short femoral neck Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally short femoral neck (which is the process of bone, connecting the femoral head with the femoral shaft). (Human Phenotype Ontology, HP_0100864)
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18 genes associated with the short femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
BMPR1B bone morphogenetic protein receptor, type IB
CANT1 calcium activated nucleotidase 1
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL2A1 collagen, type II, alpha 1
COMP cartilage oligomeric matrix protein
CTC1 CTS telomere maintenance complex component 1
FGFR3 fibroblast growth factor receptor 3
IFT140 intraflagellar transport 140
IHH indian hedgehog
MATN3 matrilin 3
MMP9 matrix metallopeptidase 9
POC1A POC1 centriolar protein A
RUNX2 runt-related transcription factor 2
SHOX short stature homeobox
SLC39A13 solute carrier family 39 (zinc transporter), member 13
TRAPPC2 trafficking protein particle complex 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4