limited hip movement Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decreased ability to move the femur at the hip joint associated with a decreased range of motion of the hip. (Human Phenotype Ontology, HP_0008800)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008800
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Genes

22 genes associated with the limited hip movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BICD2 bicaudal D homolog 2 (Drosophila)
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL2A1 collagen, type II, alpha 1
COMP cartilage oligomeric matrix protein
DST dystonin
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FBN2 fibrillin 2
FGFR3 fibroblast growth factor receptor 3
GPC6 glypican 6
HSPG2 heparan sulfate proteoglycan 2
KAT6B K(lysine) acetyltransferase 6B
MMP2 matrix metallopeptidase 2
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
PIEZO2 piezo-type mechanosensitive ion channel component 2
PTH1R parathyroid hormone 1 receptor
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SPEG SPEG complex locus
TNNT1 troponin T type 1 (skeletal, slow)
TPM2 tropomyosin 2 (beta)
TRPV4 transient receptor potential cation channel, subfamily V, member 4
ZBTB20 zinc finger and BTB domain containing 20