polygenic inheritance Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of multifactorial inheritance governed by the simultaneous action of many (more than three) gene loci. (Human Phenotype Ontology, HP_0010982)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010982
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Genes

15 genes associated with the polygenic inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
APOL1 apolipoprotein L, 1
BAX BCL2-associated X protein
BCR breakpoint cluster region
CST3 cystatin C
FLT3 fms-related tyrosine kinase 3
IRF6 interferon regulatory factor 6
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit)
NBN nibrin
NLRP1 NLR family, pyrin domain containing 1
PPARG peroxisome proliferator-activated receptor gamma
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SHANK3 SH3 and multiple ankyrin repeat domains 3
STOX1 storkhead box 1
TP53 tumor protein p53