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Heritable Phenotypic Marker : pma peroneal muscular atrophy

Primary Identifier	MGI:97628	Organism	mouse, laboratory
Chromosome	5	Mgi Type	heritable phenotypic marker

description

FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Used to study clubfoot and neurogenic-type arthrogryposis multiplex congenita-2.
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]

synonyms:
peroneal muscular atrophy,
MGD-MRK-13368,
pma

earliestPublication:
Esaki K, et al. (1981) [A new mutant in the mouse: peroneal muscular atrophy (author's transl)]. Jikken Dobutsu 30(2):151-5

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Involved In Mutations

0 Transgenic Expressors

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

Other

0 Driver For

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