ZMP
ppp1caa
Ensembl ID:
ZFIN ID:
Description:
protein phosphatase 1, catalytic subunit, alpha [Source:RefSeq peptide;Acc:NP_999976]
Human Orthologues:
PPP1CA, PPP1CC
Human Descriptions:
protein phosphatase 1, catalytic subunit, alpha isozyme [Source:HGNC Symbol;Acc:9281]
protein phosphatase 1, catalytic subunit, gamma isozyme [Source:HGNC Symbol;Acc:9283]
protein phosphatase 1, catalytic subunit, gamma isozyme [Source:HGNC Symbol;Acc:9283]
Mouse Orthologues:
Ppp1ca, Ppp1cc
Mouse Descriptions:
protein phosphatase 1, catalytic subunit, alpha isoform Gene [Source:MGI Symbol;Acc:MGI:103016]
protein phosphatase 1, catalytic subunit, gamma isoform Gene [Source:MGI Symbol;Acc:MGI:104872]
protein phosphatase 1, catalytic subunit, gamma isoform Gene [Source:MGI Symbol;Acc:MGI:104872]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8688 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26083 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40087 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8688
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 |
---|---|---|---|---|---|
ENSDART00000025046 | Nonsense | 70 | 331 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 31048639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30766678 |
GRCz11 | 3 | 30897520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTNNNNNNNNNNNATCTGCAGGTGATGTCCATGGTCAGTACTA[T/A]GATCTTCTTCGTCTCTTCGAGTATGGGGGCTTTCCTCCTGAGAGTAACTA
Long Flanking Sequence:
TGCAGAAATTTTTTTTTTGTCCATCCTTGAGTCTATTTATTTTTTTGTGTAAATGTATTTTATAATTATTCAGTTTTTAAATTAATTTCAGTAATTTTATTGACTAATATGAAAATGTTCTTTGATTTATTTACAGTACAGTTTGTAAAGATTTTTTTTTAGTAGATATGTTATATGAGAGACTTGCTTTGTTTACCAAATAAGTGAATCTATCTGGATTTGCGTTGTAGACATAAAAAGATAAAAAAAAAAAGTATATATATTTTTTCCTATATTAAGTTTTTAATTATGATACCCCCAAAATCAATCCACTTAAATTCACAGATTTTTTTAAAACAAAATTGTCTGCTTAAATAGAAAAAAAATGTCTGCAGATTCTGTCATGGGAGAAGAGTAATTAATGTGTAAAAGATTTTTTGGAAATATCCACCCTGATCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAATCTGCAGGTGATGTCCATGGTCAGTACTA[T/A]GATCTTCTTCGTCTCTTCGAGTATGGGGGCTTTCCTCCTGAGAGTAACTACTTGTTCCTGGGGGACTATGTGGACAGAGGGAAGCAGTCCCTAGAGACAATCTGCCTCCTGTTGGCCTACAAAGTCAAATATCCTGAAAACTTCTTCCTGCTGCGTGGCAACCACGAGTGCGCCTCTATCAATCGTATATATGGCTTCTATGATGAGTGTTAGTATCAGTTTGAAAAACAAATTTGATCATCTACAAAAGACACCCTTCAGTATTCACATGTCATTCTGATCTGTTCAGGTAAGCGGCGGTATAACATTAAGCTGTGGAAGACCTTCACGGACTGTTTCAACTGTTTACCTGTGGCTGCCATTGTAGACGAGAAGATCTTCTGTTGCCATGGAGGTGAGTGCAGCCGGAGGTCTTCTGTCCCCATGACAATTTTAATGTCCGTCACAACTCCTTTATTGACATTTTGCAATTTCCCTGGAGAAGTATAAATATAACTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26083
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 |
---|---|---|---|---|---|
ENSDART00000025046 | Nonsense | 114 | 331 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 31048507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30766546 |
GRCz11 | 3 | 30897388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAGTCCCTAGAGACAATCTGCCTCCTGTTGGCCTACAAAGTCAAATA[T/A]CCTGAAAACTTCTTCCTGCTGCGTGGCAACCACGAGTGCGCCTCTATCAA
Long Flanking Sequence:
ACAGTACAGTTTGTAAAGATTTTTTTTTAGTAGATATGTTATATGAGAGACTTGCTTTGTTTACCAAATAAGTGAATCTATCTGGATTTGCGTTGTAGACATAAAAAGATAAAAAAAAAAAGTATATATATTTTTTCCTATATTAAGTTTTTAATTATGATACCCCCAAAATCAATCCACTTAAATTCACAGATTTTTTTAAAACAAAATTGTCTGCTTAAATAGAAAAAAAATGTCTGCAGATTCTGTCATGGGAGAAGAGTAATTAATGTGTAAAAGATTTTTTGGAAATATCCACCCTGATCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAATCTGCAGGTGATGTCCATGGTCAGTACTATGATCTTCTTCGTCTCTTCGAGTATGGGGGCTTTCCTCCTGAGAGTAACTACTTGTTCCTGGGGGACTATGTGGACAGAGGGAAGCAGTCCCTAGAGACAATCTGCCTCCTGTTGGCCTACAAAGTCAAATA[T/A]CCTGAAAACTTCTTCCTGCTGCGTGGCAACCACGAGTGCGCCTCTATCAATCGTATATATGGCTTCTATGATGAGTGTTAGTATCAGTTTGAAAAACAAATTTGATCATCTACAAAAGACACCCTTCAGTATTCACATGTCATTCTGATCTGTTCAGGTAAGCGGCGGTATAACATTAAGCTGTGGAAGACCTTCACGGACTGTTTCAACTGTTTACCTGTGGCTGCCATTGTAGACGAGAAGATCTTCTGTTGCCATGGAGGTGAGTGCAGCCGGAGGTCTTCTGTCCCCATGACAATTTTAATGTCCGTCACAACTCCTTTATTGACATTTTGCAATTTCCCTGGAGAAGTATAAATATAACTGTTTATAGCCGCATCACTGGAAGACCATAAAGTTTGGTTCACTTGACTTTTACGAAAACCCAGGGATCCACCAGGGGACTTAGAGTCCTCATAAAGATGTTGAGTGTACATTACATTTGAACTGCTGTGTGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40087
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 |
---|---|---|---|---|---|
ENSDART00000025046 | Nonsense | 137 | 331 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 31048438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30766477 |
GRCz11 | 3 | 30897319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCGTGGCAACCACGAGTGCGCCTCTATCAATCGTATATATGGCTTCTA[T/A]GATGAGTGTTAGTATCAGTTTGAAAAACAAATTTGATCATCTACAAAAGA
Long Flanking Sequence:
AAGTGAATCTATCTGGATTTGCGTTGTAGACATAAAAAGATAAAAAAAAAAAGTATATATATTTTTTCCTATATTAAGTTTTTAATTATGATACCCCCAAAATCAATCCACTTAAATTCACAGATTTTTTTAAAACAAAATTGTCTGCTTAAATAGAAAAAAAATGTCTGCAGATTCTGTCATGGGAGAAGAGTAATTAATGTGTAAAAGATTTTTTGGAAATATCCACCCTGATCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAATCTGCAGGTGATGTCCATGGTCAGTACTATGATCTTCTTCGTCTCTTCGAGTATGGGGGCTTTCCTCCTGAGAGTAACTACTTGTTCCTGGGGGACTATGTGGACAGAGGGAAGCAGTCCCTAGAGACAATCTGCCTCCTGTTGGCCTACAAAGTCAAATATCCTGAAAACTTCTTCCTGCTGCGTGGCAACCACGAGTGCGCCTCTATCAATCGTATATATGGCTTCTA[T/A]GATGAGTGTTAGTATCAGTTTGAAAAACAAATTTGATCATCTACAAAAGACACCCTTCAGTATTCACATGTCATTCTGATCTGTTCAGGTAAGCGGCGGTATAACATTAAGCTGTGGAAGACCTTCACGGACTGTTTCAACTGTTTACCTGTGGCTGCCATTGTAGACGAGAAGATCTTCTGTTGCCATGGAGGTGAGTGCAGCCGGAGGTCTTCTGTCCCCATGACAATTTTAATGTCCGTCACAACTCCTTTATTGACATTTTGCAATTTCCCTGGAGAAGTATAAATATAACTGTTTATAGCCGCATCACTGGAAGACCATAAAGTTTGGTTCACTTGACTTTTACGAAAACCCAGGGATCCACCAGGGGACTTAGAGTCCTCATAAAGATGTTGAGTGTACATTACATTTGAACTGCTGTGTGCTTTGCCGATGACGTGGGAGTAATCTGTTCTGGAAGTGAACCATAATTAATTTTATTTGATTTTCTTTTTTTT
Associated Phenotype:
Not determined