Busch Lab

ZMP

NP_999974.1

Ensembl ID:
ENSDARG00000007561
Description:
cadherin-23 [Source:RefSeq peptide;Acc:NP_999974]
Mouse Orthologue:
Cdh23
Mouse Description:
cadherin 23 (otocadherin) Gene [Source:MGI Symbol;Acc:MGI:1890219]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa6329 Nonsense Mutation detected in F1 DNA Not yet available
sa35577 Nonsense Mutation detected in F1 DNA Not yet available
sa31961 Nonsense Available for shipment Available now
sa35578 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45500 Nonsense Mutation detected in F1 DNA Not yet available
sa42289 Nonsense Mutation detected in F1 DNA Not yet available
sa28193 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa28194 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6329
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
ENSDART00000016602 Nonsense 328 2678 7 51
Genomic Location (Zv9):
Chromosome 13 (position 43745982)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 42961188
GRCz11 13 43085754
KASP Assay ID:
554-4508.1 (used for ordering genotyping assays)
KASP Sequence:
TTCCCCAGTGTTTATAACRTGTCTCTGGAGGAGAGCGTACCCCGTGATTA[T/A]CTGGTGRTCAGACTCAACTGCACGGATAATGACGCGGGTCTAAATGCAGA
Long Flanking Sequence:
ACTAGTCTCTGAAATTGTTATATTGGGGCTGAAAAGTTTGGAGACCCCTGTTTTACTCTCTCTGTAACAAAAGCATGCTGTGTGCTGATGCCCTCTGCTGGTTTCCTCCCTCAGGTGCAAGTCCAGGACCCCGACGAAGCAGCCAATGGTGCTGTAACAATGGCCCTTCAGATGGGGATGCCGAGGCTGGACTTCAGGCTTAACATCACCACAGGAATTCTGGTGTCCACCGTAGTGCTGGACCGGGAGCAGATCGGCCAGTATTATCTGAGGATTATTGCATATGACGCAGGCCAGTTTCCCCGCACGTCCACAAGCACTCTCACTATCACAGGTAAGCACTGCAAAATCACGGCCCACACGTGTTTTTCTGCAAATCCTGAATAATCGTAATGTTTTCCACTCTTTCTGTGTGCAGTTTTGGACGTGAATGATGAGACGCCCACTTTCTTCCCCAGTGTTTATAACGTGTCTCTGGAGGAGAGCGTACCCCGTGATTA[T/A]CTGGTGGTCAGACTCAACTGCACGGATAATGACGCGGGTCTAAATGCAGAGCTCAGCTATTTTATCACAGGTCAGTTCAGGAGGTCACAGGTCAGGGTGTGTAAATGGGTTTTTTGCTGACACAGCAACACTTTGCAATTTTGGCTTGGGACTCACTGTGAGCAGATGTGTCCAAAATCTACACTCCAAAAATTACTTTGCTCCTTGTTGAATTTGCTTATTTGAAATGAGCTGCTGAAACAACACAATTCTTAAGTTGTTTTGAGACAACCTAAATGTTTTATGTTGAATCCACTTAAATTTAGCAAAACAATTAAGTTAACTTAATTGATTTGTGTTGGGAAGGTCATCCGCTGTGTAAAACATATGCTGGATTAGTTGGCGGTTCATTCCGCTGTGGTGACTCCAGATTAATAAAGAGACTAAGCCAAAAAGAAAATGAATGAATGATTGAATGATTTTGTTTTATGTTTTATGTTTTATGCATGGCGGCGGATGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35577
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
ENSDART00000016602 Nonsense 589 2678 13 51
Genomic Location (Zv9):
Chromosome 13 (position 43778961)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 42994077
GRCz11 13 43115840
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGACGTGAGTACTGGTCTGCTAACCACGGTGGACTATTTGGACTAC[G/T]AGACCAAGACGAGTTATTTAATGAACGTCTCAGCCACAGATCAGTCACCG
Long Flanking Sequence:
TGGGCTTTTGCTACCTTTCTACACCTCCGTTTCTTCATGTCTTCAATACTTTTTTCCATGCGTCATTTCCTTTTATAACACAACTTAATTTCCAAACTAATCAATATTGTTTTCTTCGCATATGTATTTTTTTTTTGTTGCTATCAACATCCTTTGAAATGTGTTTTCTGAGAAAAATGGTGACGTTTTCAATACATATTTTCACCTTTGTATCTTCTAAATGTGACTTTTGTCACTGTTTTGGAACACACTAGCTTATAGATGTCCTTAAGGCTAACATACCGATACTAACATCTAAAAAACTTTATTTTAATTTCACAAGACCTTTAAATTCTAAAAATGTCCAAATTATGTCCCGTATGATGACCCAAGCCTTTCCTGTTTTCCTCTGTTCAGGGGATGGGGGCGCTGTGGCCTATTCTCTGGTCTCTGGCTCTGATCGTAAATTTGAGGTGGACGTGAGTACTGGTCTGCTAACCACGGTGGACTATTTGGACTAC[G/T]AGACCAAGACGAGTTATTTAATGAACGTCTCAGCCACAGATCAGTCACCGCCATTCCACCGCAGCTACTGCACCGTGTACGTCACGTTACTCAATGAACTGGACGAAGCGGTGGCCTTTCTTTCAGCTGGATATGAAGTTTCACTGAGAGAGAACATCGCTACAGGAACAGAGGTGGTGCAGGTGAAGGCGCAATCCGCTGATAACCTGAACCAGCTGTCGTACCGATTTGACCCCGACACCTCGCCTGCTGCCCTCGCGCTCTTTAAGATTGACAGTGTCACGGTAAGCGAACACAATATTGCACAAAAGAACAATCTGTTTTGAGAATGTGGTGATTTTAAAGGCATAGTTCATCCAAAAATTAACTCATCATTTATTCTCAGGGTTCCCACGCTTCTTGAAAGTGCTTGAAAACAAACATAGGTCCTTTAAAGAAATTTTAGTTTCTTTCTTCTGGTAAAAAACAAAGGAAGAAAGAAACTCAAATAGGTTTAGAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31961
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
ENSDART00000016602 Nonsense 848 2678 18 51
Genomic Location (Zv9):
Chromosome 13 (position 43786259)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 43001375
GRCz11 13 43123138
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTAGATGTGAACGATAACCCTCCCGTACTGCAGAGTCCTCGAGGGTA[C/A]AACGTCAGCGTCAGTGAGGTCAGAACACAGCACCTCAAACCAGAGACGCC
Long Flanking Sequence:
TTTCAACATTTTTGGTCAAACAATTGACCTTGGTGACCCTCAAACTTTTAAGTGGTAGTGTGTTTCAGTCAGCAATGGCTGAAACTAGACAAATATTAACATTTAATTAGAGGGGATAAAGGCCTGGTTATCTGTATATTAAATATGTTGGCAGCTCGTTTTTGGAACTTTTACTGCCTTCATTTACTGTCAGTCATTTCATTTAAAATGTATTTGGTAACTTCAGCAGACATCTCTATATATGGTCACAGTGTGGAGTTGCGTGACTTTGGACATGTTTCCTTGTACTGTTAAAAGCATCAGATTTTGCATAACTACTTCTGATGTGTATGTGTGGTTGTTTGCTAAGCTCAGCAAGCATGTCTATTTGTTTTCATGTGCTTTAATCAGGTGCGGGCGATGGATAATGGTTCTCCTCCGAGGTACACCGATGTTTCGCTGACGGTGAATATTGTAGATGTGAACGATAACCCTCCCGTACTGCAGAGTCCTCGAGGGTA[C/A]AACGTCAGCGTCAGTGAGGTCAGAACACAGCACCTCAAACCAGAGACGCCATCAGCACCCTGGCTGTCAATCATTCGCATATTTGCATAAAAGACAAAAATATTCGCATATTTGCATAAAAGACAAAAATAAAGATAAAAGTAATTTGTTTAATTTATATTTATTAATTTTGTTTTTGTTTATTTATTTTCTTGCTAATTTATATATATATATATATATATATAGTGTTGGGCAAAAGTTAATCGCGATTAATCAAATCTAAAATAAAAGTGTTTTGACATGTTTTTACACGTTTATTTATATTTAAATATAAAATATATGTGTATATGATACAAATTTATATATTAATTAAAATTAATATATAACAAAATTGTTACGTGTAGTTTTACTTTTATTTATGTTTGTATTATATAAACATAATGACTATATAGTACACACATATATCTTGTGTCAAAACAAATTTTTATTTTTAATGCAAAAACTTGCGATTATTTATGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35578
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016602 Essential Splice Site 931 2678 20 51
Genomic Location (Zv9):
Chromosome 13 (position 43818281)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 43033397
GRCz11 13 43155160
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATTAAAAGTATTTTTTTAATGTCTTGCTGCTTGTGATCTACTTCCAT[A/G]GACATCCACCACCGTTTGGGTGCGTATAATTGATGAAAACGACAACGCAC
Long Flanking Sequence:
CTCTCGCACACCCCCATACTGAATATAACCCCAAACCATGATTTTTCCTTCACCAAACATGACTGATGTCTGAGAATATTGGGTCCATGTGGGTTCCAATAGGTCTTCTGCAGTATTTGTGATGATTGGAATGCAGTTCGATGGATGATTCAAGGGAAAAATCTACCTTTTGCCACTATTTCAAATGATCAACTAGAAGTCAAGTTATTGTTTGTTGCTCTTACAACTGTGATCAACGACAAGACTTTTGTCAGGTAGTTGTACATATGCCATGACAAGTTGCACAATGTTTTCCAAAAATATGGAGTGTTTATAAGAAAGTGTCTGGTGCATATGAAGATGAATGTGTGTATTTCCTACAAGTGGTTTGTCAAGCCCCCTCACCAACATTCCTAAGGGTAGAAAATTAGTGGAGGACACTTTATATATTTGTCCCGTTAGATTTTCCTACTTATTAAAAGTATTTTTTTAATGTCTTGCTGCTTGTGATCTACTTCCAT[A/G]GACATCCACCACCGTTTGGGTGCGTATAATTGATGAAAACGACAACGCACCGGAGTTTCCAGAGGAAGAGTACGTGACGGAGCTCAGAGAGGGACCAAACACTGTAGGAGCCATCATCGCCACAGTCACCGCCATTGACCCGGACGAAGGACTCAATGGAACCATCCGTTATGCCATCTCTAAGGGCAACCTGGCACAGACCTTTCAGATCAATAGCGTAACGGTGAGGATGACACACCACAAACCAGAGCCGGGGTTGTTAGAGACATTGCTGTGTTTGTGTACATAAATCATCCAAATATTCAGAAGTTTTAAAGCACTTGATTTATATATATATTTTTTGCCCAAACAGTTTTTTTTTCTCTATTCAAAAAGTTAAACATTACACAGATAATGAATTTACATAATTACTTTCATTCAAACATACAAAATTTGCATAATAGCCCAGTGAAACCTCACCTTTTATATCCCAGTTGAAATGTGAGTTTGAAAATTCCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45500
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
ENSDART00000016602 Nonsense 1038 2678 21 51
Genomic Location (Zv9):
Chromosome 13 (position 43822621)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 43037737
GRCz11 13 43159500
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATGTGCTGACGGTCACAGCCACAGATCAGTGTCCGATACCCCTGCTC[A/T]GACTGACCTCCAGCACCACAGTAAGTTCACTATCTACTACACACGTTTAT
Long Flanking Sequence:
ATGAATCGCCAACTATTTCAGCATATCTTTTATGCAGCGGATGCCCTTCCAGCCGCAATTCACTATATAGTGCATGTTTTTGGACTGTGGGGGAAACTGGAGGACTCAGAGACAACATGGGGAAAACATGCAAACTCCACATAGAAATGCCAACTGGCCCAGCAGGGACTCGAACCAGCGACCTTCTTGCTGTGAGGCGACAGTGTAACAGAATCATTAAAATAATAAATTCTTTCACACTTTAAAATACACTAAGGTCATCATAAAATAGACCCTTAAACACAAATTCAACCAAAGTCATAAAAAAAACATATTTGTTACTCCATCCTGGAGTGAACATTTATCCGAAAATCCACTCCTTCATCTGTGTTTGTTGATTGTGTGTGTTTGTGTGTTCACAGGGTCAGATCGTGGTGGTTAGTGCGCTGGATTACGAGATCAGCAATGGTCACTATGTGCTGACGGTCACAGCCACAGATCAGTGTCCGATACCCCTGCTC[A/T]GACTGACCTCCAGCACCACAGTAAGTTCACTATCTACTACACACGTTTATAATCCTCATAGTTGCTTTTTTTATTCAACTAATGTTTAATTGTATAGTGCTTTTCACAATGATTATCATTTCAAAGCAGCTTTACAAAAAGTCCATATTATTACATTACAATCAAATAAAAATAATAAAAACTTGAACTAATTAACTAGTAACTAATAGCTTTTAACAGTAAAGGTTATTATATATAAACATGGGTTACCTGCAGTTACAGCAGGGAAAATAAGTATTGAGCAAGTCATGTTTTTTTCCTGGGAATAATATTTCTAAAGGAGCTGTTGACATGGAATTAAACCAGGTTTAGGTTATAACCCAAACAATACAAACATTAAAATAAAACAAAACTAAGCAAATGATATAAGGAGAAAATGCTGAACTACTGAAATGTATTTAATACTTTATATAAAAGGCTTTATTTGGTGATGGCTGCTTAAAGACGCCTCTCATATGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42289
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
ENSDART00000016602 Nonsense 1132 2678 23 51
Genomic Location (Zv9):
Chromosome 13 (position 43825445)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 43040561
GRCz11 13 43162324
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGAGTGAGGAAAGACATTGAGCTTGACAGAGAAACAATTGCCTATTA[C/A]AACATCACTATTACCGCCAAAGATTTGGGAACGCCTTCGCTCAATGCTAC
Long Flanking Sequence:
AAATGGTTACATGTTTAATACTAATTTCCCCTACTGTATATAGTATACAGATGATGTCTGTGTACATTTTCAAAGAAATCCTTGTCGATAACATATCCACACACTGTCCTGTCCTTCAGGTCCTGGTGAATGTGATAGATGTCAACGATAACCCACCCATCTTCCCGAGGCCATTTGAGGGACCGTTTGAGATCACAGAGGGTCAGCCGGGCCCTCGTGTCTGGACCGTCAAAGCCACAGATGCTGATTCGGGATCCAATGGAAAAGTGGAGTACAGCATCACCGCAGGGGACCTGAAAAGTGTGTATCTGTGATGCACAGCTCAGATTTATTTAGAAAAATTTATATTGTTGTTGTTTTCTTTTCCACAAAATACAAAAATGATCTGTCTATCTCCTTTTGTCTATCTCTTTGCCAGATGAGTTTGTAATCTCCTCAGTTGAGGGAGAGTTAAGAGTGAGGAAAGACATTGAGCTTGACAGAGAAACAATTGCCTATTA[C/A]AACATCACTATTACCGCCAAAGATTTGGGAACGCCTTCGCTCAATGCTACGGTATGGCAAGCACACCCTCATCGCACTTCATAATTTACTACACAAAAAATGATGAACTGATGGGTAAGTGCATACTTCTGAGTATGTAAAAAGGCAGTATGTCAGCGTTGGAACATGCTGAATTACTTCTTGATGGCACAAACACAAATTGCAGTTTTGTTTAAGCTAAATTAGTTACAGATCCATTGGTAATTAAATTAGTTTGATGCTTATGTTTTCAAACAGTAGTTTAAGATGTTACAGATGCAAATGTTGATCTTCATTCATTCATTTTCCTTCAGTTTAGTCCCTTATTTATCAGAGGTTGCCGGCAACACAAAAATAAGAATCTTATGGAACTTAACCAAACAGAAGTAGTCCTTGACTCACCCAAATAAATACAAACAAGAATTCAAACAAATAACTGACAGTCTCCCTCATCATGAACCCATATACAGATGGATCAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28193
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016602 Splice Site, Nonsense 1668 2678 32 51
Genomic Location (Zv9):
Chromosome 13 (position 43843465)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 43058581
GRCz11 13 43180344
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCTATATTCAGTCTAAATTGTGATCTTCCAAATCTTTACCCGCAGGT[A/T]AAATTGTGGCCAATCGGACGGTGGATTTTGAGCAAGTGCAGTGGTTGAAC
Long Flanking Sequence:
TAAAATATAATTTATATCATATAAACAATTTTTTGAGTGGTTAAAGTTGCTTTTTTTATTGTAATATGGAGATTTAATTTGACAGAAAAAAGCTACTAAACCAGCCTGGAAATATCTGTCTTTCCTGGAAATCTCAGACTCTATCATCATGATTTCCCTCCACAGCCAAACTGACCATAAATGTGCTGGATGTGAATGACAATGCTCCTCGTTTCCGTCCTTTCGGTGTGGCGAACTTTTCCGAGAGCATTCTAGAGGGTGCTGTGCCTGGTACCACACTGCTGTCAGTCACAGCTGTGGATCCTGATAAAGGACCCAACGGACAGATCATCTACCAGCTCCTAAACCTGCCTCGTGGAAACTACATCAGACTTGAAGACCCATCTACAGGTTACACAAACACTCATTTGCATTTCTGCGGGTGAAATTTCTTATAAGGCCTTGTTATATAACTCTATATTCAGTCTAAATTGTGATCTTCCAAATCTTTACCCGCAGGT[A/T]AAATTGTGGCCAATCGGACGGTGGATTTTGAGCAAGTGCAGTGGTTGAACTTCACGGTTCGTGCTCAGGATCATGGCTCGCCTCCTCGCTTCACTGAGCTTCCTGTCTATCTACGCATCATTGATGTTAATGACAACAACCCAGTTTTTCAGCAGCCGTTATATCAAGTATGTCAGCACAGGCCAGAGTAAGGCTTTTCCAAAAGTCCATAGCTTATGTTCAGGAAGTTATTTAAGGTGTTTATGTGTATTTTTTGGTGTTTACTGTGTATATTATCATTATTATAATTTTTTTTGCTAATTTGATACAGTTCATTGTTTCAGGCATACATTCTAAGCATTACTGTAGCTTTAGCATGATAGGAATAATAAAATTTTTGAAATTATTATTATAATTAAATTGCACCATTTTGCTGTTTTTATTTATTTATTGTTATTAAATTCATTTTTGTTAAACCTAATAAATTTCCACAATTTTTGGTAAATTTATTTTTTAAATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28194
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016602 Essential Splice Site 2228 2678 42 51
Genomic Location (Zv9):
Chromosome 13 (position 43863686)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 43078802
GRCz11 13 43200565
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGATCAGTGTATTTGAATTTCATGTCCTGATCATTTGTTTTTTTTTC[A/G]GGTGAGACTGACGGAATCATCTGCACGTTTGACCTCTTTATGGCTTACGC
Long Flanking Sequence:
TTAATATAGTTAATTTAATTATTTAAGTTATATATTAATAATAAAATATATATTACTATAAAATATTAATTGACATATTTCCTATGTGTTTATTATTTAAATTATGACATATTTATACATTTTACATATTTATTTACATATGTATTATTTAAATTATTTATTTTTTATTTTATTCATTGTAGAAATCCTTTACATTTTAACATATGTTTTTATGATTATTACATACTTTTTAAAGCCCAGAGGAAATCACTGTCTCTCTTTCTGTCAGGTGTTGCTGCAGATGCTAAAGTGGGATCGGATCTGATCCGGGTTCAGGCCATTGACAATGACATTGGCAACAACAGTCTGGTTCTCTATCACATTCTGTCCATCCGCTACATCAAACTGCACTCCAATGACTCTGAAGAAATGGGAAACGTCTTCATCATCGGTCTGTATGTTCTACTCTCTCGCTGATCAGTGTATTTGAATTTCATGTCCTGATCATTTGTTTTTTTTTC[A/G]GGTGAGACTGACGGAATCATCTGCACGTTTGACCTCTTTATGGCTTACGCTCCGGGTTATTTTATCGTGGAGGTTTTGGCAAGAGATCTGGCCGGACACAGCGACGTAGCTCTGGTGAGCATTTACATTCTGAGAGACGACCAGCGGGTGAAAATCGTCATCAATGAGATCCCAGAGCGAGTCCGGCTCTTTCAGGAGGAGTTCATAAACCTGCTGTCCAACATCACAGGAGCCATAGTCAACACTGATGATGTGCAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTGATTATTGACATGAGAACTATTATAACTGACTTGTGTGTAAGATTGAACACTTCTCTTGTGATGCAAATGAGTGAATGGGATGTTTTATTCTTTTAGTTCCATGTGGATAAAAAAGGAAGAGTGAACTTCGCTCAGACTGATGTGCTGATTCATGTGGTCAACAAGCAGACCAACCGTATTCTGGATGTGGAGAAGTAAGGGT
Associated Phenotype:
Not determined