The CLN8 gene homepage

General information
Gene symbol CLN8
Gene name ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
Chromosome 8
Chromosomal band p23.3
Imprinted Unknown
Genomic reference LRG_691
Transcript reference NM_018941.3
Associated with diseases NCL
Citation reference(s) -
Curators (1) Y Yang
Total number of public variants reported 24
Unique public DNA variants reported 24
Individuals with public variants 24
Hidden variants -
Date created February 04, 2015
Date last updated June 09, 2017
Version CLN8:170609

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL LRG_691
HGNC 2079
Entrez Gene 2055
PubMed articles CLN8
OMIM - Gene 607837
OMIM - Diseases NCL (Neuronal Ceroid-Lipofuscinoses)
HGMD CLN8
GeneCards CLN8
GeneTests CLN8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000118 8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) NM_018941.3 NP_061764.2 24


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