ZMP
ppm1aa
Ensembl ID:
ZFIN ID:
Description:
protein phosphatase 1A [Source:RefSeq peptide;Acc:NP_571504]
Human Orthologue:
PPM1A
Human Description:
protein phosphatase, Mg2+/Mn2+ dependent, 1A [Source:HGNC Symbol;Acc:9275]
Mouse Orthologue:
Ppm1a
Mouse Description:
protein phosphatase 1A, magnesium dependent, alpha isoform Gene [Source:MGI Symbol;Acc:MGI:99878]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35528 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17877 | Essential Splice Site | Available for shipment | Available now |
sa31939 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35528
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040451 | Nonsense | 35 | 384 | 2 | 6 |
ENSDART00000076527 | Nonsense | 35 | 384 | 2 | 6 |
ENSDART00000126658 | Nonsense | 35 | 390 | 1 | 5 |
ENSDART00000127843 | None | None | 218 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 31773373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31419321 |
GRCz11 | 13 | 31549771 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGAACAGTCTTCGCTACGGCCTGAGCAGCATGCAGGGCTGGCGTGTT[G/T]AGATGGAAGATGCGCACACCGCTGTCATCGGCCTGCCCAACAGTCTGGAC
Long Flanking Sequence:
ATGAATCACATTGGTGTTTTGTTTCTTAAATAAATCAAGAGAGTCAGTCACTGATTCAATCATCCATTGATAAAAACGCTCAACTTGTTTCATTGTGAATAAATCTGCATGTTTGAATGAATCACTTGAATGCATAATTAAAAGTATCCATTAAGACAAGAACTTATTGCCACTGACTGGTGGTTTTTAGTGATATTTATGCACAACTTCTCCAAACCAGCCTTGGTATCAGCACAAAAACACATTCAGCAAAATGTCAGTTTATTTATGTCATTATTTTTAACCAAGAACGTGTATATTGATGTCAGACTGCTGCATAGCCCTATAAAGAGTTGACATTGTTCTGCTGTTACTCATATTTCTTGAACTTTTCTGTTCTAGATTTTTAAGCAGCAGACATGGGTGCATTTCTGGATAAGCCAAAGATGGAGAAACATAACGCTCATGGGGATGGGAACAGTCTTCGCTACGGCCTGAGCAGCATGCAGGGCTGGCGTGTT[G/T]AGATGGAAGATGCGCACACCGCTGTCATCGGCCTGCCCAACAGTCTGGACCTCTGGTCGTTCTTTGCCGTTTATGATGGTCACGCGGGATCACAGGTGGCACGTTACTGCTGCGAGCACCTTCTGGAGCACATCACCAGCAACCCTGACTTCCAGGGTGGAGGCGGAGGAGGGGGACCAGCTGTGGAGCCCAGTGTGGACAGCGTGAAGTCGGGAATTCGCACTGGTTTCCTTCAGATCGACGATCACATGCGACAGATTTCGGAAAAGAAGCATGGTGGAGCTGACCGCAGCGGCTCGACAGCTGTCGGAGTGATGATTTCACCTCGCCATATCTACTTTATCAACTGCGGAGATTCGCGCGGGTTGCTGAGTCGCGGAGGGGCGGTGCACTTCTTCACACAGGACCACAAACCCAGCAACCCTCTCGAGAAGGAAAGGATCCAGAACGCTGGAGGGTCTGTGATGATCCAACGTGTCAATGGGTCTCTGGCGGTGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17877
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040451 | Essential Splice Site | 362 | 384 | 4 | 6 |
ENSDART00000076527 | Essential Splice Site | 362 | 384 | 4 | 6 |
ENSDART00000126658 | Essential Splice Site | 362 | 390 | 3 | 5 |
ENSDART00000127843 | Essential Splice Site | 190 | 218 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 31775877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31421825 |
GRCz11 | 13 | 31552275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAWCTGAGAGCATCCCAAACCTACCCCCTGGAGGAGAACTGGCCAGCAA[G/T]TGAGTACCATACTYACCCAAACCCYGGCGATCTGTCCATGCAAGACTTTA
Long Flanking Sequence:
AGATATATTGTGCATCCCTAATTACAAGAATAGTGAAACCTAATTCTATAGTAAAGAATATCTTATCTTCATAACAACTTAGTCTTCAAGTTAAATTTTAGCTTCTATCTTTCCTCAGTGTTTCCAATTGGTTTAAATTATTGACTCAATTGAAATTTTATTGAACCTCTCCCTTCTTCTGTGTATTAACAGGGAAGTCGTGACAACATGAGTGTTGTGCTGGTGTGTTTCGTCAGTGCACCGAAGGTTTCCCCTGAAGCTGTTAAAAGGGAAGCTGAGCTTGATAAATACCTAGAGAGCCGAGTAGAAGGTTTGAGCTCAATCTACTGTCATTAATTAATCAGCTGTTCATCTGGATCATGCTTGATCAAAGTTGTTGTTATAACAGAGATCCTGAAGAGGCAGGGAGACGAAGGTGTGCCCGACCTGGTACATGTGATGCGCACGTTAGCATCTGAGAGCATCCCAAACCTACCCCCTGGAGGAGAACTGGCCAGCAA[G/T]TGAGTACCATACTTACCCAAACCCCGGCGATCTGTCCATGCAAGACTTTAGCAAACCATTAGTGAGTAATTCTCAGGAGTGATTCTCATGTCAATTCACAAGTTTTAGATCAATAAGTTCCGGTTACATTTGGTATTGAGATGTGATGTTCATACAGTTACAAACATGTTTTTTTTTTAATTTGCTGATTCTGCAAGTTTTGCATATACGCACACCTATTGTTTCCAAGAAACACTAATGGCCCATTTCCACTGAGTGGTACGGTACGGTACGGTTCGGTACGCTTTTATGGCCTTTTCCATTGTCAAAACACGTACCTAATCAAACCGTACCGTACCACTTTTTTGGCACCCTTTCAAAAGGGTCCCAAATACGAAAGGGTACCAAAAGGAGGAGCTAGACGCGCAGCTAAATGCTATTGGTTTACAGAGATACGTCATTCGCTTACGCAACAAGCCAGAATGTAAACAAAGGGCCCACCATGTTTGAAATACACAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31939
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 |
---|---|---|---|---|---|
ENSDART00000040451 | Essential Splice Site | 362 | 384 | 4 | 6 |
ENSDART00000076527 | Essential Splice Site | 362 | 384 | 4 | 6 |
ENSDART00000126658 | Essential Splice Site | 362 | 390 | 3 | 5 |
ENSDART00000127843 | Essential Splice Site | 190 | 218 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 31775878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31421826 |
GRCz11 | 13 | 31552276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGAGAGCATCCCAAACCTACCCCCTGGAGGAGAACTGGCCAGCAAG[T/C]GAGTACCATACTTACCCAAACCCCGGCGATCTGTCCATGCAAGACTTTAG
Long Flanking Sequence:
GATATATTGTGCATCCCTAATTACAAGAATAGTGAAACCTAATTCTATAGTAAAGAATATCTTATCTTCATAACAACTTAGTCTTCAAGTTAAATTTTAGCTTCTATCTTTCCTCAGTGTTTCCAATTGGTTTAAATTATTGACTCAATTGAAATTTTATTGAACCTCTCCCTTCTTCTGTGTATTAACAGGGAAGTCGTGACAACATGAGTGTTGTGCTGGTGTGTTTCGTCAGTGCACCGAAGGTTTCCCCTGAAGCTGTTAAAAGGGAAGCTGAGCTTGATAAATACCTAGAGAGCCGAGTAGAAGGTTTGAGCTCAATCTACTGTCATTAATTAATCAGCTGTTCATCTGGATCATGCTTGATCAAAGTTGTTGTTATAACAGAGATCCTGAAGAGGCAGGGAGACGAAGGTGTGCCCGACCTGGTACATGTGATGCGCACGTTAGCATCTGAGAGCATCCCAAACCTACCCCCTGGAGGAGAACTGGCCAGCAAG[T/C]GAGTACCATACTTACCCAAACCCCGGCGATCTGTCCATGCAAGACTTTAGCAAACCATTAGTGAGTAATTCTCAGGAGTGATTCTCATGTCAATTCACAAGTTTTAGATCAATAAGTTCCGGTTACATTTGGTATTGAGATGTGATGTTCATACAGTTACAAACATGTTTTTTTTTTAATTTGCTGATTCTGCAAGTTTTGCATATACGCACACCTATTGTTTCCAAGAAACACTAATGGCCCATTTCCACTGAGTGGTACGGTACGGTACGGTTCGGTACGCTTTTATGGCCTTTTCCATTGTCAAAACACGTACCTAATCAAACCGTACCGTACCACTTTTTTGGCACCCTTTCAAAAGGGTCCCAAATACGAAAGGGTACCAAAAGGAGGAGCTAGACGCGCAGCTAAATGCTATTGGTTTACAGAGATACGTCATTCGCTTACGCAACAAGCCAGAATGTAAACAAAGGGCCCACCATGTTTGAAATACACAGCGA
Associated Phenotype:
Not determined