abnormal cutaneous microfibril morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the fiber-like strand of fibrillin that forms the scaffold of the cutaneous elastic fibers found in the extracellular matrix of the skin (Mammalian Phenotype Ontology, MP_0008419)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008419
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1 gene mutations causing the abnormal cutaneous microfibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FBN1 fibrillin 1