ZMP
PDE4B (1 of 3)
Ensembl ID:
Description:
phosphodiesterase 4B, cAMP-specific [Source:HGNC Symbol;Acc:8781]
Human Orthologue:
PDE4B
Human Description:
phosphodiesterase 4B, cAMP-specific [Source:HGNC Symbol;Acc:8781]
Mouse Orthologue:
Pde4b
Mouse Description:
phosphodiesterase 4B, cAMP specific Gene [Source:MGI Symbol;Acc:MGI:99557]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44638 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38555 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40714 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44638
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028612 | Essential Splice Site | 388 | 783 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 30547903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30868819 |
GRCz11 | 6 | 30855733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGCTCGATTTGGCGTCAAAACTGACAAAGAGGATTTACTGTCAAAGG[T/C]AAGGAGAAGACTGACTAATACTGGCTCTTTAGTGTGTTGGGATGTGAAAA
Long Flanking Sequence:
CATAGTGGAGATGTGAGCTATTCAGCTGTGGCATTGCACCTGGGCCAAAAGCATCTACTTACGTCACTCAGGGAAACACGATATGTGGCCACCGGTCTCCAAACAATGGGCTTTTGTGCGGGCATGGATGTGTGTAGTCTGTGTGGAAACTACAATGAGGAGATTGAGTAATCTGGAATGTGATCTGTCAGCATTTGACACACTTGTGAATGATATGTGTAGAGAGGTTTGCGAGCCGTCCTATTCTGTTTTACATGAAGATATCTGTAAAGTTAAAAACCACCAGGTTGTTCTAATCCTTGGGTTCTTACTGTTCCTCACAGACAAACAGAACGATGTGGAGATTCCCTCGCCTACACCAAAAGCCCGCGAGAAGAAGAAAAAACAGCAGCTGATGACTCAGATCAGTGGTGTGAAGAAAGTGTCCCACGGGCCCAGCCTCAACTGCGGCATCGCTCGATTTGGCGTCAAAACTGACAAAGAGGATTTACTGTCAAAGG[T/C]AAGGAGAAGACTGACTAATACTGGCTCTTTAGTGTGTTGGGATGTGAAAATGTACAAATGTATTTTAATCTCATTTCCTGACTCTTCTCTTTCCAGGAATTAGAAGACCTGAATAGATGGGGCTTGAATATCTTTACTGTTTCAGAGTATTCAAACAACCGGCCTCTTACTTGCATTATGTATGCCATCTTCCAGGTCAGTTCTGTTCAGTTGCCTATGGTGACTTTCCACAAATTTCAACAAACGTTGTAGCGAAATGTACTAATGATGCTTCTTTCTGTAACAGGAACGAGACTTGCTTAAGACTTTCAAGATCCCGACAGATACCTTTGTGACGTATATGATGACCCTTGAGGATCACTACCACCAAGATGTGGCCTATCATAACAGTCTTCATGCTGCTGATGTGGCCCAGTCAACTCACATACTTCTGTCCACACCTGCACTAGATGTAAGAACACTTTGTTTTCTTTAGACACAAGGTTTTCCTAGAGTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38555
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 |
---|---|---|---|---|---|
ENSDART00000028612 | Nonsense | 396 | 783 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 30547783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30868699 |
GRCz11 | 6 | 30855613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATTTCCTGACTCTTCTCTTTCCAGGAATTAGAAGACCTGAATAGATG[G/A]GGCTTGAATATCTTTACTGTTTCAGAGTATTCAAACAACCGGCCTCTTAC
Long Flanking Sequence:
GGCATGGATGTGTGTAGTCTGTGTGGAAACTACAATGAGGAGATTGAGTAATCTGGAATGTGATCTGTCAGCATTTGACACACTTGTGAATGATATGTGTAGAGAGGTTTGCGAGCCGTCCTATTCTGTTTTACATGAAGATATCTGTAAAGTTAAAAACCACCAGGTTGTTCTAATCCTTGGGTTCTTACTGTTCCTCACAGACAAACAGAACGATGTGGAGATTCCCTCGCCTACACCAAAAGCCCGCGAGAAGAAGAAAAAACAGCAGCTGATGACTCAGATCAGTGGTGTGAAGAAAGTGTCCCACGGGCCCAGCCTCAACTGCGGCATCGCTCGATTTGGCGTCAAAACTGACAAAGAGGATTTACTGTCAAAGGTAAGGAGAAGACTGACTAATACTGGCTCTTTAGTGTGTTGGGATGTGAAAATGTACAAATGTATTTTAATCTCATTTCCTGACTCTTCTCTTTCCAGGAATTAGAAGACCTGAATAGATG[G/A]GGCTTGAATATCTTTACTGTTTCAGAGTATTCAAACAACCGGCCTCTTACTTGCATTATGTATGCCATCTTCCAGGTCAGTTCTGTTCAGTTGCCTATGGTGACTTTCCACAAATTTCAACAAACGTTGTAGCGAAATGTACTAATGATGCTTCTTTCTGTAACAGGAACGAGACTTGCTTAAGACTTTCAAGATCCCGACAGATACCTTTGTGACGTATATGATGACCCTTGAGGATCACTACCACCAAGATGTGGCCTATCATAACAGTCTTCATGCTGCTGATGTGGCCCAGTCAACTCACATACTTCTGTCCACACCTGCACTAGATGTAAGAACACTTTGTTTTCTTTAGACACAAGGTTTTCCTAGAGTTTTTCCTCAAAGGAAGCATGTTGCTCAACATTTTGAATCTTTCTTAAACAGGCTGTCTTCACCGATCTCGAAATCCTGGCAGCCATTTTTGCGGCAGCCATCCATGATGTGGACCATCCTGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40714
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 |
---|---|---|---|---|---|
ENSDART00000028612 | Essential Splice Site | 602 | 783 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 30546774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30867690 |
GRCz11 | 6 | 30854604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACAAGCTCGGGAGTCTTGCTTCTGGACAACTACACAGACAGGATACAG[G/A]TACAGTAAAGGCTTCCTGATCTCCATTCCCTCAGTAAAACCAGTTGTTAG
Long Flanking Sequence:
AGTTCCTCATCAATACAAGTGAGTATTCTCAATTCCCAGCCTACTTTAGATACACAAGTCATGGAGATACATGGATTAATGTCCCATTCGCTCATTTTTTACAGACTCTGAGTTGGCCCTCATGTATAATGATGAGTCGGTTTTGGAAAATCACCACTTAGCTGTGGGCTTCAAGCTTCTCCAAGAGGACAACTGTGACATTTTCCAGAACCTCACAAAGAAACAGAGAACGTCACTCCGAAGGATGGTCATCGACATGGTGAGTTCCTTCCATCCTTCCTTCCTTCCATCCATCCTCCCATTCTTCCTTTCTTTTTCTTTAACCCTGGAATGATTTACATGCTAACACATTATTGTTCAATGTTTCCTTTTCACAGGTACTAGCCACTGACATGTCTAAACACATGAGCTTACTGGCCGATCTGAAGACCATGGTGGAAACGAAGAAAGTGACAAGCTCGGGAGTCTTGCTTCTGGACAACTACACAGACAGGATACAG[G/A]TACAGTAAAGGCTTCCTGATCTCCATTCCCTCAGTAAAACCAGTTGTTAGATAAACTTCAGACCATGATGACTTACAGTTGCTTAAATTTGTAAATTTACTCCAGGTTTTGCGGAACATGGTTCACTGCGCAGATCTGAGCAATCCCACCAAGTCTCTAGAGCTATACCGCCAGTGGACTGACCGCATCATGGAAGAGTTCTTTCACCAGGGTGACAGAGAAAGAGAGCGTGGCATGGAAATCAGCCCTATGTGCGATAAACACACTGCCTCTGTGGAGAAATCCCAGGTTAGTTCCTGTCTAAGATTCTGCAGAACCATGTTTTAAGCATCCTACAAAGTCTAATGATATTTTTTTCTCACTCTTTCTTCAGGTGGGATTCATCGACTACATCGTCCACCCGTTGTGGGAAACCTGGGCTGACTTGGTCCATCCGGATGCCCAGGATATCCTGGACACGCTGGAGGATAATCGGAACTGGTACCAGAGCATGATCCCTC
Associated Phenotype:
Not determined