ZMP
pogzb
Ensembl ID:
ZFIN ID:
Human Orthologue:
POGZ
Human Description:
pogo transposable element with ZNF domain [Source:HGNC Symbol;Acc:18801]
Mouse Orthologue:
Pogz
Mouse Description:
pogo transposable element with ZNF domain Gene [Source:MGI Symbol;Acc:MGI:2442117]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15926 | Nonsense | Available for shipment | Available now |
sa14074 | Essential Splice Site | Available for shipment | Available now |
sa12020 | Nonsense | Available for shipment | Available now |
sa16289 | Splice Site, Nonsense | Available for shipment | Available now |
sa9652 | Essential Splice Site | Available for shipment | Available now |
sa15093 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15926
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113473 | Nonsense | 292 | 1320 | 7 | 22 |
ENSDART00000128542 | Nonsense | 308 | 1349 | 7 | 18 |
ENSDART00000132087 | None | None | 1031 | None | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 40789956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 38174756 |
GRCz11 | 16 | 38124788 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTMTATTTACAGTGACAATAAAGCAAGGAAATGGACCCCTAGACATG[C/T]AAAACCTAATGAATCTTGTGAAGTCTGTGAACCTTCCTGGTGGGGCTCAG
Long Flanking Sequence:
TCTACAAAATAAACAGAAAGAACAAATACATTTAAGTTGAAGTGACATGCAAGTACTTTTTTCCAATAATAAAGGAATCATAATTCAATTCAAGTAGGCCTATTACAACATAAAATATAGTATTTCTGAAAATTGTTTTTATGTCATGAATTTGAGTTATGAATTACAGTATCGCAATACTACTTGGTATCACGATACTTCAGCTTGTATAGTATCGTAACATGAATTAATGGTATTGCGACAACCCTAGTCTGAACCAGATATAAGAGACATATCCGGTAAATTAAATTAAATCATTTGAAATAAAGTTTTGTAAATGCCTGGCATTCTTCTACAAGATACAAATAAAGAAATCAAGTATTTAATAATTGTTTGCTACTATGTGTATTTTTCACAGTTGCTTGGTCAATCAGCATTCAGAATTACAATTATCTGTTTTAAAATTGAATTTATTTATATTTACAGTGACAATAAAGCAAGGAAATGGACCCCTAGACATG[C/T]AAAACCTAATGAATCTTGTGAAGTCTGTGAACCTTCCTGGTGGGGCTCAGGCGCAGACATTTGTAGTCATGAGCAATCAAAATACCAAAAATGGTCCTGTTGTTTCTTCTGCTGTTCCTATCATCTCACAAAATGTCATCCAAAGTAAGTTTGTTGTTCTGACTATTACATTGATTTCCTATTAGAGTAAAGCCATGCTGATAAATTCCAAATTATGTTTTTGCAGCGATCCCACTTCCAAATGCAACCTCATCAACAACCACCACTCATTTGTGTCCTCGTTGTGGAGCTCAGTTCAGAATGATTGAGGCTCTACGCGGTCATATGTGTGTAAGTACATACTTTGTGAGGAGACTGTAAATGTGTTTGGTCACCTAAAAAACGAATCCCTTTCTCTCTTAGTTTTGCTGCCCTGATCTGGTCCACATGACTGAAACAAGCAGTACCCCAACAGCTGTGAAACCCCCAGCAACACCACCTAAGAGTGCCTCTGTTGTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14074
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113473 | Essential Splice Site | 469 | 1320 | 9 | 22 |
ENSDART00000128542 | Essential Splice Site | 485 | 1349 | 9 | 18 |
ENSDART00000132087 | Essential Splice Site | 95 | 1031 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 40790644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 38175444 |
GRCz11 | 16 | 38125476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCATTCAGATGCCTGACCTGTAGCAAGAAACTAAAGAATAATATTAGG[T/A]ACGATTATGGACTGATTTTAGAAGTCTTATTGTAAATATCTAGTTGAAAA
Long Flanking Sequence:
TAAAGCCATGCTGATAAATTCCAAATTATGTTTTTGCAGCGATCCCACTTCCAAATGCAACCTCATCAACAACCACCACTCATTTGTGTCCTCGTTGTGGAGCTCAGTTCAGAATGATTGAGGCTCTACGCGGTCATATGTGTGTAAGTACATACTTTGTGAGGAGACTGTAAATGTGTTTGGTCACCTAAAAAACGAATCCCTTTCTCTCTTAGTTTTGCTGCCCTGATCTGGTCCACATGACTGAAACAAGCAGTACCCCAACAGCTGTGAAACCCCCAGCAACACCACCTAAGAGTGCCTCTGTTGTGCCTAGTGCCAAGGTGGATAGCCCACCTAGCAAAACAGGAGATAGCCATCCCAGACTCGTCATGCTGGTTGATGATTTCTACTACGGCACATTTGAGGGAAATCGAGTCTATGTACCAATGGACAACTCAAAAGAACCATTATCATTCAGATGCCTGACCTGTAGCAAGAAACTAAAGAATAATATTAGG[T/A]ACGATTATGGACTGATTTTAGAAGTCTTATTGTAAATATCTAGTTGAAAATGATAGGTTTTATTTTAAGTAATTTCCTAGTCTTTGTTTATTCTGTCTTTGATATGTTGGAACTGTGCCATTAGTGATCACTTGTTTTCTTTGAAGACTTATGAACCATATGAGGTACCATGTTGAACTGGATCAACAAAATGGGGAAATGGACAACCACACATCCTGTCAGCATTGTTTCCGTCGCTTTCCTACACCGTTTCGTCTGCAGTGCCACCTTGAGAGTGTCCATACCTCCATTGAATCATCTAGTAAGAACTATTTCTATTTTATTAATCTTTTTGTTTAAGGGTGCCACATACAGCATTTGTTTAATAAGTTAAATTGTTCTCTGATATATACATAGTAGGTTTATGGCTTTGGTATTTAAAAAAAAATCTCCAGAAACAGTTTTATAAGCACTTTTATTACTCCATAAAGTACCAACAGAATCAAAAGATCCATGATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12020
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113473 | Nonsense | 596 | 1320 | 12 | 22 |
ENSDART00000128542 | Nonsense | 612 | 1349 | 12 | 18 |
ENSDART00000132087 | Nonsense | 222 | 1031 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 40792949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 38177749 |
GRCz11 | 16 | 38127781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTCTGTGCCAGTATTGCCTGAAGGTTTTCAAGCATTCCACCAGTTAC[C/T]AGCAACAYTATGTTCGTCATCAGGYRAGGATAGGAAGCATMAAATTTTAA
Long Flanking Sequence:
AATAAGGAGGGGTCAATGAGGCAATGTTCAGTCCCAACAAATGTTTAGTAAAGTTCTTCATTCACCATTGTTCTGCAATGCTGCAAAGATAGTAAATGATAAAAGTTTGTATTTTGGTTTGCCACAGTGTCTATAAACTGCAGGACTCTCAATTTGTCAGCAGTTTAAGTAACTGTTGTGCTTTTGTGTTCAGCCAAGTGTAAGATATGTGAGTGGTCCTTTGAGAATGAGCCAGTGTTCCTGCAGCACATGAAGAACTCCCACAAACCCGGAGAGATGCCTTATGTATGCCAGGTAAACTAAACAAATTTGACTGACAAATGGATGAATCACAAGGAGAGTGGGAATATAGCATATAATGCCCTTGAAATTTTCAGGTGTGTGAATACCGTTCCTCCTTCTACTCTGATGTGTTTAACCACTTTCGTACCTGGCATGAGGATACCCGCCACCTTCTGTGCCAGTATTGCCTGAAGGTTTTCAAGCATTCCACCAGTTAC[C/T]AGCAACATTATGTTCGTCATCAGGTAAGGATAGGAAGCATAAAATTTTAATTAAAAATAAAACTAATTAATGCATATAGACATTCAAGACTTTCACCAGGTTTTAATTTCATCATGGTTAAAAAAAACCCAAAAAAAACTTGTTTTACAGTTCTTAATGGTCCTCATCATTTGTGTAACATTTGTAATTTTTTATAGCATTGGAATCTTTGATTGTGTTTTAATATAGCACATTATCCTAAACAGTGATCACTCTTGTATGTATAAATCATAGAATTGGATAAAACCATCATCATCATGGAAGTTCCTTGATTATTACAGCAGAATGAAAGTATAGTTTTTAGCCACACCAAGTTAGATAATAGCAACTTTTCATTTTCTGTTGGTCTTTGTACATAAAGCAACTCCAGAATAGTCAGGTGGTTTTTGCAAGATCGAATACGCTTGCGGCCTGAAGTTAACGCAAATTATTTCTATTATTTATTACATTTCCCATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16289
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113473 | Splice Site, Nonsense | 603 | 1320 | 12 | 22 |
ENSDART00000128542 | Splice Site, Nonsense | 619 | 1349 | 12 | 18 |
ENSDART00000132087 | Splice Site, Nonsense | 229 | 1031 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 40792970)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 38177770 |
GRCz11 | 16 | 38127802 |
KASP Assay ID:
2261-0111.1 (used for ordering genotyping assays)
KASP Sequence:
TGAAGGTTTTCAAGCATTCCACCAGTTACYAGCAACAYTATGTTCGTCAT[C/T]AGGYRAGGATAGGAAGCATMAAATTTTAATTAAARAYAAAACTAAWTAAT
Long Flanking Sequence:
CAATGTTCAGTCCCAACAAATGTTTAGTAAAGTTCTTCATTCACCATTGTTCTGCAATGCTGCAAAGATAGTAAATGATAAAAGTTTGTATTTTGGTTTGCCACAGTGTCTATAAACTGCAGGACTCTCAATTTGTCAGCAGTTTAAGTAACTGTTGTGCTTTTGTGTTCAGCCAAGTGTAAGATATGTGAGTGGTCCTTTGAGAATGAGCCAGTGTTCCTGCAGCACATGAAGAACTCCCACAAACCCGGAGAGATGCCTTATGTATGCCAGGTAAACTAAACAAATTTGACTGACAAATGGATGAATCACAAGGAGAGTGGGAATATAGCATATAATGCCCTTGAAATTTTCAGGTGTGTGAATACCGTTCCTCCTTCTACTCTGATGTGTTTAACCACTTTCGTACCTGGCATGAGGATACCCGCCACCTTCTGTGCCAGTATTGCCTGAAGGTTTTCAAGCATTCCACCAGTTACCAGCAACATTATGTTCGTCAT[C/T]AGGTAAGGATAGGAAGCATAAAATTTTAATTAAAAATAAAACTAATTAATGCATATAGACATTCAAGACTTTCACCAGGTTTTAATTTCATCATGGTTAAAAAAAACCCAAAAAAAACTTGTTTTACAGTTCTTAATGGTCCTCATCATTTGTGTAACATTTGTAATTTTTTATAGCATTGGAATCTTTGATTGTGTTTTAATATAGCACATTATCCTAAACAGTGATCACTCTTGTATGTATAAATCATAGAATTGGATAAAACCATCATCATCATGGAAGTTCCTTGATTATTACAGCAGAATGAAAGTATAGTTTTTAGCCACACCAAGTTAGATAATAGCAACTTTTCATTTTCTGTTGGTCTTTGTACATAAAGCAACTCCAGAATAGTCAGGTGGTTTTTGCAAGATCGAATACGCTTGCGGCCTGAAGTTAACGCAAATTATTTCTATTATTTATTACATTTCCCATTTATTGTATTTTATTAACATCTACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9652
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113473 | Essential Splice Site | 769 | 1320 | None | 22 |
ENSDART00000128542 | Essential Splice Site | 793 | 1349 | None | 18 |
ENSDART00000132087 | Essential Splice Site | 404 | 1031 | None | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 40795682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 38180482 |
GRCz11 | 16 | 38130514 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCATGTYCCTGGAAGGGCTCCAAAACCTTCTAAAAAGGGGCCTCCAAGG[T/C]AATGTAATATTTGKATTTTGAGTTCTGTTTTGCTCAGTCTGAAACTGTAC
Long Flanking Sequence:
CACGTGCTGTTCTCGTGCTTATGCAAATCACATGATCAAGTAAGTTGAGTCAAACATATATTTTCACATAAATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATTTATGTGAAATTATATGGCAAAGTGATGTAAAGCTTTAAGCATCAAAATTGGTACTTTGTATCGGTTGATCACCATGACAAGAAATCAGTACTTGGTGTTGCCTGTAAAAATCCTGATCGGAGCGGCTCAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGAAGAATATATATGTACAGAAGAAAACAGTTTCATTGGAAATTGCAGCTTGAAGTTTAGTCACATATTGCAATTTATTTTTTTAATTTCAGCAATCATGTTCCTGGAAGGGCTCCAAAACCTTCTAAAAAGGGGCCTCCAAGG[T/C]AATGTAATATTTGGATTTTGAGTTCTGTTTTGCTCAGTCTGAAACTGTACCTTATGGGTATTTTGGTGTTCTTTTTGTAGCGTTGTGAAGCTGACTTGTGCAGGTTGTGAATACTCCACTCCTCACGGAAATTTGATGGCCAAACATCTCATCAAGTTCCCTGATCACTCCTACTGTTTATTCATGCGCAAAGGTGGGTGTTCTCTAGCTCAGTAGAACATTACAGCATACTTGTATTTTTACTGCATTTCTCTTACTGCATGGGCCTCTTAACCTGCATGCTCGTTTTTCTTTCTCTGCTTTCGTACTTCTGTAGTTAGAGGGTATCCAACTCTGTTGTAGGTGTCTTTAATTGCATGTTTATACTAATACAGCATTGACACAAAAGTAAAAATACAGTGAACTAAATTACTGGCATCATGGCATATTCATCAAATTTAACCTTTTCACTTACAAATTATCACTTATCATTGTGTCTTAACTTCTTACATGTGCAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15093
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113473 | Nonsense | 944 | 1320 | 21 | 22 |
ENSDART00000128542 | Nonsense | 951 | 1349 | 18 | 18 |
ENSDART00000132087 | Nonsense | 579 | 1031 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 40799227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 38184027 |
GRCz11 | 16 | 38134059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAAAGCAGCAAAAGAGATGRACACCAAACCGCAGCTCATCAAGACCTG[G/A]ATTCAAGACAAGGAGGATCAGTTAAATGAATGCTGCAGCAGTATCTGTGG
Long Flanking Sequence:
TTTAAAAAATTTAATTAGTCCTAGTTATACTTAAGTCAAGTAATTGCAACCTGTGATGTATTCTTCCCCACATTTAACATGTTATCCAGATTTTAGAAAGTGTCACATTATTTCTCTTCCAGGGACGGCACAGAGCCAGGACTTAAACATAAAACAGAAATGTTGGAAAGAGGCCAGGCCAAATCCTCAGTGGACATCAGTAATGTTTCACAGGGTGCCACTGCTGGCCAGGACGAAGACGTGGACCAAGAAATGGCTCCTCTGGAAGACGAAGACACAGAAACAGACACTGATACGGTTGAAAGCAGCGAGGAAGTCCCACTTCGAACAGTGGCTAGTGAGAAAGAAAAGCGATCACTAACCAAACCAACACAGCCTGTGAGAAACAGAGAGGAGTCTTTGACTATTCACCAGCGGCGAATACTTCTTCTTGCACTATGTGCCGGGATCCAAAAAGCAGCAAAAGAGATGGACACCAAACCGCAGCTCATCAAGACCTG[G/A]ATTCAAGACAAGGAGGATCAGTTAAATGAATGCTGCAGCAGTATCTGTGGAGAGGCTGTTGATCGTCTAGTACAGTGGGTTCTGACACAACGAGAACAGCAGCGTCCTATCAATGAGGCGAGATTGTTTGAAAAAGCTTCAGAGCTCCAAAGCCAGACCAATGAAACAAGTTCATTCCGTATTTCATACGAGTGGGCTGTGAACTTCATGATGCAGCACAAACTGGGCTTGGATACCTGTTTCACAGTACAAAGGGAACTCCCTAGTGCCATGGAAGAGAACTGTCGTTGCTTCAAAGAATTGGTGCATGGTCAAGTTAAGACCAACAACGTTCCACAGTGTGTCATTGGGGTTATGGACCAGCTTTCCGTGTTTGTGGACATCAATATGTTGAATGAGAAAAACAAGGTAAGACGAGACACAGCTATTCAGTTTACCGGGTCTGGGAAGCCTTTCGTAAAGATTTACCTTGCAATGCTTGCAAATGGTACGATGCTTCC
Associated Phenotype:
Not determined