ZMP
zgc:153454
Ensembl ID:
ZFIN ID:
Description:
Mediator of RNA polymerase II transcription subunit 13-like [Source:UniProtKB/Swiss-Prot;Acc:A2VCZ5]
Human Orthologue:
MED13
Human Description:
mediator complex subunit 13 [Source:HGNC Symbol;Acc:22474]
Mouse Orthologue:
Med13
Mouse Description:
mediator complex subunit 13 Gene [Source:MGI Symbol;Acc:MGI:3029632]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22623 | Nonsense | Available for shipment | Available now |
| sa22622 | Nonsense | Available for shipment | Available now |
| sa35864 | Essential Splice Site | Available for shipment | Available now |
| sa28439 | Nonsense | Available for shipment | Available now |
| sa12757 | Nonsense | Available for shipment | Available now |
| sa30993 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32028 | Nonsense | Available for shipment | Available now |
| sa35863 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22623
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 |
|---|---|---|---|---|---|
| ENSDART00000110267 | Nonsense | 220 | 2102 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19062355)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20164981 |
| GRCz11 | 15 | 20100713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTACAGTCATCCTCTCTCCGTATGGTCTGAGCGGGACTCTGACGGGC[C/T]AGTCCTTCAAGCTCTCGGATCCACCAACCCAGAAGCTAATCGAGGAATGG
Long Flanking Sequence:
AAATACAAAATGGTCATTATAAATTATTTTAGCGCTAAAAAGCATAGTTCTTTCTTGCATTAAAACTGTCCAGTTAAAATCCAAACATTTTAAACAAGGCAAAGATAAATATCCATCCATTTGCATTTTAAATTGTGCATCAAACATTTGCTAGCATTTATTAACATTAGAACTTTTTTTTTAAATCATACGATTTCCTAAATATAATCCCAACATCCATTAGCTTTCAAAAACATTTCATAACCCATTATTAAATCTATTTTTTTACTGATTTTCTATTTTATGATCTAACATGAACTTGTGCAACTCTGAAATACAGATAGATCATTTGACTGTCATTTTATGGTTACTTTTGTGGCTCTAAGCATTGTCCTCATGTTTCCACAAAGAGAACTGAGACTTTACCAGGAAGTATCATTCTTGCAATTACACTGCAGTATTTGCTATATTTTCCTACAGTCATCCTCTCTCCGTATGGTCTGAGCGGGACTCTGACGGGC[C/T]AGTCCTTCAAGCTCTCGGATCCACCAACCCAGAAGCTAATCGAGGAATGGAAGCAGTTTTATCCCATCGGCCCCAACACCAAAGAGGTCACAGACGACAAGATGGATGACCTCGACTGGGAGGACGATTCCTTAGCCGCCGTTGAAGTCGTTGTCGGTAAGACAGATATTCAGCTTTATGTATTGTGATTTCATGGTCGCCTCGAGTGATTTGGAGTGCGAGTAATAATTAATGTGATGCAGCTGGTGTGAGGATGGTGTACCCAGCCAGCCTGGTGCTGGTGGCCCAGTCAGACATCCCGCTGGTGGCTACAGTGAGCTCTTCCTCCTCCTCGGGCTCTTATGCTGGAGCTCCGCATAATCAGCTGGTCCATGGAGACACTGGCATCTCTTCAGTCACGCTGACTCCTCCCACTTCACCTGAAGAGGCACAAGCAGGTACCATTACTACTGTCTAAATTATTTCAAATGCTGTCATTCGTTAAGAATAATTAAAGTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22622
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110267 | Nonsense | 236 | 2102 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19062305)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20164931 |
| GRCz11 | 15 | 20100663 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCCTTCAAGCTCTCGGATCCACCAACCCAGAAGCTAATCGAGGAATG[G/A]AAGCAGTTTTATCCCATCGGCCCCAACACCAAAGAGGTCACAGACGACAA
Long Flanking Sequence:
TTTCTTGCATTAAAACTGTCCAGTTAAAATCCAAACATTTTAAACAAGGCAAAGATAAATATCCATCCATTTGCATTTTAAATTGTGCATCAAACATTTGCTAGCATTTATTAACATTAGAACTTTTTTTTTAAATCATACGATTTCCTAAATATAATCCCAACATCCATTAGCTTTCAAAAACATTTCATAACCCATTATTAAATCTATTTTTTTACTGATTTTCTATTTTATGATCTAACATGAACTTGTGCAACTCTGAAATACAGATAGATCATTTGACTGTCATTTTATGGTTACTTTTGTGGCTCTAAGCATTGTCCTCATGTTTCCACAAAGAGAACTGAGACTTTACCAGGAAGTATCATTCTTGCAATTACACTGCAGTATTTGCTATATTTTCCTACAGTCATCCTCTCTCCGTATGGTCTGAGCGGGACTCTGACGGGCCAGTCCTTCAAGCTCTCGGATCCACCAACCCAGAAGCTAATCGAGGAATG[G/A]AAGCAGTTTTATCCCATCGGCCCCAACACCAAAGAGGTCACAGACGACAAGATGGATGACCTCGACTGGGAGGACGATTCCTTAGCCGCCGTTGAAGTCGTTGTCGGTAAGACAGATATTCAGCTTTATGTATTGTGATTTCATGGTCGCCTCGAGTGATTTGGAGTGCGAGTAATAATTAATGTGATGCAGCTGGTGTGAGGATGGTGTACCCAGCCAGCCTGGTGCTGGTGGCCCAGTCAGACATCCCGCTGGTGGCTACAGTGAGCTCTTCCTCCTCCTCGGGCTCTTATGCTGGAGCTCCGCATAATCAGCTGGTCCATGGAGACACTGGCATCTCTTCAGTCACGCTGACTCCTCCCACTTCACCTGAAGAGGCACAAGCAGGTACCATTACTACTGTCTAAATTATTTCAAATGCTGTCATTCGTTAAGAATAATTAAAGTAGTGTATATGGGCTTGACTTCATTTGGGTTATATTTAATCCCTGCTTATATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35864
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 |
|---|---|---|---|---|---|
| ENSDART00000110267 | Essential Splice Site | 390 | 2102 | 7 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19059170)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20161796 |
| GRCz11 | 15 | 20097528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGAGCGAGTCTGGCAGGAGTGCAATATTAACCGAGCACAGAACAAG[T/C]AAGAATGTAAAATCTACATCATGACTGATTAGCCAGAGCAAATAACCTGG
Long Flanking Sequence:
CAATCGCAGCCCTTTCTGTCAAGCGTGTGACCAATCATAGGCGTTTAACAGCTCGCTTGACAACCCCTAAAAAGCAAACGGGATAACATTTACGTTTGCTTAAAATAATAATTTAAAATAATAATTAATATTACATATATTAATACACAATATTGTTGTTATTATTATTCATTCATTTCATTTTTTTCTATTAATGTTTTAATAGATGAATTATGTTCTATGATAAATTATGTATAACAAGACCAGTACAATCAACAGCACTTGCTCATTCTAAGTTGCTGTCAAAACCATTAGTTATGTAATGTCTTGTATGTTTTTTTTTTCTTTCCCTTGTTGCAGTCTCTCAGCCTGCCCAGAAGTGGGTAAAGCTCTCAGCAATGTCAGGCGTCTTTAGTGTGGACAGCAGCAGCCATCACGGAGGAAAGATCCCCCGCCGGCTAGCCAGTCAAATGGTGGAGCGAGTCTGGCAGGAGTGCAATATTAACCGAGCACAGAACAAG[T/C]AAGAATGTAAAATCTACATCATGACTGATTAGCCAGAGCAAATAACCTGGCAGTGAGAAATGGATTGAGTAAGAACAAAGCAAGTTCAGGCATTCGCTTTGATTTGTTTTTGTGCAGGAGAAAGTTTTCGACTATGTCTAATGGAGTTTGCGAGGAAGAAACCGACAAAGCTTCTGTTTGGGACTTTGTGGAGTCGTCTCAAAGGTCACAGTGCAGCTGCTCAAGGTATGCTCACAGGCTTCACTTTTGCAACAAAAAAGTATTTTTATTTAATAGAGACATAATTTTCATTCTACCTTGGCTTCAATGATTATTTCATCAATAGAAACCTGCCTAAAACAGAAACTATATTTAGTTCATTTAGTATATTTAGTATGCTGTGTGTGTGTTTTTGTGCTAGTCCTTGTTGGCTGTTCAGGCCTCTCATTGATAAATCAATGGTATTGTAATGTTCAGTTGGTGGTAGGCCTGTCACAATATCTATATTTTAGTGTTTGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28439
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 |
|---|---|---|---|---|---|
| ENSDART00000110267 | Nonsense | 432 | 2102 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19056810)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20159436 |
| GRCz11 | 15 | 20095168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATAACATTTCTATCTTTCATTTTTCATTCCAGGCTTAAAAACCAGAAA[C/T]AGCGGGCATGTAGCACCCCAGGGCATCCTCCATCTGCTGGCCAGCCTCCT
Long Flanking Sequence:
AATGATGTCAACTGACACTGTATTTACAATCTACTGTAGAGTATTTACGAGGAGATCTCAGAACTGTATTCACTGAAGCAATAAAATGAATCCCATATATTGCTTCAGCGTTTTGTTGTTTGTGATGAGCAAGTGATGAGTAAGTCACTCATCAGAGCCCAACATAAATACCTTTGATTGGACACTGCATTCATAAGATCAATAAAAACATGTGCTTGACACTATTTATTTTTACATTTAATTTTATTATCATGACTGCACTTGTAATTTATTTGAATTATTCATTTCCTCCTCATTATTTTGGACTCTAGAGCAAAAGCTAACATAATGCAAATTAGTTTTAAACCCAAACATTAAAGACTCATTTTACACATTACATGAAAGTTAAAATCCCCAAAAAAGGATAACAGAGACACTCAAACTAAAACGTGTGAACGAATAAATGCTGGTTGATAACATTTCTATCTTTCATTTTTCATTCCAGGCTTAAAAACCAGAAA[C/T]AGCGGGCATGTAGCACCCCAGGGCATCCTCCATCTGCTGGCCAGCCTCCTCAGCCCTCTACCAAACACAAGATGGCGGAGAAGCTGGAGAAGGGGGACAAGCAGCAGAAAAGGCCGCTGACGCCCTTCCACCACCGCAGCTCTCTGTGTGAAGAACAACCCAGCTTGGAGCAGGGAGAGAGCGTTCACCGACTGTGTCTGCAGGGTCATGAGGACAGCAGGTATCCCAGCCTCCACCACGCAGACGTCACCTCCAGCAAGACGCCAATGCTCCACAGCTCTGCGGATGAGATGGCAGGCTCCCCTCAGCCGCCACCGCTCAGCCCGCACCCCTGTGAACGTATGGAGGAACCAGCCGATGGCATGAAGAGTTCATCCTCACCCCTGCACCAACACTTTTACCCTCCTTCCTCTGAGCCCTGCCTGGAGCCCCAGAAACCCCCAGATGAATCCACATTAGACCCATTGCCCTTACCATGCCCACCTCCATACCCAGAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12757
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 |
|---|---|---|---|---|---|
| ENSDART00000110267 | Nonsense | 484 | 2102 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19056654)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20159280 |
| GRCz11 | 15 | 20095012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAAAGGCCGCTGACGCCCTTCCACCACCGCAGCTCTCWGTGTGAAGAA[C/T]AACCCAGCTTGGAGCAGGGAGAGAGCGTTCACCGACTGTGTCTGCAGGGY
Long Flanking Sequence:
GCCCAACATAAATACCTTTGATTGGACACTGCATTCATAAGATCAATAAAAACATGTGCTTGACACTATTTATTTTTACATTTAATTTTATTATCATGACTGCACTTGTAATTTATTTGAATTATTCATTTCCTCCTCATTATTTTGGACTCTAGAGCAAAAGCTAACATAATGCAAATTAGTTTTAAACCCAAACATTAAAGACTCATTTTACACATTACATGAAAGTTAAAATCCCCAAAAAAGGATAACAGAGACACTCAAACTAAAACGTGTGAACGAATAAATGCTGGTTGATAACATTTCTATCTTTCATTTTTCATTCCAGGCTTAAAAACCAGAAACAGCGGGCATGTAGCACCCCAGGGCATCCTCCATCTGCTGGCCAGCCTCCTCAGCCCTCTACCAAACACAAGATGGCGGAGAAGCTGGAGAAGGGGGACAAGCAGCAGAAAAGGCCGCTGACGCCCTTCCACCACCGCAGCTCTCTGTGTGAAGAA[C/T]AACCCAGCTTGGAGCAGGGAGAGAGCGTTCACCGACTGTGTCTGCAGGGTCATGAGGACAGCAGGTATCCCAGCCTCCACCACGCAGACGTCACCTCCAGCAAGACGCCAATGCTCCACAGCTCTGCGGATGAGATGGCAGGCTCCCCTCAGCCGCCACCGCTCAGCCCGCACCCCTGTGAACGTATGGAGGAACCAGCCGATGGCATGAAGAGTTCATCCTCACCCCTGCACCAACACTTTTACCCTCCTTCCTCTGAGCCCTGCCTGGAGCCCCAGAAACCCCCAGATGAATCCACATTAGACCCATTGCCCTTACCATGCCCACCTCCATACCCAGAGACACTAGAGGCCACCATATACGTGGGCTCAGCCATAAACCCCAATGAAGATACGACACATAACCCCTGGAAGTACTTTAGGGTGCCTGGTGGGAGGAATTCAGATTTCCACACACCTCATCTTCCTGTGGTTGCGCACTTTGAGGATGGGAACAGGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30993
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110267 | Essential Splice Site | 1373 | 2102 | 19 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19036281)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20138907 |
| GRCz11 | 15 | 20074639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATAAAAGACTATAGAAATAAATGTGACTTGATTGATTATTGTTTGGCA[G/A]TCTTGTCGGCTTGGTCAGCACAGGCCCATTGCCAAGTCTCACGCTGATGG
Long Flanking Sequence:
AGTAATTTAATAAGTAATCCAATAAATTGGCTAATAAATCATTAAAATGTAAAGTTTGACATCAGCCTGATTTGGAAAATGATATACTGGTGCGATGCACTGTACAATTTGACAAATAAAATGAATGTAACTTAATAATATTAAAATACTTCTGTTTATGAATTAATAAAGCAGAAGAAATTTTTGATAATAATGGTGATAATACATTTTATTTGGGCCACATGAAGTTGCTATGTTTTTTTTTCCTGTTTTTATATTCTATTATAAGTTGGATACTTTTCCGTTTTATCCATATACAAACTCATACAGGCAATAAATACTATATAGCATAGCTTAACTGAATAATAGCTTGTCTCATTGCAACGTGTAAACTACATCATCACCCAGTTCAGCTTAATTAAGACACTTTAAACATTATTTTATGTAAAGCTGCTTTGAAGAAAATATGTTGTATAAAAGACTATAGAAATAAATGTGACTTGATTGATTATTGTTTGGCA[G/A]TCTTGTCGGCTTGGTCAGCACAGGCCCATTGCCAAGTCTCACGCTGATGGCATTGTGACAGTGAGCGATGCTGGATCAAAAGCTCTTACTGATCAGACTCTCATCGACTGGCTTCCAAAAACCATCAACAGCAGCAGCAGCAGTGAGGCTTTAAACAAGCTCAAACTCTACGCCCATGTGTGCCGACATGACTTGGGTATGTGCAGAAACTGAATGTTCTTTGATGTACTGCAGACCACATCGATAAATGTAAAGTTTCTATAATATTTAATGTCTCCTCAGCATCCTGTCTGGCTTCCCAGTCATTGGACGGCTCACTTCTTACCCAGCGAAACCCAGCCAGCTCTTCGCAAACTTCCAGTTCCAGCAGCCCAGTCACAACCGCACAGAATGTCACCCCAACCACCAACAGCAACAGCAACACCAACACTAACACCACTCCGACCTCCACTTCCACCTCCAGCAGCTCTTCCTCTTGTCCTCAGGGCGTAGGCAACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32028
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 |
|---|---|---|---|---|---|
| ENSDART00000110267 | Nonsense | 1652 | 2102 | 22 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19032998)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20135624 |
| GRCz11 | 15 | 20071356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTACTTGCTGCAGCCGGTCTGGAGTGAGGAGCGCCATATATATGCA[C/T]AGCACCTGAAGTCTTTGGCTTTCTCAGTTTACACACAGTGCAGACGGCGT
Long Flanking Sequence:
TAATTTCCCTTTCTAAGCACTGTAGTTCATTTCTAATGGCCAGACTGCTTTACTACTGATGGTTTTTTGATGAATAATGTTGGTTCTTTTCAGATGTTTCCTCTAATCTATGATTTTTTCCGTCACAGTACGATGGAGAGAGAAAAGGTTGGGGTCCCGACTGATGGAGACTCTCATGCAGTCACCTATCCTCCTGCCATAGTGATCTACATCGTGAACCCCTTCAGCTATGAGGAAAACTGCCAAGGCAGCAGTTCCAGCGTGTGGACGATAGCTCTTCTTCGCTGTTATCTGGAGATGCTTCAGCTTCTTCCTCCACATATCAGGAATGCTGTATATGTCCAAGTAAAAAGACATCGAATATGAGATTACTTTTTCCCCCTACTATTTCCTCTTTGCTTGGATCATCTGAACATTCTGTGTATTTTTTTTTCTATTAGATAATTCCCAGTCAGTACTTGCTGCAGCCGGTCTGGAGTGAGGAGCGCCATATATATGCA[C/T]AGCACCTGAAGTCTTTGGCTTTCTCAGTTTACACACAGTGCAGACGGCGTCTGCCAACCTCTACTAATGTCAAAACGCTAACAGGTTTCGGCCCCGGCCTGGCAATCGACACTGCACTACAGAGCAAAGAGGTACACATGATAATTGCCAGCATCGCAGGCAAATGGGCTTTCAAACTGGTGTGCTTGAAGTGTTTGTAAAAGTAGCATCTATTCAAGCATTTATACAAGGTTTACCAAAATTTTTATTCGAAATTTAAACAAATCTGTGCCAAATGTGGTGTTTCTTTCTTTATAAAGATAAAGTAGGTGTCCACAAGGGAGATCAATATTGTCACTGGAAAAATTATATTAGAAAAAAAAGATTTTAATAAGAGCATGTTTGATTATTTATTTACTTTGTAATAAATGTCATAACTGGTAAATTTGTATTGAAATGTTATTTTCTTAATAAAAAAATAGAAGGGAGGTCTGAGGAAAATTAACAACATACTTGTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35863
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110267 | Essential Splice Site | 1870 | 2102 | 25 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 19028495)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 20131121 |
| GRCz11 | 15 | 20066853 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTGTCTAGTTGCCATGGAACCACAGGCTTCCTTTGTAATCATGCCAG[G/A]TAATTAATGTGGCGCTTTCACACAGAGCACTTGTACTTTGTCATTGTTCA
Long Flanking Sequence:
TATCTGAAACGCATTAAAAAGAAACTGTGTAAAACAGTGTCATAATAAATAAAAATATAGTTAAAATCACATAATTTTGTTCATCACATAGTTATCCATTTGTGTGCTGTGGGTAAAAGGTGTGTTTCAAACTACTGAACAAAATGACTTTACTCCTGAATGATTCATTCCTTCCAAATGTGCAGTAGCTGTTCAATTCATTATTATTATTTTTAATATTATTATTATTATTTTTAAATTGTAAAATAAAACAATGTCAGTTATTCCTGAAATCTTACAGCTCTTGTCTGGTAGCACATGTCCTAGCTTATTGGTCTAACTGCTGTTTCTGTCTCAATCAGATTGGAGTATTCTGTTGAGTAGGCGGAACCTGCAGTCTCTCGGCAGACGACTGAAGGAAATGTGCAGGATGTGTGGCATCTCTGCCGCCGACAGTCCCAGCATCCTCAGCACCTGTCTAGTTGCCATGGAACCACAGGCTTCCTTTGTAATCATGCCAG[G/A]TAATTAATGTGGCGCTTTCACACAGAGCACTTGTACTTTGTCATTGTTCAGTTTATCCTTTCAGAAACTTCAATGAAAGTTCAGTACTTAGTCACTATTTCCCTTTCCTTCTCTGTCTCTCCATAGACTCCGTGTCCACGGGCTCCGTGTTTGGCCGCAGCACGACTCTGAACATGCAGACATCCCAGTTAAACACTCCTCAGGACACCTCCTGCACACATATTCTTGTGTTCCCCACTTCTGCTGGCCTCCAGGCCTTCAGCGGTAGGACACTTTCACTTTGGATTTTGTGTGTAAACTAAATTAAGTGCAGGACACTGAAGGCAAAATTTCTTTTTTTATGCACATGTCAATTTTGAGGTTTTGTGCTTTTCATAATGTGACTCATATAAATAAAACATTCAAGAAGTATTTCAAGTGTTTCTTTGACACACTTTATTTACAATTTGCTAATTTGTGTACATTTTAAGTACAAAAATCTAAACTTTCTGTAAAATCAA
Associated Phenotype:
Not determined