ZMP
si:ch211-165e15.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate dystonin (DST) [Source:UniProtKB/TrEMBL;Acc:B8A457]
Human Orthologue:
DST
Human Description:
dystonin [Source:HGNC Symbol;Acc:1090]
Mouse Orthologue:
Dst
Mouse Description:
dystonin Gene [Source:MGI Symbol;Acc:MGI:104627]
Alleles
There are 22 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15356 | Nonsense | Available for shipment | Available now |
sa14777 | Nonsense | Available for shipment | Available now |
sa12257 | Nonsense | Available for shipment | Available now |
sa16177 | Essential Splice Site | Available for shipment | Available now |
sa10442 | Essential Splice Site | Available for shipment | Available now |
sa11822 | Nonsense | Available for shipment | Available now |
sa11890 | Nonsense | Available for shipment | Available now |
sa22197 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15356
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Nonsense | 829 | 7146 | 23 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1408764)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1405934 |
GRCz11 | 13 | 1537457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTCAGATCACCATCGGCAAAGAGGACGAGTGTGTTCTGGTGAGCAACT[C/A]GCACAGAGCCAAGTGGAAAGTCATCAGTMCGTCTGGAAATGAGGCCATGG
Long Flanking Sequence:
GGACTACCTGAAGAGCCTCCAAGATGCCATTCACAGGAAGTACAGCTGTGACAGAAGCAGCAGTCTACACCGGCTGGAGGATCTCATTCAGGAGTCGATGGTGGGTCACACGTGCACACGCTAAACGTCTCGTTCCGGAGGCTTCTCCGTATATCTTGTGTGTATCGTGCACTTGAGTGGATCACTACTCCAGCGCTGATGCATGACTGATGTTTCTCCACAGGATGAGAAGGAGCAGCTCCTGAAGTACAGCAGTACTGTGGGTGGGTTAGTGGGCCGAGCAAAAGCCATCGTTCAGCTCAAGGCTAGAAACCCAGAGAATCCCATCAGGACGTCCATACCTGTCAAAGCCATCTGTGACTACCGGCAGATAGAGGTGCGCTCACTATAGGATCTGCTTCTGCTGTTCATGTTTACAGAGATGCAGTAATGCATTGTGTGACCTGTCTGTCCTCAGATCACCATCGGCAAAGAGGACGAGTGTGTTCTGGTGAGCAACT[C/A]GCACAGAGCCAAGTGGAAAGTCATCAGTACGTCTGGAAATGAGGCCATGGTGCCTTCAGTCTGCTTCAGTGTTCCTCCACCCAATAAAGAAGCCACTGAAATGGCAAGCAGGTGAAGAAATCCCCACTCACTCACTCACTCACTCACTCACTCACTCACTCAATCATTTCACTCATTCATTCATTCATTCATTCATTCTCTCACTCACTCATTCACTCATTCATTCACCTACTCATTCATTCACTCACTCACTCACTCACCCACTCATTCACTCATTCACTTATTCATTCACCTCACTCACTCACTCACTCACCTACTCATTCACTCACTCACCCATTCACTCATTCAATCATTTCACTCATTAACTAATTAATTAATTCCTTCATTCATTCATTCATTCATTCATTCATTCATTCATTGTCAATCTGTCATTCACTCTTTCATTCACTCACTCATTCACTCACCCACTAATTCATTCATTCATTCATTTTTTCATTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14777
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Nonsense | 2380 | 7146 | 43 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1434776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1431946 |
GRCz11 | 13 | 1563469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGATATTAAGCATGCATCTACCGAAAAAGCAAGTGTAAGCAGTAGTT[T/A]GGAGCTCTATTTAMAGTCCAATTCTGAYATTCACTCTAAAACTTCTTCTA
Long Flanking Sequence:
CAATGTGTTTGATAAAGTTTCCAAGACAAGCCAGGGATCAGATAAAGCCATGCAGGTCTCTAGTGACGTGGGAAGTCTGAGCTCTAGTTCGGAGCTGCCATTAACCATAATTTCTGACATTCAACCTAAAGCAATTTCAACACAAGCCAATGTGTTTGATGACGTTTCTAAGACAAGGCAGGGATCAGATGAAGCCATTGAGGTATCTACCGACACAGAAGCAGTAAGAGGTAGTCAGGATCTTTATTTACCATCCATTTGTGACATTCAACCTGAAGCTATTTCTACAAAAGATAAAATGTCACATGATGTTTCTAGGACAAGACAGGGATCCGATGAACCCATGCAGATATCTGCTGACATAGCAAGTAAGAACAGTAATCAGGAACCCCCTTTACCTATCATTTCTGACAATATGTTAAATATTGTTTCTGAGGCAAGTCAGGCATCAGATGATATTAAGCATGCATCTACCGAAAAAGCAAGTGTAAGCAGTAGTT[T/A]GGAGCTCTATTTACAGTCCAATTCTGACATTCACTCTAAAACTTCTTCTACAAATATGTTTGATAACGTTTCTGAGATGAGCCGAGTATCGGATGAACCCATGAAGATATCTACTGGCATAGCAAGTTTGAGCAGTAGTCAGGAACCCTCTTTACCCATCATTTGTGACTTTCAACCTAAAGGTATTTCGACAAACAGTGTGATGGATAATGTTTCTAAGACTAATGGAATGGTGGATGATTGTGATGTAAAGTGTGCTAGTTCTCCATCTTATGTTAGGCAGGTGACATATTTCGGGACCTCAGCGAGTCAAGTTGTAAGCCCTGTACAGAGTGATTCTGGGATATCCTGTTCCTCACAAAGTGACATCTGTTCAGATGAAAGAAAATCAGAGAGTGTACTTAATCCTGGACAGGAATTCAAAGAGTCTGAAATAACACATGTGAATTTAGACAAAGGATCCTCTGGGAACTCAAGTACTTTGCTACCATTGGTAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12257
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Nonsense | 2464 | 7146 | 46 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1435325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1432495 |
GRCz11 | 13 | 1564018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGTTRCACAAGTTAGTTCACTCACCGAACCACAGTCAGACYTGTCTT[T/A]GTGTGGTGCAAATSCTCAGCCAMMAATTGAGACAACAGAGGTCAGTTTAA
Long Flanking Sequence:
TACAAATATGTTTGATAACGTTTCTGAGATGAGCCGAGTATCGGATGAACCCATGAAGATATCTACTGGCATAGCAAGTTTGAGCAGTAGTCAGGAACCCTCTTTACCCATCATTTGTGACTTTCAACCTAAAGGTATTTCGACAAACAGTGTGATGGATAATGTTTCTAAGACTAATGGAATGGTGGATGATTGTGATGTAAAGTGTGCTAGTTCTCCATCTTATGTTAGGCAGGTGACATATTTCGGGACCTCAGCGAGTCAAGTTGTAAGCCCTGTACAGAGTGATTCTGGGATATCCTGTTCCTCACAAAGTGACATCTGTTCAGATGAAAGAAAATCAGAGAGTGTACTTAATCCTGGACAGGAATTCAAAGAGTCTGAAATAACACATGTGAATTTAGACAAAGGATCCTCTGGGAACTCAAGTACTTTGCTACCATTGGTAGAAGATGTTGCACAAGTTAGTTCACTCACCGAACCACAGTCAGACTTGTCTT[T/A]GTGTGGTGCAAATGCTCAGCCACCAATTGAGACAACAGAGGTCAGTTTAAGTGCCGACGGTCATCCTACATTTGTTCAAAATTTGCTGAATGATAAAAAGTATATGTCATCTCAGACCAATGCATTGTGTACTGCTAAATACCCAAGTCATATAAGAAAGAACCTAGATGTCAAACATTGCAATGAAGATCCAAGTGTGGATGACCCAAGTACAGAGAATACAGTTAAAGAGTTGTCTGACATACAAGGAATGTTCAGAAATTCCTCTGAATTGCAACCAGGCCACGATAGTCCAAGTCCTTCTGTAAGTGTTATGCTTGACAAGAAAAATGAACAAACTGCAGGCATATTCACACAGTCTCAAGGTGGAGATACAGTAGTTAATGAAGTTGCTCACCAGGGTGACCTTGATTTACCTCATATATCAAAGGCCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGTTTTAAGATCTACCTTAAATGAGTTAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16177
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Essential Splice Site | 2478 | 7146 | 47 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1435746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1432916 |
GRCz11 | 13 | 1564439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KATACAGYAGTTAATGAAGTTGCTYACCAGGGYGACCTTGATTTACCTCA[T/A]AWATCAAAGGYCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGT
Long Flanking Sequence:
AACTCAAGTACTTTGCTACCATTGGTAGAAGATGTTGCACAAGTTAGTTCACTCACCGAACCACAGTCAGACTTGTCTTTGTGTGGTGCAAATGCTCAGCCACCAATTGAGACAACAGAGGTCAGTTTAAGTGCCGACGGTCATCCTACATTTGTTCAAAATTTGCTGAATGATAAAAAGTATATGTCATCTCAGACCAATGCATTGTGTACTGCTAAATACCCAAGTCATATAAGAAAGAACCTAGATGTCAAACATTGCAATGAAGATCCAAGTGTGGATGACCCAAGTACAGAGAATACAGTTAAAGAGTTGTCTGACATACAAGGAATGTTCAGAAATTCCTCTGAATTGCAACCAGGCCACGATAGTCCAAGTCCTTCTGTAAGTGTTATGCTTGACAAGAAAAATGAACAAACTGCAGGCATATTCACACAGTCTCAAGGTGGAGATACAGTAGTTAATGAAGTTGCTCACCAGGGTGACCTTGATTTACCTCA[T/A]ATATCAAAGGCCACAGATGCATGTTCTCCAAAATCAATGGGAGGAAGTGTTTTAAGATCTACCTTAAATGAGTTAAGCCTAATGAAGTTGGATGTTGGAAGTGTGGATGATACTCAAAAACAAAAAGTGGAGTTTGGAATAATGAATGTATATTTCAACAAAGGGATATCTGAGAGCTTAAGTACTTCACTACCAATGGTAGAAGATGTTGCACAAGTTAGTTCACTCACAGAATCACAGTCAACCTCATGTGGTGCAAATGCCCAGTCACCAATCAGGATGGGAACAGAGGTCAGTTTAAGGACTGATGGTCATCCCACATCAGCTCAAAATTTGCTAAATGGTAAAGAGTATATGTCATCTGAAACAAATGCATTGCATACATATAAATGCCCTAGTGGTATAAGTGAGAACCCAGATTTCAAGCCTTGGAATGAAGATCCAAATGTGGATGATCCAAGTATACAAAATACAGTTAAACAGTTGGCTAAGTGTGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10442
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Essential Splice Site | 3410 | 7146 | 58 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1444038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1441208 |
GRCz11 | 13 | 1572731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACGCCATTCATTTGTGCTTATTTGYGCCCCAAAWATGAACATTTGTGC[T/A]GGATTGGTGATATGAAACCTTAKTTTYTGGACTGTGTGAYGTYACTCTTC
Long Flanking Sequence:
CTGGAAAACATCCATACACTCTCTCATTCACACACACTCATACACTATGGCCAATTTAGTTCATCGATTCCCCTATAGCGCATGTGTTTGGACTGACTATGCTTGAACTGCTTGATCAAAGTAAGCACAGAGTAAACAGGGTGTTCGCAGGGGTCTTAAAAAGCCTTAAATTCACTCAAATATTGCATTGTAGGTATTAAATCATTTTTAAACGGGTCTTAATTTTCCTATTTACATGTGAAGCTTTCTAATTAGGGCAACACCCAATCACCAAAAAAAACAACACAAAAAATCTCAATAGAACCTTTAACAAAACTCTATTTTAAACTCCATTTACCAATATGGTTTAGTTGTGATTTTAATTATTATTAGGGATGCACTGAATTCTGAAAAAATATGAAAAGAGCTCAAAATATATATTTTAAAAATAAAAATAAACAATCCCCAAAACTACGCCATTCATTTGTGCTTATTTGCGCCCCAAAAATGAACATTTGTGC[T/A]GGATTGGTGATATGAAACCTTATTTTTTGGACTGTGTGACGTCACTCTTCACCCCACGTTGCTCAAAGAGTTTGTTTGTGCTCGAGTTTGTGCTCGTTTAGATTCTGCCATTAATCATTTTTGACATCGCACAGTCAAAAAGATAACATAATTAAGTTTATTGTAGTTTTTAAAGAGTTTTTGTCTTGTTTCTAGCTTAAATTTCTACAAATTTTTAAACCAAGAAGCTTTTTCTTGACAAGCGAAACATATGGTCTTGTTTTCAGAAATAATATGCCAAAATTAAGTGAGGTTTTCTTTAAAACAAGTAAAATAATCTGCCAATGGGATAAGTAAAATGATCTTATGACAAAAGGCAAAACTAGATTATTTTGCTTACCCCATTGTCAGATTATTTAGCTTTAATCTTAATGACTTTAATCTTTGAGCTTAAACGCTTAATTTTAACATATTTTGTTTTAAAACAAGACATTATATTTTACTTGTCTAGAAAATGCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11822
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Nonsense | 3417 | 7146 | 58 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1444061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1441231 |
GRCz11 | 13 | 1572754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGYGCCCCAAAWATGAACATTTGTGCWGGATTGGTGATATGAAACCTTA[T/G]TTTYTGGACTGTGTGAYGTYACTCTTCACCCCACGTTGCTCWAAGAGTTT
Long Flanking Sequence:
TCATTCACACACACTCATACACTATGGCCAATTTAGTTCATCGATTCCCCTATAGCGCATGTGTTTGGACTGACTATGCTTGAACTGCTTGATCAAAGTAAGCACAGAGTAAACAGGGTGTTCGCAGGGGTCTTAAAAAGCCTTAAATTCACTCAAATATTGCATTGTAGGTATTAAATCATTTTTAAACGGGTCTTAATTTTCCTATTTACATGTGAAGCTTTCTAATTAGGGCAACACCCAATCACCAAAAAAAACAACACAAAAAATCTCAATAGAACCTTTAACAAAACTCTATTTTAAACTCCATTTACCAATATGGTTTAGTTGTGATTTTAATTATTATTAGGGATGCACTGAATTCTGAAAAAATATGAAAAGAGCTCAAAATATATATTTTAAAAATAAAAATAAACAATCCCCAAAACTACGCCATTCATTTGTGCTTATTTGCGCCCCAAAAATGAACATTTGTGCTGGATTGGTGATATGAAACCTTA[T/G]TTTTTGGACTGTGTGACGTCACTCTTCACCCCACGTTGCTCAAAGAGTTTGTTTGTGCTCGAGTTTGTGCTCGTTTAGATTCTGCCATTAATCATTTTTGACATCGCACAGTCAAAAAGATAACATAATTAAGTTTATTGTAGTTTTTAAAGAGTTTTTGTCTTGTTTCTAGCTTAAATTTCTACAAATTTTTAAACCAAGAAGCTTTTTCTTGACAAGCGAAACATATGGTCTTGTTTTCAGAAATAATATGCCAAAATTAAGTGAGGTTTTCTTTAAAACAAGTAAAATAATCTGCCAATGGGATAAGTAAAATGATCTTATGACAAAAGGCAAAACTAGATTATTTTGCTTACCCCATTGTCAGATTATTTAGCTTTAATCTTAATGACTTTAATCTTTGAGCTTAAACGCTTAATTTTAACATATTTTGTTTTAAAACAAGACATTATATTTTACTTGTCTAGAAAATGCTTCTTAATTCAAGAATTTGTAGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11890
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Nonsense | 4667 | 7146 | 76 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1470993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1468163 |
GRCz11 | 13 | 1599686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGAGGGCACTGAAATACAAGGAGAACGCTGAGAAGCTGAACTCGTGGT[T/A]GCAGGAGTGTGAAGACACGGAGAASACGGTGAAGCTCAGCGTAAGCTCGG
Long Flanking Sequence:
TTGGGTTGTTAACAACTAAAATCTTATCTTAAAATGACGTCTGACCAAGATTTCTAATGTAACAATGTTATATTTCATCTTGTGTTCGCCAGCTAAGCGGATCGAGCAGCTCAACTCGGCTTTCGCCAGCTCTCAGCAGTTCCACCAGACATCGAAAGACTTCCAATCCTGGCTGAATCAAACTCTACAAGACCAATGCAATCCACAACCCATCTCTGCTGATGTGCAGAAGCTCAAACAGAGTCTCAAAGACAACAGCGCTGTTCAGAAAACCATTAATGACCACGAAGAACCTTACAGAACCATCATGAAAGAGGGAGAAGCTCTCCTCCAGAGCACCGAAGGCGCAGAAAAGGTGGCTCTTCAAGGACAGCTCTCTGCTTTAAAGTCCAACTGGGAAGATGTGAAGAAAAGCAACGCGGAACAAGCAGAAAAGCTTCAGACGGCAATGCAGAGGGCACTGAAATACAAGGAGAACGCTGAGAAGCTGAACTCGTGGT[T/A]GCAGGAGTGTGAAGACACGGAGAACACGGTGAAGCTCAGCGTAAGCTCGGTCGAGATTGAAGGATCGCTCTCGCAATTAAAGGCCATCCAGAAGGACATCGATAAGCATAGAGGACACATAGAAATGATGAACAGTGCGGCAGACGGCCTCCTGGAGGTCATCACAACAGATGGAGATGCAATTAAGGAGGACAAGCTATCAATTGGTAAAAGAGCTGATAAGCTGACGGAAGATCTGACGCTCAAGCGAGAGGCGTTAGAAAGCATCTCGCAGAAGCTGAAAGAGTTCAATGACCTCCAGAAGGAAGCTAAAGGACAATTGGAGAGCGCAAGGAAAGTGCTGGATGTTCACTCCTCATTGGGTGTCCAGGCTTTCAGCAATAAAAGCCTGAGCAATATGAAGGCTCAGCAGAACGCTTTGGAGAGCGTCCACAAGCAGATCGAGCATCTCAAAAGTATCGCACAAGGACTCGTTGTTGATGCATGCGAGGCCGAAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22197
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092780 | Essential Splice Site | 5020 | 7146 | 76 | 125 |
ENSDART00000133961 | None | None | 310 | None | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 1472055)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1469225 |
GRCz11 | 13 | 1600748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCGGATTGGAAACAGAAGTCATTAATCAGCAACTGGAGTCCTTCAAGG[T/A]AAGATTTGATGTGTTGTAGCGATCTGACTGGGTAGAGGTGCCAACCTATA
Long Flanking Sequence:
GGTGGACGATGCTTGCTCCAGTTTGGAGAGCAAACTTCTTGGAATCGGACAGTTCCAGAACAGCATTCGGGAGATGTTTGCAAGCTTCGCAGACTTGGACGATGAGCTAGATGGCATGGCTCCTGTGGGACGAGATCTTGAGATCTTGAGAGATCAGAAAAGTGCCATCGAAGCGTTCGTAGCCAAGCTTCAGGATCTGACGCGCAACACATCCAACGGGAGAGACAGTTGCAGGAAGATGCTGGAGTCGGAGGCTTCGCCGGATCTGCTGGGTCTGAGGAGAGACTTGGAGACGCTTGGAAAACAGTGTGGAAAGCTGATGGACAGAGCCACCGCGAGAAAGGAGCAGGTTGAGGAGACGCTCGGTCATCTGGAGGAGTTTTACAGCAAGACGCAGGAGTTTACCAGCAACCTGAGCACTGCGGAAAGGCAAGAGGAGTCCCAGGGGTCTGTCGGATTGGAAACAGAAGTCATTAATCAGCAACTGGAGTCCTTCAAGG[T/A]AAGATTTGATGTGTTGTAGCGATCTGACTGGGTAGAGGTGCCAACCTATACATTTATAGGTACAAATTAAAACATTTCTGCTGCTGTAGCCCATCCGCCTCAAGGTTGGCCGTGTTGTTTGTTCAGAGATGCTCTTCTGCAGACCTCGGCTGTAACGAGTGCTTATTTGAGTTACTGTTGCCTTTCTATCAGCTGGAACCAGTCTGGCCATTCTCCTCTGACCACAACAAGGCATTTGCACCCACAGAACTGCCGCTCACTGGATATTTCCTCTTTGTTGGACCATTCTCTGTAAATCCTAGAGATGGTTGTGCGTGAAAATCCTAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCCGTCTGGTACCAACAACCATGCCACATTCGAAGTTACTTAAATCCCCTTTCTTATCCATTCTGATGCTCAGTTTGAACTGCAGCAGATCGTCTTGACCATGTCTGCATGTCTAAATGCATTGAGTTGCTGCCATGCGAT
Associated Phenotype:
Not determined