Pectus Excavatum Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A defect of the chest wall characterized by a depression of the sternum, giving the chest (pectus) a caved-in (excavatum) appearance. (Human Phenotype Ontology, HP_0000767)
External Link https://www.disgenet.org/browser/0/1/0/C1864796
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Genes

9 genes associated with the disease Pectus Excavatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
AR androgen receptor
CDAN1 codanin 1
GAL3ST4 galactose-3-O-sulfotransferase 4
KRT7 keratin 7, type II
SCLY selenocysteine lyase
TAL1 T-cell acute lymphocytic leukemia 1
TP63 tumor protein p63
TSPYL2 TSPY-like 2