Busch Lab

ZMP

si:ch211-210g13.5

Ensembl ID:
ENSDARG00000062575
ZFIN ID:
ZDB-GENE-030131-5675
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
sa40030 Nonsense Mutation detected in F1 DNA Not yet available
sa38379 Nonsense Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
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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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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

Mutation Details

Allele Name:
sa40030
Status:
Mutation detected in F1 DNA
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
ENSDART00000090676 Nonsense 475 1122 2 6
ENSDART00000131584 Nonsense 361 1000 4 8

The following transcripts of ENSDARG00000062575 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 17101487)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 17307820
GRCz11 3 17457620
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGGTTGTAGTCTGGGATGGTCCTGACTGTGAGCCTGTGGTCTATGTT[G/T]GAAGCTCTGTTGCATCCCAGCTGGCCTTTTGTAAAATTCTTGATGTCATT
Long Flanking Sequence:
ACTGCTATGGTGAAGGCATTGATTTAGACACATTTGTAGAGGCATACTGTGAACTGTGCACACGCTCCGAGATCTTTTTCCTGCTGGTGCAGTTTTCCAGCAACAAAGAATACCTGGACTCTAAAGACTTGATGATCTTTGTGGAGGTGGAGCAGGGAGTGGAGGGTGTCACAGAGGAAATGTGTCGGGAGATTGTGCATAAGTACGAACCCTCTGCTGAAGGACGTAATAATGGCTACTTGTCCATAGATGGCTTCACACACTACCTCCTGTCATCCGAGTGCCACATTTTTGACCCGCAGCACAAGCATGTTTGTCAGGACATGACGCAGCCCCTTTCACACTACTACATCAATTCTTCTCACAATGCCTCACTTTTAGAAGATCACTACTGGGGCTCTTCTGACCTCAGCAGCTATGTTCGAGCACTGCGAATGGGTTGTCGAAGCCTAGAGGTTGTAGTCTGGGATGGTCCTGACTGTGAGCCTGTGGTCTATGTT[G/T]GAAGCTCTGTTGCATCCCAGCTGGCCTTTTGTAAAATTCTTGATGTCATTAACCAGTATGCCTTTGAGAGTTCAGAGTATCCACTAATCCTCTGTCTTGTCACACATTGTAGTGTTCCCCAGCAGAGAGTCATGGCTCAACATCTGAAGAAGATTCTTGGAGACAAACTGCACATCGAGTCTCCCAATCTGGAGGACCACTATTTGCCCTCCCCTGATAAACTCAAGGGAAAGGTACTCATTAAAGGGAAGCGCTTGCCAACAGATTCACAAGACTCTGAAGGAGAGGTCACAGATGAAGAAGAAGGTTTTGAGATGTCCAGGAGAATGATGGGTGTAGATGATAAGGATCACCTTAACGGGATTGGCTGCAAACGATTACGACTCTGCAAGGAACTTTCTGACCTAGTCACCCTTTGCAAGTCCGTTCAGTTCCGTGACTTTGAGATGTCAAAACGCGAACAGAAGCATTGGGAGATTTGCTCCTTTAATGAGGTTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38379
Status:
Mutation detected in F1 DNA
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
ENSDART00000090676 Nonsense 856 1122 2 6
ENSDART00000131584 Nonsense 742 1000 4 8

The following transcripts of ENSDARG00000062575 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 17102630)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 17308963
GRCz11 3 17458763
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGCCTGCTTCCCGGTTACCGGCATGTACCACTGCAGTCACTTACAGGG[G/T]AGTTTTTGCCCAACACCACGCTGTTCGTTCACGTTGCTATTACAAACCGA
Long Flanking Sequence:
TGGCTATGAATTACCAAACTCCAGGTTTGATGATGGATTTGAACCTTGGCTGGTTTAGGCAAAATGGCAACTGTGGCTATGTCCTGCGTCCTGCTATAATGCGTGAAGAGGTGTCCTATTTCAGTGCCAATGCTCGTGACTCGCTTCCTGGAGTCTCAGCACAGCTCCTTCACATTAAGGTGATCAGCGGTCAAAACCTACCAAAGCCTCGAGGCTCTGCTGCTAAAGGAGATGTGGTAGAGCCATACATCTATGTGGAGATCCATGGAATCCCTGCAGACTGCGCAGAACAACGCACAAAAACTGTCTCGCAGAATGGTGACAATCCAATATTTGATGAAAGCTTTGAGTTCCAGATCAACCTCCCTGAGCTAGCTGTTTTGCGGTTTGTTGTCCTTGATGATGACTACATTGGCGATGAATTTATTGGCCAGTACACGATTCCTTTTGAGTGCCTGCTTCCCGGTTACCGGCATGTACCACTGCAGTCACTTACAGGG[G/T]AGTTTTTGCCCAACACCACGCTGTTCGTTCACGTTGCTATTACAAACCGACGAGGTGGGGGCAAGGCCCATAAGAGGGGTCTCTCTGTGAGAAAGGGCAGAAAAGCAAGGGAATACACCTCTACAAAGACCACAGGGATCAAAGTGGTAGATGAGCTCTTCAGGGCGTCCACCCAGCCACTACGAGAAGCAACAGACCTACGGGAAAATGTACAGGTATGAACTTTGGTCTTTTTAGGGTTGGTGTGTTTAAAGGGGTGGTGTAATGCTATTTCATGCATTCAGAAATTATTTTACACTGTTAAGAGTTAAAGGACTATCATGTTTAAGCATTCCAGTGGGAACCTTAGTGTCAAAACATCATCAAGTTGACATTGACGTCTATTTAACATCCACACATTGGATTGATGCCCTTCTGATCACCACCATAATGACACAAAAAGTATTATAAAATAAGATATAAAATATAATAAGAAGCTTTATTAATCTGAAATCTTAAAT
Associated Phenotype:
Not determined