ZMP
si:dkeyp-1d11.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
PDE8B
Human Description:
phosphodiesterase 8B [Source:HGNC Symbol;Acc:8794]
Mouse Orthologue:
Pde8b
Mouse Description:
phosphodiesterase 8B Gene [Source:MGI Symbol;Acc:MGI:2443999]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17719 | Essential Splice Site | Available for shipment | Available now |
sa9848 | Nonsense | Available for shipment | Available now |
sa9852 | Nonsense | Available for shipment | Available now |
sa32333 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17719
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 |
---|---|---|---|---|---|
ENSDART00000093339 | Essential Splice Site | 272 | 874 | 7 | 22 |
ENSDART00000134519 | None | None | 500 | None | 12 |
ENSDART00000143409 | Essential Splice Site | 178 | 273 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 7618722)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 7941189 |
GRCz11 | 21 | 7678857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGTGTCAGGAGGCCGTGGAGATCAGCAGTGAGGATCATGTCATACAAG[T/C]GAGTTCTRGGAGACAAACACRGTCTTCCTACTGGGATTTGCTTACATTRA
Long Flanking Sequence:
GCGAAAGTGAACTTACTTTACGTCATGTAAATAGCAAATGCGCTATGGCGCGACGCAGCTGGCTCTTAAAGGGAATGGGAGATGAGACTCTTATTGGTTTATTCTTAAAACACACCTATAACTCGTTAAGAAAAAAACTCAACCCTTTTAGACCATGCGCCATGGCACAAAGCGGATTTTCTCGTCCTTAAGTTAGCAAAAATGCGTTCTGACATGCCCTGAAAGCGTTTGCGTTTTGCGCTTTGCGCATGGACCGTCAAAATAGAGCCCTAAGTTTTCAAGGGTTGAATCCTACAGGTGTAACGGTAGCAAAAGTTGTGCATTTTAAAACCAAAAATACATGCTTAAATGTAGCCTGTGGCCGCTGCTGTGAGATGGATGCAGAAGCTGTCATGTTTGTTTGTGTTTCTGTGCTTGCAGGGCTTGTAACGCTGTGTTTACTGCACTAGAACAGTGTCAGGAGGCCGTGGAGATCAGCAGTGAGGATCATGTCATACAAG[T/C]GAGTTCTAGGAGACAAACACGGTCTTCCTACTGGGATTTGCTTACATTAAAGCAGGCTCTTTTTGTTCAAAGAAACTTCCTGGAGGAGAATGCATTAGCGTGTGTCCACATTTCCATTTATTTTTTTCCCATAGGGATTTGTAATGTGATAAGACTTAAGACATGAACAAACCAGTCAACCAGCAAACTTTACAAGCTTTGATTTGAGGGAAAGAAGTTTATTCAAATCTGAGAAAAAGACTAATGTATAAGGATGTGAGTTTAACAAGGTTAATGAGTGGAAGCATTGCTTATGACACAGTCACGTTACGTTTTTTCTCAGTGGTTTTGGTGCATTCCTTACAACACTATTTACATTTGCACAACATTTCATTTCATTTTCTTGTCGGCTTAGTCCCTTTATTAGTCCGGAGTCGCCAAAGCGGAATGAACCGCCAATTCCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACACACACTCATACACTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9848
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 |
---|---|---|---|---|---|
ENSDART00000093339 | Nonsense | 383 | 874 | 11 | 22 |
ENSDART00000134519 | Nonsense | 9 | 500 | 1 | 12 |
ENSDART00000143409 | None | None | 273 | None | 9 |
ENSDART00000093339 | Nonsense | 383 | 874 | 11 | 22 |
ENSDART00000134519 | Nonsense | 9 | 500 | 1 | 12 |
ENSDART00000143409 | None | None | 273 | None | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 7605245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 7927712 |
GRCz11 | 21 | 7665380 |
KASP Assay ID:
2261-5224.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAGGTTCACAAGCTGAGCAAAGAAGAGAAATGCTGTGGTGAACACTCA[C/T]AATCAGGTACAGTAGCTGTCYTTGAAGCGTTGTTTGTTTACTAWGTGTGT
Long Flanking Sequence:
GAAATGACCATAAAAGCATACCGAACTGTACCGTACCATATCACTCAGTGAAAACGGGCCGTAAGCTGCCATCACCAAAAAAGCCTTTTATGTAAGGTATTAAATACGTTTCAGTAATTCAGTGATTTCTCCTTTTGTCATTCCATTGTTATTACGCATAACTCATTATTTTATATTATGTTTTTTCTTAATGTTTGCATAGTTTGGGGTTTTACCAAAATTAGGTTTAATTCCATGTCAACAGCTCCTTCATAAAAATTATTCCTAGGAAAAAACATGAAGTGTTCAATACACCCCCCTCCCCCCCTCCCTGTATATCAGTAGGCTGGGTCTAATCAACCCTCCAAATGTCATTCTAACTTTGTTGCCAGATAATTAAAACTGTGTTGAGTGAGATGATTAGGATCATTGTGTTTGTTTCCGAGAGCCAGCTGATCAGAGATCTGTGTTTGCAGGTTCACAAGCTGAGCAAAGAAGAGAAATGCTGTGGTGAACACTCA[C/T]AATCAGGTACAGTAGCTGTCTTTGAAGCGTTGTTTGTTTACTATGTGTGTTTTGGATCCATCATGCAATGTTGCATAATTAGCACACTGCAGTCGATAATGACTCTTTATAGATTTGGTTTATGTGGCATGCTGTGAAACAAAAGCAGGAATGAAAAGGCACAAATCAATGTGGCTTTGATAAACAGTCAGTGATCGTGGTGCAGAATAGATGGGTGGCAGCAGTGCACCCTGGAAATTGTGATCAGACTTCAATAAAAAAACTTTGAAAACCGCAACACTTTAGCAACCCCATAGCAACACTCCTTTTGAAGAGCTAACTGAATAACATCTCGATCAGAACCACTTAATACCCACCCACCTATCCATTTATTCATCCATCTATTCATCTATCCATCCATCTGTTTATCCATCCATCTGTTTATCCATCCATCCATCCATCTGTTTATCCATCCATCTGTTTATCCATCCATCCATCCATCCATCCATCCATCTATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9852
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093339 | Nonsense | 495 | 874 | 15 | 22 |
ENSDART00000134519 | Nonsense | 121 | 500 | 5 | 12 |
ENSDART00000143409 | None | None | 273 | None | 9 |
ENSDART00000093339 | Nonsense | 495 | 874 | 15 | 22 |
ENSDART00000134519 | Nonsense | 121 | 500 | 5 | 12 |
ENSDART00000143409 | None | None | 273 | None | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 7597235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 7919702 |
GRCz11 | 21 | 7657370 |
KASP Assay ID:
2261-5223.1 (used for ordering genotyping assays)
KASP Sequence:
TTCACTCAGATTTACTGTTGTGTATTTCTTCTTCACTGCAGGACGGACTC[A/T]GAAGGCTCTCCGGGAACGAGTACRTCTTCTCCAAAAGTGCTTTACAAAGT
Long Flanking Sequence:
GTATATGTGTGAGTGTATGTACAGATGTGTGTGTTAGTGTGTGTATGTATCTATGTAAGTATGTATGTGTGTGTTAGTGTCTGTGTTAAGTATGTGTGTGACTGTGTCTATGTGTATGTGACTGTGTATTTGCTGTGCGTATGTGTGTTGCGTACATGCATGACTATGGCACACACACACACACACACACACACACACACACACACACATACACTAGAGTGTGATTATCCTGCATCTGCTTCATCTCACTCAGAGTTTGTTTTAAGTGCTGGATTGTTGAAGCTGAGTCTGGATCAGTTTTTCGGTGTGTGTTTAATATCCTGCAGCTCTGATAAACGGCTCTTCTCCTGAGAGAGAGAGTGAATCATGGCTAGCGTGTCAGTGCGCTGCTTAAGTCTGCTGTTATGATTATGTTGGCTTGAAACAATATTTTGGCCTTTTCTCTTTGATTTCACTCAGATTTACTGTTGTGTATTTCTTCTTCACTGCAGGACGGACTC[A/T]GAAGGCTCTCCGGGAACGAGTACATCTTCTCCAAAAGTGCTTTACAAAGTAGGTTCATTGTCATTATGGGCAATTGTGTGTAGAATTTCGAGGAAATAAATGAATTTAATCCATTTTTGAATAAGGCTTTAAAATAAAAAGTCAAGCGCTAGGAATACTTTCCAGATGCCAGACCTTTTTCTTGTCTGCTGCATGGAGGGTGCCATAGCGACCAGCGTCTTCCGGCAGAATGTTTAGAACTTCCGTTTACAGCGTTTACAACCGGTAATTTGCGCTCCGAAAATGGGTTTCGTTAGCACTTTGAGTAGATTACGGAGTGTTTTTGTGACACACAACTTTAAAAGGTGCGTGTTAAAGCCGTTATAATCTGTCAGATCTGTGGTTCAAGCGCGAGAGAAAAACGTTCTCCTATTTAACGTGTCTGCCGTCCGAAATACAGTGTGTGTGTGTGTGTGTGTTCCCGGCCTGTTAGCTGACACACACACAAACACACACACGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32333
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093339 | Nonsense | 588 | 874 | 17 | 22 |
ENSDART00000134519 | Nonsense | 214 | 500 | 7 | 12 |
ENSDART00000143409 | None | None | 273 | None | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 7593063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 7915530 |
GRCz11 | 21 | 7653198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTCTGAACTGCTCCGAGTCCACGCTGCGCTTGTGGCTGCAGGTGATC[G/T]AGACCAACTATCACTCCTCAAACTCCTACCATAACTCCACACACGCCGCT
Long Flanking Sequence:
GTCCCTGATTAATTAGGGTTTGCCACAGCGGAATGAACTGCCATATTACATGTTATGTAATGTAACACACAATTTCTAAAAAAAAAAAAACAAGACAATTAACGTTTAATTTCTCCTGTAATTGTCAGACATGAGTCAGAGTCAGCTGGGTGTGCCCGTCCCGCTGAATGACATCCCGCCGTCCATCGCAGAGCTGCTGAATGAAGAGGAGCAGTGGGAGTTCAACATCCTGGAGCTGGAGGCAGCCACACACAAGAGGTACCAACAGGACATCAGCATTTCTTTCATTTCATTGTCTGAAATGTAGTATTAACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGCGCATGTAGGCCACTGTCGTACCTGGGTCTGAAGATCTTCTCTGCGTTTGGCGTGTGCGAGTTTCTGAACTGCTCCGAGTCCACGCTGCGCTTGTGGCTGCAGGTGATC[G/T]AGACCAACTATCACTCCTCAAACTCCTACCATAACTCCACACACGCCGCTGACGTGCTGCACGCCACCGCTTACTTCCTGCGCAAGGAGAGAGTCAAGGTAAACTCACACAAAGCCTTTTTAAAGGTCCCGTCCAGTGCTTTGAAATGTGCATTTTCTGTTCAACGTTTGACATAATCTCAATTGAAACATGAGGAGAGGGTGGGACATAGAGATAGAGAAGCGTCTTGAAGGGGGTAGGGCATGTTAGATTCTAGAGAGCATTTGATTGGTCAAGATATGATGAGAACCTGAAGTATGAGGAGATGTAAAAAGGTCGTTGATCCATTTAGGCGGAAGTGACAAACTGCAAGCTCTGGATGTTTATGTCAGTTTTTTAGTTTCTAAACGTGAATGTTGTCACTGTTCTGAAGCGCACAAGATTATAGATATTCTTAAAACTACCAGACTGAAACTAACTTTATTTTTGTTTCATGGGATCTTTAACACGGACTGATGATT
Associated Phenotype:
Not determined