ZMP
pax6b
Ensembl ID:
ZFIN ID:
Description:
paired box gene 6b [Source:RefSeq peptide;Acc:NP_571716]
Human Orthologue:
PAX6
Human Description:
paired box 6 [Source:HGNC Symbol;Acc:8620]
Mouse Orthologue:
Pax6
Mouse Description:
paired box gene 6 Gene [Source:MGI Symbol;Acc:MGI:97490]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11497 | Essential Splice Site | Available for shipment | Available now |
sa9552 | Essential Splice Site | Available for shipment | Available now |
sa15822 | Nonsense | Available for shipment | Available now |
sa86 | Nonsense | Available for shipment | Available now |
sa13392 | Essential Splice Site | Available for shipment | Available now |
sa20883 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11497
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014572 | Essential Splice Site | 66 | 382 | 4 | 11 |
ENSDART00000053407 | Essential Splice Site | 66 | 437 | 3 | 11 |
ENSDART00000067248 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000134696 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000143282 | Essential Splice Site | 66 | 384 | 4 | 12 |
ENSDART00000144765 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000145946 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000146704 | Essential Splice Site | 48 | 68 | 5 | 6 |
ENSDART00000014572 | Essential Splice Site | 66 | 382 | 4 | 11 |
ENSDART00000053407 | Essential Splice Site | 66 | 437 | 3 | 11 |
ENSDART00000067248 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000134696 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000143282 | Essential Splice Site | 66 | 384 | 4 | 12 |
ENSDART00000144765 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000145946 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000146704 | Essential Splice Site | 48 | 68 | 5 | 6 |
The following transcripts of ENSDARG00000045936 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 16647433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15630131 |
GRCz11 | 7 | 15882104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCGCACACAGCGGAGCGMGACCCTGCGACATCTCCAGGATTTTGCAG[G/A]TGACTTGTGAAGCCCATTCGCACATCCAYRAGCTTTACAGCTTCTAGTTA
Long Flanking Sequence:
GTCGATTGATTCCAGCATTCTGCTGCTGATTTATAGGGCACAACGAGCTGTGAAACAGCATTCACGACTCTTAATTTAACAAACGCAGAACTTGGCTTGGATTGCTGACCAGTGATTTAGAAAATAATTATAAGTTTCCTTTGTTGCTGTCGCAATTGTACAGTTACTGATTCCACTATGTTATATAACAAGGACATTGTGATGTAAAAGAAACAGTTTTTATGCTCTAATCTGACTTGGCTTGTCAGTAACGCTGATCAAAGGAAAGCACCAAGAAGTGGAGCTTTATTCTGGACAATGGGACACCTATTGAGGGAATGTTTTCGAGGGGAAAGACGAGCCAATTTGTTCTGTATCCGTGTGCCACAGGTCACAGTGGCGTCAACCAGCTTGGCGGGGTGTTTGTGAACGGCAGACCGTTACCGGACTCCACCAGACAGAAGATCGTCGAACTCGCACACAGCGGAGCGCGACCCTGCGACATCTCCAGGATTTTGCAG[G/A]TGACTTGTGAAGCCCATTCGCACATCCATGAGCTTTACAGCTTCTAGTTAAGATGGCCACACGCAATCACCATGTTGCAAAATTATAGCAAAGCCAAATTAATTACAATTATTTTAAGCACACTCTTCAAAATAAAGGGATTGGCATTGATAGTTCCCTGAAGAACATTTAACATCCACTGAAACGGATGGTATTTTAAAGCAGGGGTTTTTAAATGTTCTTCATATTAATATTATAATGGTTCTTAGAACTTTTGAGTGAATGTGCTTTATTTTCAAGAGTGTATTCAGAGATTAAAGGGGTAGTTCATCCAAAAAATCTAAATTACCATGTGACTTTCTTCCGTTGAACACAATAGAAGATATTTTGATAAATGCTGGTTGAAGGTTCCTATTGATGGTAGGAAAAAATACTATGAAAGTCAATGGGTACAATCAACTAGCATTCTTCAAAATATCTCTCTAACAGAAGAAACTCAAAATGAACAAGTAAAAACTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9552
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014572 | Essential Splice Site | 66 | 382 | 4 | 11 |
ENSDART00000053407 | Essential Splice Site | 66 | 437 | 3 | 11 |
ENSDART00000067248 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000134696 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000143282 | Essential Splice Site | 66 | 384 | 4 | 12 |
ENSDART00000144765 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000145946 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000146704 | Essential Splice Site | 48 | 68 | 5 | 6 |
ENSDART00000014572 | Essential Splice Site | 66 | 382 | 4 | 11 |
ENSDART00000053407 | Essential Splice Site | 66 | 437 | 3 | 11 |
ENSDART00000067248 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000134696 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000143282 | Essential Splice Site | 66 | 384 | 4 | 12 |
ENSDART00000144765 | Essential Splice Site | 48 | 81 | 4 | 6 |
ENSDART00000145946 | Essential Splice Site | 66 | 437 | 4 | 12 |
ENSDART00000146704 | Essential Splice Site | 48 | 68 | 5 | 6 |
The following transcripts of ENSDARG00000045936 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 16647433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15630131 |
GRCz11 | 7 | 15882104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCGCACACAGCGGAGCGMGACCCTGCGACATCTCCAGGATTTTGCAG[G/A]TGACTTGTGAAGCCCATTCGCACATCCAYRAGCTTTACAGCTTCTAGTTA
Long Flanking Sequence:
GTCGATTGATTCCAGCATTCTGCTGCTGATTTATAGGGCACAACGAGCTGTGAAACAGCATTCACGACTCTTAATTTAACAAACGCAGAACTTGGCTTGGATTGCTGACCAGTGATTTAGAAAATAATTATAAGTTTCCTTTGTTGCTGTCGCAATTGTACAGTTACTGATTCCACTATGTTATATAACAAGGACATTGTGATGTAAAAGAAACAGTTTTTATGCTCTAATCTGACTTGGCTTGTCAGTAACGCTGATCAAAGGAAAGCACCAAGAAGTGGAGCTTTATTCTGGACAATGGGACACCTATTGAGGGAATGTTTTCGAGGGGAAAGACGAGCCAATTTGTTCTGTATCCGTGTGCCACAGGTCACAGTGGCGTCAACCAGCTTGGCGGGGTGTTTGTGAACGGCAGACCGTTACCGGACTCCACCAGACAGAAGATCGTCGAACTCGCACACAGCGGAGCGCGACCCTGCGACATCTCCAGGATTTTGCAG[G/A]TGACTTGTGAAGCCCATTCGCACATCCATGAGCTTTACAGCTTCTAGTTAAGATGGCCACACGCAATCACCATGTTGCAAAATTATAGCAAAGCCAAATTAATTACAATTATTTTAAGCACACTCTTCAAAATAAAGGGATTGGCATTGATAGTTCCCTGAAGAACATTTAACATCCACTGAAACGGATGGTATTTTAAAGCAGGGGTTTTTAAATGTTCTTCATATTAATATTATAATGGTTCTTAGAACTTTTGAGTGAATGTGCTTTATTTTCAAGAGTGTATTCAGAGATTAAAGGGGTAGTTCATCCAAAAAATCTAAATTACCATGTGACTTTCTTCCGTTGAACACAATAGAAGATATTTTGATAAATGCTGGTTGAAGGTTCCTATTGATGGTAGGAAAAAATACTATGAAAGTCAATGGGTACAATCAACTAGCATTCTTCAAAATATCTCTCTAACAGAAGAAACTCAAAATGAACAAGTAAAAACTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15822
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014572 | Nonsense | 68 | 382 | 5 | 11 |
ENSDART00000053407 | Nonsense | 68 | 437 | 4 | 11 |
ENSDART00000067248 | Nonsense | 68 | 437 | 5 | 12 |
ENSDART00000134696 | Nonsense | 63 | 81 | 6 | 6 |
ENSDART00000143282 | Nonsense | 68 | 384 | 5 | 12 |
ENSDART00000144765 | Nonsense | 63 | 81 | 6 | 6 |
ENSDART00000145946 | Nonsense | 68 | 437 | 5 | 12 |
ENSDART00000146704 | Nonsense | 50 | 68 | 6 | 6 |
The following transcripts of ENSDARG00000045936 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 16648195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15630893 |
GRCz11 | 7 | 15882866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCTTAAATAATRTMTGTGAATTGTGTATATTGCTGTCCATTCAGGTGT[C/A]GAATGGGTGCGTGAGCAAGATTCTRGGGAGGTATTATGAGACGGGCTCCA
Long Flanking Sequence:
ATGTGCTTTATTTTCAAGAGTGTATTCAGAGATTAAAGGGGTAGTTCATCCAAAAAATCTAAATTACCATGTGACTTTCTTCCGTTGAACACAATAGAAGATATTTTGATAAATGCTGGTTGAAGGTTCCTATTGATGGTAGGAAAAAATACTATGAAAGTCAATGGGTACAATCAACTAGCATTCTTCAAAATATCTCTCTAACAGAAGAAACTCAAAATGAACAAGTAAAAACTTTTTGTGTGAACTATCCCTTTAAGCATGCGTTTCTCATTCAAAAAAGGTGGACACTAATGCAAAAAAAGTGTGACCCTAATTAGTCCTGAAACCATCCTAGCAATTTTAAGGCATATTTTCTGTGTTCGTAGACCCATGATGATGCAAAAGTCCAACTGGACAATAAGAACGTAAGCGTATAATCGTTTGACGTACATTACATTAGTTCACTCTAGTCTTAAATAATGTATGTGAATTGTGTATATTGCTGTCCATTCAGGTGT[C/A]GAATGGGTGCGTGAGCAAGATTCTGGGGAGGTATTATGAGACGGGCTCCATCCGACCGCGAGCCATCGGAGGCAGCAAGCCCAGAGTAGCGACGCCTGAAGTGGTGGGCAAAATCGCACAGTACAAGAGGGAGTGTCCATCTATATTTGCCTGGGAGATTCGGGACAGGCTGCTGTCGGAGGGTGTGTGCACCAACGATAACATACCGAGCGTGAGTGCAAATCAAACTTCATTTACATCATTTCATCAATACTTTGGTGGATAAATTTTTAATTTATCCACATTACAAGAAATTATACCTATGGAGCACTGTGTAAAGTGTTTAGTGCTTGACTTAACCTTTAATGTTGAATCAGATAAAGCTCAAGTAATTTTAAAGGGACAGTTCACCCCAAAATTTGAACTTTGCCATTGTTTACTCAACCAAACAAGGTTGAGTTTTGTTTGTTCTGTTGAAAACAAAAGAACATATTTTGAAAAACTTTGGAAACCACTGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa86
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014572 | Nonsense | 109 | 382 | 5 | 11 |
ENSDART00000053407 | Nonsense | 109 | 437 | 4 | 11 |
ENSDART00000067248 | Nonsense | 109 | 437 | 5 | 12 |
ENSDART00000134696 | None | None | 81 | None | 6 |
ENSDART00000143282 | Nonsense | 109 | 384 | 5 | 12 |
ENSDART00000144765 | None | None | 81 | None | 6 |
ENSDART00000145946 | Nonsense | 109 | 437 | 5 | 12 |
ENSDART00000146704 | None | None | 68 | None | 6 |
The following transcripts of ENSDARG00000045936 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 16648319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15631017 |
GRCz11 | 7 | 15882990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAAGCCCAGAGTAGCGACGCCTGAAGTGGTGGGCAAAATCGCACAGTA[C/A]AAGAGGGAGTGTCCATCTATATTTGCCTGGGAGATTCGGGACAGGCTGCT
Long Flanking Sequence:
GGTTCCTATTGATGGTAGGAAAAAATACTATGAAAGTCAATGGGTACAATCAACTAGCATTCTTCAAAATATCTCTCTAACAGAAGAAACTCAAAATGAACAAGTAAAAACTTTTTGTGTGAACTATCCCTTTAAGCATGCGTTTCTCATTCAAAAAAGGTGGACACTAATGCAAAAAAAGTGTGACCCTAATTAGTCCTGAAACCATCCTAGCAATTTTAAGGCATATTTTCTGTGTTCGTAGACCCATGATGATGCAAAAGTCCAACTGGACAATAAGAACGTAAGCGTATAATCGTTTGACGTACATTACATTAGTTCACTCTAGTCTTAAATAATGTATGTGAATTGTGTATATTGCTGTCCATTCAGGTGTCGAATGGGTGCGTGAGCAAGATTCTGGGGAGGTATTATGAGACGGGCTCCATCCGACCGCGAGCCATCGGAGGCAGCAAGCCCAGAGTAGCGACGCCTGAAGTGGTGGGCAAAATCGCACAGTA[C/A]AAGAGGGAGTGTCCATCTATATTTGCCTGGGAGATTCGGGACAGGCTGCTGTCGGAGGGTGTGTGCACCAACGATAACATACCGAGCGTGAGTGCAAATCAAACTTCATTTACATCATTTCATCAATACTTTGGTGGATAAATTTTTAATTTATCCACATTACAAGAAATTATACCTATGGAGCACTGTGTAAAGTGTTTAGTGCTTGACTTAACCTTTAATGTTGAATCAGATAAAGCTCAAGTAATTTTAAAGGGACAGTTCACCCCAAAATTTGAACTTTGCCATTGTTTACTCAACCAAACAAGGTTGAGTTTTGTTTGTTCTGTTGAAAACAAAAGAACATATTTTGAAAAACTTTGGAAACCACTGACTTCCATACTATTTGTTTTTCCTACTATAAAAGTCAATGGTAACCAGTTTCCAACATTCTTCAAAATATCTTCTTTTCTGTTCGACAATCAAAAATGGTTTGAGACAAGTAAGGTTAAGAAAATAAT
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
Stage | Entity | Quality | Tag |
---|---|---|---|
Hatching:Long-pec ZFS:0000033 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa13392
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014572 | Essential Splice Site | 194 | 382 | 7 | 11 |
ENSDART00000053407 | Essential Splice Site | 194 | 437 | 6 | 11 |
ENSDART00000067248 | None | 194 | 437 | 7 | 12 |
ENSDART00000134696 | None | None | 81 | None | 6 |
ENSDART00000143282 | Essential Splice Site | 194 | 384 | 7 | 12 |
ENSDART00000144765 | None | None | 81 | None | 6 |
ENSDART00000145946 | Essential Splice Site | 194 | 437 | 7 | 12 |
ENSDART00000146704 | None | None | 68 | None | 6 |
The following transcripts of ENSDARG00000045936 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 16654435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15637133 |
GRCz11 | 7 | 15889106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRGTGTGAGAAGTCTGCCYGATCTTGCAACTATATATGTTAWATTTTWGC[A/T]GACGGTTGCCRGCAACAGRACAACGGTGGTGAAAACACAAACTCCATCAG
Long Flanking Sequence:
CATTTTTGTTTAATTGAAGATAAATATATATTTGGTTACATACATTTTACAATGAGGTTGCACTAGTTAGTTTATCTATTTACTAACATCAACAAACAATCAACAATACTTTCATTACAGCATTTATTAATCTTCATTTATTATTAAAGTTCAAAGCGATGCTTGTTAGCATAGGTTAATGTGCTGTGAGTTAACAAGAACTAATAACAAATGACTGCATTTTTAAAAAAGATGAATAAATAGTGTACTAAATGTATTGTTTATTATGTGTTCATGATAGTAAATGCATTAACAATTATTAACTAATGGAGCTTTACTGTAAAGTGAGATGTAATAATAATAACACATAAAAAAAAACGGAAAAAATAAAGCAATCTAGTTGCCATTTATTTCTTTTTAACTTTTGTTTCAGATTTAAGTTAAACTAAAGTAACAATACCACATGCAACATGGTGTGAGAAGTCTGCCCGATCTTGCAACTATATATGTTATATTTTTGC[A/T]GACGGTTGCCAGCAACAGGACAACGGTGGTGAAAACACAAACTCCATCAGCTCAAACGGCGAGGACTCAGACGAGACTCAAATGCGTCTGCAGCTGAAAAGAAAACTGCAGAGAAACAGAACGTCCTTCACGCAGGAGCAGATCGAGGCACTTGAGAAAGGTGAACGATCACAACTTTATTTGTATGTATACATAAATATATATATAACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAACAGTTGAAGTCAGAATTATTAGCCCCCCTGTTCATTCGTTTAGTCTTTTTTAAATATTTGCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTGAATTTTTACAGAATCATTTTTAAGGTTCAAATTATTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20883
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 |
---|---|---|---|---|---|
ENSDART00000014572 | None | None | 382 | None | 11 |
ENSDART00000053407 | Essential Splice Site | 325 | 437 | 8 | 11 |
ENSDART00000067248 | Essential Splice Site | 325 | 437 | 9 | 12 |
ENSDART00000134696 | None | None | 81 | None | 6 |
ENSDART00000143282 | None | None | 384 | None | 12 |
ENSDART00000144765 | None | None | 81 | None | 6 |
ENSDART00000145946 | Essential Splice Site | 325 | 437 | 9 | 12 |
ENSDART00000146704 | None | None | 68 | None | 6 |
The following transcripts of ENSDARG00000045936 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 16655611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15638309 |
GRCz11 | 7 | 15890282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTCAACACCAGCGTCTATCAGGCCATCCCACAACCCACCACACCTGG[T/C]AAACCACAACACAACACAACACATTAATTATTTCATTTTCCTTCGGCTTA
Long Flanking Sequence:
AATGCCTTATTTGCATATTTTAACACTCCATTTTAGAACACTTCTAATACAAAGGAAGCTTGCAATTCTTAATGTAATTAAAGAACTGGGGAAGTTTGATAAAAACTATTACATTTGTTTTTTTACCCTGTTCACCTGCAGTGTCTCACCTTTAAAAAAAAGTAACCCAGTTGCGCATCTCCTTTCAGAGTTTGAAAGAACACACTATCCAGACGTTTTCGCAAGAGAGAGACTTGCGGCAAAAATTGACCTCCCGGAAGCAAGAATACAGGTGAAAATGAGTTAATAGTTGAATTTTGCAAATATTGTTGTGTTTATATCTTTGGCTAACTTTATCTGTGTCTGCAGGTCTGGTTTTCAAACAGAAGAGCCAAGTGGAGGAGAGAGGAGAAACTGAGGAACCAGAGACGACAAGCCAGCAACTCCTCCAGTCACATTCCCATCAGCAGCAGCTTCAACACCAGCGTCTATCAGGCCATCCCACAACCCACCACACCTGG[T/C]AAACCACAACACAACACAACACATTAATTATTTCATTTTCCTTCGGCTTAGTCTCTATTTCAGAGGTGAACTACCAACTATTCCAGCATATTACAACACAACACAACACAACACAACAAAACAAAACACAACACAACATATTAATTAATTCATTTTCCTTCGGCTTAGTCTCTATTTCAGAGGTGAACTACCAACTATTCCAGCATATTACAACACAACACAACACAACACAACAAAACAAAACACAACACAACATATTAATTAATTCATTTTCCTTCGGCTTAGTCTCTATTTCAGAGGTAAACCACCAACTATTCCAGCATATTCCAACACAACACTACACAACACAACACAATACGTATAATTTCCTTCGGCTCAGTCTCTGTTTCAGAGGTTGCCACAGCGGAATGAGCCACCTGCTATTCCAGCATATATTTTATGCAGTGGAGGCCCTTCAAGCCATAACTCAATATTGGGAAACCCCCAACAAACAGAACACA
Associated Phenotype:
Not determined