ZMP
si:ch211-8a9.3
Ensembl ID:
ZFIN ID:
Description:
piggyBac transposable element-derived protein 5 [Source:RefSeq peptide;Acc:NP_001139077]
Human Orthologue:
PGBD5
Human Description:
piggyBac transposable element derived 5 [Source:HGNC Symbol;Acc:19405]
Mouse Orthologue:
Pgbd5
Mouse Description:
piggyBac transposable element derived 5 Gene [Source:MGI Symbol;Acc:MGI:2429955]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42197 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35479 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9658 | Nonsense | Available for shipment | Available now |
sa14201 | Essential Splice Site | Available for shipment | Available now |
sa6298 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42198 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42197
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000028285 | Essential Splice Site | 103 | 518 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 24247277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23892937 |
GRCz11 | 13 | 24023387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCGATACGCTGCGGGACCTCAGCCTGCCTCACTACCAGGACACGCACG[G/A]TAAGTTGGTGTAACGGTGATGAACGCTGATTAGTGTAAATGCAATGCAGC
Long Flanking Sequence:
CGCACGGCGGACAGCTCCCACGGCGCTCACCTTTGTTTCCCCGCCGCTAGTGAGACCTGCGGCCGCTGTTCAGGCGCAGCGGAGGGGCTCGGCAGAGCAGACTGGATGCCGGATTGGACTCTTTTTAAGGAGGTCATTTGCATGCCGAAGCTCGCCGGGTGTAGCAGCTCAACGTCGGGACTGACAAACGATGGCGGAGTGTGGAAGGAGGGGACTGTCGCTGCTCGAGGAGGCGCGATCTCGCTACGAGAGCCTGCAGATTTCCGATGATGTGTTCGGGGAGTCAGGCGACGACAGCAGCGAGAACCCCTTCTACAGTACCACCGGAGACTCCAATTCGGATAACTACCCGGAGACGAATGCGGACGATGCGAGAGTCAATGAAACTCGAAGTCAGAGCTGCGTTCCTCCCGGCTCTGTGTCTAGCGGGCAGGCGCAGGAGGAGGGATGGGGCGATACGCTGCGGGACCTCAGCCTGCCTCACTACCAGGACACGCACG[G/A]TAAGTTGGTGTAACGGTGATGAACGCTGATTAGTGTAAATGCAATGCAGCTTCGTCCTCCTTGAGAGGCCTGCTTGCTCGACGAGTAATTAAGCTCACAGATGGGACTCTCTGATGACTACACTGGTTTGCTTTGATCTCTCTCATCAGATGGCTCCAACAGATGACACAATTCCTTGAAATATGGATCAGGGGTGATTATTAGCTTGCTTTGTGAATTCATGCATGCACATAGGGGACGTGAGTGAGCAGGCCAAATTTTGGGGTTTCAGTCCAGCTGAGGATGCTTTTTGTGTCTGCCAGACTCTGAGCAGCTGTGATTTTGAGTATGATTAGCTCAGTTTCAGGGCAGAGAGGGCATTTGCATGGGCGGATGAGAGGAGGCTCTTATTTCTGAGAATTTCACACTTTGAAGTGATAAGATGGCTCTTTCAGAGATTTAGTGCAAATGCTTTCTTATGAAGTGATGTACTGTGCAGACATGTACTGTATATTTAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35479
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000028285 | Nonsense | 175 | 518 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 24258036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23903696 |
GRCz11 | 13 | 24034146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAATGAAAGCATTTCTAGGCTACGTTACATCTACTAGCGTGAACCGCTG[T/A]GAGTCGGTGTTAAGCATCTGGAGCAGTGGTTTCTTCAGTAACCGCAGCAT
Long Flanking Sequence:
CATTATTTTCTGTAGTCATGTGCATAGCAAAATTGTTGCAAACCATTTATGTGTTGATTTTAAACAAAACATATTAAATTTAGTAATGTTCAGCTTCATTTGTTACTTTAAGTTCAGCCCAAATAAATTGTTTACAGCCACTTAACATAAAAAAGAGTAAATCCAAGGAATCATCTTTGAATTTTTTTTTTCAATGCAATGTGCTTTTAAGAAGTTACACAATTAAAAAATATCTAAAAACAACAACAACAAAAAAATATCTTAAAACATACCTTTTATTTTATAGGTCCAACACAGAAAATGTCAGCCACCGCTACAGCCATGGACTTCTTCCAGCTGTTTGTACCGGACAACGTCATTCAGAACATGGTGACCCAGACCAACATGTATGCCAAGAAGTTCCAGGAGCGTTTCGGCAGTGATGAAGGCTGGACCAACGTGACACTTGCAGAAATGAAAGCATTTCTAGGCTACGTTACATCTACTAGCGTGAACCGCTG[T/A]GAGTCGGTGTTAAGCATCTGGAGCAGTGGTTTCTTCAGTAACCGCAGCATCGCGCTCAAAATGAGCCAGGCGCGCTTCGAAAAGATCCTCAAATACTTCCATGTTGTAGCCTTCCGCTCCAGCCAGGGTGGCAGTCAAGGCCTCTACAAGATCCAGCCCTTCCTGGACTCTCTTCAGCAGAGCTTCAGCTCTTCCTTCAGGCCCTCGCAGACACAGGTAAAACACACACATCACTCATTATCCCCAGTAAAACATATCTGTTCATTTACAGCTCATGTTTGGGACATTCAAGGGTTAAGGCCCAATCCCATTTGTATTTTTGTACCGCTACCCCTTCCCCTTGGCCCTTGAAACAGAAGGAGCAGGGTGTCAAAATGTACCCCTAAGAAATGGAACAGCACTACAACACCTGCACACGTCATCATAAGTCATTATGATCTCTTGCTTCACTACACCTTACTGACAGGGTATTCCAGTGTCATCGAGTGTCAGAATGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9658
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028285 | Nonsense | 401 | 518 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 24273900)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23919560 |
GRCz11 | 13 | 24050010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCAGTCTCATGTTAAGATGAGAGGAAATATGTCCATAATCAACTGGTA[C/A]AACAAAGGCAACTTCAGGTTTCTCACTAATGCCTACTCTCCTACTAAAGA
Long Flanking Sequence:
TGGCGAAACAAAAGATGTAATAGCAGTTCAAACACTCCAGAGTAAATCCTACAGGACTTCTGACAGCACTGCACAAGCACATAAAATGAAAACCTTCAAGGGAAGATTAGTCACACAGTTGTCCTCTTTCTCTTGCGGCAAGGATGAATATGAGTAATCAGCACATCTCAATCAGACCTTAGATTCAGGCTAAAGCATCTGACGATGCTGTAGAGAAGACATCTGCTCACAGCTTCACACATGCAGTCCTCTATTCATCCAATCAGCTTTCAAATGTCAGCACTTGTTGTGCCGTGCACTGAATACTCAGGCTGTATATTCATTCTCAGATGGGCTATTATTTTTATTTCTGCAGGCATCTACTGCTGCGGGCTGCTGAGCATCAGGAAGAGTGATTGTACAGGCCTTCCACAGTCAATGCTGATCAATACAGAGGCTCCACAGCAGCGTGGCCAGTCTCATGTTAAGATGAGAGGAAATATGTCCATAATCAACTGGTA[C/A]AACAAAGGCAACTTCAGGTTTCTCACTAATGCCTACTCTCCTACTAAAGAAGGTAAGAAAAACACACAAAAGACTGGCTTTACATTTCCTCTAGCTTAAATGTGAAGTAGTTTCTATCTACCTACTGAAATTATAAAAGTAAAACCTTTCCAAAATACCTCTTAGATTCACCATGTCTTGTAATCCACTATTTCTTACTATTCAGAATCCATATGCACCCACTAACAGGTCAAATCTTCTTCTCTCTCCTTCAAGTTTACAGCAAACCTGAATGCCAAAATGCCAAATTTTAGATATATATAAATAGTCTATGCCAGTGTTTCTCAACTGGTGGGTCGCGACCCACTTAACATTTTCAGTGGATCGCGGAGTGTGTGGTCAAAAAAAACAACAAAAGTTAAATTTTTTACTTATTTTGCTTATACTAGACTTTTATTTTGAAATGCTTTCGCGACAACCCTACCATTTGACATGTGAAATTTCATTTAATTATAGCAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14201
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028285 | Essential Splice Site | 419 | 518 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 24273954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23919614 |
GRCz11 | 13 | 24050064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGGCAACTTCAGGTTTCTCACTAATGCCTACTCTCCTACTAAAGAAGG[T/G]AAGAAAAACAYACAAAAGACWGGYTYTACATTTCCTYTAGCTTAAATGTG
Long Flanking Sequence:
GACTTCTGACAGCACTGCACAAGCACATAAAATGAAAACCTTCAAGGGAAGATTAGTCACACAGTTGTCCTCTTTCTCTTGCGGCAAGGATGAATATGAGTAATCAGCACATCTCAATCAGACCTTAGATTCAGGCTAAAGCATCTGACGATGCTGTAGAGAAGACATCTGCTCACAGCTTCACACATGCAGTCCTCTATTCATCCAATCAGCTTTCAAATGTCAGCACTTGTTGTGCCGTGCACTGAATACTCAGGCTGTATATTCATTCTCAGATGGGCTATTATTTTTATTTCTGCAGGCATCTACTGCTGCGGGCTGCTGAGCATCAGGAAGAGTGATTGTACAGGCCTTCCACAGTCAATGCTGATCAATACAGAGGCTCCACAGCAGCGTGGCCAGTCTCATGTTAAGATGAGAGGAAATATGTCCATAATCAACTGGTACAACAAAGGCAACTTCAGGTTTCTCACTAATGCCTACTCTCCTACTAAAGAAGG[T/G]AAGAAAAACACACAAAAGACTGGCTTTACATTTCCTCTAGCTTAAATGTGAAGTAGTTTCTATCTACCTACTGAAATTATAAAAGTAAAACCTTTCCAAAATACCTCTTAGATTCACCATGTCTTGTAATCCACTATTTCTTACTATTCAGAATCCATATGCACCCACTAACAGGTCAAATCTTCTTCTCTCTCCTTCAAGTTTACAGCAAACCTGAATGCCAAAATGCCAAATTTTAGATATATATAAATAGTCTATGCCAGTGTTTCTCAACTGGTGGGTCGCGACCCACTTAACATTTTCAGTGGATCGCGGAGTGTGTGGTCAAAAAAAACAACAAAAGTTAAATTTTTTACTTATTTTGCTTATACTAGACTTTTATTTTGAAATGCTTTCGCGACAACCCTACCATTTGACATGTGAAATTTCATTTAATTATAGCAACAAATATGTCGAAGCCCAAGTAGGACCCCGAACATGTAAAGTATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6298
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000028285 | Nonsense | 431 | 518 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 24277807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23923467 |
GRCz11 | 13 | 24053917 |
KASP Assay ID:
554-4635.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCCTACTGTAGGTGTGATCATTAAGAGGAAGAGTGGAGAAATCCCATG[T/A]CCCCTTGCTGTGGAGGCCTTCGCTGCACACCTGAGTTACATCTGCAAATA
Long Flanking Sequence:
AAGAGAAATAGTGGATTTCTTTTTTTCTTCTTCTTCTTTAACCCATTGAAAAGAAACAGTGTATAACAGTGTCATAATGAATAAAATTATTGTTAAAAATTAAATTATGTTTTGTTTGTGTGTAAATGATGTGGGTAAATGGTGTGTTTCAATCTGGCTACCATCGCAAACGTATTTTAAACTTGTGGGCAGCACTATAAAGTATATATACCGTTCAAGTCAGAATTATGAGCCCCCCTTTGATTTTTTTTTTTTTTAGCTGATTCTAGTTAGTTAGTGATTTTAGGTTGTTAAATAATAATTCTTGTTAGCTTGTGATGCTAGCTAATGATTCATGTTAGCTTGTGACACTAGGTTGTTAGCTGATTTTTGTTAGTTTGTGATGCAAGCGTGTGACGTTAGATTGTTAGCTCATCATTTTGTTACGAGGACAGAATGACATTTCTTTATTCTCCTACTGTAGGTGTGATCATTAAGAGGAAGAGTGGAGAAATCCCATG[T/A]CCCCTTGCTGTGGAGGCCTTCGCTGCACACCTGAGTTACATCTGCAAATATGATGACAAGTACAGCAAGTGAGTTTGACCAGGAATCAAAGCAAGAGTTCAGTCCCCTAAAAAAATTAGCTGGTGATTTGCCTTCCCTCAGGACATCTAAAATGTACGTGACTCCCTCCAATCAGACCATTAAAGAAGATTTCTAGCTGAAATTAAGTCAATGGCTACTGGCACATTGAGCGTTTAAGCATAATAAGCAAACAATTGGTCTGTACAAGAAACAAAAGATTGTGGGCTTGGATTAATATAATGTTTCTTACCTAAGACCTCAGTGTACCATCAGGAACCTCTAGTGTTTCAAAACTGAATTTATCAATAATATTTATGATTTTTTTTATCAATAATTTACTTTACTTTAGCCTCATGCACACCAGGACGTTTAATGTTCATGCTTATCTCATGTTTAAGCAAGACCTTTTTTTATTTAATGCCTAGTGATTGCCTAGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42198
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000028285 | Nonsense | 452 | 518 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 24277870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23923530 |
GRCz11 | 13 | 24053980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCCTTCGCTGCACACCTGAGTTACATCTGCAAATATGATGACAAGTA[C/A]AGCAAGTGAGTTTGACCAGGAATCAAAGCAAGAGTTCAGTCCCCTAAAAA
Long Flanking Sequence:
TAACAGTGTCATAATGAATAAAATTATTGTTAAAAATTAAATTATGTTTTGTTTGTGTGTAAATGATGTGGGTAAATGGTGTGTTTCAATCTGGCTACCATCGCAAACGTATTTTAAACTTGTGGGCAGCACTATAAAGTATATATACCGTTCAAGTCAGAATTATGAGCCCCCCTTTGATTTTTTTTTTTTTTAGCTGATTCTAGTTAGTTAGTGATTTTAGGTTGTTAAATAATAATTCTTGTTAGCTTGTGATGCTAGCTAATGATTCATGTTAGCTTGTGACACTAGGTTGTTAGCTGATTTTTGTTAGTTTGTGATGCAAGCGTGTGACGTTAGATTGTTAGCTCATCATTTTGTTACGAGGACAGAATGACATTTCTTTATTCTCCTACTGTAGGTGTGATCATTAAGAGGAAGAGTGGAGAAATCCCATGTCCCCTTGCTGTGGAGGCCTTCGCTGCACACCTGAGTTACATCTGCAAATATGATGACAAGTA[C/A]AGCAAGTGAGTTTGACCAGGAATCAAAGCAAGAGTTCAGTCCCCTAAAAAAATTAGCTGGTGATTTGCCTTCCCTCAGGACATCTAAAATGTACGTGACTCCCTCCAATCAGACCATTAAAGAAGATTTCTAGCTGAAATTAAGTCAATGGCTACTGGCACATTGAGCGTTTAAGCATAATAAGCAAACAATTGGTCTGTACAAGAAACAAAAGATTGTGGGCTTGGATTAATATAATGTTTCTTACCTAAGACCTCAGTGTACCATCAGGAACCTCTAGTGTTTCAAAACTGAATTTATCAATAATATTTATGATTTTTTTTATCAATAATTTACTTTACTTTAGCCTCATGCACACCAGGACGTTTAATGTTCATGCTTATCTCATGTTTAAGCAAGACCTTTTTTTATTTAATGCCTAGTGATTGCCTAGTAAATGTGCAAAACCACTTCCTGACACAGATGCTGCTTTATGAGAAACTAAATCACTGCTGTACACA
Associated Phenotype:
Not determined