Congenital Emphysema Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0265797
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Genes

40 genes associated with the disease Congenital Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APRT adenine phosphoribosyltransferase
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
CXCL10 chemokine (C-X-C motif) ligand 10
DEFB1 defensin, beta 1
DNASE1 deoxyribonuclease I
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
ELN elastin
HAS2 hyaluronan synthase 2
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HMGB1 high mobility group box 1
HSPA4 heat shock 70kDa protein 4
IFNA1 interferon, alpha 1
IFNA13 interferon, alpha 13
IFNG interferon, gamma
IFNK interferon, kappa
IL17A interleukin 17A
IL6 interleukin 6
MFAP1 microfibrillar-associated protein 1
MICA MHC class I polypeptide-related sequence A
MICB MHC class I polypeptide-related sequence B
MMP2 matrix metallopeptidase 2
MMP9 matrix metallopeptidase 9
MSH5 mutS homolog 5
PITX1 paired-like homeodomain 1
RPP21 ribonuclease P/MRP 21kDa subunit
RTRAF RNA transcription, translation and transport factor
S100A7 S100 calcium binding protein A7
SOAT1 sterol O-acyltransferase 1
SOCS1 suppressor of cytokine signaling 1
TIMP1 TIMP metallopeptidase inhibitor 1
TLR4 toll-like receptor 4
TLR9 toll-like receptor 9
TNF tumor necrosis factor
TNFRSF12A tumor necrosis factor receptor superfamily, member 12A
TNFRSF8 tumor necrosis factor receptor superfamily, member 8
TREX1 three prime repair exonuclease 1
TRIM21 tripartite motif containing 21
TRIM39 tripartite motif containing 39
TRIM39-RPP21 TRIM39-RPP21 readthrough
WWTR1 WW domain containing transcription regulator 1