complement deficiency Gene Set

Dataset	GWASdb SNP-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation. (Human Disease Ontology, DOID_626)
External Link	http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:626
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Genes

9 genes associated with the disease complement deficiency in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol	Name	Standardized Value
HSPA1L	heat shock 70kDa protein 1-like	3.02852
TAP2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)	2.90657
NOTCH4	notch 4	2.80274
BTNL2	butyrophilin-like 2	2.73163
NCR3	natural cytotoxicity triggering receptor 3	2.61485
GTF2H4	general transcription factor IIH, polypeptide 4, 52kDa	2.53675
TNXB	tenascin XB	2.0844
CFH	complement factor H	1.5865
C3	complement component 3	1.48714