NUP155, nucleoporin 155, 9631

N. diseases: 13; N. variants: 1
Disease: Atrial Fibrillation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.130 GeneticVariation disease BEFREE In conclusion, our results indicate that lamin A/C mutation p.Arg399Cys weakens the interaction between nuclear lamina (lamin A/C) and the nuclear pore complex (NUP155), leading to the development of AF. 30488537 2019
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.130 Biomarker disease BEFREE NUP155 is a nuclear pore complex protein that has been identified as a clinical driver of atrial fibrillation, yet the precise mechanism is unknown. 29848314 2018
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.130 Biomarker disease BEFREE These human and mouse studies indicate that loss of NUP155 function causes AF by altering mRNA and protein transport and link the NPC to cardiovascular disease. 19070573 2008
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.130 AlteredExpression disease LHGDN These human and mouse studies indicate that loss of NUP155 function causes AF by altering mRNA and protein transport and link the NPC to cardiovascular disease. 19070573 2008
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.130 Biomarker disease HPO