cutis laxa Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A skin disease characterized by skin that is loose, hanging, wrinkled and lacking in elasticity; it can also affect connective tissue in other parts of the body, including the heart, blood vessels, joints, intestines and lungs. (Human Disease Ontology, DOID_3144)
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Genes

5 genes involed in the disease cutis laxa from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ATP6V0A2 ATPase, H+ transporting, lysosomal V0 subunit a2
ATP7A ATPase, Cu++ transporting, alpha polypeptide
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
ELN elastin
FBLN5 fibulin 5