Greig Cephalopolysyndactyly Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face. (Human Disease Ontology, DOID_14761)
External Link	https://www.disgenet.org/browser/0/1/0/C0265306
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Genes

13 genes associated with the disease Greig Cephalopolysyndactyly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
AGO2	argonaute RISC catalytic component 2
EGF	epidermal growth factor
EGFR	epidermal growth factor receptor
GCK	glucokinase (hexokinase 4)
GLI1	GLI family zinc finger 1
GLI3	GLI family zinc finger 3
HPD	4-hydroxyphenylpyruvate dioxygenase
IL6	interleukin 6
PGAM2	phosphoglycerate mutase 2 (muscle)
TARP	TCR gamma alternate reading frame protein
TRG	T cell receptor gamma locus
VSX1	visual system homeobox 1
WISP3	WNT1 inducible signaling pathway protein 3