soft skin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Subjective impression of increased softness upon palpitation of the skin. (Human Phenotype Ontology, HP_0000977)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000977
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Genes

18 genes associated with the soft skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
ATP7A ATPase, Cu++ transporting, alpha polypeptide
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL3A1 collagen, type III, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
EDA ectodysplasin A
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
FKBP14 FK506 binding protein 14, 22 kDa
KIF22 kinesin family member 22
MTAP methylthioadenosine phosphorylase
PAX2 paired box 2
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
TGFBR1 transforming growth factor, beta receptor 1
TNXB tenascin XB