CLN3
ceroid-lipofuscinosis, neuronal 3
BTS, JNCL
Human CLN3 (1201), Mouse Cln3 (12752), Rat Cln3 (293485), domestic guinea pig Cln3 (100727617), domestic cat CLN3 (101089821), cow CLN3 (504799), sheep CLN3 (101112942), Domestic Rabbit CLN3 (100009244), Zebrafish cln3 (492340), fruit fly cln3 (39981) ...More
- 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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