ZMP
f5
Ensembl ID:
ZFIN ID:
Description:
coagulation factor V [Source:RefSeq peptide;Acc:NP_001007209]
Human Orthologue:
F5
Human Description:
coagulation factor V (proaccelerin, labile factor) [Source:HGNC Symbol;Acc:3542]
Mouse Orthologue:
F5
Mouse Description:
coagulation factor V Gene [Source:MGI Symbol;Acc:MGI:88382]
Alleles
There are 13 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13037 | Nonsense | Available for shipment | Available now |
| sa21530 | Essential Splice Site | Available for shipment | Available now |
| sa21531 | Essential Splice Site | Available for shipment | Available now |
| sa41467 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7198 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13751 | Nonsense | Available for shipment | Available now |
| sa13402 | Essential Splice Site | Available for shipment | Available now |
| sa2508 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa13037
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 66 | 2101 | 2 | 25 |
| ENSDART00000128539 | None | None | 406 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35101085)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34320596 |
| GRCz11 | 9 | 34129781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAA[C/T]AGCCAAAAGCTCATCCCTTGTCCTCAGGTAYACCGRTCACTTAACTTTAA
Long Flanking Sequence:
AATTTCAAATATCTATGTAACAAAATAGTTTTGTATACATATTTTTTCTATGTATGTGTATCACATATACATAATAATTACATATATATATATATATATATATGTATATGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATACACACACATAAATTTGTAAAAACAAACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAA[C/T]AGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCTAGGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGGGTGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21530
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078065 | Essential Splice Site | 75 | 2101 | None | 25 |
| ENSDART00000128539 | Essential Splice Site | None | 406 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35101193)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34320704 |
| GRCz11 | 9 | 34129889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCT[A/G]GGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGT
Long Flanking Sequence:
TGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATACACACACATAAATTTGTAAAAACAAACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAACAGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCT[A/G]GGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGGGTGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAAAGCTGTCAGTCCCTGATAAATATTTACTTTTTGTTCCGAAAAATCTTAAGCAAAATTACTTTTTCCCCTAAAAATGCATGTCTGTTAGTTTCATTAAATCCTTTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21531
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Essential Splice Site | 115 | 2101 | 3 | 25 |
| ENSDART00000128539 | Essential Splice Site | None | 406 | 3 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35101318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34320829 |
| GRCz11 | 9 | 34130014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGG[G/T]TGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTT
Long Flanking Sequence:
AACTTTATATTTAGACCCAATTTCATTGCAATTAATTGCAATTAAAGAGAGAGAGAACGAAAGTGAGAGAGAGTGAGAGAGAATAATTCATTCACTCACTCACTCACTCACTCACTTACTCACTCACTCACTCACTCACTCACTCACTCGCTCACTCACTCGCTCACTCACTCACTCACTGCTCATACTTATTTACTGTTGTTGTATTTCAGAACCGGACAATCATATAAAAAAGTAGTATACAGGGAATATAATGAGGGATTCAAACAGCCAAAAGCTCATCCCTTGTCCTCAGGTATACCGGTCACTTAACTTTAAAACCCATTCAGTATAAAGCAAAGCATGAATCTAACAATTGCTCAAAACAAATGTTCTAGGGTTACTTGGGCCTACATTGCGTGGACAAGAGGGTGACACAATCATCGTCACGTTCAGGAACATGGCAGATCATCCTTGCAGCCTCCACCCCCATGGCATTGCTTACGGGAAGCAGTCAGAGG[G/T]TGTGTATTCAGATGTGATTGCGGTAACAGTATGACCCATGTAGCAATGTTGTAACATACACCATAATTTTAACAAGCAGACACTGTGCTTTGAAATGACAGAGATGATGCATTTCAAGTGGAATTTTGTTTAGAGGACATTATGGATTATTTTAGTGCTCATCGTTTAGCTGAGTAAACAGTTTGAGCAACACAAACATTTGTGTTTGATGTCTTTGGAAATATTAACCCAAGATACAAATTAACCAAAGGCTGTACCTAAGTCCAAAGCTGTCAGTCCCTGATAAATATTTACTTTTTGTTCCGAAAAATCTTAAGCAAAATTACTTTTTCCCCTAAAAATGCATGTCTGTTAGTTTCATTAAATCCTTTATCCTTCAATGTTTCCATTAGGGTCTTTATACTTTGACAACACGTCACTCCTTGAGAAAAATGATGATGTAATTCAACCTGGTGAAGAGCACACTTACCAGTGGGACGTGACGTCTGATGTGACCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41467
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 195 | 2101 | 5 | 25 |
| ENSDART00000128539 | None | None | 406 | 5 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35104061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34323572 |
| GRCz11 | 9 | 34132757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGATTAATGTGTCCTTGTCCCACAGGCACCCTAGACGACTCAGGAAAT[C/T]AGATTCATTTCCATCAAGAGTCTGTGCTGCTGTTTGGAGTATTTGATGAG
Long Flanking Sequence:
ATGTAGCTTTCTTCAAAATATTTTCTTTTGTGTTTAACAAAATAGTTAATCAAATAGTTTTAAACAAGTAAAGGGGGTGAGTAAATGATGATGGCATTTTCATTTTTGGTTGAACTATTTCTTTAAACTAGACTAGATTCTAATGCATATCAATGAAGTCTCCATGGCTGATTCTGAAATGTTATTTCATAGTTAGTAAGAGAGGCTTAAGCCATGTTTGTTTCTCCTTTATGAAAGATCGAAGACACAGTACTCAACACAGTGTCTAACAAAGTGTGCAGTGTAAATTGGTCTTAATAAACCAATATACTGAATGATGCATCATCATAATCATCATCATTAACATCATCCTGCACAAGCTGAACTCATTTTCAAGCGTTACAGTGTAAATGCGTGCAGTTTTTTGAGTTTCCCAGAACTTATGCAACTATAAACAGCTCTGTTTGTTTAGATGATTAATGTGTCCTTGTCCCACAGGCACCCTAGACGACTCAGGAAAT[C/T]AGATTCATTTCCATCAAGAGTCTGTGCTGCTGTTTGGAGTATTTGATGAGAACAAGAGCTGGTACAGCACTGGGGACTCTCCACAGCCTCTGAATGTCAAATACACAATAAACGGCTACACAAATGGCTCAGTACCAGGTTGGTTCGATACAGTTTTTTGCAAAAGTCTTAGGCCACTAGCATTTTCACCAACAAAAAAAGTTTTGGTGTAGTATGCGAGTAGAAATATATTTTCCAAACATTATTTTTGCTATTTTTGATATTTATAGTCACCATCATCGAATACAACTTGAAAAACATGACGAAATAGAACAAACTGATACAGACTAAATCCAGTAGAACATCTTCAAGACACTTCAGGAACCTGACACTGTAAAAAGGTTTTAGGCACTTGTGTAAGAATGCTGTAAAGTGTGTATGCTTCAAAAATAATGCCTTAAAGGGGACCTATCATGCCGATTTTCTCAAGATGTAAAGTAAGTCTCTGATGTCCCTAGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7198
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 630 | 2101 | 12 | 25 |
| ENSDART00000128539 | None | None | 406 | 12 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35110453)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34329964 |
| GRCz11 | 9 | 34139149 |
KASP Assay ID:
554-4876.1 (used for ordering genotyping assays)
KASP Sequence:
ATTACATCCAGACTGCTACTTTCTATGGTCATACATTTGAGCTAAAAAAC[A/T]GAGAAGAGGATATACTCAGTCTATTTCCTATGACKGGTGAAACTATCACG
Long Flanking Sequence:
CTTTTTTTTTTTTAGCTCACTGACAAACTACCATTAAAATGTTTGTAAAAGAGTTGCTCCTTATGTTAAATGTTTCAAAAAATGTGGCTTAAGCTGCTGTCAACACTTCTCTATTTCAGCTAAAAGCTGACAAGGAGCAGCATGCCATGTTTACCGTTTTTGATGAGAACAAGAGCTGGTACCAAGATGAGAACATTAACACATACTGCAGTGATCCCAAAAAAGTGAAGAAAGACGATCCCGAGTTTTACAAGTCAAATGTCATGCACAGTGAGTGATTTTCTGCTATTATTTCTGATATCATCATATTGCTGTTGATTGATATATGCTACGATGTGTTTATAAAAACTCTTACAGCAATCAATGGTTATGTATATGAAAGCGGCCAAGAATTGGGATTTTGTCATGGTGAAATTGTGACTTGGCATGTGTCGAGTGTTGGGGAACAGGATTACATCCAGACTGCTACTTTCTATGGTCATACATTTGAGCTAAAAAAC[A/T]GAGAAGAGGATATACTCAGTCTATTTCCTATGACTGGTGAAACTATCACGATGAACATGGTTAATATAGGTATGTTTGTCTGATTAGACTATCCAAATTACTTGTAATAAATTAGTTTTAGAATTTAAATATTAACTATACAAACATACACATTGTACAACAAAAACTGAATGCAACCTCAATATCTCCACTTTACAGGTATTTGGCTTTTGGCATCATTGAACTCGCATGATTCCACTAAAGGGATGAGGGTGAAATTCAAAGACCTCGAATGCTTCAGAGATTATGTAATAGAATATGATTATGAGGACGGGAAATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAACCGGTCCGTGCAAGACCTGACGTGGTCGACGAGTACTCTGATTTATTTGCTGAAACCCTCAACTTAAGGACGTTCAACAATGTTAAAGATGAAGTTGAGATAATCGACTTGACATTTCTAGATCAAGATGATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13751
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 799 | 2101 | 13 | 25 |
| ENSDART00000128539 | None | None | 406 | 13 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35111089)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34330600 |
| GRCz11 | 9 | 34139785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTTTATTAATGGAGGAAGGWGATTTAGACAAGGGAGAATCTTCTAAT[A/T]AAGWCTTGAATGACAGCACWGACAAGKCATTGCTAGAGACAACAACTACT
Long Flanking Sequence:
CTATACAAACATACACATTGTACAACAAAAACTGAATGCAACCTCAATATCTCCACTTTACAGGTATTTGGCTTTTGGCATCATTGAACTCGCATGATTCCACTAAAGGGATGAGGGTGAAATTCAAAGACCTCGAATGCTTCAGAGATTATGTAATAGAATATGATTATGAGGACGGGAAATTCACTGCATGGAAACCACCGACTATTAATGAAATCAAAAAAGAGGAACCGGTCCGTGCAAGACCTGACGTGGTCGACGAGTACTCTGATTTATTTGCTGAAACCCTCAACTTAAGGACGTTCAACAATGTTAAAGATGAAGTTGAGATAATCGACTTGACATTTCTAGATCAAGATGATGGTTTGTTGCCCATTGTTGAAGAAAAAAGCCTGGGATCAAGCAACGAGAACTTACACAATGCTACTTTACAATCTTTCATTGAGACTCATGGTTTATTAATGGAGGAAGGTGATTTAGACAAGGGAGAATCTTCTAAT[A/T]AAGTCTTGAATGACAGCACAGACAAGGCATTGCTAGAGACAACAACTACTTTTGATTCCAATAGAGTTGTCGCATTAAACAACGAAACGGACAGTATAATTTTAGATTTTCCAATTGTAGAAAGAAAGGTTCGTAGTGCACCATCAAAGCCAATGAACGAACCTGAAAGTGTCACTATGAACTTTAAAACAACAGAACATATCAATTCATCATTAGAGAGAATCAATGCTATATATTCCCCAATAACTGAAACAAACATCAACACAATGACTGAGACACACACTGATTTCAGTATCACTCCATTTGATGGTTCAACTGGAGAAATGAACTTCACACTAGAGGATGACACCGCACTTCTAAATTCATCTGAATCAGAGCCCCTGCAATCAAACCAAAACTCCGAAAACAGAATAGCTTTTCAAGAAGAGCTAAATGCAAAAGATGGCACAGATGTTGACAGTAATAATTCTGTGAAAAATCAGATCTTCAAATACAACGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13402
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078065 | Essential Splice Site | 1467 | 2101 | None | 25 |
| ENSDART00000128539 | Essential Splice Site | None | 406 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35114295)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34333806 |
| GRCz11 | 9 | 34142991 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACRTTTTMAATAAATRAATCTAAARCTAATTTGCTAATTCCTGTTTGCAA[A/C]GGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAA
Long Flanking Sequence:
AAATTTACTGTAAAATAACAGTCCTTAAATTACAGAAATTTACCATAAAACAACGGCTGTTAAATTACAAAATTTCCTTAAATTTTTAATTTCCGGTAAATTTCTGTTTTTTAATATCTGTTATTTTACAGTAAATTTCTGTAATTTAACGGACGTTATTTTATGTCTTTTTCCAGTACCCTAGTACTAAACCGAAGGAGATGAATGAATAAATAGTGTTTTTTTTTTAAGTGAGACATTTAATTCCTAACTGAATTTGATGAGCCAAGACAAGTTTAGCATTTTTAACATATTAGGAATACAAATAAGACTGAATGTGTGCATGTTTTAAAATAATATTTGGAAATAATTAAAAATTATAACTTCCCACCTAGAATTCGACTACATCATTCTGTTTCTTCAAATGTTATTTAAAAATAAGTCCCTCAAAATCATCAGAATTTCTGGAGAACGTTTTAAATAAATGAATCTAAAACTAATTTGCTAATTCCTGTTTGCAA[A/C]GGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTACCTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACACCTGGGAATTCTTGGTCCGCTCATTAAAGCGGAAGTTGATCAGACCGTTATGGTAAACCACACACTTGTGAAGAAATCAGAATTGGAAAGCATCACGTCTATAAAATGAATATTAACAATTGCATTCTGGTTTTCCATGCTAGGTATTTTTCAGGAACCGTGCAAGTCGTCCATACTCTTTGCATGCAAATGGAGTAAAATACTTAAAACAAATGGAAGGCCTGAGTTATGATGATGAATCTCCATACTGGTACAAACAGGACGATGCTGTTCCACCCAATGGCACCTTTACCTACATGTGGACCATAAATCCCAAATCTGGACCTCAAAATAATGAATCTGACTGCCGAACTTGGACCTACTACTCTGCAGTGAATCCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2508
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000078065 | Nonsense | 1489 | 2101 | 14 | 25 |
| ENSDART00000128539 | None | None | 406 | 14 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 35114363)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34333874 |
| GRCz11 | 9 | 34143059 |
KASP Assay ID:
554-3064.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTA[C/A]CTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACA
Long Flanking Sequence:
AAAATTTCCTTAAATTTTTAATTTCCGGTAAATTTCTGTTTTTTAATATCTGTTATTTTACAGTAAATTTCTGTAATTTAACGGACGTTATTTTATGTCTTTTTCCAGTACCCTAGTACTAAACCGAAGGAGATGAATGAATAAATAGTGTTTTTTTTTTAAGTGAGACATTTAATTCCTAACTGAATTTGATGAGCCAAGACAAGTTTAGCATTTTTAACATATTAGGAATACAAATAAGACTGAATGTGTGCATGTTTTAAAATAATATTTGGAAATAATTAAAAATTATAACTTCCCACCTAGAATTCGACTACATCATTCTGTTTCTTCAAATGTTATTTAAAAATAAGTCCCTCAAAATCATCAGAATTTCTGGAGAACGTTTTAAATAAATGAATCTAAAACTAATTTGCTAATTCCTGTTTGCAAAGGCGACTTGATAAAACAGCTCAAAATGAGAGGCCCACGGTTTTCAGAAAAGTGGTGTTCCGAAGGTA[C/A]CTGGACAGCACCTTTAGCATCCGAGACATCCGAGGAGAAATGGACGAACACCTGGGAATTCTTGGTCCGCTCATTAAAGCGGAAGTTGATCAGACCGTTATGGTAAACCACACACTTGTGAAGAAATCAGAATTGGAAAGCATCACGTCTATAAAATGAATATTAACAATTGCATTCTGGTTTTCCATGCTAGGTATTTTTCAGGAACCGTGCAAGTCGTCCATACTCTTTGCATGCAAATGGAGTAAAATACTTAAAACAAATGGAAGGCCTGAGTTATGATGATGAATCTCCATACTGGTACAAACAGGACGATGCTGTTCCACCCAATGGCACCTTTACCTACATGTGGACCATAAATCCCAAATCTGGACCTCAAAATAATGAATCTGACTGCCGAACTTGGACCTACTACTCTGCAGTGAATCCTGTACGCATGAATCTTATCATAATATGGTTTTTATTCCTCCAAGGAGCAAGCCAATAATCACAGATTGCTA
Associated Phenotype:
Not determined