ZMP
dock8
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate dedicator of cytokinesis 8 (DOCK8) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
DOCK8
Human Description:
dedicator of cytokinesis 8 [Source:HGNC Symbol;Acc:19191]
Mouse Orthologue:
Dock8
Mouse Description:
dedicator of cytokinesis 8 Gene [Source:MGI Symbol;Acc:MGI:1921396]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13478 | Essential Splice Site | Available for shipment | Available now |
| sa12347 | Essential Splice Site | Available for shipment | Available now |
| sa12014 | Nonsense | Available for shipment | Available now |
| sa21325 | Nonsense | Available for shipment | Available now |
| sa34432 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30642 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8963 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13478
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099021 | Essential Splice Site | 54 | 2090 | 3 | 48 |
| ENSDART00000137583 | None | None | 189 | None | 5 |
| ENSDART00000144637 | None | 1 | 2034 | 1 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31243932)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30386658 |
| GRCz11 | 8 | 30395890 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCATACTTTTCACTACTTGCTTTTGATATTATGATGTGGTTTTCTTTCT[A/C]GYCTCAATCATATGAAGCGGTTGAGCCRGTGGACCTGGATGAGTTCCKGA
Long Flanking Sequence:
AGTATACCTGATTATGTGTGCCTGGGCTACCCTGTCGAATGGATTAATCCGAGCGTACTATTTTATGTGTGCCTGGGTTACACTATCAAATGGCATACCTTGTCGAATAGCTTAACCCTAGACTGAATTATTAAGTATTAAGTATTAACTGACTTAATACTAAAAATGCACTCTATGTCTCCATGTAACAAATTATAAAATGTTTCAGGCTGATTAGAAAAATAATCCAGCATATGCCTGAGCAAGTAAATAACATTCAACATATTTGGATGCATGTAAACTCATTGTTGAAGAAATTATAAAATTTTAAAGTAGCACAACTGGGGCACTTTAGGGAATTATATTGGTTAACTGAAATAATAAAATATGATAGTTAATGAATTGTAAAAAATATTTATTAAATTTATTTAGGCAAGAGAAAACTGGCAATACTAATGCTCTTGGACACTCATCATACTTTTCACTACTTGCTTTTGATATTATGATGTGGTTTTCTTTCT[A/C]GCCTCAATCATATGAAGCGGTTGAGCCAGTGGACCTGGATGAGTTCCTGATGTCTCAGCTGCGCAGTGGCGATGCCGAGGTCATGCAGGAGTTGGGTGAGTTTCCTGATGACGACCTGGATGTTGAGCTTGTGGAGAGGGAATGCAGGACCATCCGCCCCACTATTGCTGAGGAAGGGTAAGTGCTGTATCATTCCAGCTGGGGTTGAGGACATCAACCCTTCTGAAAAAAATATGAATAGATGCTTTTTTGGTATTAAATAATAATGCAGGTACTAGTAACGAAGACATAAATCATATGATTGCTCAGATTGTTTTAAAATGAAAATGTATATTAATTTAAAGTTGCAAAAATAAACGTTTTCACCACAAAATGTCATCTTTCTGACAGTTTTTAATTCCAAAAAGGCTTTTTATGGCACAAACTGTTAGTAAATCTGGGCCTATTTATATACTGTTACAATCAATGGTAATAAAAACTTTTTTAGAAAATAATGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12347
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099021 | Essential Splice Site | 294 | 2090 | 8 | 48 |
| ENSDART00000137583 | None | None | 189 | None | 5 |
| ENSDART00000144637 | Essential Splice Site | 241 | 2034 | 6 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31234673)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30377399 |
| GRCz11 | 8 | 30386631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTCTCTTTGCAACAATGGCCCTCTATGACCTGAAGGAGAAGAAGAAGG[T/G]CAGTTTCTGATGGTTACTTTAWAAGCTAAGAATAAAATTACAAATATGTG
Long Flanking Sequence:
GTTTAAACACAGTAACAATTTGTTAAATCATGTTTCTAGCTTGGTTCTACTTAGTCTGTTACTTGTAGCATTTTTTCAACATGCTAAAATTATAATTATGTCAAACATGCTAAAAATGAGTTAGCCTGTTACTTGTAGCATTGTATCCACATGTTAAAAAAATAATTTTTAATATTAGCAAAATGCTAAAAGTGTTAAATCAAGTTTCAATTGTTTCTAGCTTGATTCTAGTTAGCCTGTTACTTTTAGCATTGTTTCCATACACACGCTTATGTTAAATTTTTTCTTGTTTTTATTTCATTCTTTAGGTAGAAACACGTGCATCTTACAATTATGGTGTATAAATTGTGCTGATTGTCTTTTCTCTTCATGCATTAAGTGTTATTAAAAATGTATATTCCTTTGAGAGAATATTTCCAATGTCTTTAACAGATTTGAGATTGAAATCGAGCCTCTCTTTGCAACAATGGCCCTCTATGACCTGAAGGAGAAGAAGAAGG[T/G]CAGTTTCTGATGGTTACTTTAAAAGCTAAGAATAAAATTACAAATATGTGATTTCACTGTTGTAGTTTGATCTGTTTTCTTAAGCTGTGGAGACATAATTAATAATTATTCTGCCTGTCAGTGTTCTTCCTGTTTGTCCTCCCACATTCCTTGACTTCAGTCTCTACAATACTGGACTTTAAAGAGAAGCCTTTTCCATAAACAACCATAACAAGTAAATGTTAAAAGAAACAATAGTTATACAAGCATAAATAGGCCTCAAAATAAGTCTGAAGAGTATAAAACAAGGGAACACAAGACATTTAAATACACACAGCCTGTCTTTACCTCAGATTTAAGAAGGTCTTGCAGTGACAGTCATGGATGTTAAGCAATCAGTAATTATACTACGTTTAGATGCAGTGCTGTGTATTTCCATATTAAACAGACAGACTGCAGATATATTTGGGAGGAATATCCTGCATTACATTAATCCTCTTTAGTGTTAGCTTTGACTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12014
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 |
|---|---|---|---|---|---|
| ENSDART00000099021 | Nonsense | 872 | 2090 | 22 | 48 |
| ENSDART00000137583 | None | None | 189 | None | 5 |
| ENSDART00000144637 | Nonsense | 816 | 2034 | 20 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31219967)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30362693 |
| GRCz11 | 8 | 30371925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTGTTTATCTACCAGGTACAGGAGGTCTGATGGCTCATCCAGAGGGT[C/T]GATACAGCACTTTAACTCGCACAACGGCCACCACTGTTGGCTTCATGCTG
Long Flanking Sequence:
TGAAATTCTCAATGAGAGCAGAGCGGATATTTTGTGCAAAGACCAAATGGTTTAACAATAAAGCCATTTTTTACAGCCATTTTGCTCAGATTTACCAATGGAGGCGATATTACTGGAGGGCACTGTACATTCTCTTCTGAGTTTTCAGTCTTGGATCATACATGTTCAGTATTGTTAGTTTTAATCTTGTTTTTTGCAGCAAATCTGGCCCAAATTGCGTTTGAGTCAGTGGTGTCGGTCATCAACAGTCTTCACAACAGTCAGGAGCTGGCAAAAGACCATCAGGGCAGAAACTGTCTCCTCGCAACATACCTGTACTTTGTGTTTCGCTTGCCAGATACTCAATATGAAATCCACACCTCAGGTACAGCAGACCCGTGGACCACCAAATGATTTAATTCCTGTTCAGAATAAAAACAGTTTTTGACTCTGAATCTTTTTTTAACTGTTATTGTGTTTATCTACCAGGTACAGGAGGTCTGATGGCTCATCCAGAGGGT[C/T]GATACAGCACTTTAACTCGCACAACGGCCACCACTGTTGGCTTCATGCTGCTGCAGTCACGAATCCGTTCCAGCAGCAACCCTGATATACCAGCACCACTGAGCCCAGAGGACACAGAGGTCAATAACATTCTAGGAAAGGTACTGTACATATACACGCATGCAACATACTGGGCTTGGGTAAAATACATTGAAAACAGGATGTTGAATTCTATTATATTAAATTTATATTATATTATATAATTCATTTTTAATAAAAATACCCACTGCGCCATCATTATTACAATCATTATTATTATTATTATTATTTTTTGCAATGTAATGTAATGATTTTGCTTTAATTTTAGGTTGCTAATTAGAATTACAATAATACAAACTATACAATTGTATTTATTTTATTTATTTTCTATTAAGGGGTGCATTTCCCGAATAAGGACATAACTTGTGGCTGAGCTCTCATCTATCATAGTATTATGCATTGTTTGGAAAAAGAATGATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21325
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099021 | Nonsense | 1456 | 2090 | 35 | 48 |
| ENSDART00000137583 | None | None | 189 | None | 5 |
| ENSDART00000144637 | Nonsense | 1400 | 2034 | 33 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31204252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30346978 |
| GRCz11 | 8 | 30356210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGCAGTTCCTCTGGCCGACTGTAAGGATAATGTGGTTGGCGGAGTGT[T/A]GAAGGTTTTGCTGCACTCGCTCACCTGTAATCAGAGCACCACCTACTTGT
Long Flanking Sequence:
TTGTTTAGCTGTTTTCTAAATATGTCCTGTGTTGGCTGTGCAGTGCAAGGTAACGACCGGACACTGGGTCTGAGAGAGAACCTACGCTGGAGGAAAGACCTTACACAGTGGCGCCAGACAAACGACAGGCAGGACAAGTGAGCGTAAAATAGTACCATCATTTCACGCTTCATGTCCATTCAACCTGCGGCACTTCTCATTTTTATAGCCGCTGCTAGTTCTCAGCTGCAGCTCAAATTGGGCTTTGCTAACTGTCTTCTTGTTGCTGTTTCTTCAGATCCAAAGCAGAGCTGGATCAAGAGGCCATAATCAGTGGGAATCTGGCGACTGAGACCAACCTCATAGTGCTGGACCTGCTGGAGATGATCGTACAGGTGACCGTGAACTCGTACTGTGGACTTGAATAATGTTTTGGCAGTGCAGAATGAATAAATGTGTGGGGTTTATTTTTCAGGCAGTTCCTCTGGCCGACTGTAAGGATAATGTGGTTGGCGGAGTGT[T/A]GAAGGTTTTGCTGCACTCGCTCACCTGTAATCAGAGCACCACCTACTTGTCGCACTGTTTCAGCACTCTGAGGGCTCTCATTGTCAAGGTACCAGGGGCAGGAATTATTTTTTTTTGTTAAAAGCCTTATATTTACCTCCTTTATGATATGTTTTACCATAAATCCAGTGCCTTTTATGGTATTTTAGGTTTTACTTAAAGGGATAGTTCACCAGAAAATGAAAAAATTACTTTAATTTTTTTTTCCTCCTGCGTCTTTTTTATATTAATGTATTACTTTCTTCTGTAGAACACAAAAGAGTATGTTTTGAAGAATGCTGGTTGTTGGGACCCATTGACTTCCATATTATGGAGAAAAATACTATGGAAGTCAGTGGGGATTTTCCAGAGCAACTTATTTTTTGTGTTCAAGTGAAGTCAATGATAATAGAACTTACTTTTTTTGGGTGAACTATCTCTTTAAATTTAACCAAATACTTTAAACAATCAAAATAAATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34432
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 |
|---|---|---|---|---|---|
| ENSDART00000099021 | Nonsense | 1615 | 2090 | 38 | 48 |
| ENSDART00000137583 | None | None | 189 | None | 5 |
| ENSDART00000144637 | Nonsense | 1559 | 2034 | 36 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31191697)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30334423 |
| GRCz11 | 8 | 30343655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTATCCTCTCAGATACAGTCAAGATGAAGGAGTTCCAGAAAGATCCC[G/T]AGATGCTTATGGACCTCATGTATAGGTACACAGCTAAACCCAAGTCTGCA
Long Flanking Sequence:
CCTTAATGCAAGCCTAAACCTAACATAAAATGTAAAAATCTCATTGACTGATTGGAACAATGCTCAAGGGTCAACATAATTGTTAATTCATTAACAGATCCTACTTGGTGAAATCCCGCTAACCCCAGGATTTTGCCCTTAGGAGCAGGATTTTACACACCTGGCCTAAAGTTTTTAGATTAGGAGAGCCCAATACTGTTTCTGGAGATCTGCCTTCTTTCAAAAGTTCAGCTCCAAACCAAAGTAAACATACCTAAATCTTTTAAATAAGATCACAAGGAGCAGTTGATATTTACAGACAGAAATGTTGAATCAGGACTGGAATTGAAGGTGTGTAGATCCCCAGAAAGAGGATTGAACACTCCTGGTGTAGATCTTTAGTCATCCAACCAATCTATTGTAATGAAATACCTCTATCTTAACAGGTAGATGAACTCCTGAGGAACCTAAACAGTATCCTCTCAGATACAGTCAAGATGAAGGAGTTCCAGAAAGATCCC[G/T]AGATGCTTATGGACCTCATGTATAGGTACACAGCTAAACCCAAGTCTGCATCTGCCTTTGGGATCCCAGGCCTGTGGTTTTCTTCTCTGCTTTCCATTTGACTGTGGTTTCTACTGTTTGTCTACTGTTTTTGGACTCACCATGGAAACCGAGTGGCACATTTGAGCCCCGCAGTGTGCCTCACATGTGCAATAACTTGTGTGAATATGCCAGTCCACACTGTTCTTTTGATATTAGGAACAAAATGTTGTTTATTTGCTCAGAGCATTAACCTATGGTTTGCTTTGGCTCCAGGATCGCGAAGGGCTACCAGACTTCTCCAGACCTGCGTCTAACCTGGCTTCAAAACATGGCAGAGAAACACAACGGCAGGAAGTGCTTCACTGAGTCGGCCATGTGTCTGGTTCACGCCGCAGCCCTGGTGGCTGAATATCTCAGCATGCTGGAGGATCACAAATACTTGCCTGTGGGCAGCGTCACCTTTCAAGTGAGTTATTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30642
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 |
|---|---|---|---|---|---|
| ENSDART00000099021 | Nonsense | 1858 | 2090 | 44 | 48 |
| ENSDART00000137583 | None | None | 189 | None | 5 |
| ENSDART00000144637 | Nonsense | 1802 | 2034 | 42 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31187036)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30329762 |
| GRCz11 | 8 | 30338994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCTGTGACAAAATGTGTTGATTTTTGCATTTCACACCAGGCGTACATA[C/T]AGATCACCTTTGTGGAGCCTTACTTTGACGACTATGAGATGAAAGACCGC
Long Flanking Sequence:
GATATCCCACCGGCTCGAGGTGAAATTTCTCTGGAAACCTGTGAAGTTCTGAAATCCGTTTGCGATTAAAGATAAATTGTGAAGTTTGAAGTATTTCTTAACTTTTCAGTCAGATGTTTTGATCGTTTTAGAAGTCTAATGTGGTCTGACATTTTCACTCACGTTTTGTTTGACCAAGACTTCTCTTTGTCTTCTACTTTTGCAGAACTTCTACAGTCAGTGCTTTGGTGATGGCGTTTTGGAAATGATTAAAGATTCCACACCAGTAGACCGAAACAAGCTGAGTCCCAACAAGGTACTTCTCATCAAATGTCCTGCCAATGTAAACACGATTACAAACGAAAGCTTTCTTCAGTGTGACCCTCATTAGCCTTGAAAGTCTGTCAGCAGTCAAATCTCCGTTGCCTCATTTAACTAATGTTACCTTTAGCGATTTATGTTTCCTTTAAGTGCCTGTGACAAAATGTGTTGATTTTTGCATTTCACACCAGGCGTACATA[C/T]AGATCACCTTTGTGGAGCCTTACTTTGACGACTATGAGATGAAAGACCGCCTCACCAACTTTGAGAAGAACTTCAACCTTCGCCGCTTCATGTACACCACGCCGTTCACAAAGAGTGGGCGGCCCAGAGGAGAACTCAACGAGCAATACAAGCGGAAAACCATCCTTACCACTATGCATGCCTTCCCCTACATCAAAACACGAATTAACGTCATTCAAAAGGAGGAGGTAATGAGCATCTGGATACAATACTCCATTCTTTGCTTCATCTGCAGGGCTAGTTTGAGAACTGTGTCTAACCTGTATAGAAATCTGACATATGGCAATATATGCTAATTACCTATGATATACAAATTCATGTTTTCATTTCACATAGATTAAATATGTCATATATGCAACATGTATTTCAAAACATTGCAAAAGTGGCAGTCTGCATACAATCTGTTCACATAGTTTCATCTGTTGGAATTACAAATATGTTCATACATGTTCAAATTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8963
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 |
|---|---|---|---|---|---|
| ENSDART00000099021 | Essential Splice Site | 1934 | 2090 | 45 | 48 |
| ENSDART00000137583 | Essential Splice Site | 37 | 189 | 2 | 5 |
| ENSDART00000144637 | Essential Splice Site | 1878 | 2034 | 43 | 46 |
Genomic Location (Zv9):
Chromosome 8 (position 31183969)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 30326695 |
| GRCz11 | 8 | 30335927 |
KASP Assay ID:
2260-0768.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTAGGATGATGWATACAAAAANTGAATTTTCTCTCTTGACATGTTTTCA[G/A]TTTGACCTCACACCAATCGAGGTGGCCATTGAGGACATGCAGAAGAAGAC
Long Flanking Sequence:
TATCTTTTTTGTGTGTCCAAAGAATGAAGAAATTATGATAACCAGATTTTTGGCTGTATTGTCTCTTTAACATTTGCTTTTTCTTTTCCTTTTAATAACAATGAGAGTACACAAAGTACTCCTGTCAGGGTTCTGCCACTCTGGTCTTGTAAATTCTTGTTGTGGTGGCAGAGTCCGGACACTGGCCCTGTCTTGTCCTGTTTCTGTCATTGTGTGTGTCTCTGGGTGCCTCGGATGCGTGCGTTCTTGTACTCGTATTTGTGTTTTGTTCTGTCAGCATTGCGCTGCTTCATTCTCAGCGTCTCCGTCTAGTTGGTTTCTGTTTTGGTTGGCACTGAGATGAGACACCCCGACCGTGACAACTCCATTTTGGTGGCATTTGTTTATTTCTTTGCCCGCAATATGGATTTGAACAGAAAATGGTTCATGGTTTCTGTGGATGATTATTTTTTTTAGGATGATGTATACAAAAATGAATTTTCTCTCTTGACATGTTTTCA[G/A]TTTGACCTCACACCAATCGAGGTGGCCATTGAGGACATGCAGAAGAAGACCCGAGAGCTGGCTGAAGCCACACACAGGGAGAAACCGGATGCTGTGATGCTTCAGATGGTTCTGCAGGGATCTGTCACAGCCACTGTCAATCAGGTCTGAAACCATTATATACACGACTGCTCTGACTTTTTTTTTGTTTGTTTGTTTTTATACACATGATGCAGTGTGGTTGATTGGATCACACGTAGATGAAGGACAACCATTTACATTTACACCTAGTGTTCTAAGTGCCCTAGTGTAGCAAACCATCTACTGTATAAATAATTCATTAATATAGAAATCCAAAGTTCAACAATAGATTTGTCAAATGAAAAATAAATATGCACAAGGATACATTAAAATAATTAAATCCATCTCTTCTGACTAATTTTGACCACTTTCCTGATTTGGGCTAGTCTACATATGGGCTTTTTCTGATGTTTTTATTCAGTGCAATTTTCATTGTGAAA
Associated Phenotype:
Not determined