ZMP
PLEKHA6
Ensembl ID:
Description:
pleckstrin homology domain containing, family A member 6 [Source:HGNC Symbol;Acc:17053]
Human Orthologue:
PLEKHA6
Human Description:
pleckstrin homology domain containing, family A member 6 [Source:HGNC Symbol;Acc:17053]
Mouse Orthologue:
Plekha6
Mouse Description:
pleckstrin homology domain containing, family A member 6 Gene [Source:MGI Symbol;Acc:MGI:2388662]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27777 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41827 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21900 | Essential Splice Site | Available for shipment | Available now |
sa41826 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41825 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16827 | Nonsense | Available for shipment | Available now |
sa35076 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35075 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27777
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032844 | Essential Splice Site | 40 | 1149 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24360697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23173294 |
GRCz11 | 11 | 23426318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGATCCAGACACACCTGGAAGAAAACGGACCTTTGAAAGCCTTGCTG[T/C]GAGTGGACTTTTGTTTATTTGTTAGTAAATATATGGCTAGCTTTATGCTG
Long Flanking Sequence:
CCCTGAACTCCAGGCTTCAGGCTTTTCATATGTCTTTTATCGAATGTAATAGCATGAATTCTGACGTTGCTCCACCGGAACTGATCTTGTTGATATTTTGACAATGAACGTGAGTATGTTCACACTTTACACAAGCGTCTTTCACAAGTGTTGACAGCCATTAATTTCCACAGCAGTCGTTTCATATGGACCTACAAAGAAAGTGGCTGTGTATTGATTGATCTCGATGTTGTAATGCTGAATTATTAATAAAGAAAGGATGTGGCTGTTGTGAAACAGGTTTGAAGCTGCAAGAATGAGTTGTAGAGCATCTTAAAAAATGAAAAGTCACATCTAGCTGCTTTAGGCTTGATTTTTTGTGTGAAAAATTTGCAGTTTTTACTTATAAATCCTCTTTTTTGTTTTGTCTTTTCAGTCAAAATGACCCTAATGGAACTGTTGGACACCAGCAAGTGATCCAGACACACCTGGAAGAAAACGGACCTTTGAAAGCCTTGCTG[T/C]GAGTGGACTTTTGTTTATTTGTTAGTAAATATATGGCTAGCTTTATGCTGCCAAGATCCGTGACCTGTGGAAGAACAGTTTTAATAAGAGACTGAGTTTTATCAACTGCGCCAAGTGTCTTCTTTTAAAGAGACTGCATTTATGGATCCAGTCCAAAAAGATTTATGATGGTTATTGTAGAAACTTAATCATATTCATTTGTTTTTGTTTTATGAATTAATATATTAAATGAGAGAAAAGCATACTTCTATTCAGCAAAGATGTGTAAACGATAAAAAAGATGAAAACGTTTGCTGAAATATATGAGGTTCATTTAAACTTTCTTTGTTAAAAAGGAAATTAATAAAAATCATGGATGCAACAAATATTTTAACTGTGTTCAATACTAACGATGATAATAGTTACAAAAAGTTACTTGACCACTAAATCAGGCATTAAAATAATTTAATGATGGACCATGTGACGCTGAAGACTAGAGTTATCTGGTGCTTGATTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41827
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 |
---|---|---|---|---|---|
ENSDART00000032844 | Essential Splice Site | 535 | 1149 | 10 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24309607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23122204 |
GRCz11 | 11 | 23375228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAAAGTATGTATTTATATATACAAATAAGTGTGTAATTGTTCTTTC[A/T]GTATGATTTCCCTGGAGATCGTCGCTCATACAGCCAAGGAATGTACCAGT
Long Flanking Sequence:
TTTAATTAGTTTATAAACTTATGTGTATTAAATAAATTGGCACAGCATAAAAGTATTGAACACATGAAGAAAGGGGAGGTAAAAAGGCAGTGAAAACCTAAACAGCAGCTGAAGTCTTTCAGAAGTTCTTTAGCAACCCTCTGCCCTTCCTCATTGTAAATTTATATTAGCTGCTTCCGTCCCACAACTAAGTCATTGAGATGATGAAGATGAAACCAGAATGGACATTTCAGCAAGAAAATGATCCAAAGAAACTCTCAAGTGCTTTCAGAGAAAAAAAATCAAGCTCTAGAATGGCCCAGCCAATCACCTGACTCGAATCCAATAGAAAATACAAAATTAATATCAGTTTTGATAGACCAAACACACAGAACTATCAAGATTTTTATGCTCTGTGTTGAAGTGTGTGAAAAAATCACACCTGAGCAGTTCATGTGTATGTATTTATACAAAAAAAAGTATGTATTTATATATACAAATAAGTGTGTAATTGTTCTTTC[A/T]GTATGATTTCCCTGGAGATCGTCGCTCATACAGCCAAGGAATGTACCAGTATAACTACCCAGCGTCCCCATCGCTCCACAGTAAAATGGTAAGAAATCCACACTTTTAACTATCCATGAATGTCATTAGCATGCTAAAAGTCAATTACAGTCTTGTCAGCTAAGAACTACCAAATCACATAATCATCGGACTGATAATCTGTATGTGCATCACAGTAGCTTGGCTTGTGAATGATGGAGTGTGTGTAATTGTCTCTTCTAATGAGTTTTATTGTGAAATCACTTCGCTTTGCTGTGATTAGCGATGGTGTGATTAGCATGTGTTTGTCTCCGTCTCCCCATGCGATGCTTGTGCTGTTTGCTGACACGCTGGGCTTTGCTGCTGCTTCATTACACACATCAGGAGGACATTTTAGATGCGCAGCTTCAGAGGAACCTGGAGTACCTTGATCAGCAGGTAGGAGGTTTGATGCAACAAATATTACAGAGACTCGATACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21900
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 |
---|---|---|---|---|---|
ENSDART00000032844 | Essential Splice Site | 581 | 1149 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24309150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23121747 |
GRCz11 | 11 | 23374771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTTTAGATGCGCAGCTTCAGAGGAACCTGGAGTACCTTGATCAGCAG[G/A]TAGGAGGTTTGATGCAACAAATATTACAGAGACTCGATACTGATACAACA
Long Flanking Sequence:
AGTATGTATTTATATATACAAATAAGTGTGTAATTGTTCTTTCAGTATGATTTCCCTGGAGATCGTCGCTCATACAGCCAAGGAATGTACCAGTATAACTACCCAGCGTCCCCATCGCTCCACAGTAAAATGGTAAGAAATCCACACTTTTAACTATCCATGAATGTCATTAGCATGCTAAAAGTCAATTACAGTCTTGTCAGCTAAGAACTACCAAATCACATAATCATCGGACTGATAATCTGTATGTGCATCACAGTAGCTTGGCTTGTGAATGATGGAGTGTGTGTAATTGTCTCTTCTAATGAGTTTTATTGTGAAATCACTTCGCTTTGCTGTGATTAGCGATGGTGTGATTAGCATGTGTTTGTCTCCGTCTCCCCATGCGATGCTTGTGCTGTTTGCTGACACGCTGGGCTTTGCTGCTGCTTCATTACACACATCAGGAGGACATTTTAGATGCGCAGCTTCAGAGGAACCTGGAGTACCTTGATCAGCAG[G/A]TAGGAGGTTTGATGCAACAAATATTACAGAGACTCGATACTGATACAACATGCTAATTATGATATGCTTTGTTCCAAAACTAAGTGAGCGACCCGTGATTTCCCATGATTAAAATAAACTGCAGATATGTTTTTTTTTAGTGCTGGGCAAAGTTTAATAGCAATTAATTGCATCCAAAGTAAAAGTTTGTTTTGCCGTAATATATATGTGTGTATTATATAAGGCACATTCTACCTATACATTTTCACTTATAAAACGTGACAGGGCCTCACTTAAGCTTGTCTTTCTCCAAAAATCATACAAAAACAAGCATAAAATCATACAATTCAATGATAGAACTCATCCTTGATCCATGTCAGGTTCTTCTCCGTCAAATGATGTCACTACCGAGTTATAGTCGCAAAGGTGTTTTGCACGAACTTTATGTTAAATTTAATGCAAAGGTGACAGGATTGACAGAAACATGGGGACAGTTGTAAATGTATTTTGATGTAAATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41826
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 |
---|---|---|---|---|---|
ENSDART00000032844 | Nonsense | 627 | 1149 | 13 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24299404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23112001 |
GRCz11 | 11 | 23365025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGAACAGAATCGACTTTTGAAAGAGCAAGAGACTGTAGTTCATCGTT[T/A]ACGAATGGAAAAGGTATGTTTATTGCTTGCAGGAGCTTCAAAAAACATTA
Long Flanking Sequence:
TTGTGTTATTATTATTATTATTTTCTGATGGCGCTTGTTTTTGTGTAGTTGTTCATGTATTCATTTAATATGTTGATATGTATTTAATTATATAAAATATTTTGAAATGTTTATTGCGTTTATACATAATAGATATATATTTAAATTATCTTTTGCCTGAAATCATATATTTTTTTAAGTGTTATATTATTCATATTAATTACATCCTGAACTGTAAACCAGAAGACTTGTTTTCACTAATCATTCTGTTTTGTTTTATTCTCTTTTACAGGTGCCTCCATTCCATGATGTGTATGGTGACTTACATCCCACTCTGAAGCTTAATGAGATTGAGACCAGTGTAAGTCTTTTTGTACAATCATGTATAGCACATCAGCATATCTATTTGCACACAACATAGACCTATAAACTCTTTAATTTTGTCCCTGTTCAGAAACTACTTGGCCGATTGTGTGAACAGAATCGACTTTTGAAAGAGCAAGAGACTGTAGTTCATCGTT[T/A]ACGAATGGAAAAGGTATGTTTATTGCTTGCAGGAGCTTCAAAAAACATTATATATTGTAATTAGTGTTATATATTTTTATAAATTGTCACAGTCTGGTGTGTAGTGTAGAGGGAAAAACAAAGTGTGGATCCAAACAAAGCATTGAAAACATTTAATGAAAAACTATAACTAAACAAAACAGAACTAAAACAAGGCAAGAAAAATCAGGAAACGCACGGGCATCATGGGGGTAACAAAGAAAAAAAAACAACAACAGACGATAAGAGGGGAGCACAAACTAAAATATATAGTTCTCGTAATCAGTCCTTGGCAATCCTCCGGCTGTTTGTGTGTGTAATCAATGGCGATCTGAAACAGCTGTGTTGGCGAAGTGCATGACAGGACTTGTAGTTCGATAGTGTGTGTGTAGTTCATTTGATGTGTGTGTAATTTACCAGTGATCTAGAGTCCTTACATTTCTGGTGATTGTTACACATATTATTATATTATATTATATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41825
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032844 | Nonsense | 832 | 1149 | 18 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24290185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23102782 |
GRCz11 | 11 | 23355806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCCTTTCCCCCCTCTGTCCCTCCCCTGCCTTTAGACAGCAATGCCTG[G/A]CAGCGCAGCATGGGCCGCAATTCAGGCATCCACCAGGAAGGCTACAAGGA
Long Flanking Sequence:
CTCCCACAGTGATACGCTACCAAAATAAACACAGAATTTTATACCTTTTTGGGTTTCTAGCGCATAGAGAGTATTCAGATAAATCAGTCCCTGACTGAACTGCACATTTCAGATTTTAAATTGTAGGTAAAACAGATCTAAGCTCACAGTTGCTTTTGCTAGCAATGATTCTTATAAAGGTATGAAGTGTGTGGGAAGTGTGCAGGTCAGTGTTTATTAGTGGTTGTGATGAGGGATTCATATTTGCTTCCCATGATTCAGTCCGCCCTCCACCTGGCTTAGTTGCTCCTGATGCACAGCTTTCTTTCCAACTTTCTCCTCCCTATCTGTATCTTTTTACTCTCTCTCTCTTCCCTTTTCCTTTTTATTTTTTCCCTTGCCTTCCTAACGTAGGAGGCTATTCCTCCACGACCTCCACTCCCAAAATCGTACCAGCCCTTGGAATCCTCCCAGTCCTTTCCCCCCTCTGTCCCTCCCCTGCCTTTAGACAGCAATGCCTG[G/A]CAGCGCAGCATGGGCCGCAATTCAGGCATCCACCAGGAAGGCTACAAGGATGACGGAGATTTCCACAGCAGAAAGGTACCTCTGAGAGGCAGCCACAAACTAAGAGAACAAGGAATCGCACTTCTAATGTGTCCATTTTCATTCCACAATCATTTTTTCCACAATCATCGACAACTAGGGATGCACCGATATGAAAATTTGGGCCAATACCAACAACACCTTATATTTAAAAGCTAATAACTGCTAAATGGATGCAATCAGGAATTGCATTTATTCCATCTATTCAGCAGTTATTAGATTTTTTTGCCTGATTACAAAAACAAAATGCAAATATGTATATATATATATATATATATATATATATATATATATATATAATTAGGGGTGTGTTATAATTCGGTTCAGTTACATTTATTATGCCATCGATTCGTTTCAATATCTCAGTGCATCACGTTGCATTGACAACGCTTTTCATAAACAATTGAATAATTTACTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16827
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 |
---|---|---|---|---|---|
ENSDART00000032844 | Nonsense | 860 | 1149 | 19 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24288118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23100715 |
GRCz11 | 11 | 23353739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWTTTTTTTNGCAGGGGGTTACATTTYATATGTTCTTTTCCAGCACAACTA[T/A]AACTCGCAGGGAGAAAAGACMAGTGACTTTGARACAGAGCAAGACAGGTT
Long Flanking Sequence:
CACTATTAAAGTCCACACTACCCATTTTATGTGTGTCTGTGTTAGATAATTTTAAAAGGTGGTAGTGTAAAAGTGTGCTTCGATTGCTTTTTCTTATTGCCATATTCTCCCCTGTAGCCTCATGCATTCCAGGCTTCTATTCACCATGCCATAGATTAACCTACAGAAGCCCTCACTGTCCCTCACATTTATTTTTTTTGGTTGTATGTTAAGAATAACTGTTATCATAAAAAAATAACTAGAGTCTGTGTCATCTGAGGATGGCTTTGTGAACATATAGGTATGGGATTGCTAAAGGCTTTTTTAAAATTATAATATGATTAAAAAATCTACTAATAATCAAATACATTTCCACTAGATCCTAAATTTGATCCTGTCAGAAGGATCTTTTGGCTTGGCTGGTTTCAATTATAGCAGAAATTCCAATAGCAATCCTGTACATTGAATTAGAATTTTTTTGCAGGGGGTTACATTTCATATGTTCTTTTCCAGCACAACTA[T/A]AACTCGCAGGGAGAAAAGACAAGTGACTTTGAGACAGAGCAAGACAGGTTATCCAACCAAAATAAAGGTAAGAAACATTTTTGATCTTATATTTAGACAACAAGAGGTTGAAAAACAGTCATATTTAAATTGTTTTACTGCAGGGAAAATAAGTATTAAACAAGTCACCATTTTTCTAAGAAAACATATGTGCTGTTGACTTGAAATTTTCACCAGATGTTGACAGCAACTAAAGAAATCCATATATGTAAAGAAAACAGATCTAATTGGTTAAAATTAAATCATGTGTAATAAAACACAGGAAAAACTATTGAACACATGAAGAAAGGGAGTTATAGAAAGGCAGTGAAAGCCCAGACAGCAGCTGAAATCTCCCAGTATTCAGCAACCCTCTGCCCTTCATCATTGTAAATTGATATTAGCTGCTTTAAACCAACTACTAAATCACCAGGATGATGAAGATGAAACCAGGGTGGACATTTCAGCAAGACAACGATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35076
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 |
---|---|---|---|---|---|
ENSDART00000032844 | Nonsense | 938 | 1149 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24286685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23099282 |
GRCz11 | 11 | 23352306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTGCTGTGTTCCCTGCAGAGGTGAAGTCAAAAATGAGTGTGGAGGAA[C/T]AGAATGAGAGGATACGAAGAAACCAGAGCAGCTCCGTCAGAGACAAGAGA
Long Flanking Sequence:
AACATGATGTGTTCGATACTTATTTTCCCTGCGGTTTTTGTAAAACTACAGTTATAGTTTAGACAACATACAAACACAACTGCAAATAAAGTCTAGAAGCAACCTCTATAGCTTTATAGTCTATAACTTTTTCTTGCAGTTGGAATCGTTCCACCGAGGACCAAGTCACCTTCAGAAGAAAAGAACAATTCTGATGCCGTCCAGCGCAGAAACGGGAAGGTGCCCAATGGCCACATTTCAAGAGTGGGTTTAATCCGTAGTAAAAATGTTTAAACAGCAACTATTTCTTGAGAGAATATAAATGACTATAGATTATATCAATTCCCATTGTTTTTAACTACGTAAATAAGATACAGATCCATATTATATGTTTAGATTTAGTAGGACTATGGGTTGACTTTTGTAAATGCATTTCATAATGTGTCGAATGTGTGTTCCAGGAGAGGCCAAAGAGTGCTGTGTTCCCTGCAGAGGTGAAGTCAAAAATGAGTGTGGAGGAA[C/T]AGAATGAGAGGATACGAAGAAACCAGAGCAGCTCCGTCAGAGACAAGAGAAGAAGCCTTAACCTTTCCAGCAACCAGCACATTGACGGCTTCAAGTCTTCGACAAGCTACAGAGTGGTTAGCCTCATATTTCTGCACATATTTGTTTGATTCTGTACTGAAACAGTGATGAATTACTCCAAGGTTAGCTGGTAGCTTATGCGTCACCACAGCTCATGTGGTTTAAGTTAAATTCTTACACCTACTTTTTATAAGGGTCAGTTTTTTTATTGTATTTCAATTATCATTTAAGCGCTTAGTACTGTATATAACAGAAGGAAAAAAAAATATAAATATTATTATATATATAATATATTATAATATATATTTATCTCTATTATATTATAAATAAAAAGAGATAAATTATTGTTATTATAAATATGTATAAATTATATCAAACAAACATACCTAAAAGTGTTTTTATATAAATTATATTTAAATTGAGATATATGTATACAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35075
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032844 | Nonsense | 1026 | 1149 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 24285064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23097661 |
GRCz11 | 11 | 23350685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAGACGACAGGTGGAGCCTGAACACTATGATCTGGATCTCAGCAAA[G/T]AGGTAAGAGATCACATGGCAGTGCTGTACATTCCATTATGAACAACTTTT
Long Flanking Sequence:
ACACTTGTAGTAGTGTGATATGGCTGTATATCGGCACTGGTGGGGGCACCAAGGTATTTGGCCTGCGGCCTCATGCCAACGCACGCCTCCCACCGATATACAGCCATATCGCACTGCTACTCGTGTGATATTGCTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTAACAATAATCATTGCATTTATTGTGTTAGTATACTGTAAGTACCTTCTCATCATTATAAAAATATATTTACTAATGGCAAACTATGCATATTTTTTGCAGTTTATGCATTGAGCCTGCTGTTCTGCTTGTTGTCCAGGTACGGAGGAGAGTTACAGCTGATGAGGTGGATATAAAGGGTCTTGAGGCAGCTGTGAGGGGAGAAGGTATGGAGTCGCCCAGGGAAGAAATTGCTCGTCTGAGACGACAGGTGGAGCCTGAACACTATGATCTGGATCTCAGCAAA[G/T]AGGTAAGAGATCACATGGCAGTGCTGTACATTCCATTATGAACAACTTTTTTTTTCTTTCATGCCATCTAGTAGTTTAAAGGCCCAGTGTGTAATTTTCACCACTAGAAGGCACATTTTCACAACAAACAAAGTCGTAGTTTGATTATGTTATGACTAAGCGTGAAATCCTGAGAGGAATCCCGTCACGTTGTTTAAATTGCAAATCCAGTTGCACCACTTTGTGGACTCATTGGTGTTCCAGTCTAAAAAGGAAGTGTGTTAAGGTGCATTGTTGGGACGTTGCTATTTTGAAGAACTGAAATAGACTGCACCGTTGACCAAATAAATTCTCTTGGTCTAAAGTCCAGCACAAAGCGCGTTAGTTATGCAGGTCCAAAACATGTACACATTGGTTAATACACACAGAATGTACAACAATACAAAAATATCTTTACATATGAAAACAATTAAAAGACTAAAATGTTTTTAAAAAATTATTATTTTCTACATAAATATAAA
Associated Phenotype:
Not determined