RECQL5, RecQ like helicase 5, 9400

N. diseases: 28; N. variants: 2
Disease: Werner Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		0.020 Biomarker disease BEFREE Collectively, our results indicate that RECQL5 plays both co-operative and complementary roles with WRN. 28180303 2017
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		0.020 Biomarker disease BEFREE In the acquired forms, genes such as LMNA, PPARG, CIDEC (cell-death-inducing DNA fragmentation factor a-like effector c) and PLIN1 are heavily involved in familial partial lipodystrophy (FPLD) type 2 (also known as the Dunnigan-Variety) and WRN along with RECQL5 in Werner Syndrome (WS). 24152769 2014