Busch Lab

ZMP

arnt2

Ensembl ID:
ENSDARG00000058449
ZFIN ID:
ZDB-GENE-001207-3
Description:
Aryl hydrocarbon receptor nuclear translocator 2 [Source:UniProtKB/Swiss-Prot;Acc:Q9DG12]
Human Orthologue:
ARNT2
Human Description:
aryl-hydrocarbon receptor nuclear translocator 2 [Source:HGNC Symbol;Acc:16876]
Mouse Orthologue:
Arnt2
Mouse Description:
aryl hydrocarbon receptor nuclear translocator 2 Gene [Source:MGI Symbol;Acc:MGI:107188]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa20863 Nonsense Available for shipment Available now
sa15572 Nonsense Available for shipment Available now
sa20864 Essential Splice Site Available for shipment Available now
sa11162 Nonsense Available for shipment Available now
sa20865 Essential Splice Site Available for shipment Available now

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26891
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129575 Essential Splice Site 65 738 3 20
ENSDART00000130997 None None 586 None 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11411904)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10489700
GRCz11 7 10731340
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGGATTTTGACGACGAGGACGGCGAGGGACCCAGCAAATTTTCAAG[G/A]TAAAACCTCACACCATTTCCAGCTTTCCAAACCACCCGATTAGACCACAA
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTGAGTATGGAAAAAAAAATCTTTTTTATAAATCTTTTTTCTGTGTGTAGGCAAAATATTATATTAATTAATAACTAAATTAAATATGAAAATCATATATGAATATATATAAATCTCAAATAATAATTAAATAATAAAAATGTTTGTATTAAATAATGCTTGTATTGTCAGTGTGTGTAGCAGTATGTTTTAAAATAGAGAGTTAAAAATACAACTAAGCCTAAATAAGGACAACATATAAAATGAAAGCAGATTAAAACCATTGACCAATATATACAGTCCATAGTGATGTTTTAATACCTCTCTAACATTTATTTAATTAATGACAAAATAATCCGTGAACAAGTATTTATTTCTGCATTTATTTCTCTGTTCGTCGTTAGGATGGATTTTGACGACGAGGACGGCGAGGGACCCAGCAAATTTTCAAG[G/A]TAAAACCTCACACCATTTCCAGCTTTCCAAACCACCCGATTAGACCACAATCCTCCATGTCCTTTGTGTTGTGTTTTCAGTTGTTTGAGCATATCTTTCAGCTGTGTGTGTTCATCTGTCATCAGCTTATGTTTTCTTTGAGTTGGTGTTGTTTTTAAGGAGCTGTAAGTCTCGACTGACGGTTCAGCGTTAGTGGAGACACACTGACCCCTGCTGGAGACTCAGGACAAACGCGCACAAAATCCATCAGTAAACGTTAAAACTTCGGGAGACTGTCAATGTTTACTCGCCCGCATGCTTTTTCATGCTGCTGACGAACATGGGGTGATTAAATGATGATGCACAAGTCAAGAAGCAGGCACAATTAAAGTGCAAAAAATGAAAATATACTAATATAAAAAAAATCTATCTATATTTTTTTAAAGGTAAATTTTATTTAATATGATAAGAATTTAATTTAATTTAAAAGGGAAAATAAAAGCATTTTTAGTAGTATCCAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa8259
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129575 Nonsense 91 738 5 20
ENSDART00000130997 None None 586 None 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11554849)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10495205
GRCz11 7 10736845
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTTGGTCTGCGTGCAGAGAGAATCACAGCGAGATCGAGCGGCGCAGA[C/T]GAAATAAAATGACGCAGTACATCACCGAGCTGTCGGACATGGTACCCACC
Long Flanking Sequence:
ATTATTTAATTACATTATAAATAAGAAATAATTTATTAATGCTTGCTGTTATAAGTTCAAATCATTAGTTTCCTGTGAATTTCTTTTTCTATTTTAAACATTTGTTTATATAAGGAATTTTTCACAGTATTTCCTATAATTTTTTTTCTTCTTGAGAAAGTCTTATTTGTTTTATTTCAGCTAGAATAAAAGCAGTTTTTAATTATTTAAAAAAACATTTGAGGTCAATATTATTAGCCTCCTTAAGCAATAATTTTCTACAAAATTTAGAAATGTTAAAAAAATTCTACAGAAATTGGAGAAAATATGTACATGTGGGCTAATAATTCTGATTTCAACTGTACATCATATTATTATGTTTAATTAATCTATATAAAACATAAAACTAACAGTAAAGTGTTGGTGCAGTGCATGTGTCTGTGTGTTTGTGACTCTCTGCTGTGTCTTATTGTTGTTGGTCTGCGTGCAGAGAGAATCACAGCGAGATCGAGCGGCGCAGA[C/T]GAAATAAAATGACGCAGTACATCACCGAGCTGTCGGACATGGTACCCACCTGCAGCGCCCTGGCCAGAAAACCAGACAAACTCACCATCCTGCGCATGGCCGTCTCTCACATGAAGTCCATGAGGGGAACCGGAAACACCTCAACCGACGGCGCCTACAAACCCTCCTTCCTCACTGAACAGGTGAGCCATCAGCAGCTGCTGTTTTCAGGGTTGCCAGATTTTTTTTTGCTAAAGTAAAGTAGCCCAAAGGCCAAACAAACTTTATTTTTAGTTGTCCCTTTAAAGGGAACTATTATGCTTTCTTTTACAAGATTTAAAATATGATGTCCAGAGGTGGGTAGAGTATCCAAAATCTATACTCAAGTAAAAGTACTTGCAGAAATTTTTACTGAAGTAAAAGTAGCAATCTTAAAAGTTAATCGAGTAAGAGTAAAAAAGTATCTGATGAAAATATTACTCAAGTAAATAGTTAGTCGTTACTTTTCAATATATATATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20863
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
ENSDART00000129575 Nonsense 270 738 8 20
ENSDART00000130997 Nonsense 119 586 3 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11591830)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10532182
GRCz11 7 10773822
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGTTTCAGGTGTGGCAGTGCACCTTTGGATCACATCTCATTGAAT[C/T]GATTGTCCAGCATGAGAAAGAGATACAGGTATGTTTGAAAGATTCACTGA
Long Flanking Sequence:
TTCGGTTTCCCCCAAAGTCCAAAGACATGCAGTATGGGTGAATTGGGCAAACTAAATTGGCCATAATATACGAGTGTGAATGTGAGTGTGTATGGGTGTTTCCCACTACTGGTTTGTGGCTGGTAGGGCATCCGCTGTGTAAAATATATATTGGAATAGTTGGTGGTCCATTCTGCTGTGGTGGCCCCTAACAAAATAAAGGGACTAAGCTGAAGGAAAGTGAATGAATGAATGAAATTCTTAATAAAAATGTGTTAAATGCATCTGTTTTTCATTGTTTAATCTAAATCTCCTTCTTGCTGAATACGTACACAATTTTTTATTATATGTATTAACATCAGAGCCGGTCACAATTAAGTTTGGTTTTTCCATATTTTAGCTTGTAACATGAATGTATGTTTATTTTAATTTGTATTTCTTAGAGATGAGAAACTAACAATGTTTTATGTGTGTTTTGTTTCAGGTGTGGCAGTGCACCTTTGGATCACATCTCATTGAAT[C/T]GATTGTCCAGCATGAGAAAGAGATACAGGTATGTTTGAAAGATTCACTGAATCACTCAAGTCACGTATGAACTTTGGCATTAAAAAAAATGATTCACTGTACTATACGCATCACTGCATGTAATTTAGATTCTTTCAAAAAAGATTCACTGAATCTTTTTCATTACATTGTGTGATTTTGATGTGCTCAAAAATGATTCACAGAGTCATTTGCATCACATCGTCATATTATTTTGATTCTATCAAAAAAGTTCACTAAAGCACTCACGTTACTGTATAACCTTTGGTACTTAAAAAAGAAAGAAAAAAAGATTCACTGTATTATTCACATCACTGCATGTATCTTAAATTCTTTCAAAAAAGATTCACTGAATCTTTTTTATCACTTAGTGAATCAGTTTTGAGCACATTAAAACCACACGTCATTTGAATCACACCTTCTTGCTTTGTGGTTTCTAAAAAAGATTCACTGTATTATTCACATCACTGCATATTATTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15572
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
ENSDART00000129575 Nonsense 368 738 11 20
ENSDART00000130997 Nonsense 217 586 6 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11614265)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10554617
GRCz11 7 10796257
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTCCTTTCRCGCCACAATTCGGATGGCATCWTCACAKTYGTGGACCCT[C/T]GATGCATCAACGTGATTGGCTACCAACCTCAGGTCATTATCACMTTGAAA
Long Flanking Sequence:
TTATGGGTGACACCATTACATTTAATGCAATTTCAGTTAAATGCCTCTTCATGTAAAATTGCTAAACTCCTCATTTGTAAGTCGTTTAGACAAAAGAATCAGCTAAATAATTAAATGAAATGACTAAATGTCTACCCTGCCCATTCCTCAATCACACACACTCAGGGGATGGAGAATTACCCTGTTTACTTCACAGTGAAGCCACATCTTTGCATTTGAATCAAACATTACATCCATTCAGTTTAATAAATACTCTCCCACATCTTAAACCATACAGACAACTGTAACTAATGTTTTGACGATCCCATGACAGTGTTGCGCAATAAAGCATGCATCTGCTGGTTTGAGAACCAGACCATCTGTTTGTATGTAAAACTCTTCATCATCTCGTCCCTCAGGTGACCAGCTCTCCTGTTTCAATGGATATGAACGGACTTTCAGTTCCGACTGAATTCCTTTCACGCCACAATTCGGATGGCATCATCACATTCGTGGACCCT[C/T]GATGCATCAACGTGATTGGCTACCAACCTCAGGTCATTATCACCTTGAAACTTCATATTAAATGAACACCACACGTTTTTATTGAAAATATAGGCTCCTTTTACAGCTCTCCTAGAGTTAAACAGATGAGTTTTACCATTTTTTAATCCATTGAGCTGATGTTTGGGTCTGACAGGAGCACTTTTAGCTTAGCTTAGCACAATTAATTGAATCGGGTTAGACCAGGGGTGTCAAACTCAATTCCTGGAGGGCTGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTTTAGGTTTCAAACAAGCCTGAAGGACTAGTTTAGATCAAAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTTTTGGAACCGAGTTTGACACCTGTGGGTTAGACCATTAGCATCTCGTTCATAAAATGACCAAAGTGTTTAAGAAAAAAAATTTCTTAAAGCTTGACTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20864
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129575 Essential Splice Site 404 738 13 20
ENSDART00000130997 Essential Splice Site 253 586 8 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11638530)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10578882
GRCz11 7 10820522
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATGGGGACAATAAAGTGTAAACAAACAAACAAATGTTTCTTGTGAAT[A/G]GGTGGTGAAGCTGAAAGGCCAGGTTCTCTCAGTGATGTACCGCTTCCGGA
Long Flanking Sequence:
GAATGACAAACTCTTTAGCCATATTGACTTTATTTACATCGGTGTATAATTATTCAGAGACACGGAACGGAACGAAACATACAGCATAATCATAATCGAGCGAACACGAACCAACACACAAGAGCACTCTGTAAAACAAGGCGTGCCGGTCGAATTTAAAGTCCACAGAACGAAGTCCGATTGGTCCACGAGGAAATGCCCTAATGAGGAGTGACAGGCTCAGGATCCAATCAGAAGGTATCTGGTAGAGAGAAAATAGTGGAACAAAAGGTGATAGTGCGAGACACAGAGCGAATGACAGACAAGGAGAGGGACAGCGAGAGGAGAAAAGCAAAAACAGAAAGGGTGAAAGCACAGAAATACAAACTCCCACAGACCGTAATGATGTTATTGATGTTTGTTTCAGCTCAGTGTATGCAAATGTGGGCTCACAGTCCAAGACAGATTTTCCCAATGGGGACAATAAAGTGTAAACAAACAAACAAATGTTTCTTGTGAAT[A/G]GGTGGTGAAGCTGAAAGGCCAGGTTCTCTCAGTGATGTACCGCTTCCGGATGAAGAACCGAGAGTGGATGCTCATCCGAACCAGCAGTTTCACCTTCCAGAATCCTTATTCAGACGAGATTGAGTACATCATCTGCACCAACACCAACGTCAAGTAAGTCCAACCTTCTCACTAAATGATAACATTCAAAGCAATACACAAACAGGCTCTTCTGATTGGATAGTTTGTGGATTTTGCAGGGGTCAAACATAACCTCGTGACCAATCTTGAGACATCTGGGCCTCCAGAGAAATCGATACCATTTATTTTTGTGTTTAACCATTCTGGTATAGGTGTCTGTTCGTCTGGTGTTGGAAGGATATGTTTGATTTATGCCAACATCTGTACTCTGAACTTGATGATGTACATTTAAAGCAGGTTGTATTTGCTTTGCTTTCAGAGGATCTTTAGGGATTGGCTTTTATTTATTTATTTTTTATGGTTGGTGTGTCTAAGAAGGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26893
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129575 Nonsense 510 738 15 20
ENSDART00000130997 Nonsense 359 586 10 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11663619)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10603971
GRCz11 7 10845611
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAAAGCATCGACAAGACTGAATCTCTGTTTTCACAGGAGAGAGACCCA[C/T]GATTCAGCGACATCTACACCGGCATCTCTACATGTATGAGCTACAGCGCA
Long Flanking Sequence:
GAGCGAGTTGGATTGTAGCAAGACAGGAGGTTGGCTAGATAAACAGGAGCTAGATTATTTAAAGCTTTATAGGTAAGAAGCAATATTTTAAAATCTATACGAAACTTAACAGGCAGCCAGTGTAAGGCGGATAAAATCGGGGTGATATGATCATATTTTCTAGACCTGGTACGAACTCTGGCTGCTGAATTTTGCACTAACTGAAATGAAATGAAATGAATTGAAGTTCGGATATATCAAGAGACATTTCTGATGATATTAAATGTTTAAAAGCTGCTTAATATTTTACTTAAAATGTAATTCAGGCTTCTTACATGAAGAGAAATGTGGCTATATTTATTTGTTTATTAAATGTGTCATTTTGCATGTATCATCATAATTTTTACTGACAGTGTTTACTGATCTTGCAGGTTCCTGTGTCCGGTGTTTCAGCCGGTGTTCATGAATCCGGCAAAAGCATCGACAAGACTGAATCTCTGTTTTCACAGGAGAGAGACCCA[C/T]GATTCAGCGACATCTACACCGGCATCTCTACATGTATGAGCTACAGCGCAAATTTAACATGCAATTCACTGGAGATTCAGCTAATTCAGTTAAAGTCTCACAAATACAATTCCTGCATGATTTACACTGTAAACACTGTATGTTTGGTGCATTTGGTTGCTATTACAAAGAGTTTGCAAGACAATTAAGTCAGAAATTCCAACTAAAATAGGTCAGATTGAGCTTCTGAGGGTTTCTAGCTTGTAAAAGTCTGTTGTTTCTGGTTATGCACTGATTCAGTGTCAGTGTTTGCCAGTTATTGGCTTATTCCTCTGTAGTTTGGGCTCTATATTATTTACAATAATAACAGTGCTAATAAAATAGATATATGTTGTTGTGCAATTTTTTTTAAACCCATGCAAATCTATAAATCACTGCCAAAAAAAATAATTTATATGTGTATGTGTGTATATATATATATATATATATATATATATATATATATATATATTATAGTTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11162
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
ENSDART00000129575 Nonsense 524 738 16 20
ENSDART00000130997 Nonsense 373 586 11 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11665279)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10605631
GRCz11 7 10847271
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCTCNNNGATGATGTWTTGTGTGTKTTTATGTGTGTTCAGCTGAAAAG[A/T]ARATGATGGTTCCCTCATCCACCTCTGGCGGGCAGCAGTTGTATTCTCAG
Long Flanking Sequence:
TAAATATTGGGACATCAACAAAATTCTAACATTTTAGGCTCTATACAACAACACAATAGATTTGAAATGAAAAGACTGAAAATGAAATGAAATGAAAGACTGCAGTCTGTCAGCTTTAATTTGAGGGGATTTAAATCCAAATCAGGTGAACAATGTAGGAATTACAACAGTTTGCATATGTGCCTCTTACTTGTTAAGGGGCCAAAAGTAACGGGACAGTTGGCTTCTAAGCTGTTCGATGGTCAGGTGTGTGTTATTCCCTCATTATGCCAGTATTTTCCCAATATTTATGGACCTAACTGTATATACGTCCTCTATTTTTGTCTTTATTCTTGTCAAATCATGTAGATTGTAGTATTTGTAAAATTAGTTTATTTTACAAATTTATTGTCTCCTCTGTGTGATCCCAAAGATAAAGCTGTAATGTGATGTTTCTCTGTCATATTTGAGCTTCTCGATGATGATGTTTTGTGTGTTTTTATGTGTGTTCAGCTGAAAAG[A/T]AGATGATGGTTCCCTCATCCACCTCTGGCGGGCAGCAGTTGTATTCTCAGGGCAGCCCGTTTCAGCCAGGACACTCCGGAAAGAGCTTCAGGTACACATTCAAAATCTGTGCGGGACTGAATTTTTAGTCCCGATCCCATCAGGTTTTATTCCACACCCGACTGCTCCCGCTGTATATTCATCCTTTGTTCACCCGCTGCCCGACCCTCCCCGTTTTCTACACAACCCGACAGTTTCTGCCTAAATTTAGATCTGGTTTCCAAAATCTCACATTTAAATTAGGCACTACCAAAAGAGAGAGAGATAACAGATAAATGCGTAGGTTGTGCAAGGATTGCAGGCTAAATGTCAGTTTTGTTTGCCTCTTTGTGATGAGACATGAGTGCTGCCTTAAGCAGTGACGTTTGGTGAGGTTTGTGGTTGGTGAGGCACTACCTCTTTCAAAGTCAGATTTACAAACATATCCACTCAATATGTTTGCCAACTACAGATTGTGTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20865
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129575 Essential Splice Site 658 738 None 20
ENSDART00000130997 Essential Splice Site 506 586 None 15

The following transcripts of ENSDARG00000058449 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 11672899)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 10613251
GRCz11 7 10854891
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCCGGAAACGCCTACTCCAACCTCGCCAATCGCAACACTGCTTTCGG[T/A]AAGAAAATCTGCTCATTCATTATAATACATGACTACATTGCTCATTGATA
Long Flanking Sequence:
GCGGTTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATAAATATATATATATATATATATATATAACTATATATATATATATAACTATATATATATATATATATAAAACTATATATATATATATATATATATATATATATATATAACTATATATATATATTTATACATATATATATATATATATATACATACACATATAGACTGAAGCTGTGGATCTGGAGTTTAGCCTAATAGGTCTAATATGGTCTCTGTTAGATCTATGTGTTATATCTCTTCATGTCTCTTGTCGTTCCTTCAGCAGCAGATTCCCGCTCAGTCTAATAAGGCTCAATCGTCTCCATTTGGCATCGGCTCCAGTCACAGCTATCAGGCAGACCCGTCATCCTACAGCCCTCTGTCTAGCCCCGCCACCTCCTCGCCCTCCGGAAACGCCTACTCCAACCTCGCCAATCGCAACACTGCTTTCGG[T/A]AAGAAAATCTGCTCATTCATTATAATACATGACTACATTGCTCATTGATAACCATGCATTATCCAAGAAGTTACTTCCAGGAACATTAGACTCATTGAAATCCTAATTTTATTATTGTTTTTGAGAGAAATAGAAATCTAAATGCGAAATGAAATCTAATTTTCCTTTTTAATGATGGTTCTTAAATGTTTTTGTAGCATTTTAGTTTTTAATACTTACTATTTATTTAGTTTTTAATAATTTTAATACTTACTATTTCTGATTTCAAGAGATATTGGGATCTCAATGTTCAAGTTGTAAACATTTTGTTGTTTAAAATGCAAATAATCACTGTACATGAAGCTAGTACTTTTTATAAAAAAAAAATGAATGTCTGGAAGATTAATAATATTGAAACTTGTCACGTTTACTTTCATCAAAACAGCTGCAAGAAACATACTCCAATTAATGTAAAAAAAAATTACATTTTCAATGTTTGCAGAGCCTTAACTCTGGAAATG
Associated Phenotype:
Not determined