ZMP
plcxd3
Ensembl ID:
ZFIN ID:
Description:
PI-PLC X domain-containing protein 3 [Source:UniProtKB/Swiss-Prot;Acc:Q58EK3]
Human Orthologue:
PLCXD3
Human Description:
phosphatidylinositol-specific phospholipase C, X domain containing 3 [Source:HGNC Symbol;Acc:31822]
Mouse Orthologue:
Plcxd3
Mouse Description:
phosphatidylinositol-specific phospholipase C, X domain containing 3 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12146 | Nonsense | Available for shipment | Available now |
sa8998 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa905 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12146
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 |
---|---|---|---|---|---|
ENSDART00000077053 | Nonsense | 54 | 322 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 32698992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31841718 |
GRCz11 | 8 | 31850950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACTCCTTCAGTTTCTACATTGAYGAAGCCTCACCAGTGGGTCCAGAG[C/T]AACCWGAAACAGTGCAGAACTTTGTKTCTGTGTTTGGCACTGTGGCTAAG
Long Flanking Sequence:
AAATTGCACATTAGTGGTGCGATCCAAAGGCATAACAGTTTGACCTGCATAACATATAAGTAACACTTACATAGCAAATACTTGCATTAAACACTGTTTAACACTATCATTGAACACTATTTATTTGAACTCTCTTACATCTATTAAAACAACAGAAGCTAGTATAAGAGCTATTACAACAGTTGGCAGAGAGTTACATCAAACATGTGAAAACTTTTGCTTTAGAGCAATTCCAGTGTTATTGATGTGACAGTAAAAGCTCAAAACATAGTCTATGTTAACATTGTTAAAACATATGTTTATATTTTCCAGAACAACTTACCACAAAGTTAAGGGATCAGAAAAATATCAATCTGTAAAGAGGTTATGTCATTTAAATGAGAAAAATAATAATATATATGCTCTTATAATGTATTATACTAATGTAGAAATCTCATCTTCCAGGTTCCCATGACTCCTTCAGTTTCTACATTGACGAAGCCTCACCAGTGGGTCCAGAG[C/T]AACCAGAAACAGTGCAGAACTTTGTGTCTGTGTTTGGCACTGTGGCTAAGAAGCTGATGAGGAAGTGGTTGGCAACACAAACCATGAACTTCACCAGCCAGCTGGAGGCAGGCATCCGCTTCTTTGACCTCCGCATATCCACCAAACCCAGAGACCCCGACAACGAGCTCTACTTTGCACATGGCCTGTTCAGCGCCACAGTACGTGAAGGCCTGGAGCAGATCAGCACCTTCCTGGCCTCTCATGCCCGCGAGGTTGTGTTCCTGGACTTCAACCACTTCTATGGTGTACAGAACCTCCATCACGAGAAGCTGGTGCAGATGCTACGCACCGTCTTCGGAGACCGACTCTGTCCAGTAGTGTTTGCTCAAGAAGTCAGCCTGAAATACCTCTGGGAGAAAGAGTACCAGGTGCTGGTCTTCTATCACAATCCAATGGCTCTGGAGGTTCCTTTCCTGTGGCCAGGTCAGATGATGCCTGCTCCTTGGGCCAACACCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8998
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 |
---|---|---|---|---|---|
ENSDART00000077053 | Nonsense | 232 | 322 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 32699527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31842253 |
GRCz11 | 8 | 31851485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGGCCAAYACCACAGATCCTGAGAAGCTCATTCTGTTCCTTCAAGCTT[C/A]AGTAAAGGATCGGAGACGTAAGGGCACCTTTTTTGTGTCCYAGGTGRTTC
Long Flanking Sequence:
TGGCACTGTGGCTAAGAAGCTGATGAGGAAGTGGTTGGCAACACAAACCATGAACTTCACCAGCCAGCTGGAGGCAGGCATCCGCTTCTTTGACCTCCGCATATCCACCAAACCCAGAGACCCCGACAACGAGCTCTACTTTGCACATGGCCTGTTCAGCGCCACAGTACGTGAAGGCCTGGAGCAGATCAGCACCTTCCTGGCCTCTCATGCCCGCGAGGTTGTGTTCCTGGACTTCAACCACTTCTATGGTGTACAGAACCTCCATCACGAGAAGCTGGTGCAGATGCTACGCACCGTCTTCGGAGACCGACTCTGTCCAGTAGTGTTTGCTCAAGAAGTCAGCCTGAAATACCTCTGGGAGAAAGAGTACCAGGTGCTGGTCTTCTATCACAATCCAATGGCTCTGGAGGTTCCTTTCCTGTGGCCAGGTCAGATGATGCCTGCTCCTTGGGCCAACACCACAGATCCTGAGAAGCTCATTCTGTTCCTTCAAGCTT[C/A]AGTAAAGGATCGGAGACGTAAGGGCACCTTTTTTGTGTCCCAGGTGGTTCTTACTCCAAAAGCAAGCACCGTCATGAAGGGAGTCACCAGTGGTTTAAGGGAGACCATTACAGAGAGGTAAGCTACTGTGTACTGTTATAAAATCAGTTCTGTTAAATAATGCTGTTGTTCCTGAATGTCTTAATTTCCATTTTTCATAGTTCTTTGAACCAATCTCTGCGACCAAAACATATGCTTACGTCATCACTAAAGGTTTGCATTACATACTTAGCCAGCACCCCTGAAAAATAAGTTACCCAAGGTATATATTAATGTCAGTGATGGGAAGTAGCGTCACTACAAGAAGTGAAGCTACTAGCTTAACTACGTTTCTCAGCAGTGTGGCAGTAGCTTTGTTAGTTTCTAAATTTCTAAATCAAATAGCATTTCTGTAGTGAAGCTTTTTTTTTAGTCAAGTAGCGCAGTAGCGTCCACACAAGCTGCATTTACTGATCGCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa905
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 |
---|---|---|---|---|---|
ENSDART00000077053 | Nonsense | 246 | 322 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 32699568)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 31842294 |
GRCz11 | 8 | 31851526 |
KASP Assay ID:
554-0812.1 (used for ordering genotyping assays)
KASP Sequence:
TTCAAGCTTCAGTAAAGGATCGGAGACGTAAGGGCACCTTTTTTGTGTCC[C/T]AGGTGGTTCTTACTCCAAAAGCAAGCACCGTCATGAAGGGAGTCACCAGT
Long Flanking Sequence:
CACAAACCATGAACTTCACCAGCCAGCTGGAGGCAGGCATCCGCTTCTTTGACCTCCGCATATCCACCAAACCCAGAGACCCCGACAACGAGCTCTACTTTGCACATGGCCTGTTCAGCGCCACAGTACGTGAAGGCCTGGAGCAGATCAGCACCTTCCTGGCCTCTCATGCCCGCGAGGTTGTGTTCCTGGACTTCAACCACTTCTATGGTGTACAGAACCTCCATCACGAGAAGCTGGTGCAGATGCTACGCACCGTCTTCGGAGACCGACTCTGTCCAGTAGTGTTTGCTCAAGAAGTCAGCCTGAAATACCTCTGGGAGAAAGAGTACCAGGTGCTGGTCTTCTATCACAATCCAATGGCTCTGGAGGTTCCTTTCCTGTGGCCAGGTCAGATGATGCCTGCTCCTTGGGCCAACACCACAGATCCTGAGAAGCTCATTCTGTTCCTTCAAGCTTCAGTAAAGGATCGGAGACGTAAGGGCACCTTTTTTGTGTCC[C/T]AGGTGGTTCTTACTCCAAAAGCAAGCACCGTCATGAAGGGAGTCACCAGTGGTTTAAGGGAGACCATTACAGAGAGGTAAGCTACTGTGTACTGTTATAAAATCAGTTCTGTTAAATAATGCTGTTGTTCCTGAATGTCTTAATTTCCATTTTTCATAGTTCTTTGAACCAATCTCTGCGACCAAAACATATGCTTACGTCATCACTAAAGGTTTGCATTACATACTTAGCCAGCACCCCTGAAAAATAAGTTACCCAAGGTATATATTAATGTCAGTGATGGGAAGTAGCGTCACTACAAGAAGTGAAGCTACTAGCTTAACTACGTTTCTCAGCAGTGTGGCAGTAGCTTTGTTAGTTTCTAAATTTCTAAATCAAATAGCATTTCTGTAGTGAAGCTTTTTTTTTAGTCAAGTAGCGCAGTAGCGTCCACACAAGCTGCATTTACTGATCGCAGATCAATAAAGGACGGCACCGACATTGACATCTAGCGGATCTAG
Associated Phenotype:
Not determined