ZMP
pld1a
Ensembl ID:
ZFIN ID:
Description:
phospholipase D1a [Source:RefSeq peptide;Acc:NP_001153567]
Human Orthologue:
PLD1
Human Description:
phospholipase D1, phosphatidylcholine-specific [Source:HGNC Symbol;Acc:9067]
Mouse Orthologue:
Pld1
Mouse Description:
phospholipase D1 Gene [Source:MGI Symbol;Acc:MGI:109585]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19763 | Nonsense | Available for shipment | Available now |
sa6842 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11536 | Nonsense | Available for shipment | Available now |
sa38333 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39837 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19763
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078686 | Nonsense | 56 | 1025 | 2 | 25 |
ENSDART00000133623 | Nonsense | 56 | 1022 | 3 | 26 |
Genomic Location (Zv9):
Chromosome 2 (position 25725967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25922163 |
GRCz11 | 2 | 25577797 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCCATCTACCGGACAGTTGGCTTTAAAGACACAGAAGCACATGTCTA[T/A]CTGACCTCTCTCCCAATTACTGCCAAGATCCTGGATGTGGAGCGCTTCAC
Long Flanking Sequence:
TGGACCAACATCTCTGAAGAATAATTCCAGTACCTTGTTGAATCTGTGCCACAAAGGATTAAGGTACTGTAGTTCTAAATGCAAAAGGTTTTCTATCCCTGTACTATTAAGGTGTACCTAATAAAGTGGCCACTGAGTGTAGTTTGGAATTGGTAAAATTTGTTTTGGGGAGGTAAAATATGATCAGAATTTTTTTTTTGCTTGCACTGTAAAGTGACTTGACTCGTGAAACAATTTGATTTGCAATGATTTTCCAAACAATAAGTTATAAAGGGTGGACGTGTGTGTCTGATAAGACATCTAGACTAAAAGTGATGTGTGTCACAGGGAGTGATATGAGGACAGCTGTGTAACATGATGAAGCACGTCACAAACAAGCGCTCGCATTCCCCACAGACATGCCTCACTCCTCCCTGTTGTTTTCTCACAGGTGCGTCCCGTATTGGGTTCTCTGCCATCTACCGGACAGTTGGCTTTAAAGACACAGAAGCACATGTCTA[T/A]CTGACCTCTCTCCCAATTACTGCCAAGATCCTGGATGTGGAGCGCTTCACCAGAACTCAAGACCGCTTCAAGTTCTCCAAACACAGGAGCGTGTCTAAGGTCTGTGGTGTAAACACTGCTTAACAGATTGAACAATGTCACAGATCTCACATCACTGCTGTGTCCACAGGCAATGCCAGCAGTGTTTAAGATAGAGCTCAAACATGGGAACTTCACCTGGATAGTGAAGAGAAAAGAGAAGCACTTCATGGAGCTGCACAGAGAGCTCCTGAAATACAAGACCCTCATGAGGATCCCACTGCCCACCCGCAGGTCAGACCCCTCTCATACTGAAAAAAAAAAAACAACTCTATCAGTGATCTACATTAGTCAATGTTTGAAGTCGATCAAAAGGTCTAAGACAAGAATAAGGGTTGTTGTTTTGTAGTTTTAGGGCAACTTTGATGAAAGGCTTTGAACCACTTTAAATGCTGACTACTGTATGTGGTCTTATTGTGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6842
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078686 | Essential Splice Site | 378 | 1025 | 11 | 25 |
ENSDART00000133623 | Essential Splice Site | 377 | 1022 | 12 | 26 |
Genomic Location (Zv9):
Chromosome 2 (position 25747166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25943362 |
GRCz11 | 2 | 25598996 |
KASP Assay ID:
554-5154.1 (used for ordering genotyping assays)
KASP Sequence:
TKAGCAAGTCATGTCATAAAATATGCCATATGTTTGTGTTTGTAATGTGC[A/T]GGCTGAGCCCTGAGATCTTTCTGAAGAGGCCTGTGGTGGAAGGCAATCGC
Long Flanking Sequence:
TCAAAGGTTTAAGTCAAGTCAACAAGAATACCATTTTATTAACATCATTTAAAATCAAAATTTAGACCTAAAAATAATTATAGACTATTAATTGGTCACCTTCCTTAAACACTTGATGTCTACTTATTATAATGTGTGCAATAAGACCAATAAAATTAATTTAAAGTTTACAGTAGGTCACTCAAAAATTTAAAATTAATTTCCCTCATGTAGTTGCAAACATTTATGGGTTTTTTCTGTTAGATACATAAAAAGATATTTTGAAGAATGTTGAAATCTGGTAGCAAATAACATTAATTTAAAAATACAAAGGGAAAATAATGGCTACAGTTTGCCAACATTCTTCAGATATTTTGTGTTCAACAAAAGAAAGAAGCTTAAACAGATTTAGATCAATTAGGGGTGAGAAATGATGACAGAAATAAAATTTTTGGGTTAAATCTCTTGTCCTGAGCAAGTCATGTCATAAAATATGCCATATGTTTGTGTTTGTAATGTGC[A/T]GGCTGAGCCCTGAGATCTTTCTGAAGAGGCCTGTGGTGGAAGGCAATCGCTGGAGGCTCGACTGCATTTTGAAACGCAAGGCTGTAAGTCTTCTGCATAGTATTCATTTCTTTTGCTACAGTGGGCTTATAATGTTCAAGCTGGCATGAAAATATGTTTAGTATCTCACAAACCTCTCAAACTAGACAAAATGTTGAGCGGGATTGGATTTTGTTCATTAAAATTGTTTAGGTCATTATTATTTGCTAATTCTGTGATCTCATATTAATGATAGAATTTTCTGCCTTTGTGCCAGAAAAAAAAACAAAACAAAAACTTTTAAACACATTTATTTTATTTATTTGAAGAAAATGACAAGTTTAGGACAATATAAAATATCCCATGTTTCAGACCATAGTTATTGAAAATACGTCAAGAAGTCAGAATTCTTAGCCCCCTTTTGATTTCTTTTTTCTTTTTTTAAACATTTCCCAAATTATGTTTAACAGAGCAAGGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11536
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078686 | Nonsense | 457 | 1025 | 13 | 25 |
ENSDART00000133623 | Nonsense | 456 | 1022 | 14 | 26 |
Genomic Location (Zv9):
Chromosome 2 (position 25749031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25945227 |
GRCz11 | 2 | 25600861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACAGGTGATGAGACACCCTGATCACGTGTCCTCCTCCGTCTACTTATG[G/A]GCACATCAYGAAAAGATTGTAGTGATTGACCAGTCAGTTGCTTTTGTTGG
Long Flanking Sequence:
TTTCTTAAAGTGTGCAGTGTGTGCAGTGTTATTTTATGGTTTATACTGGTCTATTTTCATTTTCTGCAAAGAAATGCTCTTAGCGGTAATATTTTTCTTTGAAATTTTGCCGACATGTTATCAATAATTTATGTAACCAAACATAAACATTTTACTCAAAACGTACTTGTAATACAATAGATTTTTTAATTTAATGAATGTTGTTGTTATTTTTACTTCATTTGTTTATTAAAATGTTTTCTCAGCTTAACTTGTGTATATATTTGCTTGTAGCAACAAGGAGTGAGGATCTTTGTTATGTTGTATAAGGAAGTGGAGCTGGCACTCGGCATCAACAGTGAATACAGCAAAAAAACACTAATGCATCTTCATCCAAACATTAAAGTAAGTCCTGTACCACATTTACTTTCCCACATTTTACGTCACACAACTATAACTATTTCTCTTTCTTAACAGGTGATGAGACACCCTGATCACGTGTCCTCCTCCGTCTACTTATG[G/A]GCACATCATGAAAAGATTGTAGTGATTGACCAGTCAGTTGCTTTTGTTGGTGGAATTGACCTGGCTTATGGCCGCTGGGATGACCGTGAGCACCGGCTGACAGATGTGGGAAGTGTAACACGATCTGTTGCTCAAGCCATAGAGCAGGTTTGTATGATGGACCTTCTATTTGTATTAGCAAATCACAAACACACACACACAAAAAAAAAACTTTTTAGCCACAAACGGGTCAGAGTGAAAATGTAACCCTTGGTTAAGCTATGAAAAAGGTAACTTCAGACATCCTTTCGATGATAGGTATATGGGAAAAGCCAGAATGTTTAACTGAAAATAAACCCATTCATATTAATACATTTGGAGTGGAAAAAGTATTCCAATATATGGTATTGTCTAGCATTTCAAACTTACAAAGGACAAACTACTTTACCAGGTGAAGTGGTATCACAAAAAAACAAACCCATAAAAATGTGTCATTATCACAGTTAGAGATGTCATTATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38333
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078686 | Nonsense | 629 | 1025 | 16 | 25 |
ENSDART00000133623 | Nonsense | 626 | 1022 | 17 | 26 |
Genomic Location (Zv9):
Chromosome 2 (position 25755154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25951350 |
GRCz11 | 2 | 25606984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTGGTCTGTAGACTTTATCGACAGGTACACAACCCCTAGAATGCCCT[G/A]GCATGATATCTCCTCAGTGGTGCATGGAAAAGCAGCCAGAGATGTGGCCA
Long Flanking Sequence:
TGATCAAAACAAACATTAGTAAACCATATTGCATAATTTATGTTAATTACCCTTCCCAAACAATAATGTTTGCACTGACACAAGCTGTTGGTACTGTAAATCTGGCTCCTTATGTTTTATAGCAATGTTCTATGTGTAATGTCTGCAGAGAGTGGCTCAGTGCACAGTCTTCAGACAGGAGTGGGAGAGCTGATGGGAAACACACGCTTCTGGCACGGCAAGGACTACTGCAACTTTGTCTTCAAAGACTGGGTTCAGCTGGACAAGCCCTTTGATGGTGAGCCACACTTTTTTTTTTTTACTTCCTCACGCTTTTACTTTTTGGATTACCTGGATTAACGATCACTTCAGTGATCGTTAATCCAGGTAATCCAAGGCTGAACAGTGTGATTAAACACAGTCTTTTAGATGCGCTTCAGATGTTTATGATGCTTTTTTTTTTTTAACACTGTGCTGGTCTGTAGACTTTATCGACAGGTACACAACCCCTAGAATGCCCT[G/A]GCATGATATCTCCTCAGTGGTGCATGGAAAAGCAGCCAGAGATGTGGCCAGGCACTTTATACAACGCTGGAACTTCACCAAGGTGAGAAATTTAGCAGCCTCCTGTCTAAGCTATGACCTACACAGTTTAAAGTTCACCACACAATTTAGATATTTTTCTTTATTTACACACACTCATACTGTACCACTGAGCAGTGCAGTGCAGTTTAGAACAGTAAAAAATTCCAAAACAGCAACAGCATATTATTTGAGTCTTTAAAATAAACTGTTAAAAGTGCAGATGATTGTGATTGTAAGTGTTGTATTGTCGTCTTTCAGGTTGTATCTCAGCTTTAATGCACTTTTTAAATAAATAAATAAAAAAAACAGCTGCTTGCCATCGTGACAGCATTAAGATTCAATGGACGGCCGATCACTTTCACTCCAAAATGGCAGAATCGTAGGGCTGTTGCTGGTCGCTGCTGTTGCAATGGAACGTTCTGTTGAGTGTCGCCTCTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39837
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 |
---|---|---|---|---|---|
ENSDART00000078686 | Nonsense | 897 | 1025 | 23 | 25 |
ENSDART00000133623 | Nonsense | 894 | 1022 | 24 | 26 |
Genomic Location (Zv9):
Chromosome 2 (position 25776539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25972735 |
GRCz11 | 2 | 25628369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTGAGGACTCTGAAACCACGCCATCAGTGATGGACGGTCAAGAGTA[C/A]CAGGCCGGCAAGTTTGCCCTTCAGCTCAGACTGGAGTGCTTCAAGTAAGA
Long Flanking Sequence:
CTGTGGGTTCTTAAAGTGACACCTCTGTTATCAAACAAAACAGTGGATGTGAATGAGAGATTCGTTGCTCTTTACTAAATAACTACCGTAATTTTAATCAATATTGGTTCGAAATTTAATCAAAAATGAACATTTTTGAAAGTTATTTTTTTACAGTATTTTACAATCATGTTTACAGGTATGAGTCAAACCAGAATAAACAAACTTGTTAATGTGTATTCTCTACATTTTGCTTATTTTGTAATAAACATTAAAAAGAAATAAAGTAAAAAATTATTTTATTTTATTGCCTCTGAATAAATAAATGAAAGAGTTTATTTTACATCTTTTACCCATCTTGAGTTTCCTGTCGTTTAGTTTTCTCTTTTTAATCACAGAATTAATTTTCTAGGCTCTGCCAACATAAATGACCGCAGCATGTTGGGCAAGAAGGACAGTGAGGTGGCTGTGATATTTGAGGACTCTGAAACCACGCCATCAGTGATGGACGGTCAAGAGTA[C/A]CAGGCCGGCAAGTTTGCCCTTCAGCTCAGACTGGAGTGCTTCAAGTAAGATTTGACAGAAAACCACCCATGCTAATGCTAATGTAATCAGCACAACTGAATCACAGCTGAAAGTCTCTGTCTTTCTGTAAACCAGGACCATTCTTGGTGCCTTTACTGACCCAAGCATTGACGTCAGCGACCCCATCAGCAACAGCTTCTACAAGGACGTCTGGATGAGCGTCTCAGGTCGAAACGTCACCATCTACGAGAAGGTATGCGGGGTTCCTTGCAGCTATTTTGTATTTTAAATTGACCTACTGTATTTGTAAATGTCTTTACATTACAGCTAATAATAAATTAGCATTCTGTAATATGACAAGTTGCATCAAAGTTAAAATAACCCAGTGATTATTCGGCTATAAGTTAAACGCTTCTTCAGTATAAGTAAATTTGGTACAACATACAGTTTAACCAAAGATAAATTAGCTTTACATTTCTTCATAAATTTCTCCAGAAAAT
Associated Phenotype:
Not determined