ZMP
dlg5
Ensembl ID:
ZFIN ID:
Description:
disks large homolog 5 [Source:RefSeq peptide;Acc:NP_001139075]
Human Orthologue:
DLG5
Human Description:
discs, large homolog 5 (Drosophila) [Source:HGNC Symbol;Acc:2904]
Mouse Orthologue:
Dlg5
Mouse Description:
discs, large homolog 5 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1918478]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45483 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35447 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13331 | Nonsense | Available for shipment | Available now |
sa22258 | Essential Splice Site | Available for shipment | Available now |
sa13023 | Essential Splice Site | Available for shipment | Available now |
sa15456 | Essential Splice Site | Available for shipment | Available now |
sa12813 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45483
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105496 | Essential Splice Site | 1177 | 1926 | None | 32 |
ENSDART00000124710 | None | 1208 | 1958 | 18 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16493273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16313308 |
GRCz11 | 13 | 16444300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTAAACCTTCAGACTCAGCACATCGAGGACTGGCCCCCTGCTCTGC[A/G]GTAACAGCCGTCATGAAGAACCCTGTTTACATGGTGCGCAGTCACAGAGT
Long Flanking Sequence:
CCCAGTAGAAACCTACATGAATATGGGAAGAACATGCAAACTCCACACAGAGATGCCAACTGGCCCAATCGGGACTTGAACCAGCGACCTTCTTGCTGTGAGGTGACATTGCTAGCCACTTTGCCACCCCCAAACAAATATTCCAAAATTAAATTATGATTTAGTTATTCATGGGTTAATGTTTTATGTAATGAAAAACATTGTGAACTGTATCTATAAGTACATCTATTTATGCATTGATAAGTGATTTTAATTAATATATTTTTTATTAGTTAATATAACTTTAATAATAAGTGCTACATAACATTCAACGTATTAAACGTTTTTTGAACATGTGAGCAGGCCCAATAAAAGAAACTGAAATGAAATATGTGAGCACAGGGGGCAGTTGAAGGGAATTGTGTGTATGTGTGTTTCTCATTGGAGTGTTTTATTGGTTATTTTGTGGTTGTGTTTAAACCTTCAGACTCAGCACATCGAGGACTGGCCCCCTGCTCTGC[A/G]GTAACAGCCGTCATGAAGAACCCTGTTTACATGGTGCGCAGTCACAGAGTTCACACTAACAACTGCCCTACTGTCGTCAGCCAGATCAATCAGCAGCACACGCACCCCAGGTACCACAGTTCCCACTGAGATAACCAGCACTTCACACACATGCAAACTCAAACATATACTTCACTTCCTTTCTAGACTGTACCTTTATTACAGTGGAGAAGTAGACTTGACACATCCTTATCTGCTCCTTTATAAAACTGTGAGCCTGTTTTACAGAAACATGCAACAGAGATTATACATATTATTATGTACTAGCCATTCATTTACCAAAATAAGAAATATTTTGACATTTACATTTTTTACATTTTGGATCAAGTCTTTATTTCAACAGTGATTTGTTAAAATTTTAATTTATTTTAGAAAGAATCGAGTATTTATCAATTCTTGTCTCACCTCAATCACTCAGTTGCCCTGAGATTGTGTTTAAAGAAATGCAATATTTTTACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35447
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105496 | Essential Splice Site | 1255 | 1926 | 18 | 32 |
ENSDART00000124710 | Essential Splice Site | 1287 | 1958 | 19 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16497559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16317594 |
GRCz11 | 13 | 16448586 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCGGGCCTCACACGGCACCAACTCCCTGCCGTCCAGTGCAAGACTCGG[T/G]CAGTTTTCTTTAATAATACATGTTGTTGTCTGTTTACTCCACGCACCAAA
Long Flanking Sequence:
TTTTTTAAATAAAACTGCTAAAAATTCCTTGCTCTGTTAAAAAGATCGCTGGGGAAATATTTGAAAAAATCAACAAAACAAAAAATCACAGAATTCGCTAATAATTTTATATTCAACAGAATATCATACTATAAAAAATTTTGCGCTAAAAGTTTCTGTGGGCTGCCTTTCCTGAGCAGTTCCACTTATTTGTTTTGATTTCTCCACTTGATTCTATTCCAAAGTTTAATGAGCATAAGTGTGGTTTATAAGTGTGTCATACTAAGTGCAAACTAGCAGTTACAGGTGATAAACAGGCTAGTTATTCATTTTCTCACCCCATGATCATGAGTGTTTACTGATTCAGTGTGCTCAGTTTCTTCTCTCCATCTTAGTCCTCAGCATCAAGGACAACTGAGTCTGGACCTAAGCCAGAAACGCTCCACGGACTATTCTGAGTCGTCCCGTAGCAGCCGGGCCTCACACGGCACCAACTCCCTGCCGTCCAGTGCAAGACTCGG[T/G]CAGTTTTCTTTAATAATACATGTTGTTGTCTGTTTACTCCACGCACCAAACTTTCATATAAGTGTATTTTTATTTTGGTCTATATCTTCTCCCTTTTGCTTTCTGAAGGTTCATCAAACAACTTGCAGTATCGCACTGAAAGGATTAAGATTCCCTCCACACCGCGATATCCTCGCTCTATTCTGGGGTCAGACAGAGGTGAGTCTACTTTCATAAATAAAGGATTTCCGAATTCATGTGATATAAAGTGGAGATCAGAATTTGGTGAATTTACACTTCTAATTTGATTTGTTCAAATATCAAACATTTTTAGTTTTAGCTCATCAAACTGTGTTCTACAACAATTCCAAAGCCCCTTTGACAAAAATAACTGTTTTGTGAAAAACATAATCAAAAATTAAATACAGCAATAAGTATATGCATGGGGACTTTTAATTTTGAATAAGCCAGCTCAGGTGCTTCTGGTGAACAGTTACGCATTATAAACTCATCACATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13331
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 |
---|---|---|---|---|---|
ENSDART00000105496 | Nonsense | 1410 | 1926 | 22 | 32 |
ENSDART00000124710 | Nonsense | 1442 | 1958 | 23 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16512030)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16332065 |
GRCz11 | 13 | 16463057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACATCAGTATAATGGAATAAACCTGCGYAATGCCACTGAACAGCAAGCA[C/T]GACTCATCATTGGCCAGCAGTGTGACACCATCACGATCATGGCCCAATAC
Long Flanking Sequence:
ATAATTACAATATCTTCAAAAAAGTTTATGTATTTCACTAATTCCATTCAAAAAGTGAAACTTGTATAATGTACATTCATTCCACACAGACTGATGTATTACAGGTGTTTATTTCTTTTAATTTTGATGACATCTAATGAAAACCCCAAAATGAATATTACTTAAAACCAATACAAAGAAGGGATTTTTAGACATTTTGGCCAACTGAAAAGTTAGAGTATGAGTAAAATATGTTTGTTTTTGCCTTTTTATATTTTCAATTATAATGAATAATGAATTTTAGATATGAGATATTTTAAATTGTGCTACTTTATTTAATAAAGCTAAGAAGTTTTTTAATTATATTACAACTAAATAATGGAAAACATGCACATATTTTTTTGATCATAGTAAAGCTGTATGCCATGTTATTGACAGTTTGCAATGTGTAACTTAAAGTTGTTCTTTCTTTACATCAGTATAATGGAATAAACCTGCGCAATGCCACTGAACAGCAAGCA[C/T]GACTCATCATTGGCCAGCAGTGTGACACCATCACGATCATGGCCCAATACAACCCACACATGTATCAGCTCGGCAACCACTCGCGCTCCAGGTACAATCCTTTCCCCATTTTATTCATTAAGCTAAATGCAGATTTGATGTATAGCTTTTAGTTTTTTTTCATGGCTGGCTTGTTTCATAGTTCCCGCCTGGAGCCAGTGAGCACTCAATCCACGCCACAGGGCAGTGGAACTGCAACCCCAGATAACCACTCTACCATAGACACCCTGAGTGAACAGGATGAAGGCACACTCACCCCATCCTCCAAACAGACCACACCCACAACCAGTCCCAACAGCTTCATCAGGTACTGCTCATACACTTAGAGAGCTGCCTTGTTGTGTACAGTCTTAGTAGGGGTGGGAACAGTGTTGGGTGTAATTGGTTACAAATGAACTACAAACTGTAATAAAATTATTAATTATTTTAATAAAATACATTTTATGCATTATTATTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22258
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 |
---|---|---|---|---|---|
ENSDART00000105496 | Essential Splice Site | 1606 | 1926 | 25 | 32 |
ENSDART00000124710 | Essential Splice Site | 1638 | 1958 | 26 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16522524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16342559 |
GRCz11 | 13 | 16473551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGTTCAACCAGGTGAAAGGCACTCCTGGAGATGGATTCTATATCAGG[T/C]ACAGTATGATATCGCATCTGCCATTGACTTACATAAGCACACATGGCCGC
Long Flanking Sequence:
GACCTATAGGTTAGTGTATGCTCTGTCAGCCACATTGAGTGTTGTGTTTAATCAATAATTGATAAACTATTACGACTCAGATAATATTTTATCTAAAACAATATTTTCTGTCTAATTTGTGTCTAAGCCCTTCGGTCTTATATGACAGCCCTCCGAATTGCTTTAGGATTTACTCTGTGAAAACAACCTCCTGGATGTACTTAAAAAGCATGACTTTGGATTCTAGCAATGCATTGGTAACTGTTGAAATTAACAGTAAAATGAACCAATGAAACATTATAGTAAAGTGTGACCTATGTGTTTAAATTAAATGTAATAACCTCCTATTATATTATTATTTGTCCTTTCAGTATGGCTCAGTTAATATGAAGAATAAGACTGTGGAGGAGGCATATCTGGAAATGCTGAAGCCTGCAGAAACAGTGACGTTAAGAGTCCAGCATCGTCTGGATGAGTTCAACCAGGTGAAAGGCACTCCTGGAGATGGATTCTATATCAGG[T/C]ACAGTATGATATCGCATCTGCCATTGACTTACATAAGCACACATGGCCGCTTAAAAGTTCCATATAACCAAATACCAGAGTTTGGACCCTGCACTCACTGCTAAATATGGATACACGAGAAAATCGCATCAACGGGAATCTTTTAATCTTTTTAATTATGTTTAAGATGGAGGGTGAGATATTGTATCTGGCAGTGCAGATTGTATCACCAAATCTCCATAATTTGTGTTCTATAATAGTAGCTGTGGTAATTAGACGGTTCGAGACAGAGATGCATTGTGTCTGTGCGGTGGAAAAAAGAATAATGGAAGAGGGCTGTTCAGAAATAGCCATGTTTGTCTTCACAAATGAAATTCTGTGGCCCGCAGCTGTTGCAGGCGCTTTTTTCTGCCCGCTCTCCCATGATGTCACCCGCAGTAAATAATCTCTGTCAATCCGTGTGTCATGAATGAGCAGGAACGAGGAGTTATGGGTGGCTGCTAAAAGCCGCCTCGTGCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13023
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 |
---|---|---|---|---|---|
ENSDART00000105496 | Essential Splice Site | 1856 | 1926 | 30 | 32 |
ENSDART00000124710 | Essential Splice Site | 1888 | 1958 | 31 | 33 |
ENSDART00000105496 | Essential Splice Site | 1856 | 1926 | 30 | 32 |
ENSDART00000124710 | Essential Splice Site | 1888 | 1958 | 31 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16532164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16352199 |
GRCz11 | 13 | 16483191 |
KASP Assay ID:
2260-6217.2 (used for ordering genotyping assays)
KASP Sequence:
ATTTACCCAATCGTCATTTTCATACGCTACAAAAAYGCAAAGCAGATAAA[G/A]TAAGTTTTCACATCCTCCTYMACACATACMTATCAAAATAATCATAAACT
Long Flanking Sequence:
TCCTCTCGAAATTGGTTTATGAATAAACTTCACTTATGTCACCTAAAACAATTATTTGAGCCCTGATGTCAATTCCAGTAGTCATAGCAAAACATATGAATAAAGTGTAATTTTTCATTAGTTTTTTTTCTTATTCTCTAAAGCTAAAAACAATGGAAAAAATACTAAATTCTCAAAATATTTTTTTCTGCCTGAATTGACTAAATTAAGCTATTTTATCATTTTGTGTGAACTATCCCTTTAATAGTCAGATAAATCTCTTTTAAATAGAATAATATCAAGAGGCATTGTTAATGTTTGTTGATTTCGCTTTGCTGTTGTTTCTCTGTTGGCGTGTGCTGTATATGTGTAACATGACTCTGTTCTGTGCCATGTTGTTCTCTCTCATAGGACTGTCACTGTTTGCTTGACATTGCACCTCATGCTATTGAAAGGCTTCACAGCGTTCACATTTACCCAATCGTCATTTTCATACGCTACAAAAACGCAAAGCAGATAAA[G/A]TAAGTTTTCACATCCTCCTCAACACATACATATCAAAATAATCATAAACTGAATTCTTGGATGTCCTTGTGGACCCTTCCAAACACACATACACGCGCACACACTCTGTTCAAGGCCTTCTTGGCACATTTTTATGCCAAGAAGTTCCTGTGCGCTCCCCCAGGGCCCTGAAGACATTTGGGAAATGGAAAGCAGTTTTACTGTGTAGGCTGCGTTTGACTTGGAAGAACTGCTGTTAAACGGATGAATATCTTGTCTCCCTTTATATAGATATAGGACAAGATATATGGCAGCGTAGGCAGCCGCTTCACTCTTTCTGTCTGTGCCTCCTTCTTTGGTTGTCTGCTGAAGGTCACTTTGTGAGATTCCAGACCTGGTTTATCAGACAGGCTCAGTTAAAGGGGATATGTCACAAGAATTTGATTTTTCCATGTTTGATTGCTATAATAGGTTCCCTGATGCATCTACCAACCCAGAGACTGGCTGCAGCAGATAGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15456
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 |
---|---|---|---|---|---|
ENSDART00000105496 | Essential Splice Site | 1856 | 1926 | 30 | 32 |
ENSDART00000124710 | Essential Splice Site | 1888 | 1958 | 31 | 33 |
ENSDART00000105496 | Essential Splice Site | 1856 | 1926 | 30 | 32 |
ENSDART00000124710 | Essential Splice Site | 1888 | 1958 | 31 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16532164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16352199 |
GRCz11 | 13 | 16483191 |
KASP Assay ID:
2260-6217.2 (used for ordering genotyping assays)
KASP Sequence:
ATTTACCCAATCGTCATTTTCATACGCTACAAAAAYGCAAAGCAGATAAA[G/A]TAAGTTTTCACATCCTCCTYMACACATACATATCAAAATAATCATAAACT
Long Flanking Sequence:
TCCTCTCGAAATTGGTTTATGAATAAACTTCACTTATGTCACCTAAAACAATTATTTGAGCCCTGATGTCAATTCCAGTAGTCATAGCAAAACATATGAATAAAGTGTAATTTTTCATTAGTTTTTTTTCTTATTCTCTAAAGCTAAAAACAATGGAAAAAATACTAAATTCTCAAAATATTTTTTTCTGCCTGAATTGACTAAATTAAGCTATTTTATCATTTTGTGTGAACTATCCCTTTAATAGTCAGATAAATCTCTTTTAAATAGAATAATATCAAGAGGCATTGTTAATGTTTGTTGATTTCGCTTTGCTGTTGTTTCTCTGTTGGCGTGTGCTGTATATGTGTAACATGACTCTGTTCTGTGCCATGTTGTTCTCTCTCATAGGACTGTCACTGTTTGCTTGACATTGCACCTCATGCTATTGAAAGGCTTCACAGCGTTCACATTTACCCAATCGTCATTTTCATACGCTACAAAAACGCAAAGCAGATAAA[G/A]TAAGTTTTCACATCCTCCTCAACACATACATATCAAAATAATCATAAACTGAATTCTTGGATGTCCTTGTGGACCCTTCCAAACACACATACACGCGCACACACTCTGTTCAAGGCCTTCTTGGCACATTTTTATGCCAAGAAGTTCCTGTGCGCTCCCCCAGGGCCCTGAAGACATTTGGGAAATGGAAAGCAGTTTTACTGTGTAGGCTGCGTTTGACTTGGAAGAACTGCTGTTAAACGGATGAATATCTTGTCTCCCTTTATATAGATATAGGACAAGATATATGGCAGCGTAGGCAGCCGCTTCACTCTTTCTGTCTGTGCCTCCTTCTTTGGTTGTCTGCTGAAGGTCACTTTGTGAGATTCCAGACCTGGTTTATCAGACAGGCTCAGTTAAAGGGGATATGTCACAAGAATTTGATTTTTCCATGTTTGATTGCTATAATAGGTTCCCTGATGCATCTACCAACCCAGAGACTGGCTGCAGCAGATAGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12813
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 |
---|---|---|---|---|---|
ENSDART00000105496 | Essential Splice Site | 1856 | 1926 | 30 | 32 |
ENSDART00000124710 | Essential Splice Site | 1888 | 1958 | 31 | 33 |
ENSDART00000105496 | Essential Splice Site | 1856 | 1926 | 30 | 32 |
ENSDART00000124710 | Essential Splice Site | 1888 | 1958 | 31 | 33 |
Genomic Location (Zv9):
Chromosome 13 (position 16532164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 16352199 |
GRCz11 | 13 | 16483191 |
KASP Assay ID:
2260-6217.2 (used for ordering genotyping assays)
KASP Sequence:
ATTTACCCAATCGTCATTTTCATACGCTACAAAAAYGCAAAGCAGATAAA[G/A]TAAGTTTTCACATCCTCCTYMACACATACMTATCAAAATAATCATAAACT
Long Flanking Sequence:
TCCTCTCGAAATTGGTTTATGAATAAACTTCACTTATGTCACCTAAAACAATTATTTGAGCCCTGATGTCAATTCCAGTAGTCATAGCAAAACATATGAATAAAGTGTAATTTTTCATTAGTTTTTTTTCTTATTCTCTAAAGCTAAAAACAATGGAAAAAATACTAAATTCTCAAAATATTTTTTTCTGCCTGAATTGACTAAATTAAGCTATTTTATCATTTTGTGTGAACTATCCCTTTAATAGTCAGATAAATCTCTTTTAAATAGAATAATATCAAGAGGCATTGTTAATGTTTGTTGATTTCGCTTTGCTGTTGTTTCTCTGTTGGCGTGTGCTGTATATGTGTAACATGACTCTGTTCTGTGCCATGTTGTTCTCTCTCATAGGACTGTCACTGTTTGCTTGACATTGCACCTCATGCTATTGAAAGGCTTCACAGCGTTCACATTTACCCAATCGTCATTTTCATACGCTACAAAAACGCAAAGCAGATAAA[G/A]TAAGTTTTCACATCCTCCTCAACACATACATATCAAAATAATCATAAACTGAATTCTTGGATGTCCTTGTGGACCCTTCCAAACACACATACACGCGCACACACTCTGTTCAAGGCCTTCTTGGCACATTTTTATGCCAAGAAGTTCCTGTGCGCTCCCCCAGGGCCCTGAAGACATTTGGGAAATGGAAAGCAGTTTTACTGTGTAGGCTGCGTTTGACTTGGAAGAACTGCTGTTAAACGGATGAATATCTTGTCTCCCTTTATATAGATATAGGACAAGATATATGGCAGCGTAGGCAGCCGCTTCACTCTTTCTGTCTGTGCCTCCTTCTTTGGTTGTCTGCTGAAGGTCACTTTGTGAGATTCCAGACCTGGTTTATCAGACAGGCTCAGTTAAAGGGGATATGTCACAAGAATTTGATTTTTCCATGTTTGATTGCTATAATAGGTTCCCTGATGCATCTACCAACCCAGAGACTGGCTGCAGCAGATAGAGAT
Associated Phenotype:
Not determined