neurofibromatosis type 1 Gene Set

Dataset PhosphoSitePlus Phosphosite-Disease Associations
Category disease or phenotype associations
Type disease
Description Neurofibromatosis type 1 (NF1) is a clinically heterogeneous, neurocutaneous, genetic disorder characterized by café-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas. (Orphanet Rare Disease Ontology, Orphanet_636)
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Genes

1 proteins associated with the disease neurofibromatosis type 1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Symbol Name
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)