ZMP
scrib
Ensembl ID:
ZFIN ID:
Description:
Protein scribble homolog [Source:UniProtKB/Swiss-Prot;Acc:Q4H4B6]
Human Orthologue:
SCRIB
Human Description:
scribbled homolog (Drosophila) [Source:HGNC Symbol;Acc:30377]
Mouse Orthologue:
Scrib
Mouse Description:
scribbled homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2145950]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34144 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21043 | Essential Splice Site | Available for shipment | Available now |
sa12569 | Nonsense | Available for shipment | Available now |
sa12522 | Nonsense | Available for shipment | Available now |
sa12563 | Nonsense | Available for shipment | Available now |
sa21044 | Nonsense | Available for shipment | Available now |
sa34145 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34144
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 |
---|---|---|---|---|---|
ENSDART00000021013 | Nonsense | 88 | 1181 | 3 | 27 |
ENSDART00000074212 | Nonsense | 141 | 1724 | 4 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43950094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40940394 |
GRCz11 | 7 | 41220467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACGCAGCTCCGAGGACTGGCTCACCTATCACTCAATGACGTGTCGCTG[C/T]AGTCTCTACCCAATGACATAGGAAAGTGAGTTGATAAGAACAAATTCAAA
Long Flanking Sequence:
ATTTTTTATTATGAAAAAATAAGTGTATTTTTATTATTTGTTTATGCCGTCAATTCTTAGAAAATTGCAATAGGCTAAAATCGGTATTGACTGGTCACACTTATCAAAAAATCAAAATTGTAAAAGACTCATCTCTGATAAGCAGGATGGGAAAGGAAAAGATTTGTACTAAAAAGAGTTTACATATGTTGTGTTAAAATGCTGTAATGTTGTATTTAGAACAGGTGAGAATTTAGCAGGCTCATTTTCCCCTTATTTTGGGGTCAGAGAGTTCACACAACCATTGGAGGATGTCAACTTTATTCATCACTTGAGTACTTCCTACTCTTTATTTACATTAGAGCAGGAAGACGTGCACTGCTAGCAGTAACAGCCTTCAGAGGCCAAACCTTTTCCATTGTGCATCTCATTTTCCTTTTGTCTCTCTCGGTCTCAGGTTGCCTGATGGCTTCACGCAGCTCCGAGGACTGGCTCACCTATCACTCAATGACGTGTCGCTG[C/T]AGTCTCTACCCAATGACATAGGAAAGTGAGTTGATAAGAACAAATTCAAAATTGCATAAAATAAATCTTAATGTGGGAACAAAACATGCATTTCCTTTTAAAATTTGCTTTAAAAGTTATTTATTCTAGGTGCTAGAAAGAACTTTCTAGTCTTTTTAACAAGAAATAAATTAGGTTCATCGTGTCACCCACGGTCCAAAAAACATGTTTATTCCATTAACCACTGGACTCATTTTAACAAAGTAAATCCACACGTAGTTCTTAAGTTTTCTTAAATATTTTATCTCATTGTAATTGTGAAAATAACCAAACCTGATTCTTACCATGAATTTAGCCTTAAGCTAAGATGGTGCTATAAAAAAAGACATTGATATTAAATAATATAATATAATAATATAACATAAAATATTTCATTAGAGTAAGTATTTTATTTGTAGTTTGCTCTGCAAATACAAAATTGCCACAATGTAAAAAAAGTAGCAGATCTTTCGTATTGTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21043
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021013 | Essential Splice Site | 592 | 1181 | 15 | 27 |
ENSDART00000074212 | Essential Splice Site | 759 | 1724 | 17 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43967441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40957741 |
GRCz11 | 7 | 41237814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCATAGCAGGAGGGAAGGGATCTACTCCCTATAAAGGTGACGATGAGG[T/G]AAGTTTCCACGAGCTTTCAGTAGTTAATTCAGGTTTGCATTACAAACATT
Long Flanking Sequence:
ATTCTGAGAGTTTTAACTGTTTTGCTGGGTTGCTGTGCTTGTTTTGTCTTTAGTTAATATTCATGTTTTTTTAATGTATGTTTGTGCAAATAGCTAGTGCATAGTTTGACCATACAGTGATCCATGAATCTGAGCCATTTCATATGTAAACGAATGCTACATGTAATACTTGTGTATCAAGGAAAGAAGGCTGCTGGTTGGGACGGTATATTTGATCTGTTTGAACACAGATGTGTTCTTATTCACATTAGATATTTCTCCTAAGCATGCATGCACTGCATGAAAACTTCATGTTTTTGTTATTTTTTTGTTGGCGTTAAACCGTGAACATTCTTGCAAACCACTTGTGTGATGTGCTGTTTTACATTCTGCACGTTTATGATTTTCTGATGGTTTTGTTCATCTGTAGCTGACCTTGAGCATCCTGAGGCAGACTGGTGGATTAGGCATCAGCATAGCAGGAGGGAAGGGATCTACTCCCTATAAAGGTGACGATGAGG[T/G]AAGTTTCCACGAGCTTTCAGTAGTTAATTCAGGTTTGCATTACAAACATTTTAATCTTGCTATTTTAATGTTGGTCAAATCTGCCAAACCAGTTTTTTTTGCATGACTAATTCCAATCTAGTTTTGTAGTGTTTTTAAATCCATTGGAATATCTCATCGCCTACATTATTGTGTGAGCTACAGTAAATGATCTTCCTAACTCAGTGTGGATGTCAATTACAAATGTCAATTATTGTTTTACTCGCGCAAGTAAAAAAGTATAGTAACAGTTTACATGCCAGTAGGCAATGCACGCTTGCATCCAGTAAAAATAAGTAAATAAAAAAAACACAACAGACACATGAAATCACAGATATTCAGTGATTGTTAATGTTGCTAAGAAAACTAGTCCTTTAATGTGTAAACTTGTGCTTCAATGTGTAAGTGTGTGTTCAGTTTTTATTAATGTACTGCTTGTCCCTTTCAGGGTATTTTCATCTCTAGGGTGTCAGAAGAAGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12569
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021013 | Nonsense | 613 | 1181 | 16 | 27 |
ENSDART00000074212 | Nonsense | 780 | 1724 | 18 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43967968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40958268 |
GRCz11 | 7 | 41238341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCTAGGGTGTCAGAAGAAGGYCCTGCGGCTCSTGCTGGTGTCAAAGTT[G/T]GAGACAAACTTCTTGAGGTAAACAWCTGTGAGGATTTGTCTACTTTGACT
Long Flanking Sequence:
ATTCAGGTTTGCATTACAAACATTTTAATCTTGCTATTTTAATGTTGGTCAAATCTGCCAAACCAGTTTTTTTTGCATGACTAATTCCAATCTAGTTTTGTAGTGTTTTTAAATCCATTGGAATATCTCATCGCCTACATTATTGTGTGAGCTACAGTAAATGATCTTCCTAACTCAGTGTGGATGTCAATTACAAATGTCAATTATTGTTTTACTCGCGCAAGTAAAAAAGTATAGTAACAGTTTACATGCCAGTAGGCAATGCACGCTTGCATCCAGTAAAAATAAGTAAATAAAAAAAACACAACAGACACATGAAATCACAGATATTCAGTGATTGTTAATGTTGCTAAGAAAACTAGTCCTTTAATGTGTAAACTTGTGCTTCAATGTGTAAGTGTGTGTTCAGTTTTTATTAATGTACTGCTTGTCCCTTTCAGGGTATTTTCATCTCTAGGGTGTCAGAAGAAGGCCCTGCGGCTCGTGCTGGTGTCAAAGTT[G/T]GAGACAAACTTCTTGAGGTAAACATCTGTGAGGATTTGTCTACTTTGACTTTCTCCTTACAGAGGCGGTCATTAAAAAGAGCTCTCTGTCCTTGTGTTCATCTGCTCTCAGGTGAATGGAGTAGACCTGCACGGAGCGGAGCATCATACAGCTGTTGAAGCTTTGCGCAATTCAGGAGCAGCCGTGGTCATGACTGTTTTGCGGGAGCGCATGGTGGAACCAGAAAACGCCATCACCACCACACCGTTGCGGCCAGAAGATGATTATTTCCCCCGGGAGAGACGCTCCAGTGGGCTTCCTTTCCTCCTGGATCCTGATTGTCCCGCTGTTAGCACTGGACCCGCACAGCGACTAGCCACTTGTCTGATCCGCAATGATAAAGGCTTAGGCTTCAGCATTGCTGGTGGGAAAGGGTCAACGCTGTACAGAGTCGGAGACACGGTAAACAAAAGATGCTCTTGCAGATATACTTGTGACTTGCCCTGTAGTGAATATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12522
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021013 | Nonsense | 640 | 1181 | 17 | 27 |
ENSDART00000074212 | Nonsense | 807 | 1724 | 19 | 40 |
ENSDART00000021013 | Nonsense | 640 | 1181 | 17 | 27 |
ENSDART00000074212 | Nonsense | 807 | 1724 | 19 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43968143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40958443 |
GRCz11 | 7 | 41238516 |
KASP Assay ID:
2259-9314.1 (used for ordering genotyping assays)
KASP Sequence:
ACCWGCACGGAGCGGAGCATCATACAGCTGTTGAAGCTTTGCGCAATTCA[G/T]GAGCAGCCGTGGTCATGACTGTTTTGCGGGAGCGCATGGTGGAACCAGAA
Long Flanking Sequence:
CAGTGTGGATGTCAATTACAAATGTCAATTATTGTTTTACTCGCGCAAGTAAAAAAGTATAGTAACAGTTTACATGCCAGTAGGCAATGCACGCTTGCATCCAGTAAAAATAAGTAAATAAAAAAAACACAACAGACACATGAAATCACAGATATTCAGTGATTGTTAATGTTGCTAAGAAAACTAGTCCTTTAATGTGTAAACTTGTGCTTCAATGTGTAAGTGTGTGTTCAGTTTTTATTAATGTACTGCTTGTCCCTTTCAGGGTATTTTCATCTCTAGGGTGTCAGAAGAAGGCCCTGCGGCTCGTGCTGGTGTCAAAGTTGGAGACAAACTTCTTGAGGTAAACATCTGTGAGGATTTGTCTACTTTGACTTTCTCCTTACAGAGGCGGTCATTAAAAAGAGCTCTCTGTCCTTGTGTTCATCTGCTCTCAGGTGAATGGAGTAGACCTGCACGGAGCGGAGCATCATACAGCTGTTGAAGCTTTGCGCAATTCA[G/T]GAGCAGCCGTGGTCATGACTGTTTTGCGGGAGCGCATGGTGGAACCAGAAAACGCCATCACCACCACACCGTTGCGGCCAGAAGATGATTATTTCCCCCGGGAGAGACGCTCCAGTGGGCTTCCTTTCCTCCTGGATCCTGATTGTCCCGCTGTTAGCACTGGACCCGCACAGCGACTAGCCACTTGTCTGATCCGCAATGATAAAGGCTTAGGCTTCAGCATTGCTGGTGGGAAAGGGTCAACGCTGTACAGAGTCGGAGACACGGTAAACAAAAGATGCTCTTGCAGATATACTTGTGACTTGCCCTGTAGTGAATATTTAATGATGTGTTCATTTCTTTGGTGTCAGGTTTTGCAGGCTTTCTTTATCTCAGTGTTTGTTTATGAAGCCCAGGACACTTCTGTCAACATGTTTAGATTCACCTTGAAATCAAAACTGGCAATTTGTACAAATTTTACATTTGCACTTAGGGTGCTATTTAGATTCAGACACCCACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12563
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021013 | Nonsense | 640 | 1181 | 17 | 27 |
ENSDART00000074212 | Nonsense | 807 | 1724 | 19 | 40 |
ENSDART00000021013 | Nonsense | 640 | 1181 | 17 | 27 |
ENSDART00000074212 | Nonsense | 807 | 1724 | 19 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43968143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40958443 |
GRCz11 | 7 | 41238516 |
KASP Assay ID:
2259-9314.1 (used for ordering genotyping assays)
KASP Sequence:
ACCWGCACGGAGCGGAGCATCATACAGCTGTTGAAGCTTTGCGCAATTCA[G/T]GAGCAGCCGTGGTCATGACTGTTTTGCGGGAGCGCATGGTGGAACCAGAA
Long Flanking Sequence:
CAGTGTGGATGTCAATTACAAATGTCAATTATTGTTTTACTCGCGCAAGTAAAAAAGTATAGTAACAGTTTACATGCCAGTAGGCAATGCACGCTTGCATCCAGTAAAAATAAGTAAATAAAAAAAACACAACAGACACATGAAATCACAGATATTCAGTGATTGTTAATGTTGCTAAGAAAACTAGTCCTTTAATGTGTAAACTTGTGCTTCAATGTGTAAGTGTGTGTTCAGTTTTTATTAATGTACTGCTTGTCCCTTTCAGGGTATTTTCATCTCTAGGGTGTCAGAAGAAGGCCCTGCGGCTCGTGCTGGTGTCAAAGTTGGAGACAAACTTCTTGAGGTAAACATCTGTGAGGATTTGTCTACTTTGACTTTCTCCTTACAGAGGCGGTCATTAAAAAGAGCTCTCTGTCCTTGTGTTCATCTGCTCTCAGGTGAATGGAGTAGACCTGCACGGAGCGGAGCATCATACAGCTGTTGAAGCTTTGCGCAATTCA[G/T]GAGCAGCCGTGGTCATGACTGTTTTGCGGGAGCGCATGGTGGAACCAGAAAACGCCATCACCACCACACCGTTGCGGCCAGAAGATGATTATTTCCCCCGGGAGAGACGCTCCAGTGGGCTTCCTTTCCTCCTGGATCCTGATTGTCCCGCTGTTAGCACTGGACCCGCACAGCGACTAGCCACTTGTCTGATCCGCAATGATAAAGGCTTAGGCTTCAGCATTGCTGGTGGGAAAGGGTCAACGCTGTACAGAGTCGGAGACACGGTAAACAAAAGATGCTCTTGCAGATATACTTGTGACTTGCCCTGTAGTGAATATTTAATGATGTGTTCATTTCTTTGGTGTCAGGTTTTGCAGGCTTTCTTTATCTCAGTGTTTGTTTATGAAGCCCAGGACACTTCTGTCAACATGTTTAGATTCACCTTGAAATCAAAACTGGCAATTTGTACAAATTTTACATTTGCACTTAGGGTGCTATTTAGATTCAGACACCCACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21044
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 |
---|---|---|---|---|---|
ENSDART00000021013 | Nonsense | 906 | 1181 | 21 | 27 |
ENSDART00000074212 | Nonsense | 1073 | 1724 | 23 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43977766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40968066 |
GRCz11 | 7 | 41248139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATCGTATCTTGGAGGTGAACAGCATTGATCTGCGTCATGCCACACAC[C/T]AGGAGGCTGTTAGAGCCTTGCTTTCCAACAAACAGGAGATCCGTATGCTT
Long Flanking Sequence:
ATACAACCAAGCCTTAAAATTACATTCTGGACCACCCTTCTATTCAATACATAAAACGTGCCAGGAACCACAAACTTTTGAATGCTCTCTTTTTATTTGTATTGGTTTCTTCCACAAATTATTTAGCACTGCATTTATCAGAACTACTCAGTACAACTAAGTTTCCTGTCACAGGAAGTGACGCTGATCAAAGCAGGTGGACCCCTGGGTTTGAGCATTGTAGGGGGCAGCGACCATGCCAGCCATCCATTTGGAATTAATGAACCTGGAGTGTTCATCTCAAAGGTAAAGTTAACATTTTAAAGTTAACATTCATGATGAGCAAGTATGTTGTATGATAATGGTTTGTTATGATTTGTTAAGAAAAAGCTTGCATCAGATGATTTCTGACCTGTTTTTATGAATAGGTCATCCCCAATGGCCTGGCCTCCCAGAGTGGACTTCGCGTGGGTGATCGTATCTTGGAGGTGAACAGCATTGATCTGCGTCATGCCACACAC[C/T]AGGAGGCTGTTAGAGCCTTGCTTTCCAACAAACAGGAGATCCGTATGCTTGTGCGCAGAGATCCTTCTCCCCCTGGCATGCAGGTATACACACTAATTATTAGCAAAACCTGCTGCATGGATGTTTGCGGTAATTTGGTTTCTTAAGGGCGAAGCTGTTTACTCAGCTTCCAGACATCCACAAACCTTTAATTTTATCTAAACCAGTGTTTCACAACTGGCGGGTCTTGACCCACAAGTGTTATTTTATTTTATTTATTTATTTTTTTTTCTTTGAAAGATGTGTAAAAGCTTTGTTTATGTTCATGAGAAAAACATGTTGTCCTAAAGATTGTTTCAGACGGGATGTGTCGCCATGGGATGTGTTTGTCCATTTGCAGGATGTGAGGGTTTAGTTAAATTTCAGTTGAGGGTATGGCAAAAACCTGTAAAATGCAAATGATTTCACTGGTGACGTGAACATGCCATGCAAAGGCATGCACACGAAGTCCTCTTTTATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34145
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 |
---|---|---|---|---|---|
ENSDART00000021013 | None | None | 1181 | None | 27 |
ENSDART00000074212 | Nonsense | 1408 | 1724 | 33 | 40 |
Genomic Location (Zv9):
Chromosome 7 (position 43991031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 40981331 |
GRCz11 | 7 | 41261404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGTAGGCACAGTCCAGAACAGCGCTCCTTCAAAGACAGACAAAAGTA[T/A]TTCGAGATCGATGTGAAGCAACAGACTCCAGACAAACCCAAACCTCGCAT
Long Flanking Sequence:
TGTCTCGCCCTTCAGTGGAGCCAAAGGTACCATCGTCTCCAGCAGAAGCACTCTGACACTGGATGCTCTTCAGCTTGAGTGGTGGTGGTGCGGGTGTACAGGTCGCTTCCAAAATCGTTTTGCAGCATGTTTTTCAGTCAAGTATGGAAACGTGATCAATCAATGTTCTGTTTGAATCAATGCGGTTATTGTTGGTGAGAAAGAGGCTTCAGGAGAGCAGTAATTACAATATTTTTATTTTAGCAATGACAGCACATTAAGCAATCACTGCATTATGATGGTGGTGGATGGAAGATTTGCTTCTTTTGTGCTATTGCTCACTTCTTGTCTGAATTTCAGATCTTTATGGGAGCTGCTCGTGCATGTCAAAGGCATGTCAAATTTGGGTGCTTGCTAGACGGTGTTTACTAAACTGTTTTCCACTTTTCTCTCTGCCAGACCCCTTCGCCTCTGGGTAGGCACAGTCCAGAACAGCGCTCCTTCAAAGACAGACAAAAGTA[T/A]TTCGAGATCGATGTGAAGCAACAGACTCCAGACAAACCCAAACCTCGCATCTCACTGGTGGGAGAAGATGACCTGAAGAAAATGAAGGAGGAAGAAGGTTTGTGTTTGTTTGGTTGTCAGTCTTACTTTTGTCAAATTTGAGTCATGCTCAATCATCTGAATGTCGTTCCTCAGCAAAGCGAATTGAACAGAGGGCGCGAGAGTTCATGTTGGATGAAGATGAGGAGGAGGAAGAAGAGGATCTTGCCAAGCAAGTGGCACATATGAAGGCTCACGGAAAGGTTGTTCTTGATGGTGTGGAGTACAAGGTAGAGAGCTTGGGTTCCCCGACTTCACGGCAGTGTGCCACACCACCAAACTATAGTGCCACACCACCCAGCCACTGCGGAAGCTCAGGGTGAGCTACTCTCAGAGCTGCTGATTTATTTGTTGTGTTCCAGATGTGTTTGTTTGTTTGTTTTGTTTTGTTTTAGAACACAAACTGAACATCAGTAATCAGT
Associated Phenotype:
Not determined