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pma
Spontaneous Allele Detail
Nomenclature
Symbol: pma
Name: peroneal muscular atrophy
MGI ID: MGI:1856996
Gene: pma  Location: unknown  Genetic Position: Chr5, Syntenic
Mutation
origin
Strain of Origin:  CF-1
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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:  6 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/26/2014
MGI 5.19
The Jackson Laboratory