UCP1, uncoupling protein 1, 7350

N. diseases: 124; N. variants: 7
Disease: Lecithin Acyltransferase Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023195
Disease: Lecithin Acyltransferase Deficiency
Lecithin Acyltransferase Deficiency 		0.010 AlteredExpression disease BEFREE Primed expression of PRDM16 and UCP in quiescent satellite cell caused by LCAT deficiency synergizes with cell cholesterol depletion to induce satellite cell-to-BAT transdifferentiation. 29369831 2018