lower limb asymmetry Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A difference in length or diameter between the left and right leg. (Human Phenotype Ontology, HP_0100559)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100559
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17 genes associated with the lower limb asymmetry phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGGF1 angiogenic factor with G patch and FHA domains 1
AKT1 v-akt murine thymoma viral oncogene homolog 1
COL2A1 collagen, type II, alpha 1
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
KCNAB2 potassium channel, voltage gated subfamily A regulatory beta subunit 2
MNX1 motor neuron and pancreas homeobox 1
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PORCN porcupine homolog (Drosophila)
PRDM16 PR domain containing 16
PTEN phosphatase and tensin homolog
RASA1 RAS p21 protein activator (GTPase activating protein) 1
SALL1 spalt-like transcription factor 1
SKI SKI proto-oncogene
TRPV4 transient receptor potential cation channel, subfamily V, member 4