ZMP
plcb3
Ensembl ID:
ZFIN ID:
Description:
1-phosphatidylinositol-4,5-bisphosphate phosphodiesterase beta-3 [Source:RefSeq peptide;Acc:NP_0011
Human Orthologue:
PLCB3
Human Description:
phospholipase C, beta 3 (phosphatidylinositol-specific) [Source:HGNC Symbol;Acc:9056]
Mouse Orthologue:
Plcb3
Mouse Description:
phospholipase C, beta 3 Gene [Source:MGI Symbol;Acc:MGI:104778]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21109 | Essential Splice Site | Available for shipment | Available now |
sa15031 | Essential Splice Site | Available for shipment | Available now |
sa9679 | Nonsense | Available for shipment | Available now |
sa41058 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12809 | Nonsense | Available for shipment | Available now |
sa15264 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21109
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 |
---|---|---|---|---|---|
ENSDART00000098563 | Essential Splice Site | 33 | 1244 | 1 | 34 |
The following transcripts of ENSDARG00000068246 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60827236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 60046201 |
GRCz11 | 7 | 60351438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCAATGAGGTCCTCAAACGGGGGAGCAAGTTTATCAAATGGGACGAG[G/A]TAAGAAGATCGCGTCCGTCTGTGATTGTTATGTGGCGTGATACTTGATCT
Long Flanking Sequence:
ACTTCCTTACTCCCCCCGTCGCTCTCTCCCTCTCTCTCTCCGTCTTTCTCGCGCTCCCATTTAGTTCGGAGAAAACATGAAGGAAAAGAGGAGCAAATTCCAGCGGGGACCAAAGCCAAGTGAAAGTTTCTCCTGAGCTGGGATCTCATCATTACTGAGCGGATGGACGGACAGGAAGGAAAATATCAATTCAAGTCCTTGCCGTGATAAGCGCTTAGATGAACAAACAATCGCCAAAGTCTTAAAGTGCGCCCGCTCGTGAATGTGTGACAGTCGCGTCCGCGTGTGTTGACCCAGGCGGACTCGAGGCGTTGGGTCAAGCTCTGGTTCCGTTGTTACACTGAAGGTCAGAAACTTCCAACCGAGAAGCTGAGGCGTCGCCACCCGTCGATTCAGCAGCCATGGCCGGGGCGAAACCGGGAGTTCACGCGTTGCAGCTCAAACCGGTGTCTGTCAATGAGGTCCTCAAACGGGGGAGCAAGTTTATCAAATGGGACGAG[G/A]TAAGAAGATCGCGTCCGTCTGTGATTGTTATGTGGCGTGATACTTGATCTGTGTTACACGTTGAAGTCATTTACAGTCAAACATCTGACACCCAGGACAGAGCTGGAGTTCAGCGCTGTTCCAAGTTTCGACTTCTTGTGCTCTGTTGATAAACACTCGACTTGTGTTTTATGTTTGCTGTTGTTTTCCCTTCATGGAACGACTTTTGAGTTGTGTAAATATTGGTTTATAATGGGGAAAACTGCCCGTTTTAAAGATACTATTTGTAAGAGCATGACATTCACGATTCGTGTCGCATATGGAACTTAACCCTTGCTAGGCTGATCTGTAGATCTGTTTTGGCAGATCATAAACACTGTTATTCAGGCCTGATTATCAGAAACATGATAATCATGACTCATGAAACCATGTTTGAGTTCGTGGCATTACTGTGTATTTTAGGGACATTAAAAGGAAAATGTAGGCTATTATCACTTTTTTTTACAAGCCATACAGTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15031
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 |
---|---|---|---|---|---|
ENSDART00000098563 | Essential Splice Site | 497 | 1244 | 14 | 34 |
The following transcripts of ENSDARG00000068246 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60759041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59978006 |
GRCz11 | 7 | 60283243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCATCCGACGCAAGGATGGGACAGAYGAACAGTCTTCACCTTTGAATGG[T/C]GTGTGTACACATGCWAGCATACCAAAATATAACCTMATCTGCTCCAGCAC
Long Flanking Sequence:
TTTTGCCATTGTGTATATCTTACCTTGGTTGTTGTTTTCTTTTAGAGCAAAGCAGCAGGCTAAAATGGCTGAATATTGTCGCTCAATGTTTGGGGATGCGCTGCTCATTGACCCACTGGACAAATATCCGGTGGGTTGTTCATCACCATAAAACCAAATTTATCAAACTTTAGTTGTCAGAAGTTTAAGACAATCTATCAATGTAAGTATGTAAGGAGCATGATGTCCAATGAACTTGATAGTTTGCGCAAAAATATAAAATGACAGATTGATCATAACCCAGAGTAAGTAATAATTGAAAATGACAGATTGATTTGGCCTTTATCATTGAGAGATCATGTTGTTTTTCAGCTGGTTCCTGGTCAACAACTCCCAAGCCCCCAGGAGCTGTTGGGGAAGATCTTGATCAAGAACAAGAAGAAACATCACCACAGGGCCTCTAACGGTGGGAGCATCCGACGCAAGGATGGGACAGATGAACAGTCTTCACCTTTGAATGG[T/C]GTGTGTACACATGCAAGCATACCAAAATATAACCTAATCTGCTCCAGCACAGAAGTGACTGTGATTTCAATGATCACAAAATGCATCAAAACAAATGTGATGATTATTTAAATGTTTATAGCAACTTGAGAACACGCATCATACTGTGTATCTATATATGATTTGGATGTGTGCATATAGAAATTAAGTTTGCACATTGAGGTACTAGCCAAGACATGAGCACAATGGTCAAACACTTTAGTTGAGCGTGTTTACAAGGAAAAATGAAAAAAACGGTAACTGTAATCTGTGTGAATGGCTTGTTAGAATGCACATCAGTGTTTCCTACATCAGCAGATCATGTTGTGTGTTGTTGGACAGGGCAACCTGTGATGTCCAATTAGTGTATTAGGCCCTCAAGAGCCAATTCCTATAATGAATCAAGCTTCTGATGCTGATGTGATTTTTATTCTAACAGCATTCTCACTCACTGAACAGTGAACAATTCCGTCACAGTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9679
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 |
---|---|---|---|---|---|
ENSDART00000098563 | Nonsense | 726 | 1244 | 21 | 34 |
The following transcripts of ENSDARG00000068246 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60750769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59969734 |
GRCz11 | 7 | 60274971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACAGATCATCTCAGGCCAGTTTCTAAATGATAAGAAGGTTGGTGTTTA[T/A]GTGGAGGTGGACATGTTTGGGCTTCCTGCAGACACTAAAAGGAAATATCG
Long Flanking Sequence:
CAGATGGTGGCACTAAACTTCCAAACCCTTGGTGAGACATGAACATAGCTGTTTTGTTCTTCATGGTTTGTCTTTAGCTGTTGTGCTTCATTTTTGCATAAGAATTCCTTAAAGTAGCTTTTACTCTGTTTCTCAGACCTGGCGATGCAGCTGAACATGGGGGTGTTTGAATACAATGGCCGCTGTGGCTATCTGCTGAAACCGGAGTTCATGAGACGCACTGACAAACACTTTGACCCCTTTACTACAGACATTGTGGATGGCATTGTAGCCAATACAGTTAAAGTCAAGGTATATTATTATTATTATTTATATTATTATTATTATTATTATTATTATTATTATTATAATTATATTTACTGTTTCAAACAACAGATGATGTGCGTTATTCTGCATTTTATATTTTCACATGTAAAATGTACAGTTTGATGACATCTAATTCCTTCACATACACAGATCATCTCAGGCCAGTTTCTAAATGATAAGAAGGTTGGTGTTTA[T/A]GTGGAGGTGGACATGTTTGGGCTTCCTGCAGACACTAAAAGGAAATATCGAACAAAAACTTCAAACAACAACTCTCTGGACCCAGTCTGGGATGATGAAACCTTTGTGTTCAATAAGGTTTGAAACTAAAGTAATATTTTACCCAAAATTTGCAATTCTGTCATGCACAAGCTTATGTGTATTCTTATGTAAAATGAATTGCATTTTGAAAAAGTATGTAATTCATTTCATTCTCTGTCTAGGTGGTGTTACCTACGCTAGCATCTCTGAGAGTGGCGGTATATGAAGAAAACGGAAAGTTTATTGGTCATCGTATCTTGCCAGTGTCAGCGTTGCGCCCAGGTGCCTATACATGGCAGTAATCTCGCTAGTCTGATACAGTAACAAACGTCTACTTGCTTGCAATAACTGTTGTGTTCGGTTATATGTGTGTGTGATAGGATATCACTACATCTGTCTAAAGAATGAACTGAACCAACCACTCATGCTGCCTTCCCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41058
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098563 | Essential Splice Site | 765 | 1244 | 21 | 34 |
The following transcripts of ENSDARG00000068246 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60750651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59969616 |
GRCz11 | 7 | 60274853 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACTCTCTGGACCCAGTCTGGGATGATGAAACCTTTGTGTTCAATAAG[G/A]TTTGAAACTAAAGTAATATTTTACCCAAAATTTGCAATTCTGTCATGCAC
Long Flanking Sequence:
TTTTACTCTGTTTCTCAGACCTGGCGATGCAGCTGAACATGGGGGTGTTTGAATACAATGGCCGCTGTGGCTATCTGCTGAAACCGGAGTTCATGAGACGCACTGACAAACACTTTGACCCCTTTACTACAGACATTGTGGATGGCATTGTAGCCAATACAGTTAAAGTCAAGGTATATTATTATTATTATTTATATTATTATTATTATTATTATTATTATTATTATTATAATTATATTTACTGTTTCAAACAACAGATGATGTGCGTTATTCTGCATTTTATATTTTCACATGTAAAATGTACAGTTTGATGACATCTAATTCCTTCACATACACAGATCATCTCAGGCCAGTTTCTAAATGATAAGAAGGTTGGTGTTTATGTGGAGGTGGACATGTTTGGGCTTCCTGCAGACACTAAAAGGAAATATCGAACAAAAACTTCAAACAACAACTCTCTGGACCCAGTCTGGGATGATGAAACCTTTGTGTTCAATAAG[G/A]TTTGAAACTAAAGTAATATTTTACCCAAAATTTGCAATTCTGTCATGCACAAGCTTATGTGTATTCTTATGTAAAATGAATTGCATTTTGAAAAAGTATGTAATTCATTTCATTCTCTGTCTAGGTGGTGTTACCTACGCTAGCATCTCTGAGAGTGGCGGTATATGAAGAAAACGGAAAGTTTATTGGTCATCGTATCTTGCCAGTGTCAGCGTTGCGCCCAGGTGCCTATACATGGCAGTAATCTCGCTAGTCTGATACAGTAACAAACGTCTACTTGCTTGCAATAACTGTTGTGTTCGGTTATATGTGTGTGTGATAGGATATCACTACATCTGTCTAAAGAATGAACTGAACCAACCACTCATGCTGCCTTCCCTGCTTGTGTACACTGAGGTACAGGACTACATTCCCAACGAGCACCAAGGTAGGCAAGGGATTTCAGGGATATCCAATACCATTTACATAACCTTCCCTCCTCCATCTGGCCTGCAACTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12809
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098563 | Nonsense | 779 | 1244 | 22 | 34 |
The following transcripts of ENSDARG00000068246 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60750485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59969450 |
GRCz11 | 7 | 60274687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTCTAGGTGGTGTTACCTACGCTAGCATCTCTGAGAGTGGCGGTATA[T/G]GAAGAAAACGGAAAGTTTATTGGTCATCGTATCTTGCCAGTGTCAGCGTW
Long Flanking Sequence:
AGTCAAGGTATATTATTATTATTATTTATATTATTATTATTATTATTATTATTATTATTATTATAATTATATTTACTGTTTCAAACAACAGATGATGTGCGTTATTCTGCATTTTATATTTTCACATGTAAAATGTACAGTTTGATGACATCTAATTCCTTCACATACACAGATCATCTCAGGCCAGTTTCTAAATGATAAGAAGGTTGGTGTTTATGTGGAGGTGGACATGTTTGGGCTTCCTGCAGACACTAAAAGGAAATATCGAACAAAAACTTCAAACAACAACTCTCTGGACCCAGTCTGGGATGATGAAACCTTTGTGTTCAATAAGGTTTGAAACTAAAGTAATATTTTACCCAAAATTTGCAATTCTGTCATGCACAAGCTTATGTGTATTCTTATGTAAAATGAATTGCATTTTGAAAAAGTATGTAATTCATTTCATTCTCTGTCTAGGTGGTGTTACCTACGCTAGCATCTCTGAGAGTGGCGGTATA[T/G]GAAGAAAACGGAAAGTTTATTGGTCATCGTATCTTGCCAGTGTCAGCGTTGCGCCCAGGTGCCTATACATGGCAGTAATCTCGCTAGTCTGATACAGTAACAAACGTCTACTTGCTTGCAATAACTGTTGTGTTCGGTTATATGTGTGTGTGATAGGATATCACTACATCTGTCTAAAGAATGAACTGAACCAACCACTCATGCTGCCTTCCCTGCTTGTGTACACTGAGGTACAGGACTACATTCCCAACGAGCACCAAGGTAGGCAAGGGATTTCAGGGATATCCAATACCATTTACATAACCTTCCCTCCTCCATCTGGCCTGCAACTGTCAACAAAAAATAACGAGATTCAGGCCCCTAAAACGTATGTTTTTTTAAATCACTATCATCATTGTCCAGTCGCATATCCACTTGTTAAGTTGTGACGTATGGATACTGTTTTTGGGTCCAAGCCGCTACTTATTTGAATTGAAAAAATATTTGTTTATGGTTTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15264
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 |
---|---|---|---|---|---|
ENSDART00000098563 | Nonsense | 796 | 1244 | 22 | 34 |
The following transcripts of ENSDARG00000068246 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 60750435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 59969400 |
GRCz11 | 7 | 60274637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KGAAGAAAACGGAAAGTTTATTGGTCATCGTATCTTGCCAGTGTCAGCGT[T/A]GCGCCCAGGTGCCTATRCATGGCAGTAATCTCGCTAGTCNNNNNNNNNAA
Long Flanking Sequence:
ATTATTATTATTATAATTATATTTACTGTTTCAAACAACAGATGATGTGCGTTATTCTGCATTTTATATTTTCACATGTAAAATGTACAGTTTGATGACATCTAATTCCTTCACATACACAGATCATCTCAGGCCAGTTTCTAAATGATAAGAAGGTTGGTGTTTATGTGGAGGTGGACATGTTTGGGCTTCCTGCAGACACTAAAAGGAAATATCGAACAAAAACTTCAAACAACAACTCTCTGGACCCAGTCTGGGATGATGAAACCTTTGTGTTCAATAAGGTTTGAAACTAAAGTAATATTTTACCCAAAATTTGCAATTCTGTCATGCACAAGCTTATGTGTATTCTTATGTAAAATGAATTGCATTTTGAAAAAGTATGTAATTCATTTCATTCTCTGTCTAGGTGGTGTTACCTACGCTAGCATCTCTGAGAGTGGCGGTATATGAAGAAAACGGAAAGTTTATTGGTCATCGTATCTTGCCAGTGTCAGCGT[T/A]GCGCCCAGGTGCCTATACATGGCAGTAATCTCGCTAGTCTGATACAGTAACAAACGTCTACTTGCTTGCAATAACTGTTGTGTTCGGTTATATGTGTGTGTGATAGGATATCACTACATCTGTCTAAAGAATGAACTGAACCAACCACTCATGCTGCCTTCCCTGCTTGTGTACACTGAGGTACAGGACTACATTCCCAACGAGCACCAAGGTAGGCAAGGGATTTCAGGGATATCCAATACCATTTACATAACCTTCCCTCCTCCATCTGGCCTGCAACTGTCAACAAAAAATAACGAGATTCAGGCCCCTAAAACGTATGTTTTTTTAAATCACTATCATCATTGTCCAGTCGCATATCCACTTGTTAAGTTGTGACGTATGGATACTGTTTTTGGGTCCAAGCCGCTACTTATTTGAATTGAAAAAATATTTGTTTATGGTTTTAGTCCCATCACACATTAAAGTGTATTTTACATAAAATCATGTAAATCAACAGT
Associated Phenotype:
Not determined