ZMP
PLA2G4C (3 of 5)
Ensembl ID:
Description:
phospholipase A2, group IVC (cytosolic, calcium-independent) [Source:HGNC Symbol;Acc:9037]
Human Orthologue:
PLA2G4C
Human Description:
phospholipase A2, group IVC (cytosolic, calcium-independent) [Source:HGNC Symbol;Acc:9037]
Mouse Orthologue:
Pla2g4c
Mouse Description:
phospholipase A2, group IVC (cytosolic, calcium-independent) Gene [Source:MGI Symbol;Acc:MGI:1196403
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11000 | Nonsense | Available for shipment | Available now |
| sa6960 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11000
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 |
|---|---|---|---|---|---|
| ENSDART00000067596 | Nonsense | 36 | 563 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 4522893)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 4172736 |
| GRCz11 | 5 | 4597253 |
KASP Assay ID:
2259-5376.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGAATATGAAGGAGGCRGCRTGTGTGAAAAAAAGGAGAAGTGAAATCT[G/A]GTCAAGCCTGAAAACACTTGGTATAAACTGTAGTCAGGTTAGTCTAACAT
Long Flanking Sequence:
TGACTGCAGTTTATTATTAGAATTTTTTTCTCTCTAATTGAATAAAAGTTCACACTGTTATTGTTTTGAACACACTCTTTCCAATAATTAACTAAAACAGCGCACATGACACAACAGTTGGCTTTCTTGTTTTTCTAATACACTACTTGAGTAAATAGTATTAATGCCAAAAACAGTGGCTCTAGAGGTGACTGATGTTGTACTGTTATTTTTTGTAAATACTTTAGCATTTCTTGTTGACTATCCTTTTGCAGATGAGTGCATCTAATGTACAGGAAAGGTAAGCAGAGATCTGTTCAGATTCACACAGTAAAAAATATATAATTCTGTGAACAACTATTGAAGAAAAACTTAGTACTCTTCAATATGGCTTCAATACATACAGTATCTATGATGTAAAATTCAGCCCAATGATGTCTTTTTGTGCAGTGAAGTGCGAATCGCACACTCTCTGAATATGAAGGAGGCGGCGTGTGTGAAAAAAAGGAGAAGTGAAATCT[G/A]GTCAAGCCTGAAAACACTTGGTATAAACTGTAGTCAGGTTAGTCTAACATCGAAAGTGTTGACTTTGATACCAATCAATACTGGAATTTTAAAAACATCCATTAAGCCATGTCTGTCAGCTGATCCGTCAATCATCAGACATATGAGCAATCCGCTGACAGCCATGGCTTTCAAACACTTCAGTGTATGTATGTCTGTATTTGCGCTTGGTGAATAGTGGTGAAGTGATTACCTTTAATGGCCAAACATCTGTGTTTAAGAAAGTGCTCAACAGTGTTCAAATATTAGCGGGAAATTGACCATTATTTTTACATTCAGTATATTTATGCAAAAGCAAGACTAGGTCAAACATGTCATATTTCTTGATTTTTCTTCAAGAACTGAAAAAAAAAAAAAATTCAGATGTAGTTAATGAATGTGTGTGTGTGTACATGCAGGATAAAGTTCCAAACATTGCATTACTGGGTTCTGGAGGAGGACAAAGAGCCATGGTGGGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6960
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 |
|---|---|---|---|---|---|
| ENSDART00000067596 | Nonsense | 421 | 563 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 4538869)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 4188059 |
| GRCz11 | 5 | 4612576 |
KASP Assay ID:
554-5340.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGATCCTGCAGTTCCYGCTGCTCTTCTGAAARGTRAAACSAGAGACTA[T/A]GAAGATGCTGGACTGTTGCTGAACTCACCCTAYTTCTCTGTGCTGAGAAC
Long Flanking Sequence:
ACTGGACAGCTCCAGAGCATATGAAGAAGTGTCCCAGTAGATATCTTACACCTTTGACACATGGCAGAGGTCTTGGAAATGTCCTTCACTTTTGACTTGTAAAACCAGACTGATGCTTTAAAGTAAGATGCGTTTTACTAAAAGACAGCAAAAAAGTTAATAGACTAGGTTTCTTTACACAGCCAGTAACAAAATTAAAAGCATAAACAAGATCAAATTATTTTACTTTACCAAAGAACACATATAGTTACCTGTAAAACAATATAAGAACCATTTACTGAATTTCAATTTCAGATTTGAAGATGTGGATAAGGATTTTTGTATGCATGGCTAAGTGGACCTGGGGCAGGAATTATGACTTTCTCTACAACATGAGAGGTGAGAAAAGACCTGCTGTTAACTGTAAATTCAGTGTGAATAATAAAACAGACTCATTTACACCATGATCCCCCAGATCCTGCAGTTCCCGCTGCTCTTCTGAAAAGTAAAACCAGAGACTA[T/A]GAAGATGCTGGACTGTTGCTGAACTCACCCTATTTCTCTGTGCTGAGAACAGAAAGAAAGATTGACATCATCATTTCTCTGGATTTCAGTGAAGGCGATCCTTTCCAGGTATTATAGTTGAAATCAGAATTATTAGCCCCCCCTGTTTATTTTTTTCTCCAATTTCTGTTTAACGGAGAGAAGATCGCTTCAACACATTTCTAAACATAATAATTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATACTTTACTAGATATTTTTAAGTCACTTCTACACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAACTAGGGCAGGTTAGGGCTAGTTATTGTATGATGATGGTTTGTTCGGTAGACTATCGAAAAAAATATATAATTTAAAGGGGCTAATAGTTTTGTCATTAAAATGTTTAAAAAAAATTAAGATCTGCTTTTATTCTAGCCGAACCAAAACAAATAAGA
Associated Phenotype:
Not determined