abnormality of the acetabulum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the acetabulum, i.e., the Acetabular part of hip bone, which together with the head of the femur forms the hip joint. (Human Phenotype Ontology, HP_0003170)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003170
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Genes

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

Symbol Name
AP3B1 adaptor-related protein complex 3, beta 1 subunit
ARSB arylsulfatase B
CANT1 calcium activated nucleotidase 1
CENPJ centromere protein J
COL10A1 collagen, type X, alpha 1
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
CRTAP cartilage associated protein
DYM dymeclin
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
EIF4A3 eukaryotic translation initiation factor 4A3
FBN1 fibrillin 1
FKBP10 FK506 binding protein 10, 65 kDa
FLNB filamin B, beta
GATA1 GATA binding protein 1 (globin transcription factor 1)
GLB1 galactosidase, beta 1
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GUSB glucuronidase, beta
HOXA11 homeobox A11
HSPG2 heparan sulfate proteoglycan 2
HYAL1 hyaluronoglucosaminidase 1
INPPL1 inositol polyphosphate phosphatase-like 1
MATN3 matrilin 3
MMP2 matrix metallopeptidase 2
RAB23 RAB23, member RAS oncogene family
SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC35D1 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
SMAD3 SMAD family member 3
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
TRPV4 transient receptor potential cation channel, subfamily V, member 4
WDR60 WD repeat domain 60