Busch Lab

ZMP

psme4b

Ensembl ID:
ENSDARG00000018742
ZFIN IDs:
ZDB-GENE-100316-4, ZDB-GENE-100316-4
Description:
proteasome (prosome, macropain) activator subunit 4b [Source:RefSeq peptide;Acc:NP_001177949]
Human Orthologue:
PSME4
Human Description:
proteasome (prosome, macropain) activator subunit 4 [Source:HGNC Symbol;Acc:20635]
Mouse Orthologue:
Psme4
Mouse Description:
proteasome (prosome, macropain) activator subunit 4 Gene [Source:MGI Symbol;Acc:MGI:2143994]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa18110 Essential Splice Site Available for shipment Available now
sa42034 Nonsense Mutation detected in F1 DNA Not yet available
sa38893 Nonsense Mutation detected in F1 DNA Not yet available
sa35298 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38894 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22097 Nonsense Available for shipment Available now
sa9120 Nonsense Mutation detected in F1 DNA Not yet available
sa13795 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa18110
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000003143 None None 285 None 7
ENSDART00000128865 Essential Splice Site 115 1827 2 45
Genomic Location (Zv9):
Chromosome 12 (position 25505941)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23874617
GRCz11 12 23995836
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATCAGCATGATGCAGAGCTTTGCACGACTCCTCGTCAACTTGCTGAAG[T/G]AMGCAAAAGTCTGACATCAACAATCACCAGACCACTGYCAAATATTTGAG
Long Flanking Sequence:
TGGAGCGACTCCTAGGTTTATATGATTTTAAAATGACTTTTTGATCCTGTTGAAGGACTAAGAAGTTACATGGTTGGGACAAAAGTCCTCCCTTAGTTCAAGATAAAGGAAAACCAAGACTTATAACAGCCAACTTTGACTATTAAAACTGAAATGGTCAAATTTAAGTATGGACCATTACACTAAATTTCCAGAGCATTATTTATCTTTTTTGCAAAAACTATTTGAGTGATTGAAATAAACTTTGCCTTTAATGTCTTCTGTGTATGTAAAATCCATTTTGCAACATTTATTAGATGATATGTAAACTGTTTGTCATGTTTCTCTCTTATTGCTGTGATATTTTTCACCTTTAAAGGTACCTTCGGCTGTACGGGAGGAAGTTCAGCAAAGAGGACCATGTGCTCTTTATCAAGCTGCTGTACGAGCTGGTCACCATCCCCAAGCTGGAGATCAGCATGATGCAGAGCTTTGCACGACTCCTCGTCAACTTGCTGAAG[T/G]ACGCAAAAGTCTGACATCAACAATCACCAGACCACTGTCAAATATTTGAGAACGGCACAGCTGATTTGTTGTCGGTCATTTACAGTTTTTATTTATATTATTTACTTGTGTAACACTTTAAAATAATGGTCCATTAGTTAATTTTAGTTCATGTATTTAATAACTTGAACAAAGTGATACATTTATTATGGTATTTATTCATGTTTGTTAACTTTAGTTAATGTTAAGTTAAATAACGTTAGTTCATGTTAACTCACAGTGCATTAACTCCTGTTAACAAGCTCGACTTTGGATTTTAATAATGAGTAGGTAATGTTCAACTATGATTAATAAATGCTTTACAATTGAACGAGGTAAAGTCATTTTTTAATGATTGAATAATACATTATTTTTATTGTTAGGGCACATTTCCACCAAAGTGTTTTTGTTCAGGTGAAAATGCCAGCATTCTTCTAAAAAATCTAAGCTGTGAGCACTTCTTAAACTTTCAAGGCTGGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42034
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000003143 None None 285 None 7
ENSDART00000128865 Nonsense 291 1827 8 45
Genomic Location (Zv9):
Chromosome 12 (position 25517676)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23886352
GRCz11 12 24007571
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTTGGCACCAGCCAGATGGTAGTTCCTAGATACTTGACTAACTCCTA[C/A]GACATTGGTCATGTGGTACTTTGGATTTCCTCCATGCTGGTAAGTTTCAT
Long Flanking Sequence:
AAGTTTCACAGGCAGTGTGTTTGTACAATTCACACAACGTGAGGTCGAATTAATTTTTTTAACCGGCGAAAATTACGGACAAACATTTTGGGTTTGGTATGCAACAACCTTAAAGGTGTTTCATATTTACCCTGGTTAATGTGTAATGTTTAAAACCAGAAAAAATAGGATAAAACCTTTTTTATTCTATGCTATATTAACAATGTAATTGTACATAATAAAAAAATAAATAAATGTGTATTTGGACAAATACCTCTTCATGCATTAAGATATTGTCTTTTAAAGCATTGTAAAGGTCTTTATTTTCATTTTTGACCAATTGCATTCATCATTCTGAATAACATCATACATGTTTTCTAAAAGAAATGATGATGCTAAATGTCTGAATTTATTCTGATATTTTCTGTCTTGCTTCAGATCTTCACCAGAATCCTGCGTAGCTTTAATCTGCCAGTTGGCACCAGCCAGATGGTAGTTCCTAGATACTTGACTAACTCCTA[C/A]GACATTGGTCATGTGGTACTTTGGATTTCCTCCATGCTGGTAAGTTTCATGAGTCACATATCTATAAAAAGGCTAATTAATAAAAGGTTTGTTTATTCACAGATCATTTTTATAGTGTTGCTTATGGCTTTTTTCAGGGTGGCCCTCAGAACCAGTCCCAAAAGCAGCTTAATGGGCTCTTCAGTAGTATAGCATCCTTCTATCACCCCTCAAACAACGGACGCTGGCTGGTAAGATGTTCTCTATTTTAGGGTAAACAACAAGAACAATATGATGCAAATGGAAATCTCGTCCTCCCACGTTCTAGAGCTGCCTACCTGCGCTGTGTTGTCATCTGAGCTTCATGTTTGCGATATGCATTGACAGATGGTTCTCTGACAGAGCGAGGACACTTCAAATTCCAGCTATTGAAACCCTGCTAACAACCTTTCAGTTTCCATCTTAGACATGCATAATTTTCACACTCTAATGATACTAAGTGCCATAAACTACAATTCGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38893
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
ENSDART00000003143 None None 285 None 7
ENSDART00000128865 Nonsense 636 1827 16 45
Genomic Location (Zv9):
Chromosome 12 (position 25530885)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23899561
GRCz11 12 24020780
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGTGTCACCCTGCTGAGTCTCTCAGGCTGTTTGTACCGCACTGCTG[T/A]AACGCCATTACTCATCTAACTGCCAGTGCGTACAAGAAAATAAAACCACA
Long Flanking Sequence:
ACGACTCAAGCCTGTCAAAAAAAACTGAATTGACCATCAGGATCTGCAGTGTGAATGCAGCCATCATGTAGCTAACCATATTTCAGCACTTTCAAAAATACTAAGCAACATAAAAGCATTTATCATTGATGGCAATAAGATATAACTATAATTATTCATTTCTTGAGCATCAAATCACATTCATTTCTTAAGGATTATATTAGATGTATTTCTGTAGGATCTTCTCTCAGTAAGGTGTGTGTGTGTGGGTGACTCATATGAGGTGTTATTACCTATAGGTGGCTCTCGAAAAAGTCTTCAACTTCGCCACCACCAACATCTTTGAGACTCGTGTCGCAGGCAGAATGGTGGCAGACATGTGCAGAGCGGCTTCTAAGGTAGTGTCTTTTCCCATTGCATGCAAGCAAACATGACTCCGAGACCGCATTGATTCAACTGTCCTCTGCTTTGTTTCAGTGTCACCCTGCTGAGTCTCTCAGGCTGTTTGTACCGCACTGCTG[T/A]AACGCCATTACTCATCTAACTGCCAGTGCGTACAAGAAAATAAAACCACATTCTGTGCCATACTGAGAGCATGTCAGCATCCTCACTTGAGTTTTTTTGGTTGTGTTTTTTGTTTTTTTAGATGAAGATGTTTCAAATGAGGAAGAACTGGATAAAGAACTGCTCTGGAACCTACAGCTTCTGTCTGAGGTGAAAAGACCACTGTATTATAATGCATATGAAATATTTGAAAAGCTGCATCACAGAATCATGTTAATTAGGCATTGTTACCCATCATAGCCTTTGTCCTGACTTTGGGACTGTTCTGTATAGTAGGCATTATTATATACCTTGTACCGTGATTCTTTGGAGTCAGCATCATATGTATTATTCATGAATGTGCAGATAATTCAATCCTTTAATGCACTGCAAATTACAATGATAAGCTTTTCATTCAACCGTGAAAATTATTGATCTAAAAAATGCATGCTGTGTGTTTTATGCTTATTAGATTATAAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35298
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
ENSDART00000003143 None None 285 None 7
ENSDART00000128865 Essential Splice Site 861 1827 22 45
Genomic Location (Zv9):
Chromosome 12 (position 25534965)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23903641
GRCz11 12 24024860
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGAAAACTACCGTGAGGCTGTCTGCAAAGTGATGAGACAGTTGCTTC[G/A]TAAGTGCTCCTCATTTATTGCATCTAACTTCACACACTTTCATTCTTTAT
Long Flanking Sequence:
TAATTTTTTAAAAGCCAACTGAACCGAGAGCATCAAATTAGAAGTTTGAACATGTCCTTAAATTGATTTCAATAATCATCAGTCGGAAACAGTACATTTATCATTTAATAGTGTTTTTACTGTATTTTTGATCAATTAAATGCAGTTTGATCAAATAAAACTGACCTTTAAACTTTTGATAAATGGTGCTTCAGTATGAAAGTTTATTTTCTTCTTAATTCTCTTCTGTGCAGTGTGCCCAGCATGGTTAATTTGGAGGAAACAAAGCTGTACATCGGTGTTGACTATGGTAAGCCACAACTGAAAAAGTCAAACTATATTTATGAAGCCCATTTCAAGTTGTTGTGATGAATGTTCAAGTAGAGACATGGGTAGTGTATCATGATGATAGAGATTAGGATATCAGCCTCACAGCCCATAAGACATTGCTGATTTTTCCACAGATCAGTCCAGAGAAAACTACCGTGAGGCTGTCTGCAAAGTGATGAGACAGTTGCTTC[G/A]TAAGTGCTCCTCATTTATTGCATCTAACTTCACACACTTTCATTCTTTATACAGTCACCCCAATGCATCTTTTAATTCTTTTCTGTAGATTATATTCTGGAGCACTCAGAGGATGACACCAAATCCCTATTTGCCATTATCAAGGTAAATGTACGCAGTTGATATTTGAGCAAAATAAATTGCATCTATTGCCAATTAATCATATAGCAGTTGAGGGAGGGATATAAGGGAAAAAGTACATCCAGGTGGTTATTAATGCATAATAAAACCAGACTGGCTTAACAGGAATTTGTCTTGTTGAAGAGCTTTATTCTGCAGAAACAACCACCCAGATTAACTTTATCCTGCTTATTACACAGCTACTTCCCACAAAACTTAAGAATTAGACACAAAACATTGTGTAAGCCATAATAGTTTTATAGTTGTAGTTTTTATAGTTCATTTTCTATTTAAATGCAAAGCTGACAGAAATGAAAACAGCTGAATGGAACATACACTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38894
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
ENSDART00000003143 None None 285 None 7
ENSDART00000128865 Essential Splice Site 1187 1827 31 45
Genomic Location (Zv9):
Chromosome 12 (position 25540985)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23909661
GRCz11 12 24030880
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCTTCTTTGTACAAAGCCTAAACCACGATGCACTTGTTGTTCGCAAG[G/A]TTGGTGGAATGCTAATGTTTTGGAAGTTTTATAGGGCGCACAGTGATGTG
Long Flanking Sequence:
ATGAATCTGTAGGTACCTGAGAATGCAGTTTTTCTAGGCCGGAGCATCACCAATTCAAGCCAACCCACTCCACACATGGGTACTCCAGAAGACCAGGAGTTGCAGCAGGGACTGGCAGTTCAACAAGCTAAAAACCGCGAGGCAGAGCAGTAAGTGCCACACACAAACACACTCTCAACATTTACGTCTCATTTAACATGGTGTGGTGAATTTGTGCTGTTTGCTTTTCCAGGAAATATGAAAAGCTTGTAAAAGATCTGTTGGAATGTCTAGATGACAGGGACCTGTAAGTGTCACACTGATTGTTTTCACTAAAACTGAACTTTTGAAAGCATCACTCATTTGTGATTATTCTGATTTGTGTCATCAGACCTTGGAAATTTGAGCACATTGCTATCGGTTTCCTGTCTCTACTGCTGAGAGATGACTATCCGCTCCCAGCTCCTGCTGTATTCTTCTTTGTACAAAGCCTAAACCACGATGCACTTGTTGTTCGCAAG[G/A]TTGGTGGAATGCTAATGTTTTGGAAGTTTTATAGGGCGCACAGTGATGTGGTGTTCCTCTGTGATATTTGTTTCTCTAAAATAGCGATGCTAGTGACTCACGACCCCCCACTATTTTCGGAGGGGGTTAAAAATGTACAAATGTTGTGCACTGAAAGTCCATTGTTGGTTTAATTTTGGAGACTGCCACTCAGATATCATCCTCCACATTCAGTCGTGACCTGTACTTATTATTAATGTACATGAGTGCAGAAAAGATGAAAAATTTAACATGATTCTGTAAAATTGATTTGATGCAACTGACACTGTTGCAGTGTCGTTAATCTAATATAATCACCCTAGGGGTCGCAATAACTTTTTTTTAATATCTCTAACTGGCAGCTACTATGTTATATATTTAAAATCTGGCAATTCTAAAAGCTTTATCAAAATTAGTAGTATTATTAAATATATTATTATTATGTTTGTATTTTTATTTATATTTTATATATTGTGCGACCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22097
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000003143 None None 285 None 7
ENSDART00000128865 Nonsense 1505 1827 40 45
Genomic Location (Zv9):
Chromosome 12 (position 25551307)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23919983
GRCz11 12 24041202
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCAGCGTATTGACATACATCTTCATGATTGATGTGGCTCTGCCCTA[C/A]ACTCTGCCCACTAAATCCCCACACATCGCCGAGTTCACCGAGCGGATCCT
Long Flanking Sequence:
CTGTTGTATAAATATTTATAACCACTTCAGAGAATATTTGAGGTCGCGAGTCACTGGCATTGGTAATTTGGGGGTCACAGGCTGAAAAGCCCCTGCCCTACATTACAGTAATATTCAACACTTCACTAATTTTACCCCATAGAGACTTGTTTTGAATTATATTTTGGGTTATTCACGGTCTGCTGAAAGTAATTGAGTTAGTTAATTCTAATAAGTTGTCTTTAAATATTCAGTGGATGGACTGTTATGAAAATAAAGCCACTTCATTGTACCCAGAATAAAGTAAAATAAAAAAGCTGTACTAATTGTTTAACACATTGTTACTCTAATAGTTCACGCAAAGCATCATGGGGGCATAGGAAACATTGGATTGGACAAACAGTTTAAACGTGGCTACTATAATCCAAAAATACACCAGCACTCGCTTTCATCCTCTTGTCGTGATTAATTCCTTTCAGCGTATTGACATACATCTTCATGATTGATGTGGCTCTGCCCTA[C/A]ACTCTGCCCACTAAATCCCCACACATCGCCGAGTTCACCGAGCGGATCCTGTCTCAGCTGAAACCCCTGATCGAAGGTGACGAGGAGATCCAAAACCACGTGGTGGAGGAGAATGGAGTTGGTGAGCAGGACGAAAGGACCCAGGCCATCAAACTGCTGAAAACAGTGTTGAAGTGGCTGATGGCCAGTGCGGGACGCTCGTTCTCCACTCCAGTCCCTCAGCAACTCCAGCTGCTGCCGCTGCTCTTTAAGGTCTCGTGTGCTTCTGTGTCTCATCTTTTATCCATTTGTGCGGAGTGCTCTTAAGTGGATTGCTGACTTGTTTTTCTCTCTGTCTGCAGATCGCGCCTGTTGAAAATGATGACAGCTATGATGAGCTGAAGAGAGACGCCAAGACATGTCTATCTCTTATGTCTCAGGGGCTTCTGTATCCTGAGCAGATCCCGATGGTACTCGCTGTGCTACATGAGGTGAGGATTCAGCCACGCCAGACTTAACCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9120
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
ENSDART00000003143 Nonsense 11 285 1 7
ENSDART00000128865 Nonsense 1553 1827 40 45
Genomic Location (Zv9):
Chromosome 12 (position 25551449)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23920125
GRCz11 12 24041344
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAACCACGTGGTGGAGGAGAATGGAGTWGGTGAGCAGGACGAAAGGACC[C/T]AGGCCATCAAACTGCTGAAAACAGTGTTGAAGTGGCTGATGGCCAGTGCG
Long Flanking Sequence:
AGACTTGTTTTGAATTATATTTTGGGTTATTCACGGTCTGCTGAAAGTAATTGAGTTAGTTAATTCTAATAAGTTGTCTTTAAATATTCAGTGGATGGACTGTTATGAAAATAAAGCCACTTCATTGTACCCAGAATAAAGTAAAATAAAAAAGCTGTACTAATTGTTTAACACATTGTTACTCTAATAGTTCACGCAAAGCATCATGGGGGCATAGGAAACATTGGATTGGACAAACAGTTTAAACGTGGCTACTATAATCCAAAAATACACCAGCACTCGCTTTCATCCTCTTGTCGTGATTAATTCCTTTCAGCGTATTGACATACATCTTCATGATTGATGTGGCTCTGCCCTACACTCTGCCCACTAAATCCCCACACATCGCCGAGTTCACCGAGCGGATCCTGTCTCAGCTGAAACCCCTGATCGAAGGTGACGAGGAGATCCAAAACCACGTGGTGGAGGAGAATGGAGTTGGTGAGCAGGACGAAAGGACC[C/T]AGGCCATCAAACTGCTGAAAACAGTGTTGAAGTGGCTGATGGCCAGTGCGGGACGCTCGTTCTCCACTCCAGTCCCTCAGCAACTCCAGCTGCTGCCGCTGCTCTTTAAGGTCTCGTGTGCTTCTGTGTCTCATCTTTTATCCATTTGTGCGGAGTGCTCTTAAGTGGATTGCTGACTTGTTTTTCTCTCTGTCTGCAGATCGCGCCTGTTGAAAATGATGACAGCTATGATGAGCTGAAGAGAGACGCCAAGACATGTCTATCTCTTATGTCTCAGGGGCTTCTGTATCCTGAGCAGATCCCGATGGTACTCGCTGTGCTACATGAGGTGAGGATTCAGCCACGCCAGACTTAACCTCTGAAGGCTAAAATTGACCTTGGTTCATTTATTATTTAATCAATGTTATTGCTTTTGTAAGATGCTATCGGTGGGAGAGAAAGGTAAACAAAAATAGTTTTTGAAATAAAGTAAAATCTGTTAAAAATATATATATTATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13795
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
ENSDART00000003143 Nonsense 140 285 3 7
ENSDART00000128865 Nonsense 1682 1827 42 45
Genomic Location (Zv9):
Chromosome 12 (position 25553875)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 23922551
GRCz11 12 24043770
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGTGTTCARGGCGTCAGAGCTCTGGTCATCAGGCTCCTGGAGGACGAG[C/T]AGCTGGAGGTACATCTGGGCCACAATCATTTATTTATTCGCTTTCATGCA
Long Flanking Sequence:
AGCAGAACATGAACCTACATTGTAAACTGGAAATATAAAAATAAATATTAATATTAAAAAATTGTTGACAGTAATTTAAGTAATTTAAACTAATATTATAGTAAGAATAATATGAATGTAAAAAATACATTTTGTGATATCAGTATTATTATATTAACTAAAATAATAAGTTATTACTACCATTATTGTTTCTGTAATACTCATCTTGTATGCAGATAATAATTTAAATTGTAGAAAATAATTATTAATTGTCCAAAATAATTAATTGTCTTATTTATTACCAACCAACACGTATCACCTTGTCCTTATTTCTACAGTTGTGAAACCATAAGCTTCTTTTTCTACATTTACAGATTGCCGGTAGCAGCTCTTGGCATGCCAGATACTCAGTGTTAACGTATCTCCAGACAATGGTGTTTTATAATCTGTTCACCATCCTGAGCAGCGAGCAGTGTGTTCAAGGCGTCAGAGCTCTGGTCATCAGGCTCCTGGAGGACGAG[C/T]AGCTGGAGGTACATCTGGGCCACAATCATTTATTTATTCGCTTTCATGCACCCTTTTCATTAAAGCTTCATCTCTGTGCGTGTCTCTGCTGTAGGTGAGAGAAATGGCTGCCACCACACTTAGCGGCTTCCTGCAGTGCAATTTTTTGGCAATGGATTCCTCCATGCAGACCCACTTTGAGGCTCTATGCAAAACCAGATTGCCCAAAAAGAGGAAAAGAGATGTGGGTTCTGTGATGGACACCATTCCTTCTGTTGGTATGATCACACTTTAATCAAACGCAGTGCTGTGCTCTGTGGACCGGAGAAGTAGGGCAGTAGAAACATTCCAAAAATTCAACAGCAAATGTCATTTAAGTTCAAGTTTAATACCAGCTCTTTTAAATTATCCTGTCATAAAAAGGTACAAAAAGAGGTTCATATTTTTAAGGATGTTTGTATGTGCATATTTTGTGGTTAATAAACAAAAATATTCAATGTACTGTCACACTGACTTTTAAT
Associated Phenotype:
Not determined