abnormality of the calcaneus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the calcaneus, also known as the heel bone, one of the or heel bone, one of the components of the tarsus of the foot which make up the heel. (Human Phenotype Ontology, HP_0008364)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008364
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Genes

14 genes associated with the abnormality of the calcaneus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
ECEL1 endothelin converting enzyme-like 1
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
FLNA filamin A, alpha
FLNB filamin B, beta
HDAC6 histone deacetylase 6
HOXD10 homeobox D10
LBR lamin B receptor
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
PHGDH phosphoglycerate dehydrogenase
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)