Down syndrome Gene Set

Dataset PhosphoSitePlus Phosphosite-Disease Associations
Category disease or phenotype associations
Type disease
Description A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. (Human Disease Ontology, DOID_14250)
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Genes

2 proteins associated with the disease Down syndrome from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Symbol Name
CRYAB crystallin, alpha B
TP53 tumor protein p53