ZMP
ppp2r5ea
Ensembl ID:
ZFIN ID:
Description:
protein phosphatase 2, regulatory subunit B', epsilon isoform a [Source:RefSeq peptide;Acc:NP_91939
Human Orthologue:
PPP2R5E
Human Description:
protein phosphatase 2, regulatory subunit B', epsilon isoform [Source:HGNC Symbol;Acc:9313]
Mouse Orthologue:
Ppp2r5e
Mouse Description:
protein phosphatase 2, regulatory subunit B (B56), epsilon isoform Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23672 | Nonsense | Available for shipment | Available now |
| sa37005 | Nonsense | Available for shipment | Available now |
| sa31043 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43413 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23672
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 |
|---|---|---|---|---|---|
| ENSDART00000009356 | Nonsense | 37 | 468 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 20320456)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 20348623 |
| GRCz11 | 20 | 20248296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTGTCAGGAAAGCCCGGCAGAAGCGAGCGCAGAGCTCATCCCAGTTC[A/T]GATCTCAGGACAAGCCCATAGAGCTGGTGGCGCTGCCTCTGCTGAAAGGT
Long Flanking Sequence:
ATTTCAGTTGTTCAGCATTGATGTTCAATAACTAATCATAGATTGTAGATGGTGTGTGTTTACTTCATTTATTTTAATCAAGTCGAGCTCTAGTACTGGTAGACATATATTGTGTTAATGTGGACATACTTCTCTTTTTACATACTAATGGGAGTCGAGTAGTCTTTCATCAGGATAGGTGTCATATTTAATTGAATATGAAGTGGAAATGTGTGAAGTCAGTGCGTTCAGTGGGCTGCATTAAATACTTTTTTCATGCCGTCTTTTTGCCACTCATTGGGTTTTGTCCAGTTAAATTAAAAATGAAGGGAGGTTACCATAAGTTTCTCGTTTTTGCACAAGATATTCTTCTTTTATCAATGACGGTCTGTTTTCCGTTCTGGCACAGGGCTATGTCTTCAGCAGCCACCACAGCCCCGTCGGTGGACAAGGTGGACGGCTTCTCCAGGAAGTCTGTCAGGAAAGCCCGGCAGAAGCGAGCGCAGAGCTCATCCCAGTTC[A/T]GATCTCAGGACAAGCCCATAGAGCTGGTGGCGCTGCCTCTGCTGAAAGGTAAGCTCGGTTTACTTGGTCAGATGAAGATAACGACTGCTGATGTCACAGCGCTTTGAGTTTTTTTAGTTGGTCAGATAGAGTTGATAAGGATTGCTATGCTATAATAACAAGGCAACACGCTGAATGCAGAAAAACCTGTCTTTGTGAGACTTTGAGAGAAAGAAAATATTTATTTTCAAGGTGAGATTAGGTAGCCTTATTGTTATTAAAAAATGATGTACATTTCAAAAGAATAGTATGGATATATAGTAAAAAAAAAAAAAAAAGATGTGACATTTTCAATATTTTTATTGCTGGGATTATTTTGTGATGAATGTAAGTAATTTAAGAAATGTAGCTTGTCACGTTATCCATAATTGTGTCAGTATAGAAATATAAAATGTTTTATATTTGCATGTTAATTTCTACTGTTCTGTTTTAAGGGTTTTAAATAAACTTCAGCAGTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37005
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 |
|---|---|---|---|---|---|
| ENSDART00000009356 | Nonsense | 155 | 468 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 20315171)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 20343338 |
| GRCz11 | 20 | 20243011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTCTGATCTTTCTCTCTCTCTCTTTCTTTTCTTTTTAAGCTTGTTTA[T/A]GAGTTCTTCATCCGTTTCTTGGAAAGTCAGGAATTTCAGCCCAGCGCTGC
Long Flanking Sequence:
TTTTTTATTTTTTTTAAGGTATATACTTTGTAGTTACAATAGTCGTTACTTAGTCTAGCTAATAAATAGGTTCTATCTCTTAATCTACCCCTGAACCTCACCTTAGCCCATTTAGTGACCTGTAAGTACATATTATATACATACACGTACTATAAAAATGAAACCAATTTCTTTATTTTTTTAAAGGGATTGCACAAAACGTAATATCTGTAAATAATTACATAGTCATTAAATGCAATCTGAAAGAGAAATATTTAATAAGTGTACATTTTTGAATTGTATTAGTAACTTGTTTAGTTTTATTTAGGAAAATTATAAAATGGTACGTCTCTAATGTTTAATAGGAACTTAGCAGCAAATTGTAAAATTTGGCTTTGGGTAAAGCATTAAAATCCCTGACATCACCATGGTTTTAGTCTTATGTAGTTGAGATAACGTTTATTTTTTCAAGTTTTCTGATCTTTCTCTCTCTCTCTTTCTTTTCTTTTTAAGCTTGTTTA[T/A]GAGTTCTTCATCCGTTTCTTGGAAAGTCAGGAATTTCAGCCCAGCGCTGCCAAAAAATACATCGATCAAAAATTTGTTTTACAGGTGAGTGATTGCCTTTGGAATGTTTCTGGACGCTTATACTACTATAAATGAAAGGAAACCAGTATTGCCAGTGAAATGCCACGATGCATCTCTCTCTAAAGTGCTTAATTGGGATTGGCGTTTTTAAATATTTTTCCCATCCGATGAATTGCATTCCCATCACCAAAAACAAAGGGTAACAATATGTAACAAAAATAATTATAATGTAACACGTAATAATTAAATAAATAATAAAAAGATAGCTGTGTAATACTAAAGCTAGTACATGAATATTCTTTACAGAGCAATGTATAATAAACTGTTAAGGTGTTCGGCTGTTAAATTTGCAGTATAATCTAGGTTAATTTAGCCCTTGCTAAAACAAAATTTGCACAAAATATTGTATATAAGATGATAATTTTAATGTTAAATTACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31043
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 |
|---|---|---|---|---|---|
| ENSDART00000009356 | Essential Splice Site | 318 | 468 | 10 | 14 |
| ENSDART00000009356 | Essential Splice Site | 318 | 468 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 20312408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 20340575 |
| GRCz11 | 20 | 20240248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCAGAGGTTTGTTGAAGTTTTGGCCAAAAACATGCAGTCAAAAGGAG[G/A]TAAGTGTTCTCATTCAGTTATTAAAGTGGTCCCATAATACTTTTAGTATT
Long Flanking Sequence:
TAAGCCTCACGTGTCTCTGCTTTTTCAGCATCATCAATGGTTTTGCGCTTCCTCTCAAAGCTGAGCACAAACAGTTCTTGGTGAAGGTGCTGCTGCCTCTGCACACAGTGAGGAGCTTATCTCTCTTCCATGCCCAGGTACAGACACCACATGTTTGGTACAAATCTGTGCATGTCTCTGCTTGCTTACCTGCGTTGCAAAGACAGAAAAAACAAATTCCTCTGTTCATGCTTGTTTGTGAATCTAAACATCTGAAATGCATTTGTTAATCTGATGTCATGTTTTCTTCTAGCTGGCCTATTGTATTGTACAGTTCCTAGAGAAAGACCCCACGTTAACAGAACCTGTGAGTGCTCCTTCATCATTATCCTCCTCATTGTTTATCAGGCCTCATTTATTTGCAGTTTTCTCTAGTTGGTCTCTGAATGTTGATGTTGCCTTTTTTGTAGGTGATCAGAGGTTTGTTGAAGTTTTGGCCAAAAACATGCAGTCAAAAGGAG[G/A]TAAGTGTTCTCATTCAGTTATTAAAGTGGTCCCATAATACTTTTAGTATTCTGCAAATGACAAACTTTATTTAATTTGAAGCTTCCCAAACAAAAACAATTGCACATTATTTGTGATTAAATTGAAACTAATTGTTTTTAAACTTTTAAAAATGTAGTGTATCTAATAAAAAAATATTATTCCACTAATTTTATATTTACAGTTAAAGTCAGAATTATTAGCCCCCCTTTGAATTTTTATTTCTTTTTTAAATATTTCCCAAATGATGTTTAACTGAGCAAGGAAATTTTTGCAGTATGTCTGATAATATTTTTTCTTCTGTAAAAAGTCTTTCTTGTTTTATTCCGGCTAGAATAAAAGCACTTTTTAATTTTTTCAACACCATTTTAAGGTCAACATTATTAGCCCCTTTAAGCTATATTTTTTTAGTAGTCTACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43413
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 |
|---|---|---|---|---|---|
| ENSDART00000009356 | Essential Splice Site | 318 | 468 | 10 | 14 |
| ENSDART00000009356 | Essential Splice Site | 318 | 468 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 20 (position 20312408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 20340575 |
| GRCz11 | 20 | 20240248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCAGAGGTTTGTTGAAGTTTTGGCCAAAAACATGCAGTCAAAAGGAG[G/A]TAAGTGTTCTCATTCAGTTATTAAAGTGGTCCCATAATACTTTTAGTATT
Long Flanking Sequence:
TAAGCCTCACGTGTCTCTGCTTTTTCAGCATCATCAATGGTTTTGCGCTTCCTCTCAAAGCTGAGCACAAACAGTTCTTGGTGAAGGTGCTGCTGCCTCTGCACACAGTGAGGAGCTTATCTCTCTTCCATGCCCAGGTACAGACACCACATGTTTGGTACAAATCTGTGCATGTCTCTGCTTGCTTACCTGCGTTGCAAAGACAGAAAAAACAAATTCCTCTGTTCATGCTTGTTTGTGAATCTAAACATCTGAAATGCATTTGTTAATCTGATGTCATGTTTTCTTCTAGCTGGCCTATTGTATTGTACAGTTCCTAGAGAAAGACCCCACGTTAACAGAACCTGTGAGTGCTCCTTCATCATTATCCTCCTCATTGTTTATCAGGCCTCATTTATTTGCAGTTTTCTCTAGTTGGTCTCTGAATGTTGATGTTGCCTTTTTTGTAGGTGATCAGAGGTTTGTTGAAGTTTTGGCCAAAAACATGCAGTCAAAAGGAG[G/A]TAAGTGTTCTCATTCAGTTATTAAAGTGGTCCCATAATACTTTTAGTATTCTGCAAATGACAAACTTTATTTAATTTGAAGCTTCCCAAACAAAAACAATTGCACATTATTTGTGATTAAATTGAAACTAATTGTTTTTAAACTTTTAAAAATGTAGTGTATCTAATAAAAAAATATTATTCCACTAATTTTATATTTACAGTTAAAGTCAGAATTATTAGCCCCCCTTTGAATTTTTATTTCTTTTTTAAATATTTCCCAAATGATGTTTAACTGAGCAAGGAAATTTTTGCAGTATGTCTGATAATATTTTTTCTTCTGTAAAAAGTCTTTCTTGTTTTATTCCGGCTAGAATAAAAGCACTTTTTAATTTTTTCAACACCATTTTAAGGTCAACATTATTAGCCCCTTTAAGCTATATTTTTTTAGTAGTCTACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATT
Associated Phenotype:
Not determined