ZMP
si:dkey-151g10.3
Ensembl ID:
ZFIN IDs:
Human Orthologue:
WNK3
Human Description:
WNK lysine deficient protein kinase 3 [Source:HGNC Symbol;Acc:14543]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15224 | Essential Splice Site | Available for shipment | Available now |
sa501 | Nonsense | Available for shipment | Available now |
sa37712 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45803 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10232 | Nonsense | Available for shipment | Available now |
sa32443 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6736
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 |
---|---|---|---|---|---|
ENSDART00000035702 | Nonsense | 574 | 1651 | 10 | 37 |
ENSDART00000132799 | None | None | 627 | None | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25492078)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25278198 |
GRCz11 | 23 | 25204739 |
KASP Assay ID:
554-4991.1 (used for ordering genotyping assays)
KASP Sequence:
AARGTGAGCTGCAACAGCAGGTGTTTATACAGCAACCTCAAAGCAAACCC[C/T]AACAAYAAGTTGGGATACARCCTCAAGTTCAGCAGCATCAGACATCAATA
Long Flanking Sequence:
CATACATGCCCCCAGTATCGCCCCAGGCACCCATGGCTGTCCTTACGTCCTCTATTCCGACTGGAGAACCAATAGCACCAGCAGGCAACATCATGCCACCCATACAGACCCAAACTAGTATTCCTCCTCTTCAACCCATGGATGTTTTGCCCCTGCAAACTGTTGTTCAAAATCAACAGCAAGTGATGCCTGAATTGCCCAGAACGCTGCAACCTAACATCCAGCAACCAACACCACAACAGCAGGCAAATGTAATGCAGCAGCATCAGACAGTCTTGTTGCCACAGCAAACTGACCAGGTTCAGCAAATTAAAGTTTTGTTACAACAGTCACAGCATGCAGAACAACCCCAGGTGGTTCTGCAGGAGCAGGCCCCACATTCCAGTGCATCTCAACAGCCATATATCCCATTACCACAGCAAGCACCGCCAACAATGACCAACCCACAGCAAAGTGAGCTGCAACAGCAGGTGTTTATACAGCAACCTCAAAGCAAACCC[C/T]AACAACAAGTTGGGATACAGCCTCAAGTTCAGCAGCATCAGACATCAATACAGCAACCCTCAGTTGATCAGTATCAACACCAGACTCAGCAACAGCAAGTGTATGTGCCACAAATGGCAGAATCACAAGACCAGAACGTGATAAAGACTGTGATACAACAGGTACCGGTGCTGCAAGCAATTCAGCAGCCATTACAATTGATAGAGCAACAACAGCAGCAGCTTCTGATTAGGCAACAAATTGAGCAACATCAGAAGGCTGCTTTACAAAACCAAATGGAGCAACATCAACAGCAAGTTTATATTCAGCCACCACAACAGCAAAAAGTGGAACAACAACAAATTCTTATGCAGCAACAGCAAAACTTGGCAGTAAAGCAACAGATAGAGCAACAGCAGCATGCATTAAAGCAACAAAAGCAAATAGAGCAGCAGCAAAAAGCCATTTTACAGCAACAGGCAGAACAGCAAAGACAGCAGCAACAGACTTTGTTTCAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15224
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 |
---|---|---|---|---|---|
ENSDART00000035702 | Essential Splice Site | 813 | 1651 | 16 | 37 |
ENSDART00000132799 | None | None | 627 | None | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25495958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25282078 |
GRCz11 | 23 | 25208619 |
KASP Assay ID:
2261-7790.1 (used for ordering genotyping assays)
KASP Sequence:
CAAGTTTGACAYTGAGGGAGATGCACCTGAAGACATTGCAGATTACATGG[T/C]AATATATNTTTTTTAGCTGCTACAGTRATTCATTTGCTTYTTGTGAAATGG
Long Flanking Sequence:
GTGGTTCCTGTTTGTTTGTCTTTTCTTTCACTTATTAGGAAAGCCTAATTCACTCTGCCAACAGGGGATCTTTATTATGGTAAGTGCTTTTGTCTAGTTGTGACAGCATATTAAACATTGAACAATGTTTTCAAACTATTAATAAAATGTCATAAAATCCAGCTCTGCTCCTACCAATGGAGATGAGGGCCAGTTGGTGTGGCCTAGTGGAAAACTAGATAAGGCAAAATGTCAGAGGAGATCATCCTGTCAGAAGACTGAAAAAACTCACTTCCAACTCTGCATGTTGCAGGTAAGGAAATCATAATATTTGCAATATTTTCTGCTCTTCTCTTTTAATTAAAAAATATATACAACAAGCACTTATGTTTATATGTTATAGGTCTCATGCACAGGAGACAACATGGTAGAATGTCAGTTGGAGACTCACAGCAACAAGATGGTCACGTTCAAGTTTGACATTGAGGGAGATGCACCTGAAGACATTGCAGATTACATGG[T/C]AATATATTTTTTTAGCTGCTACAGTGATTCATTTGCTTCTTGTGAAATGGCATGCTAAGAAAATCTGTAATAGCTGATCCTGACCTGTGGCTTTTTCATTCGGAGTGTGTCTTCATCAGTAGATTTCTTCACAATATGTTTTGTGCAGGTGGAGGAGGACTTCGTCCTTGAGCCTGAAAAAGAAAAATTTGTTGAGGAGCTGAGATGTATAGTGAAGAAAGCTCAAGCAATATTAAGTACTCAGTCGCAGGTTTGTCATTCAATGTTGTGTGTTGCTATTGTTGAAAAAATTCTCCATTTGTTTTTTGTAATGTATTTTTATTTGAAATTTATTCCTACTATATTTCAGATATCCGTCTCAATATTCCAATATGCTTATTTCTGATTATTCTAATGTGCTAATCTCTTATTCAGAGTTAAAAACAAATATGCTATGTCGTTTTTGTGGAAACCATTATGCAGCTTACGGGATTGTTTAGAACTGCATTTGTTTGAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa501
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 |
---|---|---|---|---|---|
ENSDART00000035702 | Nonsense | 860 | 1651 | 20 | 37 |
ENSDART00000132799 | None | None | 627 | None | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25496585)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25282705 |
GRCz11 | 23 | 25209246 |
KASP Assay ID:
554-0219.1 (used for ordering genotyping assays)
KASP Sequence:
AAACAATGATTAATTTTATATAGTAGCATATGTTGTTCTTTTTATTATTT[C/A]AATTTTTTTGTCACAGACTGGATCCCTGGAGCAGCTCCAAGTGAGCACCC
Long Flanking Sequence:
CTTCACAATATGTTTTGTGCAGGTGGAGGAGGACTTCGTCCTTGAGCCTGAAAAAGAAAAATTTGTTGAGGAGCTGAGATGTATAGTGAAGAAAGCTCAAGCAATATTAAGTACTCAGTCGCAGGTTTGTCATTCAATGTTGTGTGTTGCTATTGTTGAAAAAATTCTCCATTTGTTTTTTGTAATGTATTTTTATTTGAAATTTATTCCTACTATATTTCAGATATCCGTCTCAATATTCCAATATGCTTATTTCTGATTATTCTAATGTGCTAATCTCTTATTCAGAGTTAAAAACAAATATGCTATGTCGTTTTTGTGGAAACCATTATGCAGCTTACGGGATTGTTTAGAACTGCATTTGTTTGAAATAAAATGTCTTTAGTGAATAGTGTTTTGCTGTTTTTTTTTTAAATGACAAAATTGCTTAAAAATAAAAATAGGGACTTCAAACAATGATTAATTTTATATAGTAGCATATGTTGTTCTTTTTATTATTT[C/A]AATTTTTTTGTCACAGACTGGATCCCTGGAGCAGCTCCAAGTGAGCACCCCATCCAGTGCAACAAGTGAGTGTAACAATCTCGCATTAGCATTTCTCTCATATTAAATCATAAAACAAATTTAAGCTCAAAATAGCATTGTTTTTTCAGCATTGCATAGGTTTCTTTTAATATTGATTACAATAAATAAAAAATATTAACCAAGGCTTTTCAAAATTAAAAATGTACACCTTTGTTACAGTTGATAAATTTACTGTTCACTGTTTTTTTTTTTTACATTTCCAAAGTGGATTCAGCCCCTCAGTCTTCTCCAGTAGGTCGCTGGCGGTTCTTCATTAACCAGACTATTCGTCACCGTGATTCACACTCCAACCAGGGAGCTTCGACTCCCCCTCCAGTGGGGGAGAACAGAGTTCCCAAGTCCATAGAAACCGAGAAAGGTAGAAAACTCATTGACACCCTTAACTTTTGGCCTGCAGTGAAATTTCCAGTAGAAGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37712
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035702 | Essential Splice Site | 1384 | 1651 | 32 | 37 |
ENSDART00000132799 | None | None | 627 | None | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25502655)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25288775 |
GRCz11 | 23 | 25215316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACAAGAGTGACAACGCTGTAGCTGTAGTGTGTGCATGGCCAAAATTG[T/A]AATTTTGGCTTTTTTAAATGAGCAGATTTTATTTAGCTTTATTGCATAAA
Long Flanking Sequence:
AGCATACTGCTGTGTATACAGTTTTGTTTAAAAGGGTGTGGAAATAGTTTAGTGTAAAAAATGGTACACAGTATGCACTGATAAGCATTTCAAACCACAGTCTTGGTACATGTTGCACAGCCAAAGGTTTGTAGTCAGTAAGAGTTTAAGGAAATTAATACTCTAAGGATGCATTAAAGACTTCTAATGCATTTTTAGAAAAGCTGATTTATATTATAATAATATTTCAATCTATTACTCTATTTCTGGTCAAATAATTGCAGTCCTGGTGAGCATAAGAGCCTTTTGTGAGAAGGAAAAAAACTTACTGACCTTAGACTTAAATGAAAGTGTACATTAAGTGATATCTTAATAAAATAAAGGCCACATACAGTATATGCTGCAGCATATTTTGATTGCTAGTTTGCCTTTTAAAGGTCAATTCTTTTCTGTGCACACACAGTTCAGAAATTTACAAGAGTGACAACGCTGTAGCTGTAGTGTGTGCATGGCCAAAATTG[T/A]AATTTTGGCTTTTTTAAATGAGCAGATTTTATTTAGCTTTATTGCATAAAGCTGAAGCTTTGCACTCTGTGCACTGTATAGGTATCTTGACTAGTATACAGTACAACTTGGTATAGGGATGCTCATTTCAGTTAATTTTCTCAACCGACAAACGCCACTGGTTAAATGAATATTAACCGTTGACTGGTCAGATTAATATAAAATTATTATTTAATAAAAAATTTATTGACGCGTCTATTTTGTGTCTGACACATAAAATATTTTAACATGTCAACAACAGCATAGCCTACAAAACATGCAGTGTTTCCAACAGCATAAAAACGAAAAAAATAAATAAATAGCCCTGCCTTAGATATTTTCACTTAAATGACAAATTTAGATTAGAAAATGAGAACACTGACACAATTCTTTTTTTAAGTACCGGCATAGACTGTTTTTTTATTTTCCACAGAAAATATGCATTTAATTAATGTTCCGCTGTAATTCTTATATTACAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45803
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 |
---|---|---|---|---|---|
ENSDART00000035702 | Essential Splice Site | 1405 | 1651 | 33 | 37 |
ENSDART00000132799 | None | None | 627 | None | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25503905)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25290025 |
GRCz11 | 23 | 25216566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAGTTTGCGGCTTTTTTCTCCACTTGTACAAATAGATGGAGGTTTAG[G/A]AGACAGACTATCACCATCTGCGCTGGTTTGGCATCAACTCGTCTGTGTCA
Long Flanking Sequence:
TATAGCTACAATATTTCCCAGAGATGTGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCAGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGAACTAAGCCGACAAGAAAATAAATGAATGAATGAATGAATGAATGAATGAATAGCTATAATAAGAGTCTCAGTTTAGTGCAGAGTTATCATGCAAAAATTTAATAAATCATTGGATTTGTTTGATTCGTAGATTAAGCTATGGAGGCTATTTTAAAAACAGATATTTTATAAGAACTAATAATAACCGTAATTTTCCAAATTGAAAACATGTTGGTTTGTTGGTTTTACACTTAATCATCAAAACTATATAATTTGTGTTTGAGTGGTGCAGAGCACGCTCTGATGGAGAGAAAATCCTGACACTCTGACTTGTTTGCAAATTAGTGGACATTTCAGACAGTTTGCGGCTTTTTTCTCCACTTGTACAAATAGATGGAGGTTTAG[G/A]AGACAGACTATCACCATCTGCGCTGGTTTGGCATCAACTCGTCTGTGTCAAACTGTGGCCACCAATATTCTTCTTTTTGCTCCTGTCATTTTGCTTCTTTTACAAATACGTCTGTGGTTGCACATGTTCCCAACGAGATAACAAACATGTGTTGCCCATTTATGCAGCAAAATTTTAAAAATACAAAATAAAATAAAAATTATTTTTTTACCGGTTAACTGATACCATTACTTAAAAATGCATCCTTTTGGTAACGGTTATTTGGTTAATGTGAGCATCTCTAACTTGGTATTATAAATATTATACAATGCATTATTCCTATTAGTGTTCTCTGGTTGTATAATGCACATTGTGTGGTTGCAAGTTGTGTATATTTCCCATAAACACTGCATATGCATATGGTATGCAGTATACTGAACATGCATAGCATGAGTAATATGGTAGTATGCCATTCCCAACATAGCCTGAACACATTATATTATTAGTCCAAAACAATAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10232
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 |
---|---|---|---|---|---|
ENSDART00000035702 | Nonsense | 1537 | 1651 | 35 | 37 |
ENSDART00000132799 | Nonsense | 358 | 627 | 5 | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25507545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25293665 |
GRCz11 | 23 | 25220206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGARCTACAGGATTTGTACAAGCAGCTCCGCTCTCTCAAAGACCACAGA[C/T]AGCCAATGTCYATGAGCCTKTCCCGCACCTCTCCTCTGCCCTCCGCACCC
Long Flanking Sequence:
AAGCTCATCTGGATATTTTCATTCAGTTAGAGCTTTTACACTGCATAAAAGGTTATTTTCGAAAATCCATAATAGGGCTCGTTTAAAGCTGTTCTTTTAAAAAAATGGCATTATAAGCTACACGTATAGACCAAGAGGCCAGTATTTCTACTATTTATAAAAGATAAATCCTTGTTTGGCCATCTTGGATTAGGAATAGATATAAACATAATGAACATAATGTTCAATAGTATTACAGCACTCTGAGTGTATGTTAGTACAATTTATTTATTCCCTTTTTTCATCTGATAGAGCATTTAGACACTGAAACTGTGACATATGACGTGAGACTTAACATGCGGATTGCGCACTGCTGTTTTATTTTTCCATTCCATAATTGCTTCATACTGACTGTTCTTTCTCTCTGTAGACACATCAAGGAGGTGGTGTCCCTGCAGGCACAGCAGAACAGAGAACTACAGGATTTGTACAAGCAGCTCCGCTCTCTCAAAGACCACAGA[C/T]AGCCAATGTCTATGAGCCTGTCCCGCACCTCTCCTCTGCCCTCCGCACCCCTCGCTATCTCCCCGCGCAGACCCCGACCCGCCAAAGCCAAGCTCCGGCCTCGGCCGCACTCTCACATGGATAACAACGGAGTCGCACACCAAGGTACTGCCATCTTTAAAAATTAGGTGCCAATCAGATTGAGTGACCTTTTTTGTGATTAATAACGTACTTTGCTCTTGCTTTTGAAAATACAAACACTCAGGGAGTCTTCAGCAGTCTAGCAGTTATTCCGGTGGGGAGCAAAGCCGGCTACATTCACACTGCAAGCCAGAGAAATCACAATCCCTGACATCTAACAGAGGTACTTAAGCTGGTGAACAGATCGCATTTTTAGATCTCCAAATTGTTATGCTAGTTATAAATGTGGAATCAGTTGGATTTTATTTAATAATCATTTTGCTGTTGTATAAAAAACATACATCTGTTCATTAAGGGTGGATTAAATTAATCAAAAGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32443
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 |
---|---|---|---|---|---|
ENSDART00000035702 | Nonsense | 1633 | 1651 | 37 | 37 |
ENSDART00000132799 | Nonsense | 481 | 627 | 7 | 8 |
ENSDART00000136675 | None | None | 133 | None | 3 |
ENSDART00000140789 | None | None | 522 | None | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 25508577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25294697 |
GRCz11 | 23 | 25221238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGTCAAAGGAAACTGTTTGTCCAGTTCAGCCCAAGCCTTCGCTGAAT[C/T]AGATTAAACAGATCCAACAAGTGCAGGAGTTGGGTGGATGGAGCCAGCCT
Long Flanking Sequence:
TATTGTTTTCAAATTAATGTTGTTCTTTTGAGCTTTCTATTTATTAATAAATATGGGGGTGGTGGGGGTCAAGATTTCCACAAATATTTAAGCAGCACTGTTTTTAACTTGTAAAATAGTAAATCTAAAAAAATTTAGCACCAAATAAGCCTATTGAAGACAGCCTATTGAAAATATAGCCATTACAGAAAAAAATATATATTTATATACTAACATGGAAATAACTATTAAATCATAATAGCATGTATTGTAATATTTTGCAATATTGGAAATTTTGATCAAACCATTTTAAAGATTCTCCATTTGTTTTTTCTCAATTTTTGTAGCTAATCACAATTCATTGTCTTTTGTAACTTTCCAATTTCTTGTTTTCAGACCACAGTCCTTCAGCCCAGGGTTCTGGCAACAGAAAGAGCACATTCACAGATGAGCTGCATAAACTTGTCGATGAGTGGTCAAAGGAAACTGTTTGTCCAGTTCAGCCCAAGCCTTCGCTGAAT[C/T]AGATTAAACAGATCCAACAAGTGCAGGAGTTGGGTGGATGGAGCCAGCCTGCTGAGGTGAAGCACCAGATGCAAACTCTCAAACACGATTATGCAGATTAGGCTGTAGGAGTATTTTGCTGTCACATTATTAGTGTATATAGCTCCATCCTCTGTCATTTTTTGAAATTTTTAAGAGTGTAAATTGTCAAAGTTTTACCCTAACATCAAATTTCAGATTGTTTGGTTTAAATAACATCATTTTTACTGTGAAAAACACCAGTAAGTGTGGCTGCATCGTAAGGCCACTGGTGGAAAAAGATTCCTAATAACTGAATACTTTTTACTCCATCTAATTTAATGATATTACTGTTTCTTAGACTCACAGACTCCACATATAAAAGTGTGCCACAGTATAGTAGATGTGCATACAGTATAAAAATAGCTTGAACCATTTTTCTGCTGTGGGCATTTTTCTGCAGAGAGCCACATGCTCAGTGTCATGTATTTATTAAATTAGTG
Associated Phenotype:
Not determined