ZMP

ENSDARG00000056535

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 are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23053	Essential Splice Site	Available for shipment	Available now
sa6469	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23053

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079030	Essential Splice Site	165	837	7	20

Genomic Location (Zv9):

Chromosome 17 (position 21285193)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	21435342
GRCz11	17	21455178

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTGTGAGCTGAACGTGGAGATAGACAAGCTTCTTAAGAACTCTGAAGG[T/A]AAATATGTTTTCATTACAAAACATTTTCATCCTAGTTTTTCAAGTAAAAG

Long Flanking Sequence:

TTTAGTTTGTGATTATTAACATTTCTTTCTCAGACCAAGAATGAACTGTGGGTAGAGTTTGAGATGACTAAAAGGTGAATGAGCTTCTGGTAATTTTTAAAAAATATTTACTTTTATGTACAATTATAAACTTGTAAAAACTTATGATAAAGGTTTTTTGCTTGTGCATGTATTCCAGCTCTGTGACACCAAGACCATGTACATCTAATGGAGTGTTGGTGGTATGAATCTTTACTTTGACAGCTTTCTTACGTGTATCATGAGTTACAGTAGAATATATTGTATTCTATGATTTCTGAATAAAACAGATTATTCTGAATGATAAAATTCTGAACTATAGATTTTCTCAAAAGGTTTCAGGTTCACTCTTGGCACAAAAAAAACAAAAAAAACAAACTAGGTTCCTACATCAGATTAACTTTTGGTTTCTCATGAAATCAGGCAGGACCTTTTTGTGAGCTGAACGTGGAGATAGACAAGCTTCTTAAGAACTCTGAAGG[T/A]AAATATGTTTTCATTACAAAACATTTTCATCCTAGTTTTTCAAGTAAAAGCTTCGATAATAATACTATTCACAAATAGATGCAGTAGAAAATAAAACGTGACCCTGGACCACGAAACCAGTTATTTGTAACAGTTTTATATATAAATAGATTTGTCCATCACATGAAAGCTAAATAAATACACTTTCTATTTATGTATACGTTAGGATAGAACTATAATTGGCCAATATACAGTACAATGTAAGTAAAATGTTTATCTAAAAACAAGAAAATCACCTTTAAAATTGTCTTCACCCGCTTCGAATGATATCACTCGATTGAATGAGCATTATCAGTGGTTATCAGCTGATAGATATGGGCCAGTAGGGGCCTTCTGCACCTACTGGTAGATTTAGAAGGCTGTTAACATCCATCCACATGGTTAATCAGCTATAGTAATAATGAAGACTCCAGATCCAGATCTGTTTTTACATTACTGTGATGGTTAAGTTTAGGGTTGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6469

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
ENSDART00000079030	Nonsense	833	837	20	20

Genomic Location (Zv9):

Chromosome 17 (position 21296852)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	21447001
GRCz11	17	21466837

KASP Assay ID:

554-5397.1 (used for ordering genotyping assays)

KASP Sequence:

AAGGAAAGACCTGTTCAGCACCAACACCACAACCAGGATCACAGAAAACA[C/T]AAAAGACRCAAAAGTAATCTGAATGCAAAACTTGATTMATCTTRAATTGT

Long Flanking Sequence:

AACTATAGATTCATATTATATTCTATGCATGAAAAGTTTATTTGCAGTGTGCTTTGAAACATCAGCTAAAATTTGTTGATTATGTATTAGTTGATCATGTATTATATTTTGGTACAATACATCAGTAAATATTTTCCAACATCCAAGAAAATAGCTCATTAATAAAAACTAATCATAAATAATGCTCTGTATGTACTGTATGTGACGCAGGAGTGAAGAGAGAGGGTGAAAAGGAGCTAAAAGAGGGAGCGGTTGATGTTGACTTCAACAGTAACACATCTCCATATGCCACTCACAAACTGACATACACACCGGAGGACTTCCAGAGGCTCATTAACCTAACTTCCTACAACATCCAGAATAACAAAGATGTCATTCTGAACGCATTAAACAAAGCACTGAACAGAAACAGAGACAAGAGGACAGGGGAAGATAGCAAAAAAGAGGAGAAAGGAAAGACCTGTTCAGCACCAACACCACAACCAGGATCACAGAAAACA[C/T]AAAAGACACAAAAGTAATCTGAATGCAAAACTTGATTAATCTTAAATTGTTGTTGTTGTTACAACCTACTCTAATCATGTTTATGTAACTTACAACTAGGGAATGTTACTTAAAACTCACTAAGTTACATACATTCAACTCACAATTGTGATTAGTGCTTGTGATAGACTCAAGGCAAGACATGCTCACTGCCAGAGCCACACATAGAGGGCAGTATATTCTGTAGTACTCTAGTATGCACTCTGCAGGAATGCTGCTCTGAAGGGCCGAGAAGTATAGTTCAGTTTCAGAGTTTCCCCTTTGGTTTGAGATACACTGCTGAAAAATAAATTGAACTTCTATTTTATTAACCAATTGTGTGTGTGATGAGAAGTATTGAGTATGTTTTACATTTGCACATAGACAGCTTTATCTGGTATATGAAGGGCAATTGCAATGACGTGTGCAATGTTTTTAAATGTAAACCTTTGCCAAAAAGCCACAGCTATTGCATTATGAGG

Associated Phenotype:

Not determined