hemoptysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Coughing up (expectoration) of blood or blood-streaked sputum from the larynx, trachea, bronchi, or lungs. (Human Phenotype Ontology, HP_0002105)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002105
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Genes

29 genes associated with the hemoptysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
C4A complement component 4A (Rodgers blood group)
CARD9 caspase recruitment domain family, member 9
CLEC7A C-type lectin domain family 7, member A
COL3A1 collagen, type III, alpha 1
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DNASE1L3 deoxyribonuclease I-like 3
ENG endoglin
GDF2 growth differentiation factor 2
HLA-B major histocompatibility complex, class I, B
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
IL10 interleukin 10
IL12B interleukin 12B
IL12RB2 interleukin 12 receptor, beta 2
IL17F interleukin 17F
IL17RA interleukin 17 receptor A
IL23R interleukin 23 receptor
MEFV Mediterranean fever
MLX MLX, MAX dimerization protein
NOD2 nucleotide-binding oligomerization domain containing 2
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SMAD4 SMAD family member 4
STAT1 signal transducer and activator of transcription 1, 91kDa
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4
TRAF3IP2 TRAF3 interacting protein 2
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2