ZMP
plcg2
Ensembl ID:
ZFIN ID:
Description:
1-phosphatidylinositol-4,5-bisphosphate phosphodiesterase gamma-2 [Source:RefSeq peptide;Acc:NP_001
Human Orthologue:
PLCG2
Human Description:
phospholipase C, gamma 2 (phosphatidylinositol-specific) [Source:HGNC Symbol;Acc:9066]
Mouse Orthologue:
Plcg2
Mouse Description:
phospholipase C, gamma 2 Gene [Source:MGI Symbol;Acc:MGI:97616]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18057 | Nonsense | Available for shipment | Available now |
sa25057 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23252 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18057
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 |
---|---|---|---|---|---|
ENSDART00000021399 | Nonsense | 484 | 1240 | 15 | 32 |
ENSDART00000080709 | Nonsense | 484 | 1240 | 16 | 33 |
ENSDART00000148127 | None | None | 120 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 12742573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13297385 |
GRCz11 | 18 | 13265897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTATTAATATTATMATTTCTGCTGAACTGTGTTTGTGTTCAGAGGTGGTA[C/A]AGGCACTACTGTGTKATTGAGAATAAAACGCTYTATTATGCGGAGGAGAANN
Long Flanking Sequence:
AAAGTTATTTGCGAGTGGAGTAAAATCTTGTTTTTTGCTGACTAGAATGATGAAGAACAGTTTTTTTCATTAGAAACTGAATTGGAAATGATGTTTTTTAGTATAGTCGTGAACTGAGGTGGGCCGGTCTTGAAACTCGAGGCTTAAAACTCCAGGGCTGAAAAGAAGTCCCACTCTGGCCCTGGAATCGATATATTGTGCAGCCCTAGTTCCAACAGCATTATGAACTAAAAGAGATTGAAAGTATAAAAACATACTAGGATCCCTTTCTTTATACAATTCTGAATCAGAGTTTCTTTAACAGCACAAAAAACTGAACATCGATCAGACCTTTGGCAGAAAGGACCTTCGAAAAGGAGATAAGCAAGGAGAGCTCTTCATCTGGGATCCAATAGATGAGGTTTTAAACTTCCTTCTCTGATTGTTTCATCTTGGCTTTCAGTTTCATCACTATTAATATTATCATTTCTGCTGAACTGTGTTTGTGTTCAGAGGTGGTA[C/A]AGGCACTACTGTGTGATTGAGAATAAAACGCTCTATTATGCGGAGGAGAATGATGAAGAGGAAGAAAAGGTGAGTCTGCACTTCAGAATGAGATTCAGGTTAATGGTGGCACAAATGAAGTCTGATTGAGACTTCTCCTCAGTCGGTCCAGTCTTGCACGGAGCTTCATCAGTCTGAGCCGTGGTTTCATGGCCGGATGTCCGAGGGCCGAATGACTGCAGAAAGACTGCTGCAGGAATACTGTGCTGAATCGGGTGGAGTTGATGGAACATTTCTGGTTCGGGAGAGTGACACCTTCGTAAATGATTGCACACTTTCATTCTGGTAATGTAGATCTCATATAAGAAGATGTTTTTTTGTTTGCATTGTTTGCATGTGTGTATGTTTATGTATATATTTACTATACTATTTACATACTATATATGAGCAATTCCAGCGTTATTGATGTGACATTTGTAGCAAAAACTCAAAACATAAATTCGCATAGAAACCATATGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25057
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 |
---|---|---|---|---|---|
ENSDART00000021399 | Nonsense | 574 | 1240 | 17 | 32 |
ENSDART00000080709 | Nonsense | 574 | 1240 | 18 | 33 |
ENSDART00000148127 | None | None | 120 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 12745613)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13300425 |
GRCz11 | 18 | 13268937 |
KASP Assay ID:
554-7429.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTCTAGAATTGTCTTTTTGCTTCTTCTAGGCGCAGTGGACGAGTT[C/T]AGCATTGTCGAATCCGTTCCTGCTTGGAAGGAGGACACACAGTTTATTTC
Long Flanking Sequence:
AGATTTATTGAGCAGAGATATTTATTAAAATTATATTTTAGTCACAGAACATTTTTAGAAATGGAAAGATAATTTCAAAATTCATTTCAATTCATACAAAATATTGCAAAAAGTTTACAAAATACAACATTTTAACAAAATTGTATTGCTATTTTTGAAAATGTTATTTAATATTTTCCCTATAAAAATATGGGCTACTAATTTATAAACTGTTATTGTAAGTTATTCTGTTAGATAAGCTCCAGATTTGGTTTTCGCACTGACTAAACTAATGTATGTATTTGCACATATATAATGCAAAGCATCCTATAAAAAAATGTATTTAAATGAAAGACTTGTGTGTGGTGTACTCATATATGCTGAGCACTATATATATCATAAGGTCCTGTATGAAAAGAATGTCCCTATTGATTCTTTTTAATGACTGTATTCTTTGGTCATGCACAGATTTTTTTTTCTAGAATTGTCTTTTTGCTTCTTCTAGGCGCAGTGGACGAGTT[C/T]AGCATTGTCGAATCCGTTCCTGCTTGGAAGGAGGACACACAGTTTATTTCCTGACAGAAAACCTGCACTTCCCCAGCGTGTATGCTCTCATCTATTATTACAGAGACAACCTGCTCCGCTGTCAGGATTTCAACCTGCGCCTCACTGAATATGTGCCTAAACCAGACACGCACCAGTTGGAAGGGTGAGTCAAAACTTGATACCAGAGACTAAAATTAACATTTATATGAACCCGATGATAACAAAAATAGGTCTTGGCAAGTGTATGAAACAGAGTTGCTTGGGAGTTTGCTGATAACTATTTTAATAAGTCTAATAATGCATGACAACACAGTATGTTTTCGATTCAAATATTATACCATGTTTTTCGTGAGAGGTTATGAGTCTTTTATCATTTAACAAACAATAATATTAGTTTTATGTAATTTTACTGTTATTGGATAAAATAATAATAATATTAGTAATAATAATAATATTAATATATACATATAAATAACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23252
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 |
---|---|---|---|---|---|
ENSDART00000021399 | Nonsense | 886 | 1240 | 24 | 32 |
ENSDART00000080709 | Nonsense | 886 | 1240 | 25 | 33 |
ENSDART00000148127 | None | None | 120 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 12757617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13312429 |
GRCz11 | 18 | 13280941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCATTTGATTTGGCCACCGAGACCACTGAAGAGCTGTACGAGTGGTAT[C/T]AGGTGGCCTGGGACATTACGCAGAGAGAGGAAAACCTAGTGTTTGAGGTC
Long Flanking Sequence:
TAAACATTAAATGCTTGTACAGTGGTCCCTCGATGTTTGCGGGAGTTACATAACACGCAATAGGCGAAATCTGCGCTCTGTGCAGTCTAATAAAACACACAACATATTAAAGCGCCTTTGGTGTTTCATTGTTTTCTATAAAACCAATCCAGAAATCGAGGGTGTATGAGATCAGTAGCATGGTCATACATACTGTAGACCACGGTGTTAACATTCATAAAAACCTTTAAATAATGTTAAGTACATGTCAGCAAATTATTTAACACTCTTCTAATGGTTTCTGGATATTTTAATGAAAACATTTTACATTTTGTTCCTGTAAATCGATTGGTCGATCGTGGGAATTTAGCTTGTTTTTCTCACTAATTTCTTTGTTTCCAGTTCGCTCTGCCAAACATGGCAAACAAGTGGTGGTAACTCTGCAGTATAAGGAGGATAAAGAGAACATGATGCCATTTGATTTGGCCACCGAGACCACTGAAGAGCTGTACGAGTGGTAT[C/T]AGGTGGCCTGGGACATTACGCAGAGAGAGGAAAACCTAGTGTTTGAGGTCTGTCTCGTTCACATTTTTTTTTTCTAAATGGGGCCGACTGGGGCTAGTTGTCACAAAGGGGAAGTTTTGAGTCACTTGTCTGGTAAATACAGTATTATTTAGTTTAGCCAGACAAATTCAGGGGTGTTTAAATACTAGGTGTAGCCATAGAGAGAAGATTTAACTATAAAGATGTTCTAAAAATACAGTATAGTCAAGTATTTTGAGTGTAAGGTTGAGGTGGGGTTTATAAATGGTGACAATTCTTTTGCAGAAAGAAAAAACGAAGGAAGTGGAGACCAGAGATGAAGTGGCCAGTGAGATGTCAGAACTGGTTGTTTACTGCCAGCCACGCAGCAAAGAAAAGGACGGCTTTGGTATAGAAAATCAATATTTTTTTAAAGAAATTAATCTTTTTGTGTATTATAATGTTATAAAATCTTTTTTTCTAATAAATACTTTCATTTTGAA
Associated Phenotype:
Not determined