ZMP
PLCE1 (1 of 2)
Ensembl ID:
Description:
phospholipase C, epsilon 1 [Source:HGNC Symbol;Acc:17175]
Human Orthologue:
PLCE1
Human Description:
phospholipase C, epsilon 1 [Source:HGNC Symbol;Acc:17175]
Mouse Orthologue:
Plce1
Mouse Description:
phospholipase C, epsilon 1 Gene [Source:MGI Symbol;Acc:MGI:1921305]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35206 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6233 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35205 | Nonsense | Available for shipment | Available now |
sa38872 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35206
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124097 | Essential Splice Site | 552 | 1157 | 13 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 6408577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5342748 |
GRCz11 | 12 | 5377705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCGTGACCTTACATATGTGTTTGTTTGTGTTTGTGTGCGTGGGAACT[A/G]GGCCTCTCCACCCTCTCTCCATCAGGCTCTGGAAGGGGGAAAGACAGAAA
Long Flanking Sequence:
TATTCAGCTTAGTAACATTTAAAGACTTAACTAGGTTAACTAGTCAAGTTAGATTAATTAGGCAAGCCATCGTATAACAATGATTTGTTCTGTAGACAATTGAAAAATAAATATTGCTTATAATAATACCCTTAAAATTATATTTGAAAAATTTAAAACTGCTTTTAATCTAGCTGAAATACAACAAATCAGATTTTCTCCAGAAGAAAAACTATTATAGGAAATACTGTGAAAAATTCCTTGCATAGTTTGGGAAATATTTAATTAAATAAATTTAATTTCTAATAATTCTGACTGTATATTTATGCTGCGTGTCATTGTAGAATTTGCTGAATTAGTGGAAAAGGGCCGTTAAATGAGATTCAGGTGTTGGGTTTTGCTGGAAACTGTAACAGTCCCAGAGGCGAGTCTTGAACAAACAAGCAGAGTTCTGGAGGAGCGTTTACCCGGCAGCCGTGACCTTACATATGTGTTTGTTTGTGTTTGTGTGCGTGGGAACT[A/G]GGCCTCTCCACCCTCTCTCCATCAGGCTCTGGAAGGGGGAAAGACAGAAAGAGCCGGAAATCCATCTTTGGCAGCGCTCCTGCTCGCGGGAGCCCCGGGGAGCCTGTGACGCTGGTCCGAGCTCCAGGGAAAGGTACGTTCGCCTGGGTTTTTTTATTTTTTTTTTTTTGCACAGGGCACGCAGGAAGCAGAACACCCACTTAGAGCACCCATGGGGAAAGAGCTCTCAAGTTTTCCATTATTTTGAAGTCCCTCGAAAGCACATAAAAATGCCTTTCTACAGAATATTTCCAGTGGCTGGCTGTCTGAGAAAACAAGCATGTGCTTTTTAAGAAGCAGCACTTTTGGAGGGCAAGTGGCTCTATGCTCTGAAAGCCTTAATGGATGTGAACTTCCTTCCAATCCAGCAGAAGCGTATCTGCCCTTTTGATCAGTTTATTTTTATTTCATTTATAGTTCAAACCCGTTTTATTTAACTTGCTCTCATCTCTTTCCATAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6233
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124097 | Nonsense | 729 | 1157 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 6405709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5345616 |
GRCz11 | 12 | 5380573 |
KASP Assay ID:
554-4591.1 (used for ordering genotyping assays)
KASP Sequence:
AAGCCTCCAGTCCTGTGGGACAGAAGCTGTCCTCTCTATCAGCACTTTTA[C/A]CCTCTGGACCGAGACCTGGAGAACATGACCCCAACGCTATACACACTCAC
Long Flanking Sequence:
CTGGTTTCTTTTGTCTTTGGCATGATGACAGCACATACTATTTAACTAGATATTTTGCAAGATACTAGTATTGAGATTCCAGTTTAAAGACATAACTAGGTTAATATTTTTATCCATTTCTTAATAAATATAGTCAATAATATTTGGTGCATTTAAACAAATCAGTTTTATAAAATATATATGCATTAAAATAAAAGTTTGGTCATCAATAAAAATCTTAAGGAATATATATATAGATATATATATAATATATATATAGATATTTGTTATTCTTCTGGTCATTTAAAGTTATATAGTGTCTTTCCCAGTTGATGTTCACCTGTCTATAAATTTAATTCAGTGATGCGCTTTAAAAGTAAGGGTATTTGTTTGATATGTTCTCCTCTAGATCTGCCGATGCAGCTGAACGCGGCTCTATTCGAGGCTAATGGTCACTGTGGTTTTGTGCTGAAGCCTCCAGTCCTGTGGGACAGAAGCTGTCCTCTCTATCAGCACTTTTA[C/A]CCTCTGGACCGAGACCTGGAGAACATGACCCCAACGCTATACACACTCACTGTAAGAATACACACAAACAGCGGCGTAGTGCAACCCCAGGTGAAAGGATGGGGGAGGAGGGGGTGTATGAGACACCTGTGATTGCTGTTGATATATTTTTGCCACTCTACAAAATCCAACATTGGTTATTGTTTACATGAACACCAGTGTCCTAATTATTTACACAATTGATCATATATGCATACAGTTAATCTCGTATTATCATACCATATGACAGCTGCAGTAAAGGGATATTTTACTCAAAAATGAAAATAATATCATATTTTACTCACCCTTTACTTGTCCAAAACCTGTTTGAGTTTCTTTCTTTCAGCTGAACACAGCAGAACATATTTTGAAGAAAGCTGGAAACCTGTAACCATTGAAAATTGCTCGCAAATTTCTAGATATTTTTGAGATAATTTTCATCAAAATATCTTCTTTTTTTGTTCATCAGAAGAATCTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35205
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124097 | Nonsense | 736 | 1157 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 6405690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5345635 |
GRCz11 | 12 | 5380592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAAGCTGTCCTCTCTATCAGCACTTTTACCCTCTGGACCGAGACCTG[G/T]AGAACATGACCCCAACGCTATACACACTCACTGTAAGAATACACACAAAC
Long Flanking Sequence:
GCATGATGACAGCACATACTATTTAACTAGATATTTTGCAAGATACTAGTATTGAGATTCCAGTTTAAAGACATAACTAGGTTAATATTTTTATCCATTTCTTAATAAATATAGTCAATAATATTTGGTGCATTTAAACAAATCAGTTTTATAAAATATATATGCATTAAAATAAAAGTTTGGTCATCAATAAAAATCTTAAGGAATATATATATAGATATATATATAATATATATATAGATATTTGTTATTCTTCTGGTCATTTAAAGTTATATAGTGTCTTTCCCAGTTGATGTTCACCTGTCTATAAATTTAATTCAGTGATGCGCTTTAAAAGTAAGGGTATTTGTTTGATATGTTCTCCTCTAGATCTGCCGATGCAGCTGAACGCGGCTCTATTCGAGGCTAATGGTCACTGTGGTTTTGTGCTGAAGCCTCCAGTCCTGTGGGACAGAAGCTGTCCTCTCTATCAGCACTTTTACCCTCTGGACCGAGACCTG[G/T]AGAACATGACCCCAACGCTATACACACTCACTGTAAGAATACACACAAACAGCGGCGTAGTGCAACCCCAGGTGAAAGGATGGGGGAGGAGGGGGTGTATGAGACACCTGTGATTGCTGTTGATATATTTTTGCCACTCTACAAAATCCAACATTGGTTATTGTTTACATGAACACCAGTGTCCTAATTATTTACACAATTGATCATATATGCATACAGTTAATCTCGTATTATCATACCATATGACAGCTGCAGTAAAGGGATATTTTACTCAAAAATGAAAATAATATCATATTTTACTCACCCTTTACTTGTCCAAAACCTGTTTGAGTTTCTTTCTTTCAGCTGAACACAGCAGAACATATTTTGAAGAAAGCTGGAAACCTGTAACCATTGAAAATTGCTCGCAAATTTCTAGATATTTTTGAGATAATTTTCATCAAAATATCTTCTTTTTTTGTTCATCAGAAGAATCTCAAAAAGGTTCAAAACCACTACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38872
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 |
---|---|---|---|---|---|
ENSDART00000124097 | Nonsense | 976 | 1157 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 6397492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 5353833 |
GRCz11 | 12 | 5388790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGCCTGAGGACGGATATGTGGGCAGAATATACCTCAAAACCAGAGAA[C/T]AGGTAGAACAAAAGCTTTCCCAGATTCTGCTTACTTACTTTTTATGTAAG
Long Flanking Sequence:
AGGGTGGGCCATTTATATGGATACACCATAATAAAATGGGAATGGTTGGTGATATTAACATCCTGTTTGTGGCACATTAGTATATGTGAGGGGTCAAACTTTTCAAGATGGGTGGGGACCATAGTGGCCATTTTGAAGTCGGCCATCTTGGATACAACTTTTGTTTTTTCAAAACGAAAAGGGTCATGTGACGCAAATTATGTTTTGTGTGTGTGTGTGTGTGTGTGTGAATTATCCTTTTTTTATTAAGTATTGATTTGTAGTTAATGTTTTAAGCTGTTAAAATAAAGATAGAAAGATTAAACATCTCTGTCTTTCTCCAGCTGTTTCCGACTGCCTCTTTTAAGTATATGCTGATGGAGGAGAGAGTGTCTCTGTCGAAGGAGAAGAAGGCTCCTCAGCAGCGTCCTCTAGCCAATGATGAGAGACTGCTGAAGCTCATTCACAGCTGGCAGCCTGAGGACGGATATGTGGGCAGAATATACCTCAAAACCAGAGAA[C/T]AGGTAGAACAAAAGCTTTCCCAGATTCTGCTTACTTACTTTTTATGTAAGGAACGTTCCTGTTGTGCAAAAATCCTGCAATTTACCTACCCGCAGTTTAAATTAATTGTTTGTTTTCTACTTTAATATATAGTTTAGTGTTTTTAGCATCATTACTCCAGCCTTCAGTCACATCATTCCTCACGAATCATATTGTAATTTGTTGATTCTCTGCTCGGTGAGCATTTAGATCATATTTAATATGTAATATTTTTGTATAGTTCATATATAATAATATTTTAGGGATGATACTTTTTTTTCCAGGATTGTTTAATCAATAGAAAACTCAAAATAACCTTCATTTGAAGCCAAAAGCTTTAAATGTTAAAGCATAGAATAATTGTAGTATAAAAGCTTTATTTAGGTAATAATAATAATAATATATCAAAATCTATATACACAATATATAATGTAATATAAAAACAATGATGTTATTTCTTGGATGATCATGTCATAAATCAA
Associated Phenotype:
Not determined