abnormality of complement system Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the complement system. (Human Phenotype Ontology, HP_0005339)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0005339
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Genes

10 genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HSPA1L heat shock 70kDa protein 1-like 2.98001
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) 2.88662
NOTCH4 notch 4 2.80956
BTNL2 butyrophilin-like 2 2.74308
NCR3 natural cytotoxicity triggering receptor 3 2.60314
GTF2H4 general transcription factor IIH, polypeptide 4, 52kDa 2.54595
TNXB tenascin XB 2.05673
CFH complement factor H 1.44665
C3 complement component 3 1.32793
FADS1 fatty acid desaturase 1 1.12851