Busch Lab

ZMP

si:ch211-233a24.2

Ensembl ID:
ENSDARG00000062330
ZFIN ID:
ZDB-GENE-090313-98
Description:
fragile site-associated protein [Source:RefSeq peptide;Acc:NP_001139056]
Human Orthologue:
KIAA1109
Human Description:
KIAA1109 [Source:HGNC Symbol;Acc:26953]
Mouse Orthologue:
4932438A13Rik
Mouse Description:
RIKEN cDNA 4932438A13 gene Gene [Source:MGI Symbol;Acc:MGI:2444631]

Alleles

There are 18 alleles of this gene:

Allele Name Consequence Status Availability
sa42156 Nonsense Mutation detected in F1 DNA Not yet available
sa15043 Essential Splice Site Available for shipment Available now
sa9351 Nonsense Mutation detected in F1 DNA Not yet available
sa13514 Essential Splice Site Available for shipment Available now
sa42157 Nonsense Mutation detected in F1 DNA Not yet available
sa35438 Nonsense Mutation detected in F1 DNA Not yet available
sa2675 Nonsense F2 line generated Not yet available
sa35439 Nonsense Mutation detected in F1 DNA Not yet available
sa17693 Nonsense Available for shipment Available now
sa13875 Essential Splice Site Available for shipment Available now
sa2712 Nonsense F2 line generated Not yet available
sa35440 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24928 Nonsense Mutation detected in F1 DNA Not yet available
sa35441 Nonsense Mutation detected in F1 DNA Not yet available
sa13491 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa42156
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
ENSDART00000090000 Nonsense 107 4871 4 83
ENSDART00000134725 Nonsense 107 4922 4 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12673667)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12672035
GRCz11 13 12804510
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTGTCATTTTCAGAATTCAGGATGGGTTACTCATATTTCGTTGGTG[G/A]AAGATGTACAACCCAAAGCAGAAGCAACATGGTCAGTGCAAAAACAGAAC
Long Flanking Sequence:
GTACAGCTTACTTTATAAGGACTATCTATAGGCGTAATGATTCTAATGCTGTATAAACTGTATGTTCTACATCTCTACCCAACTCTAGCCATAAACACAACACTCTCAAGAACAATCTGCATTTACATTTGCAAAATACTTCAAAATACTTTATTTTGTGTGATTTATGAGCCACTTTTCCACTCATGGACCACAAATAAAACGTTGTCGCAAGGTCAGAATTTACTGGTAATATACTTGGGGGGACATTTGGTCCTCAGAAAGCAAGGAATAAAAGGTGGTACTTGGTACACGTGTGTGTTTTTGTGTGTATAGCTTATAGACACAAACACACACACACACACACAAACACACGCAAATAAACTTTTGAGACTCTGCTTATTGCTGTTGTCTGTGAGACCTTTTTCATTTGATATGGGTTATATTTCATCTTTATTTACTCTGTTGTTTATATTTGTCATTTTCAGAATTCAGGATGGGTTACTCATATTTCGTTGGTG[G/A]AAGATGTACAACCCAAAGCAGAAGCAACATGGTCAGTGCAAAAACAGAACAAACAGCAAAGAATTGTTCAATTTGAGCACATCATGTCAGTCTCAATAGTCTCAGTCTCAGTACACCAATCCCACAATATCTGTAAATGCTTGTCATTTTAGTTGCTCTATGGTTGGGTTTATCTGTGCTTGGGTTGTTTATTAATTTATATGCTGTTTTAAAGGGATAGATTTTCACCCAAAAAATGTAAATTCTGTCAACATTTACTCGCCTTCCACTTTTGAGGATATTTTAAAGAACGTTGGACGTCTATGGCTACCAGTTTACAATATTCTTTAAAATATATTTGTTTGTATTCAATAGGCAGGGTGTCTGCGGGGTCTTAAAAAGTCTTAAAATGTCTTAAATTTCAAAAACAAAATTTTAGGCCTTAAAAAGTCTTAAATTCACTGAAATATAAGGGTCTATCACACACCCGGCGCAATAAGGTGCAAGATGTGTTTGGTGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15043
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090000 Essential Splice Site 454 4871 13 83
ENSDART00000134725 Essential Splice Site 454 4922 13 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12700640)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12699008
GRCz11 13 12831483
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAAASCGTTCTGCATAATAACAGCTGTTGTATGTTTACTTTTTTCCA[G/A]TTTCATGTGATAGCCAGTTATCCTCGCGTGTGGAACATGCCTCAGTCCTG
Long Flanking Sequence:
TTAGCAGCGATTTGCACAGACTGGATCGCTGGTGATTGTGACGCTAAGAACAGAACACAGCCTAATATTGCAACAAGAGGGTCAGGAGGAAATTAGTCTTAAGTACTGTTTAGCAAGAAGAAAACACCTCAATCCAAAATTTACACATATTTTGAGCAAAACCAAAATAAATGTACATGAACAAACAAACGCAACAAAGTTCACATGTTAAACTAACATTAGATACATTTAAATAAACATTATGCATCTTCAGGGTGGCGCTGAATACATTTATAATTTTTTATTTTGCGCCATTTTGCTTTTGAAACAAGTGATGAATAAATATTTAGAATTTTTTTTTGTGATGATTGTAAAACTGTCCTAAATTTCTTAAATGTTCAGCTAACTTCTTATTTGCTAAAAAGTTGTATTATATTTTTTCTTCAAATACTACGTAAAGGATAACGCAACAATCAAACCGTTCTGCATAATAACAGCTGTTGTATGTTTACTTTTTTCCA[G/A]TTTCATGTGATAGCCAGTTATCCTCGCGTGTGGAACATGCCTCAGTCCTGGCAGTGTGAAATTGAGGTTTACAAAGCCACGTATCACTTTATCTATGCACAGAAAAACTTCTTCACAGGTGATGTTTCTCTCTTATCTGTAAGTCCCTATGCGGTGAAGTATGTCCTCAAGCTGACCTCCTCCTGTTGTCATCTGTAGATCTGATCCAAGACTGGGCCAGTGACAGTGAACCGGACATCTACTCATTCGTTCCATATTCATGGAAGTTTAAAATTCTTTTCCACCAGTTTGAGATGATTTGGGCCGCCAATCAGCACAACTGGATCGACTGCTCCACCAAACAGCAGGAGAACGGTAGGAGAGTTTCATAACAGATGCACTTATATATATATATTAATTATATTATATATATATATATATATATATATATATATATATATATATATATATATTATATATATTAGGGCAGGGCGATTTAGCAAAAAAAAAAATCTAGGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9351
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
ENSDART00000090000 Nonsense 872 4871 21 83
ENSDART00000134725 Nonsense 872 4922 21 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12716801)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12715169
GRCz11 13 12847644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTCCGATWGAWGCYGTGTTGCGTGACGGGCAWCTGAGCCTCTCGGGTT[T/A]GCAGATGAGAGCTCATGCCATGTTCTCGGCGGAGGGTTTGCCGGCGGGCA
Long Flanking Sequence:
TTAAACCACATTGAACTCACCTAAACTGAACTTCAGTTGTGAAAACTGAACTGACAGTTTCAATTTGCTAGAACTGAATTGAATTTAATTATTTGTGTGACATTTAAAAAAAAATGTCATAATAGTGCATTGTTAAAACTCCAATTACAATCTTAGCATAGTAACGTCTCATAGAATCACGATATTTCCTTCGGGATCCATAAATCTTGTCTCCCTCTGCAGCACTGTAGCAGCGACGGTCCAGAAGGTCCTACAGGCTTCATGGAGCGTCTGTGCTTCGAGATGAAGAAAGGTTACAAGGAGACCATGCTACAGCTTGTCCTCTCGCCTGTACATGTGTTTGTCAGCGATAACTATCAGGTGGAAGTGACCTCATTCATATTCATTGATTTCAGTTGCTGCTATTTTTGCTAATATTCCCCCCCTGTATGTGTGTGTGTGTTTTTAGCGGCCTCCGATTGATGCCGTGTTGCGTGACGGGCATCTGAGCCTCTCGGGTT[T/A]GCAGATGAGAGCTCATGCCATGTTCTCGGCGGAGGGTTTGCCGGCGGGCAGCGACACCCTGGAGTACGCGTGGCTCATTGACGTTCAGGCTGGAGCTCTTACGGGAAGAGTCAGTGTGCCGCAGGTGACTCATTCATTTGTTTACTAGAAATGTGTGACGTCTGGAAAGAATCATTTATGGGAATATTTGTGGCGTGATGAAGTCGCACGAAGATTCAAGCCAAATCCATTGTTGAATTCAAATGAATGAACATGTTTCTTTGTACTTATCATACAAGGTTAGGAGGCTTGTGGGTTGGACAGAAGAAAAAAGTAAGAATGCGAAGGTTGAATTTTTGATAGAGCCCTTGTGTGAAATTTATACTGTAGTGCTGCCCACTGAGCTTCTTTTTATAACGTGAATTGTATTGGAAGGTACTGTAAACACCAATTGAAATGGTTGTTTGTATACGCAGAGGAGCATGTCAGAGTTTGTCGCAGGTAATCAGAAGAATGCTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13514
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090000 Essential Splice Site 1171 4871 25 83
ENSDART00000134725 Essential Splice Site 1171 4922 25 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12730262)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12728630
GRCz11 13 12861105
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCCCGGAGAATGGATCGTCACCAAGGAAACTCCTAAAATCCCAGATG[G/A]TATGTTTGCTTTTAATGGACTAAATCATGATGCCTATTGCTTRTTGTGTG
Long Flanking Sequence:
ACATCCACTTAGTGTATTTACATGTCATAGTATATATGGAATAAAAAAATTATCATGGTTGATGATTTATTTAATGGTAATCTTATATACTTTCTTACCACCCAGTCCTTCCATAACAAGGACTGGGTGGTAAGTCCTTCTGTTTCTTGATCTTTTTTTTTTAATCATAAAGATCATGGTTTGAGCTTTATAACTATTCTCTAATGTTATAGTGCCAACACACCTATTTGCTAAATGTATTTATGTGTGTTTTAGACTTTGGTTCCTTTGGCCTGAGGAGAAATACAAGCGAAGTCGGAACCGCTGTGGCTGTCTTGGTGGCTGTCGTTTTTTTGGGGGCACCATCGGTGGCCTGGACTTCTTCCGATTGGAGGAAATCACACCCTCGTCAAGCTCAGCCTTCTCCGGTATCAGCGCAGAGTGTGATATGTCCTATGGCCAGTCATTATTACATCCCGGAGAATGGATCGTCACCAAGGAAACTCCTAAAATCCCAGATG[G/A]TATGTTTGCTTTTAATGGACTAAATCATGATGCCTATTGCTTGTTGTGTGCATTGTAGTAACTGATAGTTATATATGCAGCTAAAGGGATTGCTGTGCGAAGAGACACGTGTTCTCCTGCACCAGTGGTGGACTTGGAGAGACGTGTCCAGCAGCACCTCAGTCTCCACGTCCCTCAGCGCTCTCACAGCTCTGCCTCTTCCTCCGAGGAAAACTCTTCCTCCAGCGCCGCGCTGCCTCTGCTGGCTGGAGAACGAGAGAGTCCTTCACCCTCTACTGAGTGAGTCAGACAGATGTGCTTTGCTCCTTCTATCTACATAGGTATTTAGAAGCAGTGTAACGGTATACTGGAATCATGGTTTGGTACAACATGAATAATAGCAAATGCCCAGTGTACATTTTTCTGTTAATTTTGAACTGGCAGAATTGTTTTGTCACAATCATTTACAGAACTGAAGAGCCTCTTGTGATGCAAAAGTACAAAATAAACAATAATAATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42157
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
ENSDART00000090000 Nonsense 1178 4871 26 83
ENSDART00000134725 Nonsense 1182 4922 26 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12730360)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12728728
GRCz11 13 12861203
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCATTGTAGTAACTGATAGTTATATATGCAGCTAAAGGGATTGCTGTG[C/T]GAAGAGACACGTGTTCTCCTGCACCAGTGGTGGACTTGGAGAGACGTGTC
Long Flanking Sequence:
CACCCAGTCCTTCCATAACAAGGACTGGGTGGTAAGTCCTTCTGTTTCTTGATCTTTTTTTTTTAATCATAAAGATCATGGTTTGAGCTTTATAACTATTCTCTAATGTTATAGTGCCAACACACCTATTTGCTAAATGTATTTATGTGTGTTTTAGACTTTGGTTCCTTTGGCCTGAGGAGAAATACAAGCGAAGTCGGAACCGCTGTGGCTGTCTTGGTGGCTGTCGTTTTTTTGGGGGCACCATCGGTGGCCTGGACTTCTTCCGATTGGAGGAAATCACACCCTCGTCAAGCTCAGCCTTCTCCGGTATCAGCGCAGAGTGTGATATGTCCTATGGCCAGTCATTATTACATCCCGGAGAATGGATCGTCACCAAGGAAACTCCTAAAATCCCAGATGGTATGTTTGCTTTTAATGGACTAAATCATGATGCCTATTGCTTGTTGTGTGCATTGTAGTAACTGATAGTTATATATGCAGCTAAAGGGATTGCTGTG[C/T]GAAGAGACACGTGTTCTCCTGCACCAGTGGTGGACTTGGAGAGACGTGTCCAGCAGCACCTCAGTCTCCACGTCCCTCAGCGCTCTCACAGCTCTGCCTCTTCCTCCGAGGAAAACTCTTCCTCCAGCGCCGCGCTGCCTCTGCTGGCTGGAGAACGAGAGAGTCCTTCACCCTCTACTGAGTGAGTCAGACAGATGTGCTTTGCTCCTTCTATCTACATAGGTATTTAGAAGCAGTGTAACGGTATACTGGAATCATGGTTTGGTACAACATGAATAATAGCAAATGCCCAGTGTACATTTTTCTGTTAATTTTGAACTGGCAGAATTGTTTTGTCACAATCATTTACAGAACTGAAGAGCCTCTTGTGATGCAAAAGTACAAAATAAACAATAATAATGAAAAATCAAACTTTATAATTACTAAACTGTATTAAAGGGCCATGAAACCCCTTGTTTCAGCTGGGTGTTTTATTTATTTATTTATTTATTTTTAATTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35438
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
ENSDART00000090000 Nonsense 1254 4871 27 83
ENSDART00000134725 Nonsense 1258 4922 27 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12735084)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12733452
GRCz11 13 12865927
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATTAATGAATGTAACAACCGATTGTCCTATCCCTGAAGGCCCACCAT[T/A]GCGCTCTCCTCTCCGCTCTCCATTAAAGCGCCAGTCCTCTGTCCAATCAG
Long Flanking Sequence:
ATTTTATGTTATTCTTTAATGTTTTAGAAAGACGTTTCTTAGGATGTATTTCTTTGACCAAAATGTATGTTTTCTATTTAGATATATTGTTACTTAAAATCTAATTTATTTTTGTGTTGGTAAAGCTATCCTAAAAGTTTTTTGTTTGTAAATAGGGTTCAAAAGAAACTGTTTGATAACATTATAAATGTCTGCACTGTCACCTTTGATCAATGTAATGCACCCTAGCTGAATAAAGTAAATTAAAGTGTTCTTTCCAAAAAACAAATTACTCTGTGATTTCTAGACTGATTGAATTTTGTAGACGGTCACAAAAAGTTTTTGTTCATCAATAACTGCAAGAATAAAACTCCAAAATAAATCCTGTTCTGAATAAAAACAGCTTCTTGAGTTGCCAACATATTTGCTTTTTTATTTATTTATTTTTAATATTTGCTGTCTTTGTGTTTTCAGATTAATGAATGTAACAACCGATTGTCCTATCCCTGAAGGCCCACCAT[T/A]GCGCTCTCCTCTCCGCTCTCCATTAAAGCGCCAGTCCTCTGTCCAATCAGCACGCCTCGGCAGCACCAAGAGCCTATCAGCAGCTGTGTTCGTAGAGAAAGCCTTGCCTCCTGCTGGTGTACAATTTAGCAGCGAGGTTTCCCGAAGCGATGAGAACGTTCTAGACTCACCAAGGCAGAGAAGAAGCTATGGCTCATTTCCTTTCACGCCGTCAGCTGATTCTAGCACTTTCCATCAGTATCGCTCCGTTGACTCCTCCATGTCCGTGGCTGACAGTGAAGCCTACTTCAGTGCTACTGAGGAGTTTGAGCCCATAAGTAGCGATGAAGGTCCTGGGACATATCCAGGGAGAAAGCGCAGACGGAGACAGCAGGGTCAGCCTCACACTGAACACAGCCGCACCTCTATATACCACAGTGTTGAAGGACCGCTGTCAATCAATGAGATCCGTCCCCCTCTGCTGCCTAGCCACACCTCCCAAGCCTCATTTGTCTCTGCGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2675
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090000 Nonsense 1380 4871 27 83
ENSDART00000134725 Nonsense 1384 4922 27 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12735461)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12733829
GRCz11 13 12866304
KASP Assay ID:
554-2464.1 (used for ordering genotyping assays)
KASP Sequence:
AAGGTCCTGGGACATATCCAGGGAGAAAGCGCAGACGGAGACAGCAGGGT[C/T]AGCCTCACACTGAACAMAGCCGCACCTCTATATACCACAGTGTTGAAGGA
Long Flanking Sequence:
AACAGCTTCTTGAGTTGCCAACATATTTGCTTTTTTATTTATTTATTTTTAATATTTGCTGTCTTTGTGTTTTCAGATTAATGAATGTAACAACCGATTGTCCTATCCCTGAAGGCCCACCATTGCGCTCTCCTCTCCGCTCTCCATTAAAGCGCCAGTCCTCTGTCCAATCAGCACGCCTCGGCAGCACCAAGAGCCTATCAGCAGCTGTGTTCGTAGAGAAAGCCTTGCCTCCTGCTGGTGTACAATTTAGCAGCGAGGTTTCCCGAAGCGATGAGAACGTTCTAGACTCACCAAGGCAGAGAAGAAGCTATGGCTCATTTCCTTTCACGCCGTCAGCTGATTCTAGCACTTTCCATCAGTATCGCTCCGTTGACTCCTCCATGTCCGTGGCTGACAGTGAAGCCTACTTCAGTGCTACTGAGGAGTTTGAGCCCATAAGTAGCGATGAAGGTCCTGGGACATATCCAGGGAGAAAGCGCAGACGGAGACAGCAGGGT[C/T]AGCCTCACACTGAACACAGCCGCACCTCTATATACCACAGTGTTGAAGGACCGCTGTCAATCAATGAGATCCGTCCCCCTCTGCTGCCTAGCCACACCTCCCAAGCCTCATTTGTCTCTGCGCTTGGATTGGAGGAGGAGGGATCTATTGAAACTGAGAAGGCGGATCCTGGAATTCTGACAACACAGCCGCATTTGATGGCTTGTTACCAGAACTATCTGGCACATTATCATGTGTCAAACTGGGCTGTTAAGCAGCCGACCAATAAGAGAACATCCAAGTCCTCTCTGCACCGCCCACTTGATTTGGACACGCCTACGAGTGAGGAGAGCTCTACCTGCTTTGATCAATTGTCCATCCCCACTTTTAAGGTATATTAATATTTATTAATAGTTTTATATAGATTTCTATATTCCTTACACCAGGGCTGCTCAACCCTGCTCCTGGAGATCTACCTTCCTGCAAAGTTTAGCTCCAACCCTCATCAAACACACCTGAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35439
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
ENSDART00000090000 Nonsense 3174 4871 54 83
ENSDART00000134725 Nonsense 3195 4922 55 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12786535)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12784903
GRCz11 13 12917378
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCGGGGTCAGATTTCCACCAGGTGGCCTATTTCCGGACTCGGATTGGTT[T/A]GCGCAATGCTCTGCAGGAGGAAATCAGTGGCAGCTCTGACAAAGAGGCTG
Long Flanking Sequence:
ATAAAACAAACAGAAAATATACGGCCATTTGCTGTTTAAAAACATCAAACCTGAACAAATAAATTTAAAGTAAAACTGAAGTAAACAAATATTCACGTTCTCTCTCATTCTGCACAAATGCTATGCACTTTTAGCGTGTTTCACTAATTTATTTAAACATGACATATTTTATACGTTTATGAACAGCTTTTTAAAGATGCATCATGAATCAAGAAGAATCATTGCATTTGAAACTCAAGTTACTTTTAAAAGTAATATGATACAATCTTAAGTCTATCTTAATAAAAATAAATAATTAACAATACCTCATATTGTGCTTTTAGATTACTTAATTTAAAAAGAAACCAAGTAATATTTTACTTACTTTAAGTGACTTGAATATATGAATTTTAGGAATAAGTTTGCCTGCGCTATCATTAAATACACTTTCTCCCTCCAGGTGTATGAGGAGGCGGGGTCAGATTTCCACCAGGTGGCCTATTTCCGGACTCGGATTGGTT[T/A]GCGCAATGCTCTGCAGGAGGAAATCAGTGGCAGCTCTGACAAAGAGGCTGTCCTGATCACACTCAGCCGTCCTATTATTTTTGCTCAACCTGTGGCTTTTGACAGAGGTCAGTCAATGTTTTGCCTTTTGTTTGTCAATGCTTCTTTATTTTGGCATTTTTGGGGGTTTGTAATTGCGTATTTACAGTTGAAGATTTTTTCAACACATTTCTAAACATAATAGTTTTAGTAACTCATTTCTAGTAACTGATTTATTTGATCTTTGCCATAATGACATGTACATACTATTTTACTAGATATTGTTTAAGACACTTCTATACGGCTTAAAGTGACATTTAAAGGCGTCACTAGGTTAATTAGGTTAGCTAGGCAGGTTAGAGTAATTAGCCAAGTTATTGTATAACAATGGTTTGTTCTGTAGACTATCGAAAAAATATAGCTTAAAGCGGCTAATAATTTTGAACTTAAAATAGTGTTTAAAAAAATAAAAACTGCTTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17693
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
ENSDART00000090000 Nonsense 3227 4871 55 83
ENSDART00000134725 Nonsense 3248 4922 56 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12787256)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12785624
GRCz11 13 12918099
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGCTCTTCTGGCWGAACTATAAGGCTGCTTATGATAACTGGAAGGAA[C/T]AACGCTTGGCTCTCAACTCCGACATTCATATGGCCACCAAAGARGTTGTA
Long Flanking Sequence:
TAGTTTTAGTAACTCATTTCTAGTAACTGATTTATTTGATCTTTGCCATAATGACATGTACATACTATTTTACTAGATATTGTTTAAGACACTTCTATACGGCTTAAAGTGACATTTAAAGGCGTCACTAGGTTAATTAGGTTAGCTAGGCAGGTTAGAGTAATTAGCCAAGTTATTGTATAACAATGGTTTGTTCTGTAGACTATCGAAAAAATATAGCTTAAAGCGGCTAATAATTTTGAACTTAAAATAGTGTTTAAAAAAATAAAAACTGCTTTTATTCTAGCCAAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATGATCAGACATACTGTAAAAAATTTCCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAGAGGAAAACTAATTTTGGGGGGCTAATAATTCTAACTTCAACTGTATGTGTGTGCTGTAGCTGTGCTCTTCTGGCTGAACTATAAGGCTGCTTATGATAACTGGAAGGAA[C/T]AACGCTTGGCTCTCAACTCCGACATTCATATGGCCACCAAAGAGGTTGTAGACAAACTGCCAGCCATTCAGCAGACCAGCGTCCAGGCCTTTAGTACACTCTTCCTACAGCTCACAGTCAATGACCTGGGCATCTGTCTGCCCATTACCAGCGCCACACAGGTGGATACTTGCACAAATGCATAATCTACACTTTTTTATGGCATCATTATGATTTTTTTGAATGTGTCCGCTCATAAAGGCTGCATTTATTTGCCCAAAATACAGTAAAATACTGTAGAATTGTACTAATTGTAATAATTACAATAAAAAAAAATCAGTTCTCATTTTGAACGTAATTTGTTTAATTTATTCCTGTGATTTTAATTTATTCCTGTGAATTTCCAGCACATTTCCCCAGTGTTGCATGATTCTTCAGAATTCGTTATAACATAATCATCTGCTGTTAAAAAAAGCTATTTTTATAGGTGTTGAAAAATTGGTCTGCTATATGTAAAGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13875
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090000 Essential Splice Site 4289 4871 74 83
ENSDART00000134725 Essential Splice Site 4340 4922 75 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12832029)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12830397
GRCz11 13 12962872
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACAGCTTAATGTSCAGATGAACATGAGCAACGTCATGGGCAATAATAC[G/A]TATGASCGAGCGAGCAGCTAATATGCTTTGATACCTGCAWCTGGTTAACA
Long Flanking Sequence:
TGTGTGTATTAAGCAATGTGTAAGCAAGGCGGACAACTAGATATTTTCGTATTATCGAGTCAAGTGATTAGACTAATTATTGAGTAATTAAATAACTTTTCAGACACAGTAATTTAAGTAATTGTTTTTGTTCACTAAAGTCTCTGCTGCATGCCAGAAATCTGAATCGCTGTCTGACCATGTTTGACCAGATTAGGCATGAACATTAACATTATGATCAAGATTATGATATGATTTTAGCTAACCGTTGGTGTATATTAATACCATTTGTTGTTCACTGGCATCTGTTAGAGCTTTCGTAACATCAAATGAGCAAGCGTATTAAATCAGTTGCATATGCCTCCTGCAGACTCTGTTACCAAGACCTCTACCCCGTCGTTCCGGAACGGAAAAGCAGCAGCGCAGCAGGGTTCACCGTGGGAGACGCTGGTGGTGTTCGCCATCAACCTGAAACAGCTTAATGTCCAGATGAACATGAGCAACGTCATGGGCAATAATAC[G/A]TATGAGCGAGCGAGCAGCTAATATGCTTTGATACCTGCATCTGGTTAACATGGCTCAGTATGATGACTAACTGTTGCACATGCGTGTGTTTCAACAGTTGGACAACGAGTGGGCTGAAGAGTCAGGGCCGTCTGTCAGTGGGCAGCAACAGAGACCGTGAGATCAGCATGTCTATTGGACTGGGACGCTCCAAACTGGACTCCAAAGGAGGAGTGGTGGGTGGAAACATTGATGTCAACACGCTGGAGATGGTCTGTAAGTATGATTTCATAGATGCACATTTTGTGGCCCAGCATCATTATTATATCTTCTATTATACATCTAATTTTCTAATTGTTATGTGGTTTAACTAATTAAAAACATTTTATCTTTGGCATTCACTACCATAAAATGCCCATCACATTGTTTGATTGCTTATAAAAGTCAATATTTTGGCAGGTAGAATGAAAATTAAAATGGGTTTACATCGATTTAATCGTTCCTACATTGTGGAAAAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2712
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090000 Nonsense 4318 4871 75 83
ENSDART00000134725 Nonsense 4369 4922 76 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12832212)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12830580
GRCz11 13 12963055
KASP Assay ID:
554-3335.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCAGTGGGCAGCAACAGAGACCGTGAGATCAGCATGTCTATTGGAYTG[G/T]GACGCTCCAAACTGGACTCCAAAGGAGGAGTGGTGGGTGGAAACATTGAT
Long Flanking Sequence:
TTGACCAGATTAGGCATGAACATTAACATTATGATCAAGATTATGATATGATTTTAGCTAACCGTTGGTGTATATTAATACCATTTGTTGTTCACTGGCATCTGTTAGAGCTTTCGTAACATCAAATGAGCAAGCGTATTAAATCAGTTGCATATGCCTCCTGCAGACTCTGTTACCAAGACCTCTACCCCGTCGTTCCGGAACGGAAAAGCAGCAGCGCAGCAGGGTTCACCGTGGGAGACGCTGGTGGTGTTCGCCATCAACCTGAAACAGCTTAATGTCCAGATGAACATGAGCAACGTCATGGGCAATAATACGTATGAGCGAGCGAGCAGCTAATATGCTTTGATACCTGCATCTGGTTAACATGGCTCAGTATGATGACTAACTGTTGCACATGCGTGTGTTTCAACAGTTGGACAACGAGTGGGCTGAAGAGTCAGGGCCGTCTGTCAGTGGGCAGCAACAGAGACCGTGAGATCAGCATGTCTATTGGACTG[G/T]GACGCTCCAAACTGGACTCCAAAGGAGGAGTGGTGGGTGGAAACATTGATGTCAACACGCTGGAGATGGTCTGTAAGTATGATTTCATAGATGCACATTTTGTGGCCCAGCATCATTATTATATCTTCTATTATACATCTAATTTTCTAATTGTTATGTGGTTTAACTAATTAAAAACATTTTATCTTTGGCATTCACTACCATAAAATGCCCATCACATTGTTTGATTGCTTATAAAAGTCAATATTTTGGCAGGTAGAATGAAAATTAAAATGGGTTTACATCGATTTAATCGTTCCTACATTGTGGAAAAAAAACAATAAGATATTTTAGTTTATTTCATTTTCATGTTTAAATAATAATTTAAATAATTTAGGCACAATTTACTTTATTTATTTATGTTGGTGAATCTATGTACATTATAATCTTCATGGGTAGTGCACATCAATAAATTAATGTCATTAAACAATATTCTAGTTAAAATTTGATTTTGTGTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35440
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090000 Essential Splice Site 4477 4871 77 83
ENSDART00000134725 Essential Splice Site 4528 4922 78 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12836944)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12835312
GRCz11 13 12967787
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCCCAAAACACCAGTCATCAACACAGACAAGGCATCTGCTGAACTCT[G/T]TAAGTGCACTTATGACCAAAGTCCAGTTTTGTGTATAGGGTCTTGTTTCC
Long Flanking Sequence:
TGATTACTGTTCTTCTAGCTCACATTTCAGAACATCCAAACCAGCAGCCCAGTCATAAGATCCAGATCACCATGGGCTCCACAGAGGCACGTCTGGACTACATGGGCTCCAGCATATTGATGGGCATCTTCAGTAACGCTGACCTGCAGCTCCAGGATGAGTGGAAGGTGAATCTATGCACAGCCGAGGCCAGTCTATCTGAGAAAAGGTAAGGCAGAAATCCCCAATAATCACATAAAGGTAACCTAACCATAACTTTAACACACATTCTCTGATCCGCAGTGAGATCTTTGTGCACGGGGACCTGCAGTGGGACATTTTCCAGGTGATCATCTCTCGCTCCACCACTCCTGACCTGATAAAGATCGGCATGAAGCTGCAGGAGTTCTTCACACAGCAGTTTGACACCAGCAAGCGAGCCCTGTCCACCTGGGGCCCGGTGCCCTACATGCCTCCCAAAACACCAGTCATCAACACAGACAAGGCATCTGCTGAACTCT[G/T]TAAGTGCACTTATGACCAAAGTCCAGTTTTGTGTATAGGGTCTTGTTTCCACTGAGCGGTATAGTACAGTACAATTCGTAACAGACCACCCTGATCAGGCTATTACACCCTTACCCCCCAATCACACTGGGCGTCAGCAATTATGCTTTCTTTTCACTTTGAATGGGTGATGTCAGGCTTTGCCGAAATGCATTGTGGATCTGTTGGCACCGCTTCAGCTGCGTTGCTCACTGCAGAAAATGGGAATTTCTAAACTTTTCAAACGTCAACGGACGCCTCAGCCTATCTGATTGCTTTATTCAAATACACCAGCTCAGACAGTAGCCGATTGCGGACTTATTTCATTGGCTGACTCTGCTATGATGATCGCGTCAGCCCCAACTTCAGACACTTTTTTTTCAGAACTTTTATAGTTCTGCGTCTAGTGATCGACGTGACCCTTGGTGCATGCCTTGTGCATAGTTTTGCATTTATGTTTCTACATGCTGATTGTCTTGCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24928
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
ENSDART00000090000 Nonsense 4556 4871 78 83
ENSDART00000134725 Nonsense 4607 4922 79 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12839994)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12838362
GRCz11 13 12970837
KASP Assay ID:
554-7847.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTGTTGTTCCATCTGGAAGAGCCCAACATCGCCTTCTGGACTGAAGCA[C/T]AGAAGATCTGGGAGGATGGTACAGATGCAGTGCTGCTGTTTTATCATTCC
Long Flanking Sequence:
TGTGAAACCACACTAATATAATAAGAAAATATAAGTTTGTAACATCAAGCAGCATAACGAGCTGTTTTGTAACGTTTAAAAATAAATAGAAGTGAATAAGACCGGAAATTTTGAGCCAAAAAGTTTCAAATGGCTGCGCCCGCCTACGGTTTACTATTTTGCTGCTACTTAAAGTGAAAATGGAAATAAACTAATTTTTTTACTATACTCAAACTATAGCTTTTACATTTGTATTTAAATAAACATGAATGTTTGTTTTTCTCTCAGATATGGATGCTGCTCATCACAGGCACTGGCCCAATGTGTTGAAGATGGTGGCCGGATGCCACATTTCCCTCTTCCAGATGCCTCTCCCGGAGGATGCCGTGCAGCTGGGTGGCTCTATGAGTCTACATGGAAACCACATGACTCTGGCTTGCTTCCACGGACCCAACTTTCGCTCCAAGTCCTGGGTGTTGTTCCATCTGGAAGAGCCCAACATCGCCTTCTGGACTGAAGCA[C/T]AGAAGATCTGGGAGGATGGTACAGATGCAGTGCTGCTGTTTTATCATTCCCTTGAAATAAAAGATATTTTATTGAAATAAAAGATCCCAAGATAATTGAAATTAAAGATCCCCTTCCTTCTAGGGTTTCTTTTGAACTCTAGAAAATGATTATTTTCTAGGGTTCAAAATTTATACAGATCTGACATTTTTCCTTCATACTTCTGTTGGAATGGGTTCGAAGTTGGCATTGAATTTCACTTGAAATGGTATTAAATTTGGAGGATCCCGGGGGTACCCTGTTTACTGAACAGATTCCAATATCCGCATTTAAAAAAATGATGTGATTTTGTCATAAGACATCATGTGATGATAAAAATGTGTTTGAATGGACAAACCAGCAGGCTGAGCACATTGTAAAACATCTGAAATGTATTTTTGGTCATTCTAAAATGCCTTAACTGTTCCAGTATTAGTGCTATTATATTATAAATGACCTCCAGAACTGTCAAGAGCATCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35441
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
ENSDART00000090000 Nonsense 4559 4871 78 83
ENSDART00000134725 Nonsense 4610 4922 79 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12840005)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12838373
GRCz11 13 12970848
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGGAAGAGCCCAACATCGCCTTCTGGACTGAAGCACAGAAGATCTG[G/A]GAGGATGGTACAGATGCAGTGCTGCTGTTTTATCATTCCCTTGAAATAAA
Long Flanking Sequence:
ACTAATATAATAAGAAAATATAAGTTTGTAACATCAAGCAGCATAACGAGCTGTTTTGTAACGTTTAAAAATAAATAGAAGTGAATAAGACCGGAAATTTTGAGCCAAAAAGTTTCAAATGGCTGCGCCCGCCTACGGTTTACTATTTTGCTGCTACTTAAAGTGAAAATGGAAATAAACTAATTTTTTTACTATACTCAAACTATAGCTTTTACATTTGTATTTAAATAAACATGAATGTTTGTTTTTCTCTCAGATATGGATGCTGCTCATCACAGGCACTGGCCCAATGTGTTGAAGATGGTGGCCGGATGCCACATTTCCCTCTTCCAGATGCCTCTCCCGGAGGATGCCGTGCAGCTGGGTGGCTCTATGAGTCTACATGGAAACCACATGACTCTGGCTTGCTTCCACGGACCCAACTTTCGCTCCAAGTCCTGGGTGTTGTTCCATCTGGAAGAGCCCAACATCGCCTTCTGGACTGAAGCACAGAAGATCTG[G/A]GAGGATGGTACAGATGCAGTGCTGCTGTTTTATCATTCCCTTGAAATAAAAGATATTTTATTGAAATAAAAGATCCCAAGATAATTGAAATTAAAGATCCCCTTCCTTCTAGGGTTTCTTTTGAACTCTAGAAAATGATTATTTTCTAGGGTTCAAAATTTATACAGATCTGACATTTTTCCTTCATACTTCTGTTGGAATGGGTTCGAAGTTGGCATTGAATTTCACTTGAAATGGTATTAAATTTGGAGGATCCCGGGGGTACCCTGTTTACTGAACAGATTCCAATATCCGCATTTAAAAAAATGATGTGATTTTGTCATAAGACATCATGTGATGATAAAAATGTGTTTGAATGGACAAACCAGCAGGCTGAGCACATTGTAAAACATCTGAAATGTATTTTTGGTCATTCTAAAATGCCTTAACTGTTCCAGTATTAGTGCTATTATATTATAAATGACCTCCAGAACTGTCAAGAGCATCTGTGCTCTGTGTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13491
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
ENSDART00000090000 Nonsense 4762 4871 82 83
ENSDART00000134725 Nonsense 4813 4922 83 84

The following transcripts of ENSDARG00000062330 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 12849590)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 12847958
GRCz11 13 12980433
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATGTTTGCATCTCGGCCTGGCCAGAAGAGCCCAACAAYGCAGCAGGAT[G/T]AGCCATCATCTGACAAGAAGGAGGAGAGAGAGAAAGAAGAAGGAGTGAAC
Long Flanking Sequence:
ATGTCCGTACAGTGCCAGAGAATAACGACATTTAAAAATGGAAGAAAAGCTTAGTAATAGATGTGATTGGCTGTCGTCACTATGACGATTACGTCAGTGTAAGCTTCAGAAACACCCTCCGTCATGTGTTGACGCCGATGGCCTATAAGAACAGGGCATTTGTATTTGTTTTTAACACTATGAAAGTCAACGGTTACAGGGTTTTTTTTAGGTTTCTTCAGAATACCTTCTTTTGTGTTCAACAGAGCTCATAAAGGTTTAGAAGCACTTGAGGTTGAGTAGTAAATTTCCATTTTTTTGGGTGAACTATTCCTTTAAAATAAACTCATTCATCATAAATTATTTTTGTGACCCTTAGAAAATATCACAATAGTTTGTGTTTAATTGTGTAATAGAAACAGTCCTACTTTAGTGAAGTGTGTGTTTTTGTCGCAGCACTCTTTGCACCGCGCATGTTTGCATCTCGGCCTGGCCAGAAGAGCCCAACAACGCAGCAGGAT[G/T]AGCCATCATCTGACAAGAAGGAGGAGAGAGAGAAAGAAGAAGGAGTGAACTACACCACAGTGGACTGGAGAGAGTTCCTCTGCAACACGTGGCATCTGGAGCCCACACTACGGTAACACTGCAGTCACATGACCTCAACATTTAGCACATGTTTAACACACCATTTGATACTTTAAGAATTTTGTAAAATGTTGGAAAAAACATAATAATAATAGTAATAGTATGCTACGTATGTCAATGGATGCATTCTGATTTGTCGTCTTTGATGTATTAAGATTGATGAGGTAGACACCTCTGTCATGGCTGCTCAATACTTGAACTATTTTAGGCGTGATGAATTACATATTTAAAAATAATCTTATTATCTGCGTTATTTCAGTTTTTATTTAGATACAGTCCAAGTTATCATTCCTCAGTATATGCGTCTGAATAGTGCACGAAAGTCCTAATATTGTGTGTGCGCACATTCTGCTGTGATTGCTTAGTGGAGCAACGTTGAT
Associated Phenotype:
Not determined