camptodactyly of toe Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Camptodactyly is a painless flexion contracture of the proximal interphalangeal (PIP) joint that is usually gradually progressive. This term refers to camptodactyly of one or more toes. (Human Phenotype Ontology, HP_0001836)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001836
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Genes

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

Symbol Name
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
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
IRF5 interferon regulatory factor 5
KIAA0319L KIAA0319-like
LIFR leukemia inhibitory factor receptor alpha
MMP2 matrix metallopeptidase 2
PEX7 peroxisomal biogenesis factor 7
PHF6 PHD finger protein 6
PHYH phytanoyl-CoA 2-hydroxylase
PIEZO2 piezo-type mechanosensitive ion channel component 2
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