ZMP
ppp6r3
Ensembl ID:
ZFIN ID:
Description:
protein phosphatase 6, regulatory subunit 3 [Source:RefSeq peptide;Acc:NP_955978]
Human Orthologue:
PPP6R3
Human Description:
protein phosphatase 6, regulatory subunit 3 [Source:HGNC Symbol;Acc:1173]
Mouse Orthologue:
Ppp6r3
Mouse Description:
protein phosphatase 6, regulatory subunit 3 Gene [Source:MGI Symbol;Acc:MGI:1921807]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16892 | Nonsense | Available for shipment | Available now |
sa18514 | Essential Splice Site | Available for shipment | Available now |
sa38016 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45846 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16892
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 |
---|---|---|---|---|---|
ENSDART00000021497 | Nonsense | 111 | 396 | 4 | 12 |
ENSDART00000129682 | Nonsense | 111 | 902 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 25 (position 10832760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10524811 |
GRCz11 | 25 | 10621617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGGCTGGGTGAAGATGAAAGTTTACTGATGAAACTCTACAGCTTCYTA[C/T]AGAACGAGCCTCCGCTCAACCCACTGCTGGCCAGTTTCTTCAGCAAAGTC
Long Flanking Sequence:
TATTCAAAAAGAATTTATTATGAAAGGTTGATTATGCAGTGGGAGTGCATCTGCATAAAATCTAATAAGCAAACTATGAATCCAATAAAGAAAAAGATACAGTTGAAATAAACTGTTTTATCGTTCTCCAAGTCTATCAGTATTCAGGTACAGTAATTGAAAATAAGATTACTCGTTATTAACGTTAAAAATGATAGAATTTTTTAATCTTTATACAATCACAGGCTTCAAAAACACATGCAACTGTTAAATTATAGTACAAGCTCAACATTGCATATCCTGCAGTGTGACCATTGCGATATCGATGCTGAAAGGATATATTGTGCAGCCCTAGTTTGTTGTCTAATTTGAAGCATGTGAGATTTATTAATTGTTGTTTTGGATTGTTGTGTTAAAGGTATCCCAACATATCCTGTGAACTCCTGACCTCAGACGTTGGCCAGATCAACGATAGGCTGGGTGAAGATGAAAGTTTACTGATGAAACTCTACAGCTTCTTA[C/T]AGAACGAGCCTCCGCTCAACCCACTGCTGGCCAGTTTCTTCAGCAAAGTCTTGAGCATACTTATTGGGAGAAAACCAGAGCAGGTGCGTGCCCAGACAGGTTATGCCAGTCCCTCCAGAATTTTGTGACCAAAAAAAATTTTTTTGTGACTAAAATGACTCTGATTTTTCCAAAAAAAAAAAATGCCTTTAATAATAAATTTATTATAGTTTTGCTGTGAAAATATACACAAATTTGCACATCTAAATTAATCCTTTTTTTTTTTGACCTTCAAGAACCATTGATCTCTTTTATATATAACGGAAACACTGAGCGAACTAAAGCCTGCTCTATCATATTGGAAAATTAAACCAATTGTTTGAAAATAAATGCTAAGTAGTCTATTTTTTTGGCAGCAATTTATTTATTTTTTATAACCCTTTTTTTTTTTCATTGAGAAAAAAACCTACATACATACAGTACCGCTCAAATCCTGACAAGAAAAAAATTGACCATATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18514
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 |
---|---|---|---|---|---|
ENSDART00000021497 | None | None | 396 | None | 12 |
ENSDART00000129682 | Essential Splice Site | 451 | 902 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 25 (position 10826388)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10518439 |
GRCz11 | 25 | 10615245 |
KASP Assay ID:
2261-9428.1 (used for ordering genotyping assays)
KASP Sequence:
AGTTAATACAAAGAATTCTTGATGCCTGGGGWWCAAACGACAARGAGCAG[T/C]GAGTAACTCTTAAATCTGATYGGTCKGTTATGTTTAATTTAAAAGGAACC
Long Flanking Sequence:
GTCATACTAGTGAGTGTTTTGAGAGTTCTGTGTAATGTTTGCAGTGTGGAAAAACTAGTGGTTAGCCATGGTTTTTCAAAAACACAATAAAAAATGAAAACAGCAATTAAGTAAGCATCTAATTATTTTGTTGCCTATATTTTCGTGCACATCACATACTTGACTTTTTTTTTAATCTACAGGACATGTACTTTAAATACTTATGGAATAATTTCCTGCACACACAAGTAGAAATCTGTACAGCGATGGTCTTAGCGATGCCTTCAACCCAAAGTGAATCTCCCGAAATCAACAGAGAAAACGACCAAGAGCCCATACGAGAAAACATCCTTATCAAACATGTGAGTTCATCATCTGTTCCCGCTGTTTGAAACCCAAAGCTGTTAGCATCGCACATTAAACTTTAATGCAATCTTCTCTGTTCTGACCCGCAGCTCTTTCAGAAGTGCCAGTTAATACAAAGAATTCTTGATGCCTGGGGATCAAACGACAAGGAGCAG[T/C]GAGTAACTCTTAAATCTGATTGGTCGGTTATGTTTAATTTAAAAGGAACCATCCTATTTTGTACACCTGGTCTTGTATGATGAAGTCTTTAATGAATCCTTCATATTTATTTGTTTTTCTCCAATCAGGACTGAGGGTGGGCGACGGAGAGGTTACATGGGTCACCTGACCAGAATAGCAAATTCTATAGTGCACAACAGTGACAAGGGCCCCAATGGGTCACAAATTCAGCAGCTCATCTCAGGTCTGTCTATTGGTGCGTTCACACCAGATGTGGAGTGTTTTACATGTTAAAGGGCACCTATGATGAAAATCTACTTTTGGAAGCTGTTTGGACAGAACTGTGTGTAGGTATAGTGTGTCCACTGTCGTACTGGGATGATATAAAGACAATAAGTCCTTTTTTTTTTATTCTGATGTTAAAATAAAATCCAAATGAATATTTGTTGATGGACTGTGCGTGACGAAGGATTTGGGGTGAGAAGGGTGCGTGATATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38016
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 |
---|---|---|---|---|---|
ENSDART00000021497 | None | None | 396 | None | 12 |
ENSDART00000129682 | Nonsense | 759 | 902 | 19 | 23 |
Genomic Location (Zv9):
Chromosome 25 (position 10820966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10513017 |
GRCz11 | 25 | 10609823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCATAGAGACGGTGGACCCTCTGGGAGTCAATGCGCCTATGCAGCAA[G/T]AAAGTAAGAATAGACTCTTACCATCCTCATTTCAATTTCGACACACACTC
Long Flanking Sequence:
ATTAGCATCAAAGCCTAAAAGGGGCAGATTCAACAATTTGTAAAACATTATTTGTGTGGTATTTTGGACTGAAACTTCACATACACACTCTTGGGACTTGTTACAGTCAAATTTTTGATGGTCGTTAATTTTTTTTTTTTACTTTGCTCAGAACAAAATTCATTTCCATTTTAATTCGCTCAGAACAAAAAGTTCAAATTGGACACATTTAATGAACAGGAAAGACATAAAAGCTGTTATACTTGCTGTTTTGACAAATAAAATAATTTTAAGCTGAATTTAAATATAAGTAGTTTATTGGACATTATGATACAGCTTGTTTGTACCCACAATACCAAATATGTAATGCAGCTCTAAACATGTAAATGTGGAAAGTTCGTTAATTTCATTTTCATCCTTTAATTAGCCCTAAGGATCCCTTGAGGTGCAATTCCCCTGTAGCCATGGAGACCAGCATAGAGACGGTGGACCCTCTGGGAGTCAATGCGCCTATGCAGCAA[G/T]AAAGTAAGAATAGACTCTTACCATCCTCATTTCAATTTCGACACACACTCGCACAGATGTTAGAATAAACAATCTTATTGTGCAGATACAGATCAGTGGCTTCCCAATGAGACCACTCCAACTTCCCCCAGAGGGAAAACAGGGGACGCCTCTGACCCCGAAGAAGAGCCTGTCAGTGACCGCATCACAGAAACAGTCACCAACGGCTCTATGAAGGAGACGGTCAGCCTTACTGTAGACGCCAAAACTGAAACTGCTGTTTTCAAAAGGTGAGTCCCAGAGCTTTTTACTCATGCAGTGCCACACATCACTTCCTCTTCCTCCCCTTTGAGACACAAGCTTCACTTCACTCTGCATGTAGACCTGATCTTTCCCTGTCACGTTATCCTCCTGTTCCTCCTGCACCTACAGCCAGCCAGACCCCGGAACTCTCTCTTTTTTTTATTTATTTGTTTGTTTTTCCTTTTAAACGGGGGCTGTTAAGATGCAGAGCTTTGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45846
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021497 | None | None | 396 | None | 12 |
ENSDART00000129682 | Nonsense | 826 | 902 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 25 (position 10817565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10509616 |
GRCz11 | 25 | 10606422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTTAAAACGCTGTCCTCTCTGATCATCCTGTAGTGAGGAAGAGAAA[C/T]AGTCTACCTCTGAAGACGCATCTGCAAAGTTGTTTGTTGCAGAGAGTGGG
Long Flanking Sequence:
ATTAATTTCTTCACATACAGTGATCTAAAACAATAACAAAAAATATAACAATCAAAAGGCTCATATAAAAAATGTTTGATACAAATATATGTACCATTGCACCCCTAGTTTCTACCGAACTCTAATTCATGGGTTTACTGATGCCATCCTAAAAAGTGAAGACTGCTGGCATGACTTTGACTTTTCACCATCATTTCGCACTCACATACTAAAGCAGCTCATCGTCTAATCCACTTGTTGTGTGGTTAATAGTCACTCCCGTCTCTGTTCGTCGTTCTGCTCACATCTTATTGTCCGCCAAACCCCATTTCAGAACATTTATTTCAATGTTTTTATTTATTTTTTTGGTTTTGCCCTGTTGCTTTCAGTGTGGTCCGTTCCATTCTGCATGTGTTGTCCAAGGGTTTAAAGTGGGGGTTTTAATTCTGTAAGCGAACTGCAATGAAAGCTGTTTTTTAAAACGCTGTCCTCTCTGATCATCCTGTAGTGAGGAAGAGAAA[C/T]AGTCTACCTCTGAAGACGCATCTGCAAAGTTGTTTGTTGCAGAGAGTGGGGACGCGGAGAAGAGCAATTGTCCTTCTAGCAACTGTCAGAAACCAGGGTGAGTCTTCATTGTATTGTAAGCAAGTAAAAAGTGTTAAGGCTGGTTTATACTTCCACGTCGAGTGATCTGCGTGACCCACGGCGCATGCCTTGCACTTAGTAGTGCATTCATACTTCTGTGTGCTGTTTGTGTTGCTCTGCAAAAACACTTCCAAAACTCTAGCTGGCATTAGGTGATGTTTTTTCTAAACGCTACAAGTAGCTAAAACTCGCTCATTCAGATGCGGAAACAACATTAATCATAAGGTAAACACAAAACAACAGTTTCCATCTGGAGCTCCTTCACAGGACTCAACACTTGTAAATGCTCGCTTCATCTGGCCCACACTTGTCATCAGTACCAATCAGACCAATCACAGAGTTTGTAGTTACATTTTTTGAGAGGTGCGCGTCAGCCACGA
Associated Phenotype:
Not determined