primary cutaneous amyloidosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An amyloidosis characterized by pruritus, skin scratching and by deposits of amyloid in the dermis. (Human Disease Ontology, DOID_0050639)
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Genes

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

Symbol Name Standardized Value
OSMR oncostatin M receptor 2.23619
IL31 interleukin 31 1.78399
YARS tyrosyl-tRNA synthetase 1.60905
EARS2 glutamyl-tRNA synthetase 2, mitochondrial 1.46759
KRT5 keratin 5, type II 0.97086
KRT14 keratin 14, type I 0.840115
KRT16 keratin 16, type I 0.799103
KRT1 keratin 1, type II 0.768393
IL31RA interleukin 31 receptor A 0.752085
OSM oncostatin M 0.685891
APCS amyloid P component, serum 0.653671
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 0.604981
RET ret proto-oncogene 0.503441
FN1 fibronectin 1 0.401945
KRT7 keratin 7, type II 0.223165
LPA lipoprotein, Lp(a) 0.197742
DNTT DNA nucleotidylexotransferase 0.168381
APOA1 apolipoprotein A-I 0.162908