CLN3

GENE INFORMATION

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Gene name

CLN3

Synonyms

Description

Homo sapiens ceroid-lipofuscinosis, neuronal 3 (CLN3), transcript variant 5, mRNA. (RefSeq mRNA)

Entrez gene 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]

Chromosome

16

Cytoband

p11.2

Chromosome location (bp)

28477974 - 28503333

Protein evidence

No evidence (all genes)

Ensembl

ENSG00000261832 (version 75.37)

Entrez gene

1201

UniProt

neXtProt

Antibodypedia

CLN3 antibodies
 

PROTEIN VIEW

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CLN3-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

CLN3-001 ENSP00000454253
ENST00000568224
Q2TA70
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