Busch Lab

ZMP

golga1

Ensembl ID:
ENSDARG00000008979
ZFIN ID:
ZDB-GENE-040426-1237
Description:
golgin A1 [Source:RefSeq peptide;Acc:NP_957132]
Human Orthologue:
GOLGA1
Human Description:
golgin A1 [Source:HGNC Symbol;Acc:4424]
Mouse Orthologue:
Golga1
Mouse Description:
golgi autoantigen, golgin subfamily a, 1 Gene [Source:MGI Symbol;Acc:MGI:1924149]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa9657 Nonsense Available for shipment Available now
sa12072 Essential Splice Site Available for shipment Available now
sa18926 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10260 Nonsense Available for shipment Available now
sa21357 Nonsense Available for shipment Available now
sa27251 Nonsense Mutation detected in F1 DNA Not yet available
sa41274 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21356 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9657
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
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Nonsense 126 862 5 23
ENSDART00000112214 Nonsense 126 341 5 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43541522)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41495094
GRCz11 8 41502727
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCCAGACAAACAGAGCCAAGATGGCAGAAGCCATGTCCTTAGCRTTA[G/T]AAAAAAAAGACCAGGAGTGGATGGAAAAACTRGCTTCACTGGAGCAGGTA
Long Flanking Sequence:
TGAGATGTAGTTTGCATACAGTTTGCTACAGTGTAAACAGCACCGACAGAATGCTACCGCAGGTATTCATGCAGTGTTGAAAAATCTGCAGTCTGAACTCGGCATAACCTTTTATATTTTGTCTATTTCTAAGGTTTCAGATATATTCTGAGCTACTTTCTAACATAAGTAATTTATTAATGCGATTCGGCAAATAACAAGCTTTTTAACCCTCCAGATCTCTTTGCTGCTAATCTGCCATTAAAAATGCATTTACTGTAAACAAGTTTATTTACACACACTGTGGGAAATATTTTCTATCTTTAAAAAAAATGCATGTGGCGCACAGAGATAATTAAAAATGATCAGAAACATTACTATTAATATACTTTAAAAAAGAGTGAAGCATTTGTTTTTATTGTTGTGTTTATTTTTCAGCATCCATGCGCAAACTTCAAGACCAGAACGAATCTTTCCAGACAAACAGAGCCAAGATGGCAGAAGCCATGTCCTTAGCATTA[G/T]AAAAAAAAGACCAGGAGTGGATGGAAAAACTAGCTTCACTGGAGCAGGTAAAGATGCTTGGTGACATATTGGATGAAGTCACTCTAAATCAGTGGTCACCAACCTTTTTTAGTCAAACATTCCTAACATTTGCCTTGCTGAAAAGCAAGATCTAACCATTTAAAAATGACAGAAAAATAAAGTTATTTTTCATTAGTATGTTCAACTTATGACCTTTAATATAACATTTTTGAACTATGTAGAATGCACTTGTTTAACCTACTTAAAATATTTTAATTAATGCAACCAAAAAAACTGCAGTAATTTGCAGTAATCAGTTATCATATGAAATGCCTGTGATTTAACAAAAAAAAAAAAGATTGGTAAAATGATTTTCAGTGATACTTTTGCTGGTAAAACATTGGCATTTGATAAATTAACTATACAATATGAGCTAAAATATTAAATAATAACTAAATAACTTAACTAAAACATTAATTATTTAATTTTCTTTTTGGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12072
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
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Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Essential Splice Site 184 862 6 23
ENSDART00000112214 Essential Splice Site 184 341 6 10
ENSDART00000098578 Essential Splice Site 184 862 6 23
ENSDART00000112214 Essential Splice Site 184 341 6 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43540158)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41493730
GRCz11 8 41501363
KASP Assay ID:
2260-0970.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGCTAGAGGGCTTTCAGCAGCAGGAACTGGCTAAAGTCAAACACATGG[T/A]ACTTTTKTGTTTTGASTTTTCTAWGCTTAGGATTTTCTGTCCTGTGATGA
Long Flanking Sequence:
TGAGGGGTTTTACAGCTTAAAACATCCTATAATAATGGTTATATTATTGGTATATATTATATGGCATAATAATGGTAAAAAAAAAATAAAGTGGACTACTTAGTGGATTTTATCTATTGCAGGCTGTTTTTAGAACGTAACTCTCACGATTAATGAGGGACCACTGTATCAACATTAGCGACATAAATCACTTGAGATACATTTCTTGTACTTATTCTTCTGTCATCTACTGAGAGATCATGATCAATGGGCTGGTGACCACTGCCCTAATTGTGTTTTGTGGGTGACTTTGGGTTAAAAGCATCTGCTAAATCATCAGCGGTAATCGTCAAATACTGTATCGTCATTCTGTCCTCTTTTTGTCAAACAGGAGAAGTTGTCTTTGACTTCTCGGCTAGACGAAATGACAGAGCAGAGTTTAAGTCTGTTCCAGAAGAGAGACGACCTGGATGAGCTAGAGGGCTTTCAGCAGCAGGAACTGGCTAAAGTCAAACACATGG[T/A]ACTTTTTTGTTTTGAGTTTTCTATGCTTAGGATTTTCTGTCCTGTGATGATTTATTTATTTATTTTATTTTTTACATTTGATTAATATATATTGATAATTGATTAGTATAAATTAGTGATTGATTAAGGTTTTGCTAAAGTGATGATCAAATGCATTATAATCATTGGAATATTACAGCACACCTCATGAAGCGGAAAAGGCTTTTATACTATACGCGCTCACCGTAGTGAAAGAAAATCCACTCTAAAATCAGACGGATAAACAGAGAAGTAGAAAGTAATTTTTTTTAGTAATTATTATAAAAAATTATATGGATTTTTATAACCATTCAAGATTTTTTTAAACAAACTTTGACACATCACTTACTTTTGTTCATATTTCGGACAATTTTTCCTATTAAAGTTTATTCAACTATCAATGACAACAGAACATGCGTTCCTCTATGAATATATATATTATTTTTTTGCAAGAATAAAAAAAAAAAAACATCTGTATTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18926
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Essential Splice Site 184 862 6 23
ENSDART00000112214 Essential Splice Site 184 341 6 10
ENSDART00000098578 Essential Splice Site 184 862 6 23
ENSDART00000112214 Essential Splice Site 184 341 6 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43540158)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41493730
GRCz11 8 41501363
KASP Assay ID:
2260-0970.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCTAGAGGGCTTTCAGCAGCAGGAACTGGCTAAAGTCAAACACATGG[T/A]ACTTTTTTGTTTTGAGTTTTCTATGCTTAGGATTTTCTGTCCTGTGATGA
Long Flanking Sequence:
TGAGGGGTTTTACAGCTTAAAACATCCTATAATAATGGTTATATTATTGGTATATATTATATGGCATAATAATGGTAAAAAAAAAATAAAGTGGACTACTTAGTGGATTTTATCTATTGCAGGCTGTTTTTAGAACGTAACTCTCACGATTAATGAGGGACCACTGTATCAACATTAGCGACATAAATCACTTGAGATACATTTCTTGTACTTATTCTTCTGTCATCTACTGAGAGATCATGATCAATGGGCTGGTGACCACTGCCCTAATTGTGTTTTGTGGGTGACTTTGGGTTAAAAGCATCTGCTAAATCATCAGCGGTAATCGTCAAATACTGTATCGTCATTCTGTCCTCTTTTTGTCAAACAGGAGAAGTTGTCTTTGACTTCTCGGCTAGACGAAATGACAGAGCAGAGTTTAAGTCTGTTCCAGAAGAGAGACGACCTGGATGAGCTAGAGGGCTTTCAGCAGCAGGAACTGGCTAAAGTCAAACACATGG[T/A]ACTTTTTTGTTTTGAGTTTTCTATGCTTAGGATTTTCTGTCCTGTGATGATTTATTTATTTATTTTATTTTTTACATTTGATTAATATATATTGATAATTGATTAGTATAAATTAGTGATTGATTAAGGTTTTGCTAAAGTGATGATCAAATGCATTATAATCATTGGAATATTACAGCACACCTCATGAAGCGGAAAAGGCTTTTATACTATACGCGCTCACCGTAGTGAAAGAAAATCCACTCTAAAATCAGACGGATAAACAGAGAAGTAGAAAGTAATTTTTTTTAGTAATTATTATAAAAAATTATATGGATTTTTATAACCATTCAAGATTTTTTTAAACAAACTTTGACACATCACTTACTTTTGTTCATATTTCGGACAATTTTTCCTATTAAAGTTTATTCAACTATCAATGACAACAGAACATGCGTTCCTCTATGAATATATATATTATTTTTTTGCAAGAATAAAAAAAAAAAAACATCTGTATTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10260
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Nonsense 356 862 11 23
ENSDART00000112214 None None 341 None 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43524846)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41478418
GRCz11 8 41486051
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGTCATCTAACGTCTGCATGTTGTGTGTGTGCATGTAGAAGTCTTCCT[T/A]GGAGCAAAGGTTAGAGGAGGCCAGAGGAGAGTTACTGCAGGAGAAAACCA
Long Flanking Sequence:
GCTTCAGTCTTGTCTTGCCAGCCCAGCCAAGTTTATTTGTGTGTTTTGTTTATGTTTTCCCCCTCAGGGTAGTTTTGTTTTGCCTTTTATTTTTATTTTATTAATAATAAATACCCATTATTTGCTGCACCCGAGTCCTCGCTCCTTTCCCTAACCACGACTGTGACACTTTCCTCGAATCTGGAGATGGCAAACCCCCCTTTTCCGGTGGAGCCCCATGGCCTTAAACTTGGAGCTGATTCTCATTCCAGCCATGTGTCACTCGGCAGCAAACTGCCCCAGTGCATGCTGAAGGTCCAAAATTTGAGCCAACAGAACAACATTGTCTGCGGATAACAGAGATGAAATCCTGTGATCTCTGAAACAGACCCTCTCCAGCCTTTGAAATTCTGTCCGTATTCTGTTTAAACCAAACAATATAATGTATATACCTGTCATCACGCTACAGTTTCAGTCATCTAACGTCTGCATGTTGTGTGTGTGCATGTAGAAGTCTTCCT[T/A]GGAGCAAAGGTTAGAGGAGGCCAGAGGAGAGTTACTGCAGGAGAAAACCAGTCACACTACAGCAGTCAGTTCACTGGAGGCACAGGTATAGTTAAATGTTTTGAAATATAGTCTATTCATGTGATGACAGTTTTTTTTTAAAGGGAAAATGTGGCATAATTACTCGCCCACCAGTTGTTTCAAACCTGACTGAGTTTCTTTCTTCTTTTAAACACAAAAATATTTAGAAAAATGCTGAACACCTGTAATCGTTTTTTTGCTATTGTGGAAATCAATGGTTACAGGTTCTCAGCTTTCCGGAAAATGTCTTCATTAGTGCTCAATAAAATAAAATCCATAAAGGTTTATAACACCTTGTGGTAGAGTAATGAATATGTATTTTTTAAGAATTTTGTTGTGCGGCTTAAAATTGATACTTTATTTATAGGATTATTTGACGAAAGGAAAGTAAAAAAAAAAATATATATATATTTTTAATAATTTCTAAAACTTTATAAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21357
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Nonsense 435 862 13 23
ENSDART00000112214 None None 341 None 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43522992)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41476564
GRCz11 8 41484197
KASP Assay ID:
2260-0967.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATCTGGAGCAGAGACTGGCGGACTGCGCTGAGAAGATGAAGAGTCTA[C/T]AACAGCAACTCAAAGACAGCCAAATGCACACAGACAAACTGGTACATCAT
Long Flanking Sequence:
ACACGTTTGCGACAATCATTCGTTCCACTAACAAAAAAATAACCATTTGCATTGACTTTTTGTGTAATCTACTAGCGCTAATACTTAAATTAGCTTTTTTTTTATTTAAAAGTAGCATTGAAAATAAAAATATGACATTTAAAACTATCGCAATCTTGGTTGGTGAAACAAACTGTAATGTATTATTATTATTATGATGGACTACATTCAAAAGGCTCTATTGATTCTGACACTGATCTCTGTTCACTGCTTTTGTAGTATTAATGCTAGGATTTAAAATAATGTTAAATAATTTAAAAAAAATTATGCTGCATGGCGTTAGAACATTGCCAGGGTGAGTACGATGACGTTTTTTTTTTCTTTTCTCATCTTCTGGTGATTGAACTCACACTTTAAGTGACTTGGACTGATTGATGTGAATGAATGAATGATGTGTGTTCTGTAAGATATCAGATCTGGAGCAGAGACTGGCGGACTGCGCTGAGAAGATGAAGAGTCTA[C/T]AACAGCAACTCAAAGACAGCCAAATGCACACAGACAAACTGGTACATCATTTCCACCAAACATCTTGCAAGCTGGCTCAGGATTTTTCTCAGTTATTCACATTTTTCCTCTGTTTTTGCTAAAACATCGCCCTCTTCTGTTAGATGTCTGCCATACAACTGTGATGCCAGCAATAAATAAAAAATAAGGGGGAGAATTATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGTTGGAGTCTGAATTATTACCCCCCCTGTTTATTTTTTCCCCAAATTTGTTTAACAGAGAGAAGATTTTTTTTTCAACACATTTCTAAACATAATAGTTTTGATAACTCATTTCTAATAACTGATTTATTTTATCTTCGCCATGATGACAGTACATATTATTTGATTAAATGTTTTCCAAGACATTTCTATGCAGCTTAAATGACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27251
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
ENSDART00000098578 Nonsense 461 862 14 23
ENSDART00000112214 None None 341 None 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43521228)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41474800
GRCz11 8 41482433
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGGTCCTATAGCAGGTGGAGTGGTCAGAGGAGCGAGAGCGGCTACAG[C/T]AGCAGGTGTCCACACAAAGACAGAGAGGCCTGGAGAAAACAGCCAGACTG
Long Flanking Sequence:
AGTTAATTAAAATTTATAGAAATGTAAAAAAATAAAAGGGAAAAAAAGTGGAAAAGAAAGAAAGAACGCAAATAGTTACATTCAGAACATGTTTCCTAATACAATTCCTTTTAGAATAATCTCAGATGATCTTATGCGTCTATAGGGACAGAACACACGCATATTTGCGAATGTATTTATTCCTATATACATATACAGAACACGCATCAGCATATATTGTATACATGCATTTATCAGTCAATTAATGCTATTTGTTCAAAGCAAAATAATTAATTAAACAGTGCCTCACTTCCATATCTAAACATAACATTTTAGAAAACCAGTGCAAAAAACTAAAGAAAGATTTTAGTTCTTAATGTAATCAATCAACTGAAGTATATGATACATTTTTGTTTAGTCTATTCAACTTCAGGGTTTTAAAAACTTTACATTAGAGTGTTGACCTCTGATTTTTGGTCCTATAGCAGGTGGAGTGGTCAGAGGAGCGAGAGCGGCTACAG[C/T]AGCAGGTGTCCACACAAAGACAGAGAGGCCTGGAGAAAACAGCCAGACTGGAGGAAGAGCTGCTTGCACTACAGAGAGACAGAGAAACGGAGGCCAACAAATATCAGGACAACCTGGTGTGTGAAAGAGCACTTTATTCACCATTATAAAATGGCCACGGAAAAGTTGCTAAAGATTTGTCTTTTGTCTGATTCTCTTAAGCGGTTACTGGAGGAGGAAAAAAACTCCCTTTTGAGGAGCAAAGCGGAGACTGATAGCACTGTAGAGAGTCTGACGGCAGAACTGGAGCAGTCTAGAGTAAGCATCATCTAATAAACGTCACGTAAAACTATTCAAAAGTCTGGAGTCAGTTTTATCTATTAGTTTAGTTTAAACTTTATTGTTTTTTCTGCTTGGCACAGAAAGGAAATTAGTTTTTAACGCTTGATTTAAGACAACAATTGCATACAGTCAACAATCACACAATAACAACACTCATCAAGACAACAACACAAGTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41274
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Essential Splice Site 809 862 22 23
ENSDART00000112214 Essential Splice Site 288 341 9 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43510269)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41463841
GRCz11 8 41471474
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGAATGAATGCTCCCATGAGTGCTCGCCTCTTTCTGCTTCTCTCTTC[A/T]GGCTTTCCAGCTCATCAGAGCCGTTTCTGTGCTCCTGCATTTCTCAAAAG
Long Flanking Sequence:
AACCATTTATGACCATCAGTTTCTCAATAATAATGGGATAAATTCAGAAACATTATGGAAGAAAAGATTGATTGGAGTAGCCTGATTTCTCTCAGAAAGCATAAAGCGAGTGTGGACATCTTTATTGGTAAAGGTATTTAAAGTTCTCAAATGTTGTTTCATTTTTACCCTGAGGAAGGCAAGTTTTGCTGAAATGAATAGGTGCTGTTTTTAAATAATAGCCATGTTAATAAATGCTTTTTATTTTTTTTTTACTTATTTTTCAACTTATAATTTCATTGTTTAAATCTTGTTTCAATGATCTATGGTAAGCTAAGCTAAATGTGCTCCGGCTAGACCCAGAGACCAGCTTAATGGATTAAAAAATGGTAAAACTCGTCTAGTTAACTCTAGGGGAGTTGTAAAATTTGCCTATTTCTTTAACAAGCACATAGCAGTGATTTGATTGCTACTTGAATGAATGCTCCCATGAGTGCTCGCCTCTTTCTGCTTCTCTCTTC[A/T]GGCTTTCCAGCTCATCAGAGCCGTTTCTGTGCTCCTGCATTTCTCAAAAGAAGAGGAGGACATGCTCAAACAGACACTGGAGTACAAGGTGTGTAACAGAGAGTCTGTAAGTATGATGGAGGATCAACATTTAGAAAGGTGTTCTTCTCTAGCCTCATCTCCTCCGCACCCTAACTAGGCCATACTGCCGAGGCAGAGAACAATGTGGGTCAGGATATGTGGCTCAACGCTCTGAATCAAACCATTAGCACTCAGTGTCATGGTCAGGAAAAGCATCTGCCAGGTATTTATAGATCAGGCCGGCAGCAGTGCTGGAAAGCAAGGAAATCGCTGCACATCACTGTGCTACATTACAACACCGCTCCAGTCCCTGCTGCTATCAGCAGGCTTAAGTGGAAGATTTGTGGTGGAGTTATTATTATGTTATGTTATGTTTTATCTTAAATTTCGATTGGAGATGTACCAAGTGTAATATTATTTTTTAAAAGCACACACACATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21356
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098578 Nonsense 861 862 23 23
ENSDART00000112214 Nonsense 340 341 10 10

The following transcripts of ENSDARG00000008979 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 43508039)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 41461611
GRCz11 8 41469244
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCTCACCCAAAGGTATCATACGACCTTCCATCTCAGGAACATCAAGCT[G/A]GAGCTGAGAAACCCAAAACGGCACATCTCTGAGACCAGGTGAAAGAGGGA
Long Flanking Sequence:
GAGGTTAAAAAAGGACAATCTTAACTTCCTTTTAACAATTAGTTAAAATTTTCGAGACTTTTTATTCACACTCAGAGACGTCACAAAGCACGCCCAGGTACAGACAGCCAGTCTACACACTGGAATCCACACAAGGATCTAATCTGCGTGACGCAGCTTCAAAAAATTTGTTTCAAACCGGAAGAACAAATTTGCTCGAAATAACACAAAAACAACCAATTTTCACTTTTTTTTTTTTGGTGAAATTTATGTCCTAATAGTGTTTTAGCAGTGTGGGACACATTTTAAGACTGTCAACAGTTCAAAATATATGTGTTTTTGTGTTTAGTGACCCTTTAAGTTTTCACTTAAAGGAGAACACACACGGAGAAAATGAGGTGTCTTACGTTTTGAAGCACTGGTCGAGACTGATGTTTTGTATGCTTTTCAGATGTCGTGGTTTGGTTCCAAGCCCTCACCCAAAGGTATCATACGACCTTCCATCTCAGGAACATCAAGCT[G/A]GAGCTGAGAAACCCAAAACGGCACATCTCTGAGACCAGGTGAAAGAGGGAACAGTAAATGATCTCAGTAGAAAAGGGAACAATTGCTGACTCGGCAGTTTCAGTCTCTGCCTCAACAGTTGCTATGTAGCTCACGCCCTTTAAAAGAACGGGACACACAAACAACTCTGCGTTTTTTCGCTAAAATATTGCAGGGACTTGAAAACCAAGGCTTTATGAACATCGTCTTTTTGTGACTTGGGGAGTTTCGTCGTCTAATGAAATGAACTCAAGTTTCATCTGCTTAAAAAAACAAAACAAAAACAAAAAACAATCATCGCTTTTTCCAACATCCTGTATTGACTCGATTATTTTAACTCTGTGAAATCAAGGCTGGGCCAATCATGAAGAGAATGATCCTCCAAAACGTCAGTGAAAATCAGGAATGGGTGTCATGAAACATTACTTTAAATCTCGTTTTTATGTGTAAATTACAAATCCATACATTCCATACAAGTATTT
Associated Phenotype:
Not determined