central sleep apnea Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A sleep apnea that is characterized by a malfunction of the basic neurological controls for breathing rate and the failure to give the signal to inhale, causing the individual to miss one or more cycles of breathing. (Human Disease Ontology, DOID_9220)
Similar Terms
Downloads & Tools

Genes

23 genes co-occuring with the disease central 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