Busch Lab

ZMP

LOC565386

Ensembl ID:
ENSDARG00000070953
Human Orthologues:
JMJD7-PLA2G4B, PLA2G4B, PLA2G4D, PLA2G4E, PLA2G4F
Human Descriptions:
JMJD7-PLA2G4B readthrough [Source:HGNC Symbol;Acc:34449]
phospholipase A2, group IVB (cytosolic) [Source:HGNC Symbol;Acc:9036]
phospholipase A2, group IVD (cytosolic) [Source:HGNC Symbol;Acc:30038]
phospholipase A2, group IVE [Source:HGNC Symbol;Acc:24791]
phospholipase A2, group IVF [Source:HGNC Symbol;Acc:27396]
Mouse Orthologues:
Pla2g4b, Pla2g4d, Pla2g4e, Pla2g4f
Mouse Descriptions:
phospholipase A2, group IVB (cytosolic) Gene [Source:MGI Symbol;Acc:MGI:2384819]
phospholipase A2, group IVD Gene [Source:MGI Symbol;Acc:MGI:1925640]
phospholipase A2, group IVE Gene [Source:MGI Symbol;Acc:MGI:1919144]
phospholipase A2, group IVF Gene [Source:MGI Symbol;Acc:MGI:2685493]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa9294 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9294
Status:
Mutation detected in F1 DNA
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
ENSDART00000104608 Nonsense 227 787 9 21
Genomic Location (Zv9):
Chromosome 17 (position 21315704)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 21465853
GRCz11 17 21485689
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CWGCAGACATTTTGTCAYCTGTTCCTATGAAACCTTTATCGGCCAAACAG[C/T]AAATGAAACTCTYCAWGCCTATTGCACWGGTACGTACTGGTAAAATCAGA
Long Flanking Sequence:
GTTTTTGGTGGTAATTTAAGTCAACAGTTATAATTTACAGTAAATTTTGTACTAATTAGAAAAAAAAATCAGTTAAAGGCGATGGAATAAGTATGTTGTAAAAATTAAGATTTTTTTTTCTGCATTTACCTCAGCTGAGAACAAGATGATGTTAAGACTGCGCGGCGCATATAAGGAAGACTGTATGATCCTGAGCTCTGATGAAAACTCAAACTGCTTGCAGAACACGTGCTTCTACATCAACAGAGATCTGGAGACTGAGTTTAGTCTCTTACCCCCAAAAGTGTGTGACCGATTACACAGATGATCTCAGAACATTTTTTAACAACTTTTACCAAATTAAATAAGGAATACAAAATAAGCAACGTATGACAAAATATGAATCTTGCTTATTTGTTTGCATTTTTTTTTCCTAGGCTGGGGCAGAAATGGATGAGAAATATGCAAATACTGCAGACATTTTGTCATCTGTTCCTATGAAACCTTTATCGGCCAAACAG[C/T]AAATGAAACTCTCCATGCCTATTGCACAGGTACGTACTGGTAAAATCAGATTTTTATTGTATATCTATACATTTTTCCAACGTACTGTAAAATAAAAAGCTAGTAACTAATTGGAGTAATAATTTATTTTAGGGTGAAGTGCATCTAGAACTGAACACAGAGGATTGGTAAACAATCTTTTCTATAACCGTTTAAATAAACTTCTTTTGCATGCAATTTATTGATCAAAACTGAATGCTTTTAATTGTGTAATTGATTATAATTAAATAAGATAAATCACAAGGAACTACCAGCATTTTCTCAACTGATTCCATGAGTCATGTGAATGTGTTTTTGTTCTAAAGCTTAGATGAAGAAATGGATGTGCGTTTGGAATTTGATATTCCAGTGGAGGAGAAGAATTTTCTGCTGAAGAGAAGAAAAGTTGTTTCACAAGCTCTTCAGAAAGCTCTGAATCTCGGCTCTGCACCAGATCCCAGCAAGGCAAGAACACAAACACT
Associated Phenotype:
Not determined