ZMP

LOC565386

Ensembl ID:

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