ZMP
si:ch73-212j7.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JKV3]
Human Orthologue:
KIAA0284
Human Description:
KIAA0284 [Source:HGNC Symbol;Acc:20362]
Mouse Orthologue:
AW555464
Mouse Description:
expressed sequence AW555464 Gene [Source:MGI Symbol;Acc:MGI:2145043]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10696 | Nonsense | Available for shipment | Available now |
| sa17237 | Nonsense | Available for shipment | Available now |
| sa23625 | Nonsense | Available for shipment | Available now |
| sa9972 | Nonsense | Available for shipment | Available now |
| sa36946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18015 | Essential Splice Site | Available for shipment | Available now |
| sa8550 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10696
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 |
|---|---|---|---|---|---|
| ENSDART00000112848 | Nonsense | 732 | 1687 | 9 | 18 |
| ENSDART00000132972 | None | None | 202 | None | 6 |
| ENSDART00000133435 | Nonsense | 159 | 234 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3153502)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3107364 |
| GRCz11 | 20 | 3120204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTWACATTTCACAGGTGTTTGGTGTTTTAGATGCGCCAGAATACAGTGGT[C/T]AGACTCTTGGAGTTTATAGGCCTGTGATTGATGATGGGGACAATGAGCAG
Long Flanking Sequence:
ATTTTGCAGGTTGGTAACTTACTTAGAATTGTCTTTATTGAATAAACTGCCAATCATTTGAATAAAAATAACATGTACATAGCCCAGAAAGACTGACCCTTAAGCAAGTCAGCAATCAAAAAACAAGTACACTGTGAAAATGGCTGTAAAAAATGGTCATTTCACAAATCTGTGAAATTAAATAGTCAACACAAAGTACCAATTTATAATTTATTTCTTGTTTTAATACATCACATAATGAGTTGACATTGTTACATATATTAACAGTGTTATGTCTAGTAATAACAGACCCCTGCAATATCCTTACGACCCACTGGGGTGATGAGGCTGTGGTCCACAGGTTGAAAACCATTGATGTAGATTATGATTAACCTTTTTTTTTAAATGCTAGGATGGGTTGCCATTATGTGGTCCAAAGAGAGGAGGACAGTATTTAAGAAATCGCATCTGTTTACATTTCACAGGTGTTTGGTGTTTTAGATGCGCCAGAATACAGTGGT[C/T]AGACTCTTGGAGTTTATAGGCCTGTGATTGATGATGGGGACAATGAGCAGCTATTCTTTAGTCAAAGCCACAGTAATGCAGCTGATGTAATGTCAACATCATCATTGGGCCATGGCAGGGACCAAGTCATCTCATTGCAGGTATTGCAATTATGTACTGCTAAGGCAACTGGGCCATTCTTTATTGAAACATAGCTTCAGTTGTGTCAGTGAACAATTAATGTACTCAATGTAAAACATACCTTTTGTAATTTAGGCACATCCTGGTGTAGTAGGGCCTAAATGGGTCTCGCGTTGGGCCAGCCTTGCAGACCCTTATAGTGATCCCGGGGCTACACAAGGATCTGTACCAGTTCCACCCCAAAGTGCAGAAAGAGGTATATTAATTCAAAATCATTAGTAGTTGTTGAGCAAAAGGGTAGTAAATACAATTTTGGTTTCATCATGGACAAGCCCACAAACTAATAATAAACTCAATTTTTCTAATTTTGTAGATGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17237
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 |
|---|---|---|---|---|---|
| ENSDART00000112848 | Nonsense | 787 | 1687 | 10 | 18 |
| ENSDART00000132972 | None | None | 202 | None | 6 |
| ENSDART00000133435 | Nonsense | 214 | 234 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3153782)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3107644 |
| GRCz11 | 20 | 3120484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TKTAAAACATAMCTTTTGTAATTTAGGCACATCCTGGTGTAGTAGGGCCT[A/T]AATGGGTCTCGCGTTGGGCCAGCCTTGCAGACCCTTATAGTGATCCCGGG
Long Flanking Sequence:
AATAACAGACCCCTGCAATATCCTTACGACCCACTGGGGTGATGAGGCTGTGGTCCACAGGTTGAAAACCATTGATGTAGATTATGATTAACCTTTTTTTTTAAATGCTAGGATGGGTTGCCATTATGTGGTCCAAAGAGAGGAGGACAGTATTTAAGAAATCGCATCTGTTTACATTTCACAGGTGTTTGGTGTTTTAGATGCGCCAGAATACAGTGGTCAGACTCTTGGAGTTTATAGGCCTGTGATTGATGATGGGGACAATGAGCAGCTATTCTTTAGTCAAAGCCACAGTAATGCAGCTGATGTAATGTCAACATCATCATTGGGCCATGGCAGGGACCAAGTCATCTCATTGCAGGTATTGCAATTATGTACTGCTAAGGCAACTGGGCCATTCTTTATTGAAACATAGCTTCAGTTGTGTCAGTGAACAATTAATGTACTCAATGTAAAACATACCTTTTGTAATTTAGGCACATCCTGGTGTAGTAGGGCCT[A/T]AATGGGTCTCGCGTTGGGCCAGCCTTGCAGACCCTTATAGTGATCCCGGGGCTACACAAGGATCTGTACCAGTTCCACCCCAAAGTGCAGAAAGAGGTATATTAATTCAAAATCATTAGTAGTTGTTGAGCAAAAGGGTAGTAAATACAATTTTGGTTTCATCATGGACAAGCCCACAAACTAATAATAAACTCAATTTTTCTAATTTTGTAGATGACAGAGTGACATTAATTATTGGTCAATGCTTGGATATCTCAGAATCAGAGGGAAGTCAAAGTTCCAGGACCAGACGGCTACTTCCTCAGGTTCCTCCTGGAGAAAAACTAGAAAACACAACCCCTAGCATCCTAATCCGACATGAAACAAACTTGGACCATGAGCCACCAGAGAAAGGTTCCAGAATGCCACAGCAGCAAGACAACACTCAGAGGCTACGTGTCCAGGATGATGTGGACCCAGACAGTCTGAGTGACACCAGCCGTTCAGATGACAGCTCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23625
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 |
|---|---|---|---|---|---|
| ENSDART00000112848 | Nonsense | 917 | 1687 | 11 | 18 |
| ENSDART00000132972 | None | None | 202 | None | 6 |
| ENSDART00000133435 | None | None | 234 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3154289)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3108151 |
| GRCz11 | 20 | 3120991 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACAGTCTGAGTGACACCAGCCGTTCAGATGACAGCTCTATCCTTGAT[A/T]GAAGCGGTAGGAGCCAAGGAAAACGAGGAACTACAAGACACCTACCTTCA
Long Flanking Sequence:
TCTCGCGTTGGGCCAGCCTTGCAGACCCTTATAGTGATCCCGGGGCTACACAAGGATCTGTACCAGTTCCACCCCAAAGTGCAGAAAGAGGTATATTAATTCAAAATCATTAGTAGTTGTTGAGCAAAAGGGTAGTAAATACAATTTTGGTTTCATCATGGACAAGCCCACAAACTAATAATAAACTCAATTTTTCTAATTTTGTAGATGACAGAGTGACATTAATTATTGGTCAATGCTTGGATATCTCAGAATCAGAGGGAAGTCAAAGTTCCAGGACCAGACGGCTACTTCCTCAGGTTCCTCCTGGAGAAAAACTAGAAAACACAACCCCTAGCATCCTAATCCGACATGAAACAAACTTGGACCATGAGCCACCAGAGAAAGGTTCCAGAATGCCACAGCAGCAAGACAACACTCAGAGGCTACGTGTCCAGGATGATGTGGACCCAGACAGTCTGAGTGACACCAGCCGTTCAGATGACAGCTCTATCCTTGAT[A/T]GAAGCGGTAGGAGCCAAGGAAAACGAGGAACTACAAGACACCTACCTTCAGAAAATGTAAACCATTCAAGAGAGCTGAGGGAGATGCCACAACCTACACCCAAACCCACTTCATTTTATATCGGTTCTGAGGATGGTTTATCCAAGTCCGATGTGTCCAAAAGCCCAGTTCTTTCACAGCCAGAGAAAGACTCTGCTTTCAAGATACCTCCAACTACTGTCTTGATACGACATTTGAGTGGCCATGAGTCTAGACGTCCAGTGAAACCCAACTCATCAGCTCCAGATCTTCAGACACATAACAAGGATGTGGTGCCCACCAAAGATACTTCAACCTCATTTGTTCGACAGGAGAGTTTTACCAAAGACAGGCCAAGTGACAACATTCAAGTCAAGAAACTGCCACATATCTCTAGTCATCCTGCTTTGCGAAGCTTGGATACAGAGGAGACACTTCAAGATACATTTACCTTTCTTAAGGAAGTAGAGAAATCTCCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9972
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112848 | Nonsense | 963 | 1687 | 11 | 18 |
| ENSDART00000132972 | None | None | 202 | None | 6 |
| ENSDART00000133435 | None | None | 234 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3154428)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3108290 |
| GRCz11 | 20 | 3121130 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACCTACACCCAAACCCACTTCATTTTATATCGGTTCTGAGGATGGTT[T/G]ATCCAAGTCCGATGTGTCCAAAAGYCCAGTTCTTTCACAGCCAGAGAAAG
Long Flanking Sequence:
TACAATTTTGGTTTCATCATGGACAAGCCCACAAACTAATAATAAACTCAATTTTTCTAATTTTGTAGATGACAGAGTGACATTAATTATTGGTCAATGCTTGGATATCTCAGAATCAGAGGGAAGTCAAAGTTCCAGGACCAGACGGCTACTTCCTCAGGTTCCTCCTGGAGAAAAACTAGAAAACACAACCCCTAGCATCCTAATCCGACATGAAACAAACTTGGACCATGAGCCACCAGAGAAAGGTTCCAGAATGCCACAGCAGCAAGACAACACTCAGAGGCTACGTGTCCAGGATGATGTGGACCCAGACAGTCTGAGTGACACCAGCCGTTCAGATGACAGCTCTATCCTTGATAGAAGCGGTAGGAGCCAAGGAAAACGAGGAACTACAAGACACCTACCTTCAGAAAATGTAAACCATTCAAGAGAGCTGAGGGAGATGCCACAACCTACACCCAAACCCACTTCATTTTATATCGGTTCTGAGGATGGTT[T/G]ATCCAAGTCCGATGTGTCCAAAAGCCCAGTTCTTTCACAGCCAGAGAAAGACTCTGCTTTCAAGATACCTCCAACTACTGTCTTGATACGACATTTGAGTGGCCATGAGTCTAGACGTCCAGTGAAACCCAACTCATCAGCTCCAGATCTTCAGACACATAACAAGGATGTGGTGCCCACCAAAGATACTTCAACCTCATTTGTTCGACAGGAGAGTTTTACCAAAGACAGGCCAAGTGACAACATTCAAGTCAAGAAACTGCCACATATCTCTAGTCATCCTGCTTTGCGAAGCTTGGATACAGAGGAGACACTTCAAGATACATTTACCTTTCTTAAGGAAGTAGAGAAATCTCCAGAGGAGAAGTTGTCTGGATGTAGTCAACGATCAAAAAAAGGAAGCTCTCCTGCACAAGAAGACTCCTTTTCTGGTGACTCAGATGTGGATACTGCCAGTACTGTAAGCATGGTCAGCAGTAAAAATGCCCCTGTCAGTTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36946
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 |
|---|---|---|---|---|---|
| ENSDART00000112848 | Nonsense | 1101 | 1687 | 11 | 18 |
| ENSDART00000132972 | None | None | 202 | None | 6 |
| ENSDART00000133435 | None | None | 234 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3154841)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3108703 |
| GRCz11 | 20 | 3121543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGTTGTCTGGATGTAGTCAACGATCAAAAAAAGGAAGCTCTCCTGCA[C/T]AAGAAGACTCCTTTTCTGGTGACTCAGATGTGGATACTGCCAGTACTGTA
Long Flanking Sequence:
AAAATGTAAACCATTCAAGAGAGCTGAGGGAGATGCCACAACCTACACCCAAACCCACTTCATTTTATATCGGTTCTGAGGATGGTTTATCCAAGTCCGATGTGTCCAAAAGCCCAGTTCTTTCACAGCCAGAGAAAGACTCTGCTTTCAAGATACCTCCAACTACTGTCTTGATACGACATTTGAGTGGCCATGAGTCTAGACGTCCAGTGAAACCCAACTCATCAGCTCCAGATCTTCAGACACATAACAAGGATGTGGTGCCCACCAAAGATACTTCAACCTCATTTGTTCGACAGGAGAGTTTTACCAAAGACAGGCCAAGTGACAACATTCAAGTCAAGAAACTGCCACATATCTCTAGTCATCCTGCTTTGCGAAGCTTGGATACAGAGGAGACACTTCAAGATACATTTACCTTTCTTAAGGAAGTAGAGAAATCTCCAGAGGAGAAGTTGTCTGGATGTAGTCAACGATCAAAAAAAGGAAGCTCTCCTGCA[C/T]AAGAAGACTCCTTTTCTGGTGACTCAGATGTGGATACTGCCAGTACTGTAAGCATGGTCAGCAGTAAAAATGCCCCTGTCAGTTCACTTAAGAAGCACACGTCTGCAAATGACACGGGTAAGGAGAAGTCATCATCTGGTTTACCTGCAAAACACAAAGCACGACAACCCACAGCTCGCGAACGACTGTCAGAGAAACGCAAAAGTCATGCCTCTGCAGATAACACCAGTAAAGCTGAACTAAGTCGTCGGCTCCAGCTTCGCCGCAGTGCTGGCAATCGTGGTTCGTTAGACCTTTCAGATAATCAGCATGGTCAGCAGCTATGGCCTGAAGCGGGTGCTTCCGACCATGAGTCAAGTTCACGGCCAAACAACCGTAAAAAACTCACTGCTCCCCTGCAGAAGGAGGACCCCAATAAGGTGACCAAAGGAAGCCATCAGGTGCTGACCAGATCCAACAGTCTTTCAGCCCCAAGACCAACACGTGCCTCCATGCTCCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18015
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 |
|---|---|---|---|---|---|
| ENSDART00000112848 | Essential Splice Site | 1378 | 1687 | 11 | 18 |
| ENSDART00000132972 | None | None | 202 | None | 6 |
| ENSDART00000133435 | None | None | 234 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3155676)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3109538 |
| GRCz11 | 20 | 3122378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACTCCTCCCRTACCCATTCTACCCAAGTTAAWCACAGTAGCACAGCTG[G/A]TAGGTATTAGTCARTTTATTTCTCTTATGCTGTGTTCACACCAGACGCGG
Long Flanking Sequence:
GGGTGCTTCCGACCATGAGTCAAGTTCACGGCCAAACAACCGTAAAAAACTCACTGCTCCCCTGCAGAAGGAGGACCCCAATAAGGTGACCAAAGGAAGCCATCAGGTGCTGACCAGATCCAACAGTCTTTCAGCCCCAAGACCAACACGTGCCTCCATGCTCCGCCGAGCTCGACTAGGTGAGGCTTCAGATAATGAGAGCGCTGAGACAGACCGGGCATCTCCAAGCTCTGAGCACAGCAAGACAGAATCGAAAAAACTCTCAAGGCTAGACATTCTTGCCATGCCTCGGAAACGCACAAGGTCCTTCACTGTTCCAAGTGACAATGAGTCAACTTCAAGTAAGCATGGCATTTCTAACCGTACTACAGAGGCAAGTAGCAGTGCAAGGAAAGGTGCTTCAAGTGAGGTGAGGCATGCTAACAGCAAAGGGACTGCAGCAGCTGGGAAACACTCCTCCCGTACCCATTCTACCCAAGTTAAACACAGTAGCACAGCTG[G/A]TAGGTATTAGTCAGTTTATTTCTCTTATGCTGTGTTCACACCAGACGCGGAACGCGCGGATAAATCGCGCTATTCGCACGTAAATAGCCGCGTGAACATTTGATATTACTCGCTTCATTCGCGCGTCAAATCCGATTCAATCGCGTGTCAAATTCACTTCAGAACAGACGCGGATTTGCGTGATGGGCAGGGCTTCTGTCTGCCTGGTGACTGTAGCTTCGTTGCTAAATGGCTAACATGGATTTTATGAAGAAAATAACAGTGTTTATGTACTTTATGAAGGCTGAAAAACAGCGTCGATACGTTTAAGACCATGTCTGGGTCCACTACATGCTTTCAGAGGTGCATCCAGCTCTGTGAGCTTATAAACTCCTTCAGAAACTGAACCTGGATCACGGAGGCTTTCAACGGTGCTTCTGACTGAGCCAAGCCCAGTTTGATGACTTGTTGTCGGTGTCCGCTGGAGGATTTCCCCTGGGACACCATCAACAGGTTCTACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8550
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112848 | Nonsense | 1521 | 1687 | 14 | 18 |
| ENSDART00000132972 | Nonsense | 66 | 202 | 2 | 6 |
| ENSDART00000133435 | None | None | 234 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 3160106)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 3113968 |
| GRCz11 | 20 | 3126808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGATTAAKCTGCAGCTGGTACAGCATATACCCGAGGCAAGTTTGAACTA[T/A]CAAAAGGTTCCTCCAGGCTCAACTAGTCCAAWAGACCAGGACTCAAATAT
Long Flanking Sequence:
TTGTTATATTTTCTCTTTTGTGCAGAGACCATATGCATCATTACAGAGTTTCCTGTTACCTCAGGTGCTGAGTTCATCTCTCATTATCACCAAGTGGTGCACAAAATTAAACATGACTTGTTTTCTGTGAGCCAATCGCATTGTACTAACAGCTGTCTGATGTCCACCTTTGAAATTGCTGCCTCACTGTTTTATTTGCTTGTGGGAATTCCCTAATGCATGGAAATTCCAACTACTCACCTCCAAATGCTGTATGTTCAAACTAGTATTTTCCATTAAAGTTGACTGACTGTGAACGTATCTGTTCACAACTGAAGTAGCATGACCATGCATACACTTCCCAGTTTTATCTCCGAAGCTTCCACTGTATGCTGAGCTCAGAGATGTTTGTCTTCTAACATCAAATATAACTTGTGATGTCCACGTGTTCTTACTAGTGCTTTCCCATCCCTGATTAATCTGCAGCTGGTACAGCATATACCCGAGGCAAGTTTGAACTA[T/A]CAAAAGGTTCCTCCAGGCTCAACTAGTCCAATAGACCAGGACTCAAATATGAACGACCATGACAGTTCCAGACGGCGTCCCTGGAACCGTGAAGAGGTCAAATTTGGTGCAATTTTTTGCTCATTACACTAATAATCTGATCCATTAGTCAAATATTGAGGGTGTTACAACCTGCATAAGCACATGCAGTGTTTTTCAGATACTGTACGAACAAATGCCGCAGTTACATGGTTTTAACCTTTGACTCTTTTTATTTTGATTACAGGTAATACTGGACAATCTCATGTTGAATCCAGTTTCCCAGCTCTCCCAGGCTATCAGGGAGAACACGGAGCAACTAGCTGAGAAAATGAAGTATGAAGTGAAATGTTTTCTATTGGGAATATCTTAGGGGTTTCCATCAACATGTTGTTGGCATCAAAATTTGAGATGACTTCGGGTTGTTGTGGACCCTGTACTGTACTGTAAACCAAATAGTTGAAATGACTAGAGAACTGCAT
Associated Phenotype:
Not determined