Busch Lab

ZMP

zfyve9

Ensembl ID:
ENSDARG00000023701
ZFIN ID:
ZDB-GENE-070705-182
Description:
Novel protein similar to human and mouse zinc finger, FYVE domain containing 9 (ZFYVE9) [Source:UniP
Human Orthologues:
AC055876.2, ZFYVE9
Human Description:
zinc finger, FYVE domain containing 9 [Source:HGNC Symbol;Acc:6775]
Mouse Orthologue:
Zfyve9
Mouse Description:
zinc finger, FYVE domain containing 9 Gene [Source:MGI Symbol;Acc:MGI:2652838]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa51 Splice Site, Nonsense Confirmed mutation in F2 line Not yet available
sa50 Nonsense Available for shipment Available now
sa19724 Nonsense Available for shipment Available now
sa44 Missense Confirmed mutation in F2 line Not yet available
sa9383 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32886 Nonsense Available for shipment Available now
sa32887 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8528 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa51
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031837 Splice Site, Nonsense 25 1216 2 17
ENSDART00000132283 None None 842 None 16
Genomic Location (Zv9):
Chromosome 2 (position 19133251)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19670069
GRCz11 2 19319133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCAGTCTTTTCAAAAAGCTAATGAGCTTTCTTCTTATCCTTTCAGAT[G/T]AAACGGACACACCAATTCTCTCGGATGCCAAGTGGACTCAGATTCTGGCC
Long Flanking Sequence:
TGTCGCCACTGAACAGTTGAACAAATGTATACCCCCTCTCCGACACTAATCTTGACAGATTAATGGGGATGAAAGGAAACATGAAACTATTAAATGGCCTCAGAAGAAAGGCAAATAGGGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTGAGTGTGTGAGTGAGTGAGTGAGTGTGTGAGTGTGTGAGTGTGTGAGTGTGTGTGAGAGAGAGAGAGAGAGAGAGAGATATCACACTTGAATGTATGTAAGGATATGGGAATGCCTGCCCACATTCCTAACCATTCATGTGTCAGTTTGACAGATGGATCCCAAGGGGATGACTAGATCGACCCACTTCCTTAGCATTTTCCAATTTAGCCTGACCTCGTTTCTCAAATTTTACTCTGTTTGTTTCAGTCTTTTCAAAAAGCTAATGAGCTTTCTTCTTATCCTTTCAGAT[G/T]AAACGGACACACCAATTCTCTCGGATGCCAAGTGGACTCAGATTCTGGCCCCTCCATCACACCTCCTTTCCCTGAATCCGGCACTAACCCACTCTGACCTCAGCCCAAGGGACAGCCCTATCAGCTTCAAGCCCCTTCTGGACACCCAGACATCAGATGGGCCCTCTTTGGTTGAGGTCACCAGGTTAAATGGGAAACAGGGACTGGGACAACAGCAAGAGGGCAAGAGTGAAGAACGGCCAGCAGATGTTTACAGTCCACCTCTGCCTCAGCCAAACATTGGCAAGCTAGTGAGCACTGACGGGCAGTTGGCAGACTTACCGTCCTTCAACAGTGGGGTGTTGGAAAATGGTTATCCAGCCAGTCCTGATCATACCGTCCAGTCTGATATCATTAGATTCAATGATGATGAGACAAATCAACCAGTCATAGACAAGAAGTGTCTCAAGGACACAGGTCCCTGTGAGCTTAAATTGGAGCAGAATGGTCATATAAGTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa50
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031837 Nonsense 95 1216 2 17
ENSDART00000132283 None None 842 None 16
Genomic Location (Zv9):
Chromosome 2 (position 19133461)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19669859
GRCz11 2 19318923
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCCTCTTTGGTTGAGGTCACCAGGTTAAATGGGAAACAGGGACTGGGA[C/T]AACAGCAAGAGGGCAAGAGTGAAGAACGGCCAGCAGATGTTTACAGTCCA
Long Flanking Sequence:
AGTGTGTGAGTGAGTGAGTGAGTGTGTGAGTGTGTGAGTGTGTGAGTGTGTGTGAGAGAGAGAGAGAGAGAGAGAGATATCACACTTGAATGTATGTAAGGATATGGGAATGCCTGCCCACATTCCTAACCATTCATGTGTCAGTTTGACAGATGGATCCCAAGGGGATGACTAGATCGACCCACTTCCTTAGCATTTTCCAATTTAGCCTGACCTCGTTTCTCAAATTTTACTCTGTTTGTTTCAGTCTTTTCAAAAAGCTAATGAGCTTTCTTCTTATCCTTTCAGATGAAACGGACACACCAATTCTCTCGGATGCCAAGTGGACTCAGATTCTGGCCCCTCCATCACACCTCCTTTCCCTGAATCCGGCACTAACCCACTCTGACCTCAGCCCAAGGGACAGCCCTATCAGCTTCAAGCCCCTTCTGGACACCCAGACATCAGATGGGCCCTCTTTGGTTGAGGTCACCAGGTTAAATGGGAAACAGGGACTGGGA[C/T]AACAGCAAGAGGGCAAGAGTGAAGAACGGCCAGCAGATGTTTACAGTCCACCTCTGCCTCAGCCAAACATTGGCAAGCTAGTGAGCACTGACGGGCAGTTGGCAGACTTACCGTCCTTCAACAGTGGGGTGTTGGAAAATGGTTATCCAGCCAGTCCTGATCATACCGTCCAGTCTGATATCATTAGATTCAATGATGATGAGACAAATCAACCAGTCATAGACAAGAAGTGTCTCAAGGACACAGGTCCCTGTGAGCTTAAATTGGAGCAGAATGGTCATATAAGTGATGCTGGTCGAGATTTTATCTCTACAGAGGAAGAATCTGAGGATAAGCCATCGATTTTGAAGAATGGTGTTAAAATGGAGACAAGTAAGGATGAAAGTGTTTCACCCTCTTGTAAGGTCGGAATAAGGGACAACAGTAATGGATTATGTCCAGAAGGAAGTTCTTCCCATAAAGGAGTATTGCACAAATCTGTAAATGGTGGCGGAGAATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19724
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
ENSDART00000031837 Nonsense 115 1216 2 17
ENSDART00000132283 None None 842 None 16
Genomic Location (Zv9):
Chromosome 2 (position 19133521)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19669799
GRCz11 2 19318863
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCAAGAGTGAAGAACGGCCAGCAGATGTTTACAGTCCACCTCTGCCT[C/T]AGCCAAACATTGGCAAGCTAGTGAGCACTGACGGGCAGTTGGCAGACTTA
Long Flanking Sequence:
AGAGAGAGAGAGAGAGATATCACACTTGAATGTATGTAAGGATATGGGAATGCCTGCCCACATTCCTAACCATTCATGTGTCAGTTTGACAGATGGATCCCAAGGGGATGACTAGATCGACCCACTTCCTTAGCATTTTCCAATTTAGCCTGACCTCGTTTCTCAAATTTTACTCTGTTTGTTTCAGTCTTTTCAAAAAGCTAATGAGCTTTCTTCTTATCCTTTCAGATGAAACGGACACACCAATTCTCTCGGATGCCAAGTGGACTCAGATTCTGGCCCCTCCATCACACCTCCTTTCCCTGAATCCGGCACTAACCCACTCTGACCTCAGCCCAAGGGACAGCCCTATCAGCTTCAAGCCCCTTCTGGACACCCAGACATCAGATGGGCCCTCTTTGGTTGAGGTCACCAGGTTAAATGGGAAACAGGGACTGGGACAACAGCAAGAGGGCAAGAGTGAAGAACGGCCAGCAGATGTTTACAGTCCACCTCTGCCT[C/T]AGCCAAACATTGGCAAGCTAGTGAGCACTGACGGGCAGTTGGCAGACTTACCGTCCTTCAACAGTGGGGTGTTGGAAAATGGTTATCCAGCCAGTCCTGATCATACCGTCCAGTCTGATATCATTAGATTCAATGATGATGAGACAAATCAACCAGTCATAGACAAGAAGTGTCTCAAGGACACAGGTCCCTGTGAGCTTAAATTGGAGCAGAATGGTCATATAAGTGATGCTGGTCGAGATTTTATCTCTACAGAGGAAGAATCTGAGGATAAGCCATCGATTTTGAAGAATGGTGTTAAAATGGAGACAAGTAAGGATGAAAGTGTTTCACCCTCTTGTAAGGTCGGAATAAGGGACAACAGTAATGGATTATGTCCAGAAGGAAGTTCTTCCCATAAAGGAGTATTGCACAAATCTGTAAATGGTGGCGGAGAATTGGATTGTGGGAGGGAGAATGATGAGGGTGCCTTTCAAAATGGTGTAATGGTTGAAAATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031837 Missense 487 1216 2 17
ENSDART00000132283 Missense 113 842 1 16
Genomic Location (Zv9):
Chromosome 2 (position 19134638)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19668682
GRCz11 2 19317746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTCTAAGAAGCCCTTGAGCTCCTTGGGGGAAGTGGCTCCAGTTTGGG[T/A]TCCTGACTCTCAAGCACCCATTTGCATGAAGTGCGAGGTCAAGTTCACTT
Long Flanking Sequence:
TCTTGTAGAGGACCTTGATGGAGATGCACAGAATCAGCTGGCAGTTTCTTCAAAAGAGGACTCTGTGACAGAGGAAAAAGAAATAGAGGAGAGCAAGCAAGAGACTTGTGATCCAGTTCGACAACTGGAATCCGGCAGAACAGGCAAACTTAACAACAGTCGGCTGCAGCCTGTCAGCATTCCCTATGGTGGGGCCCGTCCAAAACAGCCTGTCAATCTAAAGCTGCAGATTCCCCAGCCTCTCTCCAACCAAGTCCAGAACGAATTTGGCACAAACAGCAAAAACAAGAACATGGAGCCTCAAAGTAGAACAGGAGGCCTTGACGCATCTTCTGAAGCTACTGAGTCTGGAGTTGTTCAGATAAATGGAGAGCATGGAAATGGTTCTTCAGGCTTAATCATCCCATCTGAGAGTCCAGACAATGACCTTCAAGCAGGCCAGCAAGGAGCTTTTTCTAAGAAGCCCTTGAGCTCCTTGGGGGAAGTGGCTCCAGTTTGGG[T/A]TCCTGACTCTCAAGCACCCATTTGCATGAAGTGCGAGGTCAAGTTCACTTTTACTAAAAGAAGGCACCATTGTCGGGCTTGTGGCAAGGTAAAGTCTCTAGTTCATTATTCAATGGTGTTTCTTTAAGGCAAGTTTATTCAGACATCTAACCCAAGTATTTAATTAACAGGCTCTAACTTGTTTGTGATACAAACATGTTATCTGAAGTTTGACAGCTTTTTTAGGAGTGGTGTGTTGATGTTTTTCCCAATCAGCCTTATTAGACTTTTTACTTTGCCAAGTAAGCATTAAAATACTGGTGTTGCAGCATACTTGAAAACCACTTATTACACTTTAATAACTGCATAGCAGTTCAGTGGCTATAGGCCACACAGCACCCTTGTATTGTGAGGTGAGTTTTGTATAAGTAAGCGCCACTCACATTTTCTTCACAAATTGAAAATCTATTTAATATTGGCTACGATCGAATGCCTTCTCCAACTCCACAAAACACATGTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9383
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031837 Essential Splice Site 550 1216 3 17
ENSDART00000132283 Essential Splice Site 176 842 2 16
Genomic Location (Zv9):
Chromosome 2 (position 19137896)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19665424
GRCz11 2 19314488
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAAAGAAGCGAGGGTTTGTGTTMCCTGCCACTGTGCATTAATAAATGG[T/A]GAGTAAYATGAAACTCAAGGGAGTGGTCAAACTGTAGGTTAGGTTAAGAG
Long Flanking Sequence:
TAGTTCTGTTTTTTATTTGCTTATCAACTTATTTATTTGAATCAAACCTGTATTTGTATTTATTATGAGTTATTTAATTGAAACATATTTAACCTTCAATCTAATTTATAATTTTAATCTTTAAATCCAATTTCTATTTATGTTTGATTATTGTTTATTTACATTTTTTTGTTAATTTCTACATTTATTTATTTTCCCTCCAAACATTAACACCCCCCACCCCCCCACCTCCCACCCCTAGAATTCCACTGTGGACCCCAACTTGAAAGCCCCCTTTGTTGTATTATTTTTCCTTTTCTGTTGTTTGGTTATTAAGCCACTGTTGATGTTATATCTAATTTTCTGATACAGATTTTTAAACAAAGCAATTTGTATGTTTTTTGATGTGTGTCTGGCCAGGTGTTCTGTGCTGCTTGTTGTAGTCTGAAAAGCAGGCTGATGTACATGGACAGGAAAGAAGCGAGGGTTTGTGTTACCTGCCACTGTGCATTAATAAATGG[T/A]GAGTAACATGAAACTCAAGGGAGTGGTCAAACTGTAGGTTAGGTTAAGAGTTTATCTTAAAGTTTTCCAAGCTGTACACTTTTTTTTTTCATGTATTCATAAACTGTATTGTAACTTAAGGGATTTAAACATGTACCGATTGTTTCGTGAGGTCAACTAAAACTTTTGGCTACGTCTAAACTAATCCGGATAAATTTGAAAATGGTGTTTTCTTATAGAAACTCTCCATGTCCATGTTTTTGTTTTCAATTCTTTTCATCATCCACATTAAAATGACTGAAAATGCTTTTGTTCAGTATTGCGCACAGACGTATCACACTTTTATCTACTTCATATCTGACTGCCGTTTATTTACTTTCTGTCTCTTTAATACGTCGCGGCAAATTATTCCAACTGTTGTCTCCCACCACTGAACAATAATTCCCAGTGAACATTCCATGCCCTTTGAAGACAGTACAAACTGACATTTAAGGTTAGAGACACCCTGGAGTACTTTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32886
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031837 Nonsense 613 1216 5 17
ENSDART00000132283 Nonsense 239 842 4 16
Genomic Location (Zv9):
Chromosome 2 (position 19140069)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19663251
GRCz11 2 19312315
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAGCTTTAAACCCTCGTCTCTGTAATGCACTTGTAGGTTCTCTTCCT[C/T]GAGAGCAAAGGAGAGTTTGGTTTGCGGATGGCATTCTGCCCAATGGGGAA
Long Flanking Sequence:
GGAAAATACAGGAAGTGGTTGTAACCAGAGCCCAAATCCCAACAACCCGGCAGAATACTGCTCCACTATCCCTCCTCTGCAGCAGGCGCAGGCTTCAGGAGCACTTAGCTCCCCACCACCAACCGTCATGGTGCCTGTCGGTGTCCTCAAACAACCAGGGTCTGAAGGTAAACTTATTTTCAATATTCATGTTTATGTTCTTTGAAGTGAAACAGAATATTGAGTAGGAGGTGGGCATATCATTTCCTTATAGCAAATAAAAGGTTAGAGGGGCGTGGTTATGAATTTTGTGGATGAAACTGTCAAACTGACATCAACAGAGTAGAACCACCAGAACCAAATATTCAGACATTGATTGAAGATTACTGAAACACTTTTTTCAGTGGATTAACACGGATTAATTGTTCACTTTAAGAATATCAGTCTGTACTAGCAAAATAAACATTGTAAATTTAGCTTTAAACCCTCGTCTCTGTAATGCACTTGTAGGTTCTCTTCCT[C/T]GAGAGCAAAGGAGAGTTTGGTTTGCGGATGGCATTCTGCCCAATGGGGAAGCTACAGACTCTTCTAAAGCCCCTGCGGCAAACCCCAACCCCTCACAGCCTGTGGCTACATCCCAAAACTCAAACAAATCCTCAGGAGCCAATGCCTCTGAGGTGACACTTTACTTTGTTCTATTTAAGCTCATCTGTAAAATTAGACACTTCATTCAGGCTTGTTTCCATCATTACAATGCTTCATTTGTATGTTTACCCTTCTGCAGGCAGTCCATGGCAGTGGAGCCCTGACTACTAGTCCAGTGGGCAGCTCTTTCAGTCTGATCCCAGAGGACGGACTTCCTCCCATCCTCATCTCCACAGGCGTCAAAGGAGGTACGGGAGGCCACATCACAGGTGCTTGCCCATCCTTCACCATTCACCATTCAGCTTTCTCCACTCCTCCAAAATATGAGTATTGCTGCTTGTTTGTGCATGTCTGTGTGCGTGTTTTTGCTTATGTCTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32887
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
ENSDART00000031837 Essential Splice Site 663 1216 5 17
ENSDART00000132283 Essential Splice Site 289 842 4 16
Genomic Location (Zv9):
Chromosome 2 (position 19140223)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19663097
GRCz11 2 19312161
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTACATCCCAAAACTCAAACAAATCCTCAGGAGCCAATGCCTCTGAGG[T/C]GACACTTTACTTTGTTCTATTTAAGCTCATCTGTAAAATTAGACACTTCA
Long Flanking Sequence:
CCAGGGTCTGAAGGTAAACTTATTTTCAATATTCATGTTTATGTTCTTTGAAGTGAAACAGAATATTGAGTAGGAGGTGGGCATATCATTTCCTTATAGCAAATAAAAGGTTAGAGGGGCGTGGTTATGAATTTTGTGGATGAAACTGTCAAACTGACATCAACAGAGTAGAACCACCAGAACCAAATATTCAGACATTGATTGAAGATTACTGAAACACTTTTTTCAGTGGATTAACACGGATTAATTGTTCACTTTAAGAATATCAGTCTGTACTAGCAAAATAAACATTGTAAATTTAGCTTTAAACCCTCGTCTCTGTAATGCACTTGTAGGTTCTCTTCCTCGAGAGCAAAGGAGAGTTTGGTTTGCGGATGGCATTCTGCCCAATGGGGAAGCTACAGACTCTTCTAAAGCCCCTGCGGCAAACCCCAACCCCTCACAGCCTGTGGCTACATCCCAAAACTCAAACAAATCCTCAGGAGCCAATGCCTCTGAGG[T/C]GACACTTTACTTTGTTCTATTTAAGCTCATCTGTAAAATTAGACACTTCATTCAGGCTTGTTTCCATCATTACAATGCTTCATTTGTATGTTTACCCTTCTGCAGGCAGTCCATGGCAGTGGAGCCCTGACTACTAGTCCAGTGGGCAGCTCTTTCAGTCTGATCCCAGAGGACGGACTTCCTCCCATCCTCATCTCCACAGGCGTCAAAGGAGGTACGGGAGGCCACATCACAGGTGCTTGCCCATCCTTCACCATTCACCATTCAGCTTTCTCCACTCCTCCAAAATATGAGTATTGCTGCTTGTTTGTGCATGTCTGTGTGCGTGTTTTTGCTTATGTCTCCACCTCTCATGCTAATAGATGGCTTTCATTGGGTTGGTTACTCATCTAGATTGTGCTGTGAGAGGAAATTGAATAGAGTCTGGCTTGAATCCATTTGTTGCTAGTTAATTTATTGATGTTGTGTGTCTGCAGACTACGCTGTTGAGGAAAGACCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8528
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
ENSDART00000031837 Essential Splice Site 987 1216 12 17
ENSDART00000132283 Essential Splice Site 613 842 11 16
Genomic Location (Zv9):
Chromosome 2 (position 19157753)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 19645567
GRCz11 2 19294631
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTAACTACCAGACGCAGGCCATTAGTATTCATCACCAGCCTCGCAAAG[G/A]TATGGCAAGATTACTTGCAAGCTAATCTTTGAAGCTTCTTTTTTCAYTTT
Long Flanking Sequence:
TTTAATATGTAGTAAATATGTTATAGTGTAATATATAATTAAATATAATTTTTTTTTTATAAAATGCTGATAATAGAAAATAATGGAAGGCACTACAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTCCTAAAGTGAAAAAGGTTGAGAACCCCTGATTTAAAGCTTACTCTCAATGTTCTTTGTTAGCCACATGCTAATTCATTCAGTTTACTAGAACATTGTATACCCTGAAATTATGAATTAAGTTTTAGGATTTTGCATAACGTTGAAATGTTATAACAAGTTTTTTTTGTCTTTTGACTTTTTCTTTTTTCAGCTTATGAAGGCAATGAATAAATCCAACGAGCATGTGCTGGCAATGGGTGCATGCTTCAACGATAGGGCAGATTCTCATCTCGTCTGCGTTCAGAATGATGATGGTAACTACCAGACGCAGGCCATTAGTATTCATCACCAGCCTCGCAAAG[G/A]TATGGCAAGATTACTTGCAAGCTAATCTTTGAAGCTTCTTTTTTCACTTTCATTACGGATCCAATATATTTCTTTAATAATATTTCTCTAAGTAAATAGGAATCATAGAGTCATTTATTACAGGTTTTTTTGATTATTAAGCACAAAAAATTCCACAAATTTATAAACCCTGGCAAACTCATCAGAAAAACCATGGAGTCTTACTAGGGTTATTACAATACTTTAAAACTGGATGACTTAAAGTTGCAGAAGGTAAATTTTACACCCTCTGGTTGAACTAAGTATTGCACTCCAAAATCAAACAACATTTTTTTTTTCACTTTGCCCGTTCTCCGATGAAGCTGCATTCACACTGCAAGCGACTCACAGTGGCAAAACGACTGTTTATTACAATGCAGAGTAAGCGACTTCAGGTGACCACTGTCTACGCTAATGACAGCTAAGGTTGACTACAAGGTGGGCATGTTGAGGAATGTGACAAAGTTGAGAATCCTTTAACT
Associated Phenotype:
Not determined