Busch Lab

ZMP

ENSDARG00000023692

Ensembl ID:
ENSDARG00000023692
Human Orthologues:
ANKRD28, ANKRD44, ANKRD50, ANKRD52
Human Descriptions:
ankyrin repeat domain 28 [Source:HGNC Symbol;Acc:29024]
ankyrin repeat domain 44 [Source:HGNC Symbol;Acc:25259]
ankyrin repeat domain 50 [Source:HGNC Symbol;Acc:29223]
ankyrin repeat domain 52 [Source:HGNC Symbol;Acc:26614]
Mouse Orthologues:
Ankrd28, Ankrd44, Ankrd50, Ankrd52, E230028L10Rik
Mouse Descriptions:
RIKEN cDNA E230028L10 gene Gene [Source:MGI Symbol;Acc:MGI:2685285]
ankyrin repeat domain 28 Gene [Source:MGI Symbol;Acc:MGI:2145661]
ankyrin repeat domain 44 Gene [Source:MGI Symbol;Acc:MGI:3045243]
ankyrin repeat domain 50 Gene [Source:MGI Symbol;Acc:MGI:2139777]
ankyrin repeat domain 52 Gene [Source:MGI Symbol;Acc:MGI:2444029]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa43196 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa16639 Nonsense Available for shipment Available now
sa4778 Essential Splice Site F2 line generated Not yet available
sa43197 Nonsense Mutation detected in F1 DNA Not yet available
sa23408 Nonsense Available for shipment Available now
hu3429 Nonsense Confirmed mutation in F2 line Not yet available
sa36748 Nonsense Available for shipment Available now
sa43198 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43196
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Splice Site, Nonsense 174 1404 5 28
Genomic Location (Zv9):
Chromosome 19 (position 1547209)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1054893
GRCz11 19 1455658
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGCTGAAGTTTCTGTATCTCTGCAAGGCCAATGCTAACATCTCTGAC[A/T]AGGTGAGACTGTTATTAGCAGAGATTCACAGATGTTTCCCTGATTACGTC
Long Flanking Sequence:
AACAACCATACCTCTAAATGATTATTATAGTTAATTTTTTGGCATTCGTTTTAAGTACTTAAACTAAATGAAAATTCACAATGTGGCCTTGATGTTGTTTTGTAAGTTAGTAATCTGTTATTTTATATAAGTGTACGCAGTTTTCCAATGCCAGTCTTGTTTTATTAGTGTAGTTTTCTGTGTGAACCTTGCACTGGGCTGAATTGTGTGTAGATCAGTATATGTGAACAGAAGAGTTCTCTGCCAGCTTGTGTTTCAGTGGGATGTTTAAGTGCTTCTGATCAGTTATTCGTCTCTCAGTATTCATCAGAGAGTCTCACACATTATTTACAGCTGACAGATCAATGCAGATGAATACAGATGCTGTAAGTGTGTGGTTTGTGTGTGTTGTTTGTGGACAGGATGAAGGTCAGACTCCTCTACACATCGCAGCTCATGAAGGAGACGAGAACATGCTGAAGTTTCTGTATCTCTGCAAGGCCAATGCTAACATCTCTGAC[A/T]AGGTGAGACTGTTATTAGCAGAGATTCACAGATGTTTCCCTGATTACGTCTACAGGTGAAGTCTGAATTATTCGCCCTTCTGTGAATGTTCAATGTTCAAATATTTCCCAAATGATGGAGGTTTGCAAACCCCAACCTTCAAAAGTGTCTATAAAATGTGTCTGTCAGCGCAGTGTTTTGTTAACAGAGTTGTGTGTTTGTGTGTCAGATGGACAGATCTCCTCTCCACATCGCAGCAGAGCGGGGACACACCAATGTAGTGGAGATCCTCACCGAGAAATTCAGGTCCTGTGTGTTAGCAAGAACCAAGGTGACTCGCTCACATACAGTATCATACAGTACTGTTGAGATATCTACACACACACACACTCTAACATTAACTAAAAACAAACACGCCCATAACCCAACAAGACCACTCCTCTTTTTGTTATCTCTGCTATTGTTGCTAGACACGCCCCTTGCTGCTGATTAGCTGCAAGTGTGTTGAAAACAAGCACCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16639
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 508 1404 14 28
Genomic Location (Zv9):
Chromosome 19 (position 1555025)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1047077
GRCz11 19 1463474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAATAGAATGGATTTTCAGTTTGACTTGAAGCTGGCGCCGCCTGCTGRT[C/T]AAAACAGTGTAAGTGCAGTACAGTCTGGCCACGCATGTTTTCATGCAAGT
Long Flanking Sequence:
TTGTCCTCTGGATGTGAGTAAAAGTGTGAACTGTGCAGGACGGAGAGACGGCGCTTCATCTGGCAGCAGAGCTCAGGACGGATGCGCTTCATCAGCCGGAGGAGGACATTACCATCATCCAGATCCTGATGGAGCATCAGGCTGACATCACTGCAGTCACACGACAGGTCTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATAGTTATCTCAGATGCAATGTGTGACTGTGGCATTTTGAAACAGAATTAATTCGAATCTAAATTGTGTTATATTAAATGTCTTTGACTTGTGTGTGTTGTATCTAAGCATTAGAAAAAAGCTAACTCAAATTGTTATCACTTTACATCAGTATGTGTAGTATGCACATAGCAGTGGTGGCTAAATAAACGTTTAGAAAAACAATCAGTGCAAAATGATTCAGAATAGAATGGATTTTCAGTTTGACTTGAAGCTGGCGCCGCCTGCTGGT[C/T]AAAACAGTGTAAGTGCAGTACAGTCTGGCCACGCATGTTTTCATGCAAGTATCTCTTGTTAAATTAAATAGAGTTAAATAACATGTTTTTTAATTTTGTTTTGTGTTTTGTTTGTTTTTTATTTTTTTGTTTTGTTTTTTGTTTGTTTGTTTGTTTGTTTTGTTGTGTTTTATTTTGTTTTTTGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAGTAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTATAAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTAGAAATGCTGATCTAGAAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTATAAATGCTGATCTAGAAATGCTGATCTAGAAATGCTGATCTGGGAATGCTGATCTATAAATGCTGATCTATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4778
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Essential Splice Site 813 1404 22 28
Genomic Location (Zv9):
Chromosome 19 (position 1563601)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1038501
GRCz11 19 1472050
KASP Assay ID:
554-3530.1 (used for ordering genotyping assays)
KASP Sequence:
CTCATTACAWGTGTCTATATATGGTTTGTAACTTGTCCATGTGTGTKTTC[A/C]GAGTGGCTGGACAGCGCTGCATTACGCTGCTGAAGCCGGCTGTCTGGAGG
Long Flanking Sequence:
TACTCCTTATCTGCTCTCACTTCTGCAGATGTATGTGCCCTCCAGAAACTTGCGCTCTGTAAATGAACGTCGCCTCGTGGTTCCATCCCAAAGAGGGAAGAAATCACTTTCTCGAACTCTCGCATTCAATCTGCCAAGTTGGTGGAATGAACTCCCTAACTGCATCAGAACGGCAGAGTCACTCGCTGTCTTCAAGAAACCACTAAAAACTCAACTATTTAGCCTCCACTTCCCTTCCTAATCTGCAATTGCCTCTCTTGCTCCACCACTAACTGTACTACAAAAATAAAATTACTAATGTTTTGCTTCTTACACTTTACACACCTGAAACTTGCCTACAGCACTTATTCATTGTTGCTTTTATAGTTGTTTAAATTGCTTCCTTGTCCACATTTGTAAGTGGCTTTGAATAAAAGTGTCTGCTAAATGACTAAATGTAAATGTAAGGGACTCATTACATGTGTCTATATATGGTTTGTAACTTGTCCATGTGTGTGTTC[A/C]GAGTGGCTGGACAGCGCTGCATTACGCTGCTGAAGCCGGCTGTCTGGAGGTGTTGTTATTTCTGGTGGAGAGTGGAGCGTCCGCCTGTGCTGAGTGTCACGGTGGACGAACGCCGCTGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATATTCCTGCTCAGACGAGAGAAAAACACACTCCGGCTGCTGGACGACAAGAAGGTCAGACTCACTGCTGCACTCCTCAGTCTGTGTCTGTTTTAGTTTCTGTCAGCTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTATTTTTGACTGTTTGGCGCCATCTAGTGTCTGAATAATGCACAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTGGCTCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43197
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 848 1404 22 28
Genomic Location (Zv9):
Chromosome 19 (position 1563708)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1038394
GRCz11 19 1472157
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTCTGGTGGAGAGTGGAGCGTCCGCCTGTGCTGAGTGTCACGGTGGA[C/T]GAACGCCGCTGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATA
Long Flanking Sequence:
TTTCTCGAACTCTCGCATTCAATCTGCCAAGTTGGTGGAATGAACTCCCTAACTGCATCAGAACGGCAGAGTCACTCGCTGTCTTCAAGAAACCACTAAAAACTCAACTATTTAGCCTCCACTTCCCTTCCTAATCTGCAATTGCCTCTCTTGCTCCACCACTAACTGTACTACAAAAATAAAATTACTAATGTTTTGCTTCTTACACTTTACACACCTGAAACTTGCCTACAGCACTTATTCATTGTTGCTTTTATAGTTGTTTAAATTGCTTCCTTGTCCACATTTGTAAGTGGCTTTGAATAAAAGTGTCTGCTAAATGACTAAATGTAAATGTAAGGGACTCATTACATGTGTCTATATATGGTTTGTAACTTGTCCATGTGTGTGTTCAGAGTGGCTGGACAGCGCTGCATTACGCTGCTGAAGCCGGCTGTCTGGAGGTGTTGTTATTTCTGGTGGAGAGTGGAGCGTCCGCCTGTGCTGAGTGTCACGGTGGA[C/T]GAACGCCGCTGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATATTCCTGCTCAGACGAGAGAAAAACACACTCCGGCTGCTGGACGACAAGAAGGTCAGACTCACTGCTGCACTCCTCAGTCTGTGTCTGTTTTAGTTTCTGTCAGCTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTATTTTTGACTGTTTGGCGCCATCTAGTGTCTGAATAATGCACAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTGGCTCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23408
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 868 1404 22 28
Genomic Location (Zv9):
Chromosome 19 (position 1563768)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1038334
GRCz11 19 1472217
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATATTCCTGCTC[A/T]GACGAGAGAAAAACACACTCCGGCTGCTGGACGACAAGAAGGTCAGACTC
Long Flanking Sequence:
GAACGGCAGAGTCACTCGCTGTCTTCAAGAAACCACTAAAAACTCAACTATTTAGCCTCCACTTCCCTTCCTAATCTGCAATTGCCTCTCTTGCTCCACCACTAACTGTACTACAAAAATAAAATTACTAATGTTTTGCTTCTTACACTTTACACACCTGAAACTTGCCTACAGCACTTATTCATTGTTGCTTTTATAGTTGTTTAAATTGCTTCCTTGTCCACATTTGTAAGTGGCTTTGAATAAAAGTGTCTGCTAAATGACTAAATGTAAATGTAAGGGACTCATTACATGTGTCTATATATGGTTTGTAACTTGTCCATGTGTGTGTTCAGAGTGGCTGGACAGCGCTGCATTACGCTGCTGAAGCCGGCTGTCTGGAGGTGTTGTTATTTCTGGTGGAGAGTGGAGCGTCCGCCTGTGCTGAGTGTCACGGTGGACGAACGCCGCTGCAGTACGCGGCTCAGCAGAACCACGAGTCCGCTGTCATATTCCTGCTC[A/T]GACGAGAGAAAAACACACTCCGGCTGCTGGACGACAAGAAGGTCAGACTCACTGCTGCACTCCTCAGTCTGTGTCTGTTTTAGTTTCTGTCAGCTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTATTTTTGACTGTTTGGCGCCATCTAGTGTCTGAATAATGCACAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTGGCTCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCAGCTGTTTGTGTTTTTGACTGTTTTGCGCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCTGCTGTTTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
hu3429
Status:
Confirmed mutation in F2 line
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
ENSDART00000103179 Nonsense 990 1404 23 28
Genomic Location (Zv9):
Chromosome 19 (position 1565418)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1036684
GRCz11 19 1473867
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGTGTTGGACTGCCTGATCGAGGGCCGGCAGAAGGGCGTGGTATCC[C/T]AACCGGCAGTGCAGACGTACCTGACGGAGGTGTGGTGTGGAGGTCTGCAG
Long Flanking Sequence:
GTCTGTTTGGTGCATCTAGTGTCTGAATAATGCGCAGGTTAGTGTATACTCCATCTTGTGTCTGAATAAAAGCAATTTTACAACAAACAGCTGATGCGTTTATAAATTCTAAAGCATTTTAAAAATTGTTCCTATTCTTGAAAGATAATCAAAAGTGTGTTTGTCCTTGTCTCTAGTTTATATTCAATCTGATGGTGTGCGGGCGAATGAATGATAATCTGTCTCTGGAGGAGCTGGTTTTACACACATCTGCTCCTCTGGATACTGCGGTGCGTCTATCTCGAGCTTTGACCCTTTGTGCGCTGAGAGAGAAGGAGCGTTCGGTGGATCTGCAGGCTGCAGCGCATCACTGTGAGCTCATGGCGTCCGATCTGCTGTCTCTATCTGCATCTGCTGGGGGTCAGGGAGCTGGCGCAGGCCCCATACTTAGGGCTCTGGACCACAGGGGGCTCAGTGTGTTGGACTGCCTGATCGAGGGCCGGCAGAAGGGCGTGGTATCC[C/T]AACCGGCAGTGCAGACGTACCTGACGGAGGTGTGGTGTGGAGGTCTGCAGTGGGACTCCTGGAAGATCCTGCTGCTGTTCTGCTGTTTACTTCTGTGTCCGCCATTGTGGCTTCTGCTCGCTCTGCCACTCACACACAGGTACAGTTTGGATTAATGCACTGGAACAACATAATTTTTGATAAATGGCAGGAGTTACGGGGAGAGAGAAAAATAGCCAATCAGAGAATGTATGTATTTAACACAGGCTCATTGTGAAAACATACTCCTGCATACATTTCTGGAGAGCATGAATTATGTACCCAGAGGTACATATGGCTGCATTTCATCTTTAAAACGAACGCTATGGGGCAGTATGACACTGCAGACGGCTTCTATTTCGATTACATTTGAAACACTGTCAGTTGGGTTTAGGGAAGGGGTTGGCGGGTCAGTCAATGCTTTTGAAAACACTATTGGTTGGGTTTAGGGAAGGGGGTGGGCGAGTCAATCGGTGCTTTTG
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa36748
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 1205 1404 24 28
Genomic Location (Zv9):
Chromosome 19 (position 1567717)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1034385
GRCz11 19 1476166
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTGATGTTGTTTCACACTGCATTTACACTGAGTCTCACCGCATTATG[C/A]CAGCCGCTTTATCCACAAGAACAGCACAATACCACGACAGAAGTGACCGT
Long Flanking Sequence:
ACCATCCCAATCGTGAAGTTCATGAGCCACCTGGTGTCCCACATCTTCCTGCTGACTCTGTTCATCCTGACCATCGTGTACCCGCCCGTGAGTCCTCTATCCCAGGCCCGTCTGATGCCCAGCTGGAGCGAGTGTCTGCTGCTCATCTGGCTGTGTGGGATGCTGGTCTCTGAGCTGACATTCCCCGGAGAGCGCACTGGATTAGCCTGGATCCGTCTGCTGCTTTTGGGTTTTTCTGCTGCTGCTCTGCTCTGCCACCTGCTGGCGGTGTTCACCCAATGGTGGCCGCCAACACACCTGCATTGTCTATTCGCTCGTAACGTACTGCTAGCCGTCGCCATGACTCTCGGTTTCATCCAGCTTCTGGAATTCCTCACATTTCATCATTTATTCGGGCCGTGGGCGATAATCATCAGAGACTTGATTAAAGATCTGTGCAGATTTGCTGTGATCCTGATGTTGTTTCACACTGCATTTACACTGAGTCTCACCGCATTATG[C/A]CAGCCGCTTTATCCACAAGAACAGCACAATACCACGACAGAAGTGACCGTTCCTGGGCCGTTAAATATGTCCGTGCTGCTTTTTTTTGCGTTGTTTGGTTTGACTGAGCCTGATAAAATCCCCGATGTGGATCGATCGCCTCCTGCTACGGCGGTGTTGGCTAAAATGGTGTTCGGTGTGTATCTGGTGGTGACGTTTATCGTGTTGATTAATCTGCTGATTGCGATGATGAGCGACACATATCAGCGAATACAGGCTCAGTCCGACACCGAGTGGAAGTTTGGCCGTGCTGTTTTGATTCGAGATATGAGCCGCAAATCTGGCATCCCGTCTCCGTTTAACCTGTTCACCAACCTGTTCTACTCCGTTAAAGTTGTCTGCAAACGTGCAGGTATGATCCGTTAGTCATCATCTGCATGTTTATAAACACTTTTTCTTGAAAATATTCTAAATGTACAGTTATTTTAGAGTTAAATTGTTAAGTTTTACCATTTTTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43198
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103179 Nonsense 1294 1404 25 28
Genomic Location (Zv9):
Chromosome 19 (position 1567994)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 1034108
GRCz11 19 1476443
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGAGCGACACATATCAGCGAATACAGGCTCAGTCCGACACCGAGTGG[A/T]AGTTTGGCCGTGCTGTTTTGATTCGAGATATGAGCCGCAAATCTGGCATC
Long Flanking Sequence:
AATGGTGGCCGCCAACACACCTGCATTGTCTATTCGCTCGTAACGTACTGCTAGCCGTCGCCATGACTCTCGGTTTCATCCAGCTTCTGGAATTCCTCACATTTCATCATTTATTCGGGCCGTGGGCGATAATCATCAGAGACTTGATTAAAGATCTGTGCAGATTTGCTGTGATCCTGATGTTGTTTCACACTGCATTTACACTGAGTCTCACCGCATTATGCCAGCCGCTTTATCCACAAGAACAGCACAATACCACGACAGAAGTGACCGTTCCTGGGCCGTTAAATATGTCCGTGCTGCTTTTTTTTGCGTTGTTTGGTTTGACTGAGCCTGATAAAATCCCCGATGTGGATCGATCGCCTCCTGCTACGGCGGTGTTGGCTAAAATGGTGTTCGGTGTGTATCTGGTGGTGACGTTTATCGTGTTGATTAATCTGCTGATTGCGATGATGAGCGACACATATCAGCGAATACAGGCTCAGTCCGACACCGAGTGG[A/T]AGTTTGGCCGTGCTGTTTTGATTCGAGATATGAGCCGCAAATCTGGCATCCCGTCTCCGTTTAACCTGTTCACCAACCTGTTCTACTCCGTTAAAGTTGTCTGCAAACGTGCAGGTATGATCCGTTAGTCATCATCTGCATGTTTATAAACACTTTTTCTTGAAAATATTCTAAATGTACAGTTATTTTAGAGTTAAATTGTTAAGTTTTACCATTTTTGGAGTTAAATAGGAAACAAAAAGGCTCATTTGGTCTGGTGAGGGGATTTTTAGCTTAGCTTAGCATAGATCATTGAATCAGATTAGACCATTAGCATCTCCAAATTGACCAAAGATTTTTATTGATCTTTCTAATGATCTTCGGGTTTGACGGGAGCACTTTTAGCTTAGTTTAGCTTAGCATATATCATTAAATCGGATTAGACCATTAGCATCTCTCGCAAAAGTTATCAAAGTGTTAATAATTTTCCAACTTTAAGAAAGTTTCCCTGTTTTACTTCT
Associated Phenotype:
Not determined