Sleep Paralysis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0456511
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Genes

11 genes associated with the disease Sleep Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
HCRT hypocretin (orexin) neuropeptide precursor
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DQB2 major histocompatibility complex, class II, DQ beta 2
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
PER2 period circadian clock 2
RBM45 RNA binding motif protein 45
REM1 RAS (RAD and GEM)-like GTP-binding 1