lipofuscinosis Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
Description	accumulation of intracellular autofluorescent material, in the form of brownish fatty pigment, in lysosomes as a normal part of senescence or aging (Mammalian Phenotype Ontology, MP_0008842)
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Genes

16 genes co-occuring with the biological term lipofuscinosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
AGER	advanced glycosylation end product-specific receptor
CLN3	ceroid-lipofuscinosis, neuronal 3
CLN5	ceroid-lipofuscinosis, neuronal 5
CLN6	ceroid-lipofuscinosis, neuronal 6, late infantile, variant
CLN8	ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
CLN9	ceroid-lipofuscinosis, neuronal 9
CTSF	cathepsin F
DNAJC5	DnaJ (Hsp40) homolog, subfamily C, member 5
GAD2	glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)
MAPK13	mitogen-activated protein kinase 13
MFSD8	major facilitator superfamily domain containing 8
PPT1	palmitoyl-protein thioesterase 1
RPS6KB1	ribosomal protein S6 kinase, 70kDa, polypeptide 1
SOD2	superoxide dismutase 2, mitochondrial
TPP1	tripeptidyl peptidase I
TRPM1	transient receptor potential cation channel, subfamily M, member 1