CLN3 Products

Description

CLN3 encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq]

Bioinformatics

Entrez	1201 Human
Uniprot	AAH02394 Human AAH02394.1 Human NP_000077 Human NP_000077.1 Human NP_001035897 Human
Product By Gene ID	1201
Alternate Names	Batten disease protein Batten, Spielmeyer-Vogt disease battenin BTSMGC102840 ceroid-lipofuscinosis, neuronal 3 JNCL Protein CLN3