ZMP
tie1
Ensembl ID:
ZFIN ID:
Description:
Tyrosine-protein kinase receptor Tie-1 [Source:UniProtKB/Swiss-Prot;Acc:O73792]
Human Orthologue:
TIE1
Human Description:
tyrosine kinase with immunoglobulin-like and EGF-like domains 1 [Source:HGNC Symbol;Acc:11809]
Mouse Orthologue:
Tie1
Mouse Description:
tyrosine kinase with immunoglobulin-like and EGF-like domains 1 Gene [Source:MGI Symbol;Acc:MGI:9990
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45257 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25341 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40727 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9781 | Nonsense | Available for shipment | Available now |
sa9143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14772 | Essential Splice Site | Available for shipment | Available now |
sa33892 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20737 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45257
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 |
---|---|---|---|---|---|
ENSDART00000003701 | Nonsense | 110 | 1122 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33703728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34021393 |
GRCz11 | 6 | 34006083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAAAGAGGATCAGACCAGCTTGGCAATGTTACACTAATTAACAACTA[C/A]AGCAAAGGTATGATTTTATGAGCAAAAAACATGTTTTGGAAAACACCACT
Long Flanking Sequence:
CTCTAGTGCCTGCATTTCTGCTGTGATTTTGCTGTAATTTAATGTACATAAGCAGCAATCTGTACAGAACAAGTTTCAGAAGGGGTTCAGCTGTAATGACTGAGGATATTTACTTTCTATTGATCGCCATGTTTTTTTCATTTCAGCAGTTGTTTTCCAAATGTTGCCGGATGATTGGATTGCATTAATATGTATGAAATATGTCCTCTTCCAGATGCTGTCATGGATCTCACCATGACCTCTAATGGGGCCACATCTGCTAATCATTTCCACCTCTCCTGCATTTCTGGAGAGCGTGACACTGATGGCATTCAGCTGAGCATCAAAAAAGACAACAGCATTGTTCTTCGTGCAGATACCCCTAGTTTCAATCTTCAGAGGCCACAGACAAAAGAAGTGGTGGCTACTGGATTTACAGGTTTTGACCACAGTGGGATTTTCTACTGTCACTCAAAAAGAGGATCAGACCAGCTTGGCAATGTTACACTAATTAACAACTA[C/A]AGCAAAGGTATGATTTTATGAGCAAAAAACATGTTTTGGAAAACACCACTATTATTGTCTTAAAGTGTAACCACAAATTTGTGAATCAGAGTGGTATGGGTTCAGTCTAGACATGCTCAAATACTCGAAAACCAAAAACAAACTACAGACCTTTATTTGCACAGGCATACAATACCCAGCAAACAATTTTGTGTTAAATAGACATCTAATAGACAGCTAAATGTAGACAGCTTGGCTAAACCAAGGCTAAACTGTCAGTGAAAATCTAATAGACATTGATCACACTTTATTTAGATAGTCTGTTTGTTGAATATAATTTTCATTGCATCTGTCAACTAATTCTCATTATTATAAGTAGACCGTTAGGTTGGGGTTAATGTAAGTTAATTGGCATGTACTTGCATAGTTTCTTATAGTCAGTTAAATGTCTGTTTAGCACCAGTATCAACACATATTAAGCAGTTTAAGTACTATTACTTAAATGGGCCATCGAAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25341
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003701 | Essential Splice Site | 246 | 1122 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33698999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34016664 |
GRCz11 | 6 | 34001354 |
KASP Assay ID:
554-7511.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATGTCTGTAGAGACTATATGCATGTAAGAGTATTTTTCTGATTTTGC[A/T]GCCTGTCGGGAAGGAATGTTTGGTCGGAACTGCCAGGAATCCTGTAAGCC
Long Flanking Sequence:
TGACTCCTATTGCTGATGTTGAAAACCGCACAGCAGTTTTGGATCTGAAGAAAGTTGATGAAAGCTATGCAGGGATTTACAGTGCCAGCTATGTTGGAGACAGTGCTCTATATAGCGCTTGGATGCGCCTCATCGTTCGTGGTATGATTTTTTGTGTCATACCTCTATTTCAAAACATTCATGACTTTAGATTGTATATTATAGTGGATTAGATTATTCATGACTTTAGATTGTATATTATATATAATATAGTATATTATATATGTTTTATTTGTCCATTTTGCAGATTGTCCAAAGAACAAATGGGGCTCAGACTGTGACAAGGAGTGTCCCGAATGCCTAAATGGAGGTGTGTGCCATGACAAAAATGGAGATTGTGTTTGTCCTCCAGGGTTTATGGGAATGCGCTGTGAGACAGGTAAATGGAAACCACTCTCATGAAACATAAAAAATATGTCTGTAGAGACTATATGCATGTAAGAGTATTTTTCTGATTTTGC[A/T]GCCTGTCGGGAAGGAATGTTTGGTCGGAACTGCCAGGAATCCTGTAAGCCGGAGAATGGATGCCAGGGCTTGAGTTTTTGCCTTACAGATCCTTATGGGTGTTCTTGTGCCAGTGGCTGGCATGGAGATCGCTGTCGTAAACGTAAGCTGAACATGAGATCACTTTATTTAATAACTGTTCCCTACATGGTGTCATCTGGACCCTATAGAAAGGATTGAGTTCTGAAGTAAAGTTTAAACAGGTGCTGCTGGAATCTGCCAGTAACAATTCAGCCTCCATCAGTCTGACCAAAATAAACATTTCTTGCTGCTCTGTTCATTTTTCTTGTCTTTTTCAAAGTCAGTTTCCACCTCAGAGTAAAAAACAAAACATGCAAGTTAAAAAAAAAGTCTTGTACTGTTACATGAGAGGAAATAAATTGCCGTTAAAGGAAAGTCATGTTGTGTAAAAACAATGGCGCAAGTTAAAAAAAAAGTGTAACTAATATAAAGTGAGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40727
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003701 | Nonsense | 352 | 1122 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33696637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34014302 |
GRCz11 | 6 | 33998992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCGCGCACCAGAGATTTTAGACATAGCCAGTAACCTGGAGGGAAACT[T/A]GAACTCAAGCCACAAGATCACATGTTCTGCAACAGGCCATCCACTGCCTA
Long Flanking Sequence:
AATACAATAAACATCCCTTTTCAGATCCAAACAAAGAGTATACAGCTAAATTGTTGCTAGATTAGACTAGAACAAGTAAACTTATGCAACAAGATAGTATGTAAAATGATGTTATAAAGTATTTCATATTTAATCGATAGAGTAAACAAGCCAAGTATACTTAAAATAAGTATATATACAAAAGATAACTACAAAGGATGTATAATTAATTATTATCATTATTATTTCGATAGCCTGTCTTGAAGGAATGTACGGTGCTGACTGTCTCCTAAGTTGCAACTGCAAGAACAAAGGCAAATGCAATCGATTTAGTGGCTGCCAATGTTCTACAGGCTGGAGAGGGCAATACTGTGAGAAATCAGGTCAGTCTTCAAGACTACTTTTCCATCTGCTTTAAAATCTGCATCGTTTGTTCCTCTTGGCGCCGCTGTCTAACCTTATCCCTCTTTCAGATCGCGCACCAGAGATTTTAGACATAGCCAGTAACCTGGAGGGAAACT[T/A]GAACTCAAGCCACAAGATCACATGTTCTGCAACAGGCCATCCACTGCCTAGCCATTTGAGCATCGAGCTACGCAAGCTGGAAAGCACCGTTCTGAAGGTGAAAGACTAATAGGTTTAAGAAGCTGCATATAAGGTGAAAGAGGGAATGTTTTAAAAAAAGTGTAAATATTGTTGTGTCTACAGATCTAATGTGGTGGCAGTCTTTTGATTCTCTACTGTTGATTACTTAGGCATTCCACACTATTTTGGACTCCAAAAAAAGCACAGCTCACTTTGAGATCCCACGTCTGTCTCCAGAGCACAATGGTTTGTGGGAATGTCGAGTCTCGACCAATGGTGGGCAGGATTCTTTGAAGTTTACCTTAACTGTGAAAGGTGAGATTACATTTTAATATTGTTTTGTTGAAACCCACATGAGCTTCATATTAGCTTCAGATGTGCAATCACATGTTCAAATCACATTCAAATGTGAAATATACGGAACAAGTTAAACGTGGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9781
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 |
---|---|---|---|---|---|
ENSDART00000003701 | Nonsense | 371 | 1122 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33696580)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34014245 |
GRCz11 | 6 | 33998935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCCACAAGATCACATGTTCTGCARCAGGCCATCCACTGCCTAGCCATT[T/A]GAGYATCGAGCTACGCAAGCTGGAAAGCACCGTTCTGAAGGTGAAAGACT
Long Flanking Sequence:
TAGATTAGACTAGAACAAGTAAACTTATGCAACAAGATAGTATGTAAAATGATGTTATAAAGTATTTCATATTTAATCGATAGAGTAAACAAGCCAAGTATACTTAAAATAAGTATATATACAAAAGATAACTACAAAGGATGTATAATTAATTATTATCATTATTATTTCGATAGCCTGTCTTGAAGGAATGTACGGTGCTGACTGTCTCCTAAGTTGCAACTGCAAGAACAAAGGCAAATGCAATCGATTTAGTGGCTGCCAATGTTCTACAGGCTGGAGAGGGCAATACTGTGAGAAATCAGGTCAGTCTTCAAGACTACTTTTCCATCTGCTTTAAAATCTGCATCGTTTGTTCCTCTTGGCGCCGCTGTCTAACCTTATCCCTCTTTCAGATCGCGCACCAGAGATTTTAGACATAGCCAGTAACCTGGAGGGAAACTTGAACTCAAGCCACAAGATCACATGTTCTGCAACAGGCCATCCACTGCCTAGCCATT[T/A]GAGCATCGAGCTACGCAAGCTGGAAAGCACCGTTCTGAAGGTGAAAGACTAATAGGTTTAAGAAGCTGCATATAAGGTGAAAGAGGGAATGTTTTAAAAAAAGTGTAAATATTGTTGTGTCTACAGATCTAATGTGGTGGCAGTCTTTTGATTCTCTACTGTTGATTACTTAGGCATTCCACACTATTTTGGACTCCAAAAAAAGCACAGCTCACTTTGAGATCCCACGTCTGTCTCCAGAGCACAATGGTTTGTGGGAATGTCGAGTCTCGACCAATGGTGGGCAGGATTCTTTGAAGTTTACCTTAACTGTGAAAGGTGAGATTACATTTTAATATTGTTTTGTTGAAACCCACATGAGCTTCATATTAGCTTCAGATGTGCAATCACATGTTCAAATCACATTCAAATGTGAAATATACGGAACAAGTTAAACGTGGCTTTCATGTGAAACTCATGTGAGCACCTGTGAACAAATGTTAAAAGTGTGGAAGTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9143
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 |
---|---|---|---|---|---|
ENSDART00000003701 | Nonsense | 508 | 1122 | 11 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33693284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34010949 |
GRCz11 | 6 | 33995639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCACATTACAAAACCTGAAGCCCTCAACCAAATACCATGTACGTGTA[C/T]AACTTGCTCGTCCAGGAGAAGGAGGAGAGGGTCCTTTGGGTCCAGAGGCC
Long Flanking Sequence:
CGACAACGTAGTACACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCAGGTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGGTAAGTGTGCTGGAGCAGGGTTGGAACTAAACTGTGCGGGGCTTCGGCCCTCCAGGAATTGAGTTTGACACCCCTGACATAGGATCATTCAAGGACTCAAACCCCTCCACAAGGATAAAGAGATGGTTCAAGGAGAGGTGATTTATTAAACGTTTAAAGTTAAGTTCATGCAGATGCAGTTGCCAAAACAATAAACATACACATGTATAACAAATAAAAACAAAACAAAACTTAAAGTTTTTGTTCTGCTACACATCTAATATTCGTAGTAAGGATTTTCTTTTGTTTTGTTTTTTTTAATTAAGTGCATGGCAGTGATCAAATCACATTACAAAACCTGAAGCCCTCAACCAAATACCATGTACGTGTA[C/T]AACTTGCTCGTCCAGGAGAAGGAGGAGAGGGTCCTTTGGGTCCAGAGGCCATCATGGAAACTGACTGTCCAGGTGAGATCAGTCAAAATACATCTAAAATATATTAGTTGTAAGAAAAGAACATATTTAGAGATGAGTTTAGCATTTACAGAACCACTATTAGAATAAGATGCCCCCCACCTGTGCCAAAAAGCCCCCATTCAGCGACCTCTTTCTGATTGCGTATTCTGTGTCGCTAGAGCCCACGGCCAGACCGGAGATTGATTCCAGCTCACTGGAGGGCCGTAATGTCACCCTCAGGTGGTCTCTGATTGGCAGGTTCCGTGAGGCCAGTGGCTTTTTAGTGCAACTCTATGGACCATATGGAGAGAAGCTGTGGGAGGAAACCACCTTCCTTAATGTGCTCTCCGTCAAGCTCTACAATCTGGAGTATCACAAGAACTACCAAGCAGTCGTCCGGCTAGTAAACTGTGGCAGCCATGGGCCCCCTTCAAGACCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14772
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 |
---|---|---|---|---|---|
ENSDART00000003701 | Essential Splice Site | 723 | 1122 | 13 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33692323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34009988 |
GRCz11 | 6 | 33994678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGKACCTGGAGAGTGGAGCAGCTTCGTACAAGCTCAGACACCTGGAGAAG[G/A]TAGGAGACTAGGAGAAAATACTGAAATAACAACATAAATTTGTTTTCTTA
Long Flanking Sequence:
CTAGTAAACTGTGGCAGCCATGGGCCCCCTTCAAGACCCCATCATATTCACATCTATAAGCAGGGTAACATAAATCTTCCATGTCCCCAAGTAGGCAAAAGAAGGATAGAACAGGAGATTAATGCTAGACAGGATGTAATGAAGCAAATATGCATACTATACTGTTCAATTAAACTGGAATAGTAAAATTGTGTATGATTCCTCTCCAGGCCCTTCTTCTCCACGAAACGTCCAGGCCGACGCCCTGTCCATTAGTGCAGTCAGGCTTCGCTGGCAGCCACCTGAAGATCCCAATGGAGGCATTGTAAAATACAGCATTGAATACCAGCCAGTGGGCCAGAGCAGCTTGCATCCTTGGGTAGACACAGACAATGGCAACAAAACCACAAAAGATGTAACATCCCTCAATGGGAGCACATTGTACCAATTCAGAGTGAGAGCTTTCTCTAAGGTACCTGGAGAGTGGAGCAGCTTCGTACAAGCTCAGACACCTGGAGAAG[G/A]TAGGAGACTAGGAGAAAATACTGAAATAACAACATAAATTTGTTTTCTTATTGTCCTTCTTATTGTCCTTCCTTAATTTCCCATGTATCAGGATTATCCAGCTTTATTCCCACCACTCAGCAAGTGGGACGGCCGTTGGCTGAGGATCATCAACTTCTTTTTGCTGTGGTTGGGTCAGTGGCTGTGACTTGTGTGACCATTCTACTGGCTCTTCTGGCCCTCTTTTACATTCGTAAATCTGTCCTTAAAAGAAGACGGACATTCACCTATCAGTCTGGATCTGTAAGTAGACATGTCATTACTTTAGACTCTACAAAATGCTGGGTCACTTTAAATTTGGATTGCATATGGACAAACTCAACTGCTAGGTTAAACTATATTTTTAACTCAACAGCTGGGTTCATCCACATTTGACCCTAATTTGAGGTGAAACAACCCAGCATTTTTTAGTGTAGTTTGATCATTTTTCAGTGTTTAAAGATCACCTATGATGAAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33892
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 |
---|---|---|---|---|---|
ENSDART00000003701 | Nonsense | 843 | 1122 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33690324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34007989 |
GRCz11 | 6 | 33992679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGTCATCGGAGAAGGGAACTTCGGTCAGGTCATCAAGGCCATGGTC[A/T]AAAAAGATGGGATAAAAATGAGTGCTGCAATTAAAATGCTCAAGGGTAAG
Long Flanking Sequence:
GATAGTTCATCCACACAAAGAAATTAGTACTCTTAAAGATTATACTTAAAGAGTATCAGTGTTTCTACCATTGTTAAAGGGAACAACTATTTTTAATGGTAAAGATAATATTATATATTAATATATATAAAAAAGTGTGTTTGATCAGGGTTGGAGTTGAACTCGGCTGGATGGCAGATCTCCAGGAACAGGGTTGAGCACCCCTGAGCTATACCGTCCCAGAAATAAATGACCTTTTAAAATATATTAAAATAGAGATCCATCATCTCATACTTCCAAACTTTTGAATGATAGTATTACATAAATGCTAAATGTCAATGCATAATTATCCTCAGGGTGAAGAGACTATCCTCCAGTTCAACTCAGGGACTCTCACACTTACCCGACGACCAAAGCCTTCCCCAGAGCCTCTTACCTATCCCATCCTGGAATGGGAGGATATAAAGTTTGAGGATGTCATCGGAGAAGGGAACTTCGGTCAGGTCATCAAGGCCATGGTC[A/T]AAAAAGATGGGATAAAAATGAGTGCTGCAATTAAAATGCTCAAGGGTAAGACAGCAAGCCAGCACAGCATTGTTAGCCAAGGTCTGTTTTTACACGATTGTAAATTTTTTTTGCTTTGTGCACCTGCAGAGTTCGCCTCAGAGAATGACCATCGAGACTTTGCTGGAGAATTGGAAGTGCTGTGCAAATTGGGACAACATACAAATATTATAAATCTTATTGGTGCCTGCGAGAACAGAGGTGATTACGCCACCTATTGGAAAGAATTAGAAATTCACATTTTAAACACAATTTGTAACATCTAACTACACATTCACATAAATATAATCATACCATTTCGATTAAATTGACATGCAGTGCTCAGAAGTAGTAAACAAAAAATATATATATTTTCTCCATAAGCCAAACCTTTAATATAGGCGAAAAACAAGCACTAATTGAAACCTATTAAAATGAAAGTCTATTTTCATTGACAATGAAAGCATATTTGCAACAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20737
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 |
---|---|---|---|---|---|
ENSDART00000003701 | Essential Splice Site | 1066 | 1122 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 33685173)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34002838 |
GRCz11 | 6 | 33987528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCCAGGGATACAGAATGGAGCAGCCCAGAAACTGTGATGATGAAGTG[T/A]AAGCAGAAGATTGATCAACTGAAGCTGTAGTAATATTGCATTTATTATCA
Long Flanking Sequence:
AACATTTCTAAAAATTCTTGTTTATTTTGAAGTAATCTGCTTTACATTTAATTATTTCTCTGAAATGGGGCGAATTTGAACAAGGTGACTTTGTCAAAGGACAGAACAGATGTCAAATCCTATTATAGTCATTAATTAAATTTCAAACAAATATAGTATTTACTATGCAGTATGCATTTTGGATGTACTTTATATACATTACAGCTTCATCACAATTATGCTGATTATTCTTTAATTGAAATGTCTGCCTTTGGGCTTTCAGATGGTCTTTTGGAGTTCTTCTATGGGAAATAGTGAGTTTAGGTAAGTGTGTTACTAGTTTCAATGAATTGCTCTCCACTTCCTCTTTGCATATTAAGCATGTTCCAGCCAGGTGAATTAGATGAGTTTGTTCTCCTCTAGGTGGGACGCCATACTGTGGGATGACCTGTGCTGAGCTCTATGAGAAGCTTCCCCAGGGATACAGAATGGAGCAGCCCAGAAACTGTGATGATGAAGTG[T/A]AAGCAGAAGATTGATCAACTGAAGCTGTAGTAATATTGCATTTATTATCACTGATATATTTACAATTATCCATGCAGGTATGAACTTATGAGGCAGTGCTGGCGAGATAGACCTTATGAGCGACCGCCATTTTCACAAATATCTGTCCAGCTTAATAGGATGCAAGAGGCACGGAAGGTAAGCGAAAAACAGACAGATGTTTCACAAACTGTACTTAAAACATTTTTGGGGGGGAGTGGTTGCTGTATAGATATAGTAAGGTGAGCAGATTTCTGAAAAAGAAACCAGGGACATAATTCTATACAGTGGTCAAAATTTCACTCAAATCTGTTGTTCATTCATTCATTCATTTTCTTTTCAGCTTATAAGGTCTGATTTCTTTAAAAGTCAGTGAACTGTAGGTAACAAACAAGTCTCAATGAATCAAGTACTCTGATTAGGTGTTTAATGACGGTTGGAACTAAACTATGCAGAGCTGTGGCCCTTCAGAAACTGAGTTT
Associated Phenotype:
Not determined