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

Symbol:	PctpR120H
Name:	phosphatidylcholine transfer protein; R120H
MGI ID:	MGI:3691424
Gene:	Pctp  Location: Chr11:89873491-89893720 bp, - strand  Genetic Position: Chr11, 54.7 cM
Alliance:	PctpR120H page

Strain of Origin:

NZO

Allele Type:    Spontaneous Mutation:    Single point mutation   Mutation details: A G-to-A transition in exon 4 resulted in the arginine to histidine substitution at amino acid 120 (p.R120H) in NZO, NZB/BINJ and NZW/LacJ strains. This mutation renders the protein inactive. (J:114974)

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

List all tumor models in MMHCdb carrying PctpR120H

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Pctp Mutation:	15 strains or lines available

Original:	J:114974 Pan HJ, et al., A polymorphism in New Zealand inbred mouse strains that inactivates phosphatidylcholine transfer protein. FEBS Lett. 2006 Oct 30;580(25):5953-8
All:	3 reference(s)