Busch Lab

ZMP

NLRC5

Ensembl ID:
ENSDARG00000024631
Description:
NLR family, CARD domain containing 5 [Source:HGNC Symbol;Acc:29933]
Human Orthologue:
NLRC5
Human Description:
NLR family, CARD domain containing 5 [Source:HGNC Symbol;Acc:29933]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa23274 Nonsense Available for shipment Available now
sa23275 Nonsense Available for shipment Available now
sa6509 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43078 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15814 Nonsense Available for shipment Available now
sa17363 Nonsense Available for shipment Available now
sa29013 Nonsense Mutation detected in F1 DNA Not yet available
sa44887 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23274
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
ENSDART00000033762 Nonsense 258 1746 3 43
Genomic Location (Zv9):
Chromosome 18 (position 17288597)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17640363
GRCz11 18 17629429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCTGATCTCTCGAGACCTGTCCTTGAAAGAATTACTTTTTCTCTTCTA[T/A]CCTGCTTGTTCGTATGTTGAAGAAGAAAAAGAAGAAGTGTTTGCATTCAT
Long Flanking Sequence:
ATGAGAGTAAATTTACATTTTTGGGTGATATACAATTTCATGATTAAACTAAAAATTGAATATGCCTTGATTTTTTTACCCCTAGATCCTTTACAGAGCTACACAGATGCTCTGAAGTCCATGGTAAAGGAAAAACATAAGACAGTGATGCAGAGTGTGGTAAAGGATATACGTCTAGATGACACATGGGTGTATTTAAAGCACAGGAACCCTCCACGAGCAAAAGACAGGACCCTCCAGCTTCAAGCCTCTCTAGACAGCCATGAAGGTGAAGAGTCAGAGCACAAAGTGTCCGTTGAGTCTCTTTTGAAAACCACTGGCAGGGTTGTTGTGCTGCTGGGCCAGGCTGGATCTGGTAAAACCCTGCTCGTGCACTGCCTCGGCCATAGCTGGGCTGAAAACACCTTCCCGTCTATTCAGCTGCTGTTTCTGCTGGAGTTCCGGCAGCTCAATCTGATCTCTCGAGACCTGTCCTTGAAAGAATTACTTTTTCTCTTCTA[T/A]CCTGCTTGTTCGTATGTTGAAGAAGAAAAAGAAGAAGTGTTTGCATTCATCCTCACACACCCGGACAAAGTCTGCTTCATATTAGATGGTTACGATGAGTTTAGAGCCAAACTCACAGATCCTAGAGAACTTGAGAGCACAGTTGATCTGAGCACACCCATGCCAATGGCCGATCTACTTTCAGGACTCTGCAGTCGTAAAATTCTTCCAGATTGCACTGTTTTGGTCACCTGCAGACCAAGAGATGTGACGGACATGTTTGGAAGCCCTGGGCTCATAACCTGTGAGCTTCAGGGGTTTGACCGATTGGGGGTGAAGGAATACGCTGAGCAGTACTTCCATGAAAAAGGAGATCTCAAAACAAATGCTGTTAACTTGTTGATGGATAACCGTCACCTCTTGTCCATGTCTCATGTGCCTGGACTCTGTCATATCTGCTGTATATGTGTGGATCATCTGTTCTCCAGTGGTGAAGTGTTGAATCATCAGCTTCCAACGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23275
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
ENSDART00000033762 Nonsense 741 1746 5 43
Genomic Location (Zv9):
Chromosome 18 (position 17290421)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17642187
GRCz11 18 17631253
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCAGTGGAGGCCTCACCGATGTTGGAGCGGCTAAACTTGCCAAGGCGT[T/A]GGAGGATTGTCCAAACATCACACACCTGAAGTAATACAGTTTGTTATGTT
Long Flanking Sequence:
AGAACATCCTTAATAATAACAGTATTAATGACTGATATAGTGCTTCCATATTGGTTTTCAGCAAATTTATCTGCATTGGTTGATGTTAGGTGCATTTCAGTCGGATTATTAATTGTGTATGGCATGTGCATTTCCCATATTTCTTTTGCTTCAACCATTTGCCAAACATCTAAGTCTCACTTAAGTTCAGTTTCACCCATGAGATCTTGTAACTTCTTAAATATAACATAACATCTTGTAACTTGTTGAATTTATTTTATTCAAGTTTCCGTAGCCGGAAATATGATGACAAATTTGCAGAGACTTTGTGCGGTATCCTGTCTAAACTCCAGGCCTTGCAACAATTAGAGTAAGTTTTTTGATGTGTACTGTGTCCAATAAGAATTGTATCTCTGTATTGTCCTGTACTGTGTTTTGCATTGGTTTATGTTTGTCTCCGAATAACAGTTTTATCAGTGGAGGCCTCACCGATGTTGGAGCGGCTAAACTTGCCAAGGCGT[T/A]GGAGGATTGTCCAAACATCACACACCTGAAGTAATACAGTTTGTTATGTTATGAACTTTATAGATTGAAATTTCAGGCGGTCTACTCTGATATAAGACACAATGTTGTTAAAAAGGTGTAGGTGCTCTATAATCAATCATTGTGTTTTATTTTCTCTGACAGTGTCAGTGATAACTCTTTGAAAGATGAGGGTATAAGAGAGATTGCAGAAACAGTGTCCAGGCTGCACAACATCTCCTCTATTTTGTGAGTGTTTTAATTTTTAACAAACTGAATATAGTCTGTAAGTTTAATGATACAGCAAGTAAATACAGCAGTTAGCAACTTATTTGTAGCACCAAAATAACAACAAAAAAAGTATTATAATATAAGCAATTTATTTCATCTTTTTCAGCTTTCATTTTAAATTTATACTGGATTTTGTATTCCTACAATGCATGTAAACTACCTGGATGTCAAAATTACATCAAATTGACATCCAGTATTGGTGTCATACAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6509
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033762 Essential Splice Site 897 1746 11 43
Genomic Location (Zv9):
Chromosome 18 (position 17296499)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17648265
GRCz11 18 17637331
KASP Assay ID:
554-4579.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAAATTTTGGACCTTCTGCCTAAACTAGGAGSAATTCAGGAGATWAAG[T/C]AAGCAAAACACTTCATCTGCAATTATTTTAGTCTGAACAGTAAGATGGTG
Long Flanking Sequence:
ATCTACATTATTGCTGACTGGCAATAAGAGAAAGCATCACAATTTCAGCCAAACAACAAACACAACCATGTTTTGCAGCAGCGGTTAAATAGTGCAAAACGGTGTTTTTGTTTTATAACTGATAGTGAAACTGGTTACTGTGGCACAACAATAGTTTTCCTTTGACCACACATACTGAACTGACAGGAATGACCTGTTTTCTTTTTCCTTTATAGCTTGAAGCAGTGTAACCTCACAGTTTCCCATGTGGCCAGCTTGTGTAATAAACTCAGAGGCTTTGCCATCCTAACGCTTTTAGAGTAAGTTCTGCAATGCACCATTAATTCCACCTTTCAAACCGAAAGTAATTTGGGTTAATACATGCACAAATGTTAAAATCAGTGCTAATGTAACATCCTGTTCCCTTATATGCCAGTTTGTCCAACAACTCTCTGGGTAACAAAGGCCTGAAGAAAATTTTGGACCTTCTGCCTAAACTAGGAGGAATTCAGGAGATAAAG[T/C]AAGCAAAACACTTCATCTGCAATTATTTTAGTCTGAACAGTAAGATGGTGTCAAGCGTTTTTAGTGGATGTGCAAATGAGTTTCCTTTTTTATAGTGCTTGTAGTGACTTTCTGTTTCCCCCCCTAAACCCTCACAGTGTCAGTGAAAATGGTGTTGATATGGAGGGTGTGGTGATGCTGGCTTCTGCCCTCTGTAAACAGTACAACTTAAAAAGAGTGGATGCAAGGTAACTTGTTAAAATAAGCCTTAACCATTATTAACAGTTTTGTTGCAAGTCTGCTTTGCTGTTCACATGCTAACGCTGTGCTCTTTCACAACAGTGAAAATGGAAAGAAAAAAGTGGTTCTTGGGTTTGACACCACCAGAGGGTACTAAAAGAATGATGACAAATTTCTGTCTAATATAGAAATGTTTATCATGGAAATGTTGCAATAACAAGTGTGCTTCATGAATGCAGGCATAATTCAGGGGAGCTGACTCAAAATGAAACCGGGATGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43078
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
ENSDART00000033762 Essential Splice Site 963 1746 15 43
Genomic Location (Zv9):
Chromosome 18 (position 17297902)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17649668
GRCz11 18 17638734
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTGTTTAAGAATCAATCAATAATTTCATACGTTGTTTTTGTTTTATT[A/G]GTTTAACCCATAGTGATATCCAACCTGCCTACATGACCAAGCTGTGTAAG
Long Flanking Sequence:
AGCAAAGGAACTCTCAAATGCTTTCAGAGAAAGAAAATCAAGGTGTAATGGCTCAGCCAGGGCTGGCGCTTCTATAGAGGTGACTTAGGCAGAATTGTGAGGGCGGCGTCTGCGCTCCCCCAACCCCCCAGACCTCACTTTTGTCCGTGACACAGAACCTCCGCCCACCCTTCGCGACACCCCACCTGGACTTCAATTTCGTCAGTGTTTTTACTTTCGGGTTGAGGGCGGTGTTATCATCATTCAGCTTGCTCCAGCCCTGGGCTCAGCCAATCACCTGACTTGAATTAAACTTATTTGTTAGATTTTTTATTTTGTTACATTTTTTATGTTTGTATTTTTTTTTTTTTACCACAATCTGGTTCAATTCCATTCAACAGTTTTTTAGAAATATTATTCCCTGGAAAAAAACAATACTTATTTTCCCTGCTTTATATTCTATCAATTTGTTAATTGTTTAAGAATCAATCAATAATTTCATACGTTGTTTTTGTTTTATT[A/G]GTTTAACCCATAGTGATATCCAACCTGCCTACATGACCAAGCTGTGTAAGCAACTGGTGAAATGCAAAAACCTACTGGACATTGAGTAAGTTGATTTTCTGCTATTTTATCAGTTGCTGAGTTCTTCACATGTTTTTTTCTAGTCTTCAATCCTTTATTTGTTGCAGCTTCTCCAATCTAAAATTAACCGACGATTCTGTTGAGAATTTGATGTTGATCCTTCCTGTCATGTTGTCTCTTCATGTACTGAAGTAAGTGGTGGTTTTGGCCTTGACCTATTAGATGACATTACCTACTGTATGTTCATTGATAATGTCCTTCTTTTCCAGCTTAAGTCATGTTGATCTGTCTACAAATGGGGCTTTGATATTGGTCAGATCTCTTGCCGATTGTCAGCGTGTCACTTCTGTCGAACTCAGGTATTTTATTTAAATCTGTATCAGGCACTAAAACAGAGATAACTTAAATATTTTGGCACAAAAATCACCAGAGCAGAAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15814
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033762 Nonsense 1130 1746 21 43
Genomic Location (Zv9):
Chromosome 18 (position 17302589)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17654355
GRCz11 18 17643421
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTACKTATTGYGCCATTTAATACTTACTCCTTCACAGCCTCATTGGCAAC[C/T]GAATGACTCAAATCGGGGYACTGCATCTGGTCAACKCAATGAATACYTGT
Long Flanking Sequence:
TTATCACAATCATCAGCACTTTTAATAGTTGATTTTACAGACTTATAATATGCTGTTGCTCTATTGGAGTTTTCATTTCAAAATGGCCGCCGCGCCATTTAGTGGCTGTTTTCCAAATTACACAAGAGTGTCGCTTCTTGGTGATTCTATGCTCTTTGGTCATTCTAAGCTCTTTGCTTTAGCTCAACCGCTCTCACTGGCAAAGAAATAATAAAAACTAAACACCATTGGGTGTTTTTTAAAAAGGGGTGGAGCTACTCTATGCTCTCTTTTTCAGTTGAGATTACGTCAAAAATGGAATACCTTTATTTCACAATGATGCTTATTGTACATCATCTTGTTATATTTTGGGAGAGGCAAGTGCCATTTCGGTCCAAAAAAATTGCTGATAAAATAAAAGTTACATTTAGGCAGAATTTAACAGGGGTATAAATAATTTTGGGCTTGACTGTACGTATTGTGCCATTTAATACTTACTCCTTCACAGCCTCATTGGCAAC[C/T]GAATGACTCAAATCGGGGCACTGCATCTGGTCAACTCAATGAATACCTGTGAAAAAGTTGTTGCTGTCGAAGTCAGGTAAAAGCCCAAGCACTACAGCACCTATTTTTCAGTTTTACTTTCAATTTGTTGATTATCTCTGAAAAATGTTGTTCATAATAACGCAATAACTCATCTAAAGGTATATGCTTTCTTGTCTGTAGTCTTGGAGTGGAGGATCAGTCTCTGATTCAGTTTGTGCAAGAACATGCCAATGGCAAGACTCTTAGGTAATTTCCCGGAATGCATGTGAGCTATAAAAAACACAATCAAAAAGTCACATGAACGATTTGATTAATTCACTCAAGTCAAAAGTGAAAGTGTGTTGGTGTTCTTCTTCCTCTTATTGTTGTCTTTTGTTCAGGCTAAGGGAGTGCAGTTTTGAGCTTGCACACTTGAAGATGCTTGTGAAAATCCTGACAAAATGCCCAAGACTCCTTTCATTAGAGTGAGTGTTTGCGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17363
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033762 Nonsense 1334 1746 29 43
Genomic Location (Zv9):
Chromosome 18 (position 17306596)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17658362
GRCz11 18 17647428
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCCACTTTCRTCACATTCTTYAGCTTTGATGACTGTGATGTAGAAGGA[C/T]AGCACCTCACTCAACTCGCACTTCCCATCCAGAAATGKCATGCCTTACWG
Long Flanking Sequence:
TTGAGAAACCTTCTAAAGAGATTACTAAATGTTTACATTACATTTTCAGGGTCCACCGTGCATCTATAAACATGATCATTGAAGCCAATTCCATTTCCAGCTCCACTTCAGTGTAAGTTACTGTACATTAATGTTTATCCCCATGGAATGTGGTTTTCTATGAATTATTGTGCATAGATAAGCTTCACAGTATTACATATTCAGAGCTAATTTGGGCCTTTTTTTTTTACAGCGGTCATTCTGAAAATGTGTTGCCTGCTCTGCAGTCTATCAGGTGTGTAGTATTTTTTGCTTATGAGGTGGTTGTGTTTATTTTTGCTTTTAATGACTTTTATTTTAATACATAGCCTCTCAAATCTGACAGCTTTTTAAAAATATTCTCAAGCCAACATAAGGTTTTGCAGTGCTAATTCATTTAAAAAAAAGGGATCTTCTTACATTTGATTTAAAATGCCACTTTCGTCACATTCTTCAGCTTTGATGACTGTGATGTAGAAGGA[C/T]AGCACCTCACTCAACTCGCACTTCCCATCCAGAAATGTCATGCCTTACTGGATTTAAAGTAAGTCACTTAGAGTTTTGTTTTATCAGATTAGATTAGAAAAGCAGATTTCTCTTTATATGATTTCTGGTATTGTGTTGTGTCCAGGTTCTCGCCACTTAAATTGGACAGAATAGGTGCAGAGTTTTTTTCTGCAGTCATTCCATTCTTAAGGAATCTCAGGAACATCACGTAAGTTTCCTTGATTTTTCAAATATATGTACTAAGTGGGCATTTCTATATTTATAGTGTTGAGTGGACATGCATTCACTACAAGACATTACTGACTTTTATTGGTGCTCTGATTCCAGAGCATGTATTTAGCCTGAATATGGACAATTTATTAATATTTGTTTTGATATTAGAATAATTTGACAAAATCAATCTTGATTTGTTATATAATATCATGCAATAAATAATACATTTATTATGAGCACAATTGTGTTGAGCACTACGGTGGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29013
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
ENSDART00000033762 Nonsense 1484 1746 34 43
Genomic Location (Zv9):
Chromosome 18 (position 17308810)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17660576
GRCz11 18 17649642
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGTCTGTGGTACTCGACCAGGAGGGTATAAATATCCTAGCTCAAGGCT[T/A]GAGTCGACTGGCCTCACTTCGGAGGCTCAGGTAATGTTAGTTGTATATTT
Long Flanking Sequence:
AGTTTTTACATTTAATTTTGAACAGCAAACGTGGTGGGAATTATTTTGCATAATTTCATTCTCTATTTACCTTACTGCATCTTTTAAATATTCCCTTTCTTTCAGCTTGTCCCAGCTTGTCTTAAGTGACCGTGGAGCTACACTATTCGGAAAAGCTTTTCAAAATGTGCCAAATCTGAAGTCATTCAGGTACCTCAAGCAGGTTTATGATTGTTACTCTATGCAGCAGAATACAGATCTCTGATTGGTCAATATCTACTTGTGCAGTATGTTGCAGTGCTCTGGTTGGACAGCAGCTCGAGGCTGTGACTTGGTCAGAGGCTTGATGCAGTGTGTTTTGCTGACAGAAATACGGTACCTCATGCTGTACAGTGTTTATAATATTACATTCACACTGACAGGGTATACTGTACTGTGCTATATTTAATACTATGCTCTCAATAATAGACTGGAGTCTGTGGTACTCGACCAGGAGGGTATAAATATCCTAGCTCAAGGCT[T/A]GAGTCGACTGGCCTCACTTCGGAGGCTCAGGTAATGTTAGTTGTATATTTTGCAAGCAGAAACCCATTCAGTTTTTTATGCTTAAGCTTGATTTTTGCTCTTTCCTTAGCTTAAACAACATTACAGTGGTGACATCTGAGACTTTTGTAAATGGCACTGGAATACTCTGTCTACTGGCCTCTTTTAAAGGTTTCAAACAGATGGAGGAGATTGAGTATGTATTGTTGTATGCAAATCACATGTACAAGTGCTAGCAGCTTTTGGAAACATGTACATTTTTTTTTTCTTATTTGAAGGTTGGAAAGTTGGCGGATGGGAGATGGTGGTACCAATGAGCTTGTGAAATACATACCTTCATGGACAGGGCTGGTAAAAATAAGGTATGGCATCTGCATTGAGCACGAGATTAGGAATAAGCGTTACCTACAACATGAGAGATATTTATAAGGTGTATGATGACCTCTAGTGGAGATCCTTAAACATATACTTCAATGGCAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44887
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000033762 Essential Splice Site 1695 1746 41 43
Genomic Location (Zv9):
Chromosome 18 (position 17314013)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17665779
GRCz11 18 17654845
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGACACTGGCTGAGATTCTTCCCTTGTGTACGAAGCTGAAAAGACTCGA[G/T]TAAGTACTGAGATGCTTACAACCATGATATTTACGTGATTACTCTGTGCT
Long Flanking Sequence:
GCTGGAACTTGAAACAGCAACCTTCTTGCTGTTTGGCAACAGTGCTAACCACTGAGCCACTGTGTCGCCCCAGCTGTAGATTTATTAAATGAAATAATACCACTATCAAAAGAGACAGAAAAGCGTTGATGTTACCAATAATTCCTAATAAATTGTGCTGTATTGAAATTGCTTGACTCTATATAATGTGATTTGGTTGTTGTACACTGTAATCCAATACTTGTTGTCTTTCAGTTTGACTTCGGTTGAGTCTTCAGATCTGGTTGGTGTGGCTTCATCCTTAAAACACTGTCCATCCATAGAGGATGTCAGGTGGGATCAGATTTTTTTAATGTAGAATTATACGTTTATGAATAAATAGATCCAGATAATGCATTGGTATATTCCTTGTGCTCCTTGTGTGTTTTCTAAATTAGTTTGTCATGGAATGGATGTGGTGACAGTCTTGCACGGACACTGGCTGAGATTCTTCCCTTGTGTACGAAGCTGAAAAGACTCGA[G/T]TAAGTACTGAGATGCTTACAACCATGATATTTACGTGATTACTCTGTGCTGATGATATTAAAACTAATGATTGCAGCCTGGAGGCTAATAACATAACCACAGCGGGAGCCACACTGATTGCCAAATGCCTCCCATTATGCCCATCCATTGAAGTTATAAGGTATGATAACTAGCCTGTAAACACTTTATCCAGCAACTGTACTGTAGAGATCAAAATTAATTGATTTATATAAATTATAAATAATCTAATCCTTATGATGTGTAAAAAAAAACTCTTGAATTAAGTATTAAGTATTACCTTCATGCTAATTAATTCTTGTAGCTTAATAATTATCAGATTAAATCACGCTCAAAAAAGGTTTGCTGGTTGTTCAAACTAGTTATTTTAAAAAAGCTGAAACAACACGATTCTTGAATTGAAGTTAACTTAATTCCTTTGATTGTTTGGAGCCCAGCATTTTTTTACAGTGAATTATCTAAGGGTCTATTTTGAGGATGAT
Associated Phenotype:
Not determined