Busch Lab

ZMP

phf20b

Ensembl ID:
ENSDARG00000038737
ZFIN ID:
ZDB-GENE-040822-33
Description:
PHD finger protein 20, b [Source:RefSeq peptide;Acc:NP_001004114]
Human Orthologue:
PHF20
Human Description:
PHD finger protein 20 [Source:HGNC Symbol;Acc:16098]
Mouse Orthologue:
Phf20
Mouse Description:
PHD finger protein 20 Gene [Source:MGI Symbol;Acc:MGI:2444148]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa13159 Nonsense Available for shipment Available now
sa37647 Nonsense Mutation detected in F1 DNA Not yet available
sa37646 Nonsense Mutation detected in F1 DNA Not yet available
sa17914 Nonsense Available for shipment Available now
sa43928 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa14382 Nonsense Available for shipment Available now
sa15420 Nonsense Available for shipment Available now
sa37645 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13159
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056570 Nonsense 54 986 3 18
ENSDART00000121468 Nonsense 54 1030 2 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15136167)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15269046
GRCz11 23 15025123
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGAAGATGAGAAAGTTCTGATCCACTACAGACAGTGGAGTCACCGCTA[T/A]GACGAGTGGTTCGACTGGAGCAGTCCGTACCTCAGACCSGTRGAGCGAAT
Long Flanking Sequence:
TATGCCTGTCTGTTGTAAAAAACGTAATGACAAAAAATACTAATTAGTGCATCTCTTTCTTACTTCCGTGTGAAGCCATGCTGCCGTTGTACATGGTGTATTCTGAGAAATTTTCTTACCCCTTAGTTGTAAGTGTGGTCCTGAAACATCTTCATTTCAATGGGCTATCTAGCCATTCCCTTAAGCCCTATGCCTTCAAGCTAAAGGGAATTGAGACACCCCTACCCCTTTATGCAAACGCCCCTTCATTACTCTACACGATGAATGTGTAGAGTAATTCTCTTTGTGAACGACTAAGCTTTGTTACTGCAGATCAAATACATACATTTCATATCAAAGCATCATATGGTCTCTTTAAAAGCAAAGGTATATGGCAGATCTTTTCCGATCTGAAGTGGCTCACTGGTGTTTTGTATTGACAGGTACGCAGCCAACATAGAAAAGATCGACTATGAAGATGAGAAAGTTCTGATCCACTACAGACAGTGGAGTCACCGCTA[T/A]GACGAGTGGTTCGACTGGAGCAGTCCGTACCTCAGACCCGTGGAGCGAATCCAGCTGAGGAAACAGGGGCTGAATGAACGACAGTGCGCTTCAGTGAGTACTTCCAGTCAGACCGTGCTGACTCATTCAGAGTCCGCATGGCCGAAGTCACACTCTTACTCATAAATGCTGCAAAATTACATTTAGATCGGTTTCTTTTCCCAGGGTTTTCAGGTCAACCAGAAAGTGCTAGCCAGCTGGTCTGACTGTCGCTACTACCCTGCTAAGATCCTGTCTCGAGACAAAGATGGTGCGTATTCATGACCTTCACAGTACCACATCTGGTTCTACAGGGTCCAGGTGCTGGATTTGTTTGTTTTTACAGAAAATAGATATTGTATGTTATTTATTTTATTTTATTCATTAAAACAAAACATATAGAGTCGAGGGCAAAATATTTTGCTCTCCTATGCAATATTTATTATTTTTCAAATATTTCTTAAGTGATATTTAAGGGTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37647
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
ENSDART00000056570 Nonsense 70 986 3 18
ENSDART00000121468 Nonsense 70 1030 2 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15136121)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15269000
GRCz11 23 15025077
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTATGACGAGTGGTTCGACTGGAGCAGTCCGTACCTCAGACCCGTGGAG[C/T]GAATCCAGCTGAGGAAACAGGGGCTGAATGAACGACAGTGCGCTTCAGTG
Long Flanking Sequence:
GTGCATCTCTTTCTTACTTCCGTGTGAAGCCATGCTGCCGTTGTACATGGTGTATTCTGAGAAATTTTCTTACCCCTTAGTTGTAAGTGTGGTCCTGAAACATCTTCATTTCAATGGGCTATCTAGCCATTCCCTTAAGCCCTATGCCTTCAAGCTAAAGGGAATTGAGACACCCCTACCCCTTTATGCAAACGCCCCTTCATTACTCTACACGATGAATGTGTAGAGTAATTCTCTTTGTGAACGACTAAGCTTTGTTACTGCAGATCAAATACATACATTTCATATCAAAGCATCATATGGTCTCTTTAAAAGCAAAGGTATATGGCAGATCTTTTCCGATCTGAAGTGGCTCACTGGTGTTTTGTATTGACAGGTACGCAGCCAACATAGAAAAGATCGACTATGAAGATGAGAAAGTTCTGATCCACTACAGACAGTGGAGTCACCGCTATGACGAGTGGTTCGACTGGAGCAGTCCGTACCTCAGACCCGTGGAG[C/T]GAATCCAGCTGAGGAAACAGGGGCTGAATGAACGACAGTGCGCTTCAGTGAGTACTTCCAGTCAGACCGTGCTGACTCATTCAGAGTCCGCATGGCCGAAGTCACACTCTTACTCATAAATGCTGCAAAATTACATTTAGATCGGTTTCTTTTCCCAGGGTTTTCAGGTCAACCAGAAAGTGCTAGCCAGCTGGTCTGACTGTCGCTACTACCCTGCTAAGATCCTGTCTCGAGACAAAGATGGTGCGTATTCATGACCTTCACAGTACCACATCTGGTTCTACAGGGTCCAGGTGCTGGATTTGTTTGTTTTTACAGAAAATAGATATTGTATGTTATTTATTTTATTTTATTCATTAAAACAAAACATATAGAGTCGAGGGCAAAATATTTTGCTCTCCTATGCAATATTTATTATTTTTCAAATATTTCTTAAGTGATATTTAAGGGTTTATGGGAAAGTTCCCAGAATTTCGGATATTTTTTCTTCTGGAGAAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37646
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
ENSDART00000056570 Nonsense 160 986 6 18
ENSDART00000121468 Nonsense 160 1030 5 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15133368)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15266247
GRCz11 23 15022324
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAGCAATCAGCAAGCTCGAAAGCGTGCCGATCAGAACGAAAAAGAAT[T/A]GAAACCCAAGGAGAATGGAAACAGCCGGCACAACAGCTCGAGACACAGCG
Long Flanking Sequence:
ATATTTCAATGTATACTAAAATTTGTTAGATATATTTAACACTGTTAAACATAATCTTTTGCAAAGCAACAAAATAAATTCATATTTCTGCTCTTCGTTAGAATGTATTGATGCCAAAATTCACATGACTTATTAACATTTTTTAATATTAAAATTGAATTCAGCTAATTTAACGTTAATGGTGATAATTCCGATCATTTTCATAAAATTATATTTTATGCACCCAACTTTCCAGTAGTTTTGAGCTGCGTTTTTTTATTTTTTATTTTTTTTATGATGTTCTAGATTTCTACACAGTGAAATTTTTTGATGGGATCATCAAGACAGTGAAGGGAATTAAAGTCAAGCCGTTCCGTAAACAGGTAAAAAGTAATTCCCTTATCTGTAATAACCAGGCCATTCATTTAAACAACGTTAATTAGTGTGTTTTGATCTACAGAGCTCTGATGGAAGGAGCAATCAGCAAGCTCGAAAGCGTGCCGATCAGAACGAAAAAGAAT[T/A]GAAACCCAAGGAGAATGGAAACAGCCGGCACAACAGCTCGAGACACAGCGTATCAGACCACGATGGAGAGAGCGAATCAGAGGCGGACGAAGACACCACAGTGATGGATGAGTCCACAGACCTCCAGAACGGCGGAGAGAAAGAAAGCACAGAAACGAAGATGGTAAACGATTCAGAGGTGAGTTCTGCTGAGCACCAGCCCAGTGAAGACCAGAACCAGCCCAGTGAAGACAAGACCGAAAACCTGGAGAATGGAAATGTAGAGATTAAAATAGAGGAGGAGGAAGAAGAAGAGATGGATGGAGGACAGGAGGAGGCTAAAGTACTTCATAATGGCATTGACAAGAACGATGAGCACAAGGGCGAAGCATCGGACGAAAGTCCTAGTTTGCCCAAGAGGACACGGAGCAGGACGGCAGATGGTGAGTTTGGTTTGGAGGAACATGCTGGTGTTAGATCTGAATTTTTGATTTGATTATGATTCAGACCCAACAGTTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17914
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
ENSDART00000056570 Nonsense 233 986 6 18
ENSDART00000121468 Nonsense 233 1030 5 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15133150)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15266029
GRCz11 23 15022106
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGATTCAGAGGTGAGTTCTGCTGAGCACCAGCCCAGTGAAGACCAGAAC[C/T]AGCCCAGTGAAGACAAGACCGAAAACCTGGAGAATRGAAATGTAGAGATT
Long Flanking Sequence:
TGCACCCAACTTTCCAGTAGTTTTGAGCTGCGTTTTTTTATTTTTTATTTTTTTTATGATGTTCTAGATTTCTACACAGTGAAATTTTTTGATGGGATCATCAAGACAGTGAAGGGAATTAAAGTCAAGCCGTTCCGTAAACAGGTAAAAAGTAATTCCCTTATCTGTAATAACCAGGCCATTCATTTAAACAACGTTAATTAGTGTGTTTTGATCTACAGAGCTCTGATGGAAGGAGCAATCAGCAAGCTCGAAAGCGTGCCGATCAGAACGAAAAAGAATTGAAACCCAAGGAGAATGGAAACAGCCGGCACAACAGCTCGAGACACAGCGTATCAGACCACGATGGAGAGAGCGAATCAGAGGCGGACGAAGACACCACAGTGATGGATGAGTCCACAGACCTCCAGAACGGCGGAGAGAAAGAAAGCACAGAAACGAAGATGGTAAACGATTCAGAGGTGAGTTCTGCTGAGCACCAGCCCAGTGAAGACCAGAAC[C/T]AGCCCAGTGAAGACAAGACCGAAAACCTGGAGAATGGAAATGTAGAGATTAAAATAGAGGAGGAGGAAGAAGAAGAGATGGATGGAGGACAGGAGGAGGCTAAAGTACTTCATAATGGCATTGACAAGAACGATGAGCACAAGGGCGAAGCATCGGACGAAAGTCCTAGTTTGCCCAAGAGGACACGGAGCAGGACGGCAGATGGTGAGTTTGGTTTGGAGGAACATGCTGGTGTTAGATCTGAATTTTTGATTTGATTATGATTCAGACCCAACAGTTTCAACCTCTCTCACGCGCCAACAGATAGCAGTTCATAAGTAGCAAGTAGAGAGGGAGACAATATTAGTGGATGAGACGGTCCACACAAATAAAAGCTAAATGAGAGGTTTTGTAATGATCAATAAGATATTAATAAGAACACTCCACATTATTATTATTATTATTATTATCATTTTGGAAATAGGTTCATTTTACAACTCCCCTAGAGTTTAACAGTTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43928
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
ENSDART00000056570 Essential Splice Site 301 986 6 18
ENSDART00000121468 Essential Splice Site 301 1030 5 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15132944)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15265823
GRCz11 23 15021900
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGAAAGTCCTAGTTTGCCCAAGAGGACACGGAGCAGGACGGCAGATGG[T/A]GAGTTTGGTTTGGAGGAACATGCTGGTGTTAGATCTGAATTTTTGATTTG
Long Flanking Sequence:
TGTTTTGATCTACAGAGCTCTGATGGAAGGAGCAATCAGCAAGCTCGAAAGCGTGCCGATCAGAACGAAAAAGAATTGAAACCCAAGGAGAATGGAAACAGCCGGCACAACAGCTCGAGACACAGCGTATCAGACCACGATGGAGAGAGCGAATCAGAGGCGGACGAAGACACCACAGTGATGGATGAGTCCACAGACCTCCAGAACGGCGGAGAGAAAGAAAGCACAGAAACGAAGATGGTAAACGATTCAGAGGTGAGTTCTGCTGAGCACCAGCCCAGTGAAGACCAGAACCAGCCCAGTGAAGACAAGACCGAAAACCTGGAGAATGGAAATGTAGAGATTAAAATAGAGGAGGAGGAAGAAGAAGAGATGGATGGAGGACAGGAGGAGGCTAAAGTACTTCATAATGGCATTGACAAGAACGATGAGCACAAGGGCGAAGCATCGGACGAAAGTCCTAGTTTGCCCAAGAGGACACGGAGCAGGACGGCAGATGG[T/A]GAGTTTGGTTTGGAGGAACATGCTGGTGTTAGATCTGAATTTTTGATTTGATTATGATTCAGACCCAACAGTTTCAACCTCTCTCACGCGCCAACAGATAGCAGTTCATAAGTAGCAAGTAGAGAGGGAGACAATATTAGTGGATGAGACGGTCCACACAAATAAAAGCTAAATGAGAGGTTTTGTAATGATCAATAAGATATTAATAAGAACACTCCACATTATTATTATTATTATTATTATCATTTTGGAAATAGGTTCATTTTACAACTCCCCTAGAGTTTAACAGTTAAGTTTCATCATTTTAGAATCCATTCAGCCGATCTTCAGTTCTGCACTTTTAACTTAGGTTACCACAACTCATTGAACCGGATTAAACCATTAGCATCTCACTAAGAAATGGAGCCCAAAGAGTTTTGAACGATGAACCTGAAATGCCTGGTTTTACACCACAATAATTCATTAGTATTTAAAAAAAAACACTCCACATTATTATTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14382
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056570 Nonsense 580 986 13 18
ENSDART00000121468 Nonsense 624 1030 13 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15117767)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15250646
GRCz11 23 15006723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTGATGTGTTGTTGTTGTGTCCTCCAGGTGAAGACAGCAGCAGTGATT[T/A]GTCCTCGGACAGTCCAGTATGGAGTGAGGACGAGTCTGACACTGAGCTGG
Long Flanking Sequence:
ATGGACAAAAGTTGTGGAAACAGTGTGCAATAAACTTTAACTGAAAAAATAGTTTGTTTTTGTAAACTTCTATTAGACGATTTGCTTCAACATTTGGAGTAGCTTTCCTTTTGTTGACGTCAACAGCTGATCTTCTGATGCTAACCTAAGGGTTTCCATAGCAACTGCATATTAATCCCCTTTCTTACCATTACCGTTGCTATGAGGGAATGATACGCCAAAAAAGCCTCTTCATTTCAGTAGGAAGTACATCAACATGCTGAAATAAAAGTCTCAGCAACTTCCAGGTCATGCTGACTTTATTGTATGATACGACTAAAAAGTGGTCAAAACTATTGAGATAAAAATGTTCTCAATTGATAAGAGTAGATGCTTGAACCTGGAAACCGTATCTTGTACGGCTCAACTTAGGAAGCAGGATATAAAAAAAGAGCTGAAATCTTCTGCTGAGAGTGATGTGTTGTTGTTGTGTCCTCCAGGTGAAGACAGCAGCAGTGATT[T/A]GTCCTCGGACAGTCCAGTATGGAGTGAGGACGAGTCTGACACTGAGCTGGATCTGAACGTCCCCCTCTCGGAGCAGGGGGTGGAAACAGTCACTCACAGCTCTGAGATCGTACGCTGTATTTGTGAAGTGCAGGAGGAGAACGACTTCATGATACAGGTCAACTACCACCCTCTGAATCTGCTTTTGACTTTCTTTTTTCGTTCGTTATGCTTTTAATATCATTTTGAAGAGTGTTTGTTTTTTTCTGTGAATTTCTTTTTCTAGTTTTTACATTTATTATGGCAACTGTTATGTTGAACATTAAACATACAGTACTATGAAACAATATTTTGAACTTTCACACATTTTAACATATCGCAATGAAATTTTTTGAAATGTATTCATAATATTGTTTCATAATACTGTTTAAAGACAAATCTGAGTTTGCTTTGCCTAAATAAATGTATCAACTGTGCACTATATTAATATAAGCTACATTAGTAATAGTTGTAATAATAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15420
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056570 Nonsense 648 986 14 18
ENSDART00000121468 Nonsense 692 1030 14 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15114580)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15247459
GRCz11 23 15003536
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTGTGACGAGTGTCTGTGCTGGCAGCATGGGACRTGTATGGGTCTCTA[T/A]GAGGACAGTGTGCCAGACAGTTACAGCTGCTATATCTGCAGAGACCCACC
Long Flanking Sequence:
TTTTTTTTATTTATCTCTGTAAAAGCTAAATACAAACAAAAAGTGAACATTGAACAAAAAGTGAACATTTAATTGTTCTATACATTTTTATTTAAAAAAAAGTAATAAGAGCCTGGAGGTATTATAGACTTTGCTAATTCAGTTTGCAGACATTTGTAGGTACAGACATCTATTGTGTGCATTCTTGGCAGTTTTTCCTGTCTTTTTAATATTGTCCATATCAATATCGGAATTATATCATATTGACCGAAATAAAGAAATATATTGTAATATAATTTTTTGCCATATCGTCCAGCCCTAATCTCATGATTATTATTATTATTATTTTAAGTGTTCCAGGAAAGATTTGTTTAGTATATAAACTATTGTTTAATGTAAAGTATATAAACTCCATTTCATTTAGTGATGATTAGTGATGGTCTTGGAGATTAAAAGATGTTTTGCTCTCTGCAGTGTGACGAGTGTCTGTGCTGGCAGCATGGGACATGTATGGGTCTCTA[T/A]GAGGACAGTGTGCCAGACAGTTACAGCTGCTATATCTGCAGAGACCCACCAGGTGAGAGACTTGATCTATCTCACTTTAGCATATATGATCTTTTTCCACCTTTTTCTGTATTAAACAGCTGCATTTTAAAATATTGAGTTGAAATTTTGGTTTAAGGAACTCCCATTCAAAACAACTGAAATCACTTCATATAATCCATATACAGTGGGGACTGTGCTTTATTTTTATTTGTCACGAAAATAAGGTTACACTTCGTATTTTAATGTGACATTAATATCACAAGTATATCTGTGGCCAAAGTCCTGTCAAGTTCACTGTGTTTTGTTCCTCCAGATTGTAGGGATAGTATACAGTTCAACCCAAAGAATGACCAGTCTGGTAGATGAAGAAGAGCCGGAGTCAGAGATTTAAATAAATAAATCAAGTTTACTGAAGATCGTTTGCAGTTTCATCCGCAGAAGCCAGCTTCAACATTCGCAATGAGTTCCTAGGCCACTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37645
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
ENSDART00000056570 Nonsense 669 986 15 18
ENSDART00000121468 Nonsense 713 1030 15 18

The following transcripts of ENSDARG00000038737 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 15112440)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 15245319
GRCz11 23 15001396
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGTTTTGTGATGTAGAAGTGTGTGTGTCTGTATGTGCAGCTCAGAGG[C/T]AGAGTCAGAGGTACTGGTACGATAAAGACTGGCTGAGCAGTGGACACATG
Long Flanking Sequence:
TGGTGTATTATATTTTATGCATAAACACTTCTCTACAAAATCATCCTAATCAAATACCAAAATTATGATTTTGTTTTGAACTTATCTGGTGAAATTATACTTGATTTTGAAATATTTATCGCAGGACAATCAAATATAGCAATGAGTTTTTTTGTTGTTGTTTTTTTCCCAATATCCTGCGATGAAAAGACTCATCTTGAGTTTTGAGTTTTTGGGTTTATTAAGGGTCAACTGAAAGTTGTTTCTAGAGGTTATATATATATATATTGAATGGATGAACTATGAGGCAAATAATGCCATTGTAGCCAGTTCTATAAAAAAAATTCACAGGTTTTTAACAGTTTAATAAAAGTTACTCTCATAATTCAAGCAAAACATCATGAATCATAGGATAAGGGTGGATATTAGTTTGTCTGGATTGTGTATATTACCCTTTCTGTGGATCTTTTATTCAGTTTTGTGATGTAGAAGTGTGTGTGTCTGTATGTGCAGCTCAGAGG[C/T]AGAGTCAGAGGTACTGGTACGATAAAGACTGGCTGAGCAGTGGACACATGTACGGCTTGTCTTTTCTGGAAGAGAACTACTCTCACCAGAACAGTAAGAAGGTGACGGCAGCACATCAGCTTCTAGGAGACGTCCACCGAGTGTTTGAGGTCCTCAACGGCCTTCAGCTCAAGATGAGCATCCTACAGTGAGTTTTTCCACACAATTTCATTCTGGGCTTTTAGCATATTGGGTTATCATTTTTTCATGTTTCACACCACTCTTATTTAGCCTGTGGTTGTGTGGTAGCCAGTGTTGATGTTTTGGAATGCTAGGAATACTTTTGCTTTAATTAACTTTTGACTCCAAATGAATGAAATGGAGAGAGCAGTACTAAAAAATGACAAAAACCACAAATGCAAAAAGTTGCAAATTATTTGCATGAAAGGGAATAATATAAATAATACATTGAAATAAGTTGAAAGACATTTTTATTTGTCATTATGTTTGCAAAAAACTAC
Associated Phenotype:
Not determined