hypermobility syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

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

Symbol Name Standardized Value
CTSC cathepsin C 2.05225
NRK Nik related kinase 1.61128
IL1RAPL2 interleukin 1 receptor accessory protein-like 2 1.57913
TNXB tenascin XB 1.51853
TNXA tenascin XA (pseudogene) 1.51018
COL5A2 collagen, type V, alpha 2 1.40833
FBF1 Fas (TNFRSF6) binding factor 1 1.34025
COL3A1 collagen, type III, alpha 1 1.01216
COL5A1 collagen, type V, alpha 1 0.883111
KRT9 keratin 9, type I 0.821667
COL6A3 collagen, type VI, alpha 3 0.792951
WDR20 WD repeat domain 20 0.745172
PEPD peptidase D 0.700321
COL1A2 collagen, type I, alpha 2 0.670732
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2 0.663975
LAX1 lymphocyte transmembrane adaptor 1 0.5645
COMP cartilage oligomeric matrix protein 0.462394
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 0.419892
MFF mitochondrial fission factor 0.419517
DLL1 delta-like 1 (Drosophila) 0.368149
IGF1 insulin-like growth factor 1 (somatomedin C) 0.366301
COL1A1 collagen, type I, alpha 1 0.362978
FLNA filamin A, alpha 0.346777
GCK glucokinase (hexokinase 4) 0.28616