ZMP
plcd1a
Ensembl ID:
ZFIN ID:
Description:
phospholipase C, delta 1a [Source:RefSeq peptide;Acc:NP_001103170]
Human Orthologue:
PLCD1
Human Description:
phospholipase C, delta 1 [Source:HGNC Symbol;Acc:9060]
Mouse Orthologue:
Plcd1
Mouse Description:
phospholipase C, delta 1 Gene [Source:MGI Symbol;Acc:MGI:97614]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24480 | Essential Splice Site | Available for shipment | Available now |
sa10380 | Nonsense | Available for shipment | Available now |
sa9594 | Nonsense | Available for shipment | Available now |
sa11302 | Nonsense | Available for shipment | Available now |
sa17762 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24480
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 |
---|---|---|---|---|---|
ENSDART00000112349 | Essential Splice Site | 163 | 775 | 3 | 15 |
ENSDART00000132340 | Essential Splice Site | 163 | 775 | 4 | 16 |
ENSDART00000139989 | Essential Splice Site | 140 | 154 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 21000508)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20247637 |
GRCz11 | 24 | 20392056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTATCAACCGCCTGCATAAACTCAATCGCCAACAGAACAGTGAACAG[T/C]ATCCTTGAACATGCATCTTTCCCAATTCCCTACAAAAAAAGTCTATTTGA
Long Flanking Sequence:
TGAGTCAGGCGTTTTGAACAAAACATTTAAATTTATGAATCAAAGAATCATTAATGTTACCACCTACTGGTGGCCTTGGAGTAGTTTATATATATTTTATATCTCATTGACAGGCCTACAGCAGCCAAGATACCAGCTGAAAATCACATTACACAAATAATACTTAGTTTATCGTTATAGAAAAATTCACCTAAAATGTAAAAGTATTGTTTTATTTTAGCATTATTACATCAATGAGTAATAATGAAATATGTCTTGCTTCTTTGACAGTTGAACTTGCGGAAATTGATTCTGTGCGTCTCGGCCGACAGTCTGAAGGACTGCAGAAATACACATATTCCTCGATTGAGAATCGCTGCTTCTCCATCATCTTCAAAGGTAGACGGGAAAACCTGGACCTGATCGCCTCTTCTGATGATGAAGCCAATTGTTGGGTCAACAGCCTGGAGAAGGTTATCAACCGCCTGCATAAACTCAATCGCCAACAGAACAGTGAACAG[T/C]ATCCTTGAACATGCATCTTTCCCAATTCCCTACAAAAAAAGTCTATTTGACTTTTCCACAGTGTATTTGAGTGTTTTAAAGTGTTCTGTGAAAGATTAAAGGAAAATAGGCTAATTTTACAACTCCCCTAGAGTAAAACAGTTGAGTTTAACCATTTGTAAATCCATAGCTGATATGCAGTTCTGTCAAGAGTACTTTTAGCTTAGCTTAGTATAGATCATTGAATCAGATTAGACCATTAGCATCTCATTCAAAAGTGACCAAAGCATTTCTATTATTTTCCTATTTAAAACGTTACTTTTATGTAGTACAATTATATACAAAATACCAATGGATTATGAAAAGTTGTCTTTTTCTAGTCTGATTTGGCTAGGAACTGTACTCTCATTCTGCCATAATAATCAAGGAACTTTGCTGCCATAGCTGCATCAGGCGCGATGATATTACACAGCACCTGAAAATTGTTCCCAGCTGCAGAAAGTAAATCTAGGTCTTTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10380
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 |
---|---|---|---|---|---|
ENSDART00000112349 | Nonsense | 401 | 775 | 8 | 15 |
ENSDART00000132340 | Nonsense | 401 | 775 | 9 | 16 |
ENSDART00000139989 | None | None | 154 | None | 4 |
ENSDART00000112349 | Nonsense | 401 | 775 | 8 | 15 |
ENSDART00000132340 | Nonsense | 401 | 775 | 9 | 16 |
ENSDART00000139989 | None | None | 154 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 21008864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20255993 |
GRCz11 | 24 | 20400412 |
KASP Assay ID:
2261-8645.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTTTGTGGATTATGWTTTCGTTTTTTTGTCACTCYAGGCCTCACCRTA[T/A]CCAGTGMTCTTGTCTTTGGAGAACCATTGTTCTTTAGAGCAGCAGAAAAT
Long Flanking Sequence:
CCATGTGTCCCACATATCTGCCACGGGTGAACACTTTTTGTCCATGTTTGTAGTTTTAATTAAATTCACTTCCAACACAGAGTGTACTATTAGCTATTAATGCATACACAGATCTGCACTTATAGTAGAAAATCCAAGTACCTTTGGAATGCTCATTTAACAAATTAAATTTGGGACAGACTAATTAATTTTTTGAATTACTTTTTAGGTTGAATATTATGTGATTTGGAATGCAGCTAATAGACGTTGTCTTTCAGAGCGCTGATGAAGAGCTGTCGCTGTGTGGAGCTGGATATCTGGGATGGAGCAAATGGGGAGCCAGTCATTTACCATGGCCACACACTCACATCCAAAGTGCCGTTTAAAGACGTCATTAAGGCTATCAAAGATTATGCTTTTAAAGTAAGTGAAATGGCACCGACTGTGTGTGAAGTAATGATTGATGGCAGAACTTTTGTGGATTATGATTTCGTTTTTTTGTCACTCCAGGCCTCACCGTA[T/A]CCAGTGATCTTGTCTTTGGAGAACCATTGTTCTTTAGAGCAGCAGAAAATCGTCGCCATGCACTTAACCACCATCCTGGGCAGTGCTTTGCTTACTCAACCGCTGGGACAAAAAATGCCCACCACATTTCCAGGACCTGAGGTTAGACCCTTTAGAATGAAAAATTTTTTGTATGCATGTTTTACTGAACAGTTTGTTGTGCACAACTGTATCTGCCCACTTTTTTAGGGCAACTGGTTCAGTTTTTTGTTTTAAATTCAGGGTTGTGCAAGGTCTTAAAGTTTTAAAATGTCTTAAATTGCAAAAACAAAAGGTCTTAAATTCACTTAAATATTTAATTTTAGGTGTTAAATCATGTTAAACATGATTAAAAACATGAAGTAATCTCACTGAGTTTAAATAAGGGTCCTGATGAGCATCAGGCGCGCTGAGGGCACGCCCCAACCTAGAACAGACAAAACATACAAAAACTTAAACCAAACCAACACAGTCCTAACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9594
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 |
---|---|---|---|---|---|
ENSDART00000112349 | Nonsense | 401 | 775 | 8 | 15 |
ENSDART00000132340 | Nonsense | 401 | 775 | 9 | 16 |
ENSDART00000139989 | None | None | 154 | None | 4 |
ENSDART00000112349 | Nonsense | 401 | 775 | 8 | 15 |
ENSDART00000132340 | Nonsense | 401 | 775 | 9 | 16 |
ENSDART00000139989 | None | None | 154 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 21008864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20255993 |
GRCz11 | 24 | 20400412 |
KASP Assay ID:
2261-8645.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTTTGTGGATTATGWTTTCGTTTTTTTGTCACTCYAGGCCTCACCRTA[T/A]CCAGTGMTCTTGTCTTTGGAGAACCATTGTTCTTTAGAGCAGCAGAAAAT
Long Flanking Sequence:
CCATGTGTCCCACATATCTGCCACGGGTGAACACTTTTTGTCCATGTTTGTAGTTTTAATTAAATTCACTTCCAACACAGAGTGTACTATTAGCTATTAATGCATACACAGATCTGCACTTATAGTAGAAAATCCAAGTACCTTTGGAATGCTCATTTAACAAATTAAATTTGGGACAGACTAATTAATTTTTTGAATTACTTTTTAGGTTGAATATTATGTGATTTGGAATGCAGCTAATAGACGTTGTCTTTCAGAGCGCTGATGAAGAGCTGTCGCTGTGTGGAGCTGGATATCTGGGATGGAGCAAATGGGGAGCCAGTCATTTACCATGGCCACACACTCACATCCAAAGTGCCGTTTAAAGACGTCATTAAGGCTATCAAAGATTATGCTTTTAAAGTAAGTGAAATGGCACCGACTGTGTGTGAAGTAATGATTGATGGCAGAACTTTTGTGGATTATGATTTCGTTTTTTTGTCACTCCAGGCCTCACCGTA[T/A]CCAGTGATCTTGTCTTTGGAGAACCATTGTTCTTTAGAGCAGCAGAAAATCGTCGCCATGCACTTAACCACCATCCTGGGCAGTGCTTTGCTTACTCAACCGCTGGGACAAAAAATGCCCACCACATTTCCAGGACCTGAGGTTAGACCCTTTAGAATGAAAAATTTTTTGTATGCATGTTTTACTGAACAGTTTGTTGTGCACAACTGTATCTGCCCACTTTTTTAGGGCAACTGGTTCAGTTTTTTGTTTTAAATTCAGGGTTGTGCAAGGTCTTAAAGTTTTAAAATGTCTTAAATTGCAAAAACAAAAGGTCTTAAATTCACTTAAATATTTAATTTTAGGTGTTAAATCATGTTAAACATGATTAAAAACATGAAGTAATCTCACTGAGTTTAAATAAGGGTCCTGATGAGCATCAGGCGCGCTGAGGGCACGCCCCAACCTAGAACAGACAAAACATACAAAAACTTAAACCAAACCAACACAGTCCTAACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11302
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 |
---|---|---|---|---|---|
ENSDART00000112349 | Nonsense | 532 | 775 | 10 | 15 |
ENSDART00000132340 | Nonsense | 532 | 775 | 11 | 16 |
ENSDART00000139989 | None | None | 154 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 21017055)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20264184 |
GRCz11 | 24 | 20408603 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTACTGCAAGAGTGTGCATTTCRCCAGCTTYGAGCAATCAAGGAAAAAA[C/T]AGGCCTTCTATGAGATGGCTTCCTTCAAGGAGGGCAAAGCCATGAACTYA
Long Flanking Sequence:
CAAAACCAGCAAGAGCTGTACCCACAGACCCGAGTTTAACCTGCTCTAACCACTATCAGTGTATTGAAGAATTAGAACACCCTCATAAACATGAAAACATACCTAATTTGTACTGTTTTAAAGTTTGGAAGGTTCCATATTAAATGTAAATTGGAAAGCAAATTTTCAAAACGCTCAACAAAGTACACCTACTCTTATTTGCATACACAAAGTTGTGGTAGATAGGGTTGAGTTCAGATCAGTGCACACAGCTATGACAAATACACTCAAAGGCCTGATTCAAATCAGTAGACCGCAGACTTGTGCCTGTTTGGCATCCCATTGTCTTTGCATGCTCCATGTGAAGTTTATTGTTTATATGTTGTGGCCTACTGTGTTTGTAATTGGTTTTGTTTCCTTTTTAGAAATCCAAAAAGATCAAGCTGGCCAAGGAGCTGTCAGACCTGGTTGTCTACTGCAAGAGTGTGCATTTCACCAGCTTCGAGCAATCAAGGAAAAAA[C/T]AGGCCTTCTATGAGATGGCTTCCTTCAAGGAGGGCAAAGCCATGAACTTAGCTGAACAATCAGGTACAAGGGTATGCAGGGTGTGCTGAGTTGTGGAGTATTTTTTAGTATTGATAATTGTATCAGTGGGTTTTGGTTTGATGTCTGAAATTGTCTGTGGTTAATAGTGTTGCTAATAGTTACATTTTTCGCATTTCTTTTTTAAAATAGGTGGCAAATCAATACTTTTAAAGAGATAATTCCCAAAAAATGGAAATTTCCTCACCATTTACTCAAACAATCTCAAGTGTTTTTTTTTTTTTTTACAATTTTTTTTTCTTCTGTTGAATACAAAACAATTTATTATGAAGAGTGTTAGAAGAAAGCAGCCATTGAAATACGTAAGAGGGACAAAAAATGGTCATGGGCCAATTGACTCCGTTTTCTTCCCCCAAAATTATTCTGTATATCTTTCTTTGTGTTCAGTAGTAGAAAGAAACTTATAGTCCCAATGAACCGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17762
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 |
---|---|---|---|---|---|
ENSDART00000112349 | Nonsense | 551 | 775 | 10 | 15 |
ENSDART00000132340 | Nonsense | 551 | 775 | 11 | 16 |
ENSDART00000139989 | None | None | 154 | None | 4 |
Genomic Location (Zv9):
Chromosome 24 (position 21017112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20264241 |
GRCz11 | 24 | 20408660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTATGAGATGGCTTCCTTCAAGGAGGGCAAAGCCATGAACTYAGCTGAA[C/T]AATCAGGTACAAGGGWATGCAGGGTGTGCTRAGTTGTGGASTATTTTTTA
Long Flanking Sequence:
AGTGTATTGAAGAATTAGAACACCCTCATAAACATGAAAACATACCTAATTTGTACTGTTTTAAAGTTTGGAAGGTTCCATATTAAATGTAAATTGGAAAGCAAATTTTCAAAACGCTCAACAAAGTACACCTACTCTTATTTGCATACACAAAGTTGTGGTAGATAGGGTTGAGTTCAGATCAGTGCACACAGCTATGACAAATACACTCAAAGGCCTGATTCAAATCAGTAGACCGCAGACTTGTGCCTGTTTGGCATCCCATTGTCTTTGCATGCTCCATGTGAAGTTTATTGTTTATATGTTGTGGCCTACTGTGTTTGTAATTGGTTTTGTTTCCTTTTTAGAAATCCAAAAAGATCAAGCTGGCCAAGGAGCTGTCAGACCTGGTTGTCTACTGCAAGAGTGTGCATTTCACCAGCTTCGAGCAATCAAGGAAAAAACAGGCCTTCTATGAGATGGCTTCCTTCAAGGAGGGCAAAGCCATGAACTTAGCTGAA[C/T]AATCAGGTACAAGGGTATGCAGGGTGTGCTGAGTTGTGGAGTATTTTTTAGTATTGATAATTGTATCAGTGGGTTTTGGTTTGATGTCTGAAATTGTCTGTGGTTAATAGTGTTGCTAATAGTTACATTTTTCGCATTTCTTTTTTAAAATAGGTGGCAAATCAATACTTTTAAAGAGATAATTCCCAAAAAATGGAAATTTCCTCACCATTTACTCAAACAATCTCAAGTGTTTTTTTTTTTTTTTACAATTTTTTTTTCTTCTGTTGAATACAAAACAATTTATTATGAAGAGTGTTAGAAGAAAGCAGCCATTGAAATACGTAAGAGGGACAAAAAATGGTCATGGGCCAATTGACTCCGTTTTCTTCCCCCAAAATTATTCTGTATATCTTTCTTTGTGTTCAGTAGTAGAAAGAAACTTATAGTCCCAATGAACCGGAAGCTGCAACCATTATTTTGTTGGATTTGTGACTCAGTTTAGCGAAACGGAATATTAA
Associated Phenotype:
Not determined