COPS4, COP9 signalosome subunit 4, 51138

N. diseases: 5; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency
0.010 GeneticVariation disease BEFREE The allele, designated csn4-2035, suppresses the adventitious root (AR) phenotype of the Arabidopsis superroot2-1 mutant, potentially by altering its auxin signaling. 28377589 2017
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.010 Biomarker disease BEFREE TA binds CSN4 and the synaptic regulator snapin in neuroblastoma cells and in brain synaptosomes. 21102408 2011
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.010 Biomarker disease BEFREE TA binds CSN4 and the synaptic regulator snapin in neuroblastoma cells and in brain synaptosomes. 21102408 2011
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
0.010 Biomarker disease BEFREE TA binds CSN4 and the synaptic regulator snapin in neuroblastoma cells and in brain synaptosomes. 21102408 2011
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
0.010 AlteredExpression disease LHGDN Aberrant expression of signaling-related proteins 14-3-3 gamma and RACK1 in fetal Down syndrome brain (trisomy 21). 11824616 2002