joint stiffness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Joint stiffness is a perceived sensation of tightness in a joint or joints when attempting to move them after a period of inactivity. Joint stiffness typically subsides over time. (Human Phenotype Ontology, HP_0001387)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001387
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Genes

23 genes associated with the joint stiffness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ADAMTSL2 ADAMTS-like 2
ARSB arylsulfatase B
BANF1 barrier to autointegration factor 1
COL2A1 collagen, type II, alpha 1
COMP cartilage oligomeric matrix protein
FBN1 fibrillin 1
GLB1 galactosidase, beta 1
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
GNS glucosamine (N-acetyl)-6-sulfatase
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
IDUA iduronidase, alpha-L-
LEMD3 LEM domain containing 3
LMNA lamin A/C
LTBP2 latent transforming growth factor beta binding protein 2
NAGLU N-acetylglucosaminidase, alpha
PRG4 proteoglycan 4
PTF1A pancreas specific transcription factor, 1a
RECQL4 RecQ protein-like 4
SGSH N-sulfoglucosamine sulfohydrolase
TMEM173 transmembrane protein 173
TPM2 tropomyosin 2 (beta)
WISP3 WNT1 inducible signaling pathway protein 3