sleep apnea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A sleep disorder characterized by repeated cessation and commencing of breathing that repeatedly disrupts sleep. (Human Disease Ontology, DOID_0050847)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010535
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Genes

16 genes associated with the sleep apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AHDC1 AT hook, DNA binding motif, containing 1
CEP57 centrosomal protein 57kDa
CREBBP CREB binding protein
DNA2 DNA replication helicase/nuclease 2
FGFR2 fibroblast growth factor receptor 2
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HRAS Harvey rat sarcoma viral oncogene homolog
IDS iduronate 2-sulfatase
IDUA iduronidase, alpha-L-
MAGEL2 melanoma antigen family L2
NDN necdin, melanoma antigen (MAGE) family member
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
SKI SKI proto-oncogene
SNRPN small nuclear ribonucleoprotein polypeptide N
SOD1 superoxide dismutase 1, soluble
TRPV4 transient receptor potential cation channel, subfamily V, member 4