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 |
---|---|---|---|
sa17877 | Essential Splice Site | Available for shipment | Available now |
sa31939 | Essential Splice Site | Available for shipment | Available now |
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