Busch Lab

ZMP

si:dkey-32e23.6

Ensembl ID:
ENSDARG00000036999
ZFIN ID:
ZDB-GENE-081104-407
Description:
Novel protein similar to vertebrate patched domain containing 2 (Ptchd2) [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
PTCHD2
Human Description:
patched domain containing 2 [Source:HGNC Symbol;Acc:29251]
Mouse Orthologue:
Ptchd2
Mouse Description:
patched domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2444403]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa41303 Nonsense Mutation detected in F1 DNA Not yet available
sa30908 Nonsense Mutation detected in F1 DNA Not yet available
sa16571 Splice Site, Nonsense Available for shipment Available now
sa9894 Essential Splice Site Available for shipment Available now
sa34506 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21392 Essential Splice Site Available for shipment Available now
sa27283 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34507 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41303
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053768 Nonsense 306 1326 1 22
ENSDART00000127709 Nonsense 276 1300 2 24
ENSDART00000131312 Nonsense 245 518 1 6
ENSDART00000053768 Nonsense 306 1326 1 22
ENSDART00000127709 Nonsense 276 1300 2 24
ENSDART00000131312 Nonsense 245 518 1 6
Genomic Location (Zv9):
Chromosome 8 (position 53354363)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51096888
GRCz11 8 51085910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTCCTGTCCTACCTCTTTCCCAGTGAGCGAGCAGGGAAGATCTACTA[T/A]GATGGAATGGGGCCTGATCTTGCTGATATACATGGTGAGTTGCGAGGTGG
Long Flanking Sequence:
AGGAAAGGAAAGGACGTCTCTGGCATAGCGAATGTCACGGAACCTACAGGGATTTTGGGAAAAGCTGAGGCGGGAGCATACAATGACAACAGGCAGTTTGGAAATGAGAAAAACAAGGAGATGAAAGAGAGGGAAAAAGACTCGAGCATATCCGCAACCCTCAATTCCAGTGATGCCGAAGATCACAAGAAACCAGACTCGCCCTTAATGAGAACCCGTAGGTTTGCGGGCTACCCCTATCTCCAGACCCAAGCCCTTTGGAGGATCGAGCTAGTGTTTGTGGCCCAGGGTGACAAGGATAACAACATCTTCACCCCCGACCGTCTTCACACCATACACCATGTGGAGAGAGTACTAATGCAGCACCCTCAGTTTCAGCAGTTCTGCTGGAAGCCATTGGAGGCGTTGCAGGATTTGCCTCTGGGACCCTCCTTCTGCTCCCCTCCGAGCTCCGTCCTGTCCTACCTCTTTCCCAGTGAGCGAGCAGGGAAGATCTACTA[T/A]GATGGAATGGGGCCTGATCTTGCTGATATACATGGTGAGTTGCGAGGTGGGGGCTGTTTATCCCACTGTCTTTGTTGTCAATAAGCTGAGCTAAACTCTCTTTACCCTTGTGTGCTGTTGAGAATGTTTTCATCCACTCTGGGGTAGGGCTGGGCGATTTATATGATTTTTTCGATTAATTCGAATTTACGTTTTGACGACGATTTAATTTTATGTTATATGTTATGTTATGTTAAATTGTGACTTTTAAAAAAATATATATATATTTAATACATAATAATGGATTAAATATCGGCGATGTACCACGCAGCACCACGCAGCACCAAGGATTTTAGAATTCTAAACAGGTTCTATACACACACCGGCGCCGCCCAGCCACGATTCAGGACGCAATTCATATTTCAGCCGCGCCACAGATCGCCATCTGATTAGTTTCATGTTAAATATCATGCGAACGTGCGCGTTTGGTGTGTGATAGTTTAAACTGTCATGTGCGCGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30908
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053768 Nonsense 306 1326 1 22
ENSDART00000127709 Nonsense 276 1300 2 24
ENSDART00000131312 Nonsense 245 518 1 6
ENSDART00000053768 Nonsense 306 1326 1 22
ENSDART00000127709 Nonsense 276 1300 2 24
ENSDART00000131312 Nonsense 245 518 1 6
Genomic Location (Zv9):
Chromosome 8 (position 53354363)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51096888
GRCz11 8 51085910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTCCTGTCCTACCTCTTTCCCAGTGAGCGAGCAGGGAAGATCTACTA[T/A]GATGGAATGGGGCCTGATCTTGCTGATATACATGGTGAGTTGCGAGGTGG
Long Flanking Sequence:
AGGAAAGGAAAGGACGTCTCTGGCATAGCGAATGTCACGGAACCTACAGGGATTTTGGGAAAAGCTGAGGCGGGAGCATACAATGACAACAGGCAGTTTGGAAATGAGAAAAACAAGGAGATGAAAGAGAGGGAAAAAGACTCGAGCATATCCGCAACCCTCAATTCCAGTGATGCCGAAGATCACAAGAAACCAGACTCGCCCTTAATGAGAACCCGTAGGTTTGCGGGCTACCCCTATCTCCAGACCCAAGCCCTTTGGAGGATCGAGCTAGTGTTTGTGGCCCAGGGTGACAAGGATAACAACATCTTCACCCCCGACCGTCTTCACACCATACACCATGTGGAGAGAGTACTAATGCAGCACCCTCAGTTTCAGCAGTTCTGCTGGAAGCCATTGGAGGCGTTGCAGGATTTGCCTCTGGGACCCTCCTTCTGCTCCCCTCCGAGCTCCGTCCTGTCCTACCTCTTTCCCAGTGAGCGAGCAGGGAAGATCTACTA[T/A]GATGGAATGGGGCCTGATCTTGCTGATATACATGGTGAGTTGCGAGGTGGGGGCTGTTTATCCCACTGTCTTTGTTGTCAATAAGCTGAGCTAAACTCTCTTTACCCTTGTGTGCTGTTGAGAATGTTTTCATCCACTCTGGGGTAGGGCTGGGCGATTTATATGATTTTTTCGATTAATTCGAATTTACGTTTTGACGACGATTTAATTTTATGTTATATGTTATGTTATGTTAAATTGTGACTTTTAAAAAAATATATATATATTTAATACATAATAATGGATTAAATATCGGCGATGTACCACGCAGCACCACGCAGCACCAAGGATTTTAGAATTCTAAACAGGTTCTATACACACACCGGCGCCGCCCAGCCACGATTCAGGACGCAATTCATATTTCAGCCGCGCCACAGATCGCCATCTGATTAGTTTCATGTTAAATATCATGCGAACGTGCGCGTTTGGTGTGTGATAGTTTAAACTGTCATGTGCGCGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16571
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053768 None None 1326 None 22
ENSDART00000127709 Splice Site, Nonsense 592 1300 9 24
ENSDART00000131312 None None 518 None 6
Genomic Location (Zv9):
Chromosome 8 (position 53370074)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51112599
GRCz11 8 51101621
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGGTAGGGGAGAGTGGAGATGGYTGCAACAAGACTTAWTCCTCTATT[T/A]AGGCATGAGCTAGAGTSMTGATATTTTTACTACATATTCTCAGTTAGACC
Long Flanking Sequence:
TACTCGAAAACAGCAGGCACAAATGGCACTGGCGAAAAATTTGAGATTTGAAAAAGCGTACACAGCGGCCTCTGGTGGATTTGCGAAAACAAAAACTGCAAAAAATGTAGCTCCTGGGAAGTATTTGATGCTCTCCAGAATTGTATACAGGGGTACGTTTTCAGAATGAGCCTGGGCTGAGTTTTTAAAACTGATAAAATCCTACTAGGTTTGACATCACTCTGGTTTGTTTAATGCACTGTTATTCCTGCTTCTTTAGGCACCACTTGCTGGATTAGCATTTTGATCTGTATATGAATAATGTTTTAGTTTAGGATTCAGTAGATTAGATTAATTTCTTTCAATCACCATTAATTAGTAAATATGCTGTAAGTTAAAATGTCGCCAATGTTACTGGTTGAAACCATAAAGTGGCGATGAGGTCTTAAAATGTATGGAAAGAGTCTTTTAAAAAGGTAGGGGAGAGTGGAGATGGTTGCAACAAGACTTATTCCTCTATT[T/A]AGGCATGAGCTAGAGTGATGATATTTTTACTACATATTCTCAGTTAGACCCTCCTTCAGTACGGAAGACATGATGTGACCATTCCTTTTGTATAAAACTTATTTTGAGGTAAAAAAAAAAATGTATTTACTAATGGTCAGAACATTTCTCATACTGTCTAATTTGTTTTTGTAAGACATTACTTGATTAATTAATTAATTTTAAAGTTGGATGTTGCTTCTTTTAATAGTCTGTATTTATATGGCCAATTTAACTAATGTAACATTTTAACCATGTAACATTTAGTGTGTTAACCAAAAAAATATTCAATTTAATGTTTTAGAATTTTTTTATTATTATTTCATTTCAATGAATGTTGCAGCCGTCCCCATGCTCGGGGTCAGTTGCAATATTCGACTTTGTGTGTTGAAGTTTAAATTCTGCATATGTTATTATTTGTACACGTCATAGCAATATGGGTGGGTATCTAATAGATGTGGGTTTATTAGGTTCAAATTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9894
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053768 Essential Splice Site 631 1326 7 22
ENSDART00000127709 Essential Splice Site 606 1300 10 24
ENSDART00000131312 None None 518 None 6
Genomic Location (Zv9):
Chromosome 8 (position 53371516)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51114041
GRCz11 8 51103063
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCTCAGATGATGATGAYGTGGCTCTGATAACKGTCGAAATGGAACCAG[G/A]TACACTGTATAAAACATTGCACAACAAATTRTGCAGGAGTGTTTTTATAN
Long Flanking Sequence:
TAGACTAGAGAAGAGGCTAATAATTTTGTCCTTAAAATGATTTAAAAAAAATAAAACAGTTTTTATTCTAACCAAAATAAAGCAAATAAGCCTTTCTCCAGAAGAAAAAAATATTATCAGACATACTGTAAAAAAAATTCCCTGCTCTGTTAAACATCATTTGAGAAATATTTAAAAAAAAAAAAAAAGAAAAAGAAAATCAAAGGGAGGCGAATCATTTTAGACTTCAACTGATGGTGTTTAAATAATCAGTGACAAAAATGTAGTTGAAACCCAGCATTACACTTACAAAAATAACGACAAAATAGCTTGGAGACACTTTAGATTCAGATTCCTGAGACTGGAATAATGACAGAACTGGTAGTTTTGGGTGGATTATCCTATTAACGCTGATATTCTTGACCCTTGCAGGTGGACCACTTTAACGAAACTGTCCAGCAGCCCAGGTCCACTCTCAGATGATGATGACGTGGCTCTGATAACTGTCGAAATGGAACCAG[G/A]TACACTGTATAAAACATTGCACAACAAATTATGCAGGAGTGTTTTTATAAGGGTGACACGGTGGCTCAGTGGTTAGCGCTGTCACCTTACAGCAAGAAGGTCGCTGATTTGAGCCAGATGGCATTTCTGTGTGGAGTTCTCCCCATGTAGGTGTGGGTTCCCTTTGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCACTATAGTGAAATTGAATGAACAAAATTGGTCGCAGTGTACGTGTGTGTTTGAATGTGAGAGTGTATGGGTGTTTTCCAGTACTGGGTTGCGGCTGGAAGAGCATCCGCTGTTGGTGGTTCATTTCACTGTGGCGACCACTGATAAATAAGAGACTAAGCTGAAGGAAAATAGATTAATGTATTTACAAGAAAATACTGTTTCAGAACGCATGCCGGATGTCATGTTTAATTCACTATGTGCATTTCTTTGGTAATATTCGTGAAATTAACTAGCAATTTTGCAGAAAAGCAATGTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34506
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
ENSDART00000053768 Essential Splice Site 830 1326 11 22
ENSDART00000127709 Essential Splice Site 805 1300 14 24
ENSDART00000131312 None None 518 None 6
Genomic Location (Zv9):
Chromosome 8 (position 53390410)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51132834
GRCz11 8 51121856
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCCTGGCAGGCTTCATCGGCTGCACACGGAGACGTGCCATCCTTTCAG[G/A]TCTGTGCTAACACACTCATTTACACACATTCATTAACACACGTGACACAT
Long Flanking Sequence:
TATTTTTGTAAATATTTATGTAAATATTTTAGTTAAACAGAAATTGTGAACACAATATGCAGGGGGGCTAATAATCCAGGATATATAAGTATTTTACTTGATATTATTATTTATTTTTATTTTATTTTAATATTATTTATATTCTGTTAAAGAGCCTAAATGTATATGACGGGTTGTGTTTTTTGTCTAAAAATAAATAAATAAATAAAAGCTATTTGTAGCCTACTGCCTGTTTCACATCTAAGATGTTCAATAAAAAGTAGGTCAAACCAAATCTTCCAGACTCCAAACTTTGCAGCAGTAGTATATCTGCGGTGCTGAATTGACCCTGATGAGTTCAGCGCTGTGATTGTGATTCTGCAGGTGGGCTGCTGACTGTCTATGTGTTCAAACTGGAGATGGGCTCCGCCGTTCCTCTTTATCGGTATTCACTAAGTGCCAGTGTACCTGCACCCTGGCAGGCTTCATCGGCTGCACACGGAGACGTGCCATCCTTTCAG[G/A]TCTGTGCTAACACACTCATTTACACACATTCATTAACACACGTGACACATCCTGAATTTAATTATATTCCTGAATATGATTTTATTTGATATGTGGAAAAAGGGATGCAGGATGGTAGCTTAGATTCAAAGGACAGTATGCTATTTATCACCACTAGAGGGTGTATATTCACAATGAACAAAAGAGTAGGTTGAAAGACTGAAAATGAGTGCGCTGAAGCAATTGTTGATGGCAGACATGCGCAGCACAAAACAAAAGTAGTGAATATATATATTTTACTTTATATATATAACATATATATAAATATATAACATGGTTCCACTGGTTTTTGGATATGTTAATGAAAAAATCGTACATATTGTGCATTTAATAAAGTAGAATTAAATTCATTATGAACGACAAACGTCATAGCAGTGTTACTTACAGTAGATCAGTGGTTTTCGCGGATGAATCACTGAGTAATGAAAGAAAAAATGAATAAGATTTTACTCACTTGATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21392
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
ENSDART00000053768 Essential Splice Site 887 1326 12 22
ENSDART00000127709 Essential Splice Site 862 1300 15 24
ENSDART00000131312 None None 518 None 6
Genomic Location (Zv9):
Chromosome 8 (position 53395421)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51137815
GRCz11 8 51126837
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCAGAGTTCGAGTTTTACGTGGCTTCGGTGGAGCAGCAGCGCAGCAG[G/A]CGAGTTTGTGTGTGTGTGTGTGTGTGCTGAAGACTGATGAGCCGTGACTG
Long Flanking Sequence:
AAGAAACAATAGTTTAAACCAAACAAACAGCTGCGATGAGCCGTTTCCTGCCTACATAATTACGCTTGGCAAATGTGTTTTTCACATTGCTTAATATTATCACTACACAGACAAAAACCATTACCGCCTGTGTGCTAATGCATCCTAGAAAAAAAAAGAAGCTTTCAATGTACACAATCTATCGCAAAGCTGTGGAATTCCATCATCCTGAGTGTAATGTGTCTGTGTGTGGCGTCTACTCATATCACCTCAGCACGCTTCAGTTGCCCTTATAGCCCCATTCTATCTGAGCTGACAAAAAAGCTGATCGATGTGTTGTCACGGTAACAGGCCTACAGCAGTCCCCATAGCAACTTCAGCACGCGGATAAGCGTGTGTGTGTCTCACGCCTATCACCCGCGGCCCCGCTGGATGCTGACGCTGCGCTCGTGTGACGGCAGCCGACGCTGGATTGCAGAGTTCGAGTTTTACGTGGCTTCGGTGGAGCAGCAGCGCAGCAG[G/A]CGAGTTTGTGTGTGTGTGTGTGTGTGCTGAAGACTGATGAGCCGTGACTGATTGAAATCATTTTTATTGCCTCTTCACTGTGCAACATTTAACCCAGTGTGTGTCTGAGTTTGACATCAGGATGTCTGAAAGTGAGCTGGAAATTGATGTGCTGTTTGTGTCAGGAAGCTGTATTTTATGGAGACGGATCAGTCTCACAAATACTACAAGTCAACTTGGGACAGTATGGAAAACGCAAATACAAAGAGAAAGTAGTGATTTAGAAATGTCCTTTGACTTGTATTTCATTGCAGACAGCATGAGCACAACATATTTCATGTTTTGTCTGGTCAACCTCATTTCATTTGTAAATAAATCCCTGTCATTCAGACCTGCAACACACTCCAAAACAAGCTGGGACAGGAGCAGCTTAGGGCAGTAATCAGGTAAACTGGTTAAATAACGATATGATTTGAAACAGGTGATGTCAACAGGTGATTATAATTATGATTTGGTACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27283
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053768 None None 1326 None 22
ENSDART00000127709 Essential Splice Site 906 1300 17 24
ENSDART00000131312 None None 518 None 6
Genomic Location (Zv9):
Chromosome 8 (position 53401820)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51144115
GRCz11 8 51133137
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTTTTTTTTCCCTTCTCTGGTAAGGTTATTCTCTTGTATATGTGCTC[A/G]GCTCCTGCCCAGGTGAAGATCTCCAGGACATCAGGCTTTAACCCCTGCAG
Long Flanking Sequence:
GGTTGGCTGGTTTTAGTTGGTCGACCAGCCTGGCTTTAGAGGGGTTTTGGTTACTTTAAGACTGGTTTTCAGCCATTTCCAGCCTGGTTTTAGCTGGACAAGCTGGGACTTTCCAGCCTGACCAGCTTAGACCAGGCTGGAAATGACAAGTTGGGACTTTCCAGCCTGACCAGCTAAGACCAGGCTGGAAATGACTGGAAACCAGTCTTAAAGTAACCAAAACCCCTCTAAAACCAGGCTGGTCGACCAACTAAAACCAGCCAACCATCCTAGGCTGGTTTGAGCTGGAATTTTCAGCAGGGTGGAGCAAGGGGTGTGCTTATTTTTCACAAGGGCCAACCCATGAGGGACTTTAAAGTAACTGATGTTGGATTTTTAGAGATCTCTTTATACATTGTGTGAGAAAAACGTATCTGACAACAAATGTTTTCCACATTGTCAACTATTGTCAGCTTTTTTTTTCCCTTCTCTGGTAAGGTTATTCTCTTGTATATGTGCTC[A/G]GCTCCTGCCCAGGTGAAGATCTCCAGGACATCAGGCTTTAACCCCTGCAGTGGAGGTAAATGTGGGAAGCCAGCCGTGCGCCCTCTAGTGGATACCGGAGCCATGGTGTTTGTGGTGTTCGGCATACTGGGGGTGAACCGCACTCAACGCTTAGACAACCATGTTATTGGAGACCTGGTAAGAAGCAATTGAAAATGAGCTCAGAAAGTCACTTGGTAAATATGTTTGGGAATATTCATAATCAATATAATCAAACTTTGCTGAAAAAAATAGGCATGCAATTTACTACATTCCCTCTATTGTCTGATTTATATTTTATACTGTAATTTTAGGGAGCTTTCACACCTGTGAATCGATTCAGTTGTTCCGAAACAGAGATTACAATTGTTACATTGTTGCTCTTTGTTCTTGGAGCGGTTCGCTTTCACATTGCAAAGTTTCTAATCGGACCAAAAGAGCTAAAACAAGTCAGGTGCGAGTAAACTCTGCTCACATTGGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34507
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053768 Essential Splice Site 990 1326 16 22
ENSDART00000127709 Essential Splice Site 965 1300 18 24
ENSDART00000131312 None None 518 None 6
Genomic Location (Zv9):
Chromosome 8 (position 53403504)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 51145790
GRCz11 8 51134812
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTATGAATTATTAATGCACTGATTTGTTGACGTTCCTCCTCCTCAAA[G/T]GGCAATGTGATCTATGACCAAGACTTTGATGTTTTTAATGAGATCGGCCA
Long Flanking Sequence:
GTAGTTCATTATTAGTTCATGTTAACTCATGGTGCATTAACTAATGTTAACAAGCATGGACTTGGATGTTAATAATGCATTAGTAAATGTTCAATTATGATTAATAAAAGCTGTACATGATTAGTTCATGTTAGTAAATGCATTAACTAATGAACCTTATTGTAAAGTGTTACCGAATTACTTTTGTTTTGTCAGCAATATTTCAATATAAACATATACTTTAATTTTCTGAAAAGTAAAATTCCATAATGTGAATATCAAATATAATCAATCATTTTTATTAGTACAGATCTTTGATCATAAAATGAGATATCATTATACTAAGATGCTTTACTGGGAACAAATAAAGGTGCTGTATGTACGTTTTTGACTCTTCTAAAGCAAGAAAAGGCCTCATTTCAATGCGCTCCCAATCTGTGCACTGTACATTGATTGTTTTCTTTTGAAGCTGATTTATGAATTATTAATGCACTGATTTGTTGACGTTCCTCCTCCTCAAA[G/T]GGCAATGTGATCTATGACCAAGACTTTGATGTTTTTAATGAGATCGGCCACTTGTGCAAGCTGTGCAAAGTCATCAGTGCCAACACCAACCTGGTGAAGCCTGGAGGAGCTCAGTGTTTGCCATCAGGTGAGCAAGAATCATTCGTTCATTCCTTTTCCTTTGTCTTAGTCCATTATTTACACAGCGGAATGAACCGCCAACTATTCCAGCATATGTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCAGTATCGGGAATCACCCATACACACTTACATTCGCACACAGACTCAAACACTATGGTTAATTTCGTTTACCCAATTCACCTATAGCGCTTGTGTTTGGACTGTGAGGGAAACCGGAGCACCCATTGAGCCACTGAGAATTTAGGAATTTGTAATGTTGCCATTTCTTTTCACAACACTTAAAAGGTGTTTAGGGACTGAAGACACAAGTGACGAAGTATTTCAGGTGTAATTTTGTCTCATTCTTCCTGC
Associated Phenotype:
Not determined