ZMP
pde4d
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phosphodiesterase 4D, cAMP-specific (Phosphodiesterase E3 dunce
Human Orthologue:
PDE4D
Human Description:
phosphodiesterase 4D, cAMP-specific [Source:HGNC Symbol;Acc:8783]
Mouse Orthologue:
Pde4d
Mouse Description:
phosphodiesterase 4D, cAMP specific Gene [Source:MGI Symbol;Acc:MGI:99555]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45318 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa117 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa18915 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9416 | Nonsense | Available for shipment | Available now |
sa14598 | Nonsense | Available for shipment | Available now |
sa41163 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45318
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 |
---|---|---|---|---|---|
ENSDART00000018934 | Nonsense | 139 | 725 | 3 | 17 |
ENSDART00000139452 | Nonsense | 48 | 665 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 17528740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16973628 |
GRCz11 | 8 | 17009340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCACAGCCAGAGGAGAGAGTCCTTTCTGTACCGTTCAGACAGTGACTA[C/A]GACCTCTCACCAAAGTCCATGTCCAGAAACTCCTCCATCGCCAGTGACAT
Long Flanking Sequence:
TAATTAAAATTTAGTTCACAACTGTTTTAACACATTTTATACAACACTCAAAAATGACATTTGTTGCTATTTCAAACTGCTTATTTAAAATGAGCTAAAACAACACAATTATTGAGTTTTTTTGGGGACAACTTGATTGTTTTATATTCAATCTACTTAAATGTGTAAAATCTAATAAGTAATAATTACTTAATTGTGTGGAACTCAGCATTTCTTACAGTCAATTGCTGTAAAAAAAAAAAAAAAAAGGAAATAAACCTGAAATAAATGTTGAATGGTATCAGCTGGTCTAGTTAAAGTCTACATCTTCTCATCTAACACAGCACTAACTGTCCTGTCCTGTCTTTTTGTCTCCTCAGCTTTGATGTGGACAATGGCACCTCTTCAGGTCGCAGTCCGCTGGATCCAATGGCCAGTCCAGGCTCAGGTCTCATCCTCCAGGCCAATTTCGTCCACAGCCAGAGGAGAGAGTCCTTTCTGTACCGTTCAGACAGTGACTA[C/A]GACCTCTCACCAAAGTCCATGTCCAGAAACTCCTCCATCGCCAGTGACATGTAAGCCAGAGTCTTTCTTATAGACAGAGAACAGTTTTGGTGGCCTGTGCACTTTTTAATAATATGCACCTTTTATTATTGCAAATTCATGTCTAGTTATGAGAGGATTTTTACATTGCATGCCGTCAGTGTCATTATAAAATGCATTCCCTATGAGCTAGTTAAATTTCAGTTCTCAATAAGAGAAAGCCAATGGTTTTGTAACGCCCCATTCACACGAGGCGTCAGCGTCAACGTTTCCCATTCACTTTGAATGGGTAACGTCAGGCGTTGCCGAACTGCATTGGTGATCCGTCGGCACCGCTTCAGAAGCGTTGCTCGCTGCAGATGTTGGGACTAGCTCAATTTTTCAAGCCCAGATGGAAGTGTCAGTCAATCAGATTGCTGGATGCAAACACACCAGCTAGACAGTGGCCTATTGCTAACTGAATTTTACTGGCTGACGCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa117
Status:
Confirmed mutation in F2 line
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018934 | Nonsense | 380 | 725 | 11 | 17 |
ENSDART00000139452 | Nonsense | 289 | 665 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 17554468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16999356 |
GRCz11 | 8 | 17035068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAACAAGGTACTTCTGTGCTGTAGGAGAGGGACTTGTTAAAGACGTTT[A/T]AAATTCCCCTCGACACGTTTATCACCTATCTGATGACTTTAGAGGACCAT
Long Flanking Sequence:
TTGAGGACGTTCCAAGTTGAACCAAAACAAAAAAAATACAATTGGCTTAGGAGAGCAAGGAAAATTCAGCAAGTACAGCAACCAGCAGAACCTGGGAATTAAAAATAATTAAATAAATAAATAATAATTATTATTATTATTATAACAATATTATATAGTCTTAAGTGTCAGGGTGATCCTTTAGATATAGTTTAAATATGCTGAATTTGATTTGTTATTGGTTATTATCAAGCAATTATGTTGCAAACTCCAAAACAGAATGATAAACATCTTTCAATTTGTGCCTTTTCAGGAGCTCGAAGATGTAAATAAATGGGGCCTTAATGTCTTCAAAGTGTCAGAATTTTCTGGAAACAGACCTTTAACGGTTATGATGTACACAATATTCCAGGTATGTGGTGTTCGCAGTGTTTTTCCATCGTGCTCTAGTTTTTGCTTGAATGTCTTTCCACTAACAAGGTACTTCTGTGCTGTAGGAGAGGGACTTGTTAAAGACGTTT[A/T]AAATTCCCCTCGACACGTTTATCACCTATCTGATGACTTTAGAGGACCATTATCATGCTGACGTTGCCTATCACAACAACATCCATGCTGCTGATGTCACACAGTCCACTCACGTCCTGCTATCAACTCCTGCCCTTGAGGTGCGATACTGCTGTCCCAGAATGCAGTGCTGCAGACACGCTCTTTTATTCTCACTGCTGGGTGTTCAAGAGAGCGGATGGCGACGTGAGATTTTATATAATCTGTCTGTGTCTGTTTTTTTTTTTTTCAGGCTGTGTTTACAGACCTTGAAATTCTCGCTGCCATATTTGCCAGTGCGATTCATGATGTTGACCATCCTGGCGTCTCCAACCAGTTCCTCATTAACACTAGTAAGTCGTTAGCTTGATTGTAATATGACAATTTGCTATATTCCTGTTTTACTGGGTTTTTTTATGCTTAATGACATCTTTTATATTTCCAAACGAGATGTTCCTACGGAGAGTCAAAAGTTTAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18915
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 |
---|---|---|---|---|---|
ENSDART00000018934 | Nonsense | 389 | 725 | 11 | 17 |
ENSDART00000139452 | Nonsense | 298 | 665 | 9 | 14 |
ENSDART00000018934 | Nonsense | 389 | 725 | 11 | 17 |
ENSDART00000139452 | Nonsense | 298 | 665 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 17554497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16999385 |
GRCz11 | 8 | 17035097 |
KASP Assay ID:
2260-0359.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGACTTGTTAAAGACGTTTAAAATTCCCCTCGACACGTTTATCACCTA[T/A]CTGATGACTTTAGAGGACCATTATCATGCTGACGTTGCCTATCACAACAA
Long Flanking Sequence:
AAAAAAATACAATTGGCTTAGGAGAGCAAGGAAAATTCAGCAAGTACAGCAACCAGCAGAACCTGGGAATTAAAAATAATTAAATAAATAAATAATAATTATTATTATTATTATAACAATATTATATAGTCTTAAGTGTCAGGGTGATCCTTTAGATATAGTTTAAATATGCTGAATTTGATTTGTTATTGGTTATTATCAAGCAATTATGTTGCAAACTCCAAAACAGAATGATAAACATCTTTCAATTTGTGCCTTTTCAGGAGCTCGAAGATGTAAATAAATGGGGCCTTAATGTCTTCAAAGTGTCAGAATTTTCTGGAAACAGACCTTTAACGGTTATGATGTACACAATATTCCAGGTATGTGGTGTTCGCAGTGTTTTTCCATCGTGCTCTAGTTTTTGCTTGAATGTCTTTCCACTAACAAGGTACTTCTGTGCTGTAGGAGAGGGACTTGTTAAAGACGTTTAAAATTCCCCTCGACACGTTTATCACCTA[T/A]CTGATGACTTTAGAGGACCATTATCATGCTGACGTTGCCTATCACAACAACATCCATGCTGCTGATGTCACACAGTCCACTCACGTCCTGCTATCAACTCCTGCCCTTGAGGTGCGATACTGCTGTCCCAGAATGCAGTGCTGCAGACACGCTCTTTTATTCTCACTGCTGGGTGTTCAAGAGAGCGGATGGCGACGTGAGATTTTATATAATCTGTCTGTGTCTGTTTTTTTTTTTTTCAGGCTGTGTTTACAGACCTTGAAATTCTCGCTGCCATATTTGCCAGTGCGATTCATGATGTTGACCATCCTGGCGTCTCCAACCAGTTCCTCATTAACACTAGTAAGTCGTTAGCTTGATTGTAATATGACAATTTGCTATATTCCTGTTTTACTGGGTTTTTTTATGCTTAATGACATCTTTTATATTTCCAAACGAGATGTTCCTACGGAGAGTCAAAAGTTTAAACTAGTTAACATTTTTAAAGGCAGATACAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9416
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 |
---|---|---|---|---|---|
ENSDART00000018934 | Nonsense | 389 | 725 | 11 | 17 |
ENSDART00000139452 | Nonsense | 298 | 665 | 9 | 14 |
ENSDART00000018934 | Nonsense | 389 | 725 | 11 | 17 |
ENSDART00000139452 | Nonsense | 298 | 665 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 17554497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16999385 |
GRCz11 | 8 | 17035097 |
KASP Assay ID:
2260-0359.1 (used for ordering genotyping assays)
KASP Sequence:
AGGGACTTGTTAAAGACGTTTAAAATTCCCCTCGACACGTTTATCACCTA[T/A]CTGATGACTTTAGAGGAYCATTATCATGCYGACGTTGCCTATCACAACAA
Long Flanking Sequence:
AAAAAAATACAATTGGCTTAGGAGAGCAAGGAAAATTCAGCAAGTACAGCAACCAGCAGAACCTGGGAATTAAAAATAATTAAATAAATAAATAATAATTATTATTATTATTATAACAATATTATATAGTCTTAAGTGTCAGGGTGATCCTTTAGATATAGTTTAAATATGCTGAATTTGATTTGTTATTGGTTATTATCAAGCAATTATGTTGCAAACTCCAAAACAGAATGATAAACATCTTTCAATTTGTGCCTTTTCAGGAGCTCGAAGATGTAAATAAATGGGGCCTTAATGTCTTCAAAGTGTCAGAATTTTCTGGAAACAGACCTTTAACGGTTATGATGTACACAATATTCCAGGTATGTGGTGTTCGCAGTGTTTTTCCATCGTGCTCTAGTTTTTGCTTGAATGTCTTTCCACTAACAAGGTACTTCTGTGCTGTAGGAGAGGGACTTGTTAAAGACGTTTAAAATTCCCCTCGACACGTTTATCACCTA[T/A]CTGATGACTTTAGAGGACCATTATCATGCTGACGTTGCCTATCACAACAACATCCATGCTGCTGATGTCACACAGTCCACTCACGTCCTGCTATCAACTCCTGCCCTTGAGGTGCGATACTGCTGTCCCAGAATGCAGTGCTGCAGACACGCTCTTTTATTCTCACTGCTGGGTGTTCAAGAGAGCGGATGGCGACGTGAGATTTTATATAATCTGTCTGTGTCTGTTTTTTTTTTTTTCAGGCTGTGTTTACAGACCTTGAAATTCTCGCTGCCATATTTGCCAGTGCGATTCATGATGTTGACCATCCTGGCGTCTCCAACCAGTTCCTCATTAACACTAGTAAGTCGTTAGCTTGATTGTAATATGACAATTTGCTATATTCCTGTTTTACTGGGTTTTTTTATGCTTAATGACATCTTTTATATTTCCAAACGAGATGTTCCTACGGAGAGTCAAAAGTTTAAACTAGTTAACATTTTTAAAGGCAGATACAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14598
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 |
---|---|---|---|---|---|
ENSDART00000018934 | Nonsense | 490 | 725 | 13 | 17 |
ENSDART00000139452 | Nonsense | 399 | 665 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 17558549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 17003437 |
GRCz11 | 8 | 17039149 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAATCATCATCTAGCTGTTGGCTTTAAGCTGCTTCAGGARGAAAACTG[T/A]GACATCTTCCAGAACCTGACCAAGAAACAGAGACAGTCGCTCCGCAAGAT
Long Flanking Sequence:
CTTATTTTGTCTACACTAGTATACTAGTATTAAGCTTAAAGTGAAATTTAAAGGCTTAACTAGGTTAACTAACTTAACTAGCAAGTTAGGGTAATTAGGCAAGCCACTGTATAACAATGTTTTGTTTTGAAGACAATCGAATTGTAATATTGCTTAGGGGGCTTATAATATTACCCTTTATAAAACTGCTTTTTTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGTAGAAAAAATATTATAAGAAATACTGTGAAAAGTTTGTTTATCTATTAAATATAATTTGTGAAGTATTTGAAATAGAAAACAGTTTTCACTGGAGGGCTAGTCATTTTGACTTCAACTGTATGTTTACTTATGTATTATACTGTATGATTGATTGTACGGTTTTGTCTTTGTCCCATCAGACTCTGAGCTGGCCCTCATGTACAATGATTCATCTGTGTTGGAGAATCATCATCTAGCTGTTGGCTTTAAGCTGCTTCAGGAGGAAAACTG[T/A]GACATCTTCCAGAACCTGACCAAGAAACAGAGACAGTCGCTCCGCAAGATGGTCATTGATATTGTGAGTCAAGCTGCTAAGTCATTAAACTTTGAGCGGATTGGTCTACGAGGACTATAATTGATCAAACTTAATTGTTTTTGCACTTTAAGCTACATGTCAGCATATAGACCATTTCAATGTGGTCATGTCATTGGCCCATGAACATTTCCTGCTTATGAAACTTGTTACATAACTGAAACAAGAGGCAATGCAATCATAATGTAATGTTAAAACAGCTATCATAACATTATTTCTCAATATGTGGCTCTTTTTGAAATTTCGGAAAGTGAAGAAATTAAAAATGTAAAACAGGAAATACATTGGGACCATTGTTTTTGTTTACATCCCTCAAAATGCTCTACATGAAAAGTAGGCATGAATGCATTTATTTAACATATTTCTCTTTAGATAAAATGATGACTATGCATGTTTTTTTTAGGTTCTGGCCACAGACATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41163
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018934 | Nonsense | 649 | 725 | 16 | 17 |
ENSDART00000139452 | Nonsense | 558 | 665 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 17563733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 17008621 |
GRCz11 | 8 | 17044333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCCAGATGCTCAGGACATCCTGGACACGCTGGAGGACAACAGAGAGTG[G/A]TACCAGAGCACCATCCCGCAGAGCCCGTCTCCAGCACTGGACACCAGCAG
Long Flanking Sequence:
ATTAGTCTAAAACAAATCTAGATGGATAGGTTGAGATGGCTGAACAAAGCATGTACAGTAAATAAAGTAGGTAGGAACGTGATTTAAAAACCTGCAAACCACCAACCACAAAAGTTTATCAACAAACAAGTTTCTTCGGCCTGTATGGATCCACAAAGACACAGTCGTTGAGACCCTGCCCATAGCATTTGGCTCAGCCAGTGCTCAGAAAGCAAAAGGTTTAATGTCCCCTCACACTTCTGCTGCTACAGTTTCGAATAAAAGCCAAAGAATATAACTTCTTATTTTTTTATAAATATCACTGTTAATTTGAAACTAGATCATATCATTGTATATTCTTACAGTATACAAACCATTCTAAAACAACAACTGTTCTCTCTTTTTGTCCGCCAGGTTGGCTTCATTGACTACATCGTGCACCCGCTGTGGGAGACGTGGGCAGACCTGGTGCACCCAGATGCTCAGGACATCCTGGACACGCTGGAGGACAACAGAGAGTG[G/A]TACCAGAGCACCATCCCGCAGAGCCCGTCTCCAGCACTGGACACCAGCAGCGAGGGCCGCCGCGCTGCAGGACAGGAGAAGTTTCAGTTCGAGCTGACTCTGGAGGAAGACGGAGAGTCAGACACCGAGAAGGACAGCGGCAGCCCTCCTGAAGAAGATGAAGAGGAGGAGGAGGAAGAGGAGAACAGCTGCAGCGACTCCAAAACACTTTGCACACAGGACTCTGAATGTACAGAGATCCCACTGGACGAGCAGGTGGGGGACGTCCCGCACGAGGACGAGTACGAACATGAGGAGAACAGGGAAATATCTGAACCCTGCGTTTTAGAGGAGGAGGAGGAAGAGGAGGAGGAGGAGGAAGAGGACACTGCCAACACATAACACAGTATGACACGCCACAACCTGGACTTTTTTGTATTAGAGATGAGAAATACTTATTTATGGGTAAGACGTTAGTTTTGTTTCATCGTTTATTTTGCGTGTCTGTCGTTCTCAAGTGC
Associated Phenotype:
Not determined