Busch Lab

ZMP

invs

Ensembl ID:
ENSDARG00000002213
ZFIN ID:
ZDB-GENE-020507-2
Description:
Inversin [Source:UniProtKB/Swiss-Prot;Acc:Q8UVC1]
Human Orthologue:
INVS
Human Description:
inversin [Source:HGNC Symbol;Acc:17870]
Mouse Orthologue:
Invs
Mouse Description:
inversin Gene [Source:MGI Symbol;Acc:MGI:1335082]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa36157 Nonsense Mutation detected in F1 DNA Not yet available
sa36158 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6435 Nonsense Mutation detected in F1 DNA Not yet available
sa12246 Nonsense Available for shipment Available now
sa36159 Nonsense Mutation detected in F1 DNA Not yet available
sa14224 Nonsense Available for shipment Available now
sa2837 Nonsense F2 line generated Not yet available
sa12856 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa36157
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
ENSDART00000015688 Nonsense 314 1025 9 18
Genomic Location (Zv9):
Chromosome 16 (position 29710034)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27547172
GRCz11 16 27481795
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTTGCAGTGTTTCTGAAACACCACTCTGTAAGAGATGAGCCTGACCTA[G/T]AGGGACGAACCGCCTTCATGTGGGCCGCTGGGAAAGGCAGTAATGATGTC
Long Flanking Sequence:
TATTTGTTTTTGTTTTTCCATTTATGTATTTATTTGATTACATACAAATTTACTAGAGCTTGACAAATTAATCATGATTAATTGCATCCAAAGTAAAATATGTGTGTGAATTATATATATTTATTATGTATATTTAATACACACATACATAAAAACAAAACTATGCACAAGTTTTCTGACATAGATATTCAAATTTATATAGAATTTGTATCATATACATATATGTTTTAAAATCTTATTGTAAACAAATATTTTCTCAAATATACGCATGCATGTGTATATGTAGATAATATACATAATAAATATACAAAGTACACACACATATATTATGTCAAAAGAATATATTATTATTTCAAGCACTGCAATTCATTTACATTAGTCCAGCGCTAAAATGTACATAAATTTCCATAACTGATTGCGTGTGGTTTTGCCTGTGTGTTGTTAAGGACACCGTTGCAGTGTTTCTGAAACACCACTCTGTAAGAGATGAGCCTGACCTA[G/T]AGGGACGAACCGCCTTCATGTGGGCCGCTGGGAAAGGCAGTAATGATGTCATCAAAATCATGCTGGATTTGAAAAAAGACATAGACATCAACATGACAGACAAATATGGAGGGACAGGTGTGTGAGAGACATGCACTCACACACACAGATTCATTTTGAACACAATTATCCATTCCTGCTTTAAACTGGTTAGTTTCAGCTCAGATCAGTGATAATTGCATTTTCTGTTCAATCAAGCAATTAGCAAGCCATATCCCATGTATGTTCCCCCATACAGCCATAACAAGAGTTGACGGTTTGCTCAATGTCTGTGTGTGTGTGAATGTGTAGCTCTTCATGCGGCTGCACTGTCAGGTCATGTGTCCACTGTGCGCTTGCTGCTGGAGCAGGGAGGAATGGTGGACCCACTGGACGTCATGAAACACACCCCTCTATTTCGTGCGTGCGAGATGGGCCATCGAGATGTCATACTAACACTCATTAAAGGTGTGTAAGTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36158
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
ENSDART00000015688 Essential Splice Site 404 1025 10 18
Genomic Location (Zv9):
Chromosome 16 (position 29710521)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27547659
GRCz11 16 27482282
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGCGTGCGAGATGGGCCATCGAGATGTCATACTAACACTCATTAAAG[G/A]TGTGTAAGTGCATGCATGCCTCCCCACTGGTGATGTTTTAAAAATAATAA
Long Flanking Sequence:
TGAGCCTGACCTAGAGGGACGAACCGCCTTCATGTGGGCCGCTGGGAAAGGCAGTAATGATGTCATCAAAATCATGCTGGATTTGAAAAAAGACATAGACATCAACATGACAGACAAATATGGAGGGACAGGTGTGTGAGAGACATGCACTCACACACACAGATTCATTTTGAACACAATTATCCATTCCTGCTTTAAACTGGTTAGTTTCAGCTCAGATCAGTGATAATTGCATTTTCTGTTCAATCAAGCAATTAGCAAGCCATATCCCATGTATGTTCCCCCATACAGCCATAACAAGAGTTGACGGTTTGCTCAATGTCTGTGTGTGTGTGAATGTGTAGCTCTTCATGCGGCTGCACTGTCAGGTCATGTGTCCACTGTGCGCTTGCTGCTGGAGCAGGGAGGAATGGTGGACCCACTGGACGTCATGAAACACACCCCTCTATTTCGTGCGTGCGAGATGGGCCATCGAGATGTCATACTAACACTCATTAAAG[G/A]TGTGTAAGTGCATGCATGCCTCCCCACTGGTGATGTTTTAAAAATAATAATCACAATAGGCAAAAACAGCATGAAATTTATAATATTTTTTCATAATAACAAATTAATTTAACAAACAATCAGTTAAAAAAAACTTACAAAATAGACATATGCTTAGAAATGCATATACACTTACTAATGCAAATACTTTATATTACAGAATGCAAGTCGTGTGTGTTTTTTAAAAATATTCCATCTTATAGTACAATACATTTAATTCAACTTTAATAATTTTTATTTAGTTGTGAGTTGAATTTAATCCAATGAATACAAGTTGTTTAAATATATCTCAAATAAAATATATTGCAATAAATGTTTGCATTGTAAGTATAAGCGTATTTAGAAATAGCTGAAGTAAGCAACCCCACAATTCATTCTAGACGTAATTGTTTGTCATATTTCAGTGTATTTCAGATTTTTTTTTGACTCAAATGGTCCCCACTATCATGAACAATATTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6435
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
ENSDART00000015688 Nonsense 447 1025 11 18
Genomic Location (Zv9):
Chromosome 16 (position 29713315)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27550453
GRCz11 16 27485076
KASP Assay ID:
554-4512.1 (used for ordering genotyping assays)
KASP Sequence:
AGGTGTGTGAGGTGCTAATGGAGAATGGGATCAGTCCTAACCTGCAGGAC[C/T]AAGCTGGACGGACACCCTTACAGTGTGCAGCGTATGCTGGCTACATAAAC
Long Flanking Sequence:
AGAGTTTATGTTTTGTTCTGATTGGCCTGATTTTCCCTGGGATTTTACACTGACAGGAATTACATGAGAATGAAGAAACATTGGTGTTAGAGGCTTATGGCTTGTCATTTCCATGTAACGAACTCTAACTATTGAGCTATGCCTACTAGGCATATGCACATTTTCATTCTATGGCACTTTTAATATTATTTCAGTCATCATCTCTGGACAAGAACAAATGTCATAACATGAGTTATCAATTTTGCTTAACTGTCACTTGAACATGACAAACCTATGTGACTACATTAGTACAAAAATTCCTAGATATCTCAATTTTAATTGTAACAGTTTCTAGTGTTCACAGCAAATCTAACCCTGTTATATATATATATATAGGAGGTGCTCGTGTTGATCTAGTAGACATAGATGGGCACTCTGCACTGCACTGGGCAGCTCTGGGTGGTAATGCAGAGGTGTGTGAGGTGCTAATGGAGAATGGGATCAGTCCTAACCTGCAGGAC[C/T]AAGCTGGACGGACACCCTTACAGTGTGCAGCGTATGCTGGCTACATAAACTGCATGGCCTTGCTCATTCAGCACGATGCAGACCCTAATATTCAGGACAAGGAGGTATGAGTGTGCAGCATGCCTGAGAACATGTATTGGCCATTACCTCTGAGTGGCCTGCTATTGAAAGCTCGAAGAATAGCACTATGTATGACTTTGGTGTGTGTTTATGTGTTAAGGGGAGAACCGCACTCCACTGGTCCTGTAATAATGGTTATCTGGATGCTGTGAAGCTGTTGCTGGGGTGTGGGGCATTTCCCAATCACATGGAGCACACTGAAGAGAGGTAACAAAGAGACAAACACTCTTGAATGGTTGGCCTGGTGGTTATGGTTCTGAAAGAGTGTCGACTCATGGCACAGATTCACTTTCTAGAACCTTCTTAAGTTTGTGTGTGTATTTTCAGGGGGAATCCAGCTGTTCACTTCAGCAAGGATGCAATAAACAACTCCTTCAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12246
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
ENSDART00000015688 Nonsense 494 1025 12 18
Genomic Location (Zv9):
Chromosome 16 (position 29713574)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27550712
GRCz11 16 27485335
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATGTGTTAAGGGGAGAACCGCACTCCACTGGTCCTGTAATAATGGTTA[T/A]CTGGATGCTGTGAAGCTGTTGCTGGGGTGTGGGGCATTTCCCAATCACAT
Long Flanking Sequence:
AACATGACAAACCTATGTGACTACATTAGTACAAAAATTCCTAGATATCTCAATTTTAATTGTAACAGTTTCTAGTGTTCACAGCAAATCTAACCCTGTTATATATATATATATAGGAGGTGCTCGTGTTGATCTAGTAGACATAGATGGGCACTCTGCACTGCACTGGGCAGCTCTGGGTGGTAATGCAGAGGTGTGTGAGGTGCTAATGGAGAATGGGATCAGTCCTAACCTGCAGGACCAAGCTGGACGGACACCCTTACAGTGTGCAGCGTATGCTGGCTACATAAACTGCATGGCCTTGCTCATTCAGCACGATGCAGACCCTAATATTCAGGACAAGGAGGTATGAGTGTGCAGCATGCCTGAGAACATGTATTGGCCATTACCTCTGAGTGGCCTGCTATTGAAAGCTCGAAGAATAGCACTATGTATGACTTTGGTGTGTGTTTATGTGTTAAGGGGAGAACCGCACTCCACTGGTCCTGTAATAATGGTTA[T/A]CTGGATGCTGTGAAGCTGTTGCTGGGGTGTGGGGCATTTCCCAATCACATGGAGCACACTGAAGAGAGGTAACAAAGAGACAAACACTCTTGAATGGTTGGCCTGGTGGTTATGGTTCTGAAAGAGTGTCGACTCATGGCACAGATTCACTTTCTAGAACCTTCTTAAGTTTGTGTGTGTATTTTCAGGGGGAATCCAGCTGTTCACTTCAGCAAGGATGCAATAAACAACTCCTTCAGGAGTGTTCAATTATTTTGGAAATAAAAAAGACACATTTTACAAAAAATCGTTGTATTAAGACAGCAAAACACAAGAATTGAAGAATATAATGCCATTCGCTTTGAGAAAAGTCATCTCAACTTTTAGGCTGCAAATATAAAATAAAAATGTACCTGCAAAATCTTGTAGCAACTTAATAAATAAAAAAAAAGACAATGGCGATTTTTGGTTTTCAAAAAAAATTTAATAAAAAATTCTGAACTTTCGTTTATCCAAAGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36159
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
ENSDART00000015688 Nonsense 690 1025 15 18
Genomic Location (Zv9):
Chromosome 16 (position 29721711)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27558849
GRCz11 16 27493472
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCCATCAGATCTCTCCCTCCAGTGACGCCAATGAGCACCAAGAAGTG[T/A]CCAGTCACCAGAGAGGAGGTGTGTGTGAGAGAAACATTTGGTCCAGACAC
Long Flanking Sequence:
AAGCCCAGACAGCAGCTGAATTATCTTAATAGTTATTCAGCAACCCTCTGCACTTCCTCATTGTAAATTAATATTAGCTACTTCAGTCCCACATCTACATTACCAGAATGATGAAGATGAAACCAAAGTGGACATTTCAGCAAGGCAAGGATCCAAAACACAGCCAAGAAAACTGCTTATATGTATTCAGAGAAAGAAAATCATGCTGGAGAATGGCCCAGCCAATCACCTAACTTGATTCCAATATAATATACCTAAATCTGGTTCAATTCCATATCAACCGCTTCTTTAGAAATATAATTCCTAGGAAAAACATGACATGTTCAATACTTATTTCCCCTGCTGTATATGGCACCATGTTACAACATGTATTGTTAATACACTTCCATAACCATAATTCTTTTCTTTTCTTCAGAGCGCAGAACAAGAGAACCTGAAACATCAGATGCTCCCTCCATCAGATCTCTCCCTCCAGTGACGCCAATGAGCACCAAGAAGTG[T/A]CCAGTCACCAGAGAGGAGGTGTGTGTGAGAGAAACATTTGGTCCAGACACGGGCATATCATTGAATTGTGGATCTGCAAATGAGCGCCGATCCCCCGCTGGCTCCAGTCGACCAGGCAGTGCCAAACCAGTCCACACAGGGGCCCATGTAGCACCAGGCCACATGGAGACTACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCCAAAAATGCCTCCCAGGACACACCACAACACAATGAGACACAGACAATGTCCAAAGGAAACAAACCCATATCAGAACACAAACCTACAGGAAGCCAGCCATCCAACAACACTTCTGTCACAAGGCAAAAAGAGAAACGACAAGAAAAAGAGACACACAGAGAAAAGGATAAAAGATCAAGGACTGAAGGAGATAAACAGACTGTCAGAGAGAAACAGAAAGGCACGGGGATTGAGAGAGACAAAGAGAGATTGATGGGCAGGACGAGAAAAAAACTAGCGGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14224
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015688 Nonsense 763 1025 15 18
Genomic Location (Zv9):
Chromosome 16 (position 29721928)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27559066
GRCz11 16 27493689
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACYACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCC[A/T]AAAATGCCTCCCAGGACACAYCACAACACAATGAGACACAGACAAYGTCC
Long Flanking Sequence:
CCAGCCAATCACCTAACTTGATTCCAATATAATATACCTAAATCTGGTTCAATTCCATATCAACCGCTTCTTTAGAAATATAATTCCTAGGAAAAACATGACATGTTCAATACTTATTTCCCCTGCTGTATATGGCACCATGTTACAACATGTATTGTTAATACACTTCCATAACCATAATTCTTTTCTTTTCTTCAGAGCGCAGAACAAGAGAACCTGAAACATCAGATGCTCCCTCCATCAGATCTCTCCCTCCAGTGACGCCAATGAGCACCAAGAAGTGTCCAGTCACCAGAGAGGAGGTGTGTGTGAGAGAAACATTTGGTCCAGACACGGGCATATCATTGAATTGTGGATCTGCAAATGAGCGCCGATCCCCCGCTGGCTCCAGTCGACCAGGCAGTGCCAAACCAGTCCACACAGGGGCCCATGTAGCACCAGGCCACATGGAGACTACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCC[A/T]AAAATGCCTCCCAGGACACACCACAACACAATGAGACACAGACAATGTCCAAAGGAAACAAACCCATATCAGAACACAAACCTACAGGAAGCCAGCCATCCAACAACACTTCTGTCACAAGGCAAAAAGAGAAACGACAAGAAAAAGAGACACACAGAGAAAAGGATAAAAGATCAAGGACTGAAGGAGATAAACAGACTGTCAGAGAGAAACAGAAAGGCACGGGGATTGAGAGAGACAAAGAGAGATTGATGGGCAGGACGAGAAAAAAACTAGCGGAGAAAGAGAAGGAAAAGAGGAGAGACGGCACTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGAGCATGGAGAAGGTACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAACAGTTGTGTATAATCATATACTTTTGTGTAATGACATTTAAACTTTGTGTTAGAGAGTTGATGCTGGAAGCCAGTCTACATTACATCTACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2837
Status:
F2 line generated
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
ENSDART00000015688 Nonsense 828 1025 15 18
Genomic Location (Zv9):
Chromosome 16 (position 29722123)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27559261
GRCz11 16 27493884
KASP Assay ID:
554-2538.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAGACRCACAGAGAAAAGGATAAAAGATCAAGGACTGARGGAGATAAA[C/T]AGACTGTCAGAGAGAAACAGAAAGGCACRGGGATTGAGAGAGACAAAGAG
Long Flanking Sequence:
CAGAGCGCAGAACAAGAGAACCTGAAACATCAGATGCTCCCTCCATCAGATCTCTCCCTCCAGTGACGCCAATGAGCACCAAGAAGTGTCCAGTCACCAGAGAGGAGGTGTGTGTGAGAGAAACATTTGGTCCAGACACGGGCATATCATTGAATTGTGGATCTGCAAATGAGCGCCGATCCCCCGCTGGCTCCAGTCGACCAGGCAGTGCCAAACCAGTCCACACAGGGGCCCATGTAGCACCAGGCCACATGGAGACTACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCCAAAAATGCCTCCCAGGACACACCACAACACAATGAGACACAGACAATGTCCAAAGGAAACAAACCCATATCAGAACACAAACCTACAGGAAGCCAGCCATCCAACAACACTTCTGTCACAAGGCAAAAAGAGAAACGACAAGAAAAAGAGACACACAGAGAAAAGGATAAAAGATCAAGGACTGAAGGAGATAAA[C/T]AGACTGTCAGAGAGAAACAGAAAGGCACGGGGATTGAGAGAGACAAAGAGAGATTGATGGGCAGGACGAGAAAAAAACTAGCGGAGAAAGAGAAGGAAAAGAGGAGAGACGGCACTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGAGCATGGAGAAGGTACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAACAGTTGTGTATAATCATATACTTTTGTGTAATGACATTTAAACTTTGTGTTAGAGAGTTGATGCTGGAAGCCAGTCTACATTACATCTACATTACGGTTACATTACATTAGATATGCACGGTGGCTCAGTGGTTTGCACGGTTGCCTCACAGCAAGAACGTCACTGGTTCAGATCCCGGTTGGGCCAGTTGGCATTTCTGTGCGGAGTTTCCCCGTTTTCGTGGGTTTCCTTCCAGGTGCTCTGGTTTCCCCCGCAATCTAAGGCATGCGCTATTAGTGAACTGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12856
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
ENSDART00000015688 Essential Splice Site 882 1025 15 18
Genomic Location (Zv9):
Chromosome 16 (position 29722288)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 27559426
GRCz11 16 27494049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGRGCATGGAGAAGG[T/A]ACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAAYA
Long Flanking Sequence:
CAAATGAGCGCCGATCCCCCGCTGGCTCCAGTCGACCAGGCAGTGCCAAACCAGTCCACACAGGGGCCCATGTAGCACCAGGCCACATGGAGACTACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCCAAAAATGCCTCCCAGGACACACCACAACACAATGAGACACAGACAATGTCCAAAGGAAACAAACCCATATCAGAACACAAACCTACAGGAAGCCAGCCATCCAACAACACTTCTGTCACAAGGCAAAAAGAGAAACGACAAGAAAAAGAGACACACAGAGAAAAGGATAAAAGATCAAGGACTGAAGGAGATAAACAGACTGTCAGAGAGAAACAGAAAGGCACGGGGATTGAGAGAGACAAAGAGAGATTGATGGGCAGGACGAGAAAAAAACTAGCGGAGAAAGAGAAGGAAAAGAGGAGAGACGGCACTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGAGCATGGAGAAGG[T/A]ACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAACAGTTGTGTATAATCATATACTTTTGTGTAATGACATTTAAACTTTGTGTTAGAGAGTTGATGCTGGAAGCCAGTCTACATTACATCTACATTACGGTTACATTACATTAGATATGCACGGTGGCTCAGTGGTTTGCACGGTTGCCTCACAGCAAGAACGTCACTGGTTCAGATCCCGGTTGGGCCAGTTGGCATTTCTGTGCGGAGTTTCCCCGTTTTCGTGGGTTTCCTTCCAGGTGCTCTGGTTTCCCCCGCAATCTAAGGCATGCGCTATTAGTGAACTGGATGAACTAAATTGGCCATAGTGTATGAGTGTGTCTGTGAATATGAGTGTGTATCGGTATTTCCCAGTACTGGGTTACAGCTGTAAGGGCATCCGCTGTCCTTCATATGCTGGAATATTTGGCAGTTCATTCCACTGTGGTGAAGTCTGATAAATCAGAGACTAAGCT
Associated Phenotype:
Not determined