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Dpmy
Spontaneous Allele Detail
Summary
Symbol: Dpmy
Name: deficient peripheral myelin
MGI ID: MGI:5697177
Gene: Dpmy  Location: unknown  Genetic Position: Chr10, Syntenic
Alliance: Dpmy page
Mutation
origin
Strain of Origin:  CBA/J
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Dpmy Mutation:  1 strain or line available
References
Original:  J:226382 Karst SY, et al., The deficient peripheral myelin mutation. MGI Direct Data Submission. 2015;
All:  1 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
04/16/2024
MGI 6.23
The Jackson Laboratory