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Symbol
Name
ID
Cln3
ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
MGI:107537
Phenotype annotations related to cellular
Darker colors indicate more annotations
Human Phenotypes
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
Disease(s) Associated with CLN3
neuronal ceroid lipofuscinosis 3

Mouse Phenotypes
abnormal lysosome morphology
abnormal cell adhesion
Availability Mouse Genotype
Cln3tm1Blda/Cln3tm1Blda
Cln3tm1Mkat/Cln3tm1Mkat
Cln3tm1Nbm/Cln3tm1Nbm

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory