Busch Lab

ZMP

LOC100332172

Ensembl ID:
ENSDARG00000074314
Human Orthologue:
TTC37
Human Description:
tetratricopeptide repeat domain 37 [Source:HGNC Symbol;Acc:23639]
Mouse Orthologue:
Ttc37
Mouse Description:
tetratricopeptide repeat domain 37 Gene [Source:MGI Symbol;Acc:MGI:2679923]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa12559 Nonsense Available for shipment Available now
sa2213 Essential Splice Site F2 line generated Not yet available
sa40552 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33706 Nonsense Mutation detected in F1 DNA Not yet available
sa33705 Nonsense Mutation detected in F1 DNA Not yet available
sa33704 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31475 Essential Splice Site Available for shipment Available now
sa18177 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa12559
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100800 Nonsense 40 1577 2 40
Genomic Location (Zv9):
Chromosome 5 (position 52554320)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50221516
GRCz11 5 50868109
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCTATTTCTCCACTTCAGGCTGTTCTAAAGCTTGAGAAGAATAACTA[T/G]AATGCCTGGGTGTTTATTGGAGTGGCAGCCACAGAGCTCCAGCAGCCGGA
Long Flanking Sequence:
TTAAATCATCTTTCTTCCCCATTCTGATGCTCTGTTTGAACTGCAGCAGATCGTCTTAATCTACTTGCCTAAATGCATTGAGTTGCTAACATGTGATTGGCTGATTAGAAATTTGTGTTAACGAGTAGTATCTAATAAAGTGGGCGATGAGTGTATAAAATACCTACATAAACACACATAAAATTACAAAAACTATGTCAAATCAAAGTTGAAACCGTGTTAGCGGCCAATGACTATAAAAATGAAACATTGTTCACAGTCAATTAAATAGTGCTAATGTTGTTTTGAAGTTATACTTACATGCAATTTCAAATTAACTATTCAAAATAGCATGGTAACGTCAAACAATATTGGGACACAAATGAACGAATGTGCAAATATAAAACTAACTTTACCTCAATTTATACCTTTCTCTTGATTGACTGAATTTATAAATGTCTTCCTCAAGTCAAATCTATTTCTCCACTTCAGGCTGTTCTAAAGCTTGAGAAGAATAACTA[T/G]AATGCCTGGGTGTTTATTGGAGTGGCAGCCACAGAGCTCCAGCAGCCGGATCAAGCACAGACTGCATACAGAAAGGCATCGGAGCTCGAGCCAGAGCAGCTGCTGGCATGGCAGGTATGTCTTCTTGATTTAACTTTAATAGAAATCTTGTGTTAAGGCAGTTTGTTTAAACGTCTTAATTTTGTATTGAAGATATTAAATGAGTATTTCTTTCACAGGGTTTAGCAAATCTGTATGAAAAAAGTGACCAAGCAGATTTCAAAGCTGAGCTTCCCAAGATTTACCAGAAACTCATTACGCTATATGAAACGTAAGTGCTCTAATGCTGAAGGGCAAATTACATTTGTTCCTCTTTATTTTTTTTATTATTGTTATTATTAGTGGTGCTTAACTACTATTAATCACATCCAAAATAAAAGTTTGCATTCAAATTAATTTGCATACAAATTTATATATAAATTTCTATATAACAACATTGTTTTGTTTTTATATATCTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2213
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100800 Essential Splice Site 184 1577 5 40
Genomic Location (Zv9):
Chromosome 5 (position 52552789)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50219985
GRCz11 5 50866578
KASP Assay ID:
554-2695.1 (used for ordering genotyping assays)
KASP Sequence:
GACTCCTGCAGGACACTGTTGACGACCAGGACAATGAAACACAGCAGCAC[G/A]TCAGAATTTCTCATATTCAAATAAAATACTCTATTTTTTCACCCAGAAAT
Long Flanking Sequence:
GATGTCCCATTTCGGTGTCATTATCAAATGAAAATGATGACAGAACATTCACATTCTTGTTCATATATAAATAAATATATGTTTAAATAAAAGCACTCTACTGCACTGGGCACCATTTGCTTCTTAACCCGTTTCTTTTTTTTTTTTTTTTTTTGCATTTGCAGCTCAGACAAAGCAAAATGTTTCGAAGTGACAAAGAAATTGGTGGAGATTTATCAGTCAGAAAAGAACTATCTACAGGTATGAGCTACAAAAAGATAAATAAAATCCTAATGTTACGGCAAATGATTTAAAGGTTCAAAATTGTGCTGATCTTTTAATTATTCAAATTTGCACAATATTTTTCAAACCCACAGGTGGCCAGAGTGTGGCGGAGGTTAATCCAGGTGAAAGAGGACGAGGAAGGGCTGGAGGATGCAGAGCTGCTGGAGCTGTGGAAGGAGATGACCAGACTCCTGCAGGACACTGTTGACGACCAGGACAATGAAACACAGCAGCAC[G/A]TCAGAATTTCTCATATTCAAATAAAATACTCTATTTTTTCACCCAGAAATACAAAATATACAAGACTTACATTTTTCATAAAGCTGACAGTGTTAGTGTTTTTTCCTCAACAGCTGATATCTGCATTTGAACGAGCTTTACAAATGACAGTAGATGTGCCCAGTGAAGCCCACAGGAGCCTTTCGCAGGATTACATTAAATGTCTTTCAAAGGTCAGCCAGCTGTATATGGTGTAAAAGCAGTAATGCGTACAATAATAATGACTGGAACAATTCGAATGTTGCATGTTTTGTGCCGTTTAGCTTCCTCATGAGGTGGCCAAGCTAAAGGAAGTATGTGACGCCACCCTGTCCCACTATCCCACACACCCATACCCTCTAGAGGCCCTCAGTGAGCACTACATCCAAACAGGTTAGTTTATTACCCTACAGAAAAAAACAAGATAAAGGCATTGTGTGTAATAATGAGTTTAACAAGTCCAAACTAACTTTACTCATTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40552
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
ENSDART00000100800 Essential Splice Site 300 1577 8 40
Genomic Location (Zv9):
Chromosome 5 (position 52548766)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50215962
GRCz11 5 50862555
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTGTCAGGATAAAAAATATGAGGATGCCATCAAAAATATTGGTCTGG[G/A]TAAGTTCATAAACACTCAGATGTTCATGAATGAATGGAGCACTAAGGTTA
Long Flanking Sequence:
ACTCCTCCACCTGGGATAAGGACTTTATTACATTCTGGAGATGGCAAACAACCTTTATTCTGGTGGAGCACCATGTCCTCCGACTTGGAGGTGCTGATTCTCATCCCTGCCGTGTCACACTCGACAGCAAACAGTCCTGTAGTTTGTATGATATAAAATAAAAACTCAAACTGGTTTGGGAAGAGAAAAGGATGAGTAAGTAATGACAATTTTTTATTTTTTTTTGGTGAAATAACCCTTTAAGCAAGATTAGGATTTTATTTAGAGGTCCATAGCATCTAAAAGCGTAAAACATAAAAAAATATGCCCCATATTTAAAAATGATAAGTAATAAATGTTGTTTTTGATTTTCTTGTCAGGTGACTGCAGTGAAGAAGCTGTTTCCTGTTTCAAGCGTCTCTTAGAACTGGATCCAAACAACTCGTATGCTCACTTTGGTCTCGGTATTAAAGCTTGTCAGGATAAAAAATATGAGGATGCCATCAAAAATATTGGTCTGG[G/A]TAAGTTCATAAACACTCAGATGTTCATGAATGAATGGAGCACTAAGGTTATAAGAAATTCATTATATCAAATTCTCCAAATGCATTTTGATCATTAAAAGTTGTTTCAATAAATCTTTTACTTAAATTCATGTTTAACTGTACAACATTAATGAAGTTCCTTGCAATTCCTAGGTATACAGTGAAAATTACAAAAAATATGTGTAACTTATTTGTTGTGTGTTTTTTTTTTTCTGCAGGACTGAAGCGTATGCGCTTCTCCATCATTGGTTGGTATAATCTTGCCCTGGCTCAGCTAAAAATGCATAAATACTCTGACAGTGCCATATCTTCCAGTCAAGGTACTGGTTATATGATTCACAGCTAACTGCTCAAGTCAGTTGCACTTAAAAACAGTTTTCAAATATGTTCCTTTTCATTTGTTCAGGGCTAAAATCGAGTGTGGGGAACGCTGATGATTGGACTCAAAAGCTCCTGAGGTTGAAACTAGAAGCTCTGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33706
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
ENSDART00000100800 Nonsense 471 1577 13 40
Genomic Location (Zv9):
Chromosome 5 (position 52545177)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50212373
GRCz11 5 50858966
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGTTCTTCCTGCTCGGGTCCCTTTATTGGAACATGGGAGAGGAAATA[C/T]GAAGAGACCGCAGCAAAACTCATTTACTCAAAGTGAGACACTTTAAAATC
Long Flanking Sequence:
TACCTTCTATAAAATGCTAAGGAAGTTAGTTTGTTTACCTACTGTATGTTCTTCATAATATTTTCTTTTGAATTTTTTTGAACAAGTAAATAGTATTTATTTTTTTCATTTTAGTGAACTATTCCTTTAAGAAATTGGATATTCCAAAAGCGAAGCAGTTCATAATAATGCCATTAATGCAATAATGCCACTGGAATGAAATGATTCTTGCAGGTTTCCACTGAGCTTTTGAGCTCTCACCCAGGATCTGTGGATGGTCTCACTTTGAAAGCACTTCTACATGTTGCTAAAGAACAGCACAAACAAGCTGAGGAGAGGTGTGAAACTCCACATATGCACACGCACACATGCATATATCATAAACAACTTGGGTGTAACCACCAGGCACTTATTTTCTCACTCTGTTACACAGCTTTCTAGAGGCTTTATCCAGAAGTCCAGATAGTGGGGAACTGTTCTTCCTGCTCGGGTCCCTTTATTGGAACATGGGAGAGGAAATA[C/T]GAAGAGACCGCAGCAAAACTCATTTACTCAAAGTGAGACACTTTAAAATCCTTTTATAGGACCCTGGTAAATATAATTTATTTCCCCCACATTTTGTTTTGTTTTTCCTTTTAGTTTTTATGTATTGTTTTTTAATTTTCTGTTTGAAATATATTTTTTAATTTTGATGGATATAATTTTAGTAATCAAAAACTATTATTTAATTGTTAGCAATATTTGAAATAAAAGTAAAATTTTTTTTAAGCAAAAAAGTAGCAAAAATAGTAGCAAAAAAACAAAAAAAAAATTCTCCCAAACTTTTGGGACTATTAAAGTTCTGCTACCTTAAAAAAAAAAAAAAAACTTAAAATTTAATGGGTTGTTTTAAATTAAAATTTAGGCAATGTCCTCATAAGGGAATGACAGAAGCTAAAAATAACACAATCTTCACATTTTATTAAATATTGTGCATTCAGTTAATGGAATGAACAATTAAGTATAATTCAATTTGATAAATTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33705
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100800 Nonsense 788 1577 19 40
Genomic Location (Zv9):
Chromosome 5 (position 52535251)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50202447
GRCz11 5 50849040
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGATGCCAGAAGCTCCCAGTCTGTGGTGTGACCTGGGTTTGAACTA[T/G]TACCATCAATCCAGACTGCTCAGCTCTCATTATCCTGAGGAGGATCCCCA
Long Flanking Sequence:
TTGACATCACAGAAGTAAAATACATTAAATATATAAAATAAAAATCAAATTATTTCTTCCAATAATCAAGGACAAACTTTGTGAATTTGCTTGTATTTATTTAAGCAGATACAGAAACATTCATTAATTCATTTTCTTTTTGGCGTAGTCCTTTTATTAATTCGGGGTTCCCACAGTGAAATAAACCGCCAACTTATCCAGCATATGTTTTATGCAGCAGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAAAGATACAAAAACATATTGAACTAATTATTAAAATGAAGACTGGAAAAATGGAAAGAAATATAAATTAGATACTGTATATAAATAAAAATACAAATGAATAGAAATAATGCCTACTGCAAAAATAAACGAATAAATGCTAATAATTTCCTCATTCTGTAATGAACCTATATTTTATTAGGTGTTTTGGTCGTGCATTAAAGCTGATGCCAGAAGCTCCCAGTCTGTGGTGTGACCTGGGTTTGAACTA[T/G]TACCATCAATCCAGACTGCTCAGCTCTCATTATCCTGAGGAGGATCCCCAGGCTCTGCTGGAGAAAGCCCTTCAGGTACTTAACCCGAATTTTTTGAATTCATAGTGATCTCATGAGTATGAGTCTTAACAGGCTGTCACTGTGATTTTGTCACTGTTCTGACAGTGTGTGAAAAAGGCAATCATGCTGGACAGTGCAAATCACACATACTGGAATGCCCTCGGGGTGGTAGCCATGACAAAGGGTAAACACAATCAGATGTGCATAATCGAATTAATCTGCATTACATAACTACAATGTGATTGGTCATTTGTGTGTTCATTATATTCTGTTTTACAATCTTAGGAATTGAAAATTTTGCACTTGCACAACACAGCTTCATCAAATCAGTCAAAGCGGAGCCAAACGTAAGTGATGCAAGAAAGGGGAACAGTTTGCTTACTTTTTAAACATTTGTGTTGATGCAAGTAATATAGAGTTGACGTCAAAATGATGAGCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33704
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
ENSDART00000100800 Essential Splice Site 839 1577 20 40
Genomic Location (Zv9):
Chromosome 5 (position 52535006)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50202202
GRCz11 5 50848795
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAATCACACATACTGGAATGCCCTCGGGGTGGTAGCCATGACAAAGG[G/A]TAAACACAATCAGATGTGCATAATCGAATTAATCTGCATTACATAACTAC
Long Flanking Sequence:
CTGGGAAAAGATACAAAAACATATTGAACTAATTATTAAAATGAAGACTGGAAAAATGGAAAGAAATATAAATTAGATACTGTATATAAATAAAAATACAAATGAATAGAAATAATGCCTACTGCAAAAATAAACGAATAAATGCTAATAATTTCCTCATTCTGTAATGAACCTATATTTTATTAGGTGTTTTGGTCGTGCATTAAAGCTGATGCCAGAAGCTCCCAGTCTGTGGTGTGACCTGGGTTTGAACTATTACCATCAATCCAGACTGCTCAGCTCTCATTATCCTGAGGAGGATCCCCAGGCTCTGCTGGAGAAAGCCCTTCAGGTACTTAACCCGAATTTTTTGAATTCATAGTGATCTCATGAGTATGAGTCTTAACAGGCTGTCACTGTGATTTTGTCACTGTTCTGACAGTGTGTGAAAAAGGCAATCATGCTGGACAGTGCAAATCACACATACTGGAATGCCCTCGGGGTGGTAGCCATGACAAAGG[G/A]TAAACACAATCAGATGTGCATAATCGAATTAATCTGCATTACATAACTACAATGTGATTGGTCATTTGTGTGTTCATTATATTCTGTTTTACAATCTTAGGAATTGAAAATTTTGCACTTGCACAACACAGCTTCATCAAATCAGTCAAAGCGGAGCCAAACGTAAGTGATGCAAGAAAGGGGAACAGTTTGCTTACTTTTTAAACATTTGTGTTGATGCAAGTAATATAGAGTTGACGTCAAAATGATGAGCCCTCCTGTGAATGTTATTTCATTTTAAAAAATAACTCCCTAGTGTCTTAACTGATATGTTATTATTTTTAACACATTTTTAGACACAATAGTTTTAAAAACTATTTTTTTTTGTCTTTGCCATGATGAAAGTACATAATATTTTAATAGTTATTTTGCCAGGTACTATTATTCAGCTTAAATTGCTAGTTAAAGACTGAACTAGGTTTTTAGGTTAACTACACTCAAAGCATCTGTTTGTTAACTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31475
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100800 Essential Splice Site 1009 1577 26 40
Genomic Location (Zv9):
Chromosome 5 (position 52530500)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50197696
GRCz11 5 50844289
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACACACACCTGCAGCTCAGGAAACAGGCCACTGAGGCTTATCACAGG[T/C]TTGCCCTTTCTAGCTAATTACACATGTCAAAAAAGATAATTAGGCTACCT
Long Flanking Sequence:
CTTACCCAATAAAATGATTATTAAAGTGCAACCAGTATGCTATTGATATCCTAAAATCTTTAACTTTCAAAGTAGGTAAATACGCTGAAATGGTACTATATGCACTGTAATACGCAATGTTAAAAAATCTGCATGCTTTTTGAATATGGAGCAAATAGTTATTGTATATTATTATATTATAATTCAAATAATGCACCACCCTCTTTGTTCATAAAAGCGTCTTTAGGCTGGAAATGGTTTAAATCCCATTATGGCTTGAATGATTTGAATGACTTGTAACGACTAGACGCATTTCAAAAATGTGTCTCCCATTGAATATTTAGGAAATTAATCATGTGACAATGACAAATTTGAAAGATGAAGAGAGGTAATGAAGCTCAGTGTTCTTTCTGTTTTTCACACCAGAGAGGATTCAGACAGACCCAGACGCCTTCATCATGCTCGGATACCTGAACACACACCTGCAGCTCAGGAAACAGGCCACTGAGGCTTATCACAGG[T/C]TTGCCCTTTCTAGCTAATTACACATGTCAAAAAAGATAATTAGGCTACCTGACATAATTTCATATTAATGGTTAATCTTTGGTTTTTTAATATTGCAGACATTTATATCTTATTTATTAGAAAAAATACTATAAAGTTTCTTGTATAAAGACAATGTTCATGCTGAGATGTTTTTTTCTACATATAATTCTATTGTGTTTTACACATTTTTATAGTTACTTATTTTAATATTTAGTTCCCCTCTGTGTTTATTATTAATTTTATACTAATTTTAATTAGTTAAATATTATGTGATTTTTTTTAATCTAATCTTGAGTTGTTTTTTAAATACTTAAATATTATTTTAAATATTTTATGGATGTTATTATTATTATTTTTATTGTTTTGTTCCAGCTATATTAATTTGTTTCTTTATTAAACTTTATAAAATAATGTTTTTTTTTTTTTTAATTTAGCATTTTTCTCGAAATATTTCCACTGATCCCCTGGCAGCCTCATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18177
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100800 Essential Splice Site 1509 1577 38 40
Genomic Location (Zv9):
Chromosome 5 (position 52507193)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 50174389
GRCz11 5 50820982
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTCCTTTTTCAAGCCTTACTGCAGTTCTCCGTGAAGATGGGYGCCAG[G/T]TAGARGACTTTAAAAATAGAGCTCTTTTGTGTTTSTGTTGTATTAATTGT
Long Flanking Sequence:
TTACAGCGCCTTCAGGCTTCTCTCTTGCACATTTTCTCCCTCTAGTTTTATTTTGTCTCTCCTCCTCTCCTCCCGTCTTTAACTGTCAGCTTATTGCCTTTATTTTAGCTGACTGCAGCTTTGCCTGTTAAATTGAATTAGACACTTTGTGGCTCGCCTTTCATTACTTTTAATTAAAGTGTGTGAGCCTTCAGCGTATCCCGACTCCAGTCATATATTAGTCTGAACTGTGCCAGCTAAAATACATCTAAAATTCTTGTTTTATAAGACTTTTGTTTCTAGTTACTCATTCTATTTCATAAAGTTGATACACCAAAACTACTGAAGTAAACATTACTTAAATATATCCAACTTCACTTTTGGTTACAGGCAGGTGTTGGCGTTTCTGATTGGAAGGATCTGGTTTCTGAAGCCACAGGTGAAGTCTTAAAAATGAGCAAATCACCGGTCGCTCTCCTTTTTCAAGCCTTACTGCAGTTCTCCGTGAAGATGGGTGCCAG[G/T]TAGAAGACTTTAAAAATAGAGCTCTTTTGTGTTTGTGTTGTATTAATTGTTACCATGGTATTCGAATCAACATGTCAGATCAGTTTGACCTGTTCTGTACCATGTGTTTGCATTACATTGTTTGCTTTAGCTTGGCATTGCATTGTTAATTAACTATATTTAACCCTTATGTACTGTTCAAATTGACTACCCTTTCATATTGGTGGCACTTATCGCCCCATTTACATTCATTATAACAATATTTTTGGATTGCAAAGCCTTGACACCAAAAAATCATGCAGTCTTGTTTGTTGGTGTTTTTCCTGTTGGAAATTTTTACTGTTGATCATCAGTTTTCATCATTAACCCTTTAGTTAGGTCTTTGCAGATAAGTTTCTGAATTTTATATGGAGTTCTATGGAGTAAAACAACAAAACATAGTGTGTGCATGAATACACTTGCGTGTACTATGTTTTGAGAGCTGTGCTGCTTATTTTTGATTTTTTCAACCATATCAAGAT
Associated Phenotype:
Not determined