pulmonary fibrosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002206
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Genes

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

Symbol Name
ALMS1 Alstrom syndrome protein 1
AP3B1 adaptor-related protein complex 3, beta 1 subunit
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
BMP15 bone morphogenetic protein 15
CAV1 caveolin 1, caveolae protein, 22kDa
CCR6 chemokine (C-C motif) receptor 6
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CTGF connective tissue growth factor
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DCTN4 dynactin 4 (p62)
DKC1 dyskeratosis congenita 1, dyskerin
FSHR follicle stimulating hormone receptor
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HPS1 Hermansky-Pudlak syndrome 1
HPS4 Hermansky-Pudlak syndrome 4
IRF5 interferon regulatory factor 5
KIAA0319L KIAA0319-like
NOP10 NOP10 ribonucleoprotein
NR5A1 nuclear receptor subfamily 5, group A, member 1
PRTN3 proteinase 3
PSMC3IP PSMC3 interacting protein
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RNF168 ring finger protein 168, E3 ubiquitin protein ligase
SFTPA2 surfactant protein A2
STX1A syntaxin 1A (brain)
TERC telomerase RNA component
TGFB1 transforming growth factor, beta 1
TINF2 TERF1 (TRF1)-interacting nuclear factor 2