abnormality of the wing of the ilium Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the ilium ala. This is the large expanded portion of the ilum which bounds the greater pelvis laterally. (Human Phenotype Ontology, HP_0011867)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011867
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Genes

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

Symbol Name
ARSB arylsulfatase B
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
CCBE1 collagen and calcium binding EGF domains 1
COL2A1 collagen, type II, alpha 1
CREBBP CREB binding protein
DDR2 discoidin domain receptor tyrosine kinase 2
DYM dymeclin
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
GALNS galactosamine (N-acetyl)-6-sulfatase
GATA1 GATA binding protein 1 (globin transcription factor 1)
GLB1 galactosidase, beta 1
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
GPC3 glypican 3
HDAC6 histone deacetylase 6
IDUA iduronidase, alpha-L-
IHH indian hedgehog
MATN3 matrilin 3
MMP13 matrix metallopeptidase 13
PCNT pericentrin
RAB23 RAB23, member RAS oncogene family
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
RUNX2 runt-related transcription factor 2
SEC23A Sec23 homolog A (S. cerevisiae)
SMAD4 SMAD family member 4
SOX9 SRY (sex determining region Y)-box 9
TBX15 T-box 15
TRAPPC2 trafficking protein particle complex 2
WNT7A wingless-type MMTV integration site family, member 7A
ZBTB20 zinc finger and BTB domain containing 20