ZMP
plcl1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phospholipase C-like 1 (PLCL1) [Source:UniProtKB/TrEMBL;Acc:B8JI
Human Orthologue:
PLCL1
Human Description:
phospholipase C-like 1 [Source:HGNC Symbol;Acc:9063]
Mouse Orthologue:
Plcl1
Mouse Description:
phospholipase C-like 1 Gene [Source:MGI Symbol;Acc:MGI:3036262]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31726 | Nonsense | Available for shipment | Available now |
sa21517 | Essential Splice Site | Available for shipment | Available now |
sa41457 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34681 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2490 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa31726
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 |
---|---|---|---|---|---|
ENSDART00000097475 | Nonsense | 244 | 1137 | 2 | 8 |
ENSDART00000136894 | None | None | 464 | None | 6 |
ENSDART00000144608 | Nonsense | 252 | 578 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 33466021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32621967 |
GRCz11 | 9 | 32432713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGAACTGGTTGGTGGCTGAGTTTGCTCTGGTTGATGAGGATGGACAC[G/T]GAATTGTGTCTGAAGATACAGCAGTGGCCACCATCTGTAAACTCTGCCCT
Long Flanking Sequence:
GTATGCCATCAGAAAAGAAGGTTAGCAGTGCTGCAGATTGCCTGGCCTTCATGCAAGGTGGCTGCGAGCTAAAGAAGGTGCGACCCAACTCGCGCATCTACTCGCGATTCTACACTCTGGACACAGAACTGGGCTGCCTACGTTGGGAACCCTCCAAGAAAGATGGAGACCGAGCCCGACTTGATATATCTGCCATTCGTGAGGTCCGCACTGGGAAAAGCACAGAGACCTTCATCCATAATGGCCCATTAGATAACCTGGCTGAAGAAGCAGCCTTCTCTATCATTCATGGGGATGATTATCAGTCCCTTGACCTTGTTGCTCTTTCTGCCGATGTGGCCAACATCTGGGTGACAGGGATGCGGTACCTGTTGTCTCACCCTGGTGCCATTGGTGGAGGTATTGGAGGGGATGGGGGTGTGGGAGAAGGCAGCATTGGAAGCAAGATGAGGAGGAACTGGTTGGTGGCTGAGTTTGCTCTGGTTGATGAGGATGGACAC[G/T]GAATTGTGTCTGAAGATACAGCAGTGGCCACCATCTGTAAACTCTGCCCTGGCATTAAAGAAGCAAAGGTAACACGTTCTCTTATAATTAATTACATTAACCACAACAACTTGCATTTCATGAGTAAATATGCTCTGAAAGAGCCAAACAATACCGAATACAAAATTGGAAGCAACCTGAAATGCATATACTGTACATGTACTGCAGCAGTTTATGTAGAATCCTACGGTCTAAGAGCTGTGAGAAATAGAAGCACTAGAAAACAACAGACACTACACTACACTACAAAACAAGACAGCCATAAATGTGAGCAGAGGCTATATGATAATTTAAATGGCTGTTGCAGAGCTGTCTCTTTTTATTTTTGCTTAACTTGACTGGTTAGCCAGCCGTGCTGAGGTGCACAGCAATAGTTGCCTTGTAAATTTGGCAGCTGTGACAGTAGTTCCATGTGTGTATGTTTGTGTGTGGACTGGACAGCTGGGGACAGAAGGAGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21517
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 |
---|---|---|---|---|---|
ENSDART00000097475 | Essential Splice Site | 266 | 1137 | 2 | 8 |
ENSDART00000136894 | None | None | 464 | None | 6 |
ENSDART00000144608 | Essential Splice Site | 274 | 578 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 33466091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32622037 |
GRCz11 | 9 | 32432783 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGTGGCCACCATCTGTAAACTCTGCCCTGGCATTAAAGAAGCAAAGG[T/C]AACACGTTCTCTTATAATTAATTACATTAACCACAACAACTTGCATTTCA
Long Flanking Sequence:
AAAGAAGGTGCGACCCAACTCGCGCATCTACTCGCGATTCTACACTCTGGACACAGAACTGGGCTGCCTACGTTGGGAACCCTCCAAGAAAGATGGAGACCGAGCCCGACTTGATATATCTGCCATTCGTGAGGTCCGCACTGGGAAAAGCACAGAGACCTTCATCCATAATGGCCCATTAGATAACCTGGCTGAAGAAGCAGCCTTCTCTATCATTCATGGGGATGATTATCAGTCCCTTGACCTTGTTGCTCTTTCTGCCGATGTGGCCAACATCTGGGTGACAGGGATGCGGTACCTGTTGTCTCACCCTGGTGCCATTGGTGGAGGTATTGGAGGGGATGGGGGTGTGGGAGAAGGCAGCATTGGAAGCAAGATGAGGAGGAACTGGTTGGTGGCTGAGTTTGCTCTGGTTGATGAGGATGGACACGGAATTGTGTCTGAAGATACAGCAGTGGCCACCATCTGTAAACTCTGCCCTGGCATTAAAGAAGCAAAGG[T/C]AACACGTTCTCTTATAATTAATTACATTAACCACAACAACTTGCATTTCATGAGTAAATATGCTCTGAAAGAGCCAAACAATACCGAATACAAAATTGGAAGCAACCTGAAATGCATATACTGTACATGTACTGCAGCAGTTTATGTAGAATCCTACGGTCTAAGAGCTGTGAGAAATAGAAGCACTAGAAAACAACAGACACTACACTACACTACAAAACAAGACAGCCATAAATGTGAGCAGAGGCTATATGATAATTTAAATGGCTGTTGCAGAGCTGTCTCTTTTTATTTTTGCTTAACTTGACTGGTTAGCCAGCCGTGCTGAGGTGCACAGCAATAGTTGCCTTGTAAATTTGGCAGCTGTGACAGTAGTTCCATGTGTGTATGTTTGTGTGTGGACTGGACAGCTGGGGACAGAAGGAGGACAGAAAGAAGCCACAGGGCCAAGTCTACACGTCTTTGTGACAGCGAGTGTGAGGCATCTGCTTCATGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41457
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 |
---|---|---|---|---|---|
ENSDART00000097475 | Nonsense | 384 | 1137 | 3 | 8 |
ENSDART00000136894 | None | None | 464 | None | 6 |
ENSDART00000144608 | Nonsense | 392 | 578 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 33467496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32623442 |
GRCz11 | 9 | 32434188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGTCAGCTGAGTGCCAGTTATTAGACCCGGAGCACCAGAATGTGTG[C/A]CAGGACATGAAGATGCCCCTGTCTCATTATTTTATCAGTGCCTCCTACCG
Long Flanking Sequence:
TTGTATATCTAGTAATAGAACAGTAGTCATAGTTTTTTATTAATTATTTGCACATAACAATTCAAAACAACAAAGGTTGGATCACTTTTACAAAGTTTAATCAATAAAAGTGTTGCCATTACTGATATTTTTCTGCCTTTCACTCAGGTGCGTTTGCGCTTCAAGGAAATTCAGAGGAGCAAAGAGAAGCTTACTTCCCATGTTACGCTGGAAGAGTTCCAGGAGGCCTACTGTGAGCTGTGTACACGACCTGATGTCTATTTTTTGCTAGTGCAACTCTCTAAAGACCGAGAGTGCCTTGACGCCCAGGACCTGCGCCTTTTCCTGGAGTCAGAACAAGGTCTGTCAATGGCCACCACTGAAGGCTGCTTGGAGCTTCTTCGCCTCTTTGAGCCCTCTGCAGCTGGACGTGAGCGAGGTCTTTTGGGCTTGGATGGCTTTGCTCGCTACCTACAGTCAGCTGAGTGCCAGTTATTAGACCCGGAGCACCAGAATGTGTG[C/A]CAGGACATGAAGATGCCCCTGTCTCATTATTTTATCAGTGCCTCCTACCGCTCCTACCTGCTGGATGACCAAGTGCATGGCCGGGCTGATCTTGGGGGTCTCACTCGAGCCCTGCAGGCTGGCTGTCGTTGTCTAGAATTGGGGGTTACGGATGGGCCAGAAGGAGAGCCACTGTTGGGTGTAGACCATGGTGCAGAAGTAAAGCATCATCACCACCACCACCATCACCACCACCACCATCATGGTTCTGTTACTCTGCGCAGTGCCCTGGAAGTAGTCAATAAGTATGCTTTTCTCACCTCACAGTATCCTTTGTTGCTGTATCTGTGTCAGCGTTGTTCACCTTCCCAGCAACGTACTCTTGCACAACACTTAAAAAAAGTTTTTGGACCCAAGCTCTATACCCCTGAGTCTCTGCCTGTTAGTTTGGGAGGTCGTGCGACTACCTTGCCATCTCCAGAACAACTGAAGGGCAAGGTGCTTCTTGTTGGAAAGAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34681
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 |
---|---|---|---|---|---|
ENSDART00000097475 | Nonsense | 539 | 1137 | 3 | 8 |
ENSDART00000136894 | None | None | 464 | None | 6 |
ENSDART00000144608 | Nonsense | 547 | 578 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 33467959)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32623905 |
GRCz11 | 9 | 32434651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCCTGTTAGTTTGGGAGGTCGTGCGACTACCTTGCCATCTCCAGAA[C/T]AACTGAAGGGCAAGGTGCTTCTTGTTGGAAAGAAGCTTCCCCCAGAGGAG
Long Flanking Sequence:
AGTGCCAGTTATTAGACCCGGAGCACCAGAATGTGTGCCAGGACATGAAGATGCCCCTGTCTCATTATTTTATCAGTGCCTCCTACCGCTCCTACCTGCTGGATGACCAAGTGCATGGCCGGGCTGATCTTGGGGGTCTCACTCGAGCCCTGCAGGCTGGCTGTCGTTGTCTAGAATTGGGGGTTACGGATGGGCCAGAAGGAGAGCCACTGTTGGGTGTAGACCATGGTGCAGAAGTAAAGCATCATCACCACCACCACCATCACCACCACCACCATCATGGTTCTGTTACTCTGCGCAGTGCCCTGGAAGTAGTCAATAAGTATGCTTTTCTCACCTCACAGTATCCTTTGTTGCTGTATCTGTGTCAGCGTTGTTCACCTTCCCAGCAACGTACTCTTGCACAACACTTAAAAAAAGTTTTTGGACCCAAGCTCTATACCCCTGAGTCTCTGCCTGTTAGTTTGGGAGGTCGTGCGACTACCTTGCCATCTCCAGAA[C/T]AACTGAAGGGCAAGGTGCTTCTTGTTGGAAAGAAGCTTCCCCCAGAGGAGGAAGGTTCGGAAGGAGAGGTTTCCGAGGAGGATGAGGAAATTGGCGGTGGTGGTCCTTTAGCTGGCCGAAGGATGACTATACCTGGGGAAGAGGAATTGGGGGTGGTCCTTGTTGTCCCACCACCCCCACAGCCAAGGCGCCTCCGCTTGCGTCATGAATTGTCTGATCTTGTTGCAGTTGCTCGTACTGGAAGTCGAAACTTTTATGCTCATCGGGCAAGTATTCTGCCATCCCAACAACATTCACCCCCATCAACTCCTTCTACGCCAGGTACACCTTTGAACATTGATCCCTCCTACTGGACCCTATGCTCTCTTGGGGAAGGGGAGGCAGGAAGGCTGGCTAGTGAGAGTCCAGAGGAGCTGGTAAGCTTTACCAAACGCAATCTAACCCGTGTGAGGCCCAGCTCAGTCAGACTTGACTCTAGCAACCCAAACCCACAAGGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2490
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000097475 | Essential Splice Site | 1045 | 1137 | 6 | 8 |
ENSDART00000136894 | Essential Splice Site | 392 | 464 | 4 | 6 |
ENSDART00000144608 | None | None | 578 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 33484397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32640343 |
GRCz11 | 9 | 32451089 |
KASP Assay ID:
554-2762.1 (used for ordering genotyping assays)
KASP Sequence:
TGAAAATGCAGATGGAGTGCAGGAGAAAATCGCTCAAGTGCAAAAAGAAG[G/A]TAAGTGGAGGAGAAGATGAGAGCAGGATGAATTTCTTCCYATCTAATGAT
Long Flanking Sequence:
AGAAAAAAATATAGCTTAAAGGGGCTAATAATTTTGTCCCTAAAATAGTTTTAAAAAATTAAAAACGGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTATCCAGAAGAAAAAATATTATCAGACATACTGTAAAAATTTCCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAATAAAACATTTGAAGGGGTATATACATCTGAATATACACACACACACACACACACATATACATTGCATTTTTAATTTTATTTTAGTTCATTTTAAATATAGTTATACTATAGCAATGTAAAATTAATTACTGTCACTTTTGATCAATTGAATGCATCCTTGCTGAATAACTCTATCAATTTCATTCAGAATTGTTAAATATTTGATCAGTTAATAATGCAATTCCTGTCTGATGCGTCCTCAGATGATCTCCGCTAACAAACAGCTGATTGAAAATGCAGATGGAGTGCAGGAGAAAATCGCTCAAGTGCAAAAAGAAG[G/A]TAAGTGGAGGAGAAGATGAGAGCAGGATGAATTTCTTCCCATCTAATGATGCTACAGTTAATGCCCCTGCAGATGCATGAAAATCTTAATAAACGGTTCACAGGTTTCTCAAAATTACATTCAAATAGTATAGCGTTATCCCAACACACACAGTCCTGTCAACACTCTCGAATATTGCAAACACATACTGAAGGGTGTTGAAAATACCTTCAAAGTTGTTTTAAAATGATGTGTTAATGTTGATGATTTAGTAAATAGGAACACTGTTTAGTTGGAATTCATTACTTCATCTTTTATCCCACTAGTCCTGCGGTACAGTGATACTTTCAAAAATAGTGAAGCTTTTCCAGTAACAAGCTACAAGCAATTTTTTTTTTTTTACAAAAGCACATTTGTTTTTGTAGCATTTCAGACTACAACAGCATGGTTATGTCAATATGTACTGCCCGTGCTACTTCGTTAGTCGACACAGTATTCAAAGAATGTAACCTTGGGATGTT
Associated Phenotype:
Not determined