Gene

pma

Species
Mus musculus
Symbol
pma
Name
peroneal muscular atrophy
Synonyms
None
Biotype
heritable phenotypic marker
Automated Description
Used to study clubfoot and neurogenic-type arthrogryposis multiplex congenita-2.
MGI Description
PHENOTYPE: Mice homozygous for a spontaneous allele display a club foot and ankle joint immobility at birth, show peroneal muscular atrophy in the hind limbs due to absence of the common peroneal nerve branch, and develop an unusual gait due to a dropped foot in adulthood. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
Not Available

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

No data available

Sequence Details

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Expression

Primary Sources
None
Other Sources
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions