ZMP
LOC100332533
Ensembl ID:
Human Orthologue:
EML3
Human Description:
echinoderm microtubule associated protein like 3 [Source:HGNC Symbol;Acc:26666]
Mouse Orthologue:
Eml3
Mouse Description:
echinoderm microtubule associated protein like 3 Gene [Source:MGI Symbol;Acc:MGI:2387612]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20885 | Nonsense | Available for shipment | Available now |
sa20886 | Essential Splice Site | Available for shipment | Available now |
sa14586 | Nonsense | Available for shipment | Available now |
sa20887 | Essential Splice Site | Available for shipment | Available now |
sa40853 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17294 | Essential Splice Site | Available for shipment | Available now |
sa18865 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9328 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20885
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 |
---|---|---|---|---|---|
ENSDART00000080834 | Nonsense | 57 | 976 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19107933)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17609316 |
GRCz11 | 7 | 17861289 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGTCCTCATTGGCCGATGCTTTACGCAGGCTCCGCCTCCATGACCAA[C/T]AGATACCCCTGCTTAAACAGCAGCTGATTGCTGGTATGAGCTTTCTTGCT
Long Flanking Sequence:
AAAGTCGGGATAAAATAAAGATGGTGTCTCGAAGGGCTACTTGGATGTCAATTAGTGTGTAAATGTATGTTTTTGACCAGTATTTTCTACTTTTGGTGGCATTTCCAGTAAGAATTTAGTAATTTAGTAAGCACATGTTCCTTAAGTCATCACTAATGTTGTCTTATTTTGTTGTAAATGATTAAATAAGTCATTATGCTGTTTCCGTTTTCCCTCTGGAATCGTTTTCCACCGGATAGAAGACGGCCATTGCGTTCAAACGTATCAATGTTTTATATTTGATTTTTAATATAGTGTGAAAGATGTTGTTTTTTTATTTGATGTGTGTGTATTTATGCTGTGTTGTTTTTTATCTAGATGATGTGTCAGCAGAAAGCAGCACAGAGTATCCCGACAAGCTTTCTACAATGGAGGTGCGTCTCCAAGCACAGGAAGATGAAATAACGCTACTGAAGTCCTCATTGGCCGATGCTTTACGCAGGCTCCGCCTCCATGACCAA[C/T]AGATACCCCTGCTTAAACAGCAGCTGATTGCTGGTATGAGCTTTCTTGCTGTTTTTACAGTGTGCTACTGTACAGATATCACATCAGGTTTATAGCACATTGACATGTATTGCAACAGATATTATTGTATTGTGTTTCCTGAACAACCTAAACAGTAAACCCTGCTGCTGCTCGAGTGCTAAATCAGTCCTGTTATGTGGATGGATTCTCTAAACCATGCAGACTGTCTACAAGTTCTCTTGATGGATTTAACCACACACCTAACAGGTACAGAGGAGTCTAGGTTTGTAATGAGCTTAACACGCTGTTATCTAAGTATATACTAGTGTTGAGTAAAAATAAAAAAAGTTCTATATTATTTTAAGCTTTATTTTAATCTTTTGAAAATAAGATTGCAAAAATAACATAACACATGAAGTGAAAATATGTGCTGTCATTTATTTATTTATTTATTTATTTATTTATTTTAAAGATTAAAGGAATAGTTTACCCAAAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20886
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080834 | Essential Splice Site | 68 | 976 | 2 | 24 |
ENSDART00000080834 | Essential Splice Site | 68 | 976 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19107968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17609351 |
GRCz11 | 7 | 17861324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCTCCATGACCAACAGATACCCCTGCTTAAACAGCAGCTGATTGCTGG[T/G]ATGAGCTTTCTTGCTGTTTTTACAGTGTGCTACTGTACAGATATCACATC
Long Flanking Sequence:
GCTACTTGGATGTCAATTAGTGTGTAAATGTATGTTTTTGACCAGTATTTTCTACTTTTGGTGGCATTTCCAGTAAGAATTTAGTAATTTAGTAAGCACATGTTCCTTAAGTCATCACTAATGTTGTCTTATTTTGTTGTAAATGATTAAATAAGTCATTATGCTGTTTCCGTTTTCCCTCTGGAATCGTTTTCCACCGGATAGAAGACGGCCATTGCGTTCAAACGTATCAATGTTTTATATTTGATTTTTAATATAGTGTGAAAGATGTTGTTTTTTTATTTGATGTGTGTGTATTTATGCTGTGTTGTTTTTTATCTAGATGATGTGTCAGCAGAAAGCAGCACAGAGTATCCCGACAAGCTTTCTACAATGGAGGTGCGTCTCCAAGCACAGGAAGATGAAATAACGCTACTGAAGTCCTCATTGGCCGATGCTTTACGCAGGCTCCGCCTCCATGACCAACAGATACCCCTGCTTAAACAGCAGCTGATTGCTGG[T/G]ATGAGCTTTCTTGCTGTTTTTACAGTGTGCTACTGTACAGATATCACATCAGGTTTATAGCACATTGACATGTATTGCAACAGATATTATTGTATTGTGTTTCCTGAACAACCTAAACAGTAAACCCTGCTGCTGCTCGAGTGCTAAATCAGTCCTGTTATGTGGATGGATTCTCTAAACCATGCAGACTGTCTACAAGTTCTCTTGATGGATTTAACCACACACCTAACAGGTACAGAGGAGTCTAGGTTTGTAATGAGCTTAACACGCTGTTATCTAAGTATATACTAGTGTTGAGTAAAAATAAAAAAAGTTCTATATTATTTTAAGCTTTATTTTAATCTTTTGAAAATAAGATTGCAAAAATAACATAACACATGAAGTGAAAATATGTGCTGTCATTTATTTATTTATTTATTTATTTATTTATTTTAAAGATTAAAGGAATAGTTTACCCAAAAATTAACTATTATTTACTCCTTCTTTACTCATTTCAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14586
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 |
---|---|---|---|---|---|
ENSDART00000080834 | Nonsense | 384 | 976 | 9 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19127599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17628982 |
GRCz11 | 7 | 17880955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCCATCTGGAGAAGCAGTTTATTTTATTGCATGTGTGRTGGTTCTGTA[T/G]CATATCAGCAACCAAAAGCAAAGACATTATCGGAAGCACACAGAYTGTGT
Long Flanking Sequence:
AGAATTTTCCTTTTTGGGTGAACTAACCCTTTAATAATTTAACTTGTTTTAGCTTGTTTTCTCGATATCATATTATTTCGGGATTGTACCCAAGACGAAATGCTTATAACAAGACTCTTCCCATTTATTTAACAAATAGTATCAATCAGCTCTCCAACAATCTGACATGGTCTCTATGTTGGCACATGCAGCACAGCACGACTATTGGCCAACAAAATCTTCAGTCTGTTCTGTCCATTTTCTCATGTTTCATTGGTGGCAGTAAAGCGCTGCCTTGTTTTATTTATAATGTACTGACACAAATGACAGCTGATTTGAAACGGGCACTTGATGCCAAACACTGAATTAGATTTCCTTTATATGATGCATACTTGTTAGCAAATGTTCCTTGACTCATATTTTTTTAGCTATGGTTACCGGGGACGGGACTGCCGAGCAAACCTTTACCTGTTGCCATCTGGAGAAGCAGTTTATTTTATTGCATGTGTGGTGGTTCTGTA[T/G]CATATCAGCAACCAAAAGCAAAGACATTATCGGAAGCACACAGACTGTGTCAGATGGTGAGTTGAGAGACTTGTGTTTCTTTTTATGTCAGTATTTTATTGACTTTACTCTTACTTCTTGGCTTCCAGTCTCGCCATTCACCCAGATAAGGTGCGCGTTGCATCTGGACAGACAGCAGGTGTGGACAAAGATGGCAAGGTGAGATATATGTATGATCTTCTCTCCCCCCACCACACAACAGCCTCAAATCATTATGCAATTCTGAGTGTGCCTCACACAGGTGAGTGGGCTTGACAAACCACCTGTAGAAAAAACTCTTTCATCGCTCTGATACGTTAACCAACAATTGGACCAGATACTTTCTAATGGTACATTCAAACTAGGGGTTGCATCGATTAATCGACTAGTCTACTTTAGTGCTTTGCCAAGACGTTTTTGATTGATGTCGACTAGTCAGGTTGCGCAGATCACGTGGTTTGACCTGACTTAAACGACAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20887
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 |
---|---|---|---|---|---|
ENSDART00000080834 | Essential Splice Site | 463 | 976 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19129299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17630682 |
GRCz11 | 7 | 17882655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGGCATATTTGAGCGAGGTGTCGGAGCCATAGCATTTTCCAATTCAG[T/A]GAGTTTTGCCTTCAATTTTGCATTCTTTCCTGCTGAAACGCGACACAGAG
Long Flanking Sequence:
CTAAAACATGTGCTTGACAGAGATGTTCTAAAATTTAAATTGTCCAATGCCCGTGCTTTTCTTATGAAAGATGAAGTTATAAATGATACAAAATGTCTTTATTGAGTTGTGGATTACTTTGAGTCTCTCCCAATGCACTCATCAATGTGAATGGATATGGTTTTTGACTATTGTCTTTACTAATTGTGGAGTGTTGACCCGCTTATCCTCTATTAATAACCACTTCACAAATCACAGACATATTTCAGTTAACCAGTTAATGCAAAATGGAGATATACTTGTGAAATCAACTACTTGTTTATAAAACTTGTGCCTAAATTTGTGGACAAAAACATTAGTAACAACTTGTCATTGTCATTGACCCACTTGTGTATTCTGTGTTTGTCAGCCTCTTCAGCCCTTTGTGCACATCTGGGACTCTAAAACGCTAGTGACACTGCAGCAGATTGGTCTCGGCATATTTGAGCGAGGTGTCGGAGCCATAGCATTTTCCAATTCAG[T/A]GAGTTTTGCCTTCAATTTTGCATTCTTTCCTGCTGAAACGCGACACAGAGAGGGAATTTAGTTTTGTTCCTATGTACAATAAATGTGAAATATTATAAAAAGATATAAAGTATTTGAGAATATTGTAATCCAGGATCCAAATACTTTTTAGTCTGTGTGTTTTTAGACTAGGAACTAAGGCTAGGCGTTGACACAGATTTGATGGTTCAATTAAAATATAGTAGATTTAGAATATAAACTTTTTTTAACTTGTAATACATTTTAATTAGGGTGACACGGTGGTGCAGTAGCTAGGGCTGTCGCCTCAAAGCAAGAAAGTCGCTGGTTCGAGCCCCAGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCAAGTGCTCTGGTTTCCCCCACAGTCAAAGACACGCTGTAGGTCAATTGGATAAGCTAAAATGTCCGTAGTGTATGTTGTTATGTCTTGTTCCTCCAGGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40853
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080834 | Essential Splice Site | 637 | 976 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19139499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17640882 |
GRCz11 | 7 | 17892855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGATCATCCGCTGGAGTGCAGACCTGGCGCCTGAAAGAGAGTGTGAGG[T/C]AAACCATGAGTCTGTGAGAATTGTGCGTTTATAGCTCTGTATAGGTTATT
Long Flanking Sequence:
GGTGGCCACAGGGGTGGCCAGAGTTCACCGAGGGGTGGCCGTGGCCACCCCTGGCCACCCCTTGGAGGCGCCCCTGCAAAGCTTGATATTGACCATATTTGGAAAGGTCATGAATATTAACATACACATCCTAAGGGTTATTTTTGTGACTATAGAAGAAAATATAAAACCGTTTCTGAAGAATCTTTGCACTTACCTAAGCCACATACCCACTTTGCAAAAATTAGAGAACAATTTAACATATTGAATCGATTTACTCTATGGTACCTTTAATGTTGTTTTAGTGATTGTTTATTTAAAAAAACTATGTTTACTCTAAAATCTCCTTTTTTCTTCTCTCCTTGCAGAGACGTTTCAGATCATGAAGCAGACCCGTGCTCATGAGGGCAGTGTGTTCACTATGTGCATCCTGCAGGGCGGCGCTATACTAAGCGGTGGCGGCAAAGACCGCAAGATCATCCGCTGGAGTGCAGACCTGGCGCCTGAAAGAGAGTGTGAGG[T/C]AAACCATGAGTCTGTGAGAATTGTGCGTTTATAGCTCTGTATAGGTTATTGAATATGAAGGTATAGCATTGATTGTATAGCTTGTAATCAGAAACATTCTGAATGCTCTATGTTCTTCCAGATTCCTGAGAAATTTGGAGCAGTGCGCACCATTGCAGATTTAGATGGAGAAGAGCTGCTCGTTGGCACAACACGAAATGCAATCCTCAGAGGGACATTTTCAGACGGTTTTGTGGCCATTGTACAGGTAAATAGACTGCATTTGTATTTCAATTAGGGTCTTTGTTGTAAATGAATACCAGAGATAAACTAAAATAACTGTTATTTATAAAAAAATAACACATATTGAATTTGAAATCGACTTTAGATAGATAAATAAAGTTGGGATAATTTAGTGTAAATAAAAAATTTAAATGGATATTTCTTCAATTGTCAGGGACATGTGGATGAAATGTGGGGTCTTGCCACACACCCCACTCAAAATATCTTTGTTACCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17294
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080834 | Essential Splice Site | 638 | 976 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19139620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17641003 |
GRCz11 | 7 | 17892976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTGTATAGCTTGTAAYCAGAAACWTTCTGAATGCTCTATGTTCTTCCA[G/T]ATTCCTGAGAAATTTKGAGCWGTGCGCACCATTGCAGATTTAGATGGAGA
Long Flanking Sequence:
ATACACATCCTAAGGGTTATTTTTGTGACTATAGAAGAAAATATAAAACCGTTTCTGAAGAATCTTTGCACTTACCTAAGCCACATACCCACTTTGCAAAAATTAGAGAACAATTTAACATATTGAATCGATTTACTCTATGGTACCTTTAATGTTGTTTTAGTGATTGTTTATTTAAAAAAACTATGTTTACTCTAAAATCTCCTTTTTTCTTCTCTCCTTGCAGAGACGTTTCAGATCATGAAGCAGACCCGTGCTCATGAGGGCAGTGTGTTCACTATGTGCATCCTGCAGGGCGGCGCTATACTAAGCGGTGGCGGCAAAGACCGCAAGATCATCCGCTGGAGTGCAGACCTGGCGCCTGAAAGAGAGTGTGAGGTAAACCATGAGTCTGTGAGAATTGTGCGTTTATAGCTCTGTATAGGTTATTGAATATGAAGGTATAGCATTGATTGTATAGCTTGTAATCAGAAACATTCTGAATGCTCTATGTTCTTCCA[G/T]ATTCCTGAGAAATTTGGAGCAGTGCGCACCATTGCAGATTTAGATGGAGAAGAGCTGCTCGTTGGCACAACACGAAATGCAATCCTCAGAGGGACATTTTCAGACGGTTTTGTGGCCATTGTACAGGTAAATAGACTGCATTTGTATTTCAATTAGGGTCTTTGTTGTAAATGAATACCAGAGATAAACTAAAATAACTGTTATTTATAAAAAAATAACACATATTGAATTTGAAATCGACTTTAGATAGATAAATAAAGTTGGGATAATTTAGTGTAAATAAAAAATTTAAATGGATATTTCTTCAATTGTCAGGGACATGTGGATGAAATGTGGGGTCTTGCCACACACCCCACTCAAAATATCTTTGTTACCTGTGGAAATGATCGTCAGCTGTGTGTGTGGAACGCAGAGGACCACAGACTGGACTGGTGCACAACACTAGAGGTCAGAGAAGTCACTGAAGGTTAAGCACACAAAGTATTTTATGTGTGTATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18865
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080834 | Essential Splice Site | 775 | 976 | 19 | 24 |
ENSDART00000080834 | Essential Splice Site | 775 | 976 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19141771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17643154 |
GRCz11 | 7 | 17895127 |
KASP Assay ID:
2259-8591.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCTGATTGACGGCAATGAACAGTTGTCTGTAATGAGATACTCACCAG[G/T]TCAGAGTTCAACAAGATCATTGTGCAATCAAAATAATAATATAATACTGT
Long Flanking Sequence:
ATATAAATGTAAAGAATAATGACTCTTGAAAAAAGGTTTCCTAAAAAGAATAACATTTTTACAGTTTTTTTTCCACTTCTGACTAAACCTGATCTTATATCAGTGTGTGATTTTAAACATTCATCAGTATAACAGTTCATTCATGTAAGTGTAAATCATCCACACAGTATTATCAAACATGTTCTGTAATGTGAAAAATGAATCAGAAACACATTCGTCTCGGCAGGACTCTGGTCTGTGTGCTGATTTCTGCCCTAATGGAGCTGTTGTGTCTGTTGGACTGAGCACTGCAAGGTAAAAAACATTTACTCACAGCACAGCCGATAACAATTACCACTTCACTTTTACAGTGTGCTTGTGAAATGTTTTTAATGGCTTTTTTGATGGTTTTCCAACCTCTCACCCATGTAGATGGGTTGTGCTGGATCTGCAGACTAAAGAAGTGGTGGCAGACCTGATTGACGGCAATGAACAGTTGTCTGTAATGAGATACTCACCAG[G/T]TCAGAGTTCAACAAGATCATTGTGCAATCAAAATAATAATATAATACTGTATAATACTAAGCATACATGGCGAATTTCACAATATACAAGTTAAACTAACAAACGATACATTGAAACCTCATGCCTCTTCAGGGTGGCATAAGTGTTTGAGGCTCATGGTATGCCAATTCAATGTACTGAACTTTTATTATTCAGCTATGCTTAGGTTTATCCTGATTTTATTCTCTGGATTGTTCTCTTGAAATGTGATCCAAATATTTGTAACTTGAAATAGATGGAAAATCTGCGATTTATGTTGTGCTTCTATGGAAATTTCAGCGTAGCTGCTATAATGACCTATTGTTTTTATGCCCACCAGGTCTCCGCAAAAGTTACGTGACTTAAAACTATCAATGGAATTTTTAAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAAAAATGTAATATAATATAATAAAATAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9328
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080834 | Essential Splice Site | 775 | 976 | 19 | 24 |
ENSDART00000080834 | Essential Splice Site | 775 | 976 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 19141771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 17643154 |
GRCz11 | 7 | 17895127 |
KASP Assay ID:
2259-8591.1 (used for ordering genotyping assays)
KASP Sequence:
AGACCTGATTGACGGCAATGAACAGTTGTCTGTAATGAGATACTCACCAG[G/T]TCAGARTTCAACAAGATCATTGTGCAATCAWAATAATAATATAATACTGT
Long Flanking Sequence:
ATATAAATGTAAAGAATAATGACTCTTGAAAAAAGGTTTCCTAAAAAGAATAACATTTTTACAGTTTTTTTTCCACTTCTGACTAAACCTGATCTTATATCAGTGTGTGATTTTAAACATTCATCAGTATAACAGTTCATTCATGTAAGTGTAAATCATCCACACAGTATTATCAAACATGTTCTGTAATGTGAAAAATGAATCAGAAACACATTCGTCTCGGCAGGACTCTGGTCTGTGTGCTGATTTCTGCCCTAATGGAGCTGTTGTGTCTGTTGGACTGAGCACTGCAAGGTAAAAAACATTTACTCACAGCACAGCCGATAACAATTACCACTTCACTTTTACAGTGTGCTTGTGAAATGTTTTTAATGGCTTTTTTGATGGTTTTCCAACCTCTCACCCATGTAGATGGGTTGTGCTGGATCTGCAGACTAAAGAAGTGGTGGCAGACCTGATTGACGGCAATGAACAGTTGTCTGTAATGAGATACTCACCAG[G/T]TCAGAGTTCAACAAGATCATTGTGCAATCAAAATAATAATATAATACTGTATAATACTAAGCATACATGGCGAATTTCACAATATACAAGTTAAACTAACAAACGATACATTGAAACCTCATGCCTCTTCAGGGTGGCATAAGTGTTTGAGGCTCATGGTATGCCAATTCAATGTACTGAACTTTTATTATTCAGCTATGCTTAGGTTTATCCTGATTTTATTCTCTGGATTGTTCTCTTGAAATGTGATCCAAATATTTGTAACTTGAAATAGATGGAAAATCTGCGATTTATGTTGTGCTTCTATGGAAATTTCAGCGTAGCTGCTATAATGACCTATTGTTTTTATGCCCACCAGGTCTCCGCAAAAGTTACGTGACTTAAAACTATCAATGGAATTTTTAAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAAAAATGTAATATAATATAATAAAATAAATG
Associated Phenotype:
Not determined