Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease BEFREE To identify candidate biomarkers, we analyzed autopsy brain and matching CSF samples from controls and three genetically distinct NCLs due to deficiencies in palmitoyl protein thioesterase 1 (CLN1 disease), tripeptidyl peptidase 1 (CLN2 disease), and CLN3 protein (CLN3 disease). 28792770 2017
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 GeneticVariation disease BEFREE The two most prevalent forms of neuronal ceroid lipofuscinosis (NCL) are the juvenile form (Batten disease, CLN3) and late infantile form (Jansky-Bielschowsky disease, CLN2). 23263384 2013
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 GeneticVariation disease BEFREE We have collected 122 late-infantile neuronal ceroid lipofuscinosis (LINCL, CLN2) and 191 juvenile NCL (JNCL, CLN3) cases, diagnosed on the basis of age-at-onset, clinical symptomatology, and pathological findings and representing the most common forms of NCL in the United States, and Europe. 9377079 1997
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 GeneticVariation disease BEFREE A variant form of late infantile neuronal ceroid lipofuscinosis (CLN5) is not an allelic form of Batten (Spielmeyer-Vogt-Sjögren, CLN3) disease: exclusion of linkage to the CLN3 region of chromosome 16. 8020979 1994
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease CTD_human
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]. 10527801 1999
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD A knock-in reporter model of Batten disease. 17855597 2007
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD Antigen presenting cell abnormalities in the Cln3(-/-) mouse model of juvenile neuronal ceroid lipofuscinosis. 27101989 2016
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD Osmoregulation of ceroid neuronal lipofuscinosis type 3 in the renal medulla. 20219947 2010
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD Altered gene expression in the eye of a mouse model for batten disease. 15326100 2004
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth. 12374761 2002
Entrez Id: 1201
Gene Symbol: CLN3
CLN3
0.540 Biomarker disease MGD A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease). 10440905 1999