genu valgum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The legs angle inward, such that the knees are close together and the ankles far apart. (Human Phenotype Ontology, HP_0002857)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002857
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Genes

75 genes associated with the genu valgum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAN aggrecan
ARSB arylsulfatase B
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATRX alpha thalassemia/mental retardation syndrome X-linked
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
B3GAT3 beta-1,3-glucuronyltransferase 3
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BCOR BCL6 corepressor
BRAF B-Raf proto-oncogene, serine/threonine kinase
CA2 carbonic anhydrase II
CBS cystathionine-beta-synthase
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
CLCN7 chloride channel, voltage-sensitive 7
CLIP2 CAP-GLY domain containing linker protein 2
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
COL9A1 collagen, type IX, alpha 1
COL9A2 collagen, type IX, alpha 2
COL9A3 collagen, type IX, alpha 3
COMP cartilage oligomeric matrix protein
CTC1 CTS telomere maintenance complex component 1
CTNS cystinosin, lysosomal cystine transporter
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DYM dymeclin
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
ELN elastin
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
EXT1 exostosin glycosyltransferase 1
EXT2 exostosin glycosyltransferase 2
FBN1 fibrillin 1
FLNA filamin A, alpha
GALNS galactosamine (N-acetyl)-6-sulfatase
GLB1 galactosidase, beta 1
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HBB hemoglobin, beta
HSPG2 heparan sulfate proteoglycan 2
IDUA iduronidase, alpha-L-
IFT172 intraflagellar transport 172
IMPAD1 inositol monophosphatase domain containing 1
KIF22 kinesin family member 22
KIF7 kinesin family member 7
KRAS Kirsten rat sarcoma viral oncogene homolog
LIFR leukemia inhibitory factor receptor alpha
LIMK1 LIM domain kinase 1
MAP2K1 mitogen-activated protein kinase kinase 1
MAP2K2 mitogen-activated protein kinase kinase 2
MATN3 matrilin 3
MPST mercaptopyruvate sulfurtransferase
NF1 neurofibromin 1
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NOTCH2 notch 2
NSD1 nuclear receptor binding SET domain protein 1
OCRL oculocerebrorenal syndrome of Lowe
ORC1 origin recognition complex, subunit 1
PEPD peptidase D
RAB23 RAB23, member RAS oncogene family
RAB33B RAB33B, member RAS oncogene family
RFC2 replication factor C (activator 1) 2, 40kDa
RUNX2 runt-related transcription factor 2
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SHOX short stature homeobox
SKI SKI proto-oncogene
SLCO5A1 solute carrier organic anion transporter family, member 5A1
SULF1 sulfatase 1
TBL2 transducin (beta)-like 2
TGFB1 transforming growth factor, beta 1
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TRPS1 trichorhinophalangeal syndrome I
TRPV4 transient receptor potential cation channel, subfamily V, member 4
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
VPS13B vacuolar protein sorting 13 homolog B (yeast)
ZBTB20 zinc finger and BTB domain containing 20