Busch Lab

ZMP

sema3d

Ensembl ID:
ENSDARG00000017369
ZFIN ID:
ZDB-GENE-990715-2
Description:
Semaphorin-3D [Source:UniProtKB/Swiss-Prot;Acc:Q9W6G6]
Human Orthologue:
SEMA3D
Human Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D [Source:HGNC
Mouse Orthologue:
Sema3d
Mouse Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D Gene [Source:

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa36576 Nonsense Mutation detected in F1 DNA Not yet available
sa30702 Nonsense Mutation detected in F1 DNA Not yet available
sa19196 Nonsense Mutation detected in F1 DNA Not yet available
sa1661 Nonsense Available for shipment Available now
sa28980 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43051 Nonsense Mutation detected in F1 DNA Not yet available
sa44882 Nonsense Mutation detected in F1 DNA Not yet available
sa15069 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa36576
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101192 Nonsense 11 291 2 8
ENSDART00000127469 Nonsense 11 766 2 18
Genomic Location (Zv9):
Chromosome 18 (position 8651036)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9228414
GRCz11 18 9186433
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAATCTCCTCGTCCATCATGAAGACTGCAGGGGAGCCGGACAGACGG[A/T]GACAGAGGAGACAGGTCAGGACGGGACGGTTTTCATGTGCTTGGTGGTCT
Long Flanking Sequence:
ATGGCACTCTTTTGCCTAATGAAGCAGAGATTCAGACATGATCGTCGCCCCAGCCTCTCACAATTCAGAATACTGTTTGTTATTCAAGCAAGAATGGGAGACGTGGACAGAACAGACGAGGGATGGTGTGAGAAAATAAAAGAGAGGCATTTGAAAGAGGGCTGAAAGTGGCCGTCCTCATCAAGCTGACCTTTTGTTTAGAGACAAACAGATTTAGAAAGCATGCGTGTTGGTGGACAAAAGAATAGACTTGAATAGAGCAGCAGCTGATGCGGGGCTGCTAAAATGCATAGACATGCCTGAAAGAGACCACAGTAAAGCAGCTGAACATTCGTTTGGGATTTAATAAGACCTCAGACGCACACACACACACAAAAGCACACACCTCCCACAATGATGCTCTGACACTCCCTCTATCTAACTGTCCACTCCATCACAGGCCCACGGCTGCAGAAATCTCCTCGTCCATCATGAAGACTGCAGGGGAGCCGGACAGACGG[A/T]GACAGAGGAGACAGGTCAGGACGGGACGGTTTTCATGTGCTTGGTGGTCTACATCAGTGATGCTCTTCTTCTCTCTGCCTGAGGGGAACTGCATGAAGGAAAGTTTGCCAAGAGTTAAACTCGGCTACAAAGGTAAAGTTTATTTAACATTCCATTTAATCCCAAAGTTAAAGCTTTTCAAAATAATCTGTTCATTATTTGGTGTTTTGCCAAATTCTGCTGTATTTATTTGAAACATCTGCTGGTATGTTTGTCATTTTTAAAGGATACGTTTTGAAGTGCATGTTGGAGTGTGATGAGAGGTTTACAGCTCACTTGTATGAGGTCAATATTTAGACTGCACATCTGACTGATTGAGTGTACATAGGGGATGTGCGGCATATCAGTAGCAGTACGCAAGCTTTGTGTTGTATTTACTTCCAGGACACATACTTGGATGGACTGGATGATAATATATGATGTAAATATGTTTTGATTATAATTTAAGATGATTTTAGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30702
Status:
Mutation detected in F1 DNA
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
ENSDART00000101192 Nonsense 15 291 2 8
ENSDART00000127469 Nonsense 15 766 2 18
Genomic Location (Zv9):
Chromosome 18 (position 8651048)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9228426
GRCz11 18 9186445
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCCATCATGAAGACTGCAGGGGAGCCGGACAGACGGAGACAGAGGAGA[C/T]AGGTCAGGACGGGACGGTTTTCATGTGCTTGGTGGTCTACATCAGTGATG
Long Flanking Sequence:
TGCCTAATGAAGCAGAGATTCAGACATGATCGTCGCCCCAGCCTCTCACAATTCAGAATACTGTTTGTTATTCAAGCAAGAATGGGAGACGTGGACAGAACAGACGAGGGATGGTGTGAGAAAATAAAAGAGAGGCATTTGAAAGAGGGCTGAAAGTGGCCGTCCTCATCAAGCTGACCTTTTGTTTAGAGACAAACAGATTTAGAAAGCATGCGTGTTGGTGGACAAAAGAATAGACTTGAATAGAGCAGCAGCTGATGCGGGGCTGCTAAAATGCATAGACATGCCTGAAAGAGACCACAGTAAAGCAGCTGAACATTCGTTTGGGATTTAATAAGACCTCAGACGCACACACACACACAAAAGCACACACCTCCCACAATGATGCTCTGACACTCCCTCTATCTAACTGTCCACTCCATCACAGGCCCACGGCTGCAGAAATCTCCTCGTCCATCATGAAGACTGCAGGGGAGCCGGACAGACGGAGACAGAGGAGA[C/T]AGGTCAGGACGGGACGGTTTTCATGTGCTTGGTGGTCTACATCAGTGATGCTCTTCTTCTCTCTGCCTGAGGGGAACTGCATGAAGGAAAGTTTGCCAAGAGTTAAACTCGGCTACAAAGGTAAAGTTTATTTAACATTCCATTTAATCCCAAAGTTAAAGCTTTTCAAAATAATCTGTTCATTATTTGGTGTTTTGCCAAATTCTGCTGTATTTATTTGAAACATCTGCTGGTATGTTTGTCATTTTTAAAGGATACGTTTTGAAGTGCATGTTGGAGTGTGATGAGAGGTTTACAGCTCACTTGTATGAGGTCAATATTTAGACTGCACATCTGACTGATTGAGTGTACATAGGGGATGTGCGGCATATCAGTAGCAGTACGCAAGCTTTGTGTTGTATTTACTTCCAGGACACATACTTGGATGGACTGGATGATAATATATGATGTAAATATGTTTTGATTATAATTTAAGATGATTTTAGTCACTGTAAAGCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19196
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101192 Nonsense 41 291 2 8
ENSDART00000127469 Nonsense 41 766 2 18
Genomic Location (Zv9):
Chromosome 18 (position 8651128)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9228506
GRCz11 18 9186525
KASP Assay ID:
2261-1870.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGTCTACATCAGTGATGCTCTTCTTCTCTCTGCCTGAGGGGAACTG[C/A]ATGAAGGAAAGTTTGCCAAGAGTTAAACTCGGCTACAAAGGTAAAGTTTA
Long Flanking Sequence:
AATGGGAGACGTGGACAGAACAGACGAGGGATGGTGTGAGAAAATAAAAGAGAGGCATTTGAAAGAGGGCTGAAAGTGGCCGTCCTCATCAAGCTGACCTTTTGTTTAGAGACAAACAGATTTAGAAAGCATGCGTGTTGGTGGACAAAAGAATAGACTTGAATAGAGCAGCAGCTGATGCGGGGCTGCTAAAATGCATAGACATGCCTGAAAGAGACCACAGTAAAGCAGCTGAACATTCGTTTGGGATTTAATAAGACCTCAGACGCACACACACACACAAAAGCACACACCTCCCACAATGATGCTCTGACACTCCCTCTATCTAACTGTCCACTCCATCACAGGCCCACGGCTGCAGAAATCTCCTCGTCCATCATGAAGACTGCAGGGGAGCCGGACAGACGGAGACAGAGGAGACAGGTCAGGACGGGACGGTTTTCATGTGCTTGGTGGTCTACATCAGTGATGCTCTTCTTCTCTCTGCCTGAGGGGAACTG[C/A]ATGAAGGAAAGTTTGCCAAGAGTTAAACTCGGCTACAAAGGTAAAGTTTATTTAACATTCCATTTAATCCCAAAGTTAAAGCTTTTCAAAATAATCTGTTCATTATTTGGTGTTTTGCCAAATTCTGCTGTATTTATTTGAAACATCTGCTGGTATGTTTGTCATTTTTAAAGGATACGTTTTGAAGTGCATGTTGGAGTGTGATGAGAGGTTTACAGCTCACTTGTATGAGGTCAATATTTAGACTGCACATCTGACTGATTGAGTGTACATAGGGGATGTGCGGCATATCAGTAGCAGTACGCAAGCTTTGTGTTGTATTTACTTCCAGGACACATACTTGGATGGACTGGATGATAATATATGATGTAAATATGTTTTGATTATAATTTAAGATGATTTTAGTCACTGTAAAGCTTTAGAATTCCTTGAAATAATAATGTTTGTGTATATCCTAAAAATACAGTATGTTTGTATTTTGCATTTGGACACTGTCTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1661
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101192 Nonsense 257 291 8 8
ENSDART00000127469 Nonsense 257 766 8 18
Genomic Location (Zv9):
Chromosome 18 (position 8677228)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9254606
GRCz11 18 9212625
KASP Assay ID:
554-1608.1 (used for ordering genotyping assays)
KASP Sequence:
ATCCCTACAGAGGGCAAGTTCATTTCTGCCCATCCCATCTCAGACACCTA[C/A]AATCCTGACGATGACAAGATTTACTTCTTTTTCCGTGAGGCTTCTCGTGA
Long Flanking Sequence:
AAAGAACCAAAAGGCAGCCGTTCTGGCATGTAACTCACATTTTCAAAGCTGAATTTCTGACTTAGTATTGTTTTTCAGGTAAACAAGAATATTCACTCAGCATGTTTCTTAACAACTGCAAACATATTATGGTATTTGTATGCTTTAGAAGAGTAAAAAACTTACATACAACACCTTTAAGCCTAGTTTTACTAACAGCCAGTGCAAAAGTTTAGTTTATTTAGGTTTTTAGGCATGGACTCAGTTGTTTTTGCAGCAGACCTTATAACATTTGCATTTATGTTAAAGGTACTCTTACTAAAGTATAGTTTATGGGAGAAGATTAATTTAAGTTTGCATTTACTGGTAACAATTTTAATAAGCGTCCACACTTTCTTACAAGATTATAAAGGGATTGGTTGGATTACCATCACAGATATAAATTAAATCTGATCAGCTTTTGTCTCTCTTATCCCTACAGAGGGCAAGTTCATTTCTGCCCATCCCATCTCAGACACCTA[C/A]AATCCTGACGATGACAAGATTTACTTCTTTTTCCGTGAGGCTTCTCGTGATGGGAGCACTACAGACAAGAGCGTGCTGTCTCGTGTCGCCCGGATCTGCAGGGTAAGGCCCGTCCTCACGCTGCCTGATCACAGAGAAACTCACCTCATCTCTCTGATCCTCCTCAGAACTGAAGATTAAATGTGCTTCCTCTGGGGGGAGAGGCTTCCTGGTACGTTTCCCTTGATGTGATCTGCTGAAAGAGGACCAAACCACTGTCAGGCTGGGTAAATCAAAGTAGAGGTCTGGCCATGTAATTGCTGCCTGGACTGTCATTCCTGATCAGATGATCAGAGTCCCTTGGGTTGAGAAATTAATGTGTTAAGTGACTCCATTGTGTTAACACACAGCTTAAAGGGATAGTTCAAAATATGACAATTTAAACACTATTTACTTCCTCAAGTGGTATAATTTTCTTATTTTCTTAATACAAGATTTTTTTTTTTTTAAAAGAAAGCTGA
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:
sa28980
Status:
Mutation detected in F1 DNA
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
ENSDART00000101192 None 291 291 8 8
ENSDART00000127469 Essential Splice Site 291 766 8 18
Genomic Location (Zv9):
Chromosome 18 (position 8677331)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9254709
GRCz11 18 9212728
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGCACTACAGACAAGAGCGTGCTGTCTCGTGTCGCCCGGATCTGCAGG[G/A]TAAGGCCCGTCCTCACGCTGCCTGATCACAGAGAAACTCACCTCATCTCT
Long Flanking Sequence:
GTTTCTTAACAACTGCAAACATATTATGGTATTTGTATGCTTTAGAAGAGTAAAAAACTTACATACAACACCTTTAAGCCTAGTTTTACTAACAGCCAGTGCAAAAGTTTAGTTTATTTAGGTTTTTAGGCATGGACTCAGTTGTTTTTGCAGCAGACCTTATAACATTTGCATTTATGTTAAAGGTACTCTTACTAAAGTATAGTTTATGGGAGAAGATTAATTTAAGTTTGCATTTACTGGTAACAATTTTAATAAGCGTCCACACTTTCTTACAAGATTATAAAGGGATTGGTTGGATTACCATCACAGATATAAATTAAATCTGATCAGCTTTTGTCTCTCTTATCCCTACAGAGGGCAAGTTCATTTCTGCCCATCCCATCTCAGACACCTACAATCCTGACGATGACAAGATTTACTTCTTTTTCCGTGAGGCTTCTCGTGATGGGAGCACTACAGACAAGAGCGTGCTGTCTCGTGTCGCCCGGATCTGCAGG[G/A]TAAGGCCCGTCCTCACGCTGCCTGATCACAGAGAAACTCACCTCATCTCTCTGATCCTCCTCAGAACTGAAGATTAAATGTGCTTCCTCTGGGGGGAGAGGCTTCCTGGTACGTTTCCCTTGATGTGATCTGCTGAAAGAGGACCAAACCACTGTCAGGCTGGGTAAATCAAAGTAGAGGTCTGGCCATGTAATTGCTGCCTGGACTGTCATTCCTGATCAGATGATCAGAGTCCCTTGGGTTGAGAAATTAATGTGTTAAGTGACTCCATTGTGTTAACACACAGCTTAAAGGGATAGTTCAAAATATGACAATTTAAACACTATTTACTTCCTCAAGTGGTATAATTTTCTTATTTTCTTAATACAAGATTTTTTTTTTTTTAAAAGAAAGCTGATATCCTGTAACCATTGACATCCATAGTAGAAATATACTATGGAAGTTAATGGTTACAGGTTTCCAACATTTTTTAAAATATCATTTTTTCAATATCAATAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43051
Status:
Mutation detected in F1 DNA
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
ENSDART00000101192 None None 291 None 8
ENSDART00000127469 Nonsense 318 766 9 18
Genomic Location (Zv9):
Chromosome 18 (position 8680960)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9258338
GRCz11 18 9216357
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACAAGTGGACAACATTTCTCAAAGCGAGACTCGTGTGCTCCATTCCT[G/T]GACCAGATGGAGTGGACACACACTTTGATGAGCTCCGTGAGTGATGTGTT
Long Flanking Sequence:
TGGCAGTAATGAGGAGATCTGTTTAAGTGTTCTCAGCATGTCTTCTCTTTCTGAGACCTTTCAGTGATCTTTTGTGCATCTAAATACGTAAAACCTGCTCATGGAGAGGGTCATTATATTCTCTTTATAAACTCTCCTTGCTCGCTTTTCTCCATTTCTTGAACAGTCTTTCTTTGTCTCTCGTGTGTGCATTTGTGCTCCTCTTTAGCCTTTGTGTTACTGAAGGGCTTGTGGTTTGCTGTCGTCTTATGCTTAATTGAATAAGCTGCTTTAATCAGAAGCAAATGCTGGGTTTACATTTTATTATGAAAGTCTATAAAATATATAATAACTGAGGATTTAAATGATAAACACATGCTTTCGGAATGACTTCACTGAAATGTCCTATATTTGCGTGTGTCTGTGTGTGTTTTTGCATGAAGAACGATGTTGGAGGTTTGAGAAGTCTTACTAACAAGTGGACAACATTTCTCAAAGCGAGACTCGTGTGCTCCATTCCT[G/T]GACCAGATGGAGTGGACACACACTTTGATGAGCTCCGTGAGTGATGTGTTTTATGTTACTTCTCCCTCCCACAAACGCATATTTTAGATTTATCAGACTTTTTAAAATGTGTGTATGTGTGTGTGTGTTACAGAGGACATCTTTCTTCTCCCTAGCAGAGATGAGAAAAACCCTATGGTGTATGGAGTGTTCACCACTACCAGGTTAGTGTGTCCAACGCAAGCTCACGGCAATTCGTAACTTTTTGATTCAGTGGTTATTTCGTATGAATTCGTACGATATAGTTTGTACAATTTAGTACGATTTGCTCATCATCCAATGACAGTTGGGGTTAGGGGTGGGGTTGGGTGTCACGACCTCCTTTCTAAAAACGGATATTTTCGTACGACTGAACTAAACTGACAAAACGTAAAATACTTACGTTTTCTTGTAAGATCAGGCTGGTGTATCAGTATTTTTATCTTGGTACTGAAGCTTGAAAAGCAACCCAAAATACAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44882
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101192 None None 291 None 8
ENSDART00000127469 Nonsense 597 766 17 18
Genomic Location (Zv9):
Chromosome 18 (position 8693646)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9271024
GRCz11 18 9229043
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTTTTTGATATGCTGATCGCTCCCTCTCTCTTTCGCTTTTGCAGTGT[T/A]AGGGAGGAATGTCGAGGAGAAGGTGTTGTACGGAGTGGAGAGTAACTCCT
Long Flanking Sequence:
GTAATGTTATTGATCAATTCTAAAATGTAATCAAGGTTAATCTGATGCATGCTCAATTAAAGGCTTTCTGATGTGTGCTTACAGAAGGGCCAGAAGGCAGGACATCAAACATGGAGACCCATCCAGCCATTGTTGGGACACAGAGGATGGTAAGAAAGCATATGAGGGCGTACAGTCTGTGTGTGTGTGTGTGTGTGTGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTCTCTGTGTGTGTGTGTGTGTGTGCGCAGCATAAAAGCACTAAAAGCTCTGTTTTGTTTTAAGATGCTGCATTGTCCTGTGGGGCTCACCTAATGGACCTCAATGTTAACCCAAAAAAATGTCTTTTTGATATGCTGATCGCTCCCTCTCTCTTTCGCTTTTGCAGTGT[T/A]AGGGAGGAATGTCGAGGAGAAGGTGTTGTACGGAGTGGAGAGTAACTCCTCTTTTCTTGAGTGCGTTTCGAAATCCCAGCAGGCCTTGATCCGCTGGTTTGTACTGAAGCCAGGAGTGGACCACCGTCAAGAGGTATCAGTAACCTAGAGTACATCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGCTGTGCGTGTGTGTTTTTTGTTCACCTACTTTGTAGCTACACTGAAAAAATATTCATTGGATTTACTAGATTTTTTAAGGTAACTGGTTGCAAACAATTCAACACAGGGTCATTCTGAAAACGTAGCCCTATATACATTTCTGGAGGTCGCAAATTATGTAGTCAGAAGTACGTGTGGCTGCATTTCATCTTTCATCTTCCTTTTCATGCTTACCAGCTGACCACTTACCTCCATGTGGACAGCTTTCCCGTTGTTACCAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15069
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101192 None None 291 None 8
ENSDART00000127469 Essential Splice Site 641 766 17 18
Genomic Location (Zv9):
Chromosome 18 (position 8693781)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 9271159
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGAWCCGCTGGTTTGTACTGAAGCCAGGAGTGGACCACCGTCAAGAGG[T/C]ATCAGTAACCTAGAGTRYATCAGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Long Flanking Sequence:
GGACACAGAGGATGGTAAGAAAGCATATGAGGGCGTACAGTCTGTGTGTGTGTGTGTGTGTGTGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTCTCTGTGTGTGTGTGTGTGTGTGCGCAGCATAAAAGCACTAAAAGCTCTGTTTTGTTTTAAGATGCTGCATTGTCCTGTGGGGCTCACCTAATGGACCTCAATGTTAACCCAAAAAAATGTCTTTTTGATATGCTGATCGCTCCCTCTCTCTTTCGCTTTTGCAGTGTTAGGGAGGAATGTCGAGGAGAAGGTGTTGTACGGAGTGGAGAGTAACTCCTCTTTTCTTGAGTGCGTTTCGAAATCCCAGCAGGCCTTGATCCGCTGGTTTGTACTGAAGCCAGGAGTGGACCACCGTCAAGAGG[T/C]ATCAGTAACCTAGAGTACATCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGCTGTGCGTGTGTGTTTTTTGTTCACCTACTTTGTAGCTACACTGAAAAAATATTCATTGGATTTACTAGATTTTTTAAGGTAACTGGTTGCAAACAATTCAACACAGGGTCATTCTGAAAACGTAGCCCTATATACATTTCTGGAGGTCGCAAATTATGTAGTCAGAAGTACGTGTGGCTGCATTTCATCTTTCATCTTCCTTTTCATGCTTACCAGCTGACCACTTACCTCCATGTGGACAGCTTTCCCGTTGTTACCAGTTTGTCCAGTGGTTTGCACCATACGTTGGCCCCAAGACCCCGACAATGGGGTTCAAGTCTGATGAAGGTTGGTTCCAAAAAGCAGGTAAAACAAAAACAAAAGGCAAAAAATAAAATAAATAAGTAAATAACAGTGT
Associated Phenotype:
Not determined