ZMP
ano2
Ensembl ID:
ZFIN ID:
Description:
anoctamin 2 [Source:RefSeq peptide;Acc:NP_001103862]
Human Orthologue:
ANO2
Human Description:
anoctamin 2 [Source:HGNC Symbol;Acc:1183]
Mouse Orthologue:
Ano2
Mouse Description:
anoctamin 2 Gene [Source:MGI Symbol;Acc:MGI:2387214]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40208 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31370 | Essential Splice Site | Available for shipment | Available now |
| sa33366 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40209 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20190 | Essential Splice Site | Available for shipment | Available now |
| sa31371 | Essential Splice Site | Available for shipment | Available now |
| sa33367 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40208
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Nonsense | 63 | 984 | 1 | 24 |
| ENSDART00000109788 | Nonsense | 77 | 998 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4145929)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4264542 |
| GRCz11 | 4 | 4273455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCTCCAATGGAAGTTATCATTTAGGAGTGGAGGAAAAAGACCCAGAA[G/T]GAGGGAAAGAGGAGCCTGCGGAGGTGGTGGTTGATGTTGGACCACCGGAC
Long Flanking Sequence:
ACGAGTGGCAACAAGATCCACGTGAGTATGATCTTCATCTCTCTACTAAAAGAATAGCAATACGCAAACAGCTCTAGAGGCAGTAACCCAGAAATAAATGGCATCAGCGGATAGTGTCTATTGCCAATCTAAATTGAAGAGTATATTGAGAGCAGCCAAATTAAGAAGCAATAGTCTGACCTACATCTATCCTCACCATACTCCCTCCCTCCCCCCTTTCTCCTGTGTTGAATTTGATATCCACACACACTGCTGATGAACACTGAGCCCGGGTACATTGTATTCTCCTCTCACCTGTTCAGGTGGCCAATAACATGATGGACATGGACCAGGACCCTCGCAAGCGGCTCTACTTTGCTGACGGCCGAAGGAAAGTGGACTATGTGCTGGTGTTCCACTACCGAAAGCGTTCCTCCATCAGGGGGTCTCCTAGTCAGCACAGACTGTCCATCATCTCCAATGGAAGTTATCATTTAGGAGTGGAGGAAAAAGACCCAGAA[G/T]GAGGGAAAGAGGAGCCTGCGGAGGTGGTGGTTGATGTTGGACCACCGGACCCTGCCGAAGGGGAGAAAATCATGATCCGGGAAGAGTTTGAGGGCAGTTTAAAGGACGCAGGGCTGGAAATTGAACGTGATAAAGAGGTGAGTGGAAGCTTAATTGATTTATATGTGGCTTTGCTGGTGTGTAACTTTTAGAACGCTAAAGAAATGATTCTATTTAGTGCGTGTGTCATTCTTAGAACGTTCTTAAACATTCTAAATATTCTTGGAACATTCTTGCAGCTTGAAAAAAAGGGTTAAATTACATGGGTTTGAGCTTAAAACAACAACAAATATCATAAACAGAAATTCAAGATGATTCCATTTGCAGGTATTTTACGTTTTTTAACACTTAAAGTCAATTTTTTCAGACTAAACAGCTTAAGTAATACATTTTAGAATCAAATTAATTTAAAAATATATCATTTTAGTGCATAAGAAAGATAAAAAGATAAAATTAGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31370
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Essential Splice Site | 142 | 984 | 3 | 24 |
| ENSDART00000109788 | Essential Splice Site | 156 | 998 | 4 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4163112)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4281725 |
| GRCz11 | 4 | 4290638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTTGTTTCCATGCTTCACTGATAATAATAAACACTGTGTCTTGTTCA[G/A]AGTTACGAGCTGAGGGAAGAAAAAGGTCTGGCCGCCACTATGAATGAAGT
Long Flanking Sequence:
CTACAGCTAATCAGGACGCAGAACACAATGCACTGTAAAATAACTAAATAAATAAAAATAAGCAAACTGCAGTAAATAAATGAGAGAAACTGAGAGCCCACAAAATGTGATCCAGGGACCACTGTATTGCTTCTACTTTAGAATGAGCTTAGCTTCTCTGACTGTGACCCATCGTCATACTGCCTGTATGTGAAGTCATTTCTCTGAAATTCTTTCCTCAGAACAAGGCTCATGGTCATGCCTTTATCCGGTTACACGCGCCTTGGCAGGTATTGAGCAGAGAGGCAGAGTTTCTCAAGATCAAGGTGCAGACCAAGAAGGTAAGATTGAGCAGAGTTTTGTCTAACTCTCGAGACAGAACCCAGCCCCTCGGGATGTCCTTATGTGAACTCCCTGCGAGTATTATGTAGCATGTCTCTTAAGTGAGCAAAGCACAAACGAATGCCACTGATTGTTGTTTCCATGCTTCACTGATAATAATAAACACTGTGTCTTGTTCA[G/A]AGTTACGAGCTGAGGGAAGAAAAAGGTCTGGCCGCCACTATGAATGAAGTGTGGCGGAAGTTAAATCAACCGTTCCAGCCCAAAGTACCCCATCAGGAGCAAGAGAACAGCCGCACCAAGTTCCTCACCCACTGTTTCTCCCGGGACAAGCTCCACCTGTGAGAGCCTAGCGTGGTTGGGGTGATATAGGGTTAAATGTCATCAGGGGCCACAAGGGATTTTCTTACATTCTTAAAGGACTTGATAGGATTTGCTTGAGTGCCAGTGGAGTCTCATGGATGTCTCATGGCTATTTTTTGCAGGTACAACATACAGTCAAAGGACACCTTCTTCGACAATGCCACAAGGAGCCGAATAGTGAGTCTATTTTTTGTTTGTTTGTGAAAGTCTTGTTCAGTCAAAATTGCACAATGAGATACCTGTTCTTTGCATGTTGAGAAGAGAACATGATATACAAGAGGGAACAAAAGCTATTTGGTATTAGCAGGTGATTGCCGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33366
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Essential Splice Site | 229 | 984 | 5 | 24 |
| ENSDART00000109788 | Essential Splice Site | 243 | 998 | 6 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4163792)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4282405 |
| GRCz11 | 4 | 4291318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGAAATCCTCAGACGCACAGCCTGCACACGGACCTGCCAAACCATGG[G/A]TTAGTAATGTGTAAATCCATAACCTAAGCATGGACTAGCGTTCAGGGAAT
Long Flanking Sequence:
GGTGATATAGGGTTAAATGTCATCAGGGGCCACAAGGGATTTTCTTACATTCTTAAAGGACTTGATAGGATTTGCTTGAGTGCCAGTGGAGTCTCATGGATGTCTCATGGCTATTTTTTGCAGGTACAACATACAGTCAAAGGACACCTTCTTCGACAATGCCACAAGGAGCCGAATAGTGAGTCTATTTTTTGTTTGTTTGTGAAAGTCTTGTTCAGTCAAAATTGCACAATGAGATACCTGTTCTTTGCATGTTGAGAAGAGAACATGATATACAAGAGGGAACAAAAGCTATTTGGTATTAGCAGGTGATTGCCGTCTCTAGGCACCGGTCTAGGGAACCAGTTCCACTGGGAATTTTCCAGGAACAATTTTCGGCTTTATTGTTTGCTTGCACCTCTCTCACTCCTTCTCTCTCTCTCTCTCTCTCTCTTGCCATCTGCCCCAGGTGTATGAAATCCTCAGACGCACAGCCTGCACACGGACCTGCCAAACCATGG[G/A]TTAGTAATGTGTAAATCCATAACCTAAGCATGGACTAGCGTTCAGGGAATCCTCAGAATAGTCAGAGCCAGAGAGTCTTTGCATGTGGGTATGGTGCAGTTGGGACAGGGTGCAACACAAGCCCATGCCATATGCTCTCTTGGACTGAACCATCGTGCAGACGGACCGCCTGGGGGATTCTCGGAGATCGGGGCTATCCAGCAGAAGGGATGGCATGATGCTCTCTTTAGTTCTCCCTCCCTTTCTTCCCTTCTCGCAGACTTCCACTTGATTTCTTTTAGACTGAGGAAATTGGGTCATAAAGTTCTGGGATTGGGATCCGAATTGAAGCCGGGTCCATTGAGGTGGAAAAAAGGGGGGTGCTGAGTGGTGGTGGTCTTTCCAGCTTGTTGCTGGGGAGCTACTTTATTAATTGAGGGCTAATCACCAGAGCGTACGTGTCGTTCCTTTGAGGACTGATTAATTACTTTGATTAAAGCCTGTGTTCCACATGTCAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40209
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Nonsense | 258 | 984 | 7 | 24 |
| ENSDART00000109788 | Nonsense | 272 | 998 | 8 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4166648)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4285261 |
| GRCz11 | 4 | 4294174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGAGTTTTTCTATGATTTCAGGGTGACTTCCACTCCTCTGGACAAGCC[G/T]AGGGAAAAAACGAAAGACAAGTATGTTGCTACCACAATGCAAATAATCAG
Long Flanking Sequence:
TGAATCATTTAATTATTTGTTATTCAATTGGCACACGTGAAGTGAACTGAATAGTGATTGCTCATACGATAGCTACATGTTTTTATTATCAATGACTGACCTATAATCTAATATATGACGCTAAATAATTATAGACAATTATAATTTCAGAAATGTGATGCTTTTTTTGCGCTATCATCGTTTAATGACGTCATGTTCTGGGAAAACTGAAACTGTTTGTTGGATGTCAGTCATGCTAACTTTAATCTCCTGGTTTTATTTCGGGAATTATTAGTTTACAAATTAAGCACTGAAATAACCTCTTTAGGTCACTCTCTCTCTTGTTTTTTGCATTTCAGGTATCACCACACTCATAGCTAACGGGGTTTATGATTCAGCATTCCCATTGCACGATGTGAGTTGATTTTCTTTAAATGTTTGGCCTTTCTTTTTCCTTCCAGGTTAACTCGAAATGAGTTTTTCTATGATTTCAGGGTGACTTCCACTCCTCTGGACAAGCC[G/T]AGGGAAAAAACGAAAGACAAGTATGTTGCTACCACAATGCAAATAATCAGAAGCGATTGCATGATTCAATTCTATGGGTTTGTGTTGCAGCTGTTACATGACGAATGGGCAAGATATGGTGCTTTTTACAAGTATCAGCCGATCGATCTCATCAGGTAAACATTTATGACCAATTTCCACCAGATGTTGCACATATACTTTGCACACACTCTCATGTGTAATCTTTAGGAAGTACTTTGGCGAGAAGATTGGTCTGTACTTTGCCTGGCTTGGTGTGTATACTCAGCTTCTGATCCCTGCATCTGTGGTGGGCATTATCGTCTTCTTCTACGGCTGGGCCACTGTGGAAACCAACGTACCTAGGTATGTGCCAATAAAACCTACCGAGGGCTGGGCACGGGTCCCTGTTGTGGGTGGACACGCGGCAGCTGCCATCCTGGGAGTAACCGACTGTGATTATAATATTCCACTGATATTAAAGCGATAATTAGAATCAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20190
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Essential Splice Site | 561 | 984 | 16 | 24 |
| ENSDART00000109788 | Essential Splice Site | 575 | 998 | 17 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4201649)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4320025 |
| GRCz11 | 4 | 4328938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGAACTCATCTCTCTGAACCCTACATAATATCACTTCATGTGTCTGC[A/T]GAGATCCCGAAAACTGAGACCAACTTTGAAGAGCGTCTGATTCTGAAGGC
Long Flanking Sequence:
TTGTCTGAAAAACAATGCTAAAGTCTGATAATATGCTTTAAAAATGTGCATTATGTGTCAGAATGCCTGTCTACGTTTAGGTCATTTAACTCGGCCAATGGCAGTTTACTGCACAACATGGGTTCGTTCATTGAATAATACTCATGCGTCACATTAAACGCTCATCTGGAAGTGATATAGAGTGTGACCAATAAAACTGAGAAATCCAAACACAAGTATTCACAAGACACATCTTAGTCCGTGTTAATACACCAGGTGGAAATGCTCTCATCTGACCACTTGCGACGGGATCACTGCAAATGCATGTTAATTCCAGGAAGCAGGAGTCTATAGGACTTTTAACCTTACGACCAGCTGAACAGAAGTTGCTAAAGAGAAACATGCCGGGACACATTTTTAGCCACCCATGTTAATTATACTTGTCAGGTTTTTCAAACTGCGTGCGGTCTATCCAGAACTCATCTCTCTGAACCCTACATAATATCACTTCATGTGTCTGC[A/T]GAGATCCCGAAAACTGAGACCAACTTTGAAGAGCGTCTGATTCTGAAGGCTTTCGTCCTGAAGTTCATGAATGCCTATGCACCGATCTTTTACGTGGCCTTCTTCAAAGGGAGGTAGGTGGACATTTGCCAAGTTCAGCCCCAAAACATTAAAAAATCATAATAATTAATTGTGGGAGATAATGAAAAGCACACAAACACGCACATATTCAGCCTCTGGCGTAAAGTCTGACTGCTGCACAAACATCTGGCTTCAAATAAGACAGGCATGTGACCCTTGGCACTGACTGTCTTGGGGCAAGACATATCCCGTAACCAAGAATTGTGTGTGTGTGTGTGTTTTACAGGTTTGCGGGCCGCCCTGGTGACTATGTATATGTCTTTCATGACTATCGAATGGAAGAAGTGAGTATGATTTTTTGAAATTATTAATTAGCACTAAGATATCATGTTCAGCATGAGATGATTTACAAAAATGAACTGGAAAATGTGACTGGAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31371
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Essential Splice Site | 825 | 984 | 23 | 24 |
| ENSDART00000109788 | Essential Splice Site | 839 | 998 | 24 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4225586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4343962 |
| GRCz10 | KN150482.1 | 7272 |
| GRCz11 | 4 | 4352875 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGCAAGAACTGAATGAGCCCTTAATGACTTTTTCATTTTGTATATTTT[A/T]GGTACAAGGACTACAGAGAGCCTCCATGGTCGAATGAGCCTTACCAGTTC
Long Flanking Sequence:
TTAAAGGAACTAAGCCGAGAAGAAAATGAATGAGTTGGCGGTTCATTCCACTGTGGTGACCCATAATAAATAAGGTACCAAGCCGAAGGGAAATGAAAATATGAATTTCCAAACAATAAAAAAAAAATGTGGCCAATTATGATCCCGACCGTCTAATAACTTTGGATTGAAACTAGTAAAAGTGGCTAATAAGCTTAAAGTTAGCGTGGCTTAAAGCTAATACAAAGCTCTGTTTATAAGCTATCAAAAACTCTCATTAGCTCTAAAGCAGGATGAAATCCACTTGGACAAATAGTTAAGTGGCACAGCAAAATTCCAGATCCGTTTTTTTCTGCACTTAAACATCCTCATCATGATTATTAATGTTGTTGTGTTGTTTTGTCCTCCTAGAAGCATGTGTGGAGCATGTGTTTCACATTTTCTCGTCTTTATTGCACTAGCTAACGGATACTTGCAAGAACTGAATGAGCCCTTAATGACTTTTTCATTTTGTATATTTT[A/T]GGTACAAGGACTACAGAGAGCCTCCATGGTCGAATGAGCCTTACCAGTTCTCCAAACAGTACTGGTCCGTGCTAGCGGCTCGGTTAGGTTTCGTCATTTTATTCCAGGTATGACATTTTTCCCGAAACATTCGTAATCAATCGCAGAAAACCCTGTTAATAGTCTGTGATTAGAGGAGTGTAAATGTAAAAGCCAAACAAATGAAAAAGCCACAGCATCGTCAGCCATTCAGCCGTGTATAAACGTTGCACGTGAAGATTAAGACTCTATATGTTGGTCAGAATAATTGCTGGAACTCACTAGAAATGTCCTGCTGTCAGCAGATGTGGGTGAAACTATTTCTATTGACATGCAATTATACCGTAAACCAAACAGTTAAAGGAATAGTTTGCCCCAAAACTAAATGTCGTTTAACCTCGGTGGCGTTCCAGACTCATAAAGTGACATTTCACAGTGATCACGGCTACCTAAAATGTAAACAAATTTTTATTATTTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33367
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 |
|---|---|---|---|---|---|
| ENSDART00000092932 | Nonsense | 872 | 984 | 24 | 24 |
| ENSDART00000109788 | Nonsense | 886 | 998 | 25 | 25 |
Genomic Location (Zv9):
Chromosome 4 (position 4228161)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4346537 |
| GRCz11 | 4 | 4355450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCACTTCCTCCAGAACCTGGTGATAATCATGAGCATGCTGGTGGCCTG[G/A]CTGATCCCGGACATGCCCAAAAACATCAGTGAGCAGTTAAAGAAGGACAA
Long Flanking Sequence:
GAAATTTTCACAGTATTTTTTATAATATTTTTTCTTCTGGAGAAAGTCTCATTTGTTTGATTTCAGCTGGAATAAAAGCAGCTTTTGATTTTTTTTTATCCCATTTAGAGGTCAATATTATTTGCACCCTTAAGGAATTATTTTTGATTGCCTACAGAACAAACCATCGATATACAATGACTTGTCTAATTACTCTAACTTTACCCTAATTAATCTAGTTAAGCCTTTAAATGTCACTTTAAACTGAATACTAGTATCCTGAAGAATATCTAGTCAAATATTATGTACTGCCAACATGACAAAGATAAAATAAATCAGTTATTAGAAATTAGTTATTAAAACTATCATGACTATAAATGTGAATAAAGAAAAACTTGAAATTGGGGGAAAACATACAGGGGGCTGTAACGTGCATGCATGAATAAAACCTGGGTTTAACCCACTGATGATCTCCACTTCCTCCAGAACCTGGTGATAATCATGAGCATGCTGGTGGCCTG[G/A]CTGATCCCGGACATGCCCAAAAACATCAGTGAGCAGTTAAAGAAGGACAAGACTCTTCTAGTGGACGTCTTCCTGAACGAAGAAAAGGAGAAGCTGCAGCTGATCCAGAGCCTGTTCTCCAAAGATCTGACCAACAAGCAGCAGGAAGAGCACCAGCAGCAGGTTTCGGATAAAACCTCGCTGCCTCTCCAGCAAAGCCAGCCTGGCTTTCTCCCTCCGTCCTCATCCCCTGCCTCTACAGCTCCTCGAACCCGAGCACGAGCCGCCAGCTTCAGTCAGTTCACCCGGCAGATGTCTATGTCTCCCCGCAGGGACGTCACCCAGCACACGGCGGTGTGACGGGACGCTGGACAAGTCTTGGAGGATTTGCTAAAGCGTGAGGCTTGAGTTTTGGGAATCAGGTGCCCGCGTTTGTTCTCCTCTTTAATTTTTGTTTGTTTTTTTTCCACACCGGAGCACTGGATAGTACATTTCGAAAGTCTATCTCGGATGTTTCAGCC
Associated Phenotype:
Not determined