Cyanosis Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule. (Human Phenotype Ontology, HP_0000961)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D003490
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Genes

16 genes/proteins associated with the disease Cyanosis from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
ADRA2B	adrenoceptor alpha 2B	2.88009
CYB5R3	cytochrome b5 reductase 3	2.88009
TGFB2	transforming growth factor, beta 2	2.88009
HBB	hemoglobin, beta	2.88009
CASP3	caspase 3, apoptosis-related cysteine peptidase	1.42401
CAT	catalase	1.41532
BAX	BCL2-associated X protein	1.30881
FOS	FBJ murine osteosarcoma viral oncogene homolog	1.28796
JUN	jun proto-oncogene	1.2437
MAP2K1	mitogen-activated protein kinase kinase 1	1.11046
TNF	tumor necrosis factor	1.10872
IL6	interleukin 6	1.09786
PRL	prolactin	1.04501
RELA	v-rel avian reticuloendotheliosis viral oncogene homolog A	1.04126
PROS1	protein S (alpha)	1.03009
PROC	protein C (inactivator of coagulation factors Va and VIIIa)	1.01966