ZMP
wu:fl04e06
Ensembl ID:
ZFIN ID:
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 |
|---|---|---|---|
| sa10413 | Nonsense | Available for shipment | Available now |
| sa18765 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| 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 |
| sa18766 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9339 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15353 | Nonsense | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa18765
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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:
sa10883
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa18766
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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:
sa9339
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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:
sa15353
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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