MFN2, mitofusin 2, 9927

N. diseases: 334; N. variants: 75
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2936719
Disease: Mechanical Allodynia
Mechanical Allodynia
0.310 AlteredExpression phenotype BEFREE The results of the present study suggest that a reduction in Mfn2 mRNA expression contributes to paclitaxel-induced mechanical allodynia. 28587902 2017
CUI: C2936719
Disease: Mechanical Allodynia
Mechanical Allodynia
0.310 Biomarker phenotype CTD_human The results of the present study suggest that a reduction in Mfn2 mRNA expression contributes to paclitaxel-induced mechanical allodynia. 28587902 2017