ZMP
si:ch211-168k14.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phospholipase D1, phosphatidylcholine-specific (PLD1) [Source:Un
Human Orthologues:
PLD1, PLD2
Human Descriptions:
phospholipase D1, phosphatidylcholine-specific [Source:HGNC Symbol;Acc:9067]
phospholipase D2 [Source:HGNC Symbol;Acc:9068]
phospholipase D2 [Source:HGNC Symbol;Acc:9068]
Mouse Orthologues:
Pld1, Pld2
Mouse Descriptions:
phospholipase D1 Gene [Source:MGI Symbol;Acc:MGI:109585]
phospholipase D2 Gene [Source:MGI Symbol;Acc:MGI:892877]
phospholipase D2 Gene [Source:MGI Symbol;Acc:MGI:892877]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21513 | Nonsense | Available for shipment | Available now |
| sa31724 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21513
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 |
|---|---|---|---|---|---|
| ENSDART00000078631 | Nonsense | 440 | 984 | 12 | 32 |
| ENSDART00000133094 | Nonsense | 444 | 452 | 13 | 13 |
| ENSDART00000140220 | None | None | 449 | None | 11 |
The following transcripts of ENSDARG00000056191 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 32582846)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 31738792 |
| GRCz11 | 9 | 31549538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAGCCTTCCTGGGAGGGATTGATTTGGCTTACGGAAGATGGGACGACTA[C/A]CAACACAGACTGGCTGATGTGGGAAGTGTGAGAAGAAGCCCTCAGCAAAG
Long Flanking Sequence:
AATTTGGACAAATGAGAAAAGAAGTTACGTTTATCAATTTCGTCAGGGTTTATATGAAATGTTCCTCACATTTGTCAAGATGTAAACCAAACTTAAAAAAAAATCTATTAACACTTTTCCCAAAAATGGTTTCCATCATTGGAATGATATGGATATATAATGTCCATCTATTTTTATAGTCTATGGTTTATATAATGAAAGGATGTGATAGGAATGATTGATTAAATAGTAAAGAATTGATTGATTGATTTAGTAATCATTATAGTAATAATACAATTTAAATACTAATCCTACTGACCAGAATTTCCCTGTGTCTCGTGCAGTTGAGAAAAGACACCTGACAAGCTGGCCATCTGTATTGATTAACAGGTCATCCGACACCCTGATCACATGCCCTCCACTGCATTGCTTTGGGCTCACCATGAGAAGTCGGTGGTGATTGACCAGTCACTAGCCTTCCTGGGAGGGATTGATTTGGCTTACGGAAGATGGGACGACTA[C/A]CAACACAGACTGGCTGATGTGGGAAGTGTGAGAAGAAGCCCTCAGCAAAGTCCTGCTATTTCCCCCAGCCTCACTCATGTAAGACCACTATTACCTGTTGCACTTTCTAAGGTAACATCATCATTAATGTAATCCGTACAATTATAAATCTCAGTCATTCTGATCTATTATTGTACTACTGTTTAGAAGGTACTTATTATATGGTCACACTTTATTTTGATGGTCCGTTTGTTGAATTTAAGTTACATCTCTTCTACATGCCGACTAATTCTCATTAGATTATAAGTAGACTGTTAGGTTAGGGTTAGTTAGTGTAAGGTGATATGTTCTTGCAAAGTTTCTTATAGTCAGTTAAATGTCTGTTAGAGTAGCAGTATCAACAGATATTAAGCAAATAGTCTGATAATACTAAAATGGACCATCAAAATAAAGTGTTACCCATTATATTCCTTTGATAGCAAAGCTAAATTTTCACAGTACTAATGCAGTTCCACCAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31724
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 |
|---|---|---|---|---|---|
| ENSDART00000078631 | Essential Splice Site | 523 | 984 | 19 | 32 |
| ENSDART00000133094 | None | None | 452 | None | 13 |
| ENSDART00000140220 | None | None | 449 | None | 11 |
| ENSDART00000078631 | Essential Splice Site | 523 | 984 | 19 | 32 |
| ENSDART00000133094 | None | None | 452 | None | 13 |
| ENSDART00000140220 | None | None | 449 | None | 11 |
The following transcripts of ENSDARG00000056191 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 32588025)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 31743971 |
| GRCz11 | 9 | 31554717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTAAGAGATTGGTGTATAACACATATTTGTGTGACTAAAATCAACAGAG[T/G]ATTCTTCGGATAGCATAGTGTGAGTACGGCGTTAGTGTCTTTTGCAGTGA
Long Flanking Sequence:
GTCTTGTTATGATAAAAACTTAAACCACCATTTATTGGCTACAGATTAAATAAGTTCCATAAGTAAAATGAACATTTATATTATTCTTAAGAAAATCGATTGTCAATAATAACTGATAAACCTTTTAAGATCTGAGGTTGCTGGTTGATTTTTCATTCGCACCCTCTGGTAACCCCTCTGGTAAGTGTTAGTTTCATACTGATTAGTTTATCAAACAATGTTTGATTCCTACATGATTACTGCATTTAAATTTAGACACTTTAAGCTTTCTATAGATATATGTCTCATGTCTGTGTGTCTTGTTTTCACATAGTTTCAGTTCATTTTAGTGATGTGTTTCTAAAAACAGTTCGCGGAGAGACAAAAGAAACAACCACAGTGTTTATTTTATTTATTTTGCAAAAGCACACACTTTTGTTGTTATTGTGTGTATACACAAAAAAGTAGACACCTAAGAGATTGGTGTATAACACATATTTGTGTGACTAAAATCAACAGAG[T/C]ATTCTTCGGATAGCATAGTGTGAGTACGGCGTTAGTGTCTTTTGCAGTGATTAAGAAAAAAAAAAAAAGATGCTGGTCACGCCGGCGTGATCTGGCGACCTCAGAGGGTTAATTACTCTTGTTTTATACTGCATTAGCCACAATGTACAGAAAAGTATACACTGCTCAATATTATTGATACATGTAAACATTTTGTGCTGTCCACATTTACAAGCATATGGATTCCAGACTGACCAAGCACAATGAACTGCTGGTACTGCAGAGAGACAGATAATAAAAACACTGTTTTAAATATTATGTATCCACCTGATACTAAAGAACTGGTATTTTTGACAACTCTAGCAAACACATACATTCACAAGATTGTTATAACACATTTAATGGTCATCATAATCTTAAATCTGTAATATTTAGATAAAAAAACTATGTACATTTATATGTATTTACTTACGGACCAACATTTTTGCATCTGCAAGCATCTAATTACATCGAGTTGTTTC
Associated Phenotype:
Not determined