ZMP
btbd11b
Ensembl ID:
ZFIN ID:
Description:
Ankyrin repeat and BTB/POZ domain-containing protein BTBD11-B [Source:UniProtKB/Swiss-Prot;Acc:P0C7A
Human Orthologue:
BTBD11
Human Description:
BTB (POZ) domain containing 11 [Source:HGNC Symbol;Acc:23844]
Mouse Orthologue:
Btbd11
Mouse Description:
BTB (POZ) domain containing 11 Gene [Source:MGI Symbol;Acc:MGI:1921257]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8602 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32195 | Nonsense | Available for shipment | Available now |
sa23258 | Nonsense | Available for shipment | Available now |
sa39195 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2959 | Essential Splice Site | F2 line generated | Not yet available |
sa23257 | Nonsense | Available for shipment | Available now |
sa16940 | Nonsense | Available for shipment | Available now |
sa12869 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8602
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091742 | Essential Splice Site | 405 | 1012 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14570426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15015844 |
GRCz11 | 18 | 14984356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACTTACAATGTTTTTATAGCACWGTAATCACCTGTTGTCTCCCCCTGC[A/G]GGCCGTTTCTRGTGCTGCCTCCTCTGATGGAGTGGATCAGAGTGGCTTTG
Long Flanking Sequence:
GTATCTTAAAATTAACATTTTTTTAAACAGTTCATTAAATTATGTAAATGAAGCTTAATATTGAAATTTAAATAAACACATTAAAAGTACTTATGAATGAATAAACAAATACAATTATTAAAACTTAAACAAAAGTGAAAGCTGACAATACAATAAGTATATGTTTGTTATAAATATGTTAATAAAAATGTAAATATGTGTATATCGAAGATTTTTCAGATAATTAAGCTGATATTAAATTTGATCTAATATTAAAGCTGAGCTTAAATAGCTTTTCTGTCTTTGAGATTTATGTGCAAACGTAATAAATTAATCACTAACTAGAATAACAAACTGATGTAAAATTACATTAAAATTATTTTTAAAATATTTAGTGCAAAAAAATGTCTAAAATCCAACCCAATTGAACATTTGAATCAAAAATAAAATAACGTGTGCAAATACAAAGTGCTACTTACAATGTTTTTATAGCACAGTAATCACCTGTTGTCTCCCCCTGC[A/G]GGCCGTTTCTGGTGCTGCCTCCTCTGATGGAGTGGATCAGAGTGGCTTTGGCACACGCGGAGCACCGCCGCAGCTTTTCAGTGGATAGCGATGATGTTCGGCAGGCGGCCAGACTCCTGCTGCCCGGGGTGGACTGTGAACCCCGCCAGCTCAAGTAAGAGCAATGCCATTAAATTACCATCCAGCCACCAGACACTGCTGCCCATCGTGAGTGAAATGAAAATGGCTCATAACAGTCTGAACAGCAAAAACAAGTGTAGTCCAGCGTTTGTTGGACCAGAACTGAGTTTTTATTGTTGTTTGCCTGAGCGTAGTGATGCAAGAATCATGTTTTATGATGGCAGATACCTAACATTGATTTTTCATCATAGAACATTTCCATAATGAAAAATAGATCAACATTGACATCAGCAACTGTTTAACCTCAATTAAATCAAGTTCACTTAGATTTTACTTCACTTATAGGAAACAGATTTGACTTTGTGTCAGTTGTCTACTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32195
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 |
---|---|---|---|---|---|
ENSDART00000091742 | Nonsense | 697 | 1012 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14555943)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15001361 |
GRCz11 | 18 | 14969873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACCTGGAGGAGAGGAATTCCCTAAAGATGGAGGCGACCCGCACGGGG[A/T]AAGCCAAACTCAAAGCGCTGAGGGAGGCCATGTATCACAGCTCCGAACAT
Long Flanking Sequence:
TTTGCAGTTGGCTTCGGCCGCAGGTAAGAAAGCTCACGCTGCAGACTGGACAACAGTGCCACTTCCGTCTCCAATTACTCAGTTATATGCCAGCAAGAGGCCACAAGAGAGGACTCAGCAGTTTGTGTGCTGTAGGGAACTTTGAGCTGGTCAGTCTGCTTTTGGAGAGAGGAGCAGACCCCATGATCGGGACCATGTACCGCAACGGCATCTCTACCGCACCACACGGAGACATGAACTCTTACAGCCTGGCCGCTGCGCATGGACACAGGTAACACACACACACAAGATGCATTAGTCAAATACACACTCGCAGCAGCTCGTGATTTATTAATAAAACCTGCAAAATCTCATCCTCGTGCTGCAGGAACGTGTTCTGCAAGCTTCTGTCGCAGTCGGAAAAGGGGAAGGCGGACGTTTTGTCTCTGCAGGAGATTCTGGCGGAGGGATCTGACCTGGAGGAGAGGAATTCCCTAAAGATGGAGGCGACCCGCACGGGG[A/T]AAGCCAAACTCAAAGCGCTGAGGGAGGCCATGTATCACAGCTCCGAACATGGATACGTCGACATCACCCTGGACATCAGAAGTCTAGGTCAGTTCCTGCTGTAGGATCCACAGTTATGTAATGTTGGTTTAAATTATTGCTTGGTATAATAAGTGGCTTGTTGAAATTTGCATGAACATACATTGAAGGAAAGACTCGAGACGAATTTGCTTTTCAGGCATCAACTGAATTCAAGTTTATGTACAGTAGAATGTTTACGGTTAATTAAAAATAATTACTATCATACGTTTTGTGCTATTATTTAAAGAAAAAAGTTCTCAGGCATGTTTTGTAATTACATAATAAAAAACTTTATTTAACGATCACACTGTAGGCTCCAAATACTCAGTAATTATTCATCTTAAATCTTTACACTTTGTCACACTCCTTCAAACCACTGGGGTCTACTCATTACTCAGCAAAAGACTTTTAATCATTTATGATATGATAAAATCTAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23258
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091742 | Nonsense | 715 | 1012 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14555887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15001305 |
GRCz11 | 18 | 14969817 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTCAAAGCGCTGAGGGAGGCCATGTATCACAGCTCCGAACATGGATA[C/A]GTCGACATCACCCTGGACATCAGAAGTCTAGGTCAGTTCCTGCTGTAGGA
Long Flanking Sequence:
TGCCACTTCCGTCTCCAATTACTCAGTTATATGCCAGCAAGAGGCCACAAGAGAGGACTCAGCAGTTTGTGTGCTGTAGGGAACTTTGAGCTGGTCAGTCTGCTTTTGGAGAGAGGAGCAGACCCCATGATCGGGACCATGTACCGCAACGGCATCTCTACCGCACCACACGGAGACATGAACTCTTACAGCCTGGCCGCTGCGCATGGACACAGGTAACACACACACACAAGATGCATTAGTCAAATACACACTCGCAGCAGCTCGTGATTTATTAATAAAACCTGCAAAATCTCATCCTCGTGCTGCAGGAACGTGTTCTGCAAGCTTCTGTCGCAGTCGGAAAAGGGGAAGGCGGACGTTTTGTCTCTGCAGGAGATTCTGGCGGAGGGATCTGACCTGGAGGAGAGGAATTCCCTAAAGATGGAGGCGACCCGCACGGGGAAAGCCAAACTCAAAGCGCTGAGGGAGGCCATGTATCACAGCTCCGAACATGGATA[C/A]GTCGACATCACCCTGGACATCAGAAGTCTAGGTCAGTTCCTGCTGTAGGATCCACAGTTATGTAATGTTGGTTTAAATTATTGCTTGGTATAATAAGTGGCTTGTTGAAATTTGCATGAACATACATTGAAGGAAAGACTCGAGACGAATTTGCTTTTCAGGCATCAACTGAATTCAAGTTTATGTACAGTAGAATGTTTACGGTTAATTAAAAATAATTACTATCATACGTTTTGTGCTATTATTTAAAGAAAAAAGTTCTCAGGCATGTTTTGTAATTACATAATAAAAAACTTTATTTAACGATCACACTGTAGGCTCCAAATACTCAGTAATTATTCATCTTAAATCTTTACACTTTGTCACACTCCTTCAAACCACTGGGGTCTACTCATTACTCAGCAAAAGACTTTTAATCATTTATGATATGATAAAATCTAGGATAAGAACTGGTCAAATTTAGTATTTTGCTGCATTTTAGCTAAATATATGTGGTATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39195
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 |
---|---|---|---|---|---|
ENSDART00000091742 | Nonsense | 779 | 1012 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14554617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15000035 |
GRCz11 | 18 | 14968547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGAATATACAGAGGAGCTCATCACACACGGCCTCCCTCTCATGTTC[C/T]AGATCCTGCGCGCCAGCAAGGTGAACTAAAACATTTACACATTTGACATC
Long Flanking Sequence:
TTACAAAATATTTACATTTCAAATATGTGTTATTTTTTTTACTTTATCTTCAGAAGTAAAACCAAAAATAGATCATTATCTTTTTTATGATGATAATAATAATAAGTTATTATTCTTTATCGCTAAATGAGAATATTTATAAATATTAGATATTTATATATATAAATATAGAATATTTTACTATATAAATATATATATTTGTTTTTATTTATTTATTTATTTTTTATTAAGTGTTGTAAAAGGCTGACTGCACACAGTTGACTGCATAACAACATTTAGTAATAAAATGATTGTCAATTTCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGGGGTGCCCTGGACGCTGCACACATGGCTGGAGTCTCTGCGAACCTGTTTCCTTCAGCACCGGCGGCCGCTGATCCAGGGTCTGCTGAAGGAGTTCAGCTCCATTGAAGAGGAGGAATATACAGAGGAGCTCATCACACACGGCCTCCCTCTCATGTTC[C/T]AGATCCTGCGCGCCAGCAAGGTGAACTAAAACATTTACACATTTGACATCATATACAGTCATACTGGACTGCAACATGATCATTTCACTCACATCTCACTTGCTTTTTAACTTTTTTTAACTGTAGTTTATTTTCTGTTGTTAAAAATTGCAACATGCAAGAGACAACACGGAAAAGTAATTTATCAACAACAAACTAACAAACTGAAATCAAAACATCACAGCAGCAAGTCCAACTAGCCAAATTCTCTGGACCAACAACTCTTTCATGCCAAAATGCTGCAGTCTTTATGGGACCCACATAATGAGCCTCAGGTGGGACACCTTCATCCACCAATCACCAGCAAACACTAAAGAAAACAAGCTAAACAAAACATAGGGCCAGCATGAGACCTACCCTGCACCCCCCAACCCCACCCCGATCTAACTTCCTCCCAACTTTTTATCCTTTTTATCCCTCCAAATTTATAGGATTTTTTTCAAAGTGTCATTTGGTTTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2959
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091742 | Essential Splice Site | 820 | 1012 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14549699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14995117 |
GRCz11 | 18 | 14963629 |
KASP Assay ID:
554-2749.1 (used for ordering genotyping assays)
KASP Sequence:
TCCCATTCCAAAACTGACCRAGATCAAGAGGAAACAGACCTCAAGACTGG[G/A]TACGTACTGTAAAGAGATCAGCTTTCATCACCAGAACAAACTGACTGACT
Long Flanking Sequence:
AGGAACTGGCTTTGACACATGTGCTGTAGATCCTGTTGAGTTTGCATGTATAGTTATTTGTGAATATTTTCAAGCTCTAAATATGCATAAATAAGTGCATGATAAATTGTGGTACAGTGTCTAAAAAGAACTGATTCTTCTCGCACAAAGCTGTTATTTGGTGTTCAGGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTATTTTATTTTTTACCTCAAATGAAGAACAAAAAACAACTTTTCAGTGGTTAAAGACGTTGTAACAAGGCAAGTCAGTCTGTGTTGTTTAGTAATGGGGTTTGATGGCAGTGGTCTTACCTGTTACTCTTTCTCCTGCTTTGCAGAACGAAGTGATTAGTCAGCAGCTGGCTGTGATATTTACTCAGTGCTACGGCCCGTATCCCATTCCAAAACTGACCGAGATCAAGAGGAAACAGACCTCAAGACTGG[G/A]TACGTACTGTAAAGAGATCAGCTTTCATCACCAGAACAAACTGACTGACTTGAATTAAACTGTGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTTTTTTTTTTGATGTCAAGGGAAATTGTCATTTGTGTGCCATTAAAAACATATTTTAAGAGATTCATGCTTACTTATTGGTATGCTTATTGGTATGACTTTAGATATCATTATTTTTTAGATATCTTTACTATTTTATCTTTATAATCTTTAGTTATCGTTTTCCTTTTTTCTCGGAAACTAATTCTATAGAATTTGCTAAAATTAAATACTTATTTAATAAACTGCTTATTATCATCTGCAAATGCAGAGTTTATTATTGCGAAATCATAAATGTGCTACAATTATATGCAGTTTTTATTTTCACTGCTTATTACCGTACCTTTTGCAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23257
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 |
---|---|---|---|---|---|
ENSDART00000091742 | Nonsense | 922 | 1012 | 16 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14545368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14990786 |
GRCz11 | 18 | 14959298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTCTCTGCATCTAAGTTCTTCCAGCTGGAGGCATTACAGAGACACTG[T/A]GAGATCATCTGCGCCAAGAACATCAACACCGAAACTTGTGTGGAGATCTA
Long Flanking Sequence:
TGGTGGAACAGATGCTCTCCACATCAGAAACACTGAGGTTATGGATGTAAGTACTAATAATGCTGTTTCAGTCCTTTTGTTATACAATCTATGTTTATATTTAAAGTTCCTATACAATGTAAAGCAATACAATTCATAATAATGCTTATGAAATTAATTAATTATTTAATAATTATCAAATATTTTTATCCCAATAAATATATGTATATATTTATTAATCTTTTTAATTATTATGATTTTTTTATGTACAATTTAAAACATTTTACCGTAACTTTTCCTAAGTTTTAGCCTTCCGTATATTCAATTTAGGTGTAAATATTTATTGACATATTGCTTTTTTAAGCTGTTGAGATATTTTTTCTGATAACCAAGGAATCCTGTGTGCTACAGTAGGTTTATATTGAGGTGTATTTGTTTTGGGCTCAGTTTCTCTCCTTCTCCATCTTCCAGCTCCTCTCTGCATCTAAGTTCTTCCAGCTGGAGGCATTACAGAGACACTG[T/A]GAGATCATCTGCGCCAAGAACATCAACACCGAAACTTGTGTGGAGATCTATAACCATGCTAAAGTAATGGCAATCTATTTCTGTTACAATCTTACATGTTCTTAGGTTTTAAAAGGTCACAAACTGCAATTTTTTTATTAATATTTTGGGGTGTTAGAAAATCATAGTTTAGAGCTAATAAGCTATTTTTTATCCTTTTTTTTTTACAAACTGTCTTAATAGGCTTCTCACATTCAAGAATTGGAATTAAACCGAGTCTGTGATTGGCTAACAGCTTTGCATATTAAAATAATAAACAGATGCTGCTGTGATGTTCATTACCATCAAAATAATATGTGATTTGAATTGAAACTGTAAAAATACAAAAAAAAAACATAAGCATCATAAAGTTTAATCACTTATATTGCCATATTATTGTTAGATCCAAAATAGTCAACAATGCATCATCTTTTGTTTTCCGTCTCTTTAAAAAAAGCTTGTGTTTTAACTGCCAGGCTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16940
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 |
---|---|---|---|---|---|
ENSDART00000091742 | Nonsense | 976 | 1012 | 17 | 17 |
ENSDART00000091742 | Nonsense | 976 | 1012 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14542346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14987764 |
GRCz11 | 18 | 14956276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAACATGGCRGTTCTCATAGAGCTTGAGCCATTTAAACAGTTGCTCTA[T/A]AACACCCCGGTGGAGAACTGCTGTCCTGACGTGTTGCATGACCTGGAGAA
Long Flanking Sequence:
CATTACAATCTTTTGCAGTGCCATAATTGAAACTGTAAGGTAACTGAAAGAGAAAATAATTTCAGGATTTTAAATGCAGTGATGCTCATCAATGTCACTTCCAAAGCAGTGAACCAATCAGAAGAACTTGGAGGCGGGGCAAGTGTTGCAAGCTTCAGTTTACAGTAGCAAGTTGGCATGACAACTATTTAATTTTTTAGTAACATGGCGGAGGCACTTTTTTTTTAAAGCATTCCTGATTGTCTGGATTTTTGTAAATGCAAAGCCTTATTCTCTGTGTATGACCACTTATATTCCAAAAGATTAAGGGGAATTAGCTTTTTTCGATTCATGAACTCTTTAATTTTCCATCCTAAATTTTGTTGCATGTGAAACATTCTTTAAATTTGCTGTGTTCCTTAGTTCCTGGAGGCACCCGAACTGTCGGCCTACATTGAAGGCTACTTCCTGAAGAACATGGCGGTTCTCATAGAGCTTGAGCCATTTAAACAGTTGCTCTA[T/A]AACACCCCGGTGGAGAACTGCTGTCCTGACGTGTTGCATGACCTGGAGAAGACGCTGGCCACACGCATTCGCTCCATTCATCTGTCGTCCTCGAAGGGCTCCATTGTCTAAAACTGCCTCCAGACCTCATCAAGCATGCTGAGATCCCAATACGTTCACTTCCTTCAGGACTAAATGTGCTCATTCAGTGGCGGTAGCAATGCACTCATCGTTCTCCATCTAGGACTATGGACGATCTCTTCTCAATAGACTCGATCTGTGCTTTAGGTTACAGCCATAAAGGAAACAATGCCATTTTAGCTTTTGACTCAAAGTTTAAAAACACCTGTGACAGATTAGGGTTTTATTGTTAATCTTGAAATAGTGCAATTCCAGTTGTGGTGTGGACGCATTAGTAAAACTTTAATGGTATTTTTTGGGCCAAAAAAGTCTATCGTCAATAGTGCAGAGATGTATTATATTATACTTACAAAAAAGCTTTTAGTTGTGGCAACTTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12869
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 |
---|---|---|---|---|---|
ENSDART00000091742 | Nonsense | 976 | 1012 | 17 | 17 |
ENSDART00000091742 | Nonsense | 976 | 1012 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 14542346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14987764 |
GRCz11 | 18 | 14956276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAACATGGCRGTTCTCATAGAGCTTGAGCCATTTAAACAGTTGCTCTA[T/A]AACACCCCGGTGGAGAACTGCTGTCCTGACGTGTTGCATGACCTGGAGAA
Long Flanking Sequence:
CATTACAATCTTTTGCAGTGCCATAATTGAAACTGTAAGGTAACTGAAAGAGAAAATAATTTCAGGATTTTAAATGCAGTGATGCTCATCAATGTCACTTCCAAAGCAGTGAACCAATCAGAAGAACTTGGAGGCGGGGCAAGTGTTGCAAGCTTCAGTTTACAGTAGCAAGTTGGCATGACAACTATTTAATTTTTTAGTAACATGGCGGAGGCACTTTTTTTTTAAAGCATTCCTGATTGTCTGGATTTTTGTAAATGCAAAGCCTTATTCTCTGTGTATGACCACTTATATTCCAAAAGATTAAGGGGAATTAGCTTTTTTCGATTCATGAACTCTTTAATTTTCCATCCTAAATTTTGTTGCATGTGAAACATTCTTTAAATTTGCTGTGTTCCTTAGTTCCTGGAGGCACCCGAACTGTCGGCCTACATTGAAGGCTACTTCCTGAAGAACATGGCGGTTCTCATAGAGCTTGAGCCATTTAAACAGTTGCTCTA[T/A]AACACCCCGGTGGAGAACTGCTGTCCTGACGTGTTGCATGACCTGGAGAAGACGCTGGCCACACGCATTCGCTCCATTCATCTGTCGTCCTCGAAGGGCTCCATTGTCTAAAACTGCCTCCAGACCTCATCAAGCATGCTGAGATCCCAATACGTTCACTTCCTTCAGGACTAAATGTGCTCATTCAGTGGCGGTAGCAATGCACTCATCGTTCTCCATCTAGGACTATGGACGATCTCTTCTCAATAGACTCGATCTGTGCTTTAGGTTACAGCCATAAAGGAAACAATGCCATTTTAGCTTTTGACTCAAAGTTTAAAAACACCTGTGACAGATTAGGGTTTTATTGTTAATCTTGAAATAGTGCAATTCCAGTTGTGGTGTGGACGCATTAGTAAAACTTTAATGGTATTTTTTGGGCCAAAAAAGTCTATCGTCAATAGTGCAGAGATGTATTATATTATACTTACAAAAAAGCTTTTAGTTGTGGCAACTTCATG
Associated Phenotype:
Not determined