGAGTTTTTTCATTTTGTGGTGTGCTAAGTTTACTATCATCAGTGAATGTAATGCAATACAAATGAATGCATTAACCTCATCCGCATTTCTGGCCCAGTTAAAGTTCATTAACAAAGAACCACACACAAGTAAATTAGTTTTGCCACCACACCCCAGCAACAACAACAACATAAAGCTCCATTAAGGCTTTCTAATGTTTACAAGTGCTGCAAAACACTTAAAAGCCTTTTGTTTTTCTGGCAGGCTGCAGTCTGAGCTTCCCGCTAGTCGTCTGTGCCGCTGTGGTACTTTTCAGAGAGAGAGAGACCCGTTCCTCTCCCCCCGAGGAGAGATGGAGCCCCGGGGGAGTCTGGGAGTGGAGGGTGACGCGAGTGCTCTAGGGGTGCTGGTGCCGAGCCCACGGAGCGAAGCGGTGACCCATGACCTGGAGGAACTGTCTCTTCAGCCCACTCAAAGCCTTCCACCCATTAAAGAGCGC[A/T]AGAACGGTGAGTGAGACCATTCGGTCAGACCCCTCAGGCCATAACTCTGCTCCCAAGCTCCTATTTCCTCCTCATTCGCTCAACTACCGCCCCGATTTGACAGTGAGAAAATAAGGCTTGCCAGAAGGTTGAGAAATTTGTTTGTGGTAAGACGTGGGGAATTACACAGGAATTGCATGCGAACGCCAGCATGTAATCATGTCTTAAGTGCTGCCTTTAACTCTTTTCCAAAGTGTTTTTGGCTCAGGTTCGAGTGCGCGACTGCTAATCTAATGTGATAGATTTTTGTGTCGAACGCGATTGCAGAAAGTCTCCGATATAGAGGGGTTTTTTTAGACTCGCAGTCATAATGTGGCTTTGGTTTGGCAGTAACTCAAAGGCACAGTCGATCATTCAGAAATGATCATCCTGTCAGAATTTATACACCATCATCATGTTTTAAAGCAGTAGGACTTTGATTCTTTTGTCAAAGACATTTTTGTTCGAATGTCTCAGCCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10883
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113531 Essential Splice Site 118 926 4 15
Genomic Location (Zv9):
Chromosome 3 (position 46373042)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48382595
GRCz11 3 46334929
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAAGCAGACCTGACCGTGCTGAACTTGTTCGCATGCACATTTTACAAGG[T/C]ACGTACCTCACCGAACAGATGTGCTAAAAAAACACCAGTCTTATAAAAAT
Long Flanking Sequence:
ACAGAGTCTCAGAGTTCAACAGTTTAACATACCAAATGCGATTTGCACATATCTATTTTAAAGATATGAAATAATGTCATGTCAGTGTTATGTAATTAACGGATGTTTATTTTTTCTTCCAGCGCTGAAGACACCTGCGGCTTTTCATGAGCAGGTCAGAAGTTTGGAAAGGGCAAGGGTAAGTTGGCTCTTCTCAGTATTACTCTTACACTTTCCATGATTCATTAACGAACTGCCCTTTAAAAACCTTATTAGTAAAGGTTATGAAAAGATCACAACACCATAAAATTTAATTAATCTGCTTAAAATCATGTGTAATCAATGCTGTTCAGTAATTAATTTATTTATACCATGTTGTTTTCTAAATATAAACCATTTTATATATTAATTTACTCAATTTATATGTATTTTTATCTTATACAGACTGAGAACTTCCTGAAACACAAAATTCGAAGCAGACCTGACCGTGCTGAACTTGTTCGCATGCACATTTTACAAGG[T/C]ACGTACCTCACCGAACAGATGTGCTAAAAAAACACCAGTCTTATAAAAATACTTTGTCTCACTTCCTGGAGACTTTATCGTGTAGCTTTCTAAATGCTCTGAAGTTGTTTATTTGTTTCAGAAACCCACGCAGAGCCTTCTTTGCAAGCTACTCAGATGAAACTGAAGAGGGCACGTCTGGCAGATGACCTCAATGAGAAGATCGCACAGAGACCTGGACCAATGGAGCTGGTGGAGAAGAACATCCTGCCTGTTGACATTGGTAAAAACGAGGGTTATTTACCTGCATAATAAGGAAGACATACCAAAAAGTGGTCCATACCTCCATACTTGTTCTAAAACATCGACAGCATTTTTGTTTATACCCTGTAAAAGAGTTTATGAAATCAATTTGTGTTGGGACAACATGAAAGAATTAAGGTAGCTTATTAGTTTTTACAAATTTAAGTAGATTGAACTTAAAACGATTAAGTTGTTCCTAAAAAATGATTAGTTGGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10111
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113531 Essential Splice Site 165 926 5 15
Genomic Location (Zv9):
Chromosome 3 (position 46373306)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48382859
GRCz11 3 46335193
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGGACCAATGGAGCTGGTGGAGAAGAACATCCTGCCTGTTGACATTGG[T/C]AAAAACGAGGGTTATTTACCTGCATAATAAGGAAGACATACCAAAAAGTG
Long Flanking Sequence:
TGAAAAGATCACAACACCATAAAATTTAATTAATCTGCTTAAAATCATGTGTAATCAATGCTGTTCAGTAATTAATTTATTTATACCATGTTGTTTTCTAAATATAAACCATTTTATATATTAATTTACTCAATTTATATGTATTTTTATCTTATACAGACTGAGAACTTCCTGAAACACAAAATTCGAAGCAGACCTGACCGTGCTGAACTTGTTCGCATGCACATTTTACAAGGTACGTACCTCACCGAACAGATGTGCTAAAAAAACACCAGTCTTATAAAAATACTTTGTCTCACTTCCTGGAGACTTTATCGTGTAGCTTTCTAAATGCTCTGAAGTTGTTTATTTGTTTCAGAAACCCACGCAGAGCCTTCTTTGCAAGCTACTCAGATGAAACTGAAGAGGGCACGTCTGGCAGATGACCTCAATGAGAAGATCGCACAGAGACCTGGACCAATGGAGCTGGTGGAGAAGAACATCCTGCCTGTTGACATTGG[T/C]AAAAACGAGGGTTATTTACCTGCATAATAAGGAAGACATACCAAAAAGTGGTCCATACCTCCATACTTGTTCTAAAACATCGACAGCATTTTTGTTTATACCCTGTAAAAGAGTTTATGAAATCAATTTGTGTTGGGACAACATGAAAGAATTAAGGTAGCTTATTAGTTTTTACAAATTTAAGTAGATTGAACTTAAAACGATTAAGTTGTTCCTAAAAAATGATTAGTTGGATTGTTTCAGCTCACTTTAAATAAGTAGTTTGAACAAACAAAAAACATAATTTTAGCGTATACTATGGATGAAAATGGCTTCGAAAATATTTTATTCTGTGTTCAACAGTGTTAATAAATTCATAAAAAATTTACTATAAGTCATTAAAAAGTAAATCAAGTGTCAAGGATAAAGTATAAACAATTTTTTGGTGAACTAACCCTTTAAAGCAGAATGGATTTTGATTAGCTGTTTTGTTACAAAGTGGATGCTTGCAAAAGACTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20120
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
ENSDART00000113531 Essential Splice Site 255 926 7 15
Genomic Location (Zv9):
Chromosome 3 (position 46376495)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48386048
GRCz11 3 46338382
KASP Assay ID:
2259-4010.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCGTCATTGCTGCTGTTCCCACAAGACCCGGACCCACCCTGGTGAAGG[T/C]AAACCATATGTCTCTAAACCACAGTGATGTCATTTCCTGTCAGTGTTTGT
Long Flanking Sequence:
GCGAAGCTCTGTCTCCAGATCAGCCAGCTAGTCACGAGTCTCAGTGCTCTGCATCTTCTCCTGTGGAAACCAGACTGCCTGATTCATCGTCTGTATCGCCTCCGACTGTCTCCAAACTCCAGGTCAGCCTCTTAACAGTCCCTACATCCAGACCACACTGTCTGTAAACCAGTACAGGAAAATTCACTGCAAATATTTACTTGAAGCATTTGATAAAAGAAAGACTGATATCAAATCCATCTATTAAAGCATAAGAAGCAATATGCTCTGCAGAACAGTATCTATCTTATCAACTGATATTTCCCCTTCCATTATGTTTTTATCACTCTTTGTGGCCATATGGCTTTTTAAAAACTGTTTATCTCACATGTGTCTACCTACATGCCAGTGCTCGGACATCCTAAACCGAACTTCAGCAGAAGATAGTCGAATAAAAATGAATGCCACTCAGACCGTCATTGCTGCTGTTCCCACAAGACCCGGACCCACCCTGGTGAAGG[T/C]AAACCATATGTCTCTAAACCACAGTGATGTCATTTCCTGTCAGTGTTTGTTTTGTGCTCTGAGATAAAGGGCAGTGACTCTGTGGTATTGCTGAGTAATTTCATAACAGCAAGTTATATGTGGAGAAATTTACCACACAGACTATCATAATGACTTTTTGTATTTAATTGTGCACTATTGTCCATCGGAAATTCAGTAAAAGTCAGCTGATCTAAACAAAATGTAATGCGTTGAATGATATAGTAATTAGTTAAAGTTATTAGTAACTAGTAAAACTATGGTAACTAGTAACCTTAACTAAGTAATGTGCACCTTTTGTAAAGATGCTTTGAAACAATAATTATTGTGAAAAGCACTTAACAAATAAACTTGATAATAAATAAATTGAATTGAATTGAATAGTACTGTTTAAATATTAACATTTAAAAATGCTATACCAATAAAACATTTTTTTTCCTCTAGTAAATAATACATTTATTCATCAAGGACAAGTTAAACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44573
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
ENSDART00000113531 Nonsense 372 926 9 15
Genomic Location (Zv9):
Chromosome 3 (position 46387946)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48397499
GRCz11 3 46349833
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCAATCTTCCTGCTCCCATTGTGGTGTCTCTGCCCAGTGTGGCTCCAT[C/A]ACGTCCCAACAACGCTCGTAAAAGCGGGTCTCTTCCCTCCTGCCTAGATG
Long Flanking Sequence:
TGCTATTTCCCCTTATTTAATGTCAGTTCAATTGAATTATTTGTTTCGGACCAGTGCAATTGAATATAATTCTGATATATCAGTTTCAGTTCTGACACTAAAATGATTTACTGCGAGCCTGATTGCATTATAACACAAGTGCGTAGCTCAGAACGGAATGCGAACATTGTGTGCTATGAATGATAGCCTTTAAATAACGTTTTCAACTATTAATCTTGTCTAAAAGACCTTTCATCACACCAGCTGTAATACAGCAGTTCCTCACATTCGTTTCCACTTTGACTTCTGTTGCCCCAAGATATACCTCTGCTTCTATTGTGTAGAAAGGCTGTTTATTGTGAATGATGAGGGGAACAGGAAGTTCCCGTTGCATTTAAAATCCCTCACACTCCTCTGCAGGCAAGTAGCTGAGAGTCCGAACAGCTGCCCCAACATCACCCTGAGCACCAGCCCCAATCTTCCTGCTCCCATTGTGGTGTCTCTGCCCAGTGTGGCTCCAT[C/A]ACGTCCCAACAACGCTCGTAAAAGCGGGTCTCTTCCCTCCTGCCTAGATGAGATGAAGGTGGGTGATGTACTCATTTGTTTATGTTCTCCATGCAAGATACGCTTCGTTTCCACTGAGCAGTGTGATTAAGTGCAGTACAGTATGGTATGGGTCACCTTGATTAAACTTCATTTCGACGTCATTCTCACTTGATGAAAGCAAGCCATATGGGTCATACAATTATCTGTATAATTATTATACAGATAAATATAATTAAAATATAATTATTTGTCTTTTACACGCTCAATTCATTATTTCAAATGTAGACATGTGGCAAGCACTCAATAATAGACAGAGAAAGCTGCATCCCTCAAATTTCTGCATGTTTAGATATGACATAAATAGCCCCATAAACAACAATGGAGGACATACAACAGGTTATTTGAGTAAACAAAAACTAGACTTTGAAGACTAAGGGCCCTGTCATACACCCGGCGTAGTGTGGCGCAAGGCGGGACGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17904
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113531 Essential Splice Site 624 926 10 15
Genomic Location (Zv9):
Chromosome 3 (position 46392178)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48401731
GRCz11 3 46354065
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACAAATCCTGCTTCCCATCARCCTGCCCAGCAACCCCATGAGYACACAG[G/A]TGATATTTCACTTCTGTTTATGGTTAGGAAAATGTATACGCTTATAAATA
Long Flanking Sequence:
ACAGCAGGGACAGTCCTACTAAAGCCCAATGCAGACTGTCTCCGGCCCAGCCTCCAGGAGGGACCTCGCCCTTCAAACTTGTATCTGAAGACATGGACATCAAGGTGTCCGAAAAAGACCAGCGCCTCCACGAGAAGGAGCGCCAGATTGAGGAGCTGATGCGCAAGCTGGAGCAGGAGCAGCGGCTGGTGGAGGAGCTGAAGATGCAGTTGGAGGTGGAGAAAAGGAGTGGAGGACACCAGGCTGAACCCTGTCCACTGGTCCAAGTCAAAGAGGAGATTGGTGCCAGCCCTAGCTGCAACTCCGGGCAGAGTCTGCAAGCTCCAGGTGTGAAACAGGAAGAGCCACATACCCAGATGGCCCACGCTCAAGTGCAGCAGTTCTATATTAAAACCCAGCAAGTCCCTCAAGTACTGCACCAGCAGGCACTTATCAGCCCGCAGTCTGCCTCACAAATCCTGCTTCCCATCAGCCTGCCCAGCAACCCCATGAGCACACAG[G/A]TGATATTTCACTTCTGTTTATGGTTAGGAAAATGTATACGCTTATAAATATTTTATTCTGAGCTTTTCTTTTCTTTTTGGCAGGCACCAACTATTCTCCAATCAACCAGTTTGGCACAAAGCATCGGACAGACTCCACTTCTGCAAACACAAACGTCCAATAATGCGATGCTACAGCAGCATTCAAATCAGACGCCTTCACCACCCCATGTGAGTATATACCACTTCTGTGTGATATTCATCAAAGACTCTAGAATACACTAGACATGTCACTCGTATAGTTTTGAATGGGGAAAAGTGTAACAGTCAATGTGTCGAACGAAGCCCTTACTACTAGTACAGGAGCCATTCATCGATCGCTATAGACCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCTACCCATATCACACACACCTGCCTGTAATTATCACGTGGTGTCCTAATTAATTGGTTCAGGTGTGTTTGATATGGGTAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9339
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
ENSDART00000113531 Nonsense 748 926 13 15
ENSDART00000113531 Nonsense 748 926 13 15
Genomic Location (Zv9):
Chromosome 3 (position 46399680)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48409233
GRCz11 3 46361567
KASP Assay ID:
2259-4012.1 (used for ordering genotyping assays)
KASP Sequence:
GCCCGAAGAGCAAAGACCCMCCYGGCTACGAGGAGGCCGTCAAACAAACC[A/T]GAGGYCTGCAAGCCMCAATGCAGGTAATTTAAAGCTATKCTCAAGTATCA
Long Flanking Sequence:
GAACATATCATGATATGGTTTTTATTTCATATTCCTCATCACTAACTTGTACAAACATGGACTCTTGTTCAGTCATTTTTTAAGTAAGATGTGAAAGTGAGTCAGTATTTTATTTGCCCCGCCCTTTTTATTGTGATTGGACGGCTGGATAAAAAGTGACAGGCGCAAACATCACATTGTACCTCAATGCGCTCTGCAATCAGGAGAGCATGCAGAACGTTTTTGGCTGCGTAGCAATTGGTTAACAAACACTCTGAACACTTATTTTTGTTTTCCATAGAACTAATTTTGATTTTCTTGAAGAAAAAAACAGGACATTGACAGAATCCATGTGTACGCTCACTTTTTGTTCTTTAGTGTAGCTAATCAATGTTTTATGTTTTGTTTAGCCTCCCTCACCCTGTCAGCTCAACTACATCCTTCAGCCATCATCATTCCCCAATCACCACAGCCCGAAGAGCAAAGACCCCCCCGGCTACGAGGAGGCCGTCAAACAAACC[A/T]GAGGTCTGCAAGCCACAATGCAGGTAATTTAAAGCTATTCTCAAGTATCAGTTTTAACTAGTATACAAATGGAGATCAATATCAGAATTGAATTGAATTGAACTGAACTGAACTGAACTGAACTGAATAGAATTGAATTGAATTGAATTGAATTGAATGGAACTGAATAAAGGATAAAAACACAATAAAGCCCTGGGCTTGTTTCCATCGTGGTCCTCGCTGCATGTTACCTTATGCTAATAATAGTAAGCTAAGTTACTTCAGATTGCTCATGGAGATTCTCCACATTATCCTGTCCTCTGATATTTTTGACTTTAATGGACGAACAGCCATTTTGGAAGACTTAAATGATTGATTGTCATTGTAAAGATGCATTATTTTAAAAATCACCAATTGTAACAACGAACTTTTCGTGCTTGCTAACTTTTATCTAGAAAACATGCTGTCATGCTGAGTCTTTCAGTCACTTTAGAACAGCTCAATATCCTTCCGTCAGTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18766
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
ENSDART00000113531 Nonsense 748 926 13 15
ENSDART00000113531 Nonsense 748 926 13 15
Genomic Location (Zv9):
Chromosome 3 (position 46399680)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48409233
GRCz11 3 46361567
KASP Assay ID:
2259-4012.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCGAAGAGCAAAGACCCCCCCGGCTACGAGGAGGCCGTCAAACAAACC[A/T]GAGGTCTGCAAGCCACAATGCAGGTAATTTAAAGCTATTCTCAAGTATCA
Long Flanking Sequence:
GAACATATCATGATATGGTTTTTATTTCATATTCCTCATCACTAACTTGTACAAACATGGACTCTTGTTCAGTCATTTTTTAAGTAAGATGTGAAAGTGAGTCAGTATTTTATTTGCCCCGCCCTTTTTATTGTGATTGGACGGCTGGATAAAAAGTGACAGGCGCAAACATCACATTGTACCTCAATGCGCTCTGCAATCAGGAGAGCATGCAGAACGTTTTTGGCTGCGTAGCAATTGGTTAACAAACACTCTGAACACTTATTTTTGTTTTCCATAGAACTAATTTTGATTTTCTTGAAGAAAAAAACAGGACATTGACAGAATCCATGTGTACGCTCACTTTTTGTTCTTTAGTGTAGCTAATCAATGTTTTATGTTTTGTTTAGCCTCCCTCACCCTGTCAGCTCAACTACATCCTTCAGCCATCATCATTCCCCAATCACCACAGCCCGAAGAGCAAAGACCCCCCCGGCTACGAGGAGGCCGTCAAACAAACC[A/T]GAGGTCTGCAAGCCACAATGCAGGTAATTTAAAGCTATTCTCAAGTATCAGTTTTAACTAGTATACAAATGGAGATCAATATCAGAATTGAATTGAATTGAACTGAACTGAACTGAACTGAACTGAATAGAATTGAATTGAATTGAATTGAATTGAATGGAACTGAATAAAGGATAAAAACACAATAAAGCCCTGGGCTTGTTTCCATCGTGGTCCTCGCTGCATGTTACCTTATGCTAATAATAGTAAGCTAAGTTACTTCAGATTGCTCATGGAGATTCTCCACATTATCCTGTCCTCTGATATTTTTGACTTTAATGGACGAACAGCCATTTTGGAAGACTTAAATGATTGATTGTCATTGTAAAGATGCATTATTTTAAAAATCACCAATTGTAACAACGAACTTTTCGTGCTTGCTAACTTTTATCTAGAAAACATGCTGTCATGCTGAGTCTTTCAGTCACTTTAGAACAGCTCAATATCCTTCCGTCAGTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15353
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
ENSDART00000113531 Nonsense 863 926 15 15
Genomic Location (Zv9):
Chromosome 3 (position 46400997)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48410550
GRCz11 3 46362884
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCCMGAACSCTGAGACTGATGGAGGAGCTTAAAAAYCAGCTTTTGGAG[C/T]GACYACACTCTCCGATGGACACCTCAGATCTGACYTTCACAGATGCGCCG
Long Flanking Sequence:
ATAAAAGGTCCTTGTTTTGGTTTAAACTGAAGGATATCTCAAAGTATGCTGCATACTTTGTAATGTCTTAGTGTAGTCTTATCTCATATTTTTCCATAAAGGTTCCCACTGCCACCAGTCAGCACATGGACGATTTGTTTGACGTCTTAATAGAGAGTGGAGGTGAGAGCTTTCAGACATTCAAATCACAAATTTCAGCTGTAATGAATATGTAACTAAACCATTTTTGTGGTCTCCCAGAAATTCCACCTCTATCCAGGCAGGATCCATCTCTGGACAAACTTCACCCTGTGACAGCCAACATCACCACCTTGCCTATCAACACGGTGCTGTCACGTCCTCCTCCACAGGTACATGTGGCCCGTCCGCCTAACCAAACCCATGTGTCTCCACTCAGCCTGGTGGCCCTGGCGTCTGATAACCAGCTGGAGGCTCTTCTGGAGGACGCAGAACCCCGAACCCTGAGACTGATGGAGGAGCTTAAAAACCAGCTTTTGGAG[C/T]GACCACACTCTCCGATGGACACCTCAGATCTGACTTTCACAGATGCGCCGCCCACCGCCCTTCAAGTACCTGGTCTCGATAACATGGAGTGGTTGGACCTCACGATCCCCGGTCCGGCTGGCATCTCCTCTCCAAACCCAGTCTTTTCATCAGATTTCTTGGATTCCACTGATCTGCCGTTACACTGGGAATGAGCTCACAATGGATGGACTGTTGTAGAGCTCAGTCATTGGGTTCTGTGCGAAAGCCAATGTGACCACTGATAGTTTAGCACCAGCTTTTCTCATTTGCGCAGGTTTGTGTGCTGTTATTGTTACAAACACTTCTTTCAAGGCAGAAAAAGAATGTAGAGACACTTTTTATCCACCTATATATTTAGGCAGCGATCTGCTTTTTAGATATATTGAAGCAGTTTTTGAAACTGTTGGCCTTTGGTATCTAAAATGTTGTTTTTAGATTATAGTAAGTGTCTTTTTTTACTGACAGGATATGTATATTAG
Associated Phenotype:
Not determined