ZMP
ppp2r1b
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform [Source:RefSeq pep
Human Orthologue:
PPP2R1B
Human Description:
protein phosphatase 2, regulatory subunit A, beta [Source:HGNC Symbol;Acc:9303]
Mouse Orthologue:
Ppp2r1b
Mouse Description:
protein phosphatase 2 (formerly 2A), regulatory subunit A (PR 65), beta isoform Gene [Source:MGI Sym
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39041 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13079 | Nonsense | Available for shipment | Available now |
sa35873 | Nonsense | Available for shipment | Available now |
sa22634 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39041
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 |
---|---|---|---|---|---|
ENSDART00000016860 | Nonsense | 200 | 589 | 5 | 15 |
The following transcripts of ENSDARG00000032430 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 20710167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21812793 |
GRCz11 | 15 | 21748525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCTGCCTCCAAGCTTGGCGAGTTTGCCAAGGTTTTGGAGCTGGATTA[T/A]GTTAAGAGTGACATCATTCCTCTCTTTACAGCGCTGGCCTCTGATGAGCA
Long Flanking Sequence:
CGAGGCGAGAAAATCAGTTAAGTACTTAAAAATGATCAAATGAAATAAAGCTTTTCTAATTTGCTTTTCTGTTTGGGCCCTCCCAGCCTCCCCTGGAGAGTTTGGCCACAGTGGAGGAAACGGTCGTGCGGGACAAGGCCGTTGATTCTCTGCGTAAGATCTCTCAGGAACATTCCCCTGTAGACCTAGAGGTTCATTTTGTACCCCTAGTGAAGCGTTTGGCCAGCGGGGACTGGTTCACCTCCCGAACATCTGCATGTGGGCTGTTTAGCGTCTGTTACCCACGAGTGTCCAGTACTGTTAAAGCGGAGATTCGTCAGTAAGTTTAAATGATTTACTGTTTTATGTGACATTTGTTTCAGAATCACCTTCTTCAGGATTTATTATTGTGTTTGTGTTCACAGGCACTTCCGCACTCTTTGCTCTGATGACACTCCTATGGTGCGTCGTGCTGCTGCCTCCAAGCTTGGCGAGTTTGCCAAGGTTTTGGAGCTGGATTA[T/A]GTTAAGAGTGACATCATTCCTCTCTTTACAGCGCTGGCCTCTGATGAGCAGGTATGCTGGTGCACATTTACTGGAGGACAATTACTGGAGTTGTTTTTTTTCCCCCGGATCTAATTTAATATTATGATTTTTAAAATGTATTTAAAGGTGTCATGAAATTAAAATAAATTTGTTTTTAGATATTAGAATTGTTAGCTTTTAGGATATCTATAAGTTTGTTTGCTCCAAAACCGTGACAAAATTCGCATTTAGAAGATATAAAACTGATATAAACATGTAAAGCTTGTAGTTTGTCACCTCTGCCTAAATAGATCAGTGATTTTATTCATGTCTCTTATCAAATCATAATCAATCAAATGCTCTCTGGTATCTGATATGTCCCGCCCCCTTCAGGATGCTTTTCATTTGCTTTTCATTTGATGCCCTTGAGCTCAACCACTCTCACTGGTAGTTCTGTGTTAAAACAAAAATTCTATTGGCAATTTATTTTAAAGGGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13079
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 |
---|---|---|---|---|---|
ENSDART00000016860 | Nonsense | 291 | 589 | 7 | 15 |
The following transcripts of ENSDARG00000032430 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 20712584)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21815210 |
GRCz11 | 15 | 21750942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCCCAGAGATCACCAAGAACGATCTGGTCCCTGCGTTCCAGAACTTGT[T/A]GAAAGATTGCGAGGYAGAGGTCCGAGCCGCTGCTGCCAACAAGGTGAAAG
Long Flanking Sequence:
TTATTAAAGGTGACAGGTGCTAACGTTGTCTTAACTGATGTTCAACACACACAAATCTGCTAAAATCTCAAAGTATTTGAGGGTTTCTTGAACTTTTAAAACATGTAAATGGAGCAATCGATAGATTATATAGATCTATTTTCCCCCATTCTTATTTGCCATTGATCCAGACATTTTATTTTTGTCTGCAGGACTCTGTGCGTCTGTTGGCGGTAGAGGCTGGCGTCAGCATTGCCACTCTTCTGCCGCAGGAAGACTTGGAGGCTCTGGTCATGCCCACCTTACGTCAGGCCGCTGAGGACAAGTCCTGGAGGGTGCGCTACATGGTGGCAGACAAATTCTCAGAAGTGGGTACTTATGAAATGCACAATTGGCCGTTGTCCACATTGCCTCTGAGACTGCGACTCACTCTGGTTGTTTTTCTGTTTGTGAAAAGTTGCAAAAAGCAGTTGGCCCAGAGATCACCAAGAACGATCTGGTCCCTGCGTTCCAGAACTTGT[T/A]GAAAGATTGCGAGGCAGAGGTCCGAGCCGCTGCTGCCAACAAGGTGAAAGGTGAGGCGTCCCTCTGCCAGCTTCCCAATGCCCCCATTTTTTTCCCTCTCTGTCTGAAAACAACAACATTATCTCATGGCCTGTTTTTCCCTGCAGTATTCTGTGAAAATTTGCCTGAAGACAGCAGGGAGACCATCATCATGACTCACATACTGCCATGCGTCAAGGTACACATTTTAATCTCGATCCACTTGTTTCTGAAATTGCGTGTGGCTGAACAGTTATGCTGCAAGGTGCCGGCCAAGTTTTCAGGAGGGGGTACTTAGAAAACTCAAGCTTGTTTTCTTGATAATGTGATATCATATCTGGGAAGGTGTCCAGGTTGTCTCTGCGAGGGATCTGCAAGAGGTCTGCTTGTTTTTGTGTTATTTTGGGGGTGTTTACATCTTCACTATAAACAAGTTTGAGCTTTTCATAGCGGACAATAGTTTCATCTACACGCAGAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35873
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 |
---|---|---|---|---|---|
ENSDART00000016860 | Nonsense | 294 | 589 | 7 | 15 |
The following transcripts of ENSDARG00000032430 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 20712594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21815220 |
GRCz11 | 15 | 21750952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACCAAGAACGATCTGGTCCCTGCGTTCCAGAACTTGTTGAAAGATTG[C/A]GAGGCAGAGGTCCGAGCCGCTGCTGCCAACAAGGTGAAAGGTGAGGCGTC
Long Flanking Sequence:
TGACAGGTGCTAACGTTGTCTTAACTGATGTTCAACACACACAAATCTGCTAAAATCTCAAAGTATTTGAGGGTTTCTTGAACTTTTAAAACATGTAAATGGAGCAATCGATAGATTATATAGATCTATTTTCCCCCATTCTTATTTGCCATTGATCCAGACATTTTATTTTTGTCTGCAGGACTCTGTGCGTCTGTTGGCGGTAGAGGCTGGCGTCAGCATTGCCACTCTTCTGCCGCAGGAAGACTTGGAGGCTCTGGTCATGCCCACCTTACGTCAGGCCGCTGAGGACAAGTCCTGGAGGGTGCGCTACATGGTGGCAGACAAATTCTCAGAAGTGGGTACTTATGAAATGCACAATTGGCCGTTGTCCACATTGCCTCTGAGACTGCGACTCACTCTGGTTGTTTTTCTGTTTGTGAAAAGTTGCAAAAAGCAGTTGGCCCAGAGATCACCAAGAACGATCTGGTCCCTGCGTTCCAGAACTTGTTGAAAGATTG[C/A]GAGGCAGAGGTCCGAGCCGCTGCTGCCAACAAGGTGAAAGGTGAGGCGTCCCTCTGCCAGCTTCCCAATGCCCCCATTTTTTTCCCTCTCTGTCTGAAAACAACAACATTATCTCATGGCCTGTTTTTCCCTGCAGTATTCTGTGAAAATTTGCCTGAAGACAGCAGGGAGACCATCATCATGACTCACATACTGCCATGCGTCAAGGTACACATTTTAATCTCGATCCACTTGTTTCTGAAATTGCGTGTGGCTGAACAGTTATGCTGCAAGGTGCCGGCCAAGTTTTCAGGAGGGGGTACTTAGAAAACTCAAGCTTGTTTTCTTGATAATGTGATATCATATCTGGGAAGGTGTCCAGGTTGTCTCTGCGAGGGATCTGCAAGAGGTCTGCTTGTTTTTGTGTTATTTTGGGGGTGTTTACATCTTCACTATAAACAAGTTTGAGCTTTTCATAGCGGACAATAGTTTCATCTACACGCAGAAATATTGCTCATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22634
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 |
---|---|---|---|---|---|
ENSDART00000016860 | Essential Splice Site | 331 | 589 | 8 | 15 |
The following transcripts of ENSDARG00000032430 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 20712802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 21815428 |
GRCz11 | 15 | 21751160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACAGCAGGGAGACCATCATCATGACTCACATACTGCCATGCGTCAAG[G/A]TACACATTTTAATCTCGATCCACTTGTTTCTGAAATTGCGTGTGGCTGAA
Long Flanking Sequence:
GCTGGCGTCAGCATTGCCACTCTTCTGCCGCAGGAAGACTTGGAGGCTCTGGTCATGCCCACCTTACGTCAGGCCGCTGAGGACAAGTCCTGGAGGGTGCGCTACATGGTGGCAGACAAATTCTCAGAAGTGGGTACTTATGAAATGCACAATTGGCCGTTGTCCACATTGCCTCTGAGACTGCGACTCACTCTGGTTGTTTTTCTGTTTGTGAAAAGTTGCAAAAAGCAGTTGGCCCAGAGATCACCAAGAACGATCTGGTCCCTGCGTTCCAGAACTTGTTGAAAGATTGCGAGGCAGAGGTCCGAGCCGCTGCTGCCAACAAGGTGAAAGGTGAGGCGTCCCTCTGCCAGCTTCCCAATGCCCCCATTTTTTTCCCTCTCTGTCTGAAAACAACAACATTATCTCATGGCCTGTTTTTCCCTGCAGTATTCTGTGAAAATTTGCCTGAAGACAGCAGGGAGACCATCATCATGACTCACATACTGCCATGCGTCAAG[G/A]TACACATTTTAATCTCGATCCACTTGTTTCTGAAATTGCGTGTGGCTGAACAGTTATGCTGCAAGGTGCCGGCCAAGTTTTCAGGAGGGGGTACTTAGAAAACTCAAGCTTGTTTTCTTGATAATGTGATATCATATCTGGGAAGGTGTCCAGGTTGTCTCTGCGAGGGATCTGCAAGAGGTCTGCTTGTTTTTGTGTTATTTTGGGGGTGTTTACATCTTCACTATAAACAAGTTTGAGCTTTTCATAGCGGACAATAGTTTCATCTACACGCAGAAATATTGCTCATGCAATTATATCTTGTTTAGTTTGCTCTTTTAATTAGGACATCATGAGCAGGTAAAATTAGACTGTCCACCCATGCAGAGGTCATGAGCAGCAGGGGTCACTGTTGTTATTTGTTATGGTTAGTGATTCGTATTTATTTATTTATTTAATTGCAATAACAAGCAATTACAATGAAAATACAGCAGAATAAGTATAATACAAACAACGCAAAA
Associated Phenotype:
Not determined