ZMP

zgc:77563

Ensembl ID:

ENSDARG00000003584

ZFIN ID:

ZDB-GENE-040426-2248

Description:

platelet-activating factor acetylhydrolase [Source:RefSeq peptide;Acc:NP_998354]

Human Orthologues:

PAFAH2, PLA2G7

Human Descriptions:

phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) [Source:HGNC Symbol
platelet-activating factor acetylhydrolase 2, 40kDa [Source:HGNC Symbol;Acc:8579]

Mouse Orthologues:

Pafah2, Pla2g7

Mouse Descriptions:

phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) Gene [Source:MGI Sy
platelet-activating factor acetylhydrolase 2 Gene [Source:MGI Symbol;Acc:MGI:2140321]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa37111	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37111

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
ENSDART00000016090	Nonsense	9	444	1	11

Genomic Location (Zv9):

Chromosome 20 (position 35495445)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	35567958
GRCz11	20	35470837

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCTCAATGGATCGCTGTTAACGTCGATGTGTTCTGTTGGCAGACTTGTT[C/T]AGCTGACTCTGGTCAAGAGGGTATATGAATGGTCAAAGTCAACGTCAGGT

Long Flanking Sequence:

ATGCTGTTTGTTTGCTCATTGACTTCCATTCTATAAATAACTTCCATTAAGTTAAAAAAATCTTTATAAAATAAGAAACAAAACATTGAGGCAGAAATATGCGCTTCAGTTATTACTAAATTAATTGTTTCACCAATACGAATCACTTTCATACGAATCTTGACTTTTGAACAGAACTGGACTGGGGGTGTTGTTCAATATGTGCTGCGTCACACCCCGTGCTCGAATGTTATTGGTTTGTGTTACTGTCCGTCTTATAAACCAGGAACGCGGACTGTCACTTTAAGTACGAAGTGTTCTTTCAACGAATCGTTCACTAAAAAGATTTGTTCAAACACACTTCGAAAAACCGATCCAAAATCAGCAGGGATATGTGACTCAATGCACACGCACATGAGTCGAGTCATGGTCAGGATGAGGCTCCGCCTGCTCACTGTGGACTTCAGCTGAGGCTCAATGGATCGCTGTTAACGTCGATGTGTTCTGTTGGCAGACTTGTT[C/T]AGCTGACTCTGGTCAAGAGGGTATATGAATGGTCAAAGTCAACGTCAGGTAAGTTATTACAAGTCAATTTTAAAAGCCGTTTGACGACTGTGATAACAGTGGCTAACATGCTAACAGTAAACAAACTCATGCCAGTGTTATCGTTGTTGTGACAGACAGCCACTTCCTATCACGTCACTCACTCATTTTCATAAAGTTTTTGAATACTTTTTTAAAAAGTCTGACTATAGTTTGAACTGCTTTTTATTATGTAAGCTAGTGTGCGTGATAGAGGTAAAGGTTTTATATTCACACATTCGTTCATTTAGAAGTCTCTATATTGTTTACCATGTTACTTTGAATATTCCAGTTGTTCTCAAACTGTGGTACATGTACCACTAGTGGTAACGTTACGTGGGCTTCCTTCTAGTGGTACGCGGATAAATCAAAAATGTCATATGTACATTATGCTACATATATTTAAATAAATTATCAAAAAAAATGTATATATGAATATGATG

Associated Phenotype:

Not determined