CLN3
ceroid-lipofuscinosis, neuronal 3
- Human(1201) Summary: This gene 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, Jul 2008]
- Mouse(12752) ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
- Rat(293485) ceroid-lipofuscinosis, neuronal 3
- domestic guinea pig(100727617) ceroid-lipofuscinosis, neuronal 3
- domestic cat(101089821) ceroid-lipofuscinosis, neuronal 3
- cow(504799) ceroid-lipofuscinosis, neuronal 3
- sheep(101112942) ceroid-lipofuscinosis, neuronal 3
- Domestic Rabbit(100009244) ceroid-lipofuscinosis, neuronal 3
- Zebrafish(492340) ceroid-lipofuscinosis, neuronal 3
- fruit fly(39981) CG5582 gene product from transcript CG5582-RA
- naked mole-rat(101722930) ceroid-lipofuscinosis, neuronal 3
- dog(479794) ceroid-lipofuscinosis, neuronal 3
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