Busch Lab

ZMP

ift81

Ensembl ID:
ENSDARG00000007444
ZFIN ID:
ZDB-GENE-040714-3
Description:
intraflagellar transport protein 81 homolog [Source:RefSeq peptide;Acc:NP_001002313]
Human Orthologue:
IFT81
Human Description:
intraflagellar transport 81 homolog (Chlamydomonas) [Source:HGNC Symbol;Acc:14313]
Mouse Orthologue:
Ift81
Mouse Description:
intraflagellar transport 81 homolog (Chlamydomonas) Gene [Source:MGI Symbol;Acc:MGI:1098597]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
hu7911 Nonsense Available for shipment Available now
sa7332 Nonsense Mutation detected in F1 DNA Not yet available
sa41136 Nonsense Mutation detected in F1 DNA Not yet available
sa31633 Essential Splice Site Available for shipment Available now
sa38673 Nonsense Mutation detected in F1 DNA Not yet available
sa14146 Nonsense Available for shipment Available now
sa34331 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
hu7911
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
ENSDART00000004288 Nonsense 11 675 1 18
ENSDART00000004288 Nonsense 11 675 1 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12159905)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11604668
GRCz11 8 11642373
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays)
KASP Sequence:
CACTAACGNNNNNNTAAYKYTTYAAGRWGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTASATTCGAC
Long Flanking Sequence:
ATCATTTTATCCAGTTAATTATATAGTGTATAGATTCCCTATATCATAATATATTATTAATTTTTTTAAACATCTTACGTTACTGATTATTGTTTAGTTTCAAAAAGAGTTAAAAGTCTTTTATGGGGACTTTTACTTTAAAAAGTAGGAAATCTCTTCACATTGTCCAACTTCCTGCTAGCAACCGGGCCTTGTGTGACAACGGTTTCTAGGCAGGATTTGTTGACGTGAGAGGGAACGTTATACGACGTTATTATACAAAAATTTATTATCGTTTTCATTCATCTAAAATCAAATATTAAACGACATTCTGTGCTTGCGCTACAAAAGCTATAATACGGTAAATAATTCGGCTGTTAGCTGCTAACGTGAGTTGGAAAAGTTATTTTGAACACATCGCAAGCTAACGGAAGTTAACGTTGTGAGAATATTTTTGTTAGCGGTAAAAGCCACTAACGTAATTCTTCAAGATGAGCGAACAGCTTAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGACTCTCTGGAGCCAATGCAGCTTCTGCAGACTTTAAGTGATGTTCTGGCTGAAATTGATCCAAAGGTAAGTTGAAGATCAAATTTAATATGACTAATAAAACCACAACCTATAGCAATACATATCTATAATAGTACATAGTATCAAAACGGTAAATAAAAGTAGGGCTTCACGTTATTTTATTTTTCTGCAGTTTCAGAAGATGGTTTAAATAGCTTTATTTGATTGTTTTTTTCTATGCAGTCTAACAGTATTCGGGTAACAGAAATTAAATAATCACAATGTAAAAAAATGCATTTCTTAACTTGCTTTGTTTTGTCTCGTTTTTAGTTACAAATATACAAACAATTTCTAAGACTAAGTAAAGATGCTGTTTAGTTTTAATCGTCCAAATAAAGTAAAAAATTAAAAAAAATTGTTTTAAGAGTTTTATCTTTTGTTTTAAGTGGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7332
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
ENSDART00000004288 Nonsense 11 675 1 18
ENSDART00000004288 Nonsense 11 675 1 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12159905)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11604668
GRCz11 8 11642373
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays)
KASP Sequence:
CACTAACGNNNNNNTAATTCTTCAARATGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGAC
Long Flanking Sequence:
ATCATTTTATCCAGTTAATTATATAGTGTATAGATTCCCTATATCATAATATATTATTAATTTTTTTAAACATCTTACGTTACTGATTATTGTTTAGTTTCAAAAAGAGTTAAAAGTCTTTTATGGGGACTTTTACTTTAAAAAGTAGGAAATCTCTTCACATTGTCCAACTTCCTGCTAGCAACCGGGCCTTGTGTGACAACGGTTTCTAGGCAGGATTTGTTGACGTGAGAGGGAACGTTATACGACGTTATTATACAAAAATTTATTATCGTTTTCATTCATCTAAAATCAAATATTAAACGACATTCTGTGCTTGCGCTACAAAAGCTATAATACGGTAAATAATTCGGCTGTTAGCTGCTAACGTGAGTTGGAAAAGTTATTTTGAACACATCGCAAGCTAACGGAAGTTAACGTTGTGAGAATATTTTTGTTAGCGGTAAAAGCCACTAACGTAATTCTTCAAGATGAGCGAACAGCTTAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGACTCTCTGGAGCCAATGCAGCTTCTGCAGACTTTAAGTGATGTTCTGGCTGAAATTGATCCAAAGGTAAGTTGAAGATCAAATTTAATATGACTAATAAAACCACAACCTATAGCAATACATATCTATAATAGTACATAGTATCAAAACGGTAAATAAAAGTAGGGCTTCACGTTATTTTATTTTTCTGCAGTTTCAGAAGATGGTTTAAATAGCTTTATTTGATTGTTTTTTTCTATGCAGTCTAACAGTATTCGGGTAACAGAAATTAAATAATCACAATGTAAAAAAATGCATTTCTTAACTTGCTTTGTTTTGTCTCGTTTTTAGTTACAAATATACAAACAATTTCTAAGACTAAGTAAAGATGCTGTTTAGTTTTAATCGTCCAAATAAAGTAAAAAATTAAAAAAAATTGTTTTAAGAGTTTTATCTTTTGTTTTAAGTGGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41136
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
ENSDART00000004288 Nonsense 70 675 2 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12161709)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11606472
GRCz11 8 11644177
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTG[G/T]GAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTGTAAGACAGA
Long Flanking Sequence:
GCAATATCGATGCTGAAACTATATGTTGTGCAGCCCTAATGTAAAGGATAGTTCACACCATACTGAAAACTTCATTTACATCATTTACTTTATTTGTTCCAAGCTGGTTTGACTTTCTTCTGTTGAACCACTGACTTGCATAGTATTTGTTTATCCCAACTTTAGAAGTCAATAGTCACAATTTTTAAGTTTTCTGCAAAATATCTACTTTAATATTTAACAGAATAAAGAATTACAAAAAGTTTCAAAACCTCTTGAAGATGAGTAAATAGTGAGCAATTTTTCATTTTTGGGTGAACAAGGCCTTTAATATTCTTTCACAGTTTCCTTTGAAACCACATTTTATTTTTAGAGAGTACTGTATAGATCTTTATTTATGTAATGTGTTCACACTGATAGTTTTTGACACTTTTTCTTTTTTCTGAATCTTTTTTCAGCAAGCCATTGATATACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTG[G/T]GAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTGTAAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATTTATTCCAGTGATTTTAAAGATGATTTTTCAACTTCATTACTCCAGTCTTCATGATCCTTCAGAAATCACTCTGATATGAATTATTATTATTATTATTGTTATTATTATTATGAATGCTATATAATAAAAGCAATAATGACTGGAGTAATAATTTCATTTGAAACTACATTTAATAAGAAAGCAGTTATTTAGAATTGTGATAAATATTTTTAAAAAGTTTACATTTAATAAATGCTACTTTGATGAACAGAATGGTTTTTTTTTTAAAACATGGAGGAAAAAAAACAATATATATATATATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTATTTTCTTCGTACTTCACACATCTAATCAGCTTTAAAATGTCGATTGAACAGAAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31633
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
ENSDART00000004288 Essential Splice Site 83 675 2 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12161751)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11606514
GRCz11 8 11644219
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATT
Long Flanking Sequence:
AAAGGATAGTTCACACCATACTGAAAACTTCATTTACATCATTTACTTTATTTGTTCCAAGCTGGTTTGACTTTCTTCTGTTGAACCACTGACTTGCATAGTATTTGTTTATCCCAACTTTAGAAGTCAATAGTCACAATTTTTAAGTTTTCTGCAAAATATCTACTTTAATATTTAACAGAATAAAGAATTACAAAAAGTTTCAAAACCTCTTGAAGATGAGTAAATAGTGAGCAATTTTTCATTTTTGGGTGAACAAGGCCTTTAATATTCTTTCACAGTTTCCTTTGAAACCACATTTTATTTTTAGAGAGTACTGTATAGATCTTTATTTATGTAATGTGTTCACACTGATAGTTTTTGACACTTTTTCTTTTTTCTGAATCTTTTTTCAGCAAGCCATTGATATACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATTTATTCCAGTGATTTTAAAGATGATTTTTCAACTTCATTACTCCAGTCTTCATGATCCTTCAGAAATCACTCTGATATGAATTATTATTATTATTATTGTTATTATTATTATGAATGCTATATAATAAAAGCAATAATGACTGGAGTAATAATTTCATTTGAAACTACATTTAATAAGAAAGCAGTTATTTAGAATTGTGATAAATATTTTTAAAAAGTTTACATTTAATAAATGCTACTTTGATGAACAGAATGGTTTTTTTTTTAAAACATGGAGGAAAAAAAACAATATATATATATATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTATTTTCTTCGTACTTCACACATCTAATCAGCTTTAAAATGTCGATTGAACAGAAGCAGTTTTCGTCAGGGTTTGGTGTCGGGCAGTAAGCCTGTGGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38673
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
ENSDART00000004288 Nonsense 296 675 8 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12166297)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11611060
GRCz11 8 11648765
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTA[C/T]AGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTT
Long Flanking Sequence:
CCTGGCCAGACAGTTAAGAGTGGAAAAAGAAAGAGAGGAATCACTCGCTCATCAGAAACAGGAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTA[C/T]AGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGGTGAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14146
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
ENSDART00000004288 Nonsense 306 675 8 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12166327)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11611090
GRCz11 8 11648795
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGGTGRTGCAGTACCTACARAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTKGAGGACAAGGTGAGCTTTTAAAGGGATAGT
Long Flanking Sequence:
AAGAGAGGAATCACTCGCTCATCAGAAACAGGAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTACAGAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTTGAGGACAAGGTGAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGTAATATTGTGAAAAAAGCAGACATTCATTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34331
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
ENSDART00000004288 Essential Splice Site 315 675 None 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12166358)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11611121
GRCz11 8 11648826
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGG[T/C]GAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTC
Long Flanking Sequence:
GAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTACAGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGG[T/C]GAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGTAATATTGTGAAAAAAGCAGACATTCATTTTTTTTTTCAGCTTAGTCCGTTTATTAATCTAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27137
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004288 Nonsense 424 675 11 18

The following transcripts of ENSDARG00000007444 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 12179297)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11624060
GRCz11 8 11661765
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACATATAAGAAAAAGCGTCAGGAGATAGCTGAGCTGAAGGCAGAGTA[T/G]GGTGTGCTACAGAGAACCGAAGAGATCCTGAGAGAACGACACACAGCTGG
Long Flanking Sequence:
AGACGTTCCAGCATGGAAATCCCATTCTCAAAGCTGAATATCTGACTTAAGCATTGTTTTGCAGATAAACAAGTATATTCACTTAGCATGTTTCTTAAATATCTGCAAACATATTATGGTACTTTTATGCTTTAGAACAGTCCAAAACCTACATACAGCACCTTTAAGTAAAATTCTCTAAACTGTGAAGTAAGCACAGTATCTGGATTTTACTGTTCTAATTAAAGTGCACACATTTACACATACATATATCATAACATAATACTGTCATTGTTACTGTCAAATTTTTGTTCATAATTGCGTTAGCGGTGCACGTTAACATTTGTTTGTGGTCATTTATCAGGATTGTGTTTGTTAATGATTGCCTATTTTCATGTCCTAATTAAAGTTTGGATTTTCGTTTGTCTCTTTCAGTTTAAGAGATATGTGGCCAAGATGCGTGGCAAGAGCAGCACATATAAGAAAAAGCGTCAGGAGATAGCTGAGCTGAAGGCAGAGTA[T/G]GGTGTGCTACAGAGAACCGAAGAGATCCTGAGAGAACGACACACAGCTGGACAACAGCAGCTGGTAATATCACACATCTTTTTTCTCTGTCCATAAGGCCGGCAAATATTTCGATTTCCTCAGTTTTTTTTAAGCCAAGGACCACAGTTTTACCTAAAAAAGTTTTCCAGTGTTTTGGTGTAGAAGAAAAGTCACCTACACCTTACATAGTCAGAGGGTGAGTAATTAAAAGTCTGCGTGAACCGGAATTTGCTGAGATATTTATTTCGTGTTGATGTACTTCTAACTGATACGGAATATTCAGTAGGAGGCGGGGCTTTCCCTCACAGCAAACTAATGAGTATTATTAATGTGCAGTTGCCATGAAAGCCCTCAGGTTGATGTCAACAGAAGCCACAGCAATGCAGAAGCAAATGGTCAGACTTTAATGGAAGATTATTAAAACAAACTTTTTTTTTCAGTGGATTAACTTGCACAGATTAATTATTCACCTTAATAAT
Associated Phenotype:
Not determined