sleep apnea Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A sleep disorder characterized by repeated cessation and commencing of breathing that repeatedly disrupts sleep. (Human Disease Ontology, DOID_0050847)
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Genes

23 genes co-occuring with the disease sleep apnea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
NPPB natriuretic peptide B 1.32716
KCNK3 potassium channel, two pore domain subfamily K, member 3 1.26691
IK IK cytokine, down-regulator of HLA II 1.17206
NPPA natriuretic peptide A 1.15496
NOTO notochord homeobox 1.09629
TIMELESS timeless circadian clock 1.07362
KCNK9 potassium channel, two pore domain subfamily K, member 9 1.07278
ARID1B AT rich interactive domain 1B (SWI1-like) 0.988535
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous) 0.954525
KLK15 kallikrein-related peptidase 15 0.813873
CHRM3 cholinergic receptor, muscarinic 3 0.763494
CPB1 carboxypeptidase B1 (tissue) 0.6939
CCNA2 cyclin A2 0.651694
TACR1 tachykinin receptor 1 0.572662
MAOA monoamine oxidase A 0.500761
ATXN3 ataxin 3 0.432646
NOS2 nitric oxide synthase 2, inducible 0.355235
FGFR3 fibroblast growth factor receptor 3 0.344574
LMNA lamin A/C 0.313189
CRP C-reactive protein, pentraxin-related 0.269398
CST3 cystatin C 0.260538
IGF1 insulin-like growth factor 1 (somatomedin C) 0.223165
EDN1 endothelin 1 0.177301