pachyonychia congenita Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050449)
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Genes

25 genes co-occuring with the disease pachyonychia congenita in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
KRT6A keratin 6A, type II 3.4568
KRT6B keratin 6B, type II 3.18034
KRT17 keratin 17, type I 2.85702
KRT16 keratin 16, type I 2.70747
KRT9 keratin 9, type I 1.65655
KRT72 keratin 72, type II 1.63321
PCSK5 proprotein convertase subtilisin/kexin type 5 1.48955
KRT86 keratin 86, type II 1.35899
KRT81 keratin 81, type II 1.3324
KRT2 keratin 2, type II 1.24298
KRTAP11-1 keratin associated protein 11-1 1.17249
KRT75 keratin 75, type II 0.789672
KRT10 keratin 10, type I 0.771661
FZD6 frizzled class receptor 6 0.747204
CPSF4 cleavage and polyadenylation specific factor 4, 30kDa 0.706754
FLG filaggrin 0.689893
SLURP1 secreted LY6/PLAUR domain containing 1 0.660404
SERPINA5 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 5 0.433021
KRT1 keratin 1, type II 0.387423
NONO non-POU domain containing, octamer-binding 0.387051
KRT5 keratin 5, type II 0.362239
DSG1 desmoglein 1 0.292257
DES desmin 0.255946
GJB6 gap junction protein, beta 6, 30kDa 0.230755
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 0.208914