ZMP
si:ch211-269e2.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate protein phosphatase 2 (Formerly 2A), regulatory subunit B family
Human Orthologue:
PPP2R3B
Human Description:
protein phosphatase 2, regulatory subunit B'', beta [Source:HGNC Symbol;Acc:13417]
Mouse Orthologue:
CAAA01108492.1.1364.1
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45364 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14604 | Nonsense | Available for shipment | Available now |
| sa21534 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45364
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 |
|---|---|---|---|---|---|
| ENSDART00000113656 | Nonsense | 310 | 583 | 7 | 13 |
| ENSDART00000114043 | Nonsense | 236 | 462 | 7 | 12 |
The following transcripts of ENSDARG00000076004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 35463098)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34682609 |
| GRCz11 | 9 | 34491794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGTTGTGTAATGATGAAAATGGTTGCCTGCAGAATGTGGCACTTCTT[G/T]AAGAGGATGAAGAGATTAACCAGTTGACAGAGTTCTTCTCCTATGAACAT
Long Flanking Sequence:
TTACACTCTAGTGACGTGTCTCTGTCAACCAATAGCATTCAGTTACATGTCTAGCTCCGTCTTTTGGCACCCTTTTCTTGTGCTAGGTACCCTTTGCAAAGGTAACTAAAAAGTGGTACGGTACGTTTCACTTTTTGGTACTTTTGACGGTTGAAACAGCCATAAATGAACTTCAAATGGTTTCAGACCTTTTTGAATTTATTTTAGTTCATCTTGATATTATTAAGGATGTCTGAATGTAAATACAAAATATAATGATATAATGAAGAATGTCGGAAATCCTAAGCTATTGCCATCCATAGTAGAAAAAAATTTCTACCGGTTTCCAACATTTTTTCAGGGGAAAAAAGAAACTCAAACAGGTTTAAAACCAGCTTGGAGAAAATGAACACCACATTTTTTTTATTGGTGTTCTGGTGTCTAGATGATTGAAAACCGCTGATTTACCTTTTGTGTTGTGTAATGATGAAAATGGTTGCCTGCAGAATGTGGCACTTCTT[G/T]AAGAGGATGAAGAGATTAACCAGTTGACAGAGTTCTTCTCCTATGAACATTTCTATGTCATCTACTGTAAATTCTGGGAGCTGGATACAGATCACGACCTGTACATTGACCAGAGAGACCTAATGCGGCATAATGATCAAGGTGACCGTCCAGATGCTCACACTCTTTTGACATGCTCTTTAATGATTGGCTGCTTTATTGCTGGAGGTGTCGTTGAATTTCCGTCCTCTCCAGCAGCACTTGACTGCATATGTTTCTGTTTGCAGCAGTATGAGTTTACTGAGCTGAATGAAGTGCGGTCAAATTTTAACATCAATTTCCTCTAGAATGACGCCATGTCTGGCACTTTAATCATTTTATCTCCTTTTAGACAGGGTCAATAATGGCTGTGTCTTTTAAAATGATAAAATAAGGACATTAAATCATTTTGTTACTGTGCAGCATGCAAGATTTGCAACCTTTGACTGCAAATTATTGGAATGTTTAAGAATATGTCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14604
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113656 | Nonsense | 324 | 583 | 7 | 13 |
| ENSDART00000114043 | Nonsense | 250 | 463 | 7 | 12 |
The following transcripts of ENSDARG00000076004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 35463054)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34682565 |
| GRCz11 | 9 | 34491750 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCTTGAAGAGGATGAAGAGATTAACCAGTTGAMAGAGTTCTTCTCCTA[T/A]GAACAKTTCTATGTCATCTACTGTAAATTCTGGGAGCTGGATACAGATCA
Long Flanking Sequence:
ACATGTCTAGCTCCGTCTTTTGGCACCCTTTTCTTGTGCTAGGTACCCTTTGCAAAGGTAACTAAAAAGTGGTACGGTACGTTTCACTTTTTGGTACTTTTGACGGTTGAAACAGCCATAAATGAACTTCAAATGGTTTCAGACCTTTTTGAATTTATTTTAGTTCATCTTGATATTATTAAGGATGTCTGAATGTAAATACAAAATATAATGATATAATGAAGAATGTCGGAAATCCTAAGCTATTGCCATCCATAGTAGAAAAAAATTTCTACCGGTTTCCAACATTTTTTCAGGGGAAAAAAGAAACTCAAACAGGTTTAAAACCAGCTTGGAGAAAATGAACACCACATTTTTTTTATTGGTGTTCTGGTGTCTAGATGATTGAAAACCGCTGATTTACCTTTTGTGTTGTGTAATGATGAAAATGGTTGCCTGCAGAATGTGGCACTTCTTGAAGAGGATGAAGAGATTAACCAGTTGACAGAGTTCTTCTCCTA[T/A]GAACATTTCTATGTCATCTACTGTAAATTCTGGGAGCTGGATACAGATCACGACCTGTACATTGACCAGAGAGACCTAATGCGGCATAATGATCAAGGTGACCGTCCAGATGCTCACACTCTTTTGACATGCTCTTTAATGATTGGCTGCTTTATTGCTGGAGGTGTCGTTGAATTTCCGTCCTCTCCAGCAGCACTTGACTGCATATGTTTCTGTTTGCAGCAGTATGAGTTTACTGAGCTGAATGAAGTGCGGTCAAATTTTAACATCAATTTCCTCTAGAATGACGCCATGTCTGGCACTTTAATCATTTTATCTCCTTTTAGACAGGGTCAATAATGGCTGTGTCTTTTAAAATGATAAAATAAGGACATTAAATCATTTTGTTACTGTGCAGCATGCAAGATTTGCAACCTTTGACTGCAAATTATTGGAATGTTTAAGAATATGTCTGTGATGTAAATTGTCTGTTGTCTTTGACAGCCATTTCCCACAGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21534
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 |
|---|---|---|---|---|---|
| ENSDART00000113656 | Nonsense | 569 | 583 | 13 | 13 |
| ENSDART00000114043 | None | None | 463 | None | 12 |
The following transcripts of ENSDARG00000076004 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 35456397)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34675908 |
| GRCz11 | 9 | 34485093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTGCACAGTGAGAAGAGACATCTGTTCGGGATCCCCAGCCCTCACTG[C/A]AACCTGGATCTGGATGAATATGAATACGAGGACGATTTCGAATGAGGAGC
Long Flanking Sequence:
GTTACGTCAAACTGACCACTTCTGAGATGGTCATTTTACTAGTAGCTACCTGTTGTTTTTTGGCCACAAACTAGTTTTATCTGCCAGTGCCGGTAGCCTAGTGTGTTGACATATAGTGCAACTGTGCTACAGGTGTCCTGACTTCCAGACCCATCTCTCTCCCACTTCACTTCCTGTCAACATACTGTCCTGTCATAATAAATGAATAATATATATGAGCATGAGCTATATCAGAAATCACCCTATACCCTTTAATAGTGCACTATTTGAGGGAGCAGCCATTTGTTGTAGTGTATGGCAACAAAAAGTATTGCCAAGTATTGAAGATGTATTTTCTTTTAGATATTTACTTCCAGAACCCAACTCTTCTTGCATTTTGTTACTAACAAACGTTTTGGTTTCAGGTACGACAATATTTTAGACCCGGCGGATCACGTGACGAGTGCATTAGAGCTGCACAGTGAGAAGAGACATCTGTTCGGGATCCCCAGCCCTCACTG[C/A]AACCTGGATCTGGATGAATATGAATACGAGGACGATTTCGAATGAGGAGCACACGAATAAATAAAGCATCATCTGGTAGTGTGTAGAACCCATCCTGCTCTCACACACCTGGTTCAGCTATCCCAGGCTAAAGAGCGATGCGGATGCACTCCTACAGGCCGCTGGATGCCGGACAGCAAACAGCAGCCAGAGACGGATTGTGCTGGTCCAGGTTTTCTGTCAGTCTGCGCACAACCAGCTTTCTAAAACCAAATGTAGCAGCAACTACACTGGAAGCCAACCACAACACTTGAAATATTGATTCTGCACTAAACATTGAAGATTTTAATGCTGGTGAGACATTCCAGAAGATTGATGATTTCAGCTTGATGGCTTCTTTCTCCTGGAGCTTTGTCCACATGCTGTGTGTGTGTGTTTGTGTTTGAGGGTCACGCTAATATGAAGTAATGCAGTAATCAGACTCTGATGTTTTACTGTGTCTGTGTGAGAGGTTTATAAGT
Associated Phenotype:
Not determined