obstructive lung disease Gene Set
Genes
22 genes associated with the obstructive lung disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ARVCF
|
armadillo repeat gene deleted in velocardiofacial syndrome
|
|
COMT
|
catechol-O-methyltransferase
|
|
CTLA4
|
cytotoxic T-lymphocyte-associated protein 4
|
|
CYBA
|
cytochrome b-245, alpha polypeptide
|
|
CYBB
|
cytochrome b-245, beta polypeptide
|
|
DNASE1L3
|
deoxyribonuclease I-like 3
|
|
DYX1C1
|
dyslexia susceptibility 1 candidate 1
|
|
GLA
|
galactosidase, alpha
|
|
GP1BB
|
glycoprotein Ib (platelet), beta polypeptide
|
|
HIRA
|
histone cell cycle regulator
|
|
HLA-DPB1
|
major histocompatibility complex, class II, DP beta 1
|
|
MMP1
|
matrix metallopeptidase 1
|
|
NCF1
|
neutrophil cytosolic factor 1
|
|
NCF2
|
neutrophil cytosolic factor 2
|
|
NCF4
|
neutrophil cytosolic factor 4, 40kDa
|
|
PRTN3
|
proteinase 3
|
|
PTPN22
|
protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
|
|
SERPINA1
|
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
|
|
TBX1
|
T-box 1
|
|
UFD1L
|
ubiquitin fusion degradation 1 like (yeast)
|
|
WAS
|
Wiskott-Aldrich syndrome
|
|
WIPF1
|
WAS/WASL interacting protein family, member 1
|
