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pma
Spontaneous Allele Detail
Summary
Symbol: pma
Name: peroneal muscular atrophy
MGI ID: MGI:1856996
Gene: pma  Location: unknown  Genetic Position: Chr5, Syntenic
Alliance: pma page
Mutation
origin
Strain of Origin:  CF-1
Mutation
description
Allele Type:    Spontaneous
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: 6 anatomical structure(s)
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 pma Mutation:  0 strains or lines available
Notes
This mutation was found in the CF1 stock during the process of inbreeding.
References
Original:  J:6590 Esaki K, et al., [A new mutant in the mouse: peroneal muscular atrophy (author's transl)]. Jikken Dobutsu. 1981 Apr;30(2):151-5
All:  7 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
02/20/2024
MGI 6.23
The Jackson Laboratory