ZMP
si:ch211-210g13.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
PLCL2
Human Description:
phospholipase C-like 2 [Source:HGNC Symbol;Acc:9064]
Mouse Orthologue:
Plcl2
Mouse Description:
phospholipase C-like 2 Gene [Source:MGI Symbol;Acc:MGI:1352756]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12851 | Nonsense | Available for shipment | Available now |
sa9500 | Nonsense | Available for shipment | Available now |
sa19973 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12851
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 |
---|---|---|---|---|---|
ENSDART00000090676 | Nonsense | 147 | 1122 | 2 | 6 |
ENSDART00000131584 | Nonsense | 33 | 1000 | 4 | 8 |
The following transcripts of ENSDARG00000062575 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 17100505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17306838 |
GRCz11 | 3 | 17456638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGGAAGGCTGTGAGATGAAGAAAGTTCGTTCTAATTCTCGCATGTA[C/A]AATCGTTACTTCCTGTTGGATCCTGACATGCGCTGGCTCCGCTGGGAACC
Long Flanking Sequence:
GTTATAAATAAGGTCTTCGCATCACTGCAGTAGTCACTAGAAGCTCAATCTGAAAGAGTGTTTTAAAATGTGGAGTTCTGCATGTGCATATTAACTGGTTCACTATAAATAGTCACTGCTTGGATGTTGGAATAAAAAATCTGACAGTTCATGTGAAGTTTTTACATATTAACTTTTCAAGTAGTTTATTAATTTCAGGATTTTCACATACATCTAGATAGGACTTAAATCTTGTATACCCAAAATAGTTGCCTGAAGAGGCTTTCTTTGAAAGTGACTTTGATGTATGGGTTGATTTTGTAATGTGTATGTCCACTACACTAACCAGCCTTCTTTATGCTCTCTCTTTAGGATGGTTCAAAACAGAGACAGTCAAGGAAGAAGACCGTCTCATTCAGCTCCATGCCAAGTGATCGCAAGATGAACAGCACAGCTGCCTGTATGGCCTTCATGATGGAAGGCTGTGAGATGAAGAAAGTTCGTTCTAATTCTCGCATGTA[C/A]AATCGTTACTTCCTGTTGGATCCTGACATGCGCTGGCTCCGCTGGGAACCATCAAAAAAAGACTCTGAGAAGGCCAAGCTTGAAATCAAGAGCATCAAAGAAGTTCGATTGGGAAAGAAAACACCTGTCCTACGCAGCAACGGACTCTCGGATCAGTTCCCAGAGGAGTGTGCATTCTCGATTATATATGGTGACAACTATGAATCCCTTGATCTGGTTGCAAGCACTGCAGATGTGGTTAGCACCTGGGTGATGGGACTGCGGTACCTGGTCTCATATGGGAGGCATATGGTGGGTGTAGCAGAACCTAGTCAACCTAGTGTACGAACGTCATGGATTGGGTCCGTGTTTGATCTAGCTGATCCAGAAAGGCAAGGACACATTGACCTATTCCGGGCCACCCAAATCATAAAGGGTCTCAATCCTGGCATGAGAGAGTCTCGCATCGAACTGAAGTTCAAAGAGCTACAAAAGGCCAAGGACTGCTATGGTGAAGGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9500
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 |
---|---|---|---|---|---|
ENSDART00000090676 | Nonsense | 376 | 1122 | 2 | 6 |
ENSDART00000131584 | Nonsense | 262 | 1000 | 4 | 8 |
The following transcripts of ENSDARG00000062575 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 17101192)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17307525 |
GRCz11 | 3 | 17457325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTGGAGGGTGTCACAGAGGAAATGTGTCGGGAGATTGTGCATAAGTA[C/A]GAACCCTCTGCTGAAGGACGTAATAATGGCTACTTGTCCATAGATGGCTT
Long Flanking Sequence:
TATGGTGACAACTATGAATCCCTTGATCTGGTTGCAAGCACTGCAGATGTGGTTAGCACCTGGGTGATGGGACTGCGGTACCTGGTCTCATATGGGAGGCATATGGTGGGTGTAGCAGAACCTAGTCAACCTAGTGTACGAACGTCATGGATTGGGTCCGTGTTTGATCTAGCTGATCCAGAAAGGCAAGGACACATTGACCTATTCCGGGCCACCCAAATCATAAAGGGTCTCAATCCTGGCATGAGAGAGTCTCGCATCGAACTGAAGTTCAAAGAGCTACAAAAGGCCAAGGACTGCTATGGTGAAGGCATTGATTTAGACACATTTGTAGAGGCATACTGTGAACTGTGCACACGCTCCGAGATCTTTTTCCTGCTGGTGCAGTTTTCCAGCAACAAAGAATACCTGGACTCTAAAGACTTGATGATCTTTGTGGAGGTGGAGCAGGGAGTGGAGGGTGTCACAGAGGAAATGTGTCGGGAGATTGTGCATAAGTA[C/A]GAACCCTCTGCTGAAGGACGTAATAATGGCTACTTGTCCATAGATGGCTTCACACACTACCTCCTGTCATCCGAGTGCCACATTTTTGACCCGCAGCACAAGCATGTTTGTCAGGACATGACGCAGCCCCTTTCACACTACTACATCAATTCTTCTCACAATGCCTCACTTTTAGAAGATCACTACTGGGGCTCTTCTGACCTCAGCAGCTATGTTCGAGCACTGCGAATGGGTTGTCGAAGCCTAGAGGTTGTAGTCTGGGATGGTCCTGACTGTGAGCCTGTGGTCTATGTTGGAAGCTCTGTTGCATCCCAGCTGGCCTTTTGTAAAATTCTTGATGTCATTAACCAGTATGCCTTTGAGAGTTCAGAGTATCCACTAATCCTCTGTCTTGTCACACATTGTAGTGTTCCCCAGCAGAGAGTCATGGCTCAACATCTGAAGAAGATTCTTGGAGACAAACTGCACATCGAGTCTCCCAATCTGGAGGACCACTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19973
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 |
---|---|---|---|---|---|
ENSDART00000090676 | Nonsense | 424 | 1122 | 2 | 6 |
ENSDART00000131584 | Nonsense | 310 | 1000 | 4 | 8 |
The following transcripts of ENSDARG00000062575 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 17101336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17307669 |
GRCz11 | 3 | 17457469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCACAAGCATGTTTGTCAGGACATGACGCAGCCCCTTTCACACTACTA[C/A]ATCAATTCTTCTCACAATGCCTCACTTTTAGAAGATCACTACTGGGGCTC
Long Flanking Sequence:
TCATGGATTGGGTCCGTGTTTGATCTAGCTGATCCAGAAAGGCAAGGACACATTGACCTATTCCGGGCCACCCAAATCATAAAGGGTCTCAATCCTGGCATGAGAGAGTCTCGCATCGAACTGAAGTTCAAAGAGCTACAAAAGGCCAAGGACTGCTATGGTGAAGGCATTGATTTAGACACATTTGTAGAGGCATACTGTGAACTGTGCACACGCTCCGAGATCTTTTTCCTGCTGGTGCAGTTTTCCAGCAACAAAGAATACCTGGACTCTAAAGACTTGATGATCTTTGTGGAGGTGGAGCAGGGAGTGGAGGGTGTCACAGAGGAAATGTGTCGGGAGATTGTGCATAAGTACGAACCCTCTGCTGAAGGACGTAATAATGGCTACTTGTCCATAGATGGCTTCACACACTACCTCCTGTCATCCGAGTGCCACATTTTTGACCCGCAGCACAAGCATGTTTGTCAGGACATGACGCAGCCCCTTTCACACTACTA[C/A]ATCAATTCTTCTCACAATGCCTCACTTTTAGAAGATCACTACTGGGGCTCTTCTGACCTCAGCAGCTATGTTCGAGCACTGCGAATGGGTTGTCGAAGCCTAGAGGTTGTAGTCTGGGATGGTCCTGACTGTGAGCCTGTGGTCTATGTTGGAAGCTCTGTTGCATCCCAGCTGGCCTTTTGTAAAATTCTTGATGTCATTAACCAGTATGCCTTTGAGAGTTCAGAGTATCCACTAATCCTCTGTCTTGTCACACATTGTAGTGTTCCCCAGCAGAGAGTCATGGCTCAACATCTGAAGAAGATTCTTGGAGACAAACTGCACATCGAGTCTCCCAATCTGGAGGACCACTATTTGCCCTCCCCTGATAAACTCAAGGGAAAGGTACTCATTAAAGGGAAGCGCTTGCCAACAGATTCACAAGACTCTGAAGGAGAGGTCACAGATGAAGAAGAAGGTTTTGAGATGTCCAGGAGAATGATGGGTGTAGATGATAAGGA
Associated Phenotype:
Not determined