melorheostosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteosclerosis that has_material_basis_in a mutation of the LEMD3 gene which results_in a hyperdense bony cortex. (Human Disease Ontology, DOID_4253)
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Genes

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

Symbol Name Standardized Value
LEMD3 LEM domain containing 3 2.45902
MRO maestro 1.29746
POSTN periostin, osteoblast specific factor 0.991065
HTN3 histatin 3 0.908142
SP7 Sp7 transcription factor 0.801974
EXT1 exostosin glycosyltransferase 1 0.726524
TGFB1 transforming growth factor, beta 1 0.672324
SPARC secreted protein, acidic, cysteine-rich (osteonectin) 0.588222
SMAD3 SMAD family member 3 0.470332
RUNX2 runt-related transcription factor 2 0.467684
FGF23 fibroblast growth factor 23 0.418019
SMAD2 SMAD family member 2 0.403438
ALPPL2 alkaline phosphatase, placental-like 2 0.246098
ALPP alkaline phosphatase, placental 0.245747
ALPL alkaline phosphatase, liver/bone/kidney 0.245046
FGF2 fibroblast growth factor 2 (basic) 0.17952
BGLAP bone gamma-carboxyglutamate (gla) protein 0.174093