ZMP
zhx3
Ensembl ID:
ZFIN ID:
Description:
zinc fingers and homeoboxes 3 [Source:RefSeq peptide;Acc:NP_942108]
Human Orthologue:
ZHX3
Human Description:
zinc fingers and homeoboxes 3 [Source:HGNC Symbol;Acc:15935]
Mouse Orthologue:
Zhx3
Mouse Description:
zinc fingers and homeoboxes 3 Gene [Source:MGI Symbol;Acc:MGI:2444772]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24246 | Nonsense | Available for shipment | Available now |
sa39392 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43907 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8691 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31080 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24245 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24246
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 |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 68 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 68 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2890035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2936292 |
GRCz11 | 23 | 2879988 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGACAAGTCCTCTGGGCAAGAAGATATCCTTAAAGATGCTGGATTTTA[C/A]ACTTGTAGACCATGTAACTTTGAGACCCAGGATCTTAATCTTTTCCTTGA
Long Flanking Sequence:
GGGCCTTAGTTGGTGTTAGAGATGCTTCAAGATGCAATGTTAAGTTAGGCCTTTTGTTTTTGTTATTGTGATATAATTAAACTGAGCTTGAATTCTGTGGTTTTTAAATGCTGTTGTTTTTGTTTTATCTTCACAGATTGATGCTTTGATGCCTGGGAAACATTGCTAATGAAGAATATGGAATACTAATAATGGACTGAAGATCATGCCCCTCAACAAGTTCTCGATCTGTGTTCTTTAAGAGAGGATAAACAAAATAATCAATTAATAGTCATTGGAGGCTAACTAAACCAAACCATGGCTAGCAAGAGGAAGTCCACTGTTCCATGCATGATACCTGTAAAAACAATTCATCTGCAGGATGACTTTGATCGTGAAATCATGTCCCCTCAGACTAAGGACATAGGGATTACCTTCACAGAGGAAGCAAGTGCAAAAAGCAGTCAAAGTTTGGACAAGTCCTCTGGGCAAGAAGATATCCTTAAAGATGCTGGATTTTA[C/A]ACTTGTAGACCATGTAACTTTGAGACCCAGGATCTTAATCTTTTCCTTGATCATGTCTACAGTGGGCACACAGATTTCCGTATGGACCCCTGTTTTCTTTGTGTGAGCTGTGGAAAAAGTTCTGCAAAATTTGAGGGCTTGGCACTGCACAATGCCCGTGTCCATCCCAGTACAATAACTACCACACTTCAACTTAAAAAGAAGGACAACAGGGTCATTGTGGAGCAGAGTCTTTGTGTTGAACCTTGTGAAAGCACTAGCTCAAGAGATACTGAAATTTCCATCACGAAGACACCAATCATGAAAATGCTGAAGAGTAAATCCGAATCCAAAAGGATTGTGGTTTCTCATCCTGCTACTGATGATCCTTCCCCCTCTATTTCTAAAGTCGTGGAGAAAAAGGACCCTCCTGCTGTAAAAGTCACCCATGTGCCCACTATTGTACATAATGGGGCAGCCACCAAAGTTTCCCTGCCATCAGCCATACAGATTGTTAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39392
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 |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 350 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 350 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2889189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2935446 |
GRCz11 | 23 | 2879142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATCAAGATCTGGTTCACAGCACAAAGGCTGAAACAAGGAATCAGCTG[G/A]TCTCCAGAGGAAATAGAAGAGGCCCGAAGAAAAATGTTCAACACAATTAT
Long Flanking Sequence:
TCTCATCCTGCTACTGATGATCCTTCCCCCTCTATTTCTAAAGTCGTGGAGAAAAAGGACCCTCCTGCTGTAAAAGTCACCCATGTGCCCACTATTGTACATAATGGGGCAGCCACCAAAGTTTCCCTGCCATCAGCCATACAGATTGTTAATGGCTCTGGGGCTTTACCCATGCTGAAGACAGCAATGACACAAGTTGTATCTGTTGTGCAGAACAGAAGTCTCAGCCAGCAATCTGCTCCAATCACTCTCTCTTCATCCCACTCCTCTCCAGGCTCCTCAACAAGTACTAAAAATCTTCCCAAAGTGATGATCCCCCTAAGCAGCATTCCTACCTACAATGCATCCATGGACAACAGCAGTTTCTTAAAGACATCTTTTAGCAAGTTCCCTTATCCAACCAAGGCTGAACTTTGCTACCTTACTGTAGTTACCAAGTACCCAGAGGAGCAGATCAAGATCTGGTTCACAGCACAAAGGCTGAAACAAGGAATCAGCTG[G/A]TCTCCAGAGGAAATAGAAGAGGCCCGAAGAAAAATGTTCAACACAATTATACAGGCAGCACCTTCCAATGGCCAGCAGCAACGGCAGGCCCACCATACTCCTGCTCAGTCTACTATCACAGTTCTTGGCACGACTGGCATCCCACACATCTTACAAGGTAGCCTGGTTGGGCAAGGAGGAGTCATAGTCACCCAGCCCATGATGGCAAATGGTATTCAGGTCAGCAGTGCCCCAGTTACCCTAGCGGTTACACCCAAACCCCAGGCTGCTGCAAAGCCTTTAATGCAGGCCAGACCTGCTGCAGCCCTGGTAGCTGATAAAGGAATCAGCATGGTTTTGGGCTCTGTTGGTAGCAGTAGTAGTGGAAATTGCAGCAGCAGCAGTAGCAGCAGCAATGCTAGTACTAGCAGCAGTTTAAGCAGTGTTAGTAGTACTAGCAACCTGTGCAACCAGACTAGTGTAATCAGTATTGGTGGAAGCAGCACTGCTAAGTCAAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43907
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 |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 726 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 726 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2888063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2934320 |
GRCz11 | 23 | 2878016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGTCCCACACAGACATCATCACCGCCAACTCCAACACGTCGTCCTCCA[C/T]GACCCCCTTCACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCT
Long Flanking Sequence:
CAGCTGCCAGTACCACTCCACCCACAACCTTAGCATCTACAACCTCAACAGACACCCCAGTACCATGTAAATCAGACTCCCCAAGTCCTGCCTCTACGAACTCTCGTGTTTTCTCTAACAGTAACTTTTTGGACCCCGGCTTTAACAAAACCAAAAAGTCCCAGGAACAACTGTCAGCCTTAAAGGAGAGCTTCCTTATAAGCCAATTTCCCAACCAAGAGGAAGTGGACAGACTTATAAACCTAACTGGTCTATCTGTGCGTGAAGTACGGAAGTGGTTCAGTGACCGCCGCTACCACTTCAGGAATCTGAAAGGTTCAAGGTCGAGTGGTGGCGGTCAGACTGTTACAACAAGTGGTAGCATCTCCCAACTTGATACGGTTGCTGCTGTAGACCTATCAGAAAACGGTTCACCCCCAGAGCGGCCCAAAACTCCACAGCAGTCACCTCTTAGTCCCACACAGACATCATCACCGCCAACTCCAACACGTCGTCCTCCA[C/T]GACCCCCTTCACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCTCACCAGGTTCGAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAAGTTGACCGGTTAAGAGCAGAAACAAAGATGACCCGACGTGAGATCCATGGTTGGTTTGCTGAGCGGCGAAGGAGGGTAGCAGCAGAGAAGAAGAAAGAGGAAGCTGAGAAGGCGGAAAGAGAAGATGATGATTATGTGGGAGAGGAAGAGGAGACTGGGGTAAAAAAGGAAGGAATAAGCAATGAGGAAACACATGAAGCTGAAGATTCCTCAGTAGAGACACAAGGTGAAGACGAGAAACTGAAGGATGAAACCGGTAATGAGCCAAAGGTTAATCCTATCAAAATCAATCTCAAAATGCTTAAGGTTACTGAATCCAGTGGAAAAGGTGAACCAGAGGGAAGTCAACCGGTTGAGGCTAGCAAGGTGCCACAGACACCTGTTCCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8691
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 737 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 737 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2888028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2934285 |
GRCz11 | 23 | 2877981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACGWCGTCCTCCMCGACCCCCTTCWCCRGATTTTACGGCTATACGCTA[C/A]AAAGAGCGAGAGCCTCACCAGGTTCGAGCTTTMGAGGCAAGCTTTACACA
Long Flanking Sequence:
TCTACAACCTCAACAGACACCCCAGTACCATGTAAATCAGACTCCCCAAGTCCTGCCTCTACGAACTCTCGTGTTTTCTCTAACAGTAACTTTTTGGACCCCGGCTTTAACAAAACCAAAAAGTCCCAGGAACAACTGTCAGCCTTAAAGGAGAGCTTCCTTATAAGCCAATTTCCCAACCAAGAGGAAGTGGACAGACTTATAAACCTAACTGGTCTATCTGTGCGTGAAGTACGGAAGTGGTTCAGTGACCGCCGCTACCACTTCAGGAATCTGAAAGGTTCAAGGTCGAGTGGTGGCGGTCAGACTGTTACAACAAGTGGTAGCATCTCCCAACTTGATACGGTTGCTGCTGTAGACCTATCAGAAAACGGTTCACCCCCAGAGCGGCCCAAAACTCCACAGCAGTCACCTCTTAGTCCCACACAGACATCATCACCGCCAACTCCAACACGTCGTCCTCCACGACCCCCTTCACCAGATTTTACGGCTATACGCTA[C/A]AAAGAGCGAGAGCCTCACCAGGTTCGAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAAGTTGACCGGTTAAGAGCAGAAACAAAGATGACCCGACGTGAGATCCATGGTTGGTTTGCTGAGCGGCGAAGGAGGGTAGCAGCAGAGAAGAAGAAAGAGGAAGCTGAGAAGGCGGAAAGAGAAGATGATGATTATGTGGGAGAGGAAGAGGAGACTGGGGTAAAAAAGGAAGGAATAAGCAATGAGGAAACACATGAAGCTGAAGATTCCTCAGTAGAGACACAAGGTGAAGACGAGAAACTGAAGGATGAAACCGGTAATGAGCCAAAGGTTAATCCTATCAAAATCAATCTCAAAATGCTTAAGGTTACTGAATCCAGTGGAAAAGGTGAACCAGAGGGAAGTCAACCGGTTGAGGCTAGCAAGGTGCCACAGACACCTGTTCCACAGACCTCTCAATACCGAGGTAAGAAAACACCAGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43906
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 |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 746 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 746 | 1075 | 1 | 2 |
ENSDART00000022413 | Nonsense | 746 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 746 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2888003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2934260 |
GRCz11 | 23 | 2877956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCTCACCAGGTT[C/T]GAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAA
Long Flanking Sequence:
TACCATGTAAATCAGACTCCCCAAGTCCTGCCTCTACGAACTCTCGTGTTTTCTCTAACAGTAACTTTTTGGACCCCGGCTTTAACAAAACCAAAAAGTCCCAGGAACAACTGTCAGCCTTAAAGGAGAGCTTCCTTATAAGCCAATTTCCCAACCAAGAGGAAGTGGACAGACTTATAAACCTAACTGGTCTATCTGTGCGTGAAGTACGGAAGTGGTTCAGTGACCGCCGCTACCACTTCAGGAATCTGAAAGGTTCAAGGTCGAGTGGTGGCGGTCAGACTGTTACAACAAGTGGTAGCATCTCCCAACTTGATACGGTTGCTGCTGTAGACCTATCAGAAAACGGTTCACCCCCAGAGCGGCCCAAAACTCCACAGCAGTCACCTCTTAGTCCCACACAGACATCATCACCGCCAACTCCAACACGTCGTCCTCCACGACCCCCTTCACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCTCACCAGGTT[C/T]GAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAAGTTGACCGGTTAAGAGCAGAAACAAAGATGACCCGACGTGAGATCCATGGTTGGTTTGCTGAGCGGCGAAGGAGGGTAGCAGCAGAGAAGAAGAAAGAGGAAGCTGAGAAGGCGGAAAGAGAAGATGATGATTATGTGGGAGAGGAAGAGGAGACTGGGGTAAAAAAGGAAGGAATAAGCAATGAGGAAACACATGAAGCTGAAGATTCCTCAGTAGAGACACAAGGTGAAGACGAGAAACTGAAGGATGAAACCGGTAATGAGCCAAAGGTTAATCCTATCAAAATCAATCTCAAAATGCTTAAGGTTACTGAATCCAGTGGAAAAGGTGAACCAGAGGGAAGTCAACCGGTTGAGGCTAGCAAGGTGCCACAGACACCTGTTCCACAGACCTCTCAATACCGAGGTAAGAAAACACCAGAACAGCTCCACCTGCTGAAACAAGTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31080
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 |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 746 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 746 | 1075 | 1 | 2 |
ENSDART00000022413 | Nonsense | 746 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 746 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2888003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2934260 |
GRCz11 | 23 | 2877956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCTCACCAGGTT[C/T]GAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAA
Long Flanking Sequence:
TACCATGTAAATCAGACTCCCCAAGTCCTGCCTCTACGAACTCTCGTGTTTTCTCTAACAGTAACTTTTTGGACCCCGGCTTTAACAAAACCAAAAAGTCCCAGGAACAACTGTCAGCCTTAAAGGAGAGCTTCCTTATAAGCCAATTTCCCAACCAAGAGGAAGTGGACAGACTTATAAACCTAACTGGTCTATCTGTGCGTGAAGTACGGAAGTGGTTCAGTGACCGCCGCTACCACTTCAGGAATCTGAAAGGTTCAAGGTCGAGTGGTGGCGGTCAGACTGTTACAACAAGTGGTAGCATCTCCCAACTTGATACGGTTGCTGCTGTAGACCTATCAGAAAACGGTTCACCCCCAGAGCGGCCCAAAACTCCACAGCAGTCACCTCTTAGTCCCACACAGACATCATCACCGCCAACTCCAACACGTCGTCCTCCACGACCCCCTTCACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCTCACCAGGTT[C/T]GAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAAGTTGACCGGTTAAGAGCAGAAACAAAGATGACCCGACGTGAGATCCATGGTTGGTTTGCTGAGCGGCGAAGGAGGGTAGCAGCAGAGAAGAAGAAAGAGGAAGCTGAGAAGGCGGAAAGAGAAGATGATGATTATGTGGGAGAGGAAGAGGAGACTGGGGTAAAAAAGGAAGGAATAAGCAATGAGGAAACACATGAAGCTGAAGATTCCTCAGTAGAGACACAAGGTGAAGACGAGAAACTGAAGGATGAAACCGGTAATGAGCCAAAGGTTAATCCTATCAAAATCAATCTCAAAATGCTTAAGGTTACTGAATCCAGTGGAAAAGGTGAACCAGAGGGAAGTCAACCGGTTGAGGCTAGCAAGGTGCCACAGACACCTGTTCCACAGACCTCTCAATACCGAGGTAAGAAAACACCAGAACAGCTCCACCTGCTGAAACAAGTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24245
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 |
---|---|---|---|---|---|
ENSDART00000022413 | Nonsense | 791 | 1083 | 1 | 1 |
ENSDART00000121899 | Nonsense | 791 | 1075 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 2887868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2934125 |
GRCz11 | 23 | 2877821 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGTGAGATCCATGGTTGGTTTGCTGAGCGGCGAAGGAGGGTAGCAGCA[G/T]AGAAGAAGAAAGAGGAAGCTGAGAAGGCGGAAAGAGAAGATGATGATTAT
Long Flanking Sequence:
TTATAAGCCAATTTCCCAACCAAGAGGAAGTGGACAGACTTATAAACCTAACTGGTCTATCTGTGCGTGAAGTACGGAAGTGGTTCAGTGACCGCCGCTACCACTTCAGGAATCTGAAAGGTTCAAGGTCGAGTGGTGGCGGTCAGACTGTTACAACAAGTGGTAGCATCTCCCAACTTGATACGGTTGCTGCTGTAGACCTATCAGAAAACGGTTCACCCCCAGAGCGGCCCAAAACTCCACAGCAGTCACCTCTTAGTCCCACACAGACATCATCACCGCCAACTCCAACACGTCGTCCTCCACGACCCCCTTCACCAGATTTTACGGCTATACGCTACAAAGAGCGAGAGCCTCACCAGGTTCGAGCTTTAGAGGCAAGCTTTACACAAGAGCCAGATCCAACTAGTGAAGAAGTTGACCGGTTAAGAGCAGAAACAAAGATGACCCGACGTGAGATCCATGGTTGGTTTGCTGAGCGGCGAAGGAGGGTAGCAGCA[G/T]AGAAGAAGAAAGAGGAAGCTGAGAAGGCGGAAAGAGAAGATGATGATTATGTGGGAGAGGAAGAGGAGACTGGGGTAAAAAAGGAAGGAATAAGCAATGAGGAAACACATGAAGCTGAAGATTCCTCAGTAGAGACACAAGGTGAAGACGAGAAACTGAAGGATGAAACCGGTAATGAGCCAAAGGTTAATCCTATCAAAATCAATCTCAAAATGCTTAAGGTTACTGAATCCAGTGGAAAAGGTGAACCAGAGGGAAGTCAACCGGTTGAGGCTAGCAAGGTGCCACAGACACCTGTTCCACAGACCTCTCAATACCGAGGTAAGAAAACACCAGAACAGCTCCACCTGCTGAAACAAGTCTTTGCACGCACCCACTGGCCTAGTAGTCCACAGTACAACGAACTGATAACTAAAACAGGTCTACCTAGGCCAGAGGTAGTACGTTGGTTTGGAGATTGCCGCTATGTCCTGAAGAATGGTCAACTGAAGTGGCTTGAG
Associated Phenotype:
Not determined