ZMP
zgc:162329
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC569946 [Source:RefSeq peptide;Acc:NP_001103949]
Human Orthologue:
TRPM1
Human Description:
transient receptor potential cation channel, subfamily M, member 1 [Source:HGNC Symbol;Acc:7146]
Mouse Orthologue:
Trpm1
Mouse Description:
transient receptor potential cation channel, subfamily M, member 1 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38126 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
| sa38127 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24717 | Essential Splice Site | Available for shipment | Available now |
| sa24718 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24719 | Nonsense | Available for shipment | Available now |
| sa9727 | Nonsense | Available for shipment | Available now |
| sa15364 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38126
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, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087497 | Missense | 4 | 297 | 4 | 8 |
| ENSDART00000123249 | Essential Splice Site | 92 | 1290 | None | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35402229)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34145494 |
| GRCz11 | 25 | 34586116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAGTATATCC[G/A]GGTGTCTCATGACACTAAGCCGGACAGTTTGCTGCATCTGATGGTGAAGG
Long Flanking Sequence:
GGGCCACTGTGTTGCCCATGTGAAACGAAGGGGGAGTAGGGGTGTGTGTGTGTGTGTGTGGGGGGGGGGGGGTTCTTCAAGGTGAAGATACTGACATAGGAAAACTCTGGTTATTTATAGTGAGTTCGGAATCATCTGATTGGTGAATTAATCGTTAGCTAATGCAGGACCAGCTGTGATCAATCATAATCACGCGATTCTCTCAAAATTGGTTTATGAATAAACTTTTTTTATTTTTTTATGTTTTTGCATAATTTTGTATATTAATGCAGATGCATTTGATGTATAAATCATTCCATTCAGTATAAAATTAGGAATTATTTCCAAATAAAGTCATCTGTCAGAATCTTACACCGGCCCATGCCTACTGCTAGACAAGTTCACTTGGCGAGGAAACAAACAACTTCTTTTAAATCTCCAATTAATCCTCAAATTTCTCTCTCTCCCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAGTATATCC[G/A]GGTGTCTCATGACACTAAGCCGGACAGTTTGCTGCATCTGATGGTGAAGGAATGGCAGCTAGAGTTGCCCACGCTGCTGATTTCGGTCCACGGTGGCCTCCAGAACTTCGACCTGCAGCCCAAACTCAAACAGGTGTTTGGTAAAGGCCTGATCAAGGCTGCGGTGACCACCGGGGCCTGGATCTTCACTGGTGGAGTCAGCACGGGTGGGTATATATCGTGTGAACTACACTGCAAAAATCTTACTTTCAGATTTATTTCGTCTTGTTTCAAGTCCAAATATCTAAAATATATCTAAAAAGAAGCACTTTCTGGACAATAACATACCAATATAAAATAGTTTTTGCTTTCATTAATAAGTTATAAAAATTCATTTCATTTTCTTTTCGGCTTAGTCCCTTAATCAATCAGGGTTCACCACAGCGGAATGAACCGCCTTAATCAGCATATGTTTACGCAGAGGATGCCTTTCCAGCTGCAACCAATCACTGGGAAACACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38127
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 |
|---|---|---|---|---|---|
| ENSDART00000087497 | Essential Splice Site | 171 | 297 | 6 | 8 |
| ENSDART00000123249 | Essential Splice Site | 258 | 1290 | 5 | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35406039)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34149304 |
| GRCz11 | 25 | 34589926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTACGCAGGCAGCTGGAGAAGCACATCTCGCTCCAGAAGATTAACACTC[G/A]TAAGTGCGGCGGCATCAGAGAATCTTATCTGCTTTAGGTCTAATGTACCT
Long Flanking Sequence:
ATCTCAGTATTTTAGTCAGTTTGTTTAATGTAAGTTGAGATGACTAGATAAGTTAATTTGACTGATTCCACTTAAATTCAAGTCTGCAAGAATTTTTTTGCGCCACAAAACATCAATTTAACTTATTTTAATAAGCTAATCAGGTTTCAACAAAATTAAGTTATACAAACTCAATAATTTTAGTCAGTTTGTTTGTAAGTTTAAATGACTAGTTAATTTAATTTAACTAAAAAATTAAACTTATATATATATATATTTTACAGTGTAACAATAGATGAGAGTCATACTTCTGATGAAATTCACGATGCATTGTTTGCTTTTTTTTCAGGTCAACAAACCATACCAGGCAATCTCCAACCCTCTGAGCAAACTAGCGGTCCTCAACAACAGCCATTCGCACTTCATCCTGTCTGATAACGGCACTTGTGGCAAATACGGAGCCGAGGTCAAGCTACGCAGGCAGCTGGAGAAGCACATCTCGCTCCAGAAGATTAACACTC[G/A]TAAGTGCGGCGGCATCAGAGAATCTTATCTGCTTTAGGTCTAATGTACCTCTGATCTCCTAAGAGGACGCATGTGAAAGCTCGCTAAGGGTTTGAACGACACCAGATATATCGAGATTATCAGTAATGGGTGGTAGGGATGTGTAATATGTATCGTTTCAGCATCGATACTATAATGTAGACTGCAAAAATTATCTTTAATTCTGTGTTTTGTGATTGATGTTTTTATTTTTAGACTTTTCACCGTTTATTTATGCTTTTGAATTGCATTATGGGAGCTTGATCTTTGTTCCAATAACTTTTAACTTTGCAGAAGATTAAAAAAGTGACTTTTATGAACATTTTTAATAGTTTAAAGTGATATCTAAGAGCTTGGAATGACCAAGAGGCGACACTCTAGTGTAATTTGGGAAACAGCCACTAGAGGGCGCGGCGCCCATATTGGAATGAAAACTCCAATAGAACAACAGCATACTATAAGTCTGTGAAATAAACTATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24717
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 |
|---|---|---|---|---|---|
| ENSDART00000087497 | Essential Splice Site | 172 | 297 | 6 | 8 |
| ENSDART00000123249 | Essential Splice Site | 259 | 1290 | 5 | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35406040)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34149305 |
| GRCz11 | 25 | 34589927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACGCAGGCAGCTGGAGAAGCACATCTCGCTCCAGAAGATTAACACTCG[T/C]AAGTGCGGCGGCATCAGAGAATCTTATCTGCTTTAGGTCTAATGTACCTC
Long Flanking Sequence:
TCTCAGTATTTTAGTCAGTTTGTTTAATGTAAGTTGAGATGACTAGATAAGTTAATTTGACTGATTCCACTTAAATTCAAGTCTGCAAGAATTTTTTTGCGCCACAAAACATCAATTTAACTTATTTTAATAAGCTAATCAGGTTTCAACAAAATTAAGTTATACAAACTCAATAATTTTAGTCAGTTTGTTTGTAAGTTTAAATGACTAGTTAATTTAATTTAACTAAAAAATTAAACTTATATATATATATATTTTACAGTGTAACAATAGATGAGAGTCATACTTCTGATGAAATTCACGATGCATTGTTTGCTTTTTTTTCAGGTCAACAAACCATACCAGGCAATCTCCAACCCTCTGAGCAAACTAGCGGTCCTCAACAACAGCCATTCGCACTTCATCCTGTCTGATAACGGCACTTGTGGCAAATACGGAGCCGAGGTCAAGCTACGCAGGCAGCTGGAGAAGCACATCTCGCTCCAGAAGATTAACACTCG[T/C]AAGTGCGGCGGCATCAGAGAATCTTATCTGCTTTAGGTCTAATGTACCTCTGATCTCCTAAGAGGACGCATGTGAAAGCTCGCTAAGGGTTTGAACGACACCAGATATATCGAGATTATCAGTAATGGGTGGTAGGGATGTGTAATATGTATCGTTTCAGCATCGATACTATAATGTAGACTGCAAAAATTATCTTTAATTCTGTGTTTTGTGATTGATGTTTTTATTTTTAGACTTTTCACCGTTTATTTATGCTTTTGAATTGCATTATGGGAGCTTGATCTTTGTTCCAATAACTTTTAACTTTGCAGAAGATTAAAAAAGTGACTTTTATGAACATTTTTAATAGTTTAAAGTGATATCTAAGAGCTTGGAATGACCAAGAGGCGACACTCTAGTGTAATTTGGGAAACAGCCACTAGAGGGCGCGGCGCCCATATTGGAATGAAAACTCCAATAGAACAACAGCATACTATAAGTCTGTGAAATAAACTATTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24718
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 |
|---|---|---|---|---|---|
| ENSDART00000087497 | None | None | 297 | None | 8 |
| ENSDART00000123249 | Essential Splice Site | 520 | 1290 | 12 | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35421911)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34165176 |
| GRCz11 | 25 | 34605798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGATTAGAGGAGTTATACAACACTGTAAGCACCACAACCATTATCATTC[T/C]GGAGCTTAACTCAAAGGAAGTACAACACAGCATCAGAGCAAGTCACTAAT
Long Flanking Sequence:
AGTTTTAAACTAAATAAAAAATTACCAACAGGCTTTTTCAAGTCAGCCTCAAAGTTTGTCTCGACAAATTTTACTAATCTAGTTAATAGTTACTATAGCATTTTTTTAATCTGGGCATTTAGAGCCATTTCTTGTTTATGGATTGAATTGCATTACTATCTAACAGCTAGTTCATTAACTCAGCAGTATCAGCTGTAAACAACACTATAGTAAGTACGGCAGGGTTTATAATCCTGCTTTAAAAAGCCAGCAGTTCTGGTCCATGACCAAAAAACTGCAATGCTGCAATCCTTCAGCATCAACAAAACGTGTTGATCTTCTCCTCTGTCGCCCCCTTCAGGTAAACTCTCTCGAGCAGGCCATGATGGACGCTTTGGTTCTGGACAGGACGGATTTCGTCAAGCTCCTGATAGAAAACGGTGTAAACATTCACCATTTTCTAACCATCCCTCGATTAGAGGAGTTATACAACACTGTAAGCACCACAACCATTATCATTC[T/C]GGAGCTTAACTCAAAGGAAGTACAACACAGCATCAGAGCAAGTCACTAATCCACTGAGGAGAAAAAAAAAATACAGGGCCTGCTGTCATATCTTTTAATATTTCTCATAATATTATTACTCAATAGCACACAATCTTATGGCTTGTGTGTCTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTTCTAACAGAAACTGGGTCCTGGCAACACTCTACATATTTTAGTAAGAGATGTTAAAAAGGTAAATAATTTATCCATGAATCTTTACAACTGATGATTTCTTAAGATAAAAATATAGCTTAAAGGAACACGTTACTTTTTAAGGCTAGTTTTACAACTTCTATACTCTCAACTCTCCATATATACAATATTCAAGTTGAGTTTACCCCCTCTTTTTATCATTTTTAACCCATTTAGCTGATCTCCAGGTCTGGCAGAAGAACTTTTAGCTTAGCATAAATCATTGATTTGGATTAGACCATTAGCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24719
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087497 | None | None | 297 | None | 8 |
| ENSDART00000123249 | Nonsense | 788 | 1290 | 19 | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35426626)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34169891 |
| GRCz11 | 25 | 34610513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATGACACGTCTCATCAGGTTGCTGTGGCCGATGAAGACAAAAAGACC[A/T]AAGATGATGAAAGATCCACTCGGGTAAAGTGGACGACTCTTCTTTTTCAA
Long Flanking Sequence:
AACACTATCGGTTGGGTTTAGAGAAGGGGGTGAGTGGGTCAGTTGATCATTAATTCAGTCGACAGTAAGTCGGCCTGGTCGGCTGAAGTGTATATTACGCCCTCTAGTGGATTTAAGCGAGAACAGGAATTTTTGATCATCAAAAAGTGTACACAGCGACCTCTGGTGGATTTGCAAAAACAAAAACTGTGAGCAGATGTACCTTTGGTTACATGTTTCCCTGTCCCCAGGACCTGGGTACGTATCCGCAGTGAGTCTGGGTTGGAGCATTTTTATGCAATATTCCAAAATGCTCCCAAAATAAGTGGATAGAAACGTAGCTCATTACAATAATGCATAATAATTTGTCCTAGCTGTGATTTGCTTTTCACTTTTGTTTCTGAATGCTCATCCAGGTCATACTCAGCCTCATTTTCCCACCTTTTATCCTGCTGTTGGACTTCCGTCTGGGAGATGACACGTCTCATCAGGTTGCTGTGGCCGATGAAGACAAAAAGACC[A/T]AAGATGATGAAAGATCCACTCGGGTAAAGTGGACGACTCTTCTTTTTCAAGCAAACCTCCCTGTAGATCTGTAAGCTGTTGAATGGACATTAAGACCTTAATTCTTAAGTTTATTTAGTTCATCTTTATTTGTATAGCACTTTCCCCCTAACCCTACTCCTCCAACCAAAGTAGAATGGAGGTACCCCAACTCATTCATGGTTATGCTTAAAATGGAGGGGTAGGGTGAAGTAGAAGCATTATGGACTAGTATTAGGTTTTGGTATTAGATTGTATTTATTGCACTTGTTGTAAATCTACCTTATTTACACCTAGGATGCCAATGCAGATGCAGCCTCTAAGAAAGGAGACGAGGAGGATGGAAATAAGAAAATGAGGCGTATTCCTATTGGGACGAAAATCTTTGAGTTCTACAACGCCCCTTTCACCAAGTTTTGGTTCAATACGGTGAGCACAATATTCAGCCATCTATTTCCCAAAGTGCTTCTCCTGTGTACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9727
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087497 | None | None | 297 | None | 8 |
| ENSDART00000123249 | Nonsense | 1095 | 1290 | 26 | 28 |
| ENSDART00000087497 | None | None | 297 | None | 8 |
| ENSDART00000123249 | Nonsense | 1095 | 1290 | 26 | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35429697)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34172962 |
| GRCz11 | 25 | 34613584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAAAGCAACACATTCTTTGAGGTTAAGTCCATCTCCAACCAGGTKTGG[A/T]AGTTCCAGAGATATCAGCTCATCATGACCTTTCACGACAGACCTGTGCTT
Long Flanking Sequence:
TAAATCGTAAGCAAAATGCTAAACATTCAACATTCAATTTTCAAGAAAAATAACCATGGTATAATGGAATTGTTTAAGTGAATCCAGCACAGATTCTGGCATGATAATGTAAAAGCTTTTTCTATACAGCACCCTGTGGGGAAAACCTATATGATGAGGATGGGAAGAAGCTTCCTCCGTGCATCCCTGGAGCTTGGCTGACTCCCGCCATCATGGCCTGTTACTTGTTGGTGGCCAACATCCTGCTGGTGAACTTGCTCATTGCCGTCTTCAAGTAAGGCTCCTACTATTACAGACTTCACTTATTAAGGGCATAAAATCAAAGAGCAAAAGATTTGTTGCAACATAAAACTCTTTTATGACCAATAAACTTTATCAAAACATGTTTATTGGTGCAACTCTGGTCAATCTCAGTAGTGTAATTCACTAGTTTCATGTGTTTTTCCTCCCATTAAAGCAACACATTCTTTGAGGTTAAGTCCATCTCCAACCAGGTGTGG[A/T]AGTTCCAGAGATATCAGCTCATCATGACCTTTCACGACAGACCTGTGCTTCCTCCACCGCTCATAATCTTGAGCCACCTCTACATCCTATTTCGCAAACTCTGCTGCCGCTGTAGCAAGAAAAAGGAGGGAGAACTGGATGAGAAAGATAAAGGACTGAGTGAGTGTCTTAAGATTATTGTACCAAATAATATGCAACTGATAAATTTGAGATGATTAATTGCTGTGTTTTCCTAATAAAGAGCTTATACTCACCCCGGATGAGCTGAAGATGCTGTACGAGTTTGAGGAGCAATGTGTAGAGGAGTATTTCAGGGAGAAAGAAGACGAGCAACTTTCCTCAAACGATGAGCGCATCAGGGTTACAAACGAAAGGTAATTTCATTACAGGAATACTAGTACATTAATGTCTGCTTGAACCGGAATCCATTTACATAATCTTGCTCCTGCTCAGGGTCGAGAACATGTCTATGCGCCTGGAGGAGGTTAATGAAAGGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15364
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087497 | None | None | 297 | None | 8 |
| ENSDART00000123249 | Nonsense | 1095 | 1290 | 26 | 28 |
| ENSDART00000087497 | None | None | 297 | None | 8 |
| ENSDART00000123249 | Nonsense | 1095 | 1290 | 26 | 28 |
Genomic Location (Zv9):
Chromosome 25 (position 35429697)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 34172962 |
| GRCz11 | 25 | 34613584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAAAGCAACACATTCTTTGAGGTTAAGTCCATCTCCAACCAGGTKTGG[A/T]AGTTCCAGAGATATCAGCTCATCATGACCYTTCACGACAGACCTGTGCTT
Long Flanking Sequence:
TAAATCGTAAGCAAAATGCTAAACATTCAACATTCAATTTTCAAGAAAAATAACCATGGTATAATGGAATTGTTTAAGTGAATCCAGCACAGATTCTGGCATGATAATGTAAAAGCTTTTTCTATACAGCACCCTGTGGGGAAAACCTATATGATGAGGATGGGAAGAAGCTTCCTCCGTGCATCCCTGGAGCTTGGCTGACTCCCGCCATCATGGCCTGTTACTTGTTGGTGGCCAACATCCTGCTGGTGAACTTGCTCATTGCCGTCTTCAAGTAAGGCTCCTACTATTACAGACTTCACTTATTAAGGGCATAAAATCAAAGAGCAAAAGATTTGTTGCAACATAAAACTCTTTTATGACCAATAAACTTTATCAAAACATGTTTATTGGTGCAACTCTGGTCAATCTCAGTAGTGTAATTCACTAGTTTCATGTGTTTTTCCTCCCATTAAAGCAACACATTCTTTGAGGTTAAGTCCATCTCCAACCAGGTGTGG[A/T]AGTTCCAGAGATATCAGCTCATCATGACCTTTCACGACAGACCTGTGCTTCCTCCACCGCTCATAATCTTGAGCCACCTCTACATCCTATTTCGCAAACTCTGCTGCCGCTGTAGCAAGAAAAAGGAGGGAGAACTGGATGAGAAAGATAAAGGACTGAGTGAGTGTCTTAAGATTATTGTACCAAATAATATGCAACTGATAAATTTGAGATGATTAATTGCTGTGTTTTCCTAATAAAGAGCTTATACTCACCCCGGATGAGCTGAAGATGCTGTACGAGTTTGAGGAGCAATGTGTAGAGGAGTATTTCAGGGAGAAAGAAGACGAGCAACTTTCCTCAAACGATGAGCGCATCAGGGTTACAAACGAAAGGTAATTTCATTACAGGAATACTAGTACATTAATGTCTGCTTGAACCGGAATCCATTTACATAATCTTGCTCCTGCTCAGGGTCGAGAACATGTCTATGCGCCTGGAGGAGGTTAATGAAAGGGAAA
Associated Phenotype:
Not determined