Busch Lab

ZMP

flna

Ensembl ID:
ENSDARG00000074201
ZFIN ID:
ZDB-GENE-030131-2145
Human Orthologue:
FLNA
Human Description:
filamin A, alpha [Source:HGNC Symbol;Acc:3754]
Mouse Orthologue:
Flna
Mouse Description:
filamin, alpha Gene [Source:MGI Symbol;Acc:MGI:95556]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa43949 Nonsense Mutation detected in F1 DNA Not yet available
sa43950 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43951 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17303 Essential Splice Site Available for shipment Available now
sa24296 Nonsense Available for shipment Available now
sa24297 Essential Splice Site Available for shipment Available now
sa32439 Nonsense Available for shipment Available now
sa24298 Essential Splice Site, Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa43949
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073442 Nonsense 349 2614 5 47
ENSDART00000135820 Nonsense 349 2553 5 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20065182)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19850289
GRCz11 23 19776632
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAAAGTCACAGCCAACAATGACAAGAACCGCACCTACTCAGTATTCTA[T/G]GTGCCAAAAGTCACTGGACAACACAAGGTACCCAGAACTGTTTGTATAAG
Long Flanking Sequence:
AGCTCTTGTTTAGTACAATTTTTACCAGTTGTATGCACTTCTGGTTGGCTTGTCTTAAATCCCATGCCTTCTTTCCTCCTAAGGTCATCACACCAGAAGAAATCGTTGATCCCAATGTGGACGAGCACTCCGTTATGACTTACCTGTCCCAGTTTCCCAAAGCCAAACTCAAGCCTGGTGCCCCTCTGAGGCCCAAACTCAATCCCAAAAAGGCCCGTGCTTATGGACCAGGTAAACCCTGAACAGCTTTGTTTGCGGTTTTAGGTTTTTTTTGATGTTTTAAAAGTTCTTGTGAAATGAAGCCTAATGGGTATTGCTCTCTGCTGTGCAGGTATTGAGCCAACAGGTAATGTTGTGATGAAGAAGGCTGTGTTCACTGTTGAGACCATCAGCGCTGGTCAGGGTGAGGTACTGGTTTATGTCGAGGACCCCGCTGGACACCGCGAGGAGGCCAAAGTCACAGCCAACAATGACAAGAACCGCACCTACTCAGTATTCTA[T/G]GTGCCAAAAGTCACTGGACAACACAAGGTACCCAGAACTGTTTGTATAAGTTAGCGATTGAATGGGTTGAAATGGAATTGGTGGCTTTTAACGTAAGGTCTGTCTTGCCTGTCTTTTTAATAGACCGATTTATGTGTGTTTTCCTAGGTGACAGTGCTGTTTGCAGGGCAACACATCTCTAAGAGCCCGTTTGAGGTGGATGTGGGAATGGCTCAGGGAGACTCCAGCAAGGTCACTGCCCAGGGCCCAGGACTCGAGCCTGCAGGCAACATTGCCAACAAAACCACATACTTTGATGTCTACACAGCTGGTACTTGCCCTCAGTGTGTCATGAATAGAATGTCTAGATGGGAAAACAGGCTTGTTTTGGTTGCTGCTGATGCTTAAAATAAATCAAATATTTTTAAATAAATGTATTAATATAAATATTCATCATCATATTTGAATTACATTTTTAATGAGCACTTTATATTTCAAAGGCAATAAATGCAATACATCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43950
Status:
Mutation detected in F1 DNA
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
ENSDART00000073442 Essential Splice Site 358 2614 5 47
ENSDART00000135820 Essential Splice Site 358 2553 5 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20065210)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19850317
GRCz11 23 19776660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCACCTACTCAGTATTCTATGTGCCAAAAGTCACTGGACAACACAAG[G/A]TACCCAGAACTGTTTGTATAAGTTAGCGATTGAATGGGTTGAAATGGAAT
Long Flanking Sequence:
TTGTATGCACTTCTGGTTGGCTTGTCTTAAATCCCATGCCTTCTTTCCTCCTAAGGTCATCACACCAGAAGAAATCGTTGATCCCAATGTGGACGAGCACTCCGTTATGACTTACCTGTCCCAGTTTCCCAAAGCCAAACTCAAGCCTGGTGCCCCTCTGAGGCCCAAACTCAATCCCAAAAAGGCCCGTGCTTATGGACCAGGTAAACCCTGAACAGCTTTGTTTGCGGTTTTAGGTTTTTTTTGATGTTTTAAAAGTTCTTGTGAAATGAAGCCTAATGGGTATTGCTCTCTGCTGTGCAGGTATTGAGCCAACAGGTAATGTTGTGATGAAGAAGGCTGTGTTCACTGTTGAGACCATCAGCGCTGGTCAGGGTGAGGTACTGGTTTATGTCGAGGACCCCGCTGGACACCGCGAGGAGGCCAAAGTCACAGCCAACAATGACAAGAACCGCACCTACTCAGTATTCTATGTGCCAAAAGTCACTGGACAACACAAG[G/A]TACCCAGAACTGTTTGTATAAGTTAGCGATTGAATGGGTTGAAATGGAATTGGTGGCTTTTAACGTAAGGTCTGTCTTGCCTGTCTTTTTAATAGACCGATTTATGTGTGTTTTCCTAGGTGACAGTGCTGTTTGCAGGGCAACACATCTCTAAGAGCCCGTTTGAGGTGGATGTGGGAATGGCTCAGGGAGACTCCAGCAAGGTCACTGCCCAGGGCCCAGGACTCGAGCCTGCAGGCAACATTGCCAACAAAACCACATACTTTGATGTCTACACAGCTGGTACTTGCCCTCAGTGTGTCATGAATAGAATGTCTAGATGGGAAAACAGGCTTGTTTTGGTTGCTGCTGATGCTTAAAATAAATCAAATATTTTTAAATAAATGTATTAATATAAATATTCATCATCATATTTGAATTACATTTTTAATGAGCACTTTATATTTCAAAGGCAATAAATGCAATACATCTATGGTAAATAAGCAAGCAAAATAATTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43951
Status:
Mutation detected in F1 DNA
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
ENSDART00000073442 Essential Splice Site 526 2614 8 47
ENSDART00000135820 Essential Splice Site 526 2553 8 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20070757)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19855864
GRCz11 23 19782207
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAAGGAGCAGGAACCGGAGACCTCAAAGTTACCATCAAAGGGCCCAG[T/C]GAGTGGACGTCTATATTAATGCTGCAGTGCTAGATGATTTATCATGCAGT
Long Flanking Sequence:
ATGCCTTTTTGTCTTTGACCCAAACACAGATTCAGAAAGTATTTTCCTGACATGTTAAAACCCTTACACTTGTATACAATTAAAAATTGGAAAATTATAAAATCTGAAATGACAATTATGAGAAAAGGTCAAAGTTATGATTTAAGTATCACAGTGTGACTGAGTTAATTTAACTGGTTGTATTTTTCCATCCATTAGAAAGTGTTATGGTAAAGTCTGTACAATATTGATAATAATAATAATAATAGGTTTTACTGTTTATTGCAGATATATAGAGCTCAACTTGTACAGCACTTTCATGAATGGATGTGTTCAACTGCTAACTACAGTTTGTTCTGACTTGCTTGTATGTTCTCACCAGCCTGTAATCCAAGCCTGTGTACAGCCAAGGGCCGCGGTCTGCAGCCTAAAGGCCTGAGGGTCAAGGAGACCGCCGAGTTTAAGGTTTACACCAAAGGAGCAGGAACCGGAGACCTCAAAGTTACCATCAAAGGGCCCAG[T/C]GAGTGGACGTCTATATTAATGCTGCAGTGCTAGATGATTTATCATGCAGTTACTCAACTGTGGTATTTCTTAAACAGAGGGTCTCGAGGAGCCCTGTAAGAAGAAGGATTTGGGAGACGGCGTGTACAGCTTTGATTATTACCCCTCCACACCTGGAAATTACATCATCACCATCACATGGGGCGGTCAACACATCCCACGCAGGTGAAATACAATATTTATATACTTATTAAAGTTAGCAAGAAGCATCATTTTTAAAGGGAAAGTTTACCCAAAAATGTAAATCTGCCATCGTTTACTCATCCTCCACCTCACCTTTGTTTCTTTTGTTGTTGATATTCTAAAGATTGTTGCTTATCAATTGCTGTTTTTTTTCCCCAACGTTTTTCGAATTATCTTATTTTTGAGACCAAATGTTGAAACCATATTGGTTTAAGATAATCCTACACCACCTAAAATTAAAACACTGAACAGTCAATTGACCCTAAATAGGAGAGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17303
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073442 Essential Splice Site 891 2614 16 47
ENSDART00000135820 Essential Splice Site 891 2553 16 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20075148)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19860255
GRCz11 23 19786598
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGATGCAAGCAAGGTTAAAGCTGAGGGGCCTGGACTTAGCCGTTCTGG[T/A]AAGATAATGGACACAAAACTAACTTGTGCGTCCCTGCTTAKAATGATGGY
Long Flanking Sequence:
GGAGTGGCCAAGACAGGCCTCAAAGCATATGATCCAACATACTTTACTGTGGATTGTGCTGAGGCTGGACAGGGTAATGGCTTTTAATCCCCTGATGCAAGTTATTCTCATTCTGTAATTTGGGAACAAATAAGCTTTATTTATTTATTTGTGGTTCTTTCTGTTTAGGCGACATCAGCATAGGCATCAAATGTGCTGCAGGTGTGGTGGGACCTGCTGAGGCTGACATAGACTTCGACATCATTAGAAATGACAACGACACATTTACTGTTAAATACACTCCTCCTGGAGCGGGCAGCTACACCATCATGGTGCTGTTTGCTGATCAGGTGAGAAGAAGTGCAAGTAAATGAGGTGATTGATCTAGTTGGGATTTTTTTTTATTCACACCAAGCTTATGTTTTCTAGACCATTCCCATGACACCCATCAGAATTAAGGTTGATCCCTCTCATGATGCAAGCAAGGTTAAAGCTGAGGGGCCTGGACTTAGCCGTTCTGG[T/A]AAGATAATGGACACAAAACTAACTTGTGCGTCCCTGCTTATAATGATGGCAGCAAATTAGACATTTTTAAGTACTTTCAAGCGTCTACCTCAGTGATTCCTAGTGTTGTTATAATCCTGCAAAATAGAAATTGTAACTTGGTAATGTATTTTGGTATCCAAAGATGTTCTTGGAAGATTTTGATAGTAGTTTTTTATTGCTATGACAGAAAAAGGAAAGGGCAAAATTAAGTCACAATAAAAATGCATAGTATTTCTTATTTAGTTTATTATGGTACTAAAAAGAACCTCTTTTAGTATTACCCCTTTTTTTAAGAAAACTGTAATGTTTTTAATAATAGTAATGGTGGTAATAAATATGTGATTTAGTTTAATACTCATTTATTTTTAATTAAATTACGATATACTTTAAAATTTAAAATCAGTGCATCTAATCTAGCCTCAAATCAGTGATAGAAAAAAATGACTTATTTCTCTTCAAGGTGTGGAGCTGAACAAACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24296
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073442 Nonsense 1294 2614 22 47
ENSDART00000135820 Nonsense 1236 2553 21 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20077163)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19862270
GRCz11 23 19788613
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCCGAGATCTGGGAGACGGCACATATCAAGTGGAGTACACGCCTTA[T/G]GAGGAGGGTGAGTGTTAGGGCTGTTTCTGTTTCAACTTAACATGATTAAA
Long Flanking Sequence:
GCACTAATGCTGGCCCTGCTGAGTTGACCATCGAGATCATCTCTGACAATGGCACTGAGGCTGAAGTCCACATTCAAGACAACGGCGACGGGACCTACACCATCACTTACGTCCCTCTCTACCCTGGAGCCTATACCCTCACCATCCGCTACGGGGACCAGGATGTGCCAAACTTCCCAGCAAGACTCCATGTGGAGCCTGCTGTGGAGACCAGTGGAGTGAAAGTGTTCGGACCCGGAGTGGAGGGCAAAGGTAGTGCAGATTTCTGAGATTTGTTTCAGGAATCCGCTGTCTGTATTTGGATATTTGGTTACTTTTGAATGTTCGCCTGTAGGTGTTTTCAGGGAAGCCACTACAGATTTCACTGTGGATGCCCGTGCGCTCACTAAAACCGGAGGCAATCACATCAAAACCTGCATCAACAACCCATCGGGCAACCGCACTGAAGCACTGATCCGAGATCTGGGAGACGGCACATATCAAGTGGAGTACACGCCTTA[T/G]GAGGAGGGTGAGTGTTAGGGCTGTTTCTGTTTCAACTTAACATGATTAAAAAAACAAAACAATTGGAATTCTTTGTGCAAATTTCTGAAAACTGTTCTATTTGATTCTTATCCATCATGGGTATTATGTGTTTAACAAACCTGTGGAATACAAGACCATATATGGGGTGCGTGCGTGATTGCGTGTTGTTTTTTTCAACAAGGAATATCACATTTTTTGTGGATTTGTATAAACAGATTTTGACATGAAGCTATTCAAGAGTGCAAATGAAAAACTTGATAATTTTCATTACATTTATTGTTCAAACATTATGTCTGGGGTATTTGAAAGATTTTTAAAAGGTGCTTTAAGTTTGTGAATCTCTCTATGAATTTTGATCTATCTGTTATTGAAAGTACAGTTGGGCTGTAGAATTATGGCTAAAATGAGAATCATGATTCGCACAATTTTCAAGATCTCGATTTTTTTTTTTTTTTTTCACGATTCTGTATATGTAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24297
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073442 Essential Splice Site 1296 2614 22 47
ENSDART00000135820 Essential Splice Site 1238 2553 21 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20077171)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19862278
GRCz11 23 19788621
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCTGGGAGACGGCACATATCAAGTGGAGTACACGCCTTATGAGGAGG[G/A]TGAGTGTTAGGGCTGTTTCTGTTTCAACTTAACATGATTAAAAAAACAAA
Long Flanking Sequence:
GCTGGCCCTGCTGAGTTGACCATCGAGATCATCTCTGACAATGGCACTGAGGCTGAAGTCCACATTCAAGACAACGGCGACGGGACCTACACCATCACTTACGTCCCTCTCTACCCTGGAGCCTATACCCTCACCATCCGCTACGGGGACCAGGATGTGCCAAACTTCCCAGCAAGACTCCATGTGGAGCCTGCTGTGGAGACCAGTGGAGTGAAAGTGTTCGGACCCGGAGTGGAGGGCAAAGGTAGTGCAGATTTCTGAGATTTGTTTCAGGAATCCGCTGTCTGTATTTGGATATTTGGTTACTTTTGAATGTTCGCCTGTAGGTGTTTTCAGGGAAGCCACTACAGATTTCACTGTGGATGCCCGTGCGCTCACTAAAACCGGAGGCAATCACATCAAAACCTGCATCAACAACCCATCGGGCAACCGCACTGAAGCACTGATCCGAGATCTGGGAGACGGCACATATCAAGTGGAGTACACGCCTTATGAGGAGG[G/A]TGAGTGTTAGGGCTGTTTCTGTTTCAACTTAACATGATTAAAAAAACAAAACAATTGGAATTCTTTGTGCAAATTTCTGAAAACTGTTCTATTTGATTCTTATCCATCATGGGTATTATGTGTTTAACAAACCTGTGGAATACAAGACCATATATGGGGTGCGTGCGTGATTGCGTGTTGTTTTTTTCAACAAGGAATATCACATTTTTTGTGGATTTGTATAAACAGATTTTGACATGAAGCTATTCAAGAGTGCAAATGAAAAACTTGATAATTTTCATTACATTTATTGTTCAAACATTATGTCTGGGGTATTTGAAAGATTTTTAAAAGGTGCTTTAAGTTTGTGAATCTCTCTATGAATTTTGATCTATCTGTTATTGAAAGTACAGTTGGGCTGTAGAATTATGGCTAAAATGAGAATCATGATTCGCACAATTTTCAAGATCTCGATTTTTTTTTTTTTTTTTCACGATTCTGTATATGTAAAATAAAGGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32439
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073442 Nonsense 1813 2614 33 47
ENSDART00000135820 Nonsense 1753 2553 32 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20087028)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19872135
GRCz11 23 19798478
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAATATGCCCCAACTGAGGCGGGCCTGCATGAGATGGACATTAAATA[T/A]GATGGAATACACATTCCAGGTAAAAGACATGTATTCTCAATGTACAAACT
Long Flanking Sequence:
TGTTGCTGATTCTATACTTGCTAGTCATTTTTTAAAGTGGTTTAAACTAATATTAAATGAACTAACAAGATTTCTTAGCTTTAAACCTCAGAAACATGCATTTTGCTTCTGGCGGCCATCTGTTCATCCGTTCAATTTCATTTTGCATGGCTTCTATCTGATTCCCTTGTGTTTCTTTACAGGCTACAGATGGGCAATTGGGTATGAATGGACTGGATGTAGCTGGACTGAGACCCTTTGACTTGGTCATTCCTTTCACCATTCAGAAAGGAGAAATTACAGGTAAACTTGTGTAAAAGTGTATTTATTTATTTTCAGAAATTCACTGATTTCTAGGTGATGATTATGTTAAACAATAGAAATATTCGTTGCCCCTCAGGTGATGTACGAATGCCCTCTGGAAAAGTGGCCAAGCCTGATATTACAGACAACAAGGATGGCACAGTCACAGTGAAATATGCCCCAACTGAGGCGGGCCTGCATGAGATGGACATTAAATA[T/A]GATGGAATACACATTCCAGGTAAAAGACATGTATTCTCAATGTACAAACTGCTGAAAAAGTTCATCATAAAGGGAAATGTTTGGTTGAGCATAGGGTTGCTCTTAATTATAAATTCTTCTGTAATTTTAGGAAGTCCATTGCAATTCTACGTGGATTATGTCAACAGCGGTCATGTGACTGCATATGGTCCTGGTCTAATTCATGGCATGGTCAATAAGCCTGCAGTCTTCACAGTCAACACAAAGGATGCTGGAGAGGGTATAGATCCTCACCTCTGTATTTGGCTTTAATAATCAATTAAGCTTTTAATTATCTATTATTGGACCCTCTTTGTGCTGTGGTTTTAGAGATCAAACATAAACATCTGCTGTTGTATGTTTATTAGGTGGTCTGTCTCTGGCCATCGAGGGGCCATCAAAGGCAGATATCAGCTGCACTGATAATCAGGACGGTACCTGCACTGTTTCATACCTCCCTGTTCTTCCCGGAGACTACAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24298
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000073442 Splice Site 2270 2614 41 47
ENSDART00000135820 Essential Splice Site 2210 2553 None 46
ENSDART00000142228 None None 353 None 7

The following transcripts of ENSDARG00000074201 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20090248)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 19875355
GRCz11 23 19801698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCGTAAAGATGGATCCAGTGGTGTCTCTTACATCGTCCAGGAGCCTGG[T/C]AAGGTTTTCCTTTTTTTAATTGTTTTTATTTATTTATTTTTTTACTTCAG
Long Flanking Sequence:
GAGGGCAGAAGCTGGTGTACCAGGTATGAGATGTTTGGTTTGTCTACATATTTGGTTAATACCCTCCAAAGGGTGCTTGGGGAAAACAATCATCCCCAATTTTCCCCAGTAATGATTTCTTTAATGGTTCTTGGTGACTCGTTTGGGGCTTTAATGTATCTGGTCATGTTCTGCAACAAACTAAATCTGAAAAATCCTCAAATGTGTTGTCATTTTGATTTATTTTACTGCTCTTGAACAAGTCAGAGTCTTCCAATCCTGAATTGTAAATATCAAACATTTTGACTTGCTTGATTTGGCTACCTCCAACTGGGGGATACCTGAAGTACATTTTAACGCCTCATATTTTATCCATCTTCAGCGGAGTTCAGCATTTGGACTCGTGAAGCAGGAGCTGGTGGTCTGTCCATCGCAGTGGAAGGACCCAGCAAAGCAGAGATTGCTTTTGAAGACCGTAAAGATGGATCCAGTGGTGTCTCTTACATCGTCCAGGAGCCTGG[T/C]AAGGTTTTCCTTTTTTTAATTGTTTTTATTTATTTATTTTTTTACTTCAGGGCTCATCCTGAAGATGACTATAAGCTGACAATTCTCTATCTGTTTTAGGCGATTATGAAGTATCCATCAAGTTCAATGACGAGCACATCCCTGACAGTCCGTTTGTGGTGCCTGTGGCCTCGCCATCTGACGATGCCCGCCGTCTCACTGTTGCCAGTCTTCAGGTGAGGCATCGAGAAAGACAGACATTTGTCCACCCAGAGAACCCCAAGTCAGCCCTTGGCACAGCAGCTAAGACAATAAAAAGGCTACCATAACACCGTTTGTTTTGGTTTATATAACATATCATTTCAAAATGACAGGTAATTGTTGGTAGGGATGGGTGAAAGGGACATAAAAGTATATCACAACATTGTCTGGTATTTATTGATTTTATTATAATAATGACCATAATCATATGCATCTACCAAGAGTTTTTTTTAAGAATATTTATTTATTATTATTATTAT
Associated Phenotype:
Not determined