lower limb amyotrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular atrophy affecting the lower limb. (Human Phenotype Ontology, HP_0007210)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007210
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10 genes associated with the lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL1 atlastin GTPase 1
FAM126A family with sequence similarity 126, member A
FGD4 FYVE, RhoGEF and PH domain containing 4
FLNC filamin C, gamma
INF2 inverted formin, FH2 and WH2 domain containing
KDM5C lysine (K)-specific demethylase 5C
KIF1A kinesin family member 1A
LMNA lamin A/C
TCAP titin-cap
TPM3 tropomyosin 3