ZMP
pde11al
Ensembl ID:
ZFIN ID:
Human Orthologue:
PDE11A
Human Description:
phosphodiesterase 11A [Source:HGNC Symbol;Acc:8773]
Mouse Orthologue:
Pde11a
Mouse Description:
phosphodiesterase 11A Gene [Source:MGI Symbol;Acc:MGI:3036251]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11083 | Nonsense | Available for shipment | Available now |
sa5892 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32085 | Nonsense | Available for shipment | Available now |
sa11067 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42705
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 |
---|---|---|---|---|---|
ENSDART00000006412 | Nonsense | 121 | 927 | 1 | 20 |
ENSDART00000133403 | None | None | 449 | None | 14 |
The following transcripts of ENSDARG00000006151 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 23269847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21379598 |
GRCz11 | 16 | 21185417 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCCAGTCGAGCATGCGGCGGCGCGCGCTCCTGCGGAAAGCCAGTTCGT[T/A]ACCGCCGACCACCGCGCACATCTTGAGCGCGCTGCTCGAGTCCCGAGTGA
Long Flanking Sequence:
TAAAAATTCTCCGTGTGAGGAGGAAGGTAGGAGAGCAGTGATATGTCAAATGGATGTGTAAAGTGTGTGCAGCATCACAGCGAGCTGCGTGTTACTGTACAAGACTCCACAACACTTCTTCTGTGGAGGCTTTTCGGCAATCGACATGACAACTTTTGATTTTTCCGAGGTGGAGGCATTTTTGGATTGCCATCCGGAGCTTTTTGAGGAATATCTCGTCAGAAAGGGAAAATGTGACAGCCTGAGCAGGTGGCTGAAAGAGCATCAGCCGTCCAAAACCTCTCCGGCGGAGGAGAAACGCGGGGTCGCGAGGGATCCATTCTGGCCCACGAACCCTGATGGATTAAAGCGCAGATCGTCCCACATGGAGCTTCGAAAGAACTTCGCCCGGTCCAAAGCGATGACGGCGCACCGGACCTACGACGAGCACGTCAGTCTCACGGCTCACGAGTCCCAGTCGAGCATGCGGCGGCGCGCGCTCCTGCGGAAAGCCAGTTCGT[T/A]ACCGCCGACCACCGCGCACATCTTGAGCGCGCTGCTCGAGTCCCGAGTGAACGTGCCTCAATATGCCTCCAGCGCCATTGACTACAAATACCGACTCAAAGAGTCCAACGAAAGGGAGTTCTTCCTTGAGCTGGTTAAGGACATTTCGAACGAACTTGACATGACGAATCTAAGTTACAAGATACTTATCAATGTTTGCATTATGGTGAACGCAGACAGGTGTTCGCTTTTCCTGGTGGAGGGACCTTCTCATAAGAGGACACTCGTGTCCAAGTTTTTTGATGTGCACTCGGGTACTACAGTGCGACCCTCTTCCAGCACTCTTGACTCGAATGAGGTGCAGGTTCCGTGGGGAAAAGGCATCATAGGTTATGTAGCAGAACACGGAGAAACCGTCAACACACCGAACGCATACGAGGTAGAACTACGACAAATAATACACAGCTGCGTATTCTGGGGAGCTTGAGGGGGTTTATCCAAAGGGATAAAAAGGGTATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11083
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006412 | Nonsense | 142 | 927 | 1 | 20 |
ENSDART00000133403 | None | None | 449 | None | 14 |
The following transcripts of ENSDARG00000006151 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 23269783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21379534 |
GRCz11 | 16 | 21185353 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCACATCTTGAGCGCGCTGCTCGAGTCCCGAGTGAACGTGCCTCAATA[T/A]GCCTCCAGCGCCATTGACTACAAATACCGACTYAAAGAGTCCAACGAAAG
Long Flanking Sequence:
GTGTGCAGCATCACAGCGAGCTGCGTGTTACTGTACAAGACTCCACAACACTTCTTCTGTGGAGGCTTTTCGGCAATCGACATGACAACTTTTGATTTTTCCGAGGTGGAGGCATTTTTGGATTGCCATCCGGAGCTTTTTGAGGAATATCTCGTCAGAAAGGGAAAATGTGACAGCCTGAGCAGGTGGCTGAAAGAGCATCAGCCGTCCAAAACCTCTCCGGCGGAGGAGAAACGCGGGGTCGCGAGGGATCCATTCTGGCCCACGAACCCTGATGGATTAAAGCGCAGATCGTCCCACATGGAGCTTCGAAAGAACTTCGCCCGGTCCAAAGCGATGACGGCGCACCGGACCTACGACGAGCACGTCAGTCTCACGGCTCACGAGTCCCAGTCGAGCATGCGGCGGCGCGCGCTCCTGCGGAAAGCCAGTTCGTTACCGCCGACCACCGCGCACATCTTGAGCGCGCTGCTCGAGTCCCGAGTGAACGTGCCTCAATA[T/A]GCCTCCAGCGCCATTGACTACAAATACCGACTCAAAGAGTCCAACGAAAGGGAGTTCTTCCTTGAGCTGGTTAAGGACATTTCGAACGAACTTGACATGACGAATCTAAGTTACAAGATACTTATCAATGTTTGCATTATGGTGAACGCAGACAGGTGTTCGCTTTTCCTGGTGGAGGGACCTTCTCATAAGAGGACACTCGTGTCCAAGTTTTTTGATGTGCACTCGGGTACTACAGTGCGACCCTCTTCCAGCACTCTTGACTCGAATGAGGTGCAGGTTCCGTGGGGAAAAGGCATCATAGGTTATGTAGCAGAACACGGAGAAACCGTCAACACACCGAACGCATACGAGGTAGAACTACGACAAATAATACACAGCTGCGTATTCTGGGGAGCTTGAGGGGGTTTATCCAAAGGGATAAAAAGGGTATGGTCAATTTAAGAACGTAGCTTTCAAAGGGTCTTTAAGCACTAGTAAATAATAAAAGTTAGTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5892
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 |
---|---|---|---|---|---|
ENSDART00000006412 | Essential Splice Site | 600 | 927 | 11 | 20 |
ENSDART00000133403 | None | None | 449 | None | 14 |
The following transcripts of ENSDARG00000006151 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 23246861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21356612 |
GRCz11 | 16 | 21162431 |
KASP Assay ID:
554-3833.1 (used for ordering genotyping assays)
KASP Sequence:
GGATGTTTTTRGAGCTTGGTGTYGTACAGAAATTCAAAATTGATTATGAG[G/A]TAAGGCAATCACCACATAAATGGAGGCCAAAATCCAACTCTGCTGACTGG
Long Flanking Sequence:
GTTACAAGTCAGGATTACCCAGCCTGGATGGACATTATCTCTCAATTTAAAGGACTGTTCAAGATATAGACATCAGTAAAGAATAGAGTTTAAAACTTTTCTCCAGAGAGATGTGATGAAAACTTCAAATTAAACCCATACATTAGAGAGAAAGATGCATAAAAGCATCTCAGCCTCTTGCGTTTCCCAGAAAATTATAGTTAGTGAGACTTGAGAGAGCTGAAGTATTAATAATTGAAATGGCACAGTGTAATATACTCTTACTGTTTGAGCCCTCGGTGGATCGAGCTCTGCTCTAGTATTTAATTGCCTTGCTACTGGAGTTGCTGAAATTGTCCCCTCTCCTGTCTCAGGCTGCTAAGATTCCCCTAAGCAGTGAGCTCGGGATCGATGAGTTCCACTTTAATGACTTTTCACTGGACAACGACGCCATGATCACGGCCTCCCTGCGGATGTTTTTGGAGCTTGGTGTCGTACAGAAATTCAAAATTGATTATGAG[G/A]TAAGGCAATCACCACATAAATGGAGGCCAAAATCCAACTCTGCTGACTGGAGGAGTGAAAGGCTGCTTACATATGCAGTGTATGTTGTGCGAAGCTGCAAGGGTTTTTATTGATGAGGGACTGTGCTACAAGTTGGTTCTTGGGGATTCTGGAGGTTGGTTGTGAATACAACTTGTATGTTTCTGTTTCTGCTCAGGTTCTGTGCCGCTGGCTGCTTACTGTGAGGAAGAACTACCGTACTGTAGCATACCACAACTGGAGGCATGCTTTTAATGTCTCGCAGTGCATGTTTATAATGATCACAGTAAGTATTTAAATTAATAATATGATCATATTGCTATCATTGTAAATTATTATTATTATATGCTAATATATTCTATGATTAAACTCAACTCAATTTATTACTAGAGCACTTTCAACAAACCACAATGGGTACTGAAATGCTGTAAATAAAACAAATAAAAACACATGCAAATATACAAAAAAACAAAATACATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32085
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 |
---|---|---|---|---|---|
ENSDART00000006412 | Nonsense | 689 | 927 | 14 | 20 |
ENSDART00000133403 | None | None | 449 | None | 14 |
The following transcripts of ENSDARG00000006151 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 23240631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21350382 |
GRCz11 | 16 | 21156201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGTCTGGCTCAGCACTGGCACTGCTGTATGGAACATCTGCCACACTT[G/T]AGCATCATCATTTCAACCACGCTGTCATGATCCTGCAGAGTGAGGTGAGC
Long Flanking Sequence:
GAATTTTGTTGGCACAGTGTTTAAGTTGTTAGCACTGTTGCCTATCAGCAAGAAGGTTGCTGGTTTGAGTCCTGGCCAAACCAGGAGGCTTTTCTGTGTAGAGTTTGCATGTTCTCCCAGTGTGTGTGCAGGTTTCCGGTGTGCTCCAGTTTTCCCCTCAGTACAAAACCATGTGATTATAGGTCAATTAGATAAAGTAATTTGGCAATAGTGTGTGTGAGTGTGGGTATTCGCCAACATTGAGGGTTGCACTCTCAGTTGTGGCAGGAAGGGGATCTGCTGTGTAAACAATTGTCGAAGAAATTGATGGATCTGAAGTTTGAAAACATAATTTCAGACATATTCTCTAAAAGTTAGATTTCTTTAAAAGTGTCAAATTAAAAAATGACTTCAAATTTTACAGCAATGTAACATTGTCCATATGCTGTAGCTAATCTCTGTTGTGTTTCCAAAGGTCTGGCTCAGCACTGGCACTGCTGTATGGAACATCTGCCACACTT[G/T]AGCATCATCATTTCAACCACGCTGTCATGATCCTGCAGAGTGAGGTGAGCACGAGCCTTATTTCAATGACATGAACTAACATGTGTGTCTGATCTGGTCTTAGGTCAGTTTTTACATGGAAGAAAAAATATCATAATATAGAAGTAATGGGCTGTTTTCTGCGATGTGTTTGAAACGATATGCTTTCATAATTGTGCCACTGTAATTGAAATAAAAGATGGATGTCTGCGCCAATAGTCTTGTGGTTAGTGTGTCAACACAAAGCAATATGCTCACTGTGACCCAAATTTGACTTCTGGCTTGAGGTTATTTACTTATCCTTTCCCTGTCTATACTTTACACGGTCCTGTTCCATTAAGTCTGGGACACACCAAGCTGATGCAAAATAAATAGCGCCAACTGTGTTGTCAGCTCTTGTCTGATCTCGTTTAAACCAAATAGCTGTGCATGAACACACCAAACGAATGGATTTAGTTCCATAATCACAACATAGGCTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11067
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 |
---|---|---|---|---|---|
ENSDART00000006412 | Essential Splice Site | 813 | 927 | None | 20 |
ENSDART00000133403 | Essential Splice Site | 342 | 449 | None | 14 |
The following transcripts of ENSDARG00000006151 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 23229843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21339594 |
GRCz11 | 16 | 21145413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGAACAAGGTGACAGGGAGAGATCGGAGCTGAAGCTGACACCAGCTG[T/A]RTGTAATCTTTCATCATCARAAAATTATGATTATTAAACTTTGCTTTGTC
Long Flanking Sequence:
TATTTTGACCTTTTTTCAACAGTTTATGTTAAACAATGGGATGGCATTTCAAATTATATATATATATATACACACACACACACACATGAATAATTATGATGTAATTAACTAGGTTAATTAGGTTAACTAGACAGGTAATTAAGCAAGTAATTGTATAATAGCGGTTTGTTCTGTAGACTATTGAGAAAAAAAATAGCTCATATATATATAGGAAAGCATATTAAATGGCATGTATTTGACAAAATTTATATTTAGAATCCAAAATAGGATTTATACAAAAAAAAAATAATAATAAATTGATTGTTAACAAACGGTTAATGGTTAAAAAAAACTGTATTTAATGTTTTTTTTTTTTTTTTTTTTGGAATGTTGTAATTTCAGACATTAAATTATATCAGTATAACACCTATGTTTCTATCTCTAGGTGGCTGAACTGGTGACCAGTGAATTCTTTGAACAAGGTGACAGGGAGAGATCGGAGCTGAAGCTGACACCAGCTG[T/A]ATGTAATCTTTCATCATCAGAAAATTATGATTATTAAACTTTGCTTTGTCATCTAAACTTCGCTTTCATTTTGCTCCTATTTTTTATTTAGGCCATTTTTGATCGCAATCGTAAAGATGAGCTTCCTGTGCTTCAGCTGGAATGGATTGATGGAATCTGTAAGCCATTATATGAGGTAAAACAATTGAATGAATCAATTGTATTAACTCCAGCTGATTACATTTTATGCAGTGATGGTAATGTATTTAACAGGCTCTTGTGAAGCTGAATAGAAAGCTTCAGCCAATGGTAGATGGAATTGATGCCAACCGAAAGAAGTGGGAGGAGCTTTGTCTGTCCTATCAGCAAACAAGGAGAGCCTCTGAATGCAACACAGTAGAGACAGACTCCACCCATGAGCCAGAATCTAGTCAGAGTGAAGCAACCAATCAGAATGAAGGCTCCACCCACGGTGTAGAGCCAAAGCAAACACCAGTAGCCAATTACAAAGAAGGGGCGTG
Associated Phenotype:
Not determined