hereditary mucosal leukokeratosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A skin disease characterized by a defect in the normal process of keratinization of the mucosa. (Human Disease Ontology, DOID_0050448)
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Genes

13 genes co-occuring with the disease hereditary mucosal leukokeratosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
KRT4 keratin 4, type II 2.26744
KRT13 keratin 13, type I 2.07259
KRT2 keratin 2, type II 1.77225
KRTAP11-1 keratin associated protein 11-1 1.69815
KRT6A keratin 6A, type II 1.4935
KRT9 keratin 9, type I 1.41139
KRT6B keratin 6B, type II 1.22042
KRT86 keratin 86, type II 1.06858
KRT1 keratin 1, type II 0.893359
KRT16 keratin 16, type I 0.888029
KRT10 keratin 10, type I 0.869187
CCNE1 cyclin E1 0.792131
KRT14 keratin 14, type I 0.578494