Busch Lab

ZMP

sema4e

Ensembl ID:
ENSDARG00000052997
ZFIN ID:
ZDB-GENE-990715-7
Description:
Semaphorin-4E [Source:UniProtKB/Swiss-Prot;Acc:Q9YHX4]
Human Orthologue:
SEMA4D
Human Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Mouse Orthologue:
Sema4d
Mouse Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa9636 Essential Splice Site Available for shipment Available now
sa9433 Nonsense Available for shipment Available now
sa33031 Nonsense Mutation detected in F1 DNA Not yet available
sa19891 Nonsense Available for shipment Available now
sa39940 Nonsense Mutation detected in F1 DNA Not yet available
sa33032 Nonsense Mutation detected in F1 DNA Not yet available
sa33033 Nonsense Mutation detected in F1 DNA Not yet available
sa38359 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9636
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056252 Essential Splice Site None 766 None 16
ENSDART00000108861 Essential Splice Site 13 762 None 15
ENSDART00000109471 Essential Splice Site None 766 None 16
Genomic Location (Zv9):
Chromosome 2 (position 50142495)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49838027
GRCz11 2 49572257
KASP Assay ID:
2259-2692.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGAACCACTGATGYGTCACAGGARAACTGAGAGACYAACTTGGAAAGG[T/A]AGGCGYATGGGAAGTTGCTGCTGGTCCGGTTTTGACTATTGCWGCATCGT
Long Flanking Sequence:
CACAAAGGTAGGAACACACTCGCATTCTACTTTTTTTTAAAGTGTGAACACAAAGTGTGTTTTTAGGTAGTAAGAAAACCAAAACGTGATTTTCTTTTGTTTACTACAATAGATAAGCTGGTTTTATCTAAGATCAGAGCTTCGAGAACATGACACTCTCCTACACTCCTCCTCTTTCACACACACACACTTGCTCACACTTGTAGTGGCTTGTCTGAGATTGAGGAGTTTCTAAAAGCATGTTTTTTTTCCTCTTTTCTCTCCAGCTGAAGAATGTCTTTTGCTTCACGCTGCAGGATTTAGGCAGTTTAGCGCTCTCTCACACAAAGCAGCAGACACCATGAGCTCCATTCACTGCAGAGCCACGACTCCCAACACACTTTCTGCTGTCTCTGACACTTAGAGCACTTTGATTTGTGCATTGGAGAGCTGGAATAGTGTGTGTGTGAAGAGGAACCACTGATGTGTCACAGGAAAACTGAGAGACTAACTTGGAAAGG[T/A]AGGCGCATGGGAAGTTGCTGCTGGTCCGGTTTTGACTATTGCTGCATCGTAAAACGTGTTTTCAGAGGAATTTAGAGCGATATTGTAATGCATTGGATTTGCATATATGGCCTCTGATTGTATTCTGCTGCACTTTTTTTGTGTGCATCTCAGTTTTTGGACATTTACACCACAAACTGATTTTTTCTTTGCAATTTTTAACCAAACTAATGCACAATGTTCTTTTTTTATTGTAGTTTAATTTATATACATTGTTTAGCATAAATGAGTACACCCCCTAGGATAATTTACAATAATATATTTGTGCATATACAATTAAAGTCAGCAATTATTAGCCCCCCTTTGTTTTGTTTTTTTTTCTTCTTTTTTAGTATTTCCCAAATGATATTTAACAGAGCAAGGAAATTTTCACAGTGGGTCTGATAAAATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGTTTCTAATTTTTTTCAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9433
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056252 Nonsense 9 766 3 16
ENSDART00000108861 None None 762 None 15
ENSDART00000109471 Nonsense 9 766 3 16
Genomic Location (Zv9):
Chromosome 2 (position 50150714)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49846246
GRCz11 2 49580476
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTATAACAAGAGCACTGAATGATGTCTCTGCTGGCTGTTCWGTG[T/A]GTTTTGTATGTCTGGAGTCCAGCAATGCTGACCGGTGGGCTKGGATCAAC
Long Flanking Sequence:
TCGAAGCATTCGTGAGCATGTCACTTGCGAAAGCAGTTTTGGTTAATGCTATTGCTAGGTGTATTTCAGGATGTGGTGAGTTTTTTTTTCTTTCTTTTTTTTTAAGCTGTTCTAGCTTTGTGTCATTCTGAGGCTTGAAAAAGCAGAATCGTGTGTCTCTGTCAAGGTCCCAGAGCAAAAGCTTTCATCCTCTGCATTAGCATCACTATAGAAGTGACAGAAATACTTCTGCCAGCACCCCTGCCTGTACTCTCTCTCTTTCTCTCTCATTCAGATGGCCTCACAGCGCTCTTTGCTGCTTCTTTGAAGGGCATTCTTTGCAGCTAAAGTCATATATCTCAGTATGGAGGATCTCCGAACTGAAGCAGGGCAGAAGACAAGGATGAGAAAGCTTTGACAGAAAGACCACAGAGGAATTTTGCAATCGCAGACCGAAATCACGGACTGATTTTTTTTTTATAACAAGAGCACTGAATGATGTCTCTGCTGGCTGTTCTGTG[T/A]GTTTTGTATGTCTGGAGTCCAGCAATGCTGACCGGTGGGCTGGGATCAACACTGGATAGCCTACCTCGGAAAACAGTGCCAATTGGAAGTAAGTTGACTTTTTGAAAATCACATTTGATTATTATTAGAAAAAAGTGCCAGTGCTGTTTGTCACTATCATTGGCTAATATTTATAAATGCACTTGGGTACTTAAAAAAATTACATTCATTAGATACATAAATAGTAGTAAATTAATATTTTATTTCCATTTTCTTATTCAAAGGTGCTGAAATTTTAAAGTGCTTTCAGCTGTATTTTTAGCAGCATATTAAGCTTAAAATCATGTTCTTATACAGTTAAAGTCAGAATGATTCACTCTTCTGTGAATTTCTTTTCAAATATTACCCAAATTATGTTTAACAGAGCAATGACTTTTTTACAGTATTTTCATAATATCTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGTTAGAATAAAAGCAGTTTTAAGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33031
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
ENSDART00000056252 Nonsense 116 766 6 16
ENSDART00000108861 Nonsense 112 762 5 15
ENSDART00000109471 Nonsense 116 766 6 16
Genomic Location (Zv9):
Chromosome 2 (position 50157196)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49852728
GRCz11 2 49586958
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCGTGTTGTTTTTGTCTTCTTCTTTAGAATGACTGCAAAAACTATATT[C/T]GAATTCTTCATAAAAAGGACGACGGCAGAATGTATGTCTGTGGAACCAAA
Long Flanking Sequence:
TGCTACCCACTGCGCCACCATGGCACCAACATTCCTGGAGAGCCATAGCTCTGCACAGTTTAGTTCCAACCCTGATTAAACACACCTGATCAAACTAAATGAGTCTTTCAGGCTCGTTTGAAACTTAGATAAGTGTGTTGGAGCAGGGTTGGAACTATACTATGCAGTGCAGGCATAGTGTGTAGCGTGCCATTTAGGAAGCAACTTGTAAATTAATCTGTTATTTACACTGTAAGTTGCAGTATTATAATCACTTATTAGCATTAATACATTTTTACTACTACTTTGGTAATTAGTGATGTAACATATTATACAAATATGAAGATGTTTAAGACTTACAAAAGCACCGTCTGAGGAAGTGGCTTTTGTATGTTTATTTACAGCAGATAAAAGGAAGTGTGTGTTGTAGCTTGGTCAGACATTGTGGTCAGAAAAGATCTTTGAGTTATTCCCCGTGTTGTTTTTGTCTTCTTCTTTAGAATGACTGCAAAAACTATATT[C/T]GAATTCTTCATAAAAAGGACGACGGCAGAATGTATGTCTGTGGAACCAAAGCGTTCAACCCCACCTGTGGCTATTTGGTAAGTGTCATCCATTTAATTCAGTGTTTGTTAGTGACCACAAATGTAGAATGTGCATCGTTTATTTGGTTGTTGCATGTTATTCTCATAGTCCTATGCGGATGGTAAGCTGACTTTAGAGATCCTCCAAGAAGATACGAAAGGGAAATGTCCGTTCGACCCTTTTCAGCGATATACATCTGCAATGGTCGGTACGTACTGCTTAGTTGTTTATTGACTAGATAATTTGTATTCATATCTGCAACACTCACAGTTTCATTTATTGCAAGTATTTTTACACATATAGTAATCTCTGCCTCGGTTTTCTCTCTCAGATGGAGCGTATTACTCTGCTACTTCAATGAACTTTCGGGGTTCAGAGCCGGTGATGATGCGCAGCACAGAGGAAAGCATTCGAACTGAGTTTACAAGCACCTGGCTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19891
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056252 Nonsense 161 766 7 16
ENSDART00000108861 Nonsense 157 762 6 15
ENSDART00000109471 Nonsense 161 766 7 16
Genomic Location (Zv9):
Chromosome 2 (position 50157424)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49852956
GRCz11 2 49587186
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGTAAGCTGACTTTAGAGATCCTCCAAGAAGATACGAAAGGGAAATG[T/A]CCGTTCGACCCTTTTCAGCGATATACATCTGCAATGGTCGGTACGTACTG
Long Flanking Sequence:
ACTGTAAGTTGCAGTATTATAATCACTTATTAGCATTAATACATTTTTACTACTACTTTGGTAATTAGTGATGTAACATATTATACAAATATGAAGATGTTTAAGACTTACAAAAGCACCGTCTGAGGAAGTGGCTTTTGTATGTTTATTTACAGCAGATAAAAGGAAGTGTGTGTTGTAGCTTGGTCAGACATTGTGGTCAGAAAAGATCTTTGAGTTATTCCCCGTGTTGTTTTTGTCTTCTTCTTTAGAATGACTGCAAAAACTATATTCGAATTCTTCATAAAAAGGACGACGGCAGAATGTATGTCTGTGGAACCAAAGCGTTCAACCCCACCTGTGGCTATTTGGTAAGTGTCATCCATTTAATTCAGTGTTTGTTAGTGACCACAAATGTAGAATGTGCATCGTTTATTTGGTTGTTGCATGTTATTCTCATAGTCCTATGCGGATGGTAAGCTGACTTTAGAGATCCTCCAAGAAGATACGAAAGGGAAATG[T/A]CCGTTCGACCCTTTTCAGCGATATACATCTGCAATGGTCGGTACGTACTGCTTAGTTGTTTATTGACTAGATAATTTGTATTCATATCTGCAACACTCACAGTTTCATTTATTGCAAGTATTTTTACACATATAGTAATCTCTGCCTCGGTTTTCTCTCTCAGATGGAGCGTATTACTCTGCTACTTCAATGAACTTTCGGGGTTCAGAGCCGGTGATGATGCGCAGCACAGAGGAAAGCATTCGAACTGAGTTTACAAGCACCTGGCTCAGTGGTGAGAAAGTGTTCATGTCTAAACTAACCACCAAACACAATGTGAAAAAATGCAAGAGCACACTCAGTACGATACCCTTGTACATAACCACAACATACTTGCAAACTGAATGCACAGCTTATCAGATTTTTAGAACAAAGGCTACTGATAAACTGTTAAAGGTCCCATGAAATTAAAGTTTTTTTAGTCAATATCAGTATGTTAGTTTAAGGATATCTATAGTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39940
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
ENSDART00000056252 Nonsense 272 766 10 16
ENSDART00000108861 Nonsense 268 762 9 15
ENSDART00000109471 Nonsense 272 766 10 16
Genomic Location (Zv9):
Chromosome 2 (position 50161013)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49856545
GRCz11 2 49590775
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAATCATTTTATCCTCCCAGGGTGACTTGGGTGGGCAGAGAACGCTA[C/T]AAAAGAAGTGGACGTCATTTCTAAAAGCTAGGTTCGACTGTCAAGTTCCA
Long Flanking Sequence:
CCATAACAAAAAAAGAGTTTTTTTCATAAAAAAAGGTTAATGTCCCTATAAAATGATTATTGGTGCCAGGCAGGGTAGTTTGAGTATCTGTTGATTGCAGTCGTTTACAGAAATTTTGCACACACACACACACACACACACAAATCTGTAGTTCTGCGGGTGAAAACATGTTTACTCTTATATTAGAGTGATGCAAAAAACTAAAATAGTTTTGTCATTTTAGAACCAAATTTTATCCACATGGCCCACATACCAGAGGGCCAATCTAATCCAGATGGGGATGATGACAAGATCTATCTGTTCTTCAGTGAGACGGCAGTGGAATATGAGTCATACACAAAGGTGGACGTGTCTCGAGTGGCTCGTGTGTGCAAGGTAAACTCCCTTGAGGTTATGCATCTATTTGAAGAAATGTTACAGGATTTCCTGTCGACCACGTATAACATCTATTCAAAATCATTTTATCCTCCCAGGGTGACTTGGGTGGGCAGAGAACGCTA[C/T]AAAAGAAGTGGACGTCATTTCTAAAAGCTAGGTTCGACTGTCAAGTTCCAAACACCAATCTCCCTCTTCTGGTGCAGGATGTTTTCCACTTGTGTCCAGATGACTGGACCACCTGTGTTTTTTATGCTGTCTTTACCCCACAATCGTAAGTTTGAGCTGTTGATTGTGAAAACAAAGCATATTTGATCATATCTTGAATTCATAACAACCACAAACAGCACCCTTGAAAATCTTTTAATTCAACAAACCTCAAGAATTATTATTAGTTATAGATTATTATTAGCTATAGGTTTAGATCAGGACTCTGGGCAGGACTTTTCATTAATTCAGAGTTTTATTATAGTGGAAATCAAAACTAGAGAACATAGATCTGCATAGCTCTGTTTGAAGGGGTCAAATGAGCAGTTTTAAACATGCTTCATGAGTTGCATTAATTCTGATGGACAGTTTAAAAACTTGAAAATGAACACTAATTCTCTATCAAAAAATCTAATATAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33032
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
ENSDART00000056252 Nonsense 637 766 16 16
ENSDART00000108861 Nonsense 633 762 15 15
ENSDART00000109471 Nonsense 637 766 16 16
Genomic Location (Zv9):
Chromosome 2 (position 50173357)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49868889
GRCz11 2 49603119
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTACATCTGCAGCTCCATCGAGACCGTCTCCCAGCGCAAATACCAGACT[C/T]AGCATGTAGCGTATGATGTAAAGATGTGGTCCGAATCTGGAACCACAGCG
Long Flanking Sequence:
GTGTGAAAGCGAACCGCTCCAATAGCAAAGAGCAACAATGTAACATTTGTAATCTCTGTTTCGGAACAACTGAATCGATTCACAGGTGTGAAAGCACCCTTAGACTTCAACATTTTTTAAATTCAACAGAAACTTTTTTTTTCTTAATGACAGGCACAGATGTATTGTTCACCACAAAACTAGCAATGTACGCTAACAAAATCAATATGGTTAGCTCTGATTTCATCTCTACTTCGAATGTTACATCTAGAACTTGTGTTACAGGTGTCAGTAAACCAGTCAACATCTCCTTTTACCACGGGAATACTGTGAAGCTGGGCTGCCAGCCTTATTCCAACCTGGCGCAGGTTGAATGGCAGTTAAACGGGGAGCCAATCAAACCATCAAATACCATCCAGATCCTCTCCGATGGCTTGATGATATTCAACGCATCTTTGGACGCCACCGGCTACTACATCTGCAGCTCCATCGAGACCGTCTCCCAGCGCAAATACCAGACT[C/T]AGCATGTAGCGTATGATGTAAAGATGTGGTCCGAATCTGGAACCACAGCGTCACTTCATCATGTTAAGGAAAAAGAGCGCACCCTAGTGGCCATGGTGGTGATACTGTCACTAGTTCTAGCTGCATTGTTGATATGGAACCTGTACAAAGGCCATTTGTCTCTGCCATGTTTACACAGGAGGGTAAAAGACACGCAAAACAGGCACGAAGACGATGCTAACCAGGTTCAGCCACAGAGACTAGCATCATCGGTAGTGAACTTCAACAGCAACAACAACCACGCCAATGACCAGAGGTATTCCAGCTCTAGAGAAACAGACAGACTCTCGACCACTGCTGGGTCCACAGGTCAGATGTCACTGAAATACATAGATGATGAATCAGAGATTTGAGACTTGTTAATATGCTACTTCGCCATTTACATGCAGACCAAGCACACTAGTGCGGATTCCTCTTATGCAGCTTTTAACACTTGACTAAACTGTGGTTTTGACCCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33033
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
ENSDART00000056252 Nonsense 720 766 16 16
ENSDART00000108861 Nonsense 716 762 15 15
ENSDART00000109471 Nonsense 720 766 16 16
Genomic Location (Zv9):
Chromosome 2 (position 50173607)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49869139
GRCz11 2 49603369
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCACGAAGACGATGCTAACCAGGTTCAGCCACAGAGACTAGCATCAT[C/A]GGTAGTGAACTTCAACAGCAACAACAACCACGCCAATGACCAGAGGTATT
Long Flanking Sequence:
AACTTGTGTTACAGGTGTCAGTAAACCAGTCAACATCTCCTTTTACCACGGGAATACTGTGAAGCTGGGCTGCCAGCCTTATTCCAACCTGGCGCAGGTTGAATGGCAGTTAAACGGGGAGCCAATCAAACCATCAAATACCATCCAGATCCTCTCCGATGGCTTGATGATATTCAACGCATCTTTGGACGCCACCGGCTACTACATCTGCAGCTCCATCGAGACCGTCTCCCAGCGCAAATACCAGACTCAGCATGTAGCGTATGATGTAAAGATGTGGTCCGAATCTGGAACCACAGCGTCACTTCATCATGTTAAGGAAAAAGAGCGCACCCTAGTGGCCATGGTGGTGATACTGTCACTAGTTCTAGCTGCATTGTTGATATGGAACCTGTACAAAGGCCATTTGTCTCTGCCATGTTTACACAGGAGGGTAAAAGACACGCAAAACAGGCACGAAGACGATGCTAACCAGGTTCAGCCACAGAGACTAGCATCAT[C/A]GGTAGTGAACTTCAACAGCAACAACAACCACGCCAATGACCAGAGGTATTCCAGCTCTAGAGAAACAGACAGACTCTCGACCACTGCTGGGTCCACAGGTCAGATGTCACTGAAATACATAGATGATGAATCAGAGATTTGAGACTTGTTAATATGCTACTTCGCCATTTACATGCAGACCAAGCACACTAGTGCGGATTCCTCTTATGCAGCTTTTAACACTTGACTAAACTGTGGTTTTGACCCATTTTGTGTGTTTGAATAATCTCTACCTTTGGAAATAAAATAAAAAATGTCTATTTTACTTCCAAATGAAATTCTTACCAATGCTTATGCACAAAAAAAAACACGTTTTGGCAAGCCAGTGATGGACAAGTAAACAAATTAAGTACTTAAAAGTAAAACAGTGAAAGTAAAAGTGCAGATACCCTAATAAAAATTAAGTAAAGTGAAAGTATAAGTCCTTTTTACAATATTATTTCAGTCAAAGTACAGAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38359
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
ENSDART00000056252 Nonsense 744 766 16 16
ENSDART00000108861 Nonsense 740 762 15 15
ENSDART00000109471 Nonsense 744 766 16 16
Genomic Location (Zv9):
Chromosome 2 (position 50173678)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 49869210
GRCz11 2 49603440
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAACCACGCCAATGACCAGAGGTATTCCAGCTCTAGAGAAACAGAC[A/T]GACTCTCGACCACTGCTGGGTCCACAGGTCAGATGTCACTGAAATACATA
Long Flanking Sequence:
GCCAGCCTTATTCCAACCTGGCGCAGGTTGAATGGCAGTTAAACGGGGAGCCAATCAAACCATCAAATACCATCCAGATCCTCTCCGATGGCTTGATGATATTCAACGCATCTTTGGACGCCACCGGCTACTACATCTGCAGCTCCATCGAGACCGTCTCCCAGCGCAAATACCAGACTCAGCATGTAGCGTATGATGTAAAGATGTGGTCCGAATCTGGAACCACAGCGTCACTTCATCATGTTAAGGAAAAAGAGCGCACCCTAGTGGCCATGGTGGTGATACTGTCACTAGTTCTAGCTGCATTGTTGATATGGAACCTGTACAAAGGCCATTTGTCTCTGCCATGTTTACACAGGAGGGTAAAAGACACGCAAAACAGGCACGAAGACGATGCTAACCAGGTTCAGCCACAGAGACTAGCATCATCGGTAGTGAACTTCAACAGCAACAACAACCACGCCAATGACCAGAGGTATTCCAGCTCTAGAGAAACAGAC[A/T]GACTCTCGACCACTGCTGGGTCCACAGGTCAGATGTCACTGAAATACATAGATGATGAATCAGAGATTTGAGACTTGTTAATATGCTACTTCGCCATTTACATGCAGACCAAGCACACTAGTGCGGATTCCTCTTATGCAGCTTTTAACACTTGACTAAACTGTGGTTTTGACCCATTTTGTGTGTTTGAATAATCTCTACCTTTGGAAATAAAATAAAAAATGTCTATTTTACTTCCAAATGAAATTCTTACCAATGCTTATGCACAAAAAAAAACACGTTTTGGCAAGCCAGTGATGGACAAGTAAACAAATTAAGTACTTAAAAGTAAAACAGTGAAAGTAAAAGTGCAGATACCCTAATAAAAATTAAGTAAAGTGAAAGTATAAGTCCTTTTTACAATATTATTTCAGTCAAAGTACAGAACTACTCGTTTTTTTTGTTTGTTTGTTTTTTACTTATAAGTACTGATATAAGTACTTATGAATGTTCATTTTGAA
Associated Phenotype:
Not determined