ZMP
tln1
Ensembl ID:
ZFIN ID:
Description:
talin-1 [Source:RefSeq peptide;Acc:NP_001009560]
Human Orthologue:
TLN1
Human Description:
talin 1 [Source:HGNC Symbol;Acc:11845]
Mouse Orthologue:
Tln1
Mouse Description:
talin 1 Gene [Source:MGI Symbol;Acc:MGI:1099832]
Alleles
There are 15 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6161 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34845 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11348 | Nonsense | Available for shipment | Available now |
sa34846 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2572 | Essential Splice Site | F2 line generated | Not yet available |
sa21664 | Essential Splice Site | Available for shipment | Available now |
sa41593 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5825 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38777 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15487 | Nonsense | Available for shipment | Available now |
sa31764 | Nonsense | Available for shipment | Available now |
sa10075 | Nonsense | Available for shipment | Available now |
sa21665 | Nonsense | Available for shipment | Available now |
sa21666 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6161
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 40 | 2538 | 2 | 56 |
ENSDART00000078135 | Nonsense | 40 | 2544 | 2 | 56 |
ENSDART00000098857 | Nonsense | 40 | 323 | 2 | 10 |
ENSDART00000098858 | Nonsense | 40 | 405 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8155703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6168865 |
GRCz11 | 10 | 6170074 |
KASP Assay ID:
554-5227.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTGGYGTACGACGCCTGTCGAATYATCAGGGAGAGAGTTCCAGAAGCA[C/T]AACTCGGCCAGCGTRAGTCCATCAGCAGTATACTCAGAACCCTGTCTTAT
Long Flanking Sequence:
TGGTTGTTACCTTGGGATAACATATCTTGCAACACAAAAAATTACTTTTGCTATTTGTTCAAACTACTTATTTAAAATAAGTTGAAACAACACATTTCTTAAGGTTTCATGTTCAATACAATTAAGTTAACTTAATAAAGTTTTGTTGTGACAACATGAAAAAATTGCGTTGAACTCAGCATTTTTTGCAGTGAATGTTGCAACTGACCAATCAGAATCTAGTTTTTAAACACTTGTGTCATACTAAACTTCACCACAAGTGGCTCCGCCTGTACTTTGTAACCAAACTTCAGTGATGCTTTTTAAAGTGAACATTGGAAATTTCTAACATCCTCATGTTTGTTTTGCAGGAGTAGCAGTGGCACAGTCCCGTATTGTCAGTCATGGTGGCGCTGTCGCTGAAGATCGGGGTGGGGAATGTGGTGAAGACGATGCAGTTTGAGCCCTCCACAGTGGTGTACGACGCCTGTCGAATCATCAGGGAGAGAGTTCCAGAAGCA[C/T]AACTCGGCCAGCGTGAGTCCATCAGCAGTATACTCAGAACCCTGTCTTATCTGATGCGTTCTGAAGTAAACAGACTGTTGACCAAACTGATGACAATGATCATTATGAACCAAGATATTGATATTGAAAAGTGGTCAAATTTAAAGTGCAGAACAAAACATTGCTTATTTTTTTTATTTTTATTTTTTTGTAATTACAATATAATTTTGCATCTATTTAGTTAAAATTCTTGCTTTTCAATTATTTGTGCAGTGTGTTTGTGTGCTGGCATACCTTTAGGCCTATCGTGGATTAATTAAAGGGATAGTTCACCCCTAAAAATAAAAGTTTACTCACTATCAAGGGGATTCAAAGAAGGGTCCCACAATACTGGGAAAATACGTCATTGCAATAATATTTTTTTTCGATATAATCTTTTCCTAAATAATGCTATTTAATTAGACATGTTTTTTCATTTGTCTTTGTAATGATGTTAAAATAAACAGGCAATAGATATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34845
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 189 | 2538 | 6 | 56 |
ENSDART00000078135 | Nonsense | 189 | 2544 | 6 | 56 |
ENSDART00000098857 | Nonsense | 189 | 323 | 6 | 10 |
ENSDART00000098858 | Nonsense | 189 | 405 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8163970)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6177132 |
GRCz11 | 10 | 6178341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGTTGGATCATGGGCGGACGCTGCGGGAGCAGGGTGTCGAGGAGTCT[G/T]AGATGCTGCTTCTTAGGAGAAAGTTCTTCTACTCAGACCAGAATGTGGAT
Long Flanking Sequence:
GGCATCACAAATTATGATGAGTACTCACTGGTGCGTGACGTGGGAGAGGAAAAGAAGGAAGAGACCACAGGAACACTGAAGAGAGACAAGACCCTCCTGAGAGATGACAAAAAAATGGAGAAACTCAAACAGAAACTTCACACAGATGACGAGCGTATGTCTCAATACATATATAGTTTGCTATTTTAGCTGGTCTTCAATACAGTACATACTGTATATTCTTAATGTATTCACATACCTAGCAAATAATTGAGCACAAAACACTTCATCATTACACTTTTTGTCACATTATACTATAGAGAAAAACCTGTTAATTACATCAATAAAAATTTTAGTTTTGTAACCAAACTCCAATAGTATTATGTATATTAGAAAAATAAATAAAATCAAACCAGTTACAGTTATATCTAGTTGAATTCGCTGATTGGGATTTTAATGTGTATTCAGTGAATTGGTTGGATCATGGGCGGACGCTGCGGGAGCAGGGTGTCGAGGAGTCT[G/T]AGATGCTGCTTCTTAGGAGAAAGTTCTTCTACTCAGACCAGAATGTGGATTCCAGAGACCCTGTACAGCTCAACCTGCTGTATGTGCAGGTAAAAACCACAGGAAATTCTCTTCGCATCGCAATCATGGCCTTATGTCATCTGTAAAATGGTGTTTTTGTTTTGCCATCTGCACTAGTGCTTTCAAATGTTTTGCTCTCAGAAAACAATCAAATACTTTTGTCACAAATGTGTAAAGAGTAAAATGATGTGCCGGTCACTCTCAATCTAACATGAGCGTGAAACCTGGCATACGCAAACCTTTTGTGCGTACGCACTACGCAGTGTTGATACATGAGGCTCCTGATCATGTGGCGCAACACCTCATCACTCTACTTGGTCAAATAGCCCTTACATAGCCTGGAGGTGTGTTTTGGGTCATTTTCCTGTTCAAAAGTAAATTATGGTCCAACTAAATGCAAACCGGATGGAATAGCATGCCGCTGCAAGTTGCTGTGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11348
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 216 | 2538 | 6 | 56 |
ENSDART00000078135 | Nonsense | 216 | 2544 | 6 | 56 |
ENSDART00000098857 | Nonsense | 216 | 323 | 6 | 10 |
ENSDART00000098858 | Nonsense | 216 | 405 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8164053)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6177215 |
GRCz11 | 10 | 6178424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGACCAGAATGTGGATTCCAGAGAYCCTGTACAGCTCAACCTGYTGTA[T/A]GTGCAGGTAAWAACCACAGGAAATYCTCTTCGCATCGYAATCATGGCCTT
Long Flanking Sequence:
AGACAAGACCCTCCTGAGAGATGACAAAAAAATGGAGAAACTCAAACAGAAACTTCACACAGATGACGAGCGTATGTCTCAATACATATATAGTTTGCTATTTTAGCTGGTCTTCAATACAGTACATACTGTATATTCTTAATGTATTCACATACCTAGCAAATAATTGAGCACAAAACACTTCATCATTACACTTTTTGTCACATTATACTATAGAGAAAAACCTGTTAATTACATCAATAAAAATTTTAGTTTTGTAACCAAACTCCAATAGTATTATGTATATTAGAAAAATAAATAAAATCAAACCAGTTACAGTTATATCTAGTTGAATTCGCTGATTGGGATTTTAATGTGTATTCAGTGAATTGGTTGGATCATGGGCGGACGCTGCGGGAGCAGGGTGTCGAGGAGTCTGAGATGCTGCTTCTTAGGAGAAAGTTCTTCTACTCAGACCAGAATGTGGATTCCAGAGACCCTGTACAGCTCAACCTGCTGTA[T/A]GTGCAGGTAAAAACCACAGGAAATTCTCTTCGCATCGCAATCATGGCCTTATGTCATCTGTAAAATGGTGTTTTTGTTTTGCCATCTGCACTAGTGCTTTCAAATGTTTTGCTCTCAGAAAACAATCAAATACTTTTGTCACAAATGTGTAAAGAGTAAAATGATGTGCCGGTCACTCTCAATCTAACATGAGCGTGAAACCTGGCATACGCAAACCTTTTGTGCGTACGCACTACGCAGTGTTGATACATGAGGCTCCTGATCATGTGGCGCAACACCTCATCACTCTACTTGGTCAAATAGCCCTTACATAGCCTGGAGGTGTGTTTTGGGTCATTTTCCTGTTCAAAAGTAAATTATGGTCCAACTAAATGCAAACCGGATGGAATAGCATGCCGCTGCAAGTTGCTGTGATAGCCATGCTGGTTCAGTATGCCTTCAATTTTGAATAAATCCCCTACAGTGACCAGCAAAGCACCCCCATTTCGCAGCTCATTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34846
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Essential Splice Site | 261 | 2538 | 7 | 56 |
ENSDART00000078135 | Essential Splice Site | 261 | 2544 | 7 | 56 |
ENSDART00000098857 | Essential Splice Site | 261 | 323 | 7 | 10 |
ENSDART00000098858 | Essential Splice Site | 261 | 405 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8165130)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6178292 |
GRCz11 | 10 | 6179501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAGTTTGGAGACCACAATGAGTCCAAACACAAACCTGGATTCCTAGA[G/A]TAAGCACTCACGTTTCTATAATTCGAAAATCCTGCTTTTGTGTGGTGTCG
Long Flanking Sequence:
AACTAACAAAAGCATAGATGGCTTTCTCAAGATCAGCCTTGCTCAGGAAGGGCCTGACTTCAGAGAGAAGGCGAAGCTGAAAAAAGCTGGCTTTAATCAGCGAATCAATCTGCTTATCAAATTTTAGACTACTAAAGTTCAGATCTGTTGATGACACAAACATCTGTGCTAATCTACAATCAAATGGCATGTTGAACATCAAATGTGATCTGAATGTCTGTAAATGTGCCACGTTATGCATGATTTTCTTAAAGGTATAAACAGACAGACAAGATTACTTCTTGTTGAAAATGTGCCTGGTTCATTAAATTACGATGTTGCTAATTCTGTTCAATTTCAGGTACATTTAAGGTATCGTGTTTTGTATTCCAGGCCCGTGATGACATTTTGAACGGCTCTCACCCTGTCTCCTTCGATAAGGCCTGTGAGTTTGCTGGATACCAGTGCCAGATTCAGTTTGGAGACCACAATGAGTCCAAACACAAACCTGGATTCCTAGA[G/A]TAAGCACTCACGTTTCTATAATTCGAAAATCCTGCTTTTGTGTGGTGTCGTTGAAAAGAAACCTCTGTGTTTGGGTTGATAATGTATAAACATTTGATCATAATTTAATTATTTCATAGTTAAGACATTTTTAAAAAAAACTCAAGAAATGATCCCAAACTGCATGAAAAATGAAAACATCTACAGTCAATATTACAATTATTGATAAGTTTTTTAAGCAGATTATCAGAGAAATATGACTCTGAATATGATTTTATAGGAAAGTTTTTAGATAAAAGTGCACTATAAGAATAAGTCAGTAAAATATACGGTTAAAAATTAGCATTTTACTTTATTTCATCATTTGTTTTTGACATACAGCAATGATTCAATGTTTTTATGTCTACACAACATATCACAGACAGCAAAAGGAACACAACCATAAACATACAGTTGAAGTCAGAATATTTAGCCCCCGTGTTTATTTTTTTCCCAATTTCTGTTTAAAAAAAAAGAGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2572
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Essential Splice Site | 398 | 2538 | 11 | 56 |
ENSDART00000078135 | Essential Splice Site | 402 | 2544 | 11 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | Essential Splice Site | 402 | 405 | 11 | 12 |
ENSDART00000013609 | Essential Splice Site | 398 | 2538 | 11 | 56 |
ENSDART00000078135 | Essential Splice Site | 402 | 2544 | 11 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | Essential Splice Site | 402 | 405 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8174609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6187771 |
GRCz11 | 10 | 6188980 |
KASP Assay ID:
554-3431.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGATTGCACAACTCATTGCTGGATACATTGACATCATTCTCAAAAAGG[T/C]AACACGCTATGACTTCTCAGGGGTGTGCAGCATTGACCAGAATGTTTTCT
Long Flanking Sequence:
CATAAATGCGTGTTTTTTTGTTTAGAGAATGTAAGAAATCTGGTGCAAATGAGCAAAACTGGTGTGAGTGTCAGTTAAAGTGTCAGAGATGAAAGAGTGTGTTTTCTGCAGGTGGTTTGTCAAGCCCACTCACATTTAGAAATGCGTAATGTTTTGGGGTTGTCTCATCTAAAGTTTCAAAATTGGCTCTTTCGTTGGTGGGAAAGTAACACTTTTACATTTGCAAACTACATAATAGACTAAATAACAGGTGGAATTTTAAAATCATAGAGACATTTTAATACGGAAAAGCATGCACTTCTGAGAGAAATGATCTGTAGTTTGCTGTATTATTTGTGCTGTAATTTTTACCTACCATTCGAAGTTACATGTCATGTGTGTACTCTTTCCTCTTCAGGACTTTGGAGACTATCAGGATGGTTACTACTCAGTTCAGACCACTGAAGGAGAACAGATTGCACAACTCATTGCTGGATACATTGACATCATTCTCAAAAAGG[T/C]AACACGCTATGACTTCTCAGGGGTGTGCAGCATTGACCAGAATGTTTTCTGTATATAAATAGGGCCTCTCCTATCATGTTTAAATAGATATAAGACTAAAACCACCAAGAGGAGGTAAAATTACGCTTATAATGTGTGATTCATTCATTCAAATGATTCAATCTAAATGAAATTTACTCTATTGAACAATTAAAAGGATCATTAAATCAGTGATTTGTTCAAAAACAGATTAATTTAATAACAAAACACCACATTGCTGCCCAGTATTGCACAAATGTTCTGCTAAAGCTTTATTTGGAAACGTTTTATTGGCGTAAGTCTAAGAAAAAGAAAAGAACAAATATTTTGACTAAAACATAACTTGCCTACTATTGACTACACTTTTACTTGTGTGATATTACATTACTATATCATGTTTTACAAATAGAATCTAGAATACATTTTACATTTTACATTTTTATTTACAAAACATGTGCTTGTTTGTTGTAAAAATTCATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21664
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Essential Splice Site | 424 | 2538 | 12 | 56 |
ENSDART00000078135 | Essential Splice Site | 428 | 2544 | 12 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8176680)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6189842 |
GRCz11 | 10 | 6191051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGAGATGAAGAGTCAACCATGTTGGAGGACTCCGTCTCTCCGAAAAAG[T/C]GAGCCCCTTTAATAGTTCATTGCATTCTGGATACACAGAAACAGATATTT
Long Flanking Sequence:
GTGACGCGGCAGAAATATGAAGTTTCCTGAATTGTAGCTGGGCACCGCGGACAGCAGCCGACTTGCAGCGCCAGTGTGTGTACACTGATAGAAACCCATGTTTCCAATTCTGAAAAGCATGGCGCATCTGGTGACCCCCTTTACACTTTTGTAGGCACTGTTCATAATTTCCTATGCATTTGTGCAGTACTGTCACTAAGCAGCTCTTTTTCATATCAGTCTTATTTTGAATGGTTGTGTATCGTGTCCATGTGAAATTGCTGCTGCTGGTTCTCTACATTATGAGGAATTCCTCAACAAACCTCCATGTTTGAGCAACTGAGAATGAAACAATCTGCTCTGGCAACTAAATGCCTCTTTCAGGTTCTTTTCATAAGCATCTTTCCTCAAGTCACTGTGTCTGAAAACCTCTTCCTCTGCAGAAAAAGAGCAAAGATCACTTCGGCCTGGAGGGAGATGAAGAGTCAACCATGTTGGAGGACTCCGTCTCTCCGAAAAAG[T/C]GAGCCCCTTTAATAGTTCATTGCATTCTGGATACACAGAAACAGATATTTCCCAGTATTTCTCTGTTGCAATCGTGATATCCCAATAATTAACCCTGAAAAAATCGAAGCAGCGCAGTCACAACCAGGTTACTGTTGTGTTTGCGATAAGGAAAAACACTGAACACATGCGGGCATTTCTTCTTTCTTTCTGTTTACTGAACTAGTCCGCAGTAACGAAAACAGGCAACAAATTAGAAACAGATGACCAACCAAAAAGTAACTCAGGGTTATACAAACACAAAATACACTTTTGGCCAACACAAAATACATACATTCCTGATATGCGAGTCCCATCTCGCACTCAATACACTACAATTACTATAGCATAAATACAGAACTGCAACATACAAAAGAGAGAGATCGACTTAGAAAGTCACTTACCAGTTTTATATTGATTTGATCCGCTGTAGTTAGGAATAACACTAACACAATGCTTTTCTCTTCTAAGGGCTTATTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41593
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Essential Splice Site | 558 | 2538 | 15 | 56 |
ENSDART00000078135 | Essential Splice Site | 562 | 2544 | 15 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8182461)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6195623 |
GRCz11 | 10 | 6196832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGATGCCATCACTGCGGGAACTGCTTCCATGGTCAATCTGACTGCAG[G/A]TGAGACGCTCGCAACATCTCACCGTTCACATCTTTGCGGCGGGTGGTTTA
Long Flanking Sequence:
GGTTTAATAGTTTTTTGTTGTTAAAATTGAAAAATTGAAGTTCCTGTTTCGAAACTTACAGATAGATGGCTAATTTGTATGTCATTGATATGTTCAGTGCTAAGATAAATAAACACTTTTGGCACTTTTTTCGAGTCTTTTCATTAGTTTAGTTTTTCCTGTAAATTATTCAATAAATACCGTACCGTGCCATTCATACCGAGGTATTATCGTACAGTGAAATTCTAATATCCCTAATAATCACCCTTGTAATCAGGATTGACATTGTTGGAAAATGGTTTCTCCTTCAATGTGTTTTTGACCCTGAAAGTTCGAAAACAGAAGAAAAAAACTGCAAAAAAACTATTTATTTTGTTAAATAAACTAAAATCCTGTGTCTCTTCTTGTTCAGGCATCTCAAGCCTGGAGGAAGAACAAAATGGATGAGTCCAAACACGAGATTCACTCTCAGGTGGATGCCATCACTGCGGGAACTGCTTCCATGGTCAATCTGACTGCAG[G/A]TGAGACGCTCGCAACATCTCACCGTTCACATCTTTGCGGCGGGTGGTTTATACTGCGAGACCTTTTTTCTGCTGAATATACAATTCATGGTGTAACTTTACACTGTGATTCGTGCGTAATTGAGTGTTTTGCAGGCAAAATATGTGCAGCTTCAGTGAGAGTAAAGGATTTTCTGTCCATCTACTGTGTCTGTCTATGATTTTCGTCTGAAACATGCCAGATGTTGTGTTGGACGCTGTAGAGCCTGGGCAGGAATTTGATTTTGTGCCTGCTGAGACTTTTTTGTTCTTCATTTAAGGAGGAAAACAAACGCAGGCATCATTATACTGTTAGTAAACTGCTGACGCTGCGTGCATGTGCTGTTTAGAGACATATGTAAACCTGTTGTTCATTTTAGCTCCATTTTACTAAAACTATTTTCTAAAATTGATCACATGACCAAATGATGTGGCCATCCTCTGGTTGATATTTTAACTGTAATGACCAATTTTTACTTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5825
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Essential Splice Site | 1438 | 2538 | 33 | 56 |
ENSDART00000078135 | Essential Splice Site | 1441 | 2544 | 33 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8240105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6253267 |
GRCz11 | 10 | 6254476 |
KASP Assay ID:
554-3889.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGTTCAGCGTCTAAAGCGCTGTGTGGTCTCACTGAAGCAGCTGCTCAG[G/A]TAAAAACRCTTATGTGTGTGTGTGTCNNNNTGTGTGAAGCTCATCTCTCCTAAA
Long Flanking Sequence:
TTTGTGTGTGTTTGTGTGTGTTTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTGTGTGTTTGTGTGTGTTTTTGTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTCTGTCTGCAGACGGTTGGAGGAATGCTGGAGAACCCAACAGAAGCAGTCAATGATTTGGGCTACTTTGACTGCATTGACAGTGTGATGGAGAACTCAAAGGTGCCACAGTGATCACAATAAAACGAAAACTAAATCACCCAATCTCAGTGTTGAGCTAATGCTTTATTAATGTTGATGTTGTTTGCAGGTTTTGGGTGAGGCCATGGCTGGCATTTCCCATAATGCCAAAAACAGTAACTTGCCAGAGTTTGGAGATTCGGTCAGTTCAGCGTCTAAAGCGCTGTGTGGTCTCACTGAAGCAGCTGCTCAG[G/A]TAAAAACACTTATGTGTGTGTGTGTCTGTGTGAAGCTCATCTCTCCTAAATTAGAGAGCTGAAGAGGTGGTGCGTGATGAAATGTACCAGTGCTATGATGCGTCAAACATCTGGACTTACAGGAGCGCATTAAATGAACAAACACATCCGCTGTTCTTCATCGCTGTCTTCTGTGCCTTTGCTCACACCTCCGTGCTTTTGTTATTTATGGGCACAAGAATACACTCTCACACACTTGTGCAAAAAGATTTCCTAATGGCTTTGATGGGCAGTGAGTCATTTAACTGCTTTCTGAGCTTAGCCCTAAAAAATTGTTCACTCAGAGCTGCCATTTCTGTAGTGATTCATTTTATTTGTCTGGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTGTGGATGGGGGGAGGAGTGTGATGTACCAATAATGTGAACTTGATTGTGTTTGTTTGGTTGTGTCTTGTGTTTCTCACAGGGGGCGTATCTGGTTGGTGTGTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38777
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 1520 | 2538 | 35 | 56 |
ENSDART00000078135 | Nonsense | 1523 | 2544 | 35 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8243369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6256531 |
GRCz11 | 10 | 6257740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCTGCCGGCTCGCCTCCTCCAAGACATCCAACCCAGTTGCTAAGAGA[C/T]AGTTCGTCCAGAGTGCCAAAGAGGTGGCCAACAGCACAGCCAACCTCGTC
Long Flanking Sequence:
ACTTGATTTAACCGGCGTCTGCTACAGTATGTGTCTAGGCTCTTTTTCTTTGCTACTGTTTGTGGGCGGGGCTGCAGTTTTCAATTTTCCCGTATTTGCACGCGCAACAACTGGGTGGGACTAACGTTTTGTATCAACATCATGCTGAAACGACTAAAGACTCGTTATCAAGATGATTCATTTGAAGCATTATGAGTCGACTCTTTTATAAATGAATCAAAAGTTTTAAACACTGTGCACTTTCAGATTTAAGCCTTAGCTGGATATTTCACTTCACTCAGTTCTCAGTTCATTCTCAAAAACCCATTACAGGGGCTCTTTAAATCCAATCTATATTAGTCACTTCAAATAACTTCATAGTGAGTCATAGTCATGTTTCATTCACCTGCATATTTTCCTAGGTTCTCTCTGCTGCCACCATCGTTGCCAAACACACTTCGGCCTTGTGCAATGCCTGCCGGCTCGCCTCCTCCAAGACATCCAACCCAGTTGCTAAGAGA[C/T]AGTTCGTCCAGAGTGCCAAAGAGGTGGCCAACAGCACAGCCAACCTCGTCAAGTCCATCAAGGCAAGTTTGGAGAATATCAGTCAGTGTTTATGTGCTAGTGTTATTGCGGTGATCATAACTCTGTGTTTGTGTGATCATGTCAGGCTCTCGACGGGGCCTTTAACCAGGAAAACAGACAGAAGTGTAAGGAAGCCACTGGGCCACTCATTGAGGCTGTGGATAACCTGACTGCCTTCGCTTCAAACCCAGAGTTCGCAAGTGTACCCGCTCAGATCAGCCCAGAGGTGTGTTAAATCACTGTTATATCACAGTAATCTTATTTATTTTATTGCTTGTCCAAAAGTTTAGGGACAGTAAGCGTTATGTAATTCCTTCTTTTATTCAGAAAGGATGTATTTAATTCATATAAGAGTGATTTCAGAAGGATCACACAACAAAGCTTATTTATTCAGTCTTCATGTGCTATTTACAGGGCTGGACTTAACTAATAAGCAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15487
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 2108 | 2538 | 46 | 56 |
ENSDART00000078135 | Nonsense | 2114 | 2544 | 46 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8263823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6276985 |
GRCz11 | 10 | 6278194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCCACCAAAGCAGCGGCCGGCAAACCTCACGATGACCCCGCCATGCTG[C/T]AGCTCAARAACTCTGCTAAGGTACAAAACATTCTCCAACACACAGCCCTT
Long Flanking Sequence:
TGAAGACATCCAGTAGTCTGCATGTTTGATTCATTTATTAAGCGCAAAGATTTGTTTTAAAGCTATTTCTTAGCTTTAAACGAATAAATGAACAATAATAACGAAGTGTGGTCAAAAACCACATATCCAAGTTATATCCAAACACACATCCTATTCTTATGCCCCATATGGTCCAAAACCAGACAAATGAACAAATCTAAACTAGTTTTTATTTAAACAAATATAAATATGCTTATAATAAATACTTCTAATAATAATAACATTATACAAATGCAAATTGTCATGAATAAATAAAAAAGTATTACTCTGATAAACATCATTTAGGAAATATCTGAAAAAGAAAAAAAATCACAGTAGGGCTTATAATTTTATCAACTGTATTTGTTGTTTGTCAGGTGGTTCTGATCAACGCTGTGAAGGACGTGGCTAAAGCTCTGGGTGACCTGATCAGCGCCACCAAAGCAGCGGCCGGCAAACCTCACGATGACCCCGCCATGCTG[C/T]AGCTCAAAAACTCTGCTAAGGTACAAAACATTCTCCAACACACAGCCCTTAGACTGTCTCTGCTCGGGGCTTTCAGTGGTTGAGCTCAATCAAAATGACTGTCCTGATTATTATGGGCTGCCAGACAACATTAGCTGACCTGAAATCATGATTCTGTGACCTACAAACCAAACTGGAAGAACTGATGACGATGATTTACGCTTGGATAAGTGGTTGTTATTGGTAGCTAAAACTAATAAAATAAATATTAGATAAACATTTTTAAAACACATTAATATTGCTTTAACAAATTTAAACACAAAATAAAACAATTCAACACAAATGTAAAAACAAATATTATATATTAATATGGCATGACTAATAACTAATGAAACCACAAGTGCACATAATAAAATTATTTAAATAAAAAATAAGAAAAAAGAAAATCTGAAAAGAAAAGATCATTTAAAATGTGAATAAATACTATGATAGTATATACGTATTGCTAACGCAACTGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31764
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 2136 | 2538 | 47 | 56 |
ENSDART00000078135 | Nonsense | 2142 | 2544 | 47 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8266596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6279758 |
GRCz11 | 10 | 6280967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGACGTCTCTACTTAAGACGGTGAAGGCGGTGGAGGATGAAGCCACT[A/T]AAGGCACACGAGCACTAGAGGCCACCATAGAGCACATCAAACAAGAGCTG
Long Flanking Sequence:
TTTAGTTATTGATATTATTTATGTTACCACTAAACCGCATGTCTTTGGGCTTGTGGGGGAAACCGGAGCACCTGGAGAAAACCCACGCCAACACGAGGAGAACATGCAAATTCCACACAGGAACGCCAACTTACCCAGCCGGGGCTTGAACCAGCGACCTTCTTGCTGCGAGGCAATTGTGCTACCCACTGCGCCACCATGCTGCCTCGATTATTCCATTTAATTTTTTTTTTATTCTTATTTCCAATCAATTTTTCTGATTTGCTTGATTTCTGAACGTCTCTTTCAATATTTCTTTCTGTGCCAGGCTTCAGCAAAGCAAACCTTTCTGTATTGCCTCTATTAATAAAACTGATTTCTCCTTTGATTTCCCATTCATGTTAAGTGGCATTGCTAATGTGTTTTTGGATTCGTGTCGTTTCTGTGGTGTTCATTAGGTGATGGTGACCAATGTGACGTCTCTACTTAAGACGGTGAAGGCGGTGGAGGATGAAGCCACT[A/T]AAGGCACACGAGCACTAGAGGCCACCATAGAGCACATCAAACAAGAGCTGGCTGTAAGAAACACACACTCTCTAAATCAGTGCATTCATGGCTACAGTTCAATCAAGTATATTAACAAATATTTCAATAATAATTATTATGAATGGTTAAGGATGTCAATATATGGATTTTGACATTTATTTTAATATTTTATATGCTCTTTTGGGGGTTCAAAAATTGTTTGTACACAATTTTCATTCACTCATTTTGTTGTCGGCTTAGTCCCTTTATTATATCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAACCCATCACTGGGAAACATCCACACACACATTCACACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCATCTGTACCACATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCAAAGGCAGGGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10075
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 2205 | 2538 | 48 | 56 |
ENSDART00000078135 | Nonsense | 2211 | 2544 | 48 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8267645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6280807 |
GRCz11 | 10 | 6282016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAACTCCTGCCRTCAGGAGGAYGTGATCGCCACWGCTAACCTAAGCAGA[C/T]GAGCTGTCGCAGACATGCTGCGCTCCTGCAAGGTGAGGCCACTTTCAMAG
Long Flanking Sequence:
CGACCTTCTTGCTGTGAGGCAACAGCACTACCTACTGCGCCACTGCCTCGCCCACACAATTGTCAAACTTTTTCAAATATTACAAAGTAATTTTTAAGACAGCAAGGACATTTTTCACAGTATTTCCTATTATATTTTTTATACTAATTAAGTTAGATTTTCTCCAGAAGTCTAACTTTCTAAATAATTTAAAATTTGTGATAAGGTCAATAAAATCAGCGCCTTTTATACATTTGCTTTAGACGGAAAAAACTTAATTCAGAAATTGAAACAAAATAAACCTTAACTTACTTAAGTCTTTGAGATCATCTTATGATTTAAACACAATCTGTGTGTCTTTCCCTCAGGTTTTCAGCAGTGCAGATCCTCCTCCAAAGACGGCCACTCCAGAGGAGTTCATCCGCATGACCAAAGGCATCACATTGGCCACAGCTAAAGCAGTGGCTGCTGGGAACTCCTGCCGTCAGGAGGACGTGATCGCCACTGCTAACCTAAGCAGA[C/T]GAGCTGTCGCAGACATGCTGCGCTCCTGCAAGGTGAGGCCACTTTCACAGTGTCAACATCACGTCTGACAATGACTCCATATGAACAGATGAACAGTCAGGACCGCTTCAAAATGATATATATGTTTGGCCCCTTAAGAGTTTATACACTAATGAGCAATGGTCTCAAACTCAATTCCTGGACAGCTCTGCACAGTTTAGCTCCAACTCAAACCTGCTTAATAGTTTCTAGTAGTCTTGAACAACTTGATTGGTTTGATCAGGTGTGATTAATTAGGGTTTGAAGCGGAGTCGGATACTTCCTTACTATATAGTACGCTAAAAATAGTATTTGAGCCGAGAAGTATGCCCCAATTCATAGAATTTAAAAACAACAGTATCCAAGAAGTACCTGGATGACCTCCTACTTCCAGCGAGTATCTAAAGTGAGCATCCAACGGATGCTACGCCATCCCATGATCCACCGCGAGAGAATTCATGAATGGGAGTGAAGCGATGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21665
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Nonsense | 2306 | 2538 | 51 | 56 |
ENSDART00000078135 | Nonsense | 2312 | 2544 | 51 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8284155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6297317 |
GRCz11 | 10 | 6298526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGGTGGATCCCGAAGACCCCACCGTCATTGCAGAAAACGAGCTGCTG[G/T]GAGCCGCAGCTGCCATTGAAGCTGCCGCGAAGAAACTAGAGCAGCTCAAA
Long Flanking Sequence:
TAACTACTAATCCACCCAAACACTGCAGAAATTGCATATCTCATCAATGGTGAAGAAAGACTTTAGATGTATTAAACTTAACTTTAGTCAACACCAAACATAATGTTGATTTCTTTTTTGTTTCGCTTTCACACTGCCCTTTTTGCAGTTAAACAGTGATTGTAAACAAAACCAAATGTGTTATGTCAGCTGTTTGTTGGACAGAAGTTGCTATATTCACACCTGCACCAAAGGGGAAAACAAACTTATGTTTGATTCAAACAAACAAAACAAGACCGATGTAATTCCCTCCTTAATGAAATAAACAGTCCAGCATCAGGTATTGGTGTAATTGTCATCATAACACTATGAGGTTTTGATGCAGCAGTAGTTCTCAGTAGTGTAGTATAACAGACACACAGCACAATCTTACAGAGGAGTTTGATTGGCTGTGATCCTGTCTAGGTACGGAGTGGGTGGATCCCGAAGACCCCACCGTCATTGCAGAAAACGAGCTGCTG[G/T]GAGCCGCAGCTGCCATTGAAGCTGCCGCGAAGAAACTAGAGCAGCTCAAACCCCGAGCCAAACCCAAGGTGAGGAAATGTTTAGACACATCCTTCAGGCTAAACTGACACTGCCTACAGCTTGACATTTCTATATTTAGCTCTGGAAATCCCACTCTGTGTTCATATATTCTTAAGCCAATACATTATCTGACCATTGTACAACTTCTCCTGTTTGTGCTTACCAGTATGGATTTGGATTTAAGGTAACTTCAATCAGCCATGACTACAGTCACTGAGCATGAATTAAAGGGATAGTTCACTCCAAAAAAATGACAAGTCTATCACCTATGCCACTTGATCCAAACTTGTCTGAGGTGCTTTAATCTGCTAAACACAAAAGAGGATCAACTGAAGAGTGTTGGAAACAAAAGCAACCCTTGACTTTCATAGTATTTTATATTCCTACTAGTATATCCCTATGAATTTGGTCACCTACTGTAGCACTTTTAGGAATAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21666
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013609 | Essential Splice Site | 2328 | 2538 | 51 | 56 |
ENSDART00000078135 | Essential Splice Site | 2334 | 2544 | 51 | 56 |
ENSDART00000098857 | None | None | 323 | None | 10 |
ENSDART00000098858 | None | None | 405 | None | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 8284225)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6297387 |
GRCz11 | 10 | 6298596 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGCCGCGAAGAAACTAGAGCAGCTCAAACCCCGAGCCAAACCCAAGG[T/C]GAGGAAATGTTTAGACACATCCTTCAGGCTAAACTGACACTGCCTACAGC
Long Flanking Sequence:
ATTAAACTTAACTTTAGTCAACACCAAACATAATGTTGATTTCTTTTTTGTTTCGCTTTCACACTGCCCTTTTTGCAGTTAAACAGTGATTGTAAACAAAACCAAATGTGTTATGTCAGCTGTTTGTTGGACAGAAGTTGCTATATTCACACCTGCACCAAAGGGGAAAACAAACTTATGTTTGATTCAAACAAACAAAACAAGACCGATGTAATTCCCTCCTTAATGAAATAAACAGTCCAGCATCAGGTATTGGTGTAATTGTCATCATAACACTATGAGGTTTTGATGCAGCAGTAGTTCTCAGTAGTGTAGTATAACAGACACACAGCACAATCTTACAGAGGAGTTTGATTGGCTGTGATCCTGTCTAGGTACGGAGTGGGTGGATCCCGAAGACCCCACCGTCATTGCAGAAAACGAGCTGCTGGGAGCCGCAGCTGCCATTGAAGCTGCCGCGAAGAAACTAGAGCAGCTCAAACCCCGAGCCAAACCCAAGG[T/C]GAGGAAATGTTTAGACACATCCTTCAGGCTAAACTGACACTGCCTACAGCTTGACATTTCTATATTTAGCTCTGGAAATCCCACTCTGTGTTCATATATTCTTAAGCCAATACATTATCTGACCATTGTACAACTTCTCCTGTTTGTGCTTACCAGTATGGATTTGGATTTAAGGTAACTTCAATCAGCCATGACTACAGTCACTGAGCATGAATTAAAGGGATAGTTCACTCCAAAAAAATGACAAGTCTATCACCTATGCCACTTGATCCAAACTTGTCTGAGGTGCTTTAATCTGCTAAACACAAAAGAGGATCAACTGAAGAGTGTTGGAAACAAAAGCAACCCTTGACTTTCATAGTATTTTATATTCCTACTAGTATATCCCTATGAATTTGGTCACCTACTGTAGCACTTTTAGGAATAAAAAGTTTATTCATTTAAATTTAAATGATTTATTGCTAAAACATTTTATATTTTTTTTGTTTCTCTTTTTTTTT
Associated Phenotype:
Not determined