ZMP
LOC571737
Ensembl ID:
Human Orthologue:
PDE9A
Human Description:
phosphodiesterase 9A [Source:HGNC Symbol;Acc:8795]
Mouse Orthologue:
Pde9a
Mouse Description:
phosphodiesterase 9A Gene [Source:MGI Symbol;Acc:MGI:1277179]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40574 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30867 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38511 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7009 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18434 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40574
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111973 | Essential Splice Site | 239 | 518 | 10 | 18 |
ENSDART00000111973 | Essential Splice Site | 239 | 518 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 59965378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 57828352 |
GRCz11 | 5 | 58498061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGTGAAGGAGTTTAACATGAACCCAATAACTCTCAAAAGATGGCTGG[T/G]AGGGCAAACTTTATTTTCTCACCTGCATTTTAGACTTTTTGAATCAACTC
Long Flanking Sequence:
ATTAAAGACTTAACTAGGTTAATTAGGTTAACAGGTTAGGGTAGTTAGGCAAGTTATTGTACACTGATGGTTTGTTCTGTTGACTACTGAAAAAAAAGCTTAAAAGGGCTAATAATTTTGACCTTAAAATGTTTTTAAAACAATTAAAAACTGCTTTCATTCTAGCTGAAATAAAATAAATAAGTCTTTCTCCAGAAGAAAAACGTATTATCAGACATACTGTGAAAAATTCTGTGCACTGTTAAACATCATTTATAAAATATTTCAAAAACAAAATAAATTCAAAGGGGGGCTAATAATTCTGACCTCAACTCTATGTATTTTATGTATGTCAGTTTCTGCCACATAAATTAATGTTTTATCTATATCTTTTGTTGTGTCTTTAAGTAAATTGATTGGATGTTGTTGTTAGATGCTCAGCTGTCTGGAATACATGTATCATGACCTTGGACTGGTGAAGGAGTTTAACATGAACCCAATAACTCTCAAAAGATGGCTGG[T/G]AGGGCAAACTTTATTTTCTCACCTGCATTTTAGACTTTTTGAATCAACTCAATTTTTATTAGACCTTACAACTGTGTATGTAACTGCTGTGTATCTGTCAAAATAAAAAGCTGGCTATTCAAGAAAATTATCGTGACAATCCTTTCCACAACTTCCGGCACTGCTTCTGCGTCAGTCAGATGATGTATGGCATGATCCACCTGTGCGGCCTTCAGGTAAGTGGATCTGTGTGTGTGTATGTGTATGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTTTGTGTGTGTGCCTTGTATTCCTCATGTTGAAGTGTCTAAATGTCCCCACATGTATAGCAATACCAGTAAACTTTAACCTTGTGTGGACATTTTTGTTCCCCTTGAGGAAAATGGCTCATAAATCACACAGAATTAAGCATTATTGTTTAACATCATAAACACGTAACAATTATGAAAATGTAAAAATGTAGTGTTTCCTTTGAGGGTTAGGTTTAGGGGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30867
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111973 | Essential Splice Site | 239 | 518 | 10 | 18 |
ENSDART00000111973 | Essential Splice Site | 239 | 518 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 59965378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 57828352 |
GRCz11 | 5 | 58498061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGTGAAGGAGTTTAACATGAACCCAATAACTCTCAAAAGATGGCTGG[T/G]AGGGCAAACTTTATTTTCTCACCTGCATTTTAGACTTTTTGAATCAACTC
Long Flanking Sequence:
ATTAAAGACTTAACTAGGTTAATTAGGTTAACAGGTTAGGGTAGTTAGGCAAGTTATTGTACACTGATGGTTTGTTCTGTTGACTACTGAAAAAAAAGCTTAAAAGGGCTAATAATTTTGACCTTAAAATGTTTTTAAAACAATTAAAAACTGCTTTCATTCTAGCTGAAATAAAATAAATAAGTCTTTCTCCAGAAGAAAAACGTATTATCAGACATACTGTGAAAAATTCTGTGCACTGTTAAACATCATTTATAAAATATTTCAAAAACAAAATAAATTCAAAGGGGGGCTAATAATTCTGACCTCAACTCTATGTATTTTATGTATGTCAGTTTCTGCCACATAAATTAATGTTTTATCTATATCTTTTGTTGTGTCTTTAAGTAAATTGATTGGATGTTGTTGTTAGATGCTCAGCTGTCTGGAATACATGTATCATGACCTTGGACTGGTGAAGGAGTTTAACATGAACCCAATAACTCTCAAAAGATGGCTGG[T/G]AGGGCAAACTTTATTTTCTCACCTGCATTTTAGACTTTTTGAATCAACTCAATTTTTATTAGACCTTACAACTGTGTATGTAACTGCTGTGTATCTGTCAAAATAAAAAGCTGGCTATTCAAGAAAATTATCGTGACAATCCTTTCCACAACTTCCGGCACTGCTTCTGCGTCAGTCAGATGATGTATGGCATGATCCACCTGTGCGGCCTTCAGGTAAGTGGATCTGTGTGTGTGTATGTGTATGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTTTGTGTGTGTGCCTTGTATTCCTCATGTTGAAGTGTCTAAATGTCCCCACATGTATAGCAATACCAGTAAACTTTAACCTTGTGTGGACATTTTTGTTCCCCTTGAGGAAAATGGCTCATAAATCACACAGAATTAAGCATTATTGTTTAACATCATAAACACGTAACAATTATGAAAATGTAAAAATGTAGTGTTTCCTTTGAGGGTTAGGTTTAGGGGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38511
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111973 | Splice Site, Nonsense | 354 | 518 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 59967813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 57830787 |
GRCz11 | 5 | 58500496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGCAACATATTCGCCAATATAGAGCCTGAATCCTTCAAACAGATACGG[C/T]AGGTACCTCTGACCCACCAAACAGATTCTGTCTCTACACTGAGAAACATT
Long Flanking Sequence:
CGACAGCACAACCTACTGCGCCATTGCGTTGCCTAATTTGTGTATTATACGTACATATTTATTTTACATCAAAATATAAATAAGTTTATATTTAAAAAAATATATATGCCTGCATGTGTGTATTTTTATGTACATAATAAATATACACAATACACACACTTAAATTATGTCAAAACAAACTTTTATTTTGGATAAAATTAATCGCAGTAAATCTTTGCCCTAATTTTAAACTATGGTATTATTATTATTATTATTATATGCAAAAAGTGTACTTTGTTGCATGTGTGTATAAATGACATCTCTGTCTTTTGTGCCGGAGATACTGTTTAAGGTTTTGTGTGTTCAGGTATCAGATTAATGCTCGCACTGAGCTGGCTGTGCGTTATAATGACATCTCTCCACTGGAGAATCATCACTGCGCTGTGGCCTTCCAGATCCTCTCCATGCCCGAGTGCAACATATTCGCCAATATAGAGCCTGAATCCTTCAAACAGATACGG[C/T]AGGTACCTCTGACCCACCAAACAGATTCTGTCTCTACACTGAGAAACATTGTACTGTACATTGTACATACTGTAAGAACATTTGTCACCCAGGACCACAAAATCAGTCATAAAGGTTACTTTTTCAATGAACCTTTTTTAAGTATTAGACATTTAAGACATTAAATATTACACTATAGACATTTATAAAAAAACTAAAAACTAACTAAATAGGTTTTCCATTGAAGTGGGGTTTGTTAGGATATGACAATATTTGGCTGAGAGACAACTATTTGAACATCTGGAATCTGTTTGAAATGTCCAAATTAAACTTTTTGGCAATGCATATTACTAATCAAGTTTTGATACATTCATGGAAGCAAAAGTACAACATTGCTTCATAAAACAGGATCTTTACTTAATATTCTAAAGGTTTTGTCATTAAAAAAATCTATAACTTTGACTTAAGATTGTGTCTTTGACTAAGTGCAAAATAGTTTGGGGTATTGCCACAAATCCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7009
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111973 | Essential Splice Site | 392 | 518 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 59969789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 57832763 |
GRCz11 | 5 | 58502472 |
KASP Assay ID:
554-5322.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGAAAGTGGACAACTTTGACTGTACTAATGAGGAGCATGTTAAATCTG[T/A]ATGTGTTTCCCRCTATTATGACTCACATTGTTTGCAAATGCTTGTTGGCT
Long Flanking Sequence:
TGGACCATTGCTGTCTAGGATAATGGCTCATTTCCACTGAGTGGTAGTACGGTACGGTTTGGGTCAGTAAGCCGTTTGACAGGATAAACGGCCATAACAAGAGTACCAAACCGTACCGTACCGTATCATTCAGTGGAAGCTGGCCATAAGAAAACTCTCAGATTTCTTCTAAAATAGTTTAATTAATTAGTGTTCTGAAGTGTCAGGGGATTGGAATGACACAAGGGTGAGTAATTAATAACAGAATTTTCATTTTTGAGTGAACTAACCCTTTTTAGTTTCACAGAATGTTCTTTATTGTGAAAATGTTTCTTTGAGGAACCAGTTCTGGTTGTTCATTGCCATTGTTTAAAAATCCTGGATGTGTTATTTGTACTTCCTCTAGGCAATCATTACACTTATTTTGGCAACTGATATGGCCAAACATGGAGAAATACTGGACTCTTTTAAGCAGAAAGTGGACAACTTTGACTGTACTAATGAGGAGCATGTTAAATCTG[T/A]ATGTGTTTCCCGCTATTATGACTCACATTGTTTGCAAATGCTTGTTGGCTCTGTGCTGTATGCTTAATTCTTTGTCTGTGTGTCTGCAGCTGAAGATGGTGTTGATCAAGTGTTGTGATATCTCCAATGAGGTGCGTCCCACTGAGGTGGCAGAGCCATGGGTGGACTGCCTGCTGGAGGAGTACTTTATGCAGGTATCATTAGCAGTCTCTCTATGCAAATGAAAATGTTTCTTACTTCATGTATTTAAATAAGTTTGCTCAAAAATGAAAATTTACTCACTTTTTACACACCTTTAGATACTTCTTTTTTTAAGTGAGTAAACCATACCTGCAAACACTCTTGTTTTCCCAAGAGTCTACCGTATTTCTCTCCCCTCTCCTGTCACCCTCCCATTTAGTTATTTTCCCATAACTCATGTGATTTCGCTTGATATTGCACCCCTAGGACACAACTAGAATCATTTGTCAACAAGGTACTAGAAACATTCCTCAGAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18434
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 |
---|---|---|---|---|---|
ENSDART00000111973 | Nonsense | 504 | 518 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 59971877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 57834851 |
GRCz11 | 5 | 58504560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCAKAYAAGCTATTATTTAGACTTATGGTTTGTCTTCTCTTTAGGCA[C/T]AKAAGAAGAAAACAGAGAGCATGTATTTGGGTGGNNNGAAGAAATAAGCA
Long Flanking Sequence:
TTTAATTAAAATATTTACATTTATCTAAAACTTTTCCATTATATACTTATGAGTAGTTTTGTGTTGTTTTCTGATGTGTGGTTTGTTTTGGCAGAGCGACAGAGAAAAGTCAGAAGGTCTTCCCGTGGCTCCATTTATGGATCGAGATAAAGTCACCAAACCAACCGCACAAATTGGCTTCATCAAATTCGTCCTCATCCCAATGTTTGAGACGGTCATGAAGGTTTGTACACTCAACAGACAGCCTGCCATGCAACTTTGAGCAGAAGTTTAATAACACATCTGTCATTTGTGTCTATACGTCCAGCTCTTTCCACAGATTGAGGAGATCATGGTTCAGCCTTTGAGGGACTCTCGTGATCACTATGAAGAGCTCAAGCAAATTGAGGATGCCATGTCAGAGGTAAAAAACACTAAAGCTTAAAAGCTTTGGCCTTATGTCCAGAATGCAAATCAGATAAGCTATTATTTAGACTTATGGTTTGTCTTCTCTTTAGGCA[C/T]AGAAGAAGAAAACAGAGAGCATGTATTTGGGTGGGAAGAAGAAATAAGCAATCTGCTTCTTTTTATGGTATGGAGAGAGAGTTCATTCTCATCGTTTATCAAAACGGCTACAAAATTGGTGTAGGAACTATTTTGTTTACTACTTTCATGAACAGTTACATCTAAATGGAATTTTACATTGCCTTCATTTAAAAATGAAATAATATTTACAGCATTCTATAATAGGCTTGATTGGTTAAAATGAGTTGCAAAGAATGAAACATATTTAAGCGTTGATAAATCTTCTTAGTTCATTTTAATGAGCAAAGAGCTGTAAACATGCTCAATTAAACATAACATTCTGAAGAAAGAAAAGTGACAGCATTCTCTTGTAAGAAGTACTCCAGTAATCTCAATTTTTTAAAGATTTTTGTACCGTATTTAACAGTAATATGATCTGAATTTCACTGTAGGACAGTTATGGTGTATTTTACTGTATTTTAAAATTGCATTGTGAATAT
Associated Phenotype:
Not determined