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Plp1jp-rsh
Spontaneous Allele Detail
Nomenclature
Symbol: Plp1jp-rsh
Name: proteolipid protein (myelin) 1; rumpshaker
MGI ID: MGI:1856067
Synonyms: jp-rsh
Gene: Plp1  Location: ChrX:136822166-136838582 bp, + strand  Genetic Position: ChrX, 59.1 cM, cytoband F1-F2
Mutation
origin
Strain of Origin:  STOCK Rb(1.3)1Bnr
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsSequence analysis of cDNA from brain showed this allele involves a T to C transition in codon 186 of exon 4. (J:2126)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 1 anatomical structures
Find Mice (IMSR)
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 Plp1 Mutation:  17 strains or lines available
References
Original:  J:14143 Cattanach BM, et al., Rump shaker, a new neurological mutation. Mouse News Lett. 1988;81:63-64
All:  25 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory