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 |
---|---|---|---|
sa11348 | Nonsense | Available for shipment | Available now |
sa21664 | Essential Splice Site | Available for shipment | Available now |
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:
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:
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:
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