band keratopathy 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_11164)
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Genes

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

Symbol Name Standardized Value
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4 1.80517
GLYR1 glyoxylate reductase 1 homolog (Arabidopsis) 1.50667
PTK6 protein tyrosine kinase 6 1.0606
COL8A2 collagen, type VIII, alpha 2 1.00035
MRAP melanocortin 2 receptor accessory protein 0.89541
VSX1 visual system homeobox 1 0.870415
WDR11 WD repeat domain 11 0.834788
DHX9 DEAH (Asp-Glu-Ala-His) box helicase 9 0.799513
PLAT plasminogen activator, tissue 0.762271
FRZB frizzled-related protein 0.709572
NDP Norrie disease (pseudoglioma) 0.701928
HLA-C major histocompatibility complex, class I, C 0.574994
FBN1 fibrillin 1 0.468819
CA2 carbonic anhydrase II 0.416896
AHR aryl hydrocarbon receptor 0.34384
NOD2 nucleotide-binding oligomerization domain containing 2 0.337242
PTH parathyroid hormone 0.312464
GFAP glial fibrillary acidic protein 0.195501