Abnormality Of The Respiratory System Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An abnormality of the respiratory system, which include the airways, lungs, and the respiratory muscles. (Human Phenotype Ontology, HP_0002086)
External Link	https://www.disgenet.org/browser/0/1/0/C4018871
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Genes

16 genes associated with the disease Abnormality Of The Respiratory System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
CD244	CD244 molecule, natural killer cell receptor 2B4
CIITA	class II, major histocompatibility complex, transactivator
FGF23	fibroblast growth factor 23
IL10	interleukin 10
KYNU	kynureninase
MPZ	myelin protein zero
NFKBIL1	nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1
NODAL	nodal growth differentiation factor
PADI4	peptidyl arginine deiminase, type IV
PLG	plasminogen
PPP1R21	protein phosphatase 1, regulatory subunit 21
PTPN22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SLC22A4	solute carrier family 22 (organic cation/zwitterion transporter), member 4
SLC35A2	solute carrier family 35 (UDP-galactose transporter), member A2
SUZ12	SUZ12 polycomb repressive complex 2 subunit
TSC1	tuberous sclerosis 1