Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4691
Gene Symbol: NCL
NCL
0.030 GeneticVariation disease BEFREE We have found that in the most common juvenile form of NCL (CLN3 disease or JNCL) this glial response is less pronounced in both mouse models and human autopsy material, with the morphological transformation of both astrocytes and microglia severely attenuated or delayed. 29041969 2017
Entrez Id: 4691
Gene Symbol: NCL
NCL
0.030 Biomarker disease BEFREE CLN3 disease (Spielmeyer-Vogt-Sjogren-Batten disease, previously known as classic juvenile neuronal ceroid lipofuscinosis, NCL) is a pediatric-onset progressive neurodegenerative disease characterized by progressive vision loss, seizures, loss of cognitive and motor function, and early death. 27766444 2017
Entrez Id: 4691
Gene Symbol: NCL
NCL
0.030 GeneticVariation disease BEFREE Studies of atypical JNCL suggest overlapping with other NCL forms. 9492089 1998