hip dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of developmental dysplasia of the hip. (Human Phenotype Ontology, HP_0001385)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001385
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15 genes associated with the hip dysplasia 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
BICD2 bicaudal D homolog 2 (Drosophila)
CCDC8 coiled-coil domain containing 8
IRX5 iroquois homeobox 5
KANSL1 KAT8 regulatory NSL complex subunit 1
NDN necdin, melanoma antigen (MAGE) family member
NIN ninein (GSK3B interacting protein)
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SNRPN small nuclear ribonucleoprotein polypeptide N
TRAPPC11 trafficking protein particle complex 11
TRPV4 transient receptor potential cation channel, subfamily V, member 4
VIPAS39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
VPS33B vacuolar protein sorting 33 homolog B (yeast)
WDR19 WD repeat domain 19