ZMP
pla2g6
Ensembl ID:
ZFIN ID:
Description:
85 kDa calcium-independent phospholipase A2 [Source:RefSeq peptide;Acc:NP_998262]
Human Orthologue:
PLA2G6
Human Description:
phospholipase A2, group VI (cytosolic, calcium-independent) [Source:HGNC Symbol;Acc:9039]
Mouse Orthologue:
Pla2g6
Mouse Description:
phospholipase A2, group VI Gene [Source:MGI Symbol;Acc:MGI:1859152]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29818 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43871 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa3189 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa29818
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044559 | Nonsense | 316 | 818 | 6 | 17 |
| ENSDART00000086336 | Nonsense | 319 | 757 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 22 (position 31668980)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 29148058 |
| GRCz11 | 22 | 29097253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGTCTTCTGCTGGACAGAGGATGCAACGTCAACTACTTGAGCAAGACT[G/T]GAGAAAGTCCTTTACACATCCTGACCAAGAGAGGGCGCTTTGAGGCCGCA
Long Flanking Sequence:
GGGGGAGGGACACATTGGCAAACTGGTAGTTTTTGCATTTTGTGGGTGCACAAAAGGGTTCTTGGAGCTTAGTATGGTTACAGTTGAACTGCTGAAGCCACATGGAATGTTTTGACAATATTTATAGTTCCTTTTCTGGACATCTCTGGACCCTGGAGGGTCAGATAGCTCTTGGATTTCATCTGTCATGAAATTGAAACGAGAGTAAATAATAACAGGTTGTTCATTTTTGAGTATTATTCTGTATATTTTCTCTCCTTTAGTTGTGCTGAAGCCATTTTATCTTCAAGCCCAAATCAGCTTCTGGCAGAGGATCCGGTTTATGGCGGGACACCTCTTCACTGGGCCAAAACTGCAGAGGTCAGGAAAAAAAACCTTTACATTTTCTAGTTCAGTGCTAAGTAATTATTGTGTGTTTATTATAATCCTGTGCTTACTCTGTTCAGATGAGCCGTCTTCTGCTGGACAGAGGATGCAACGTCAACTACTTGAGCAAGACT[G/T]GAGAAAGTCCTTTACACATCCTGACCAAGAGAGGGCGCTTTGAGGCCGCAATGACCCTGCTGACACACGGAGCTGATGCTAATATTAGGGGTCAGGATGGTAACACTGCCCTGCATCTTGCTATGAAGGTATGGAGGAGGAGCTCATAAAGACTGTCAAGATCATTTATATGGATATACAGTTGAAGTCAGAATTATTAGCCCCCTGTTTATTTCCCCCAAATATTATTTCCCCTGTTTATTTCCCGCTTGGAAATATTAAAAAAAAAAGGGGGGGGGGGGGGGAGAGCTAATAATTCTGACTTCAACTATATGTGCACATTTATTTATATATATATATATATATATATATATATATATATATATATATATATTGTTAGGGCCGTCAATTAATAAAAAAAATTTGCTAATTAATCACACTTTTTTTGTGATTTATCACAAAAAGTCATATTTAAAACAGAAATAAAAACACAGGCATGGAAGTGCCAATTTGAAATTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43871
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044559 | Nonsense | 406 | 818 | 8 | 17 |
| ENSDART00000086336 | None | None | 757 | None | 15 |
Genomic Location (Zv9):
Chromosome 22 (position 31679149)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 29158227 |
| GRCz11 | 22 | 29107422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACTCCGACTGAAGGCTCCAACCGTAAGGTGCTGTTGAACATGCTGTG[T/A]AGTGTAGGTGTCGAACGCTGCCATCCTCCATCCCTCAACAGCCCTACTCA
Long Flanking Sequence:
TTATTTTAGTAGGATATTTACATAAAAAGTGCTGATAAAGTAATGTTTTTTTATAGTTAATTATATTGTAAGTGATATTGTTATTGCAACACTCAGTAACAACATCGCATATTTTTTCCAGTATTGTGCAGCCCTAATTATTATTATTTTTTTTTTTTGAGGTCTACAAAACTTACATTGACAGTTTAAATTGTTCATCATCATCATAAGGAGTGGCTCTTTTCTATGAAAAACAGCTGAAGCTGTCTGACAAGTCCTAATGTTTAGATTGGCCGACAAAAGATCATCGCAGCAAACCATTTAATGCCTGCATTTCGTGCATTTAACCATAAGAATGAAATGTCATGTTCTACCCATGCTGTTTTGTTTTCTCATTCATGCATTCAGTCAGCACGTACTCACCTTTTCTTTCTTGTCTTGCGTGTGCATGGTGTGGCATGCGTTTAATCCTGCACTCCGACTGAAGGCTCCAACCGTAAGGTGCTGTTGAACATGCTGTG[T/A]AGTGTAGGTGTCGAACGCTGCCATCCTCCATCCCTCAACAGCCCTACTCACAGTCTCAGAAAAGCTCCGCCCCCTGGCATAGGTAAAGCTCCACCCCCAAACAAATGCATATTTCCTGTTGACATTTTTCAGTGCTTTATTGTGTTTCTCAACGCGTTTATACTCAAATGTTTGTCAGCGAAACAAGTGTGACTAGCTAAAGTTTGGATAGCTGTTACCTAAAAAGGCAGTTAGCTACTGCTAACCTGGGGCTGGGTGTTGATACAAATGTCACTATGTTGTTTAATTCTGATTCACAAGCTCTCGGATTTGATTCATGATTCAATTTTGTGAATATAGATTTATTACAAATAAATATTTCTTAAAAAATGGTCAGTGAACAGTTTGGTTCGAGTGCATGTTTGCATTAATACTAGTGCTGGACAAAAATTAATCGTGATTAATTGCATCCAAAATAAATTTTGTTTCAACATGATATTTGCGTGTGTATTATGCATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3189
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000044559 | Nonsense | 589 | 818 | 12 | 17 |
| ENSDART00000086336 | Nonsense | 553 | 757 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 22 (position 31690421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 29169499 |
| GRCz11 | 22 | 29118694 |
KASP Assay ID:
554-3303.1 (used for ordering genotyping assays)
KASP Sequence:
AGCGTTCTTGCAGACAGACACCCTGGAGAACTGCATCTGTTTCGCAATTA[C/A]GACCCGCCGGCCCTTCAGAGAGACCCTCCATACAAGTCTACRGCCACATT
Long Flanking Sequence:
AGCCAAGTTTAGTGTTAAATTTTCTTCAAACTTGCCTCCTAAGTGCAAAGTCTGCCAGTATTTACAAGCAATAAGAAGACCCTAGCAAAGACCTACAGTAGATTTCTAAAACCAGCTAACCTTAATACAATAATATTTACAAGCTATGGCCCATCAATGGCCCAGTACACCCTCGCAATATTCTAATGTTGCAGTCATCCAGAACTTACTGTGAACCCCCATATACCTGCCTAGCAAAAAACAATTCTAGAGCTTAATCGAAAATTCAGAAAGTGTAAGCAATGCTTTAGTGACAACTCCCAACAGCCAATAAATTCCCTAATTACACATCTGAACTCCTTAAGATGTAGCAGTGACTTTTGCATTGTCAATCACCACACATATTCTTCAGAAAGAGGCTTGTTTTTAACTCACCTCCCATCTGTTTTTCTGTTTAGAGTAATGGTGACTAGCGTTCTTGCAGACAGACACCCTGGAGAACTGCATCTGTTTCGCAATTA[C/A]GACCCGCCGGCCCTTCAGAGAGACCCTCCATACAAGTCTACGGCCACATTCCAGCCTCTTACTGTGCCACAAGGTAAATCTCTTTTGATTCTTGGGATGAAGCTGTTGTAATTATCTTTGTGGCACTGAAAAGCAAACTCATGTTCTTCCTCCCGTACTTTATATGAGCATTTTGATACGCTCCTGGATTCTCAGTTATCAAATGCTGCGTGAAGCTTCATTGTCGCTGTTGCAGGGTGGGAGGATGAAGATCTTTTGCTAGTAGGATATACTCGACCTCCCAGAAAGCGTAGGAAGGTGACTGATGAAGGTGTGTGTGAAAGAGAAAATGTGTATGTGGAATGAAAAGGTCACAGTATGCAAGTGTCCTGGTGTTCACATTGAGCAATCATACCTCATGTTGGATCTAATCGGTCGTTTAGTTTGCTGGAGGCTAATCATCTTTTGCCCTTTTAGGTCTATATTGGGCTCCTGCTCATTCGCATTGTGTTTCTTTCAGA
Associated Phenotype:
Not determined