ZMP
si:dkeyp-73b1.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A9C3V7]
Human Orthologue:
C2orf67
Human Description:
chromosome 2 open reading frame 67 [Source:HGNC Symbol;Acc:26310]
Mouse Orthologue:
1110028C15Rik
Mouse Description:
RIKEN cDNA 1110028C15 gene Gene [Source:MGI Symbol;Acc:MGI:1915941]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34713 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa27451 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45368 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44708 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41492 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7204 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa13455 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34713
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 |
|---|---|---|---|---|---|
| ENSDART00000108893 | Nonsense | 40 | 821 | 1 | 15 |
| ENSDART00000147652 | None | None | 615 | None | 15 |
| ENSDART00000148262 | None | None | 206 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39789711)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38927607 |
| GRCz11 | 9 | 38737402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCTTTGTTTCAGGACTCGCATCCCAAAGGTTTTCTGCTGTCAAGCCCA[G/T]AACCACTGCTCAGCCTCCTCTCTTTAAACAAGAACTCACCGGGTTCTCCA
Long Flanking Sequence:
TTGCAGGAATATGGGACTGTTAAAAGGTGAGCTTTCCGTTATTCCAATCTTTCCGTTATTTTCATACTGCGCTAATCGCGAAAAGTGAAGCGTTAGTTTAACCGTTTAAATATTTGCCGTTATTCTCTATTTTGTTGTAAAGGCTACCATAATTATCTGTTGTAACAGACGATGTCTTTTAGCCGACCAGAATGATCAATTAAACAGTTTCGGATGATGTTATAAGATTCATCAACAGTCCCAGGACAGGAAAAGGGGAATTACTCCTGCTCTCATTCAGTCATCAGATCAAAACCTTCATTGATTTCATCCACTGCTTTGAGTCACTTAAAAGTAGTGAGAGTACGGGCAGTGTGGATGTGGAGAATAGCTTTGCGCAGAAGATGTGGCAGCACTCTCCTTCATTGGTTCACCTGGACCTCCTGGCATCTAAAGGTTCTCCTCAGCTCTCGCCTTTGTTTCAGGACTCGCATCCCAAAGGTTTTCTGCTGTCAAGCCCA[G/T]AACCACTGCTCAGCCTCCTCTCTTTAAACAAGAACTCACCGGGTTCTCCAGCAGGTGCTCCACAGATGTGTTTCATGCCCATTCTTCAAGACAATGGACAAGATTATGTAGAACCTACTAGCACTCAAAGGCATGGTTGTTCATCAAAACATTGGCCAGTTAGCACTAAACCACTTTCCTCAGAGCAATCACAATGTAGGAAGAACAATGCTTTAAACCATACACGGGTTGGTGCTATGGGGGAAATGGAGGAAGGGTTGATGATTCAGTCATTGTGGCATCTCTCCCAGCATGTTTCATTGGCGAATCGAGCCGGTCGTTTACAACAGAGGGTGTTGGCAGTGCTTGGTGAACATGCTTCTAGGCACTACAGCCAACAACTGGATGGTTTGAAGAAGAAACTTCTTGAAGCACGCTGCTCCCCCAAATTCTCAATGACATCAGACCCTCTTTTTGAGACTGCAAAGATAGATCAGGCTCTCAGAAGAAACTTCCAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27451
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 |
|---|---|---|---|---|---|
| ENSDART00000108893 | Nonsense | 231 | 821 | 1 | 15 |
| ENSDART00000147652 | Nonsense | 18 | 615 | 1 | 15 |
| ENSDART00000148262 | Nonsense | 122 | 206 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39790284)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38928180 |
| GRCz11 | 9 | 38737975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAACTTAGAGATGTGCAGAATGTAGCTCACAGTGGTCATGCTGTTCTG[C/T]AAGGACTGCTGGAGTCTCTGGACTCAGATGCCACAGCTAGCAGCTCAGAT
Long Flanking Sequence:
TCATGCCCATTCTTCAAGACAATGGACAAGATTATGTAGAACCTACTAGCACTCAAAGGCATGGTTGTTCATCAAAACATTGGCCAGTTAGCACTAAACCACTTTCCTCAGAGCAATCACAATGTAGGAAGAACAATGCTTTAAACCATACACGGGTTGGTGCTATGGGGGAAATGGAGGAAGGGTTGATGATTCAGTCATTGTGGCATCTCTCCCAGCATGTTTCATTGGCGAATCGAGCCGGTCGTTTACAACAGAGGGTGTTGGCAGTGCTTGGTGAACATGCTTCTAGGCACTACAGCCAACAACTGGATGGTTTGAAGAAGAAACTTCTTGAAGCACGCTGCTCCCCCAAATTCTCAATGACATCAGACCCTCTTTTTGAGACTGCAAAGATAGATCAGGCTCTCAGAAGAAACTTCCAGTTCACTCAAACACATAAGCAACCTCTGAAACTTAGAGATGTGCAGAATGTAGCTCACAGTGGTCATGCTGTTCTG[C/T]AAGGACTGCTGGAGTCTCTGGACTCAGATGCCACAGCTAGCAGCTCAGATGAGGAGGGGGACCATGAAGACACAAACGCGACCTCAGACCTCCCAAAGTGAGTACCATGCGATGTTAAATAGGCTTTCTAACGAAAAGTGATGCTCTTGCTAATTTATGTTTGACACGTGGAAGAAATTACAACTAAATCAGAGACCTTTTATTCTTCACACAACAGTTAATGAATGTTTAGCATTATAAATGATTACAAAACACCATAAAAGTGGATAGTATAAATTATTTGGTATTTTACCATTTTATTTTTTTAAAATTAAAAGTTATTATTTTGCTGACTGTTTACTCTTAAACTTTCTTTAAAAATTCAGCCTTCCTATCACAAAATTACTTTTTAAAAATATTGGGGATGCTCCAATCGATTGGCTGAAGATTGGTATTGGCTGATAATCACATTTTATGACTCTATTTTATGTCTATACTCGCTAATCTGGCCAATCTCATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45368
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 |
|---|---|---|---|---|---|
| ENSDART00000108893 | Nonsense | 271 | 821 | 2 | 15 |
| ENSDART00000147652 | Nonsense | 58 | 615 | 2 | 15 |
| ENSDART00000148262 | Nonsense | 162 | 206 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39796170)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38934066 |
| GRCz11 | 9 | 38743861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTTTCTTTCTTTCTGGGAGGGTAGTTGTGATGTTTGTGAGGTGAGAT[G/A]GCTGAAGGACAGAGCTGAACTCTGCAGTCGCTGGACATGGATGCAGATGA
Long Flanking Sequence:
TTCATTTGATAAAGTTGACTGTTGGGTTTTACAGTTTGTGTATTCTTGGTTGTTGGTGGTTTTCCCTGTTGGGAAGAGCTCAAATTTGTTCATTTTCCTTTAAGTTCCCAGATCTCACTCAAAAAGTGGACCTTTAAGATATTGGACCAATATTTCCAAGGAATATCCAGCACTTTGATTTAAGACACTGGTGGTGGTATGAGGAGACGCCCCTCATGATTGTGAAGCACTTTGGGTGTATGGCCATGTACAATAAATGCGCTATATAAATACACATTACATTACATTACCTAAAGGGCGTCCAACTAAGGACTATCCTGTTGTACAGTACCTAATAAAGTGGCCAGTTAGTGTTTACAAGAAAATCTTGAATATAGAAAAAGACTCCTTGCTTTTTCGGACTGTCTTTGTGTGTAGTGAACTGCAAGTGGATAAAAATCTCAGATGATGACCTTTTCTTTCTTTCTGGGAGGGTAGTTGTGATGTTTGTGAGGTGAGAT[G/A]GCTGAAGGACAGAGCTGAACTCTGCAGTCGCTGGACATGGATGCAGATGAGACAGTCTGAGTTGGACTCTCAGATTCAGAGGATTGAAAAACTCCATCTACAGATCCTCGCTAAAAAGGTAAAGCAACAGTACATATTGAACTAGTACATTCAGTACATATTATACAGTACATATCAGTACAAAATAAAAGTTATGATCGTACTGTTGGCTAAAATCAATATTTAAGAATTGTTGGTGAACTGGAATGACTAAAAAGGCATTTACTGAATTCCTTTGTCTTATTAGATGGGATAGCCCCTTGAGATGAGCCATCTCATTTTCTATAGGGGCCATAAAAATTACATAAATCCAAATCAAGTACAATACACCAAAACAAATAGACAATTAAAAAAAAAAGTTATATATATGTGTATATTTGACTTTTGACAAATGTATATTCCTATAGGCAATAATTCAAACTAAATTCTTTCACAACACTATCATCGTTTTAATTTTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44708
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 |
|---|---|---|---|---|---|
| ENSDART00000108893 | Nonsense | 414 | 821 | 5 | 15 |
| ENSDART00000147652 | Nonsense | 201 | 615 | 5 | 15 |
| ENSDART00000148262 | None | None | 206 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39800480)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38938376 |
| GRCz11 | 9 | 38748171 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTCAAGCGACATTCACTTGTGTCTCTTGTTCCCAGTGGATCACAGTG[T/A]TTACCTAAAGCCAAGAAGAGGAAGCGAATATGTCAAAGACGACTTTATGT
Long Flanking Sequence:
CAAGCTTGTGCTTTGAAACCTCAAACACAATTAAAAATTCATCTGGTTCAACTGTTTGCTCTGTCATTTCAGAAATGTTTTTGTTATATTTTTTGAAGAATTGGTTACATATGTAATGTTTAAGAATTTCATTCATAGAAAATCTGTCATTTTTGTGCTCCAGAGGCACATGCAGGGAAGCGGTTTGTCTTGATTTCATTCTTGCTTTTTGTATTCATTGGAGCACTGCAGACACATCCTCATTCTGATACATATTAGTGTAAATTTATGTAAATCTCATGTGAATGTCAGGATGAATCATTCGCCTTGTGGAAATCTGAATGAGTTTGAAAGACCTTGAATTAGCAAGATGAAAGAATTTGAGAGGTGAAAAGAACTGATGAAATTTACCTGCTATTTTTGTCATATGTCATATCAGATTTATAAAGATTGAACTCCTACTCTACTTTTGCAGTCAAGCGACATTCACTTGTGTCTCTTGTTCCCAGTGGATCACAGTG[T/A]TTACCTAAAGCCAAGAAGAGGAAGCGAATATGTCAAAGACGACTTTATGTCCCTCAGGTGGATGCCACCTTTATGTCAGCCCGGACTCGACCCCTTCTGAACCATCACAAGCGTAGACTTTTCCTCATGGACCCATTGTCTCATAGAGAACAGGTTGGTATTTTATTTATAGCCACATTGGTCTGAAAGTATCTTTTTAGATAACCGGTCAATAAATGGTGTTTGTCAGATTTTAAAATGTTTTTGTTTAAAGAAGACTCACTAAGAGTGCATTTATTTGATCAAGAAACACCAAGCAGTAATGTTCATGCTAATGCCTTTTCAAGAGTTCCCACTTAGATATGCTTGGCACTTATAGCAGGTTTGGCATGCTGTCCCGGGAGAGAACCCTGAGCTCGGAGATATTTGAGCCCAGGGCTCCCGCCCGGTCTAGAAGCATATCAGGAGAACCGAGATCAGGTAGGTCTCGATCGCTCCCCCTTTAGAAGGGGAGAAAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41492
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108893 | Nonsense | 453 | 821 | 5 | 15 |
| ENSDART00000147652 | Nonsense | 240 | 615 | 5 | 15 |
| ENSDART00000148262 | None | None | 206 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39800595)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38938491 |
| GRCz11 | 9 | 38748286 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCTTTATGTCAGCCCGGACTCGACCCCTTCTGAACCATCACAAGCGT[A/T]GACTTTTCCTCATGGACCCATTGTCTCATAGAGAACAGGTTGGTATTTTA
Long Flanking Sequence:
ATGTTTAAGAATTTCATTCATAGAAAATCTGTCATTTTTGTGCTCCAGAGGCACATGCAGGGAAGCGGTTTGTCTTGATTTCATTCTTGCTTTTTGTATTCATTGGAGCACTGCAGACACATCCTCATTCTGATACATATTAGTGTAAATTTATGTAAATCTCATGTGAATGTCAGGATGAATCATTCGCCTTGTGGAAATCTGAATGAGTTTGAAAGACCTTGAATTAGCAAGATGAAAGAATTTGAGAGGTGAAAAGAACTGATGAAATTTACCTGCTATTTTTGTCATATGTCATATCAGATTTATAAAGATTGAACTCCTACTCTACTTTTGCAGTCAAGCGACATTCACTTGTGTCTCTTGTTCCCAGTGGATCACAGTGTTTACCTAAAGCCAAGAAGAGGAAGCGAATATGTCAAAGACGACTTTATGTCCCTCAGGTGGATGCCACCTTTATGTCAGCCCGGACTCGACCCCTTCTGAACCATCACAAGCGT[A/T]GACTTTTCCTCATGGACCCATTGTCTCATAGAGAACAGGTTGGTATTTTATTTATAGCCACATTGGTCTGAAAGTATCTTTTTAGATAACCGGTCAATAAATGGTGTTTGTCAGATTTTAAAATGTTTTTGTTTAAAGAAGACTCACTAAGAGTGCATTTATTTGATCAAGAAACACCAAGCAGTAATGTTCATGCTAATGCCTTTTCAAGAGTTCCCACTTAGATATGCTTGGCACTTATAGCAGGTTTGGCATGCTGTCCCGGGAGAGAACCCTGAGCTCGGAGATATTTGAGCCCAGGGCTCCCGCCCGGTCTAGAAGCATATCAGGAGAACCGAGATCAGGTAGGTCTCGATCGCTCCCCCTTTAGAAGGGGAGAAAAAGGAGGAGATGGGGTGGAAGGGGGGATTCTTCCAAAATGAAGATAGTGCAATGAGGAGAAAGTGATCCATTTATACTAAGCTAGGATCATTCTGATTGGATTATTACTGATTACGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7204
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108893 | Essential Splice Site | 557 | 821 | 7 | 15 |
| ENSDART00000147652 | Essential Splice Site | 344 | 615 | 7 | 15 |
| ENSDART00000148262 | None | None | 206 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39805970)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38943866 |
| GRCz11 | 9 | 38753661 |
KASP Assay ID:
554-4485.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCATCACTGTCTMAGGTCTAGAGGCAGAGYCTCCCGATCATTATTCCG[T/C]AAGAGAAATCTTTTCATTTTTATGTGAATGCATTTACAGTAGGTACACCC
Long Flanking Sequence:
ATTCACTCATCTTTTAATACGTTTTGGTGTGATTTATTACCTGCTATTAAAAAACTAAAATGTTTTGAATGAGAAGCTGTAATGTATCCTTGGCAGGATGAATTTTGTCATGGCGCCATGGAAGAATGAATGTAGCGGAAACCATGTAATTAACTTCAGCCTTGAATCTCTCATCAGTACAATCAAATTTGGAAAAGTTAAGGTTAATAGTTACTATAACTTTATTAGTTACTAATAACTTTAATTAACTAGTAACTAATAGCTTTTAACAATCAAAGTTATTGTATATAAACATAGTTAACCTGCAGTTATATGGTATATTGGTGATTTATTTGTGTATTTTGTGTGATCTATCCTTTAGAAACGACTTCGTCCTTCCATCTTCAGAATGCGCTGTTTGAAGAAAGTGTGCTTCAGCAATCTCTCCTCTTGAAGACTGAGCTCTCCAGTCCTCATCACTGTCTCAGGTCTAGAGGCAGAGTCTCCCGATCATTATTCCG[T/C]AAGAGAAATCTTTTCATTTTTATGTGAATGCATTTACAGTAGGTACACCCAGCCTTATATCACGAGAAAACGTAACTATTTTAGGTTTTATTTATTTTAGGTTTTTGTCAGTTTAATACGTATGAATTTGTACAAATTCAGTCGCACATAAATGTACAATTTTGAAAAGGAGATGTGGCATCCAACCCCACCCTTAAACCCAACCATCATTGGTGAATAAGCAAATCTTACTAAATTGTACAAATGAGATTGTACAAATTCATTCGCATTAGCCACTAAATCAAAAAGCTATGAATTGTGATGAGATAACGTTGTTACACCTGTTTGGTATGTATATGCTTTAAATGTGTTACTTCTTTGTTTGTTTGTTTTGTTTGCTTTTCTGATAGGTTTGCTTTTATTTGTTGTTTAATGTTATATAGATGGAGTGCATTATGGTTTTTGATACCAGATCCCCCACTTATGATCACTACACATGCAGTGGAATGCAGTTTATAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13455
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 |
|---|---|---|---|---|---|
| ENSDART00000108893 | Nonsense | 616 | 821 | 9 | 15 |
| ENSDART00000147652 | Nonsense | 403 | 615 | 9 | 15 |
| ENSDART00000148262 | None | None | 206 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 39815065)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38952961 |
| GRCz11 | 9 | 38762756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTGCTTTGTTGCAGGCATRCAGGTCTCCAGGGTTACACCGCAGCCYTA[T/A]CTGRTGTCCAAGAGTGATGACAGTCATGTAGAGGAAYCTTCAGAGGATGT
Long Flanking Sequence:
GAGCACACAGAAACCGGCTGTAATTTTGCTGTCTTTATCAAATATTTGCAAGCTATGGATAAAATATGGATTATTAGATTATCAGATCTATTTGCATGAGTAAATCCCTCTGTGGTGGGAATTATTGTGATAACGGTATTAAATCCTGCTTTGTTTACGATGTATGTGTTCAGAAGTTCCCTTTGTGGAATGAGAAAACCAATTACTGCCCTCTACACTCGTTTTACCTTTCTATCAGACGGCTTTAATTTGTTGTGTTCATGTGCAGCTTTTTGGTACAGACTGGACCAGATCCAAGCCGACGCAAAGCGACAACAGTTGGTTTTCGTCAGTTGTTTGGCATCGGCTTGGTGTGTTCCAGGCCTAAACATGCTTTCTGCTGACAGAATTTTTATTTACATTTATTCCCCCCTGTGTTTCACTTATGCGAACAAGTAGTTTAAGGAGTAACAGTGCTTTGTTGCAGGCATGCAGGTCTCCAGGGTTACACCGCAGCCTTA[T/A]CTGGTGTCCAAGAGTGATGACAGTCATGTAGAGGAACCTTCAGAGGATGTGAACATCTCTTACTGTACACCATCACAACAGAGAATTTCACAGGTCTGCCCTTTGATCAAACCTCAAGAGAAACACTGCATATTTCAGTTTGCAAAAATCCAAACAATGATCAATGTCCCTTACCATAAAAGGAAACGTTTACATAATTACAGGTTTATATTATGAAGAAAATAATCAAACATTATCCCTTTTTCTTTAGTTTTCATTGAACAGAAGAAATTGGGATTGCATCGATAACATTGTCATTCCCATGTCTCTCTTCTCCTCTGTGAAAGTGGAAAAGCTTCAGTATAAGAACATACTGACGCCCAGGTATTAGGTGTTTTGATATTTGATAATAACATCAGAAAAGCATCAGCATTTGTTTGTGTAGATGTACACTAGTCAGTAATTCCTTTTTTCTTTATATTGAGTTTGATTTTAGGTTTTATTTAAAAATAAATTAAGTT
Associated Phenotype:
Not determined