ZMP
NP_957396.1
Ensembl ID:
Description:
cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A [Source:RefSeq peptide;Acc:NP_95739
Human Orthologue:
PDE10A
Human Description:
phosphodiesterase 10A [Source:HGNC Symbol;Acc:8772]
Mouse Orthologue:
Pde10a
Mouse Description:
phosphodiesterase 10A Gene [Source:MGI Symbol;Acc:MGI:1345143]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35407 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38918 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28054 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17787 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35407
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 |
---|---|---|---|---|---|
ENSDART00000007500 | Nonsense | 372 | 843 | 13 | 23 |
ENSDART00000144312 | Nonsense | 351 | 734 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 4255699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4472619 |
GRCz11 | 13 | 4601115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAACATCTGTTCTGCTTTTCATAGAGAAGTAGATCTCTACACTGGCTA[C/A]ACGACGCGGAATATCCTGTGCATGCCCATAGTCAGCCGCGGGACTGTGAT
Long Flanking Sequence:
ATAAATCATGCATTGGAAGCTGATTTGAACTTTTACCCCCACAGGTTTTCGATTGAGAAAGGAATAGCAGGTCAAGTGGCCCGAACAGGAGAAGTTTTGAATATTCCGGATGCCTATGCAGACCCCCGTTTCAACAGGTAGAACTTTCATTTATCACATAACATTTGTGACCCTGCACACACAAAAATTGTCTTATCATGCACGAGAATTACTAAAATACTTTGCATGAGTCAAAAATAAATGTTTATTATATTATTAAGTAAACATATATATAGATACTTTGAAATACATCAAAACTTTTTTTTGTTTAGAAATATGCACTGCCAAGAACTTAATGTGGACAGCTTTAAAAGTAATTTTCCCATAATTTACTGTAGATTCCCATTATTTACCCTCCTGTCCTTTTTTGTCCTTTTGCGGTGTGTGTGTATTTGTGTCTGTGTGCATTTCTTTAACATCTGTTCTGCTTTTCATAGAGAAGTAGATCTCTACACTGGCTA[C/A]ACGACGCGGAATATCCTGTGCATGCCCATAGTCAGCCGCGGGACTGTGATCGGTGTTGTACAAATGGTGAACAAGCTGGGAGGAAGTGCCTTCACTAAAACTGACGAGAACAACTTTAAGATGTTCGCCGTCTTCTGTGCTTTGGCCTTACACTGTGCAAATGTAAGTGCGGACCTACAGTCTGATCAAACAAAACAATTCACTTATTATGTAAATGAATGATTTTACATTGTACTTACTAAACAAAATAAGAAAAAAATATACTATTTTTACTATGCTATTGAACTTAACCCTTGTGTATTGTTCAAATTAACTACCCTTTCAGTATGTTTGGGGCTGTTTTTACCCCATTGACTTTCATTATAACGACATTTTGTAGATTGCAAATGACAGCATATAATCATGCATTCTTGATTGTTGGTGGTTTTTCCTGTTAGTAAGAGGTCAGATTTGTTATTATTACTGTTGATCATCCAGCCTGATCTCACAAGGAAACGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38918
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 |
---|---|---|---|---|---|
ENSDART00000007500 | Essential Splice Site | 427 | 843 | 14 | 23 |
ENSDART00000144312 | Essential Splice Site | 406 | 734 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 4256743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4473663 |
GRCz11 | 13 | 4602159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTTTGCATCTGCGTAAAAGACACATGGGGCGTTTGTGTTTGTGTGTA[G/A]ATGTATCACCGGATAAGACATTCAGAGTGCATTTACCGGGTGACCATGGA
Long Flanking Sequence:
AAACTTTGCAATCAAAAAATGTCATTACAATGAAAGTCAATGGGGCAAAATCGTCCCCAACAAAAAAAAGGGTAGTCAATTTTAGAGTGTATTGTTGAGTTTTTGAAAACTTTCAAAGCATTTTCCTCAAAATAATTGTCAAAATAAGAATTGTCACCAAGAATCCTTCCATTTACTGAAACAAAGAGAAAGTTGTGACTAAATTAAGACTCAAAATCACCTCAGAGTGGTTGAAAACATCCACAACGGCCCATAAGGGTTAATAGTGTGGTGTCATTTACCACTAGTAAAAAGAGGAAAACATTGATTGTCTGTACAGAACTGTAATTCTGTTAACGTGAAAACACTCAATTATTTTTCTAGCTGAATAAAGAACGATATTAAATAAGAAAAATATTTATGACAGTGAATGCAAGCGCTGTTTTCCAATGGTTCCGCTATTTTGCATGTACATTTTGCATCTGCGTAAAAGACACATGGGGCGTTTGTGTTTGTGTGTA[G/A]ATGTATCACCGGATAAGACATTCAGAGTGCATTTACCGGGTGACCATGGAGAAGCTTTCGTACCACAGCATCTGTACGTCAGAGGAGTGGAAGACCCTCACTCAACTCACCCTCCCTTCAGCCATATATAAAGAGATCGAACTGTGAGTTTTACTCTCTCATATATGATACATCAATCCCACATAATGGAATACACATGCTAAAATGCTTTTCTTACTTAATAGTTACTCGTTTTTGTCTTGTTTCTAGTCCAAATATCCAAAAATACTTAAGTCGAGAAGCATTTTCTAGTTTTGTATTGAGAAACGTGTCAAAATTAAGTGAGTTTGTTCCCTTAAAACAAGCAAAATAATCTGCCAACATTTAAATAATGGATTGTGTTTGTATGTGTTTTAACTATTCTTAAACTTAACCAGTGTGTATTGTTCAAGTTATATGCAATTAAACTGCTCTGAATCAACAGATTGAGGAGTTTGGGGTTATTTTGATAGTTCTTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28054
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007500 | Nonsense | 742 | 843 | 21 | 23 |
ENSDART00000144312 | Nonsense | 722 | 734 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 4269760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4486680 |
GRCz11 | 13 | 4615176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGGGTTTTACAATGCAGTGGCTATTCCCTGTTACACCACTCTGTCT[G/T]AGCTGTTTCCTCCCTCCGTTCCTTTGCTTGAAGCTTGCAGGTAAGTTAGT
Long Flanking Sequence:
CCATTCCACCTAGCCTGCTTTACTGAGCAGAAGTTGCTTTTATATTCACATTGGGTTATTTCTGAGCAATGACATCCTGTGACGTGCTACCTATATTGTTTACCGCTACGATATTCGCTATGAAATAGCATGTACGTGTGGCTTAGTAATAAGTGAAATTCCTGCACGCCGCTGGCCAAGCACTATGACTTGAACTAGTGGGTTGTCTGCTGTCATGTCGCGGTGCGCGCGTTCACGAATTCTGGATGCGTGGCTTTAAAACACAGTCCCTCCCCTGCCGTCCAGAGCTAACATATTAACCGATTAACATTTTGGCAGATCACCTACTGCACCTTTAACTGTTATGTTTAGTTGTAAATCCATCATTAGGATAGCTTTTATGTTTTGTTGTAGAGTAAATGTTAAATGGACGTTTAGTTATACTATAGTCCTGTTTTTCCCCATGTTCTCAGGTGGGGTTTTACAATGCAGTGGCTATTCCCTGTTACACCACTCTGTCT[G/T]AGCTGTTTCCTCCCTCCGTTCCTTTGCTTGAAGCTTGCAGGTAAGTTAGTCCGAGACATTTAACACTAAACTAATTATAGAGATTTATATTTATGAATCAGTTTAACATCACAGTACTGGGATGAGTACATATAATCAGTTCATACACACATCAGTTATTTAAAACAACTTGTATTTGCCAGCCATAAAAACGATATACTCGAGCTTAATGAACTATATTACTGAGAGGAAGCGTAGCGGATTTGTGATTTTAATATCATTTGTGCATGATTTAAATGTGTTAGTTACAGAATTACACTAAAAACTAGTTCCATTAGCCATTAGTTGGACCCAATATTTCAAAACTAAAAACTAATAATAATGAATGCACTCAATAAACCAAAGATTGTATTTATGGGTAATTCTTCAACTACGGGCACTTTTATGTCCTTTGATCATATATCCAAAAATATATATCATTTCATTCAAGTTTCTCTTTGTTTGTCAAACTAATAATAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17787
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 |
---|---|---|---|---|---|
ENSDART00000007500 | Nonsense | 837 | 843 | 23 | 23 |
ENSDART00000144312 | None | None | 734 | None | 20 |
Genomic Location (Zv9):
Chromosome 13 (position 4274986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4491816 |
GRCz11 | 13 | 4620402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGCAGAGACGGGAGGAAGTGCAGAGGGCAGGCGGACGAGGATACTTTC[A/T]RAAAAAAAATAAACAAAACATAATGTTACCTCAGYGGGTGATGGAGGCGC
Long Flanking Sequence:
TTCCTCAGATTTTAGTTCATATTGACATGCTCAAAAATGACATTGTTTCATTAATTTTACAACATTGCATGTACAAAGATCTGAAAGGGGTTTGATATCAGAACATATTACCTACCAATTAAAATTGCATTATTTCAATCAATCAATCAATCAATCAATCAATAAATCAATCAATCAGCCAGTAGTTTAAACTGGAGAAATTGCTGTTACTTTAGTCTTATTGCAGTCTTGTAAAGAATGCTTTGTGTTTTTCAGGGAAAACCTGTCCCAGTGGGAGCGCATTGTGCAAGGGGAGGACGTCTCTGCGTGGTCATCAACCGAGGAGGCTGAAGTGAGCGAAACATCAGACAGTGGACCAGTTAAAGTGGACAACTGAATCTGTGGCACCTTTCCCACAGCACCACCCACAACCTGCCAGAGACACTGGACTTCCTGTGGACAGTCCCACTTCCTGCAGAGACGGGAGGAAGTGCAGAGGGCAGGCGGACGAGGATACTTTC[A/T]GAAAAAAAATAAACAAAACATAATGTTACCTCAGCGGGTGATGGAGGCGCACACTCTAATGACATCAGGGCTCCCTTGTTGATGGCTGGGACTCAAGTCCGGTTCAGCAGAATGGGCGTCATTATTGGCAGTACTTTCCCTTAAGAGGTTGCTTTCTTTTAGGCTTTCTTTTTCAGTTTATTTCGTGGTCTTACGTTTTGAAGAGGCCTTAAAAACGAACCCGAGTTACGATCTGACTCGTAACCAGAAGACGGTTCGTCTAGTTTAATATGGTACATTTTATCCTGCTGTGGTCGAAAACGTTGTACGCGAAGCTACTTGAGTGGATTTCTTTTTTTAAAGATAGACACAAGGAATGTTTAGTCAAAGTTAAGGTGCATGAGGCACAAAAAAAACATCGTTCTGGTGGATGTTTTCTATCATATTTTGAGCAAAGCTGTTTTGCAGTACTTGAATGAAGAAATACAGCCTATTCTGAGTGGAGATGAAAACAAAAAATC
Associated Phenotype:
Not determined