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

Symbol:	Pmp22Tr-1H
Name:	peripheral myelin protein 22; trembler 1 Harwell
MGI ID:	MGI:1862010
Synonyms:	Gena51, GENA 51, H12R, Tr-m1H
Gene:	Pmp22  Location: Chr11:63019808-63050373 bp, + strand  Genetic Position: Chr11, 38.99 cM
Alliance:	Pmp22Tr-1H page

Strain of Origin:

BALB/cAnNCrl

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: This allele involves an A to G transition at position 35 in codon 12 producing a histidine to arginine substitution. (J:63755) Inheritance:    Dominant

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

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Pmp22 Mutation:	32 strains or lines available

Original:	J:63816 Nolan PM, et al., A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat Genet. 2000 Aug;25(4):440-3
All:	3 reference(s)