ZMP
dhx57
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57 (DHX57) [Source:Un
Human Orthologue:
DHX57
Human Description:
DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57 [Source:HGNC Symbol;Acc:20086]
Mouse Orthologue:
Dhx57
Mouse Description:
DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57 Gene [Source:MGI Symbol;Acc:MGI:2147067]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9815 | Nonsense | Available for shipment | Available now |
| sa30968 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa22221 | Nonsense | Available for shipment | Available now |
| sa17834 | Nonsense | Available for shipment | Available now |
| sa16244 | Essential Splice Site | Available for shipment | Available now |
| sa17853 | Essential Splice Site | Available for shipment | Available now |
| sa35420 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9815
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 |
|---|---|---|---|---|---|
| ENSDART00000080351 | Nonsense | 135 | 1430 | 1 | 22 |
| ENSDART00000143226 | None | None | 1034 | None | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7716129)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 8020649 |
| GRCz11 | 13 | 8352672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAAACTACAGGTCAAAGAACTTCTTCGGGAACTTCAGAATCAGGAGTA[T/A]CAAACCCCWAAYAGGTGAACTTRTGTTTGCTTCTATAGAAACAGCAGTCA
Long Flanking Sequence:
GTTAAAAAGCTGCTTTTGTACATAATGTTTTTCAGGAAGTGCTTCAAAACACTTGATTTATGTGATTCATGGATGCTCTAAAAGGTAGCTGAAGTCATGAGTGGAAGGAGAAGGAGCAAACCCAATCGGGGTGGTGGTCGGTTTAATAAACCCAGGGGAGGTAGAGGAGGAGGTGGTGGAGGTGGAGGTGGAGGTGGAGGCAAGAAATTTGCCAGTGGAGGCTGGGATGATGGAGATGATTTCAGCCTGGATTTTGGTCCCAGTCGCTCATTCAAGCCTCCCTCCTCTAGAGGTTCAAGAGGTGGAGGTGTCCGCGGGGCTCAGGGTGGAAGAGGCAGAGGAAGATCTCTGGGACTACCTAGAAAACACGATGATGACGAGGAGAAGAGATCCAGGTTTAGATCAGAACAAGTGCCTCTTCCCTTGCAGAAGATTCACATGACGTCAGAGAACAAACTACAGGTCAAAGAACTTCTTCGGGAACTTCAGAATCAGGAGTA[T/A]CAAACCCCTAACAGGTGAACTTGTGTTTGCTTCTATAGAAACAGCAGTCACCATTTATTTAGTAGTTTTATGTTCATATAATTCATTCATTTTAAAACACAATGCGAACAACTAATTTCAAGATCTATCAAAACATTACAAAATTTGGTTTGAATAGAATCTATGATTGGCTATTACATTTTTGGTTTCGTCTATTTAGCCAACAAAGCATTCAAAATGTTCTAATCAAATTAAAAAAAACAATAGCAACATGTATTATTATCTAGTTACACTCAACTCCTCAAACAGACATTTATATTGGTTTACATAGTTTTTAATGCTGAATAATGTGTTCTTGTCATGTAGTGGCTCTGATTATGAAGGTGGAGAGGAGGAAGAGGATGAGGAGTATGATGAGCTGGACCATCGAGAGGAAGGTCAGTACTGGATAACCCATGATGATGGAGTAGAATATGCGGAGACTGATGACTGGATGGAAGACCCTGTTGAGGAAAAGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30968
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 |
|---|---|---|---|---|---|
| ENSDART00000080351 | Nonsense | 269 | 1430 | 3 | 22 |
| ENSDART00000143226 | None | None | 1034 | None | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7712144)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 8016664 |
| GRCz11 | 13 | 8348687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCCCGCAAACATCTGATCCCCCTTCACAGGGGGAATGTGTAGCTTTG[C/T]GACAGGAAGAGGCCTTTGCTTTGACGGCAATCTACGGCGAAAGGTTCTGC
Long Flanking Sequence:
CCTTATTGTTACATCATTTTAAAACAAAATGTAGCTTAAAGCAGCAAATGCTGTTATAAAAAGTATTAATTACCCTGTTCATGGTTGAGAAGTCCCTCTCACAGTTAACACTGCTGACTGGGAATGTCAGGGCAATAGAAGTTATTTTAAACGTAAAATAGAAAACTATCCTTTAAAAACTAGAGAGTGGGCCAGTTTGTCTCAAGCGCTATTAGTACACAAGTACACAACTAGAACATTGATATTTGCATACTTACTAAATAAATATACTTGCTTGTACCCTCCATATATTAGCAACTCAGTATTACCCATGTTGCAGGTATGGGTTTGACCGTGAGCGCAGCAGACAAACTTTGGAAGCCGGAGAAGGAAGTGGATGCGGTGAGGTTGGAGCAACATTAGAGCTCCTCCTATCCCAAATGTTTACAGAACGATTTGGCTCTAGCGCCCTCAGCCCGCAAACATCTGATCCCCCTTCACAGGGGGAATGTGTAGCTTTG[C/T]GACAGGAAGAGGCCTTTGCTTTGACGGCAATCTACGGCGAAAGGTTCTGCGAGCGCATCAGTAATCGGGTTTGGACTATTCAGCTTGATTTGCTGTGGTTGGATGAAAGACGGATCAAACTTTCTGACTCTAAGCATTCTAAAAAGCAGTCAGAGTCCAATCAGATTTGCAAGTTTTACTTAAGGGGGGCAGGTTGTAAGTTTGGGAATCGCTGCAAGTTCAAGCACCAAGTTCACGAATCAAGCACTTCAAGAGATCTTTGTAAGGCAAGTCAACCGGGGTTTAGCAACGCAGATGCTCCAATTTACCAGCTGGAGATTCGTTTCCAACCAGGCAGTTTATATCCTTTTCAACCTCCACTTGTGGCCTTCAGTAGTACAGATGAATCCCTCTCAGGGGCTGGACGTCTCAGTGTCACAGAGTATCTGTTCGGTCAGTCACTCAGTGCTGCAGAGGAAGGTGAGCCAGTGGTCTACACCCTTATTTCCAGCCTGGAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22221
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 |
|---|---|---|---|---|---|
| ENSDART00000080351 | Nonsense | 270 | 1430 | 3 | 22 |
| ENSDART00000143226 | None | None | 1034 | None | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7712141)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 8016661 |
| GRCz11 | 13 | 8348684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCGCAAACATCTGATCCCCCTTCACAGGGGGAATGTGTAGCTTTGCGA[C/T]AGGAAGAGGCCTTTGCTTTGACGGCAATCTACGGCGAAAGGTTCTGCGAG
Long Flanking Sequence:
TATTGTTACATCATTTTAAAACAAAATGTAGCTTAAAGCAGCAAATGCTGTTATAAAAAGTATTAATTACCCTGTTCATGGTTGAGAAGTCCCTCTCACAGTTAACACTGCTGACTGGGAATGTCAGGGCAATAGAAGTTATTTTAAACGTAAAATAGAAAACTATCCTTTAAAAACTAGAGAGTGGGCCAGTTTGTCTCAAGCGCTATTAGTACACAAGTACACAACTAGAACATTGATATTTGCATACTTACTAAATAAATATACTTGCTTGTACCCTCCATATATTAGCAACTCAGTATTACCCATGTTGCAGGTATGGGTTTGACCGTGAGCGCAGCAGACAAACTTTGGAAGCCGGAGAAGGAAGTGGATGCGGTGAGGTTGGAGCAACATTAGAGCTCCTCCTATCCCAAATGTTTACAGAACGATTTGGCTCTAGCGCCCTCAGCCCGCAAACATCTGATCCCCCTTCACAGGGGGAATGTGTAGCTTTGCGA[C/T]AGGAAGAGGCCTTTGCTTTGACGGCAATCTACGGCGAAAGGTTCTGCGAGCGCATCAGTAATCGGGTTTGGACTATTCAGCTTGATTTGCTGTGGTTGGATGAAAGACGGATCAAACTTTCTGACTCTAAGCATTCTAAAAAGCAGTCAGAGTCCAATCAGATTTGCAAGTTTTACTTAAGGGGGGCAGGTTGTAAGTTTGGGAATCGCTGCAAGTTCAAGCACCAAGTTCACGAATCAAGCACTTCAAGAGATCTTTGTAAGGCAAGTCAACCGGGGTTTAGCAACGCAGATGCTCCAATTTACCAGCTGGAGATTCGTTTCCAACCAGGCAGTTTATATCCTTTTCAACCTCCACTTGTGGCCTTCAGTAGTACAGATGAATCCCTCTCAGGGGCTGGACGTCTCAGTGTCACAGAGTATCTGTTCGGTCAGTCACTCAGTGCTGCAGAGGAAGGTGAGCCAGTGGTCTACACCCTTATTTCCAGCCTGGAAGAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17834
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 |
|---|---|---|---|---|---|
| ENSDART00000080351 | Nonsense | 537 | 1430 | 4 | 22 |
| ENSDART00000143226 | Nonsense | 141 | 1034 | 2 | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7711250)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 8015770 |
| GRCz11 | 13 | 8347793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGATGAAGAGGAATGTATCCCAGTAGAAAACGAGAGCTATGTTAACT[T/A]GAGGAAGAGGATGGTGAAGAAGACTGAAATCAGAACTGAGCAAATGCAGG
Long Flanking Sequence:
CAGGGGCTGGACGTCTCAGTGTCACAGAGTATCTGTTCGGTCAGTCACTCAGTGCTGCAGAGGAAGGTGAGCCAGTGGTCTACACCCTTATTTCCAGCCTGGAAGAGGATGGTCCTGTCAGGGAGCTGCTGTCAGCTGCTCATCACAAGTATAGTGCCCCACCTCCTGTGCTGGCTCCTCCCACTGTCACACCGGCAAAGAGTCGAAGCAATAAAAACAATGTAGACAACAGGACTTCAGCAACTAGAGATCAGTCAACCTCAACTAGCATCAGCGAGATCACGAACCACAGAGTGAAACAAAAAGAAGGTAAGGAGCCGAACACCCTAAAGCCTCCATTATTTAATCATACTTGATATAATATTTCACTATATAATGAAAGTTTTGTGTTCAATTAGTTGCACAAATCCTAAGTGAGGATATTGATGATGTACAAGATGAAGGGGATGATGAAGATGAAGAGGAATGTATCCCAGTAGAAAACGAGAGCTATGTTAACT[T/A]GAGGAAGAGGATGGTGAAGAAGACTGAAATCAGAACTGAGCAAATGCAGGAAGAGAACAAGAAGCTGTGCAGAGAGTTCAAAAGGAAACGGGTAACACAATTCTACACCCTACGAATGAATTATTGTTGTCTAAAACCAGGCATTTCAGTTTCATTGTCCAACACCTGCACGACCAGAGCTTTTACTTCATAATGTCAGCAAGTGCGCTGTTTTCTTTCTTTTTGATTGGCCAACATGATTGGGTTCATACCAATGGTGAAAGATTCGAATGAGGCAAATTCTGCACCTTTGTGGCAAACGCATTGCAAATTCTGCATCGTTCGCACTGCACAATGCCCTGACTTAAATGCAAAAATACTTAATTCCCTGTTTGGTGTAAGTAATTAATTAATAATAATTAATAATAATTCCTTACATTTATATAGCGCTTTTCTAGGCACTCAAAGCGCTTTTACACAATGGGGGGGGATCTCCTCATCCACCACCAGTGTGCAGCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16244
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 |
|---|---|---|---|---|---|
| ENSDART00000080351 | Essential Splice Site | 716 | 1430 | 7 | 22 |
| ENSDART00000143226 | Essential Splice Site | 320 | 1034 | 5 | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7706673)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 8011193 |
| GRCz11 | 13 | 8343216 |
KASP Assay ID:
2260-6038.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGTCACACATGTGATCGTGGATGAGGTCCATGAACGAACAGAAGAGAG[G/A]TKTGTGGAAAGCTCAAATGCACATAAATAAACCGTCACATRAAGTGAWTC
Long Flanking Sequence:
TTGCCGTTAAAAACAAATAGTATTCTAGAATTTAGTTTATTCATGTGATGGTGATTTTTTTCACCAGCCATCACCAACTGAATTATCATAGTTGCTGTAGTTCCTGTTATGAATGTTTTGTGTAAACCATGGACTTAAAAAAATCAATTGAATGCAAGTTGAAAAAGTTTGTAAAACATTGTAATGTCTTTTTTCCTGTTCAGTTTAAAACATTAATAAAAAACAATAATAAAATATTTATTTTCTTTCCATTTAAAAAAATTTTATTTTGTTGTATTATTTTTTTTTCTCTTTGAATGTCTGATTTTTGCATGGTAGTGTTATGCGGTAATACCTAGCCTTCTAATAGAAGTTTTTGTGTTTTGTTGCATCCAGTCCTCTATCACCAGGCTGATGTTCTGCACAACTGGTGTTCTTTTGAGGAGGTTAGAAGGTGATCCTGAGCTCAGCGGTGTCACACATGTGATCGTGGATGAGGTCCATGAACGAACAGAAGAGAG[G/A]TGTGTGGAAAGCTCAAATGCACATAAATAAACCGTCACATGAAGTGAATCTGACAGTAGCACAATACTTGTCTTGCAGTGACTTCCTGTTGCTGGTTTTGAAGGATCTGATTGTAAAAAGGACAGATCTGAAAGTAATTATGATGAGTGCAACCTTGAATGCTGAACTGTTCTCACAGTATTTCAACAACTGCCCCTGCATCCATATACCAGGTAAACCCCACATCATTTATCTTTCATTACACATTTATTTTTATGTACAGCTCTTGAAAAAAACAACATTTTGAAGTTATTAAAACTTGATTCTCTGGGATTTGCCATTAATGGGTGCTTGCCATTACTAAGAGTTATCATTTACATAATTTATTTGAATAGGATGATAGCAGAGTAAATAATAAATATACAAAAACATACTTATTATTATTTACTCTCCTAATGTCCTTTCAAAATAAACTAACAATAAAAAAATACAATTTATATATACGTTATATTTATTATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17853
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 |
|---|---|---|---|---|---|
| ENSDART00000080351 | Essential Splice Site | 716 | 1430 | 8 | 22 |
| ENSDART00000143226 | Essential Splice Site | 320 | 1034 | 6 | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7706595)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 8011115 |
| GRCz11 | 13 | 8343138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAACCGTCACATRAAGTGAWTCTGACAGTRGCACAATACTTGTCTTGCA[G/A]TGACTTCCTGTTGCTGGTTTTGAAGGATCTGATTGTAAAAAGGACAGATC
Long Flanking Sequence:
TGAATTATCATAGTTGCTGTAGTTCCTGTTATGAATGTTTTGTGTAAACCATGGACTTAAAAAAATCAATTGAATGCAAGTTGAAAAAGTTTGTAAAACATTGTAATGTCTTTTTTCCTGTTCAGTTTAAAACATTAATAAAAAACAATAATAAAATATTTATTTTCTTTCCATTTAAAAAAATTTTATTTTGTTGTATTATTTTTTTTTCTCTTTGAATGTCTGATTTTTGCATGGTAGTGTTATGCGGTAATACCTAGCCTTCTAATAGAAGTTTTTGTGTTTTGTTGCATCCAGTCCTCTATCACCAGGCTGATGTTCTGCACAACTGGTGTTCTTTTGAGGAGGTTAGAAGGTGATCCTGAGCTCAGCGGTGTCACACATGTGATCGTGGATGAGGTCCATGAACGAACAGAAGAGAGGTGTGTGGAAAGCTCAAATGCACATAAATAAACCGTCACATGAAGTGAATCTGACAGTAGCACAATACTTGTCTTGCA[G/A]TGACTTCCTGTTGCTGGTTTTGAAGGATCTGATTGTAAAAAGGACAGATCTGAAAGTAATTATGATGAGTGCAACCTTGAATGCTGAACTGTTCTCACAGTATTTCAACAACTGCCCCTGCATCCATATACCAGGTAAACCCCACATCATTTATCTTTCATTACACATTTATTTTTATGTACAGCTCTTGAAAAAAACAACATTTTGAAGTTATTAAAACTTGATTCTCTGGGATTTGCCATTAATGGGTGCTTGCCATTACTAAGAGTTATCATTTACATAATTTATTTGAATAGGATGATAGCAGAGTAAATAATAAATATACAAAAACATACTTATTATTATTTACTCTCCTAATGTCCTTTCAAAATAAACTAACAATAAAAAAATACAATTTATATATACGTTATATTTATTATACATTATATATGAGCAATATCACACAAATAGAAGTGTTTATGGGCACTGGTGGGAGCCGTGCATTGGCTCGAGGCCACAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35420
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080351 | Nonsense | 1393 | 1430 | 22 | 22 |
| ENSDART00000143226 | Nonsense | 997 | 1034 | 20 | 20 |
| ENSDART00000147153 | None | None | 25 | None | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 7684450)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 7988970 |
| GRCz11 | 13 | 8320993 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTTCAACCTGTTTATGCAGGTAGCTGAGCTGGTGAAAGAGCTGCGAT[G/A]GGAGCTGGATCAGCTTTTAGAAGAGAAGATCAAAAATCCCAGTATGGATC
Long Flanking Sequence:
ATGATGTCTATCGACGATGGCATTGTCTGTCGACCTAACTCTAACACACACTGACTACTCGACGCTGCTCAAAGGCTGGTGTATCAGCTTGGTGTATCCCTGTGTTTAGAATAATAGAAGAAAAACTATTGTCTAACTAGTGTCTGCAAAAGACTTGATATTAGAGCACCTTCCAGCATGACAATGTCCCTAAACATACAACCAAAGCTGAAAATATTAATGTGTTAAAATTGCCCTGACCTAAAGTCCAGACCTAAACCAAATGGGGTATACGTACGACTTTATTTTTTAGCAAATGTTCAACGGATATGAATTATTTTACAAGGCACTGTAGTATAATAGTCTGCTAAGGTGGTGTAACAGTGGTTTGATGGCTCTAAACATGAATATACTGTAGCCATAGATGCTGGAATGATGGTCAGAAGAAAACAATACAGTGTAAGCTTTTATTAATTTCAACCTGTTTATGCAGGTAGCTGAGCTGGTGAAAGAGCTGCGAT[G/A]GGAGCTGGATCAGCTTTTAGAAGAGAAGATCAAAAATCCCAGTATGGATCTGATCAGCTGTCCTAGAGGATCTCGCATCATACACACAATTGTGTCACTTATTTCAACACAGTAACGGTTTGTCAACCAAATACAGAGGGGATGTTCACCTGAATACCTTATAACACGAGTTCAAGATTTTGTTGACGTTCATTTTAGGTTCATTTTCTTTCACAGACTAGTTTGTAGAGTTTTGATATTGTGTGATTCTACACAAACAGGATCTGAATCAGAGTCCACATTGGACTGCTTTCAATAAATATCTATATTGAAAAAAATTCTAACAGAAAGCATGTGCATGAATCTTGAATGTATGGCTGAGAGGAATATGAACGCACTTATTGTTAAATATTATAAAAGGCAATGGTGTTTTGAATTCGTAACTTCTATGATGATGATGTGGGACTACTACTATAGCTTTGATAATGCATTATCAAAGGTATTGAACATAAAATGTCAAA
Associated Phenotype:
Not determined