ZMP
stab2
Ensembl ID:
ZFIN ID:
Description:
stabilin 2 [Source:RefSeq peptide;Acc:NP_001103503]
Human Orthologue:
STAB2
Human Description:
stabilin 2 [Source:HGNC Symbol;Acc:18629]
Mouse Orthologue:
Stab2
Mouse Description:
stabilin 2 Gene [Source:MGI Symbol;Acc:MGI:2178743]
Alleles
There are 21 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11372 | Essential Splice Site | Available for shipment | Available now |
sa11212 | Nonsense | Available for shipment | Available now |
sa15213 | Nonsense | Available for shipment | Available now |
hu7897 | Essential Splice Site | Available for shipment | Available now |
sa1575 | Essential Splice Site | Available for shipment | Available now |
sa11760 | Nonsense | Available for shipment | Available now |
sa31380 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11372
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 |
---|---|---|---|---|---|
ENSDART00000067253 | Essential Splice Site | 70 | 2508 | 2 | 67 |
ENSDART00000102534 | Essential Splice Site | 70 | 2509 | 2 | 68 |
ENSDART00000136000 | Essential Splice Site | 70 | 2444 | 2 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9787234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10723861 |
GRCz11 | 4 | 10722710 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAATGGATACGCTAAGATGCCACCAGGCACAAGCGATAGGGACTGCAGG[T/C]ACATATTYGTGTTTGTGTGTGTGNNNNTGGTTTTGTTTGCTTYACGAGAA
Long Flanking Sequence:
TCAATCTTCACTTCCCTACAGGGATATTTTTGCTACAAATGTTTACATTTTAGAGTAAAAATGTAGTAAATGTGGCACTTTAAGAGTTACTCACTCAGAAATTCCCTGATTTGACATGTATTGTTTAACATGCACTCGGGAATGCTGGGTAAAATAATCCCTAGAATGTCATTGGCCAGGCGCAAAGTCATGAACGAATCAGGTTAATCTCCTCGGAAAATCAGCGACAGGTGTCAAGATTCAATGTGATTTTCCTACTTTTCTAGTTTTGGGATATGCAGTATGAAAGAGAGCACATTTGTTTGCATTCTGTTGTTGTTGTGATTATTAATATCCCTTGTACATATGTGTGTGATTGTGTCTGTTTTCAGAAGCGCTGTGATAAGGATATCACGATGGTAACTAAATCCAAGTGTCATTCCTGCTCCTTATCACATTTAGCGAAGTGTCCCAATGGATACGCTAAGATGCCACCAGGCACAAGCGATAGGGACTGCAGG[T/C]ACATATTCGTGTTTGTGTGTGTGTGCATGGTTTTGTTTGCTTCACGAGAACCAGAGGTGTCTACTTAGACAGTAAAATCTCTAATCAGTGATGAAGATTACAGAATGTCATTAGCTATGCTTCCATGCATTTATTTTTTTCATGCACATGTTGGATAGAAAAAAATATGATGTGCATAAAATCCTAAAATGGGCTTTAAAATGTTTTCAAATAGGGTGGGTCATTTTTGGTAAGAGTTTACTCACAGTCTTTGTATACAAATAATAAAACTCAATGGAAGAAGACACCCTTACTATATGCTTGTACTGTACAGTGCTTAAAAATCATCATACCCTGTGAAAATACATACCTTCACTCACATTCCCCCCTGCTTTCATAACACCTACAGGATAAAGCTAGAGAAAGGCACAGAAGGTTGCAAAGTTATTCGGAATATGAATTGGTTTCAGGCTGGATGACAAATTAAGTAATTATTTCAAAGGGGTGTGATGATTTTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11212
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 |
---|---|---|---|---|---|
ENSDART00000067253 | Nonsense | 197 | 2508 | 7 | 67 |
ENSDART00000102534 | Nonsense | 197 | 2509 | 7 | 68 |
ENSDART00000136000 | Nonsense | 197 | 2444 | 7 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9792492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10729119 |
GRCz11 | 4 | 10727968 |
KASP Assay ID:
2259-4575.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGTGAGTGTANTTTTTTCTTCTCAGAGCTCCCAGCATGTGCTGCTTTG[C/T]AGTGTGGGCCGGATTCTCRTTGTMTCGAGGAAATGTTGACAGGGCAGCTT
Long Flanking Sequence:
ATGGTATAGCAGGCAATGGGACTTGCACTTGCGCAGTGAGCTTGCTTTCCTTGTTTTGCTCTGTCTGAATCAAGCACACTGCTGTCAATCAAACTTTTGGAGGTGTTTATTTATTTTATTTCATTTTTTGCAGTCTGGTTTTACAGGAGCAGCTTGCGAGGAATGCAAAACAGACTTATATGGACCCACTTGCAGTAATGGTAGAGAAAACCTTTTATTCTGTACTTCTGAATGAATTGGTTTGGGGTACTTTTGTGTTTGTATTCAGTCTATTGAATTTCTTGTGCTGGTTAGTGTGTCGTTGCAAGAATGGACTGTGTAGCAGCGGTTTGAAAGGAACAGGAGAGTGCACATGTTTTTCTGGGTACACCGGCCTAGACTGCGCCCAAGGTAAACCCTTGAACTCTTAAATTTCTCTTTGAGTGGGACATTGCACATTAAAGCAGCATTTGAGTGAGTGTATTTTTTTCTTCTCAGAGCTCCCAGCATGTGCTGCTTTG[C/T]AGTGTGGGCCGGATTCTCGTTGTATCGAGGAAATGTTGACAGGGCAGCTTGTGTGCAAGTGCAAACCTGGTTATCAAGGGGATGGAGTACAGTGTACATGTGAGTATATACTAAAATTACATATTATATTTTTAGTAATGTTTAACTTCATTTGTTTGTTTAAATTCAGCCCATATAAATTGTTTGCAACCAGATAGCTTAGTTTTTTTTTTAGCAAATCCAATGAATCATTTTTTTTTTCAGTGTGTGATAACAATTTAATGTGTCTTAATGTGTCAGTTATATGACATTATAACAATAATTGGTTATTGTCTTAAAAAACACTTAAAATGGGTCATTGATTTAAACATAATATGAGTTCAAATGCAAGATTTTTAAATATATATTTATAAAAGCATATTAGAAGCTATAGAAGAGCGTATTAATTAGTGTTTCAAGGAACCTACTGATGAACATTTGTTGTTAGCATATTAACAAAACATTTTTATTGACATTTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15213
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 |
---|---|---|---|---|---|
ENSDART00000067253 | Nonsense | 221 | 2508 | 7 | 67 |
ENSDART00000102534 | Nonsense | 221 | 2509 | 7 | 68 |
ENSDART00000136000 | Nonsense | 221 | 2444 | 7 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9792566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10729193 |
GRCz11 | 4 | 10728042 |
KASP Assay ID:
2259-4576.1 (used for ordering genotyping assays)
KASP Sequence:
MTCGAGGAAATGTTGACAGGGCAGCTTGTGTGCAAGTGYAAACCTGGTTA[T/A]CAAGGGGATGGAGTACAGTGTACATGTGAGTATATACTAAAATTACATAT
Long Flanking Sequence:
CACACTGCTGTCAATCAAACTTTTGGAGGTGTTTATTTATTTTATTTCATTTTTTGCAGTCTGGTTTTACAGGAGCAGCTTGCGAGGAATGCAAAACAGACTTATATGGACCCACTTGCAGTAATGGTAGAGAAAACCTTTTATTCTGTACTTCTGAATGAATTGGTTTGGGGTACTTTTGTGTTTGTATTCAGTCTATTGAATTTCTTGTGCTGGTTAGTGTGTCGTTGCAAGAATGGACTGTGTAGCAGCGGTTTGAAAGGAACAGGAGAGTGCACATGTTTTTCTGGGTACACCGGCCTAGACTGCGCCCAAGGTAAACCCTTGAACTCTTAAATTTCTCTTTGAGTGGGACATTGCACATTAAAGCAGCATTTGAGTGAGTGTATTTTTTTCTTCTCAGAGCTCCCAGCATGTGCTGCTTTGCAGTGTGGGCCGGATTCTCGTTGTATCGAGGAAATGTTGACAGGGCAGCTTGTGTGCAAGTGCAAACCTGGTTA[T/A]CAAGGGGATGGAGTACAGTGTACATGTGAGTATATACTAAAATTACATATTATATTTTTAGTAATGTTTAACTTCATTTGTTTGTTTAAATTCAGCCCATATAAATTGTTTGCAACCAGATAGCTTAGTTTTTTTTTTAGCAAATCCAATGAATCATTTTTTTTTTCAGTGTGTGATAACAATTTAATGTGTCTTAATGTGTCAGTTATATGACATTATAACAATAATTGGTTATTGTCTTAAAAAACACTTAAAATGGGTCATTGATTTAAACATAATATGAGTTCAAATGCAAGATTTTTAAATATATATTTATAAAAGCATATTAGAAGCTATAGAAGAGCGTATTAATTAGTGTTTCAAGGAACCTACTGATGAACATTTGTTGTTAGCATATTAACAAAACATTTTTATTGACATTTACTTATATGCAGTTCAGTGATCATACTTAATTGTAATCCATAATTGAAATTTACGTTTGATCTCAATCTAAAATTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7897
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 |
---|---|---|---|---|---|
ENSDART00000067253 | Essential Splice Site | 684 | 2508 | 20 | 67 |
ENSDART00000102534 | Essential Splice Site | 684 | 2509 | 20 | 68 |
ENSDART00000136000 | Essential Splice Site | 684 | 2444 | 20 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9801682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10738309 |
GRCz11 | 4 | 10737158 |
KASP Assay ID:
554-2405.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCTCAGTGACACTACTTTGATGCTTTTCCCCACCTTTTTATGACTCCA[G/A]AAGGCATACARWAGAGGCTGTGTTTTCAATAAGAAGCAACTTGGCCTGAG
Long Flanking Sequence:
GCCCTTCATAAGAAAAAAGTTTGGGTACTCCTGGTCTAAATTTGTAAGACCTCCTAAACTAAATTTGGAACGTTTAAAAGAGCATAACAGGATATTATAATGACGACATGTAAACCATAAACACAGTGACACCACTACAACACCAGAGAGGGCACTTTAAGATAACTAACTTCTTCAACATGTACATGATTCACCTTATTTTTTCTCTCTTTACAACACAGGTCGCCTTCCAGCTGTTTGTAATAATTGATCATTGTCTCTTTGTCACAGGCTCCATGTGTTAGCTGTACACTTATCTCCAAATCTACTTGTCCAACTGGTGAATCACTGGTAACTTTTTTCAATATTAGTGCATTTTAAAATTTAAAACAATAAAGATTACATAAAAATGATTATGAAAGCTTTGTTTAAAATTCCACCCTTTAGGTTGGCATTAATTTTCATAAAAATGTGCTCAGTGACACTACTTTGATGCTTTTCCCCACCTTTTTATGACTCCA[G/A]AAGGCATACAGAAGAGGCTGTGTTTTCAATAAGAAGCAACTTGGCCTGAGCTTACCCAGCATTGGCTGTTCCCACATCTGCAATGACACAAAGACTGTGAGTATTTATTTAACTTTAGACATTTTGTGTCTAACACATTTATGCATCATTTGCAGCTGCGTCTAGCTTATCAAAAGTCGTATTACCCGTTATTTGTCTTGACTAGACTCCTCAGTGCTGTAAAGGTTTTTTTGGACCTGACTGTTCCCCATGCCCGGGTGGTTTTACCACCCCCTGTTCCTCTCACGGGACGGTAAATCCTACACACATTCATACCTTGTGTACTATGTAGTATTTTTTTATTAAATAAGCTCCTATTGTCTTTTGTTTTAGTGCTCAGAAGGCATTGATGGAAACGGCACGTGCCAGTGTGAGCCCAAGTTCAAAGGATCGCGCTGCCAATACTGCGCTGACTCCAACAAATATGGCCCGAACTGTGACAAAAGTACAAATTCATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1575
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067253 | Essential Splice Site | 1005 | 2508 | 28 | 67 |
ENSDART00000102534 | Essential Splice Site | 1005 | 2509 | 28 | 68 |
ENSDART00000136000 | Essential Splice Site | 1005 | 2444 | 28 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9805820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10742447 |
GRCz11 | 4 | 10741296 |
KASP Assay ID:
554-1518.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAGRTGTCGACAAACCCAGATCTTCTGGGTTTTAACCAGTGGATCTCC[G/T]TAAGTTACACTTTAGTGTGTTTTTTATGTTGACATTTGTTTAAAAGCAAC
Long Flanking Sequence:
ATTTTACCAACAGTGATCAGATTGTATAACCAAAGTCATACCAGATGAATTGTGCTGAACTGAATTAGATATTAGATATGGACAAGTGTTTACTCGTTGTTTTTTGGAAATAAGGTGTGCAGTATGAAATGTAATTTTATTAGGGTTTTTATATGTATATGTAACTTATTTATCTATTTTTACTATGGAGAGCTCTGCTGTGACATGTGAATTTCCCTTTGGGGATTAATAAAGTCAAACCTAAACCTAAACCTAGTTACTGTTTACTATGTAGTCTGGGAGTGGCACAATTCTGTCTGCGCTGTCTGCGTTTCTCTTATTGTCGAATACATTTTAATTATGCTATGCAGAGGTGGGGCATTACTAAACGATATACTCTCTCAGATGCTATTGCTTCAAAGGAGTTTTTGATTTGATAAATATTCTATGTATTGTTTCATTTTGCTTTTCAGGAGGTGTCGACAAACCCAGATCTTCTGGGTTTTAACCAGTGGATCTCC[G/T]TAAGTTACACTTTAGTGTGTTTTTTATGTTGACATTTGTTTAAAAGCAACTATAGCTAATAGTTATCATTGATTTGCCAAGTATTTCAGAGGCTGTGTGTGCAGGTAGCAACGTTAAATAACCCCTGTTCATATGAATCTGCTGAAATGACTAAAGCTTATAGATGTCAGGCCAAAACCTTTGCTCAACTTTTTTGTAAAATTGCTTTTTTCAAAATCTAAAATTTAGAAAATTGTATTTTGTGGCCACAAATATACAATACTGCTTTGTTTTGTTGTTGTTGTGTGACTTGTGTCAGAAATGGTGTTGGCTAAAAACCCCTTTGGTTGCGATTTTGCAATTGAGCCACTAGATGGAGACAAGGCACTGTCTATTTTTTGTCGGTAACTGAATCATTCACACTTTTTTCATCAAAAGCATGAAATATTGACTGAGTATTTGCATTTGTTTGCTAAATTATACAAAAACAACGCTGTCAAGCACACACCTTTTTTTTGATC
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:
sa11760
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067253 | Nonsense | 1196 | 2508 | 34 | 67 |
ENSDART00000102534 | Nonsense | 1196 | 2509 | 34 | 68 |
ENSDART00000136000 | Nonsense | 1196 | 2444 | 34 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9809205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10745832 |
GRCz11 | 4 | 10744681 |
KASP Assay ID:
2259-4578.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCTAGGATTTGAATGTGACCAWGTATCACATTATACTGACYGAGATTT[T/G]AAAAGAYGTAGATTTGGTGGAKGGACTGTACAAGGACACCATGCTGGGCT
Long Flanking Sequence:
ATCAATTATTAAATTAAATTGTCAAATTATAGACTAGTTTGTTGATTTTAGTGTTTCACATTATTGAGCCATTTTAACCATGTTCCAATAATTTTGTGCTGTAAATGTTTCTGGGTTGTTTTTTTTTCTCTGTAGTGGGTGTAGCACCATAATCATGCACATGCTAACGGTATATCTAATATATTACTGAAAAGCAAAGATCTTACTCTACTTATCTTGCATTTATCCAGAACCACAACCTGACAAACGAAATGGAGGAATCTTTGGGTTTTACAGTGTTTGCTCCAACAGACAACGCAATACAAGATTACCTAAAAAGAACAGGCAAAGAATCATTGGTATCATACAAACACACTAATATGCATAGCCTTATTTAATATTATGCAGTATAGCATCTCATTCTTGCATCATGTATTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCTAGGATTTGAATGTGACCATGTATCACATTATACTGACTGAGATTT[T/G]AAAAGACGTAGATTTGGTGGATGGACTGTACAAGGACACCATGCTGGGCTTCCAATACCAACTGGGATTTTTCCGTCAAGATAAGAGAGTGCGTGCCAGATATGTTAATGTTTGCTGTCGGTTCAAACTACTTCTATAAAATAATAAGCCATTTGTTGAGTTTTTAGAGATTAAATTGAGCTTATTAAGCCAATATTTGAGTTTATTTTGGGACAGCTTATTTGTTTTATGTTCAATCTAACAACTTAAATGTCTTCATGTTGTCGCAACACAACTCATTTCTGTCATAAATATTTAATCATTGATATATTTGGGATTTTTCTATCGTAGTTGCTTGTAAATGAGGCTGAGGTGAATGTGACAGACTTGGAGACCAGTAAAGGCGTCATTCACATCATATCTGCTGTCCTCAACATCCCCAGCAATCGCTGTGACAAAGCTACCAGTATTCTTTTCTCGGTACAGTACAACTGTTTAACCTAGTAGATATTACAGTCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31380
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 |
---|---|---|---|---|---|
ENSDART00000067253 | Nonsense | 2308 | 2508 | 63 | 67 |
ENSDART00000102534 | Nonsense | 2309 | 2509 | 64 | 68 |
ENSDART00000136000 | Nonsense | 2296 | 2444 | 62 | 64 |
Genomic Location (Zv9):
Chromosome 4 (position 9824565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10761192 |
GRCz11 | 4 | 10760041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGCATCAGGAAAAGCATTCGTGAATCGCCTTCGGAACATCACTATC[C/T]AGTCCACTCTGTTTGTACCTGATAACGATGGTCTCTATAGCAACCAGGTG
Long Flanking Sequence:
ACTGACTTAACTAGTAGCTTACTACCTGCCTATTATTAATATATTGGTTGTTTATTAGTACTTATATATTCTGCATGATCTTATTTTACATCACAGGTGTCAAACTTAGTTCCTGGAGGACTGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATAAGCTAATTGAGTCCTTCAGTTGTGTTTGAAACCTACAGGTAAGTGTGTTGAAGCAGGGTTGAAACTACACTGTGTGGAACTACATCTCCTCAGGAACTGGATTTGACATCTGTGTTCTACATCCATAATCCTACCTAATATCTACTACCCTGATAACTATTGATAAGCAACAAATTAGTAGTTTATTGAGGTAAAAGTCATACTTGATAGTTTATTAATAGCAAGAATTGTACCGTGTGACCGACTGTTCTGTCTTTTTCAGCAAATCCTGAATTTTTCAACATCTGCATCAGGAAAAGCATTCGTGAATCGCCTTCGGAACATCACTATC[C/T]AGTCCACTCTGTTTGTACCTGATAACGATGGTCTCTATAGCAACCAGGTGACTCCCACATCCTTCTGCTACACTTCTCAATATTTTGTTTCTATATTTTAAAATGCCATTTCATTTTACTTCAGCACATCACTATGTTTGACAGAGAAATGTAGGTTTGATAGTATTAAGACAACATGGTTTTGTCAGATGATACAGTTTTCTTTTGTAGAATAATGTCTAATAGTACGGTTATCAAAACTGCTAGATATGTTTTTGCAATTGTTCTTTTTTGTGAAAGGATTTTTGATTATTAGTAAAAAACTAAATAAAGAAGTACAACCCAGCATTTATTTAAAATTGAATTTGTGTAAATGTTAAAGTCTTTATTGAAAACATTCAACACAACGTTTACGTTTTATGAACTTTTACGACATTTAAAATAGTTAAGATTTATAAAAATATATGTAATATTTTGATTTAGTCACTAATTCGTAAGAGTTTGTATGAACTATTATTATA
Associated Phenotype:
Not determined