Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Pld4mpc96H
Name:	phospholipase D family member 4; muta-ped-c3pde 96, Harwell
MGI ID:	MGI:5791986
Gene:	Pld4  Location: Chr12:112727089-112735420 bp, + strand  Genetic Position: Chr12, 61.2 cM
Alliance:	Pld4mpc96H page

Strain of Origin:	C57BL/6J
Project Collection:	Harwell ENU Mutagenesis

Allele Type:    Chemically induced (ENU) (Not Specified) Mutation:    Single point mutation   Mutation details: ENU mutagenesis induced a C to T point mutation that results in the amino acid substitution of phenylalanine for leucine at position 158 (L158F). (J:234901)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

1 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Pld4 Mutation:	26 strains or lines available

Original:	J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
All:	1 reference(s)