ZMP
plcd1b
Ensembl ID:
ZFIN ID:
Description:
phospholipase C, delta 1b [Source:RefSeq peptide;Acc:NP_956362]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38324 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13963 | Nonsense | Available for shipment | Available now |
sa32897 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
e52 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38324
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 |
---|---|---|---|---|---|
ENSDART00000046098 | Nonsense | 77 | 749 | 3 | 15 |
ENSDART00000142174 | Nonsense | 100 | 282 | 3 | 5 |
ENSDART00000144587 | Nonsense | 77 | 259 | 3 | 5 |
The following transcripts of ENSDARG00000034080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 21217802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 21763217 |
GRCz11 | 2 | 21421279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCCCTCAGTCTCTATTGAGGACATTGAGGAAGTCCGAACAGGTCGA[C/T]AAACAGACAGTCTGAGGAAATACACAGAGGAGACATTGGAGGGTCGAGCG
Long Flanking Sequence:
TATGACCCTGGACTACAAAAATAGTCATAAGGTTTATATTTTGTAATAATAATTTTAAATACATAGTCTGGAAGCTGAATAAATGCGCTCCATTGATGTATGGTTTCGAGTGATAGGATAACATTTAGCTGAAATACAACGATCTAAAAATCTGGGGTCTGAGGCTTTGAAACAAATCTAAATATTGAAAATAACTGACTTTTAAATATGATCAAATTAGGTTCTTAGCAATAAACATATAATAATATAAGTTTTGATTTATTTATGGAAGGAAACTTCCAAGATGCCGTCATGGAAGATGATCTTTCATAATATTCTAATCATTTTTAACATAAAATAAAAAGGATCATTTTGACCCAAACTGTGTATTTTAGGCTTTTCCCACAAATATACCACTGCAACACAAGACATTTTTCAGGTCTCATTTCATGTGGTATGCTAATGCATCTCTTTCTCCCTCAGTCTCTATTGAGGACATTGAGGAAGTCCGAACAGGTCGA[C/T]AAACAGACAGTCTGAGGAAATACACAGAGGAGACATTGGAGGGTCGAGCGTTCTCCATCTTGTTTAAGGGTCGTCAGAAAAGCCTGGACCTAATCGCCAGCACTGAGGAAGAAGCCAAGAAATGGGTCAGCGGTTTGGAGAAAGTCATCTCAAGCTTGAACAACCTCAGTTCACAGAAGAAGACGGAGCAGTATCCTTTTCATTAAGTGAAATTCTAGCATTGTTCCTCAAGTGTCTCTGTTAGTTGTTCTTACATCAGGGTTTTAGCTGGATCTACAGCTCCTTGCGGAAAGCAGACAAAAACCTGGACAACAAGATGAGTCTGAAAGAGGTCAAGAGCTTTCTGAAAGACATCAACGTTGAAGTGCACGAAGACTACGCTGAAATGCTCTTTAAGGTGATATGGGAATTTGATCATCTGTAATGTTTTCACACCGTGTCCTAACTAAATAAGTTTTTTTCCTAACCATCTACAACAGCAATGTGCAGATTTTCTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13963
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 |
---|---|---|---|---|---|
ENSDART00000046098 | Nonsense | 89 | 749 | 3 | 15 |
ENSDART00000142174 | None | 112 | 282 | 3 | 5 |
ENSDART00000144587 | None | 89 | 259 | 3 | 5 |
The following transcripts of ENSDARG00000034080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 21217765)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 21763180 |
GRCz11 | 2 | 21421242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGAACAGGTCGACAAACAGACAGTCTGAGGAAATACACAGAGGAGACAT[T/A]GGAGGGTCGAGCGTTCTCCATCTTGTTTAAGGGTCGTCAGAAAAGCCTGG
Long Flanking Sequence:
ATTTTGTAATAATAATTTTAAATACATAGTCTGGAAGCTGAATAAATGCGCTCCATTGATGTATGGTTTCGAGTGATAGGATAACATTTAGCTGAAATACAACGATCTAAAAATCTGGGGTCTGAGGCTTTGAAACAAATCTAAATATTGAAAATAACTGACTTTTAAATATGATCAAATTAGGTTCTTAGCAATAAACATATAATAATATAAGTTTTGATTTATTTATGGAAGGAAACTTCCAAGATGCCGTCATGGAAGATGATCTTTCATAATATTCTAATCATTTTTAACATAAAATAAAAAGGATCATTTTGACCCAAACTGTGTATTTTAGGCTTTTCCCACAAATATACCACTGCAACACAAGACATTTTTCAGGTCTCATTTCATGTGGTATGCTAATGCATCTCTTTCTCCCTCAGTCTCTATTGAGGACATTGAGGAAGTCCGAACAGGTCGACAAACAGACAGTCTGAGGAAATACACAGAGGAGACAT[T/A]GGAGGGTCGAGCGTTCTCCATCTTGTTTAAGGGTCGTCAGAAAAGCCTGGACCTAATCGCCAGCACTGAGGAAGAAGCCAAGAAATGGGTCAGCGGTTTGGAGAAAGTCATCTCAAGCTTGAACAACCTCAGTTCACAGAAGAAGACGGAGCAGTATCCTTTTCATTAAGTGAAATTCTAGCATTGTTCCTCAAGTGTCTCTGTTAGTTGTTCTTACATCAGGGTTTTAGCTGGATCTACAGCTCCTTGCGGAAAGCAGACAAAAACCTGGACAACAAGATGAGTCTGAAAGAGGTCAAGAGCTTTCTGAAAGACATCAACGTTGAAGTGCACGAAGACTACGCTGAAATGCTCTTTAAGGTGATATGGGAATTTGATCATCTGTAATGTTTTCACACCGTGTCCTAACTAAATAAGTTTTTTTCCTAACCATCTACAACAGCAATGTGCAGATTTTCTATTTTAGAAAGAGTTTCTATTAATGCAACGTCATGACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32897
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046098 | Essential Splice Site | 183 | 749 | 4 | 15 |
ENSDART00000142174 | Essential Splice Site | 206 | 282 | 4 | 5 |
ENSDART00000144587 | Essential Splice Site | 183 | 259 | 4 | 5 |
The following transcripts of ENSDARG00000034080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 21217403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 21762818 |
GRCz11 | 2 | 21420880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACATCAACGTTGAAGTGCACGAAGACTACGCTGAAATGCTCTTTAAGG[T/G]GATATGGGAATTTGATCATCTGTAATGTTTTCACACCGTGTCCTAACTAA
Long Flanking Sequence:
AACACAAGACATTTTTCAGGTCTCATTTCATGTGGTATGCTAATGCATCTCTTTCTCCCTCAGTCTCTATTGAGGACATTGAGGAAGTCCGAACAGGTCGACAAACAGACAGTCTGAGGAAATACACAGAGGAGACATTGGAGGGTCGAGCGTTCTCCATCTTGTTTAAGGGTCGTCAGAAAAGCCTGGACCTAATCGCCAGCACTGAGGAAGAAGCCAAGAAATGGGTCAGCGGTTTGGAGAAAGTCATCTCAAGCTTGAACAACCTCAGTTCACAGAAGAAGACGGAGCAGTATCCTTTTCATTAAGTGAAATTCTAGCATTGTTCCTCAAGTGTCTCTGTTAGTTGTTCTTACATCAGGGTTTTAGCTGGATCTACAGCTCCTTGCGGAAAGCAGACAAAAACCTGGACAACAAGATGAGTCTGAAAGAGGTCAAGAGCTTTCTGAAAGACATCAACGTTGAAGTGCACGAAGACTACGCTGAAATGCTCTTTAAGG[T/G]GATATGGGAATTTGATCATCTGTAATGTTTTCACACCGTGTCCTAACTAAATAAGTTTTTTTCCTAACCATCTACAACAGCAATGTGCAGATTTTCTATTTTAGAAAGAGTTTCTATTAATGCAACGTCATGACAAAACAACACCATAAACATCTATGATAATTTTCTCCTCAGGTACCGATTATGTGCTTTTTTATGTGAATTGCTGATATTTGTGAGTTTGAACATCGTTTACCTGGCATGTATTGCCATTCTAATGAAAGTAACAGCAAATAGTTCACCTCAGATCTTGAAAATTAAATAACTAGCAAGCGGTTAAAAAATGAAAATCAACTGTCACTGAGCCTATTAGGGCTGCAACTAACGATTATTTTAATAATCGATTAATTTGTCGATTATTTTTCTGATTAATCTGATTGAAAACAAACAAGAAAAGCATTCATCTCCAACTGTAAGATTTGAGATACCTAAGATACTTTGATGTCTTTGACAATACAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
e52
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 |
---|---|---|---|---|---|
ENSDART00000046098 | Nonsense | 301 | 749 | 6 | 15 |
ENSDART00000142174 | None | None | 282 | None | 5 |
ENSDART00000144587 | None | None | 259 | None | 5 |
The following transcripts of ENSDARG00000034080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 21210083)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 21755853 |
GRCz11 | 2 | 21413915 |
KASP Assay ID:
554-0031.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCTCATAAAAGTGTTTACCATGACATGAACCAGCCTCTCAGCCATTA[C/A]TTCATCTCCTCCTCTCACAACACATACCTGATGGAGGACCAGCTCAAAGG
Long Flanking Sequence:
NNNNNNNNNTCACATCACATGATTAGTTTGTTTATTAAAGATTAAAAGATAAAGATATTTTTAATCATTATGATGACCATGCTATTTTACGTTTGATATTGTATGTATGATATTCATATTGCAATGTATATTGCAGCAAAAGAAAATATCGCAATCCAATATTGTGCAGCCCTATTCTGAAGAATCATGTGAGACTGAAGACTGATTAAACTAATTATAAAATAATATTAAAATAATTGTATCCATGGTTAATATAGAGAATTCTTTTAGAATCTTACTAAATCTAACTTTTAAGTTAAGTAAATGTACTTGGTTTTAGTCAGTTGACTTGCAAGTCCAATGCATAATGGCTTATCTGTGTTTTCAATTCTTCTAGCCAAAGCCAAACAGCAAATGACCCAGGATGGCTTCCTGATGTACTTGCACCAGCCGGAGGGGCTGATCTTTAACCAGGCTCATAAAAGTGTTTACCATGACATGAACCAGCCTCTCAGCCATTA[C/A]TTCATCTCCTCCTCTCACAACACATACCTGATGGAGGACCAGCTCAAAGGACCCAGCAGCACTGAGGCCTACATAAGGTAATCCTGTTGATCATTCTGTATTTGTTTACATTATGTAGTTTGAACATGAATTACAATTCCAGTCTCGCATCTAAATAAATACTTTCTGTAAGGTCTTGTGCAATGAGATATTTGTGCAAATCTGGTTTATTGGTTTTACATTAGATTAGGTAGTGAGCACCAAAGGCAAAACTGGAACTGCTTTAACAAAACAATTCATGAATATGGTGCTTAAATGAATACACCCAATGAATGTGCTGGGAGAATAATGAAGAGTTCAGATGCAAAAACCTCTAAGTGCCATCTGGAATTTTCTTCTACAGTGAGCATTTTCTTTAGCCTCTTAAGTTTATGTTCTGTTTTTTTCCTGTGAAAAAAAATCAATGGAAATAACCTATGCTTTGCCATAAAAGTGAAATTACTAAATCAAACTACAAATCA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |