larsen syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities. (Human Disease Ontology, DOID_14764)
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Genes

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

Symbol Name Standardized Value
FLNB filamin B, beta 2.50284
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3 1.8936
GALNS galactosamine (N-acetyl)-6-sulfatase 1.49306
DNM2 dynamin 2 1.18582
OFD1 oral-facial-digital syndrome 1 1.14985
CLPS colipase, pancreatic 1.00499
F13A1 coagulation factor XIII, A1 polypeptide 0.850764
FBN2 fibrillin 2 0.803616
SQSTM1 sequestosome 1 0.696707
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 0.629635
COL7A1 collagen, type VII, alpha 1 0.592506
TGFBR2 transforming growth factor, beta receptor II (70/80kDa) 0.500379