erythrokeratodermia variabilis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050467)
Similar Terms
Downloads & Tools

Genes

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

Symbol Name Standardized Value
GJB3 gap junction protein, beta 3, 31kDa 3.43111
GJB4 gap junction protein, beta 4, 30.3kDa 3.2569
GJB5 gap junction protein, beta 5, 31.1kDa 1.60726
GJB2 gap junction protein, beta 2, 26kDa 1.14985
GJC3 gap junction protein, gamma 3, 30.2kDa 1.09377
GJA4 gap junction protein, alpha 4, 37kDa 1.04588
GJB6 gap junction protein, beta 6, 30kDa 0.993596
LOR loricrin 0.931656
ANKK1 ankyrin repeat and kinase domain containing 1 0.812642
IGBP1 immunoglobulin (CD79A) binding protein 1 0.776159
MATN1 matrilin 1, cartilage matrix protein 0.738271
ELOVL4 ELOVL fatty acid elongase 4 0.718443
ALDH3A2 aldehyde dehydrogenase 3 family, member A2 0.711587
KRT1 keratin 1, type II 0.543542
GJA1 gap junction protein, alpha 1, 43kDa 0.495793
TGM1 transglutaminase 1 0.440914
STS steroid sulfatase (microsomal), isozyme S 0.418768
GJB1 gap junction protein, beta 1, 32kDa 0.375179