ZMP
ercc6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens ERCC6, excision repair cross-complementing rodent repair deficien
Mouse Orthologue:
Ercc6
Mouse Description:
excision repair cross-complementing rodent repair deficiency, complementation group 6 Gene [Source:M
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22329 | Nonsense | Available for shipment | Available now |
sa22330 | Essential Splice Site | Available for shipment | Available now |
sa1301 | Nonsense | Available for shipment | Available now |
sa35517 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2690 | Nonsense | F2 line generated | Not yet available |
sa22331 | Nonsense | Available for shipment | Available now |
sa35518 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22329
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112380 | Nonsense | 88 | 1390 | 1 | 19 |
ENSDART00000134027 | Nonsense | 88 | 204 | 2 | 4 |
ENSDART00000134809 | None | None | 560 | None | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31098963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30744911 |
GRCz11 | 13 | 30875361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCACAGCTCTCAGGCCGCTGAGCTCCAAGGTCTGGGTGTGGATGTTTA[C/A]GACCAAGATGTCCTGGAGCAGGGTGTGTTGCAGCAGGTGGACAGAGCCAT
Long Flanking Sequence:
AGTAAAATCTGAGACTGTTGTAATGTTAAATTGTGTATGTCTGTTTATTTGTTCTTTAACAGTCATTGTAATTGCTCAAAACACATTTTTACAATTAAAAATGTGATTCTTGAAAAAGCGACTCTTTTTAGTTATTCTTGATATAGGCTAAAATACTCTTACTTTGGTGTTCAGTTACTCAAATTTTACAACCAAACTTTACACTCTTAGACCATTCTAATTCACAGTGACATAGCAATGCCAGTAGAAGGTACCGAGGACCAGGCCCTGTCACCCCTGTCCAGCCCTGTGAGTGCTCTTACTCCTGGAGCTCCAGAAGACAATGGCCTTTCCATCCCTGGAAGTAGTAGGGAAGAGCCAGCGGCTGCCTGTCCGGAGACTGTCGGGGCACAGAATTCGAGAAAATCACAACCTCTGCTCCAGATCAACCGTCAGGAGATCCTATCGGTGGACCACAGCTCTCAGGCCGCTGAGCTCCAAGGTCTGGGTGTGGATGTTTA[C/A]GACCAAGATGTCCTGGAGCAGGGTGTGTTGCAGCAGGTGGACAGAGCCATTCAGGAAGCCAACCAGGCTGCGGCTAAAGCTGAGGCCCAGAAAGAATACGAGTCTGTACTGGATGACGTCAGGTGAATTTATGGCTGCCTTACTTGCTCTTGTAATATTGTGCAATATGTGTCAAAAAATGAATAGCTCAAATTTGAGGTTGATCTACAGTAATGTGGTTGGTTTGTAAAACATTTCAGGTCATGTACAAGTGCTTTGAAACACATCAACAAAATATTGGAGCAGTTAACCCCTCATGCTGCCTCTAGCAAGGATATCAGTCGGAAAATTGAGTCTGTTAAACGGCAAAAAGAGAATAAGGTGAGTATATGCTGGATTGTTAGTTTTGCTGGGTTTAGCCTGTACTGCTGCATTATATGAAATTCTAGTCGGAAATGCTGTCTTCATTTGATCAAAAATACATTATAAACGTTAAATTCATTTAGAAATGTTCATGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22330
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112380 | Essential Splice Site | 129 | 1390 | 2 | 19 |
ENSDART00000134027 | Essential Splice Site | 129 | 204 | 3 | 4 |
ENSDART00000134809 | None | None | 560 | None | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31099201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30745149 |
GRCz11 | 13 | 30875599 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAATTTGAGGTTGATCTACAGTAATGTGGTTGGTTTGTAAAACATTTC[A/T]GGTCATGTACAAGTGCTTTGAAACACATCAACAAAATATTGGAGCAGTTA
Long Flanking Sequence:
TGCCAGTAGAAGGTACCGAGGACCAGGCCCTGTCACCCCTGTCCAGCCCTGTGAGTGCTCTTACTCCTGGAGCTCCAGAAGACAATGGCCTTTCCATCCCTGGAAGTAGTAGGGAAGAGCCAGCGGCTGCCTGTCCGGAGACTGTCGGGGCACAGAATTCGAGAAAATCACAACCTCTGCTCCAGATCAACCGTCAGGAGATCCTATCGGTGGACCACAGCTCTCAGGCCGCTGAGCTCCAAGGTCTGGGTGTGGATGTTTACGACCAAGATGTCCTGGAGCAGGGTGTGTTGCAGCAGGTGGACAGAGCCATTCAGGAAGCCAACCAGGCTGCGGCTAAAGCTGAGGCCCAGAAAGAATACGAGTCTGTACTGGATGACGTCAGGTGAATTTATGGCTGCCTTACTTGCTCTTGTAATATTGTGCAATATGTGTCAAAAAATGAATAGCTCAAATTTGAGGTTGATCTACAGTAATGTGGTTGGTTTGTAAAACATTTC[A/T]GGTCATGTACAAGTGCTTTGAAACACATCAACAAAATATTGGAGCAGTTAACCCCTCATGCTGCCTCTAGCAAGGATATCAGTCGGAAAATTGAGTCTGTTAAACGGCAAAAAGAGAATAAGGTGAGTATATGCTGGATTGTTAGTTTTGCTGGGTTTAGCCTGTACTGCTGCATTATATGAAATTCTAGTCGGAAATGCTGTCTTCATTTGATCAAAAATACATTATAAACGTTAAATTCATTTAGAAATGTTCATGCTGTGTTTTTGTGGATTCCATACGATTTTTAAAAAGTATGTTTTGTTAAGTACTAGTTTTATTCATCAACAACACAATAATTAAATTGACAGTAAAATCTTGTTAAATCATATTAAAAAATATTTCTATTTCAAATAAATGCTTTTATTAGTTGCATGTATTTTCCCCCACAAAAATATAAAGCAGAAAAAAAAATTCAACATTGATTATAAAAAGAACCCTCATTAATAGTAATTTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1301
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 |
---|---|---|---|---|---|
ENSDART00000112380 | Nonsense | 180 | 1390 | 3 | 19 |
ENSDART00000134027 | Nonsense | 179 | 204 | 4 | 4 |
ENSDART00000134809 | None | None | 560 | None | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31100139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30746087 |
GRCz11 | 13 | 30876537 |
KASP Assay ID:
554-1216.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCTGTTATCCTTTTACAGGAGAAGCAGTTAAAAAAGATCAGAGCCAAG[C/T]AGAAGAGATTGCAAGCTCTTCTTGACGGAGAGGATATACAGAAGCTTGAG
Long Flanking Sequence:
AAAGCAGAAAAAAAAATTCAACATTGATTATAAAAAGAACCCTCATTAATAGTAATTTTTGAAATATTTAATGATTTAACACCAATTAAAATAGATTATGACAGCAATTCAGTATTTTAAAAATATTTCTGAAGGTCCATGTGATGCTGAAGACTGCAATAATGATCATGTAAATTCAGCTTGAAATCACAGGAATAAATTATATTTTAAATCTATTCATACTCATTTAAAAATGTAATAGCTCACAGTTTTACTGATTTACAAATAAATTAGGCTTTGTTAAGGAGAAGATAATTACTTTAAAGCAAATAATGTTTGACTTTTAGTATCTATAATTGGTTTGTATTATTTTAAAAATATATATTTGAACTTTATTTTCTATTGAAATAAGAGCATGCTATATTTCAGTGATGCATTGCATAAAAAGATCTTAGCACACAATACTTAAAAAGCCTGTTATCCTTTTACAGGAGAAGCAGTTAAAAAAGATCAGAGCCAAG[C/T]AGAAGAGATTGCAAGCTCTTCTTGACGGAGAGGATATACAGAAGCTTGAGGCAGAATTATTGATTGAGGATGACGAGGGTAAGTATGAAGCGCAGGCCTTTACATGATTTGTATTATCATCATATGCTTTTTTAATCTTGCTCAGCAATCACTTTGTGTATATGGGCACCTTAAATTATACATTTAGAGAATAGTTATATCATAGAAAGTGTAAATCAGTTCATTTATCTTGTTGTTTTATGTTTGCTTTGTAGTTTATAGTATGTATACAACCGAGTTCTTTAGACCATTTTGGGGGATGTAAACAAAAACAATGGTCCCAATGTATTTCCTGTTTTACATATGTAATTTCTATAGCTTTCAAAAATACAAAAAGAGCTACATATTGATAAATAATGTTATGATAGCTGATTTAACATTAAGTTATGATTGAATTGCCTCTGGTTACAGTTATGAAATAGTTTGATAACAAGCAGGAAATGTTCATGACCAATGACATC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa35517
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 |
---|---|---|---|---|---|
ENSDART00000112380 | Nonsense | 193 | 1390 | 3 | 19 |
ENSDART00000134027 | Nonsense | 192 | 204 | 4 | 4 |
ENSDART00000134809 | None | None | 560 | None | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31100178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30746126 |
GRCz11 | 13 | 30876576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAGCCAAGCAGAAGAGATTGCAAGCTCTTCTTGACGGAGAGGATATA[C/T]AGAAGCTTGAGGCAGAATTATTGATTGAGGATGACGAGGGTAAGTATGAA
Long Flanking Sequence:
CCCTCATTAATAGTAATTTTTGAAATATTTAATGATTTAACACCAATTAAAATAGATTATGACAGCAATTCAGTATTTTAAAAATATTTCTGAAGGTCCATGTGATGCTGAAGACTGCAATAATGATCATGTAAATTCAGCTTGAAATCACAGGAATAAATTATATTTTAAATCTATTCATACTCATTTAAAAATGTAATAGCTCACAGTTTTACTGATTTACAAATAAATTAGGCTTTGTTAAGGAGAAGATAATTACTTTAAAGCAAATAATGTTTGACTTTTAGTATCTATAATTGGTTTGTATTATTTTAAAAATATATATTTGAACTTTATTTTCTATTGAAATAAGAGCATGCTATATTTCAGTGATGCATTGCATAAAAAGATCTTAGCACACAATACTTAAAAAGCCTGTTATCCTTTTACAGGAGAAGCAGTTAAAAAAGATCAGAGCCAAGCAGAAGAGATTGCAAGCTCTTCTTGACGGAGAGGATATA[C/T]AGAAGCTTGAGGCAGAATTATTGATTGAGGATGACGAGGGTAAGTATGAAGCGCAGGCCTTTACATGATTTGTATTATCATCATATGCTTTTTTAATCTTGCTCAGCAATCACTTTGTGTATATGGGCACCTTAAATTATACATTTAGAGAATAGTTATATCATAGAAAGTGTAAATCAGTTCATTTATCTTGTTGTTTTATGTTTGCTTTGTAGTTTATAGTATGTATACAACCGAGTTCTTTAGACCATTTTGGGGGATGTAAACAAAAACAATGGTCCCAATGTATTTCCTGTTTTACATATGTAATTTCTATAGCTTTCAAAAATACAAAAAGAGCTACATATTGATAAATAATGTTATGATAGCTGATTTAACATTAAGTTATGATTGAATTGCCTCTGGTTACAGTTATGAAATAGTTTGATAACAAGCAGGAAATGTTCATGACCAATGACATCACAACATTGAAATGGTATTTAAGTATGCTTCCAATATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2690
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000112380 | Nonsense | 496 | 1390 | 6 | 19 |
ENSDART00000134027 | None | None | 204 | None | 4 |
ENSDART00000134809 | Nonsense | 55 | 560 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31107314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30753262 |
GRCz11 | 13 | 30883712 |
KASP Assay ID:
554-2791.1 (used for ordering genotyping assays)
KASP Sequence:
CCTTTGCTTTTGTTGTCCAGGTATCAACAGACAGGTGTCAGGTGGATGTG[G/A]GAACTGCACTGCCAGCAAGCAGGAGGCATTCTGGGAGACGAGATGGGCCT
Long Flanking Sequence:
GAGAAAAAGAGGCAAAGAGAGAAGCAGGCGAGGAGGAATCCGACGAGAGCGATGCAGAGTTTGATGAAGGATTTAAAATACCTGGTTTCCTCTGGAAGAAGCTCTTCAAGTATGGCTCGCATAAATCACACATACTCTTATATTAAAAGAAAGGAATCGATCATGATAAGTCATGTTGTTTTTGCAAATGCAATGTGAAATATTAAATGTGTGCGCAAATTACTTACAATTTAACTTTAACGAGTCCCGAAAGGAGGAGGGATGATGTCTTTTAGGCCTAGAAAGTAGGACTGTGCTGCGGTGTTCTGGATGTGTTTTACAGCACATCAATTGGGCAACACTTATGGCCCATTTATCCGGAATCAATAGTGATAATGGCTCTATGATTAATTCATCAGCCGCTGTGTTTGTGTTTGTGTTTGTGCTGGAGCTGCGCTTTGTGTGACAAAACCTTTGCTTTTGTTGTCCAGGTATCAACAGACAGGTGTCAGGTGGATGTG[G/A]GAACTGCACTGCCAGCAAGCAGGAGGCATTCTGGGAGACGAGATGGGCCTGGGCAAGACCATCCAGATAATTGCTTTCCTGGCAGGCCTGAGCTACAGCAAGCTGAAAACACGTGGCTCCAATTACAGGCAAGGGACCCTACATGCTTGTACAGTTTCATATCTACTGTATGATAGGAAATCGAATTCTGTCTCAGAGTAAGATTTAAATTTATATATAAAAGGTTAACTATTCACAGTTTCTCTGAATTTCACTTGCCGTTGGTTTGAGCAAATTAATAATATTGGTTTATTCCATAAAGGTTTGATTAAATTTAATATGATTTCCATATATATATATATATATAAATATCCTCTAGGATTTTTTCCAGCTGTGGCGGCAGACTCTGTTGGCCATTTTACACAGATCTATCACTACATGTGGCGTTATTTCATTGACAAATGTCATGGGCGCAGATTGCATTCATGTAATAGCCTATGTCAATCTCTGCTTGAGCGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22331
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 |
---|---|---|---|---|---|
ENSDART00000112380 | Nonsense | 619 | 1390 | 8 | 19 |
ENSDART00000134027 | None | None | 204 | None | 4 |
ENSDART00000134809 | Nonsense | 178 | 560 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31116210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30762158 |
GRCz11 | 13 | 30892608 |
KASP Assay ID:
2260-6564.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATACATACGCATTATGCAAGATTACATCCAGAGATACGACTGGCATTA[T/A]GTCATCCTGGATGAGGGCCACAAGATAAGGAACCCAAATGCTGGGGTCAC
Long Flanking Sequence:
GGCAACCCGGGGTGCTGAAATATAATTGGCTAGATTGGCAGTGGACGGGTAAAGAACCAAAACAAAGACAGCATTTCGGCACGGAAAACACATTTTCAAAGCGGAAAAACTTAAGCATTGATTTTCAGAAGAATGATCACTTGGCATGTTTCTTAAATTTCTGAAAACATATTATGGTATTTTTATGCTTTAGAAGAGTGAAAAACTTAGATGCAGCACCTTTAACAAAAATAAATTAAAACAAGACCAGTGTAGAAGGTTTGCACCCTAAAGTTGTAAATATGAATGAATCTGTTTTTGAAAAAATGGAGTAAGTCAATAATTTATCGATCCATTCATAAAGTCACTTTTGAGTTGTACGAATGTTTTAATTCACTTTGTTTTCCTTATTATCAGGAGAAGCTCATTCCAGAAATTGTGGCCAGTCACGGCATCCTCATCACCTCCTACTCATACATACGCATTATGCAAGATTACATCCAGAGATACGACTGGCATTA[T/A]GTCATCCTGGATGAGGGCCACAAGATAAGGAACCCAAATGCTGGGGTCACTACAGCATGCAAGCAGGTGATCATTTCTTTTCCTTCTATTCTTTTTTTACTCTGTAAAAAGCAGTTATTTACTTAAAAGTGGCTTGCCTTAAAATGTACAAGTTTTTTTTGCTTGAGGACGTGAATACACCTGTTTTAAACTTAAGTTGACTAAACTTAATTTTTATAATTATGCACACTTCTTTTCCGTAATAATTTTTAAACTTGGCGGCATGGTGGCTCAGTGGTTAGCCCTGTCGTCTCACAGCTAGAAGGCTACTGGTTTAAGTCCAAGGTGACATTTCTGTGTGGAGTTTTCATGTTCTCCCCGTGTTCACGTGGGTTCCTCCGGGTGCTCCGGTTTCTCCCACTGTCCAAAGATTTGTAAACAAAAAAATTGGCCATACTGTATGTGTGTGTGTGAATGTAAGTAAGTAAGGGTGTGTCCAATAATGGGTTGGGGCTGGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35518
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112380 | Splice Site, Nonsense | 641 | 1390 | 8 | 19 |
ENSDART00000134027 | None | None | 204 | None | 4 |
ENSDART00000134809 | Splice Site, Nonsense | 200 | 560 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 31116274)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30762222 |
GRCz11 | 13 | 30892672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCCACAAGATAAGGAACCCAAATGCTGGGGTCACTACAGCATGCAAG[C/T]AGGTGATCATTTCTTTTCCTTCTATTCTTTTTTTACTCTGTAAAAAGCAG
Long Flanking Sequence:
AAGACAGCATTTCGGCACGGAAAACACATTTTCAAAGCGGAAAAACTTAAGCATTGATTTTCAGAAGAATGATCACTTGGCATGTTTCTTAAATTTCTGAAAACATATTATGGTATTTTTATGCTTTAGAAGAGTGAAAAACTTAGATGCAGCACCTTTAACAAAAATAAATTAAAACAAGACCAGTGTAGAAGGTTTGCACCCTAAAGTTGTAAATATGAATGAATCTGTTTTTGAAAAAATGGAGTAAGTCAATAATTTATCGATCCATTCATAAAGTCACTTTTGAGTTGTACGAATGTTTTAATTCACTTTGTTTTCCTTATTATCAGGAGAAGCTCATTCCAGAAATTGTGGCCAGTCACGGCATCCTCATCACCTCCTACTCATACATACGCATTATGCAAGATTACATCCAGAGATACGACTGGCATTATGTCATCCTGGATGAGGGCCACAAGATAAGGAACCCAAATGCTGGGGTCACTACAGCATGCAAG[C/T]AGGTGATCATTTCTTTTCCTTCTATTCTTTTTTTACTCTGTAAAAAGCAGTTATTTACTTAAAAGTGGCTTGCCTTAAAATGTACAAGTTTTTTTTGCTTGAGGACGTGAATACACCTGTTTTAAACTTAAGTTGACTAAACTTAATTTTTATAATTATGCACACTTCTTTTCCGTAATAATTTTTAAACTTGGCGGCATGGTGGCTCAGTGGTTAGCCCTGTCGTCTCACAGCTAGAAGGCTACTGGTTTAAGTCCAAGGTGACATTTCTGTGTGGAGTTTTCATGTTCTCCCCGTGTTCACGTGGGTTCCTCCGGGTGCTCCGGTTTCTCCCACTGTCCAAAGATTTGTAAACAAAAAAATTGGCCATACTGTATGTGTGTGTGTGAATGTAAGTAAGTAAGGGTGTGTCCAATAATGGGTTGGGGCTGGAAGGGCACCAGCTGCATAAAACATATGCTAGAATAGTTGGTGGTTCACTCTGTTGTGGCAACCCTTGA
Associated Phenotype:
Not determined