transthyretin amyloidosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An amyloidosis that is characterized by a loss of sensation in the extremities, cardiomyopathy, nephropathy, vitreous opacities, and CNS amyloidosis resulting from abnormal deposits of amyloid protein in the body's organs and tissues and has_material_basis_in autosomal dominant inheritance of mutations in the TTR gene. (Human Disease Ontology, DOID_0050638)
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Genes

20 genes co-occuring with the disease transthyretin amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TTR transthyretin 2.66569
LYZ lysozyme 0.868777
GSN gelsolin 0.860999
APCS amyloid P component, serum 0.828639
SAA2 serum amyloid A2 0.78066
APOA1 apolipoprotein A-I 0.705547
MBTPS2 membrane-bound transcription factor peptidase, site 2 0.699517
EFNA5 ephrin-A5 0.592895
ASPN asporin 0.566443
SAA1 serum amyloid A1 0.503441
IAPP islet amyloid polypeptide 0.443923
B2M beta-2-microglobulin 0.393001
TNNT2 troponin T type 2 (cardiac) 0.390397
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 0.321909
SDC2 syndecan 2 0.317545
COL2A1 collagen, type II, alpha 1 0.279011
FBN1 fibrillin 1 0.272597
APOA2 apolipoprotein A-II 0.232836
APOE apolipoprotein E 0.188938
NPPB natriuretic peptide B 0.185313