Hip Contracture Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Permanent fixation of the hip in primary positions, with limited passive or active motion at the hip joint. (Human Phenotype Ontology, HP_0003273)
External Link https://www.disgenet.org/browser/0/1/0/C0019553
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Genes

33 genes associated with the disease Hip Contracture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
BIN1 bridging integrator 1
COL2A1 collagen, type II, alpha 1
ERLIN2 ER lipid raft associated 2
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FKBP10 FK506 binding protein 10, 65 kDa
HACD1 3-hydroxyacyl-CoA dehydratase 1
HLA-B major histocompatibility complex, class I, B
HSPG2 heparan sulfate proteoglycan 2
ITGA7 integrin, alpha 7
KAT6B K(lysine) acetyltransferase 6B
LGI4 leucine-rich repeat LGI family, member 4
MAP3K20 mitogen-activated protein kinase kinase kinase 20
MAP3K7 mitogen-activated protein kinase kinase kinase 7
MMP2 matrix metallopeptidase 2
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
MYL2 myosin, light chain 2, regulatory, cardiac, slow
NALCN sodium leak channel, non selective
PIGY phosphatidylinositol glycan anchor biosynthesis, class Y
PNPT1 polyribonucleotide nucleotidyltransferase 1
PTH1R parathyroid hormone 1 receptor
RYR1 ryanodine receptor 1 (skeletal)
SELENON selenoprotein N
SLC10A7 solute carrier family 10, member 7
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC6A9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9
SPEG SPEG complex locus
TNNT1 troponin T type 1 (skeletal, slow)
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTN titin
ZBTB20 zinc finger and BTB domain containing 20