amyloidosis Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An acquired metabolic disease that involves abnormal deposited of amyloid proteins in organs and/or tissues. (Human Disease Ontology, DOID_9120)
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Genes

26 genes involed in the disease amyloidosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10
APOA1 apolipoprotein A-I
APOE apolipoprotein E
APP amyloid beta (A4) precursor protein
B2M beta-2-microglobulin
CST3 cystatin C
FGA fibrinogen alpha chain
GSN gelsolin
IL31RA interleukin 31 receptor A
ITM2B integral membrane protein 2B
LYZ lysozyme
MEFV Mediterranean fever
NLRP3 NLR family, pyrin domain containing 3
OSMR oncostatin M receptor
PLD3 phospholipase D family, member 3
PPP5C protein phosphatase 5, catalytic subunit
PRNP prion protein
PSEN1 presenilin 1
PSEN2 presenilin 2
SAA1 serum amyloid A1
SAA2 serum amyloid A2
SORL1 sortilin-related receptor, L(DLR class) A repeats containing
TACSTD2 tumor-associated calcium signal transducer 2
TGFBI transforming growth factor, beta-induced, 68kDa
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TTR transthyretin