Busch Lab

ZMP

LOC100334568

Ensembl ID:
ENSDARG00000056806
Human Orthologue:
PDE5A
Human Description:
phosphodiesterase 5A, cGMP-specific [Source:HGNC Symbol;Acc:8784]
Mouse Orthologue:
Pde5a
Mouse Description:
phosphodiesterase 5A, cGMP-specific Gene [Source:MGI Symbol;Acc:MGI:2651499]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa8885 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa19451 Nonsense Available for shipment Available now
sa39571 Nonsense Mutation detected in F1 DNA Not yet available
sa45068 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32625 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32624 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30581 Nonsense Mutation detected in F1 DNA Not yet available
sa32623 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa8885
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079359 Essential Splice Site 315 922 2 21
Genomic Location (Zv9):
Chromosome 1 (position 13158074)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13586816
GRCz11 1 14273329
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATGTAGTCAGGACTGGGAGACCTCTTACCGTCAAGGATGCCCATGAGG[T/C]ACAGTAYGAGGGATGTTCTTGTCTAAACCTTCTCYAAGTCATTTCAGGTC
Long Flanking Sequence:
ATCTCGAGCTCTCGTCCACCCTGTCACGATGCAAAGACCACAGTCCTGCCTCTCTGTCCATCAGACTGATCATCCTGAGAGTTTGGACCAGGGCGGAGGTCATTTTCCTCGATCATTACAGCCTATACACTTTACATTTTCACCCTGTCGGTCGAGATCAAGGTGTTCAAGTTTTCTGGGCTCCCCAAGACCTGCGGGACAGTGTAGAAGAGGCGAGTCCTGTGCCTTCATGATGCAGCTCTTCAGTGGTCTGATTGGAGCTCTACAGGACAAAAACCTGCATCTTCAGGTCCTGCAGCACCTCTGTGAGGTCACTGAGGCTCAACGCGTCAGTCTCTCGATGACAACGGTAGACAAAACAGGTGGAAAGTGTTTAGGTCCCGTCCTTCAATCAGATGCAGACTCTGTTCACAGCAACGCACAGACCAAATGGAACAAGTCCATTATGGAATATGTAGTCAGGACTGGGAGACCTCTTACCGTCAAGGATGCCCATGAGG[T/C]ACAGTATGAGGGATGTTCTTGTCTAAACCTTCTCCAAGTCATTTCAGGTCACTGATGAATGTCCAGGATTTCCCTTGTAACAGAAGTGCTAATTGCTCAGTCATTTCAGGACAGATCTAAAGTTCACTGCCCTCGAAACAGAGCGTTAATTCAAGATGCTGTACTGTACACTTTCCTAATGAGGCAGGTTATTCAGAGCTCATCTAGAGCTTTTAACAGTTTAACTTCTTTAAACCTGGAAGGACTTGAATGGTCTTACTAAGGTCATACAGTAGTAATGGTAAATGTGCAAACAAATACTCATATAGTGACATCACAATGGCATTTTTTAATTGAGCATTTTGTATTAAAGAGGCAAAGTAGGCCTATATTTAGTGCTGTTGTTTGTAATTTATATTACATTATTGCAGTTTTGGAGGATGATAATGTTATAATATATGGATAAAAAAGCTGTAAGCTGATATATAGATCAATATGGAATCTGCTTATACCATACTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19451
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079359 Nonsense 413 922 6 21
Genomic Location (Zv9):
Chromosome 1 (position 13151868)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13580610
GRCz11 1 14267123
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGATTGACAGGTGCTGTTGGAGTTGGCTCAGCTGGTGTCACATGACTA[T/A]CCATCTGTGGACGCCATGCTCGGTGAACTGGCTGCCGTTATTCTACCAAT
Long Flanking Sequence:
TTTTATAGCATTGATATTGTGTTGTAATTAAAATACAATCAGTTAAATAAACTTTAGCATTATTTAGTTGTTTAAGCATAAAATGAGATGAAAGACAGTGTAACTGCTAGCGCCGTCAGTAGCAGGAGGCTAACCAAGAAACTCCATTGAAAATACTGGGGTAAAATAAACTGTCATATTTTAAAGACATGGCAGGGGAAATGTAGTTTAAAGCAGTGCTTCTTGTTCGGTCTGAGACCCACTTCATATTGAATATCTATCAGGCAGTGAAGATTCCTGAATTTTAAGGAAATCAGACCTTAAACGTGGCAATTTTATCATGGAAAGAGTTCACCGGAAGCCCTGAGGCTGGCTGGCTGGCTGAAAATGAAAAGCCCATGTGCAAACACCCCATTGTTACTTTAAGAACTCCTCATAAAATTGATCCTTTTTATAATTCACTGTTGTGGATTTGATTGACAGGTGCTGTTGGAGTTGGCTCAGCTGGTGTCACATGACTA[T/A]CCATCTGTGGACGCCATGCTCGGTGAACTGGCTGCCGTTATTCTACCAATTACAAAAGCACAATTCTGCACTGTTTTCATTTCAGATGACAGCTCCACGGTAGTACACAAGTCAATACAATTAATTGGATGATTGCTAACTTTTAAAACCAAAAAGGATTTGTTTATTTGCATGCTTATAGTAATGGTTTTAATCTTGTTGTCCTAAATAATCTTCTTATATGAACTACTAAGAAGCTGATACTGATAGATTCTTATTTATTGTTGACTTGCAGAGGCTTTTCTCAAGGATGGTCCGTATAGAGTATGAGGAAATCGAATGTTCTGTTCATTGTTCCTCAAGGTAAGTGAAATAGGGTTTCTTAAATCTTAATTCATTAGCTTTTAGACAATTTGTCCTCATAAAGGACTCAAATTAGAGCAGGAGGTATTCAGTGTTGTATTTTTTGTGTTGTTTTTTAGTACAATCAGTAGAGTTAAATTTAATAGAGTTAAATTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39571
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
ENSDART00000079359 Nonsense 485 922 8 21
Genomic Location (Zv9):
Chromosome 1 (position 13149421)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13578163
GRCz11 1 14264676
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGGATTGTGACACTGACGACGTCAGCTACATCTATGCAATGCATGTG[C/T]AAAACTCAATGGAGACGCTCAATATTGTCAACCGGCCTGTAAGTTGATTT
Long Flanking Sequence:
ACATGCGCTATAGATGAATCAGGTGAAATGAATAAACTAAATTGTCCGTAGTGTATGAGTGTGAATGAGTGTGTATGAATGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAACATATGCTGTAATAGTTGGCTGTTCATTCCACTGTGGCGACCCCTGATGAATAAAGAGACAGAAGGAAAATTAATGAATGTATTCTTTACTTGGTTTTAAAAAGTGTTGAATTGGCTTTACTTACAGAAAGCGAGGCAAAAGTACATCATCATTTGTTCACAATTACCAAAATAAGAGTTAGTTTGTTTTGATTGAGCCCATTATGTTGAAAATAACACAGAGTTCAGTATTACTTATTTAGCAAACCAAAAAAGAATGTACTTTAGTGTACTTACGCATACAGTGAATTTTTAGTAAGTGTAAAATATGCAACTCTTGCCTTTTAGGGATTGTGACACTGACGACGTCAGCTACATCTATGCAATGCATGTG[C/T]AAAACTCAATGGAGACGCTCAATATTGTCAACCGGCCTGTAAGTTGATTTGATTGATTCGTTTGCTATAACTTAGGAATTTCAGTAGAAGTATAGGTAAAGATACTTTTCCTAATTTATTAAATTAGATCACGTGTTAACTTTGAAACCTGTGACTGCTTTTTTCATAGTTTTTCTTCCTTTTTTATTAATCTTGTTTCCTGGAAAACCATATCAGCATTTGACCAAAAAGTACCTCATATGTGGGATTTTCCATGTTCGTACGTGACATGTGCTGTTTTTGTGTGTTCTTCAGATTTCCATGGTCTCTCCGATTAGAAGTTTGATTGGTGCTCCTCTGAGAGGCAAACAGAGCAGTAACGTCATAGGTAAATATTCACATTCTTATATTGTTCTGTCGAACCAAAGCCATCATGATTTCCCACAAGAACATCTAGCTCAAGTCGTTCTCTTTTATAACGAGGGAGATAATATTATATTATACTGCATACTGAGAGGATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45068
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079359 Essential Splice Site 688 922 14 21
Genomic Location (Zv9):
Chromosome 1 (position 13145320)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13574062
GRCz11 1 14260575
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGCTTTTACACTCAGCGCGATTACTTAATATTTCTTGTGCTTTAATCC[A/G]GAGCAATTTGAGCAGTCTGGAGGTTCTCGCGCTCATGATTGCCAGTCTGA
Long Flanking Sequence:
TGACTCAGGCTGTCGTGCGCATGTTTCTGGATCTCAATTTGCCACAGGAATTTAAAATCGATTACAAGGTTTCAAGTTGAATCACACTTTTATAACCAACGTCACAACAATCAAGCCTTGAGTAACTCTTGTGTAAGCAGTGGATCTAGAGTTTTTGTATGTCCGTTTGTTTTTCAGGCTTTGTGTCAGTGGGTTCTGAGTGTGCAGAAGTGCTACAGGAGCAATGTGGTCTATCATAACTGGAGTCATGCACTGCGCACCGCTCAGTGTATGTTTGCAATGCTGCAGACAAAGGAACTAAAGGTCAGTCTGTTGATAAGAGACTAGTTTAATCTCTTAAACCCCAGTAGTGCATGCTGGGTTAATAAGTTAAATGGTTTATTCTTTGAAAATTGGATTAGGCTAATTATTGGTTAATTAATCCCTGTCCTGACAAATCTCTGATATTTCGTTGCTTTTACACTCAGCGCGATTACTTAATATTTCTTGTGCTTTAATCC[A/G]GAGCAATTTGAGCAGTCTGGAGGTTCTCGCGCTCATGATTGCCAGTCTGAGTCATGATCTTGACCACAGAGGTGTGAATAACTCCTACATACAGAGGTAAATTCTGCTATTCCTACCAGAACTCAATTCTGACTATGGTGGCATTATAAACACCTGTCTAAAGTTCATTAATGCTGTGCAGCTTCATTTGACTGGTTTTGGAGCCATATTTAAATACTGCGTATATCCGCTTGTTAAGTGTGACGTCACGCAAAGCGGCTTTCGGATCCAAGTGCTCAATCTCACTGAATGGCGAGAGTCATCAAATGGTAATAATAAATGTTTACAAAGCCATGTAATACTTTCGAAAATCACGATCGCAATATATATATATATTTGTATATATGTCCATGCCTAATATCTGATGGCCAGAAAGGGATACATTTTTTATAAAATGGTAAAATTTAGCTGTTTGTGATGCAGCAAGTCCAGAGATTGTTATGTACACTATGAATTTATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32625
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079359 Essential Splice Site 748 922 15 21
Genomic Location (Zv9):
Chromosome 1 (position 13144533)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13573275
GRCz11 1 14259788
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCGAGCACCATCATTATGACATGTGCCTTCTCATTCTTAACAACCCTG[T/C]AAGATCATGTAGCATAAATTAATCCATCCATCCATCCATCCATCCATCAT
Long Flanking Sequence:
GAATGGCGAGAGTCATCAAATGGTAATAATAAATGTTTACAAAGCCATGTAATACTTTCGAAAATCACGATCGCAATATATATATATATTTGTATATATGTCCATGCCTAATATCTGATGGCCAGAAAGGGATACATTTTTTATAAAATGGTAAAATTTAGCTGTTTGTGATGCAGCAAGTCCAGAGATTGTTATGTACACTATGAATTTATATAAAATTCCCTTTAAAGTGTGATAGGACTAATAAGTGGTCATAAACCAATATTTTCTCAATTCAAATGAGTAGCAGCTTGGACCTGGAAACAGTATTACACACGTCACCGATACGATCACGATACCGTCACGACTTAACAAGCGGATTATGTTTAAATTGACTCAATTTTATTTCATCCTTTCTGTTGTTTGTCTTAGGAGTAACCAGCCTCTGGCACAACTGTATGGTCAATCCTCCCTCGAGCACCATCATTATGACATGTGCCTTCTCATTCTTAACAACCCTG[T/C]AAGATCATGTAGCATAAATTAATCCATCCATCCATCCATCCATCCATCATTCCATCCATCTCAATCCTCATATCTTGCTATCTTCATCCATCTACCCATGCATCCATCCCCCATCCATCCATCCATATGTTTATTAATTCATTCATTTGTTTCTCCATCTATGCATACCCTTTTGTTTGTCTGTTCTACCATTTCTCCATACATTCATTCATCCACTCTGATTTTTGTAAAAATGTCTATTCAGTTCATATTCTCCCCCCACCCATCAATCCATCCTTCCATCTGTTTGTCCATCAATTCCATCCTTTTAGTTGTTCATCCTTACATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATTCATCCAACTGTGATCCACTAATTGGTACATTTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32624
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079359 Essential Splice Site 808 922 17 21
Genomic Location (Zv9):
Chromosome 1 (position 13142882)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13571624
GRCz11 1 14258137
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAATAACAGCTGTCTGTGGAAGGATGAAGGACACAGAGAACTCCTAAG[G/A]TACAAACATTTTAAATAACAATAACGCACAATATTCAAACATTTACTCAT
Long Flanking Sequence:
TATATTTGTTCATCTATCCAATTATTCATTCATCCACTTAGATTTTTGTAAAAAACATCTATACATATTCTATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATCCATCCATCCATCCATCCAATACTTTTGTCCTTACATCTATAATTCTCTTTATTCATATATTGACGTCCATGCGCATCTGTTCCATATATATCTCGCTCTTCTCTCTCAGGGCAGTCAGATTCTCAGTTCACTCTCAGTAAACGAATACATGGCCTGTTTGCAGATGATTGAGAAGAACATTCTGGCAACAGACCTTGCCATTTTTTTTGAGTAAGCTTATTTTTCTTTCCAAATCAAGCTGTAAACATGGATGTACAAAGAAAATATTAATGTGCTGAGTGTTTGTGTTTTTACCTATAGGAAGAGAACTAAATTCTTCAAACTTGCTGAGAATAACAGCTGTCTGTGGAAGGATGAAGGACACAGAGAACTCCTAAG[G/A]TACAAACATTTTAAATAACAATAACGCACAATATTCAAACATTTACTCATACAAACCACTATAAATCTACATATGTTGCTTATGACACTTACACATAGTAATTTTTTGCCTGTTTGCGCCGATCTGCAGTCATTTTATCTACAATAAGAAAAAAACAGCATGAAAACAGGAAACCCCAGCCACATTTGCTTGCTTATGACCACTTCCTGCTTCTATATTAACTGATGTTCTTGTTGTAAATAGGTCAATGCTAATGACAGCGAGTGACATATGTGCAATAACCAAACCATGGCCTGTTCAGAAGCGGGTGAGCATCTCCCACACACACATTCACGTGCGTGCAGATGCACTACAACCACGCATGCATGCAAACACACACACACACACACACATACATGCACATACACAAATGACTCGTTCTTTATCTCAACCTCAACAGATCGCTGAGCTTGTAGCAACTGAATTTTATGCGCAAGGAGACAGAGAGAAGCGTGAACTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30581
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079359 Nonsense 839 922 19 21
Genomic Location (Zv9):
Chromosome 1 (position 13142413)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13571155
GRCz11 1 14257668
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTATCTCAACCTCAACAGATCGCTGAGCTTGTAGCAACTGAATTTTA[T/A]GCGCAAGGAGACAGAGAGAAGCGTGAACTCAACATTCAACCCATTGTAAG
Long Flanking Sequence:
GGAAGGATGAAGGACACAGAGAACTCCTAAGGTACAAACATTTTAAATAACAATAACGCACAATATTCAAACATTTACTCATACAAACCACTATAAATCTACATATGTTGCTTATGACACTTACACATAGTAATTTTTTGCCTGTTTGCGCCGATCTGCAGTCATTTTATCTACAATAAGAAAAAAACAGCATGAAAACAGGAAACCCCAGCCACATTTGCTTGCTTATGACCACTTCCTGCTTCTATATTAACTGATGTTCTTGTTGTAAATAGGTCAATGCTAATGACAGCGAGTGACATATGTGCAATAACCAAACCATGGCCTGTTCAGAAGCGGGTGAGCATCTCCCACACACACATTCACGTGCGTGCAGATGCACTACAACCACGCATGCATGCAAACACACACACACACACACACATACATGCACATACACAAATGACTCGTTCTTTATCTCAACCTCAACAGATCGCTGAGCTTGTAGCAACTGAATTTTA[T/A]GCGCAAGGAGACAGAGAGAAGCGTGAACTCAACATTCAACCCATTGTAAGTCAACCATCCTATTTCATCATTCTCTTTATACAGCAAGACAAGTAGCTTCAGATAAGTGTTGCAATCAGTTTGAATAATACGTTGAATCTCTTTCTCACAGGATGTGATGGACCGTGAAAATGCGTCTCGCTTACCTCAGATGCAGGTTGATTATATTGACGGGATTTGCTCACCGCTCTATGAGGTGAAGGCCTGCCCGCACACATCCTGTTACAAATGTGTGTCAGTGTGTGTGTCTAGTGAGACATTTCTGCTGCATTGCTGTGCCTCTGGGTGTTTCAGAAGAAGCAGAAGGTCTGTAGTGTGTTTACAGTTTCTTTGTGTCTGTTTTTTCAGGCCTTGGCTTTCATTTGTGAGTCCTGCTCTCCTCTGAAAGAAGGTTGTAGCAAGAACAGAAAACACTGGCAAGAAATGGTGGACGATAGAAAGGAGGACAACATTAAAGAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32623
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
ENSDART00000079359 Nonsense 920 922 21 21
Genomic Location (Zv9):
Chromosome 1 (position 13141914)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 13570656
GRCz11 1 14257169
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTGGCAAGAAATGGTGGACGATAGAAAGGAGGACAACATTAAAGAA[C/T]AAGAAAATTAAAAATATAAGCAAGTTAAAACTGAAATCCATCAAGAAAGG
Long Flanking Sequence:
ATGCGCAAGGAGACAGAGAGAAGCGTGAACTCAACATTCAACCCATTGTAAGTCAACCATCCTATTTCATCATTCTCTTTATACAGCAAGACAAGTAGCTTCAGATAAGTGTTGCAATCAGTTTGAATAATACGTTGAATCTCTTTCTCACAGGATGTGATGGACCGTGAAAATGCGTCTCGCTTACCTCAGATGCAGGTTGATTATATTGACGGGATTTGCTCACCGCTCTATGAGGTGAAGGCCTGCCCGCACACATCCTGTTACAAATGTGTGTCAGTGTGTGTGTCTAGTGAGACATTTCTGCTGCATTGCTGTGCCTCTGGGTGTTTCAGAAGAAGCAGAAGGTCTGTAGTGTGTTTACAGTTTCTTTGTGTCTGTTTTTTCAGGCCTTGGCTTTCATTTGTGAGTCCTGCTCTCCTCTGAAAGAAGGTTGTAGCAAGAACAGAAAACACTGGCAAGAAATGGTGGACGATAGAAAGGAGGACAACATTAAAGAA[C/T]AAGAAAATTAAAAATATAAGCAAGTTAAAACTGAAATCCATCAAGAAAGGAAGCGGGACTCTAAGTTGTGTCTGATATTCAGATTTTAGTAATTATTTCTCATTTGCAAAGATGAAAAATGGTGCAACTGTATAACACATAGTCTTGAAGTATTAGGAAACTATCATAATCACTGGTGTCATGCTCATCTATTCTTGATCTTTACGTTTTTTAACATTACACAAAGTTGACCAGCTTTGTCATACTCGTGGATCGATGAATAAAAATAAATGAATAAATCATCATTTATTATTTTTAATATTGTGTTGAAATGTTTCAGAAAATATATTGATAATCTTTATGCTTTAAAATAGGATCACTTTTAATTCAATTGTTTTGAAAAGCTGATGTTGTTGTTGAAGGGATTTCCAATAAAAATATATATATTTTAATAAAAAAAACATTGCAATGATCTCTCTGTTGAGTTTTTATAAAACAAGTTAATAGTGTTGTATTTATTG
Associated Phenotype:
Not determined