joint contractures involving the joints of the feet Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Contractures of one ore more joints of the feet meaning chronic loss of joint motion due to structural changes in non-bony tissue. (Human Phenotype Ontology, HP_0100492)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100492
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Genes

29 genes associated with the joint contractures involving the joints of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
BCOR BCL6 corepressor
CAV1 caveolin 1, caveolae protein, 22kDa
CCR6 chemokine (C-C motif) receptor 6
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CTGF connective tissue growth factor
ERCC1 excision repair cross-complementation group 1
FBN1 fibrillin 1
FGFR3 fibroblast growth factor receptor 3
FLNA filamin A, alpha
GLI3 GLI family zinc finger 3
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HSPG2 heparan sulfate proteoglycan 2
IRF5 interferon regulatory factor 5
KIAA0319L KIAA0319-like
LIFR leukemia inhibitory factor receptor alpha
MMP2 matrix metallopeptidase 2
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NOD2 nucleotide-binding oligomerization domain containing 2
PEX7 peroxisomal biogenesis factor 7
PHF6 PHD finger protein 6
PHYH phytanoyl-CoA 2-hydroxylase
PIEZO2 piezo-type mechanosensitive ion channel component 2
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
SALL1 spalt-like transcription factor 1
SCARF2 scavenger receptor class F, member 2
SKI SKI proto-oncogene
TBX2 T-box 2
TBX4 T-box 4