×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
BEFREE
Two types of NCL have so-far been found almost exclusively in Finland: Finnish variant late infantile NCL, vLINCL (CLN5), and the Northern epilepsy syndrome or Progressive epilepsy with mental retardation, EPMR (CLN8 ).
11332769
2001
×
Entrez Id:
1203
Gene Symbol:
CLN5
CLN5
0.010
Biomarker
disease
BEFREE
Two types of NCL have so-far been found almost exclusively in Finland: Finnish variant late infantile NCL, vLINCL (CLN5 ), and the Northern epilepsy syndrome or Progressive epilepsy with mental retardation, EPMR (CLN8 ).
11332769
2001
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
GeneticVariation
disease
CLINVAR
The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum.
10861296
2000
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
GENOMICS_ENGLAND
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.
10508524
1999
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
MGD
An early-onset congenic strain of the motor neuron degeneration (mnd) mouse.
10191135
1999
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
MGD
Retinal degeneration in motor neuron degeneration (mnd) mutant mice.
8282051
1993
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
MGD
Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease).
7683855
1993
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
MGD
Autosomal dominance in a late-onset motor neuron disease in the mouse.
3783318
1986
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
MGD
Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS).
1639406
1992
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
Biomarker
disease
CTD_human
×
Entrez Id:
2055
Gene Symbol:
CLN8
CLN8
0.940
CausalMutation
disease
CLINVAR