ZMP
zgc:165518
Ensembl ID:
ZFIN ID:
Description:
Zgc:165518 protein [Source:UniProtKB/TrEMBL;Acc:A6H8S7]
Human Orthologue:
A2ML1
Human Description:
alpha-2-macroglobulin-like 1 [Source:HGNC Symbol;Acc:23336]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33068 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11732 | Essential Splice Site | Available for shipment | Available now |
sa39964 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39963 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17689 | Essential Splice Site | Available for shipment | Available now |
sa17770 | Essential Splice Site | Available for shipment | Available now |
sa15226 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33068
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110602 | Essential Splice Site | 47 | 1454 | 2 | 34 |
ENSDART00000114289 | Essential Splice Site | 47 | 1455 | 2 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 630205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 139503 |
GRCz11 | 3 | 76885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTCCTGCATGGCCACATGTGTGGATCTGACCAAATCTGTTTTCCTGC[A/T]GGCTCTTCATGGTGGCGTTTCCTTCACTGATCGAGTCCGGCTCTGATGCC
Long Flanking Sequence:
CTTGCCTGTAGGTTTCAAACAAGCCTGAAGGACCCCACCAGTATGGTCTGGTGTTTAATTATGGTTAAAGCTGAACTGCAGAGCTGCAGCCCTTCTGGAGCCGAGTCTGACACCTGGGCTGTAAAGTGTCGTCAGGTAGCCATCTTGTAGAGCAGAATGTAAACCATTCCACTGAAATAAACTGGAAAATGGTTCATTATTGCTGCTGAAAATGATCATGTCACTTTGGGCTGAGCTAATCAGAAAATAACATTTTGTAATTTCTGCTGGAGTATGTGAAGTTGCACTTTAACTTTTATTTCACCACCCGTTAAATTCAGCTTGCCAAGTTATTACCTGATCACGAAGTCCTCTTTATGATTAAGCTGCTAGGTGTTTCTTCATGGTTTAGTCTGCATTAACTGGCAGAAGCTTGTATTTGATGGTTGATTACCTGCAGTATGTCCTGAGTGTCTCCTGCATGGCCACATGTGTGGATCTGACCAAATCTGTTTTCCTGC[A/T]GGCTCTTCATGGTGGCGTTTCCTTCACTGATCGAGTCCGGCTCTGATGCCAAACTGTGTGTTAGTCTTCTGAAACACACGGGGAGTCTCACAATAACCATTTCTCTGGTCGATGACCAAAAAACAGAAACCCAACTTGTGCGTCAGACGTCCCGGAGGAAGCTTCACCAGTGTTTTACCTTCCAGGTCTGATTCTTTAACCTGCACCAAAACAGAAGTTGGGTTTGTGTGAAAGTGACTTCACTCAAAGTTCAGTCTCCACTTTTTTTTAAAACGCGTTTGAGATCTTTCAACTGTTGAACCCAAAGGAATATGTGTTGAACAAACAAATCCGTAGACTTCCATTGTTTTGTTGCTAAGGATGTCAAGGGCTTCTACCAACCCCCCCATACCCCCCCCCCCCCCCCCACCAAATCTTCCATGTCTTTGTGTTGAGCAGAACATTCAAGTTTATTTCAGGGTAAGTGTTGACTTCTAGTTGAGGAATCCACTATGATATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11732
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 |
---|---|---|---|---|---|
ENSDART00000110602 | Essential Splice Site | 680 | 1454 | 15 | 34 |
ENSDART00000114289 | Essential Splice Site | 680 | 1455 | 15 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 624992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 134290 |
GRCz11 | 3 | 71672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGACCCCGTCGAGCTGTTCCAACAGATCAGGCTTATAACACCTTCAAGG[T/C]AGAATSCTATTTTTAAAGTGGTTCYTGCTTGTTCTTGGTTTTWCATTGGT
Long Flanking Sequence:
CTTCACGTGGGGAGTGTGACATGTCTTTCATTGTTTGTTGCAGGTTTCTCTACAGTTCTCTCCTGCTTCTGCTGTTCCTGGAGAGGGAAGTGTTTTGACAGTCTCTGCTCAAGCAGGATCTCTGTGTGGCCTCAGTGCTATAGATCAGAGCGTCCTGATCCTGCAGTCAGGAGGACGTCTTACTGCAGAGGCGGTAATTTGTGTTTGTAAACTGCAGACCTTCTAAATTGTTTAAATGTGCCTGGAAGAAAAGCTAAACTGCTGCATTTTTGATTTGGACTTTCCGAATGTATTGCAGTTGTTGAATTCTGAGTTTTGCTCCCTTGTTTATCAGGGTTTTACAAGTCTTTGCTTGCGTTTCCCTCCCCTTAAGGTGTTTGGTTTACTCCCAGTGCAATCACTATATGATTATCCACCTGGTGTTGAAGATCAACAGGACTGCCTGCAAGTTCGACCCCGTCGAGCTGTTCCAACAGATCAGGCTTATAACACCTTCAAGG[T/C]AGAATGCTATTTTTAAAGTGGTTCTTGCTTGTTCTTGGTTTTTCATTGGTTTAGTTTTGAACAGGGTGTGGGGATTAAGATGGCAACAAATCTGCCGGTTCGAGAACCTGAGTGCCTCACATACAGGAGGCTAAATTTCTATCGCAACTTCCGTCGTAAGTATTTTAATCTAAAATTTGCCAGCTGCAATGCATAGAGTAAAAAAAAAAAGTTAAACTTTAATTCCCTCTTCTCCAAGGTCCTATGTTATTTGCTATGGATAAGGTTCTTGCTGCACCTGCAGCAGTATCCGAAATTGCTGGCTCCCCTTCTGGTTCACCTGTTGACGTGACCATCAGAACGTTTTTTCCAGAGACCTGGATCTGGCAACTCACTCCAGTGGGGTTGGTGAAACTTTATATTATTATTATTTTTTTTTTTTTTAACCCTACCGCCCCACACCCGTATATTTTTGTGGTCCTTGTCTTCAGAGACTCGGGGTCCACATCAGTTGCCCTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39964
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110602 | Nonsense | 1156 | 1454 | 27 | 34 |
ENSDART00000114289 | Nonsense | 1157 | 1455 | 27 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 622369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 131667 |
GRCz11 | 3 | 69049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGGAACACCTATGTCACTGCTCTGCTCGCCTACACCTTCAGTCTGGCT[G/T]GAGAGACCAGCACTCGAGCACAGCTTTTAAATTCCTTGCGAAACACTGCC
Long Flanking Sequence:
CATAGATCCCAACGTTCTTCAGAGTGCAAAGGACTGGTTGATAAGCAAGCAGGGTTCAAATGGCTGTTTTGTGCAACAGGGGACTCTCTACCACAATGACATGAGAGTACGTAACACTTCCACCTATTATAACCAAGCTGCAAGTGATAAGTTCTGATGCTGTTGTGTCTTAGGGTGGAGTTGGTGATAACGTGACCATGACTGGCTACATCGTTGCAGCACTGCTTGAAATTGGAGTCCCTGTCACGGTACGGGTTTAACTTTTTATCATCTGTAGGTGAAATGGATTGACTTATGTTGGCTAGTATTGTCAGTTTGGTTTTGAGCCATTGCGTTTAACCTTGGTCAAATTTAGTTTTCAATAGTTCCATGCTTGAAGTTTCTTCGTTTTCTTCCAGGATCCTGTCATTACTAAGGCTCTGTCGTTTTTGAGGCCTCTTGTTGGGAATCTGGGGAACACCTATGTCACTGCTCTGCTCGCCTACACCTTCAGTCTGGCT[G/T]GAGAGACCAGCACTCGAGCACAGCTTTTAAATTCCTTGCGAAACACTGCCATTTCTGAAGGTGAACATTAGCCACCTATTTGCTTTGTTAAATTGAGATGGAGCAATAAGTGTTCATCAGGCTGCTGTGTTAAGCTTTGCCAACAGCAAAGATATGCATTTTTAGAAACTATTAATATAAACTCCCCTCTCCTGTTCTCTTAGGTACTACTCTCCACTGGTCTCAGACTACATCAGGGGACACTCTGGCAGTGGAGATCAGTGCATATGTGCTGTTAGCAGTTCTCAATGTACAGCCTGTGACCACTGCTACACTGGGCTATGCTAACCGCATTGTCAACTGGCTTGTGGCCCAGCAGAATCCCTATGGTGGTTTCACCTCCACTCAGGTGACTTAAGCGAACAAACATTAAGCATTTGTTGTGCTTTTAAAGTCCATTAGAGTCTTTATTATGCTAATGCACTGTGTAGCTCATCTTGTAGCTGGACCTGATTTGACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39963
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 |
---|---|---|---|---|---|
ENSDART00000110602 | Essential Splice Site | 1379 | 1454 | 31 | 34 |
ENSDART00000114289 | Essential Splice Site | 1380 | 1455 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 620857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 130155 |
GRCz11 | 3 | 67537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGGTGGACATCAAGGTGTTGTCAGGATTCACTGCAGACACCTCACTG[G/A]TTTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGGAACTTGCTGAA
Long Flanking Sequence:
TCCTGTTGTGGTTGCCAAAACACTGAGTGTTGTTGCAAAGGTGACTGGAAACTGCAAGGCGTCACCAGTCAATCTGATGTTGACCTTCACAGTCAAGTAAGGATGTCTTTCAGCTTTACATATGACGTTAAGGCTAGCCAATTCTTTGCCAAGGCTTTACTTTCTGCACTTCTAGAGTAGAGCAGTGGCCAAAAAGCATTTGCAAAACTTTGTATCATTTATACAGTTGCAATGGTGATTTTGCATAAGATGGATGACTTGTGTATTTTAAAGTGGACACTGTTCAGCAATGCCGTTCTTCATGTACGGTTTATACTGTGCTAGCTCCCGTCATAAACATTTCTAAAGCACATCTATGCCACTCCAGTGTTGGAGCAAGATAGCTTGTTCCTTAACATGACCTGTCTTTCCATGTCAGATACACTGGTCCAAAACCAACTACTAACATGCTTCTGGTGGACATCAAGGTGTTGTCAGGATTCACTGCAGACACCTCACTG[G/A]TTTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGGAACTTGCTGAATATTTATTGTATTTTTCCTTGTTCCCCTCACAGCTTGGATCTCCACCCAATTTCTCTCCATTGGTGCAAAGGGTGGATACTGAAGGTGATCGTGTGCTTGTCTATCTACAAGAGGTGAGATGGTAGTTACTTACACTTAATGATAAATTATGCCATTTTTAAAGCTTAAGGTTGGCGAAATGGTAGACTTCAAAGTACTTTGACTTTCTGGCTAAAACATTTAACTCGCACCCTTTAATTTTTGAAATTTAGACTATATCCCTCTTGTTTGCACGAGCATTTATTTATATTAAACCAAAGTCAAGAGTAGGGCGAAGCAGTGTTGCAGTTGGTAGTGCTGTCGCCAGTAACCCTTCTGTCTGCAGGTTCCCAAAGGCGTCCCAGTGACCTACAGTATACAGCTGACACAGACTGTTGCAGTGAAGAATCTCAAGCCAGCAGTCATCAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17689
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 |
---|---|---|---|---|---|
ENSDART00000110602 | Essential Splice Site | 1379 | 1454 | 31 | 34 |
ENSDART00000114289 | Essential Splice Site | 1380 | 1455 | 31 | 34 |
ENSDART00000110602 | Essential Splice Site | 1379 | 1454 | 31 | 34 |
ENSDART00000114289 | Essential Splice Site | 1380 | 1455 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 620856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 130154 |
GRCz11 | 3 | 67536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGGTGGACATCAARGTGTTGTCAGGATTCACTGCAGACACMTCACTGG[T/C]TTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGRAACTTGCTGAAT
Long Flanking Sequence:
CCTGTTGTGGTTGCCAAAACACTGAGTGTTGTTGCAAAGGTGACTGGAAACTGCAAGGCGTCACCAGTCAATCTGATGTTGACCTTCACAGTCAAGTAAGGATGTCTTTCAGCTTTACATATGACGTTAAGGCTAGCCAATTCTTTGCCAAGGCTTTACTTTCTGCACTTCTAGAGTAGAGCAGTGGCCAAAAAGCATTTGCAAAACTTTGTATCATTTATACAGTTGCAATGGTGATTTTGCATAAGATGGATGACTTGTGTATTTTAAAGTGGACACTGTTCAGCAATGCCGTTCTTCATGTACGGTTTATACTGTGCTAGCTCCCGTCATAAACATTTCTAAAGCACATCTATGCCACTCCAGTGTTGGAGCAAGATAGCTTGTTCCTTAACATGACCTGTCTTTCCATGTCAGATACACTGGTCCAAAACCAACTACTAACATGCTTCTGGTGGACATCAAGGTGTTGTCAGGATTCACTGCAGACACCTCACTGG[T/C]TTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGGAACTTGCTGAATATTTATTGTATTTTTCCTTGTTCCCCTCACAGCTTGGATCTCCACCCAATTTCTCTCCATTGGTGCAAAGGGTGGATACTGAAGGTGATCGTGTGCTTGTCTATCTACAAGAGGTGAGATGGTAGTTACTTACACTTAATGATAAATTATGCCATTTTTAAAGCTTAAGGTTGGCGAAATGGTAGACTTCAAAGTACTTTGACTTTCTGGCTAAAACATTTAACTCGCACCCTTTAATTTTTGAAATTTAGACTATATCCCTCTTGTTTGCACGAGCATTTATTTATATTAAACCAAAGTCAAGAGTAGGGCGAAGCAGTGTTGCAGTTGGTAGTGCTGTCGCCAGTAACCCTTCTGTCTGCAGGTTCCCAAAGGCGTCCCAGTGACCTACAGTATACAGCTGACACAGACTGTTGCAGTGAAGAATCTCAAGCCAGCAGTCATCAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17770
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 |
---|---|---|---|---|---|
ENSDART00000110602 | Essential Splice Site | 1379 | 1454 | 31 | 34 |
ENSDART00000114289 | Essential Splice Site | 1380 | 1455 | 31 | 34 |
ENSDART00000110602 | Essential Splice Site | 1379 | 1454 | 31 | 34 |
ENSDART00000114289 | Essential Splice Site | 1380 | 1455 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 620856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 130154 |
GRCz11 | 3 | 67536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGGTGGACATCAARGTGTTGTCAGGATTCACTGCAGACACMTCACTGG[T/C]TTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGRAACTTGCTGAAT
Long Flanking Sequence:
CCTGTTGTGGTTGCCAAAACACTGAGTGTTGTTGCAAAGGTGACTGGAAACTGCAAGGCGTCACCAGTCAATCTGATGTTGACCTTCACAGTCAAGTAAGGATGTCTTTCAGCTTTACATATGACGTTAAGGCTAGCCAATTCTTTGCCAAGGCTTTACTTTCTGCACTTCTAGAGTAGAGCAGTGGCCAAAAAGCATTTGCAAAACTTTGTATCATTTATACAGTTGCAATGGTGATTTTGCATAAGATGGATGACTTGTGTATTTTAAAGTGGACACTGTTCAGCAATGCCGTTCTTCATGTACGGTTTATACTGTGCTAGCTCCCGTCATAAACATTTCTAAAGCACATCTATGCCACTCCAGTGTTGGAGCAAGATAGCTTGTTCCTTAACATGACCTGTCTTTCCATGTCAGATACACTGGTCCAAAACCAACTACTAACATGCTTCTGGTGGACATCAAGGTGTTGTCAGGATTCACTGCAGACACCTCACTGG[T/C]TTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGGAACTTGCTGAATATTTATTGTATTTTTCCTTGTTCCCCTCACAGCTTGGATCTCCACCCAATTTCTCTCCATTGGTGCAAAGGGTGGATACTGAAGGTGATCGTGTGCTTGTCTATCTACAAGAGGTGAGATGGTAGTTACTTACACTTAATGATAAATTATGCCATTTTTAAAGCTTAAGGTTGGCGAAATGGTAGACTTCAAAGTACTTTGACTTTCTGGCTAAAACATTTAACTCGCACCCTTTAATTTTTGAAATTTAGACTATATCCCTCTTGTTTGCACGAGCATTTATTTATATTAAACCAAAGTCAAGAGTAGGGCGAAGCAGTGTTGCAGTTGGTAGTGCTGTCGCCAGTAACCCTTCTGTCTGCAGGTTCCCAAAGGCGTCCCAGTGACCTACAGTATACAGCTGACACAGACTGTTGCAGTGAAGAATCTCAAGCCAGCAGTCATCAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15226
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110602 | Essential Splice Site | 1406 | 1454 | 32 | 34 |
ENSDART00000114289 | Essential Splice Site | 1407 | 1455 | 32 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 620692)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 129990 |
GRCz11 | 3 | 67372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCARAGGGTGGATACTGAAGGTGATCGTGTGCTTGTCTATCTACAAGAG[G/C]TGAGATRGTWGTTACTTRCACTTAATGATAAATTATGCCATTTTTAAAGC
Long Flanking Sequence:
GCACTTCTAGAGTAGAGCAGTGGCCAAAAAGCATTTGCAAAACTTTGTATCATTTATACAGTTGCAATGGTGATTTTGCATAAGATGGATGACTTGTGTATTTTAAAGTGGACACTGTTCAGCAATGCCGTTCTTCATGTACGGTTTATACTGTGCTAGCTCCCGTCATAAACATTTCTAAAGCACATCTATGCCACTCCAGTGTTGGAGCAAGATAGCTTGTTCCTTAACATGACCTGTCTTTCCATGTCAGATACACTGGTCCAAAACCAACTACTAACATGCTTCTGGTGGACATCAAGGTGTTGTCAGGATTCACTGCAGACACCTCACTGGTTTGTATTCGTTTTGAGGGTGACTTTTTGGGATCTTTGGAACTTGCTGAATATTTATTGTATTTTTCCTTGTTCCCCTCACAGCTTGGATCTCCACCCAATTTCTCTCCATTGGTGCAAAGGGTGGATACTGAAGGTGATCGTGTGCTTGTCTATCTACAAGAG[G/C]TGAGATGGTAGTTACTTACACTTAATGATAAATTATGCCATTTTTAAAGCTTAAGGTTGGCGAAATGGTAGACTTCAAAGTACTTTGACTTTCTGGCTAAAACATTTAACTCGCACCCTTTAATTTTTGAAATTTAGACTATATCCCTCTTGTTTGCACGAGCATTTATTTATATTAAACCAAAGTCAAGAGTAGGGCGAAGCAGTGTTGCAGTTGGTAGTGCTGTCGCCAGTAACCCTTCTGTCTGCAGGTTCCCAAAGGCGTCCCAGTGACCTACAGTATACAGCTGACACAGACTGTTGCAGTGAAGAATCTCAAGCCAGCAGTCATCAATGTTTATGACTATTATCAGAGAAGTATGCATCTTTATTATTGACCATTTTGATTTGATTTCAGACGGTGTTTCATACTCTGCTTTCTCTTTCAGGTGAAAGTTTTGAGACCACATACACTTCTGTCTGTTCATGATTGGGATTCAGTTCTGGCTACTCCATGTATTT
Associated Phenotype:
Not determined