ZMP
ppp3cca
Ensembl ID:
ZFIN ID:
Description:
protein phosphatase 3, catalytic subunit, gamma isoform-like [Source:RefSeq peptide;Acc:NP_00116010
Human Orthologue:
PPP3CC
Human Description:
protein phosphatase 3, catalytic subunit, gamma isozyme [Source:HGNC Symbol;Acc:9316]
Mouse Orthologue:
Ppp3cc
Mouse Description:
protein phosphatase 3, catalytic subunit, gamma isoform Gene [Source:MGI Symbol;Acc:MGI:107162]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33612 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20428 | Nonsense | Available for shipment | Available now |
sa16822 | Essential Splice Site | Available for shipment | Available now |
sa45205 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33612
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 |
---|---|---|---|---|---|
ENSDART00000080412 | Essential Splice Site | 126 | 499 | 3 | 13 |
ENSDART00000132740 | Essential Splice Site | 126 | 499 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 29620775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27376073 |
GRCz11 | 5 | 27976226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATCTCTTTCTGGGCGATTATGTAGACAGGGGATACTTCAGTATTGAGG[T/G]GAGTAAGAGGTTTTTTTCTTTAGATATTCTGTTAACTAAGTTACTTTGTA
Long Flanking Sequence:
TGCTGCTTTTGAGCACGAATTAATAGATGTCACAAACCCCTCTGGCTTTAGATACATTCTGCTTTATAAATGGATCCAGCCTCTGTATTTTCAAATATAGTGTCGTTGTTGCTAAGTGACAGAGCGGTCTTGTACATGTGGCCGCTGCTGGCTAGATGATGCAGGTAGGATGGCTGTAAGTGTTTGAAGCGTTTGGTCTCATTCCAGTCCCACACTTGCCTAAGGCATTTCATAAAATGTGATACAGGAAATCTTGTACAGTTTTGTTTGTGCTCAACATTGACTTTTGATCCAAAATGATGAAGCCTTTATGTATCACACTGAAAACGACCTAACATGCTAATCATTCTGTTTTGCTTGTCTTTCACCTGTAGTGTGTGGTGACGTTCATGGGCAGTTTTTTGACCTCATGAAGCTCTTCGAAGTTGGTGGTTCTCCTGACAACACGCGCTATCTCTTTCTGGGCGATTATGTAGACAGGGGATACTTCAGTATTGAGG[T/G]GAGTAAGAGGTTTTTTTCTTTAGATATTCTGTTAACTAAGTTACTTTGTAATTACATGTCAGCTAACTCTTGGTAGAGTGTTAGTGTGCTGCCTTCTAATATCTGTCAACTGCTTTTTTTTCATAGACTCCTAATAGTTATTATTTTAATCGTATTGACTTTGACTATGCGGTAGTAAAGCTTGTTTTTTTTTTTTTTTTGATTGTTCTAGAACTTCTGATTTAGTTGCCTATGGGAGAAATGACTACAAATGATAAATGGCAGAAAATGGACAAACTAGTTGATTTTAATGAGACCAGAAGTCTCGAGCCAAAGAGATTCCAATGGCTGTACCTACTTGTACGTTAATGCCCCATTCACATGGGGCGTCAGCGTCGACGCTTCCCATCATCTTTGATTAGGTGACATCATACGTTGCCGAACTGAACTGTGGGTCTGTTGTGGCTGCTCCAGCGGAGTTGCTCATTGCAGAAGTTGTGAATTTCTCAACTTTCCAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20428
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080412 | Nonsense | 256 | 499 | 6 | 13 |
ENSDART00000132740 | Nonsense | 256 | 499 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 29595680)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27350978 |
GRCz11 | 5 | 27951131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAGACGGCAGAGCACTTTAACCACAACTCCGTCAGAGGCTGCTCCTA[T/G]TTCTTCAGGTACAACAGGAAAGGGTCATCCAGTTCATACATGTACAGTGA
Long Flanking Sequence:
TCCCTATAAATTATATCTGATATTTAATGATTCAGTGGAGGATGGAGTCTCTCCAGGCTTTCTTCGATCAACCAAACTCAATGTGTCCTGTCTTTGTTTTCTCACAGGTAAAATAAAGTATTCAGAGAGGGTTTATGATGCATGTATGGAGGCCTTTGACTGCTTGCCTCTTGCAGCTCTTCTAAATCAGCAGTTCCTCTGTGTTCATGGTGGCCTCTCGCCAGAAATTAACTGCTTAGACGACATTAGGAAAGTAAGTGTCCATTTTTGTTGTTGTTGTTGCTCTGTTTTTTTCCCTTTAAGCCTTTTTACAGCATTTTACAAGACGTGTTGATTCCTCTTTCTCTGCCTTTGCGCTATGTTGTGCAGTTAGACAGGTTTAAGGAGCCCCCGGCATTCGGGCCTATGTGTGATTTGATCTGGGCTGACCCGGGAGAGGACTACGGCAGTGAGAAGACGGCAGAGCACTTTAACCACAACTCCGTCAGAGGCTGCTCCTA[T/G]TTCTTCAGGTACAACAGGAAAGGGTCATCCAGTTCATACATGTACAGTGACTTAGATTTTTTTGACAAAATAACAGCTTAATTGACACAGAATATAGCTTGACTGATTTCTATTTTTATTTACATGACAAACTTTTATTTAATTAAATGAAATATTTATAAATATTTCATATAATGATAAACAATAATAATAACAACAATAATAAAAATATAATAAATAAAATATTTAAATTGTTGTCAATATTATTTGATTACTTTAGATCTAATACTTTAGATTACATTACTTTAGATTCTAATAGTTTTAAACATGTAAAAAAAATCCAAGTTTTTGATGTTATTTTTTTATTTTATTAGTTTTTCTCTGTGCATTTTTTGTCCATTTCAAAATTAGAAAATGTTATTTTATGTGATATAATAAAAAATATTATCAAGCTGTTTTTGATGTGAACTTCATGTAGCAAATAGATATTTACATTTATAAAATATTATTATTATTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16822
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080412 | Essential Splice Site | 259 | 499 | 6 | 13 |
ENSDART00000132740 | Essential Splice Site | 259 | 499 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 29595670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27350968 |
GRCz11 | 5 | 27951121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGCACTTTAAYCACAACWCCGTCAGAGGCTGCWCCTATTTCTTCAGG[T/C]ACAAMAGGAAAGGGTCATCCAGTTCATAYATGTACAGTGACTTAGATTTT
Long Flanking Sequence:
TTATATCTGATATTTAATGATTCAGTGGAGGATGGAGTCTCTCCAGGCTTTCTTCGATCAACCAAACTCAATGTGTCCTGTCTTTGTTTTCTCACAGGTAAAATAAAGTATTCAGAGAGGGTTTATGATGCATGTATGGAGGCCTTTGACTGCTTGCCTCTTGCAGCTCTTCTAAATCAGCAGTTCCTCTGTGTTCATGGTGGCCTCTCGCCAGAAATTAACTGCTTAGACGACATTAGGAAAGTAAGTGTCCATTTTTGTTGTTGTTGTTGCTCTGTTTTTTTCCCTTTAAGCCTTTTTACAGCATTTTACAAGACGTGTTGATTCCTCTTTCTCTGCCTTTGCGCTATGTTGTGCAGTTAGACAGGTTTAAGGAGCCCCCGGCATTCGGGCCTATGTGTGATTTGATCTGGGCTGACCCGGGAGAGGACTACGGCAGTGAGAAGACGGCAGAGCACTTTAACCACAACTCCGTCAGAGGCTGCTCCTATTTCTTCAGG[T/C]ACAACAGGAAAGGGTCATCCAGTTCATACATGTACAGTGACTTAGATTTTTTTGACAAAATAACAGCTTAATTGACACAGAATATAGCTTGACTGATTTCTATTTTTATTTACATGACAAACTTTTATTTAATTAAATGAAATATTTATAAATATTTCATATAATGATAAACAATAATAATAACAACAATAATAAAAATATAATAAATAAAATATTTAAATTGTTGTCAATATTATTTGATTACTTTAGATCTAATACTTTAGATTACATTACTTTAGATTCTAATAGTTTTAAACATGTAAAAAAAATCCAAGTTTTTGATGTTATTTTTTTATTTTATTAGTTTTTCTCTGTGCATTTTTTGTCCATTTCAAAATTAGAAAATGTTATTTTATGTGATATAATAAAAAATATTATCAAGCTGTTTTTGATGTGAACTTCATGTAGCAAATAGATATTTACATTTATAAAATATTATTATTATTATTATTATTACACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45205
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 |
---|---|---|---|---|---|
ENSDART00000080412 | Essential Splice Site | 384 | 499 | 10 | 13 |
ENSDART00000132740 | Essential Splice Site | 384 | 499 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 29588530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27343828 |
GRCz11 | 5 | 27943981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTGTTCTGATGATGAACTCATGTCAGAGGGAGATGACTTGTGCGAAG[G/A]TGAGGAGGTTTTCTTGTTTATGCACTCTGCAAATGCGTTTATCCAAAGAA
Long Flanking Sequence:
CTGCTCTCCTCACCCGTACTGGTTGCCCAACTTCATGGATGTGTTTACATGGTCATTACCGTTTGTGGGCGAGAAAGGTAAGTGTCCAGACTGTGAATCTATTTGACAGAGCATTTGGAAGAGAGGCTAGAATGACCTTGTTGGTGGCTTGTCTTTGGTAGCTGACTGTGTCCTCTCAGTGGGAAGAATGCAGAGAGAAAGAGCCCTGAAACGTCATATTAACGTCATAAAATGTGTGCCAGCACGTTCAAGGGCATCATTTATAAAATCATCTGAGACTTCCTAAGTTTTTCAGTTTAATTTTTAAAGTCTTTGTGTACATTGTTTCATACAGCTTCATAACGTAGAAGTTGAGTTCGTATTTTAAAAAGAAGCAAATGGATTTACTGGATGTATTTTCCAAGAATGCTCTTTGTCTACAGTGACTGAGATGTTGGTGAATGTCCTGAATATCTGTTCTGATGATGAACTCATGTCAGAGGGAGATGACTTGTGCGAAG[G/A]TGAGGAGGTTTTCTTGTTTATGCACTCTGCAAATGCGTTTATCCAAAGAAATTAACATTGTCTTGAAGTTACACTTTTTATCTGTTGATATGCAAGACAGGGGTGGAAATTTATGCCCAACTAATTCAATGTAAGATGCTATAATACCCCTCCACAATTCAAATAACTCACTGTAATCCGTGTTTAAGATCTTTATTGATACGAGAGCAATCAATAAAAAAAATAAATAAAATTAGGTAGAATATTCACATTTAATATAGTTTATATACTTTATTGTTCAGTAGTAGGCTACTTACGGTATTTTATGCAGTTGTTGTGTAATGCATGAATGCCACATTTGAGCAACATTAAAGTGCATCTATTATGTATTATAAAAGGCTCTTATTTTGGTTTTGTGAGTCCCCAACAACAGGCTTGTATGCATGCAAGATCAAAAAACACATTCATTGTCTTTTAATATGCATTTATTCATTCATTCATTCATTTGTTTTCTTTTTGGC
Associated Phenotype:
Not determined