ZMP
PLA2G4C (5 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 |
---|---|---|---|
sa8473 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18037 | Nonsense | Available for shipment | Available now |
sa32237 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8473
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 |
---|---|---|---|---|---|
ENSDART00000053320 | Nonsense | 21 | 529 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 11849289)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 11045641 |
GRCz11 | 19 | 10964547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACATYGCACTGCTGGGTTCTGGAGGAAGTGAAAGAGCAATGGTGAGTT[T/A]GCTGGAATCACTGGACGCTCTGGCTCAAACTGATCTSATGGACTGCATGA
Long Flanking Sequence:
AGCTAATGCGGGACCGGCTGTGGTCAATCATAAGCACATGATCCTCTCGAAATTAGTTTATAAGTAAAATTCAATTAGAAGATCTAAAACAGTAATAAACCTCTAAAGCTTGCAGTTTGTCACTTCCGCCTAAATGGGTCAATACTTGTTTCACATCACCTTGTACTTCAGTTTCTCATCAAATCTTAACCATTGAAATGCTCTCTAGTATCTGACATGCCCCGCCATCTTAAAGACACTTCTCATTTTCTTTCTATTTGGTGCGCTTGAGCTCCTGAGAGCAGAGTGATGAGAAAAACAAACCGCAATTGGATGTTTTTAAAAAAGGGAGAAGCTACTCTATGTCCTGTGCACTCTTCATGTTTCAGTTGAGATTATGTCGAACATTAAGTGAAAAATGCACATTTAAAAGCCCTTGACAGGATCTACATTTTCACAGGACCAGGTGCCCAACATCGCACTGCTGGGTTCTGGAGGAAGTGAAAGAGCAATGGTGAGTT[T/A]GCTGGAATCACTGGACGCTCTGGCTCAAACTGATCTCATGGACTGCATGATGTATCTTGCTGGAATCTCAGGATCAACCTGGTAAATAAACAAATACATTCAGATAATCAGATCCAGCTGAATATAAACAAATGATGAACTTTTCCCCCCTTCATTAGGTGTATGGCATCTTTATACAAAGAACCCAATTGGTCCAATAAGCTTAAAGTAGTGAAGGATGACGTCATACAGAAACTTGTTGGTCGTGACGTCAGTTTGATGGACAAATATGTGGCCCTCAAAGAATACTACAGAGTGAAGGATAACTTTAGTTTGACAGAAGTCTGGGCTGTGCTGTTTATAAGCAAGATGGTCAAAGAGGTGAGAGAAGTTCTATGTCATGTTTCTTGCGTAAATTAAGCATTATGACATTCAATGAAGCTCTTGAAATGTATAATTCACCTAAAAATTAAAGTTCTCCTCACCATTTACTCACACTAAATTGAACCTAAACTTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18037
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053320 | Nonsense | 210 | 529 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 11852835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 11042095 |
GRCz11 | 19 | 10961020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTTATTYATCGGCAGGTCTGTGTGGTAGTAGTCTTGCTGATCCTGTA[A/T]AAATATTGGAGGAACTGATATATATAATCAAACGTAAGTTCCCTTTATCA
Long Flanking Sequence:
CTGTGGCGACCGCAGATTAATAAAGGGACAAAGCTGAAAAGAAAATGAATGAATGAATAAGCCAAAAAGAAAATGAATAAATGAGAGCAAATTTGTTTTCCCATTTCGAAATAAAATTTTAAAGCTATGTCATGGCGATGAGATAATCTAATAAATTCCAGCAAGCTAAACTGGCGCTCTAGGCAAACGACGATAACTCTGTGGCACCCCTACTACTCTGCCACCCAAGGTCGGCTCAATGGACGCACCGGCCCTGCCTGAGTCTGTGTTTGTGCTGCTGGTGTGAAAATCACCTGTAGTGCACAGACTGAAACCCCCTTTTTCATGCAAACCCTTCCCTTCTTTGCCACACGATACTCCCACCAAAACAAAGCTGGACTCACCCACTTTTTGAAAACCAGAGAATGTAAAAACACCCTGCTGAGACCCTGCTGAGGACCATTTATTTCTTTATTTATTTATCGGCAGGTCTGTGTGGTAGTAGTCTTGCTGATCCTGTA[A/T]AAATATTGGAGGAACTGATATATATAATCAAACGTAAGTTCCCTTTATCACTACCATTTCATTTTGAAAACTGTTTGTAATTAATCATTATCCATCAATGTGATATGGTATAAGATTAATATGCAACCTTTTCCTCTTAGATTTATTTGGGTCTGAGTCTGAAATGATGGCGGACGTCTCGTCTTCAGAAACAAAACAAACAGACATTCAGTCCCTCAGTGCTCAACACCTGGACAGGGCTGGCAAACTGCTCTTGACACTTGTGCAAGTGAATCTTCTGGTTTTAAAAAATGAAGATCCTTCGTCTCAGGTTAAAACCCTGAATGACTTACTGAGAGGTAATGATTATGATGATAACATGTTTAAGCTGAGCATAAGAGCAAAATCATTTGGTCAGAAAATGGGAATACATGCTATATTTCTTTGATAAAACTCAATTTAAAATCTTGCTAACATCAGGTTTTGCTTCATTTAGCATCATCACGCATTTGTAAATAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32237
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 |
---|---|---|---|---|---|
ENSDART00000053320 | Essential Splice Site | 483 | 529 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 11855725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 11039205 |
GRCz11 | 19 | 10958130 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCGACTGTGATACACATTCCTCTTTTCAACAGAGTCAACTGTGGTAG[T/C]AAAGGTAATGTCATATTATTTATTTTTAAAGAATGGAGTAAAAATCTTGT
Long Flanking Sequence:
ACACCCCTGCCATAAAGGGTTAAAATAACTGCTTTTATCTTTTAATAATGCACACACACACACATTTACCTCAGAGAAGGAGGTTTCTAGAATCTGTGAACATGAAGTGAGGCATTATGCTGATGGCGGGATCATCATCAACTCACCTTTTTTACCGGTGCTGAGGAAAGAGAGACACGCTGACCTCATAATCTCCCTCGATTTCAACGAGGACGATCCATTTGAGGTATGGAAAATGATTCTTTTAATAACCTGCATAGAGAATGCTAAATATTATCCCTGCTCCGTTCACACAAACATTCTTTATCATAAATCTTCTTGTTATTTCAGTCTCTCACAAAAACAGCTGAAATGTGCAAAAAGCTACACATTGATTTCCCTGAAGTTCCTGAAGAGATACAAAAGGAAAAGGATTTTCCAAGGGATTTTTATGTGTTTGAAGGCTGCAATACTCCGACTGTGATACACATTCCTCTTTTCAACAGAGTCAACTGTGGTAG[T/C]AAAGGTAATGTCATATTATTTATTTTTAAAGAATGGAGTAAAAATCTTGTCATAAAATATACCACATATTAACCTGGTAAACTACTATACAATTATTTTCCTGTTCAGTACTCAAATGTGCTGTACCACAAGATTTCTTGACTGTCATTTACTAGTAAAGATGTTGTGTGTCATTATAATAGCTATGCGCTGTCAAGTAAAATACGGACACACCTTATGTTGGGTTAATTTAAATTACTTTTTAATCCAGCGGTTGGGTTTGTCTATATATGACCCAACATTGGGTTAAAACAATCCAGCATTTCTATAGTAGTTGTAGCTAGTTAGATATGAAGGAAATCCGACCATGAAAACTGACAAATGTCCTAAAATGTCTGTTTTATAGCTGAAATGGAAAAGTTGAAGAGAAAATACAGCACCGTCCAAGGGCCCTACTCCATTGAAAAGATTGATGAACTGTTGAAGAAAGCTGGAGTGAACATCACAAATAACAAAGAGAA
Associated Phenotype:
Not determined