epidermal atrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description acquired diminution of the size of epidermal layer of the skin, associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes (Mammalian Phenotype Ontology, MP_0001221)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001221
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3 gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASL argininosuccinate lyase
TWIST2 twist family bHLH transcription factor 2
ZMPSTE24 zinc metallopeptidase STE24