Atypical Hemolytic Uremic Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C2931788
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Genes

54 genes associated with the disease Atypical Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
BAAT bile acid CoA:amino acid N-acyltransferase
C17ORF67 chromosome 17 open reading frame 67
C3 complement component 3
C3AR1 complement component 3a receptor 1
C4BPA complement component 4 binding protein, alpha
C4BPB complement component 4 binding protein, beta
C5 complement component 5
C5AR1 complement component 5a receptor 1
CABIN1 calcineurin binding protein 1
CAPG capping protein (actin filament), gelsolin-like
CD36 CD36 molecule (thrombospondin receptor)
CD40LG CD40 ligand
CD46 CD46 molecule, complement regulatory protein
CFB complement factor B
CFH complement factor H
CFHR1 complement factor H-related 1
CFHR3 complement factor H-related 3
CFHR4 complement factor H-related 4
CFHR5 complement factor H-related 5
CFI complement factor I
CPB1 carboxypeptidase B1 (tissue)
CR1 complement component (3b/4b) receptor 1 (Knops blood group)
CRISP2 cysteine-rich secretory protein 2
CRP C-reactive protein, pentraxin-related
CRYGD crystallin, gamma D
DGKE diacylglycerol kinase, epsilon 64kDa
ETFA electron-transfer-flavoprotein, alpha polypeptide
FHL1 four and a half LIM domains 1
G6PD glucose-6-phosphate dehydrogenase
GPI glucose-6-phosphate isomerase
GPR182 G protein-coupled receptor 182
GRHPR glyoxylate reductase/hydroxypyruvate reductase
HP haptoglobin
IL5 interleukin 5
KRT20 keratin 20, type I
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MS4A1 membrane-spanning 4-domains, subfamily A, member 1
MTOR mechanistic target of rapamycin (serine/threonine kinase)
MUC1 mucin 1, cell surface associated
NFE2L2 nuclear factor, erythroid 2-like 2
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
PIGA phosphatidylinositol glycan anchor biosynthesis, class A
PLG plasminogen
PRSS55 protease, serine, 55
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
SPTA1 spectrin, alpha, erythrocytic 1
SPZ1 spermatogenic leucine zipper 1
THBD thrombomodulin
THBS1 thrombospondin 1
TNF tumor necrosis factor
TRIM25 tripartite motif containing 25
VTN vitronectin
VWF von Willebrand factor