long toe Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Digits that appear disproportionately long compared to the foot. (Human Phenotype Ontology, HP_0010511)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010511
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14 genes associated with the long toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B4GALT7 xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
CPT2 carnitine palmitoyltransferase 2
FAM20C family with sequence similarity 20, member C
FLNA filamin A, alpha
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
IRX5 iroquois homeobox 5
NPR2 natriuretic peptide receptor 2
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
SCARF2 scavenger receptor class F, member 2
SMS spermine synthase
TBX2 T-box 2
TBX4 T-box 4
UBE3B ubiquitin protein ligase E3B
VPS13B vacuolar protein sorting 13 homolog B (yeast)