Busch Lab

ZMP

ENSDARG00000018566

Ensembl ID:
ENSDARG00000018566
Human Orthologue:
FLNC
Human Description:
filamin C, gamma [Source:HGNC Symbol;Acc:3756]
Mouse Orthologue:
Flnc
Mouse Description:
filamin C, gamma Gene [Source:MGI Symbol;Acc:MGI:95557]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa24724 Nonsense Available for shipment Available now
sa38132 Nonsense Mutation detected in F1 DNA Not yet available
sa39492 Nonsense Mutation detected in F1 DNA Not yet available
sa6812 Nonsense Mutation detected in F1 DNA Not yet available
sa18138 Nonsense Available for shipment Available now
sa15040 Essential Splice Site Available for shipment Available now
sa38133 Nonsense Mutation detected in F1 DNA Not yet available
sa38134 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24724
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
ENSDART00000046218 Nonsense 53 2719 1 48
Genomic Location (Zv9):
Chromosome 25 (position 36081461)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34515729
GRCz11 25 35020687
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGACGCGCCGTGGAAGAAGATCCAACAGAACACCTTCACCAGGTGGTG[C/A]AATGAACACCTCAAATGCGTTAATAAGGGCGTCACTGACCTGCAGAAAGA
Long Flanking Sequence:
TCATTTCAAACAGAGTTTCACTCCTGCAAACTGCGCAGAGACTTTTCCTATCTGAAGAAGAAAAAAAGTGATATTCCTCCGAGTGTCCATTAAGAAGAAGCGACTACATTCAGCAAGGGGTTGAGAATTAAAAACGCGAGGCCGACCGCCTTGTAAACCGTAAATCGGATAATCTATCATCGTCCTGACAGAAGATCACTTTTCGCAAGTGTCCGCGAAAGCTCGTCTGTTTTTCTGCAACTTTTTGATCTGCTGAACGGCGCGCGCGCTCCTGACACTCACGCGCAAAAGTGACGAGCTGCGAACTTCCAGCGTTATTAGTATAAAAGCAGCAGTCCCACCATGAGCAATTACACACATTTAGACGACCTGCCGCCGCAGTATTACCAAGGCACAGACCTTGGAGAAGAGGAAGAGGAGGAGATGCCGGCGACCGAGAAAGACCTGGCCGAGGACGCGCCGTGGAAGAAGATCCAACAGAACACCTTCACCAGGTGGTG[C/A]AATGAACACCTCAAATGCGTTAATAAGGGCGTCACTGACCTGCAGAAAGACCTGGGCGATGGCCTCAAACTCATCTCGCTTTTGGAAGTCCTCAGTCAGAAGAAAATGTACAGAAAACATCACGTCAGGCCAAACTTCAGACAGATGAAGCTGGAGAACGTGTCGGTGGCGCTGGAGTTTCTGGACAGGGAGAGAATCAAACTGGTGTCAATAGGTAAGATCTGCTCATCTTCAGTCTAACTACTGTTTGTGATAACAAAATATTAGCAAATTGAGAGTTTATTGTAATTGTGATTCAAGTTTTCCCGCTAAATTATGCTTTTGAATTGCATTATGGGATCTTTATCTTTTCTAAGTTTTTAATGTTGACATAATGATAAGCCGTTATTTTCTGTTAATATACATACTTAATTCTCTATATATTATTTGTTAAACTACATATCGTCTCAAACTATTAAAAAAGTCACGCTTTGAGAGTTGAGATATTTTGTCAATGTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38132
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
ENSDART00000046218 Nonsense 91 2719 1 48
Genomic Location (Zv9):
Chromosome 25 (position 36081573)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34515841
GRCz11 25 35020799
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCAAACTCATCTCGCTTTTGGAAGTCCTCAGTCAGAAGAAAATGTAC[A/T]GAAAACATCACGTCAGGCCAAACTTCAGACAGATGAAGCTGGAGAACGTG
Long Flanking Sequence:
GCAAGGGGTTGAGAATTAAAAACGCGAGGCCGACCGCCTTGTAAACCGTAAATCGGATAATCTATCATCGTCCTGACAGAAGATCACTTTTCGCAAGTGTCCGCGAAAGCTCGTCTGTTTTTCTGCAACTTTTTGATCTGCTGAACGGCGCGCGCGCTCCTGACACTCACGCGCAAAAGTGACGAGCTGCGAACTTCCAGCGTTATTAGTATAAAAGCAGCAGTCCCACCATGAGCAATTACACACATTTAGACGACCTGCCGCCGCAGTATTACCAAGGCACAGACCTTGGAGAAGAGGAAGAGGAGGAGATGCCGGCGACCGAGAAAGACCTGGCCGAGGACGCGCCGTGGAAGAAGATCCAACAGAACACCTTCACCAGGTGGTGCAATGAACACCTCAAATGCGTTAATAAGGGCGTCACTGACCTGCAGAAAGACCTGGGCGATGGCCTCAAACTCATCTCGCTTTTGGAAGTCCTCAGTCAGAAGAAAATGTAC[A/T]GAAAACATCACGTCAGGCCAAACTTCAGACAGATGAAGCTGGAGAACGTGTCGGTGGCGCTGGAGTTTCTGGACAGGGAGAGAATCAAACTGGTGTCAATAGGTAAGATCTGCTCATCTTCAGTCTAACTACTGTTTGTGATAACAAAATATTAGCAAATTGAGAGTTTATTGTAATTGTGATTCAAGTTTTCCCGCTAAATTATGCTTTTGAATTGCATTATGGGATCTTTATCTTTTCTAAGTTTTTAATGTTGACATAATGATAAGCCGTTATTTTCTGTTAATATACATACTTAATTCTCTATATATTATTTGTTAAACTACATATCGTCTCAAACTATTAAAAAAGTCACGCTTTGAGAGTTGAGATATTTTGTCAATGTCAATCTTATTTATATAGCACTATTAAACACAACCAAAGGTTGAACAATGTGCTGCACAATATAAATCACAAAGAGAAAGATAACAAATTAAAGCTAAAACAAACAATTCTCACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39492
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046218 Nonsense 192 2719 2 48
Genomic Location (Zv9):
Chromosome 25 (position 36085102)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34519370
GRCz11 25 35024328
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAGAACAAAGTGCCAGAGCTGCCTATTAACAACTTCAACAAGGACTG[G/A]AGGGATGGCAAGGCTCTTGGCGCCCTAGTGGACAACTGTGCCCCTGGTAA
Long Flanking Sequence:
TTTTGGTGGATTTACTTGAGAGCAGGCACTCGTGAGAAAGATTTGAGATCTAAAAAAAAAGGTGCACAGTGGCCTTTGGCAGATTCGTGAAAACGTAACATAGCAGTTATTGCTGGAAATTTCCAAAGTACCAGCCATTTTGTAAATGTAGAATCATCTGTTGAGTACACTGGCATCCCAACTATTTGAAGTCTTCTCATGATTGGAAAGGATGTCAAGTTGACCGTAGAGTTTGTCAGTTTGTTAAGTAACATGGATCCATTTGCCCAAACATTTTTCTTGCCTTTGACCTTTATAGACAGCAAAGCCATTGTAGACGGGAACCTGAAGCTGATTCTGGGTCTCATCTGGACGCTTATTCTCCATTATTCCATCTCCATGCCCATGTGGGATGATGAGGACGACGAGGAGGTTAAGAAACTGACTCCCAAACAGAGATTGCTGGGCTGGATTCAGAACAAAGTGCCAGAGCTGCCTATTAACAACTTCAACAAGGACTG[G/A]AGGGATGGCAAGGCTCTTGGCGCCCTAGTGGACAACTGTGCCCCTGGTAAGCAGACATTCTCACATTATCAGGTGTAGCTGCTTGCTTGGTTTGACCTTGGGCGGTTGTGATTAGGTGAGGCAAACATTTCATGTTAAACCTTGATCATGTTACGTTTAGCTTGTTTGTTATAGAGTTTAAAGAGATTGTTCACACAAAAAAAATAATAAAAACAGACCATAATTCTCATATTTGGATGGAAACATAGCTAATATGTAACGGTTACCAGTGTTCTTCAAAAATAAGCTCAGAAATGTTTGGACCCACTTGAGGGTGAGTAACTGAGCATGTTTTCATTTTGGGGTGAACTATTCCTTAATATGCCAGTGCACTTGAGCCTTATTTAGTTACTGAAACTCATTCATGACCTGCTTCCTGCGCCACTCTTTGGTCGCAGAGGACAGGGTAGTGAACTAAAGTGTTTACTTCAGTGCAGCTGATATGAAACAGTCCCTGTGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6812
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046218 Nonsense 216 2719 3 48
Genomic Location (Zv9):
Chromosome 25 (position 36085855)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34520123
GRCz11 25 35025081
KASP Assay ID:
554-4147.1 (used for ordering genotyping assays)
KASP Sequence:
CATATAACTTTAACTCTTTATGTAGGTCTGTGCCCTGACTGGCAAACATG[G/A]GACCCCAACCAGCCWGTGGAAAATGCTCGTGAGGCCATGCAGCAGGCCGA
Long Flanking Sequence:
TATGTAACGGTTACCAGTGTTCTTCAAAAATAAGCTCAGAAATGTTTGGACCCACTTGAGGGTGAGTAACTGAGCATGTTTTCATTTTGGGGTGAACTATTCCTTAATATGCCAGTGCACTTGAGCCTTATTTAGTTACTGAAACTCATTCATGACCTGCTTCCTGCGCCACTCTTTGGTCGCAGAGGACAGGGTAGTGAACTAAAGTGTTTACTTCAGTGCAGCTGATATGAAACAGTCCCTGTGCGACAGTCATGACCATACAGGGTGCTGCTGGCTTTTGACAGATCACAGCATTACAGTTATCTTTGTACATTTAGGCTACAGTATATGTTTCTTTAGATGGTTTTTCTAAACAATTATTAAACTGCAGACAAGGTTTATGGTACGCCTGATTCTCAGTGGTTTCTTCATTTTTATGTGCAGCTGTGGTCTAAAACATCATTCTATCATATAACTTTAACTCTTTATGTAGGTCTGTGCCCTGACTGGCAAACATG[G/A]GACCCCAACCAGCCAGTGGAAAATGCTCGTGAGGCCATGCAGCAGGCCGATGACTGGCTCGGAGTGCCACAGGTGAACATCCCCTCAATATCAACACCACTTGTACAACAAATGTGTAATAGGCTCCATTTCCACTTGGTATTAAACATGTGGTTTAAGTGATCCATTCACAAGTGGTCAACCGTGACGCATTACCACCTCATATTAGCATGTGTTCAAATTCATCTCTTGTGGCCACTTTTGCTTGGATTTCGTTGAGACCCTGCCCTCTCATTTTATTACATTCTACAGACTCACTTTCATGGGAGTGCTCTGTGAAGCCCAGAAGTAAGGAAAAATTTAGTATATTAAAAGAAAATGACTCAAAATTGGATTAAAAATATCATAATAACAGGTGTAAACGGTGCTTACACACTGCTTCCATGAGCGTTTGTGTGGTTTCAGCACTTTGGCATACAGTGGTGCCTGCTCCATTATCTTCACTGGATAACCGTGAGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18138
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046218 Nonsense 898 2719 18 48
Genomic Location (Zv9):
Chromosome 25 (position 36090761)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34525029
GRCz11 25 35029987
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTCAAAGTCAAGGTGGACCCATCTCATGATGCTGGTAAAGTCAGAGCT[G/T]AAGGTCCTGGAATTWACAAGACAGGTGGGTGTMATCCACAACTTTAAGAA
Long Flanking Sequence:
CCCTGACAAAGTCAAGGTCTATGGACCTGGAGTTGAGAAAACCGGCCTGAAGGCAAATGAGCCCACTTACTTTACTGTCGACTGTAGTGAAGCTGGCCAAGGTTTGCATAATGAGTTAATTTTTACATGGCATAAATAAATGAGTGTTAGTATGGCTAACTAGTTGTACTATCCTTTAGGAGATGTCAGCATTGGGATCAAATGTGCCCCTGGTGTGGTGGGTCCAGCAGAGGCGGATATAGATTTTGACATCATAAAAAATGACAATGACACCTTTACTGTCAAGTATACACCTCCTGGCCCTGGCCGTTACACCATCATGGTTGTCTTTGCAGATCAGGTAAAGCAGTGGACGAACATGCTTCTTGCTTAGACCCAATGGTGCACTAATGCTAATTGAACTCGTCATTTCAAAAAAAAAAATCTTTACACAGGAAATCCCCAGCAGCCCATTCAAAGTCAAGGTGGACCCATCTCATGATGCTGGTAAAGTCAGAGCT[G/T]AAGGTCCTGGAATTAACAAGACAGGTGGGTGTAATCCACAACTTTAAGAACGTGAGCCCTGGAGAAATTCCAATCAACTGACACAGCTCTACTTTACAGGCGTTCAGGTGGAAATTCCAACCCATTTCACCATCTTCACCAAAGGAGCAGGAAAGGCAAAACCAGAGGTGCATTTCAAAACAGCTGCCAAAGGAAATGCTGTAAAGGATTTTGAGATCATTGATAACCATGACTACTCCTACACTGTGAAGTACACAGCTCTTCATCAGGTCAGGGTTCGCTGTCGTCTGTTGTATTTTGAGTTTGATTTGAACAAATTTTATTTATGGAAGTAACTGTTATGTCTTATTAAATGCCAAATCTTTCGCAAATAGGGTGAGATGGCTATTGTGGTCACACACGGTGGGGATCCCATTCCCAAAAGTCCTTTCAAGATCACAGTCGCCCCTTCACTTGATCTTGGCAAAGTCAAAGTTCAAGGTCTTAATGAAAGTAAGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15040
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046218 Essential Splice Site 906 2719 19 48
Genomic Location (Zv9):
Chromosome 25 (position 36090859)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34525127
GRCz11 25 35030085
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACGTGAGCCCTGGAGAAATTCCRATCAACWRACACAGCTCTRCTTTAC[A/T]GGCGTTCAGGTGGAAATTCCAACCCATTTCACCATCTTCACCAAAGGAGC
Long Flanking Sequence:
AAGGTTTGCATAATGAGTTAATTTTTACATGGCATAAATAAATGAGTGTTAGTATGGCTAACTAGTTGTACTATCCTTTAGGAGATGTCAGCATTGGGATCAAATGTGCCCCTGGTGTGGTGGGTCCAGCAGAGGCGGATATAGATTTTGACATCATAAAAAATGACAATGACACCTTTACTGTCAAGTATACACCTCCTGGCCCTGGCCGTTACACCATCATGGTTGTCTTTGCAGATCAGGTAAAGCAGTGGACGAACATGCTTCTTGCTTAGACCCAATGGTGCACTAATGCTAATTGAACTCGTCATTTCAAAAAAAAAAATCTTTACACAGGAAATCCCCAGCAGCCCATTCAAAGTCAAGGTGGACCCATCTCATGATGCTGGTAAAGTCAGAGCTGAAGGTCCTGGAATTAACAAGACAGGTGGGTGTAATCCACAACTTTAAGAACGTGAGCCCTGGAGAAATTCCAATCAACTGACACAGCTCTACTTTAC[A/T]GGCGTTCAGGTGGAAATTCCAACCCATTTCACCATCTTCACCAAAGGAGCAGGAAAGGCAAAACCAGAGGTGCATTTCAAAACAGCTGCCAAAGGAAATGCTGTAAAGGATTTTGAGATCATTGATAACCATGACTACTCCTACACTGTGAAGTACACAGCTCTTCATCAGGTCAGGGTTCGCTGTCGTCTGTTGTATTTTGAGTTTGATTTGAACAAATTTTATTTATGGAAGTAACTGTTATGTCTTATTAAATGCCAAATCTTTCGCAAATAGGGTGAGATGGCTATTGTGGTCACACACGGTGGGGATCCCATTCCCAAAAGTCCTTTCAAGATCACAGTCGCCCCTTCACTTGATCTTGGCAAAGTCAAAGTTCAAGGTCTTAATGAAAGTAAGCATTTTAACTCAACACTTTTCTTACTTTATAAAGAATTATACTTTATTAAGAATTATACTTTATAAGAATTAAAAGTCAGCTTAATCAATTTCAAATTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38133
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046218 Nonsense 1346 2719 23 48
Genomic Location (Zv9):
Chromosome 25 (position 36092704)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34526972
GRCz11 25 35031930
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATCACTGATAAGGGTGATGGCACATATAGAGTGGAATATACAGCTTTC[G/T]AGGATGGTATGTAACTAAAACGCTTATATAAGAAACACACACACACACAC
Long Flanking Sequence:
GAGAGGCTGAACTCACCATTGAGATTGTGTCAGATTCAGGGGCTCAAGCTGAAGTTTGCATTCAAAACAACAAAGATGGGACATTTTCTGTCACCTACACCCCACTCTTTCATGGGGTACACACTATTACCATTAAATATGGAGGTCAGCAGGTGCCCAAGAGTCCCATACATGTGAAAGTGGAGCCATCTGTGGACACTAGTGGAATTAAAGTCTATGGACCAGGAGTTGAGCCCAAAGGTACGGTTAAAAAATAAAATATTAGCAGTTTTATGCGATTATTTTTTAAACCGTAAATCAATTAAATATTGTCTGTGTTTGTCACCCAAGGGGTCCTCAGGGAGGTGACAACACACTTCATTGTGGATGCACGGGCCCATGCCAAGACCAAAGGAGGCAATCATGTTAAGATTCGTATCATCAATCCATCAGGCGCAAACACGGATGCATATATCACTGATAAGGGTGATGGCACATATAGAGTGGAATATACAGCTTTC[G/T]AGGATGGTATGTAACTAAAACGCTTATATAAGAAACACACACACACACACACATATATATTCAGAGCTTTGGAGGGATAATGAATGAGAGTATTTGGCAGATGAAGGGAGAGAGGTTATAAATAGCAAATGCATTGTAAAAAGAGATCATGAAATAGTTGTGTCCCTGACAAGGGCCAGCTTGTATTAAACCCGACAACAGCTGCAGGTCACTGTTAAAGCAGATCATTAGAAGCACTGCAGAACCTGAAAACGTTTAAACTTTAAAAGGTTCTGATTTCATACATTCAGTTCAATATGTGATATTTGAAAGACTGTAAGTTATGAGGTAGAAATGGCATAAAGTGAGAGTTCTTCAAGTTGAAATAGTTTTTGGATTTTTATAGGTTTGCACCTGATTGAGGTCTTTTATGATGAAGTTGCTGTTCCTAAAAGTCCCTTTAAGGTGTCAGTTGTTGAAGGTTGTGACCCAACACGTGTCCGGGCTTATGGTCCAGGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38134
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046218 Nonsense 2670 2719 48 48
Genomic Location (Zv9):
Chromosome 25 (position 36101222)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34535490
GRCz11 25 35040448
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCTTTCTTTCAGGTACAAACATGCTCATGGTTGGTGTCCACGGTCCT[A/T]GAACTCCATGTGAAGATGTGACAGTCAAGCATATGGGAAACAAGCTTTAC
Long Flanking Sequence:
GATCAAGGATGCCTAAACTCGCTCCTGGAGGGCCGGTGTCCTGCATAGTTTAGATCCAACCCCAATCAGAGACACTTGGGCTAGCTAATCAAGCTCTAAGTAGGTTTGCTAGAAATGTCCTGGCAGGTGCGTTGAGGCAAGTTGGAACTGTACTATACAGGACACCAGCCCTCCAGGACCGGGTTTGGGCAGCCTTTGTCTAAACCACAGCTGTCAAATCCAGTTCCTGGAGGGCCGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACTTAATAAAAGTAATTGAGCCCTTCAGTTTGCTTTGAAACCTAGAGGTAATTGTGTTGAAGCAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTCCAGGAACTGGATTTAACACCCATGCCAAAGATTGTCACCCTAATTATGCAAAGTCTTTCTTACTTTCTTTCTTTCTTTCTTTCTTTCTTTCAGGTACAAACATGCTCATGGTTGGTGTCCACGGTCCT[A/T]GAACTCCATGTGAAGATGTGACAGTCAAGCATATGGGAAACAAGCTTTACAACGTGACCTACACCGTGAAGGAGAAAGGAAACTATGTAGTGATTGTTAAATGGGGGGACGAAACTATACCAGGGAGTCCTTTCCATGTAAGCGCTCCTTAAACACAAAGTCAAACGCTTAGAGTTTCTAATTCAGAAAAAAAGCTTAATCCAGGGAAAAGAATGTGGAGTAAAAGGCTTATTTTAAGACTGAATCTTATTTCAGAGGCTAATGACTTTTATTTAATGCTACCCTGTTTGACGCAAGTGTATTTTAATACTGTTTCGGATGCTGTTTATTGTAAGGGTGACAATTTAAGTTTAATAATAATTAAATGGGTATATCCACCTAATTCTGTTTTGTTTAACCACCTAAAAAGAATATATGTGTATTTTACTGAGGGAGATTTATTGTTCTTCGAGGCACTTTTGATGGTGATGGGACATCACAGCAATATTGGTTTTGTGTTC
Associated Phenotype:
Not determined