ZMP
si:dkeyp-38b6.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate protein phosphatase 2 (Formerly 2A), regulatory subunit B'', alp
Human Orthologue:
PPP2R3A
Human Description:
protein phosphatase 2, regulatory subunit B'', alpha [Source:HGNC Symbol;Acc:9307]
Mouse Orthologues:
CAAA01108492.1.1364.1, Ppp2r3a
Mouse Description:
protein phosphatase 2, regulatory subunit B'', alpha Gene [Source:MGI Symbol;Acc:MGI:2442104]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11938 | Nonsense | Available for shipment | Available now |
sa39836 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14576 | Nonsense | Available for shipment | Available now |
sa19761 | Essential Splice Site | Available for shipment | Available now |
sa9325 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11938
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110922 | None | None | 1141 | None | 15 |
ENSDART00000131977 | None | None | 520 | None | 13 |
ENSDART00000139080 | Nonsense | 381 | 716 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 25394971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25591167 |
GRCz11 | 2 | 25246801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTTACAGGCAGTTTGAAACCTATTCAGAGTGTCCCTGGTTTGTCAGCA[C/T]GAACACCTCCATCAACTAATGGGTTCTCCCATGGCAGCTTGCCTACAGCC
Long Flanking Sequence:
AAAACCTAATAACCCGCATTCTGGAGAAGACCAAGGCAGACAGCAGTGCCTCAGGAGAAGACATAAAAGCCTGTCTTGACATTCTGCTCAAGTGCTCAGAAGATCTGAAGAAGTGCACAGACATCATCAAACAGTGCATCAAAAGAAAGTCAATGGGTGGAACTAGTGATGACTCAGGGAATCCTGAAATCATTTATAAAAATGTGATGGCCCGACTCTCCAACTACCTAAAGAGACTTCCTCTTGAGCTGGAACAGGGACAAAGTATAAGGCAGGAGCACAGTGAGCTTGCTGAACTAGTCAATAGTATACACGGACTACAACAAATCCCCTTCTCGCCTATCTTTGGCAATGAACAACCTCCACGATATGAGGACGTTGTTCAGTCTCCTCCACCTACGAAGCCTCGAAATAAACCCTCCCAGCCAGAACCTTCAGAGGGTTCTAGGGAACTTACAGGCAGTTTGAAACCTATTCAGAGTGTCCCTGGTTTGTCAGCA[C/T]GAACACCTCCATCAACTAATGGGTTCTCCCATGGCAGCTTGCCTACAGCCTCCAGTAGCAGTTCAACACCATTTATCTGCCAGCATACAGTTTCAACCAGCCGACCAGACACATTTTCTTCTGCAAATTCTTTCTTGTCTATCAGTAATGAAAACCTTTGTAAGGATCCAATGGAGGCTCTGTACATTGAGGAAGAAGATTCAGATATAGGAAGGATGCCGGACAGGCCAGTTAAAGGGGATGGGAAGCACAGCTGTAATCTTTCGGAGTCCAGACAATACTCCAAAAGAACTACTGGCTACTCAGAGCCTAGTGGTGGTGTTTCGGATAAACTACATGAGCTTAGCAGAAACGGAACCACATTCAAGCCGCAAAATGACTCTACTGTCAACCAGATGTACCTGCCAAAAAGCACAGATTCTAAACTGTTCTCAAGGTCCACCTCACACACGAGTAAAGGGGGAGCCGATGATATTGATAAACTCCTGATGGACCTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39836
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110922 | Nonsense | 452 | 1141 | 2 | 15 |
ENSDART00000131977 | None | None | 520 | None | 13 |
ENSDART00000139080 | Nonsense | 472 | 716 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 25395244)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25591440 |
GRCz11 | 2 | 25247074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGCCAGTTAAAGGGGATGGGAAGCACAGCTGTAATCTTTCGGAGTCC[A/T]GACAATACTCCAAAAGAACTACTGGCTACTCAGAGCCTAGTGGTGGTGTT
Long Flanking Sequence:
AGGAGCACAGTGAGCTTGCTGAACTAGTCAATAGTATACACGGACTACAACAAATCCCCTTCTCGCCTATCTTTGGCAATGAACAACCTCCACGATATGAGGACGTTGTTCAGTCTCCTCCACCTACGAAGCCTCGAAATAAACCCTCCCAGCCAGAACCTTCAGAGGGTTCTAGGGAACTTACAGGCAGTTTGAAACCTATTCAGAGTGTCCCTGGTTTGTCAGCACGAACACCTCCATCAACTAATGGGTTCTCCCATGGCAGCTTGCCTACAGCCTCCAGTAGCAGTTCAACACCATTTATCTGCCAGCATACAGTTTCAACCAGCCGACCAGACACATTTTCTTCTGCAAATTCTTTCTTGTCTATCAGTAATGAAAACCTTTGTAAGGATCCAATGGAGGCTCTGTACATTGAGGAAGAAGATTCAGATATAGGAAGGATGCCGGACAGGCCAGTTAAAGGGGATGGGAAGCACAGCTGTAATCTTTCGGAGTCC[A/T]GACAATACTCCAAAAGAACTACTGGCTACTCAGAGCCTAGTGGTGGTGTTTCGGATAAACTACATGAGCTTAGCAGAAACGGAACCACATTCAAGCCGCAAAATGACTCTACTGTCAACCAGATGTACCTGCCAAAAAGCACAGATTCTAAACTGTTCTCAAGGTCCACCTCACACACGAGTAAAGGGGGAGCCGATGATATTGATAAACTCCTGATGGACCTGGAGTGTCTTTCCCAGAACATGCAAAAGGAACCTCCATTGCCTCCTAAGCTTAAAAATTGTGCCCTACAGACAAGTTCCCCCCAGCATTTGATTGGTAACTCTGTGGTTAAGGATCTACCTGTTGTAGGTTTCTCTGGACCCTCGGTGGCCAAGCCACCAGAGCCAGGGGTTGAGTCTACTGAAGAGGATGATGGAGCTCTTCTGCTCAGGATTCTGGAGAGCATTGAAAGCTTTGCTCAGGAGCTGGTGGAGAGTGGAGCCGGGAGAGGAACTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14576
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110922 | Nonsense | 727 | 1141 | 4 | 15 |
ENSDART00000131977 | Nonsense | 104 | 520 | 2 | 13 |
ENSDART00000139080 | None | None | 716 | None | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 25428557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25624753 |
GRCz11 | 2 | 25280387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCCACGCTTCTACTTCCCCAAAGGCCTTCMAAACTGTGCAGCCAACTA[C/A]GACGAGGCCATTGCCAAAATCGAAGCGGCYTTCACTGAGTTCGAAGAGGA
Long Flanking Sequence:
TTTTTGCAAAGTTCAACAGGGTATACTGTATATGACCAAAAGGAAATTAAAGCTAGCATTTAATTAGCTTTGTTTGTGTGGTAAGAACACCTAAACATCTTATTGCTGGGTGATTTGCAGTACCTTTTTCCACATCCTCCATTTGCTTCAGACACATCCTCAGCTGAACTATTTAAGATATGTTTTGGAAAGTCACTTCTATTTTCCTCTTCTCTTCAGCTCAATGTTTTTAAAGCCTTGTAAAAAAAACTTAAGGCCTAAAAGTTGTTGCACGTATTGATATCCTGTTTCTTTCTATCGTCTCTTTTTGTATTTCAATAGATCCAACCTGAAAAGAAACCTGGAACTCCTCCTCCAACACTATCACCTGCACCGTCCTCGCCGACCCCACGGCCACCCAGCCCTCCTCCAGCCAAAGTAGTGGCCACACCACCACCCTCCTCCATAAACATTCCACGCTTCTACTTCCCCAAAGGCCTTCCAAACTGTGCAGCCAACTA[C/A]GACGAGGCCATTGCCAAAATCGAAGCGGCCTTCACTGAGTTCGAAGAGGAGAAAGCTGACATTTATGAAATGGGAAAGATAGCAAAGGTGCATGCAAATTGGGAATTGTTTTGCTTAAAATGAGATTTAGAATATTGGAGATTCTCTCCGTAGTCTTGGATTGATGGCAATAAACATGCAAGCTGACACTTGTTTTGCAAAGTCCTCGCTTGGAGATTTGCATTGCCGATTTGTATTGGCATGGCACAATGATGGATGCCAGCTCATAACATTGTGCTTTATTTGCACTGATTTTGAATAATATATAAACGATGGAATATAAAAAGGAAGCATCAACAGAATAACTCATCCTGACATTTACACTCATTTATATTTGGATTTTGAATATCATATCATTTAGATTTTAGTAATAGAATGCAAATGTGATATCAGCTGCGTTATTTTATTTCTGTGAAAAAAAATAAGATTGTGTATGTGGCTTTATATACCAGGGCTATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19761
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110922 | Essential Splice Site | 978 | 1141 | 11 | 15 |
ENSDART00000131977 | Essential Splice Site | 355 | 520 | 9 | 13 |
ENSDART00000139080 | None | None | 716 | None | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 25435286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25631482 |
GRCz11 | 2 | 25287116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTTGTTTGGTTCCTCATTTCAGAGGAGGACAAAAAGAACCCCACAAG[G/A]TAAAAAGGCAGATGCAAATGCTGCTGTCACCAAGTTTTACTTTAGATCAG
Long Flanking Sequence:
TATTTCTCTTATGAGCACTTCTATGTTATTTACTGTAAGTTCTGGGAGCTTGACAGTGACCATGACCTCTTCATTGACCCCAAGGACCTGGCCAGGTACAATGACCATGGTAAGTACACAGTAAATCCATTCGAAACAAGTCTCATTTATTAAACTTTATCATTGTTTTAGCGAATATTCACACAATAGTTAAGTTTGTTGGTAAACTATGCCTTTCATTAGCCTACTTTTGATGTGTGTCTGCTCTGTTCTTCTTTGCAAAGCTTCATCAAGCAGAATCATTGAGAGGCTGTTTTCAGGAGCTGTCACAAGGTAGGAGCTGCTGTGGAGAACAAAGGTCATTTCTGAGATTTTGACTTTTGAGTGTTTTATAAGTGGCTTAAGACCTGTTTTTTTTTTTTTCTTCTAAGGGGAAACTCAGTGCAGAGAGAGGGGAGAATGAGCTATGCAGAGTTTGTTTGGTTCCTCATTTCAGAGGAGGACAAAAAGAACCCCACAAG[G/A]TAAAAAGGCAGATGCAAATGCTGCTGTCACCAAGTTTTACTTTAGATCAGCTTTGAGAACCTATGCTGTTACAGGTTAAGGTAATTAACATAAATCCCAAAATAAAAAAACTCATTGTTTAAACTGTTATTTTAGCTTATTTTATCTTTGAGTGGTATTGACGGTGGTATAGAATTTTCATTTTAAAGTTGTGTTTTTGTTAATGTATTAAGTTTTTATATGTATGTAGCATTAATTCATGTTTACCTTAATATTTATTTTTTTGTTTAGGTATTTGAGTTTTAAGTCACTACATTAAGAAAAATTACAAAAAGGTTTTGCTATCTTAAAATTAATAATTGCTTTGGAAACAATCAAATAAATAAGATTCAAAATTAGAATAAAATGTAATTAAAAATAAATCTTGATAGGTTTCTTTTTCAAACAAATAAAAATGAAAAAAAGCTCACAAACATGCTGAAACCATGAAAATAAAGTAATAAAAAAAAATTAAGTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9325
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 |
---|---|---|---|---|---|
ENSDART00000110922 | Nonsense | 1084 | 1141 | 14 | 15 |
ENSDART00000131977 | Nonsense | 461 | 520 | 12 | 13 |
ENSDART00000139080 | None | None | 716 | None | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 25437683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25633879 |
GRCz11 | 2 | 25289513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAATTGTAAGTGTGTGTGTGCGAATCAGGATTTGGATAGTGACGGTCCA[G/T]AGCCCTCAGACTGGGACAAGTATGCCTCTGAAGAGTATGAGATTCTTGTG
Long Flanking Sequence:
GAGGACACTGATATAGCATAATATCATTATAGTCATCATTTTTGGTGTGAATAAGCCTTTATTTCTTTTCATATCAGTTAAATGCTCACAAGAGAAAAAATGTGTAGGTACTACACATTTACTGAAATGTTTTGAATAAAAATGTGACATGCTGATAAATTGTTTACTTTGAATACTCTGAAATCTGCTTTGACTAAAAAGTAAATGAACGCATATGCAATTGTAAAGAACCGGTGACATATCTTGGCAGGTAAAATTACTCTTCGAGATCTGAAGCGCTGCAGGATGGCACACATTTTCTACGACACATTCTTCAATCTGGAGAAGTACCTGGACCATGAGCAAAGAGATCCCTTTGCAGTGCAGAAGGTACGAGTTTCCTGGGTTGCATCTATATCTAGATCCACTGTGCTGAATGTCATCTATGTTTGCACTCTGTGAGTGTGTTCAGTAATTGTAAGTGTGTGTGTGCGAATCAGGATTTGGATAGTGACGGTCCA[G/T]AGCCCTCAGACTGGGACAAGTATGCCTCTGAAGAGTATGAGATTCTTGTGGCAGAGGAGACAGCCAACGAACAGCTACGCGAGGGGTGAGTCAATGCGCTCTGTAATGGAATGAATTTGCTACAGACTTCACAACATTGCACAGCGCTGAGATACGGTCTATATGTGGCTGAATTTCATACGGTGGGAAGCGTAACTGTTGCGTGCTTGCTTTTGCAGGTCTTTCGATGACGATTACGAGTCCGATGAGCTCACAGTCTCCTCAGACATTGGAAATAAAATGGATAAGCTGGTCATATCTGATTTATCGGCATAATCTGCCGTTTTTTTGTCTACACACAGTGATGTTGAATGGAGAACCACCACGCCATATTTTCCCCTCACGTGTCAAAAAGGGAAAAAAGGAGAAAGTTTTTCTACGTTTCATTAAGGACAATTGTGTGTGTGTGCATGTGTGCAATAGAACTAATTCTAAAACCAAAAGGTTTCAGACACCCACAA
Associated Phenotype:
Not determined